Tetradentate cyclometalated platinum(II) complex based on 1,1,4,4-tetramethyl-1,2,3,4-tetrahydronaphthalene or derivative structure thereof, and use thereof

Abstract

The present invention relates to the technical field of organic electroluminescence preparation, and specifically to a tetradentate cyclometalated platinum(II) complex based on 1,1,4,4-tetramethyl-1,2,3,4-tetrahydronaphthalene or a derivative structure thereof, and a use thereof. By means of the introduction of 1,1,4,4-tetramethyl-1,2,3,4-tetrahydronaphthalene and the derivative structure thereof to increase steric hindrance, the present invention can avoid red shift or luminescence quenching caused by molecular aggregation. Deuteration at the periphery of a cyclometalated ligand can improve the stability of a material, enabling a phosphorescent material of the present invention to exhibit good chemical and thermal stability, and facilitating the fabrication of an evaporated OLED device. An organic electroluminescent device fabricated by using the complex of the present invention as a light-emitting layer material shows significant improvement in both current efficiency and service life, and has great application prospects in the fields of OLED display and illumination.

Description

Tetradentate cyclic platinum(II) complexes based on the structure of 1,1,4,4-tetramethyl-1,2,3,4-tetrahydronaphthalene and its derivatives and their applications Technical Field

[0001] This invention belongs to the field of organic electroluminescence preparation technology, specifically relating to a tetradentate cyclic platinum(II) complex based on the structure of 1,1,4,4-tetramethyl-1,2,3,4-tetrahydronaphthalene and its derivatives, and its applications. Background Technology

[0002] Organic light-emitting diodes (OLEDs) are a new generation of full-color display and lighting technology. Compared to liquid crystal displays (LCDs), which suffer from slow response times, narrow viewing angles, the need for backlighting, and high energy consumption, OLEDs, as self-emissive devices, do not require backlighting, making them energy-efficient. They also feature low driving voltage, fast response times, high resolution and contrast, wide viewing angles, and excellent low-temperature performance. OLED devices can be made thinner and can be fabricated into flexible structures. Furthermore, they offer advantages such as low production costs, simple manufacturing processes, and the ability to be mass-produced. Therefore, OLEDs have broad and enormous application prospects in high-end electronics and aerospace. With increasing investment, further research and development, and upgrades to production equipment, OLEDs have a very wide range of application scenarios and development prospects in the future.

[0003] The core of OLED development lies in the design and development of luminescent materials. Early OLED devices primarily used small organic molecule fluorescent materials as their luminescent agents. However, spin statistical quantum mechanics shows that under electroluminescence, the generated singlet and triplet excitons account for only 25% and 75%, respectively. Since traditional fluorescent materials can only utilize excitons in the singlet state, their maximum theoretical internal quantum efficiency is only 25%, with the remaining 75% of triplet excitons lost through non-radiative transitions. In 1998, Professor Forrest of Princeton University and Professor Thompson of the University of Southern California discovered the phosphorescence electroluminescence phenomenon of heavy metal organic complex molecules at room temperature. Due to the strong spin-orbit coupling of heavy metal atoms, excitons can more easily undergo intersystem crossing (ISC) from the singlet to the triplet state. This allows OLED devices to fully utilize all singlet and triplet excitons generated by electro-excitation, enabling the theoretical internal quantum efficiency of the luminescent material to reach 100% (Nature, 1998, 395, 151).

[0004] Currently, almost all OLED devices utilize a host-guest emission mechanism in their emitting layers. This involves doping a host material with a guest emitting material. The host material generally has a higher energy level than the guest material, transferring energy from the host to the guest material, thus exciting it to emit light. Commonly used organic phosphorescent guest materials are typically heavy metal atoms such as iridium(III), platinum(II), and Pd(II). Currently, the number of heavy metal phosphorescent organic complex molecules, specifically iridium(III) cyclic complexes, is limited. The abundance of platinum in the Earth's crust and its annual global production are approximately ten times that of iridium. The price of IrCl3·H2O, used to prepare iridium(III) complex phosphorescent materials, is also significantly higher than that of PtCl2 used to prepare platinum(II) complex phosphorescent materials. Furthermore, the preparation of iridium(III) complex phosphorescent materials involves four steps: iridium(III) dimer formation, iridium(III) intermediate ligand exchange, mer-iridium(III) complex synthesis, and mer-to-fac-iridium(III) complex isomer conversion. This significantly reduces the overall yield and the utilization rate of the raw material IrCl3·H2O, thus increasing the preparation cost of iridium(III) complex phosphorescent materials. In contrast, the preparation of platinum(II) complex phosphorescent materials only involves the final step of ligand metallization design of platinum salts, resulting in high platinum utilization and further reducing the preparation cost. In conclusion, the preparation cost of platinum(II) complex phosphorescent materials is far lower than that of iridium(III) complex phosphorescent materials.

[0005] However, the development of platinum complex materials and devices still faces some technical challenges, such as improving the chemical and thermal stability of materials, avoiding redshift or luminescence quenching caused by molecular aggregation, and improving device operating life. Therefore, there is an urgent need to develop novel phosphorescent platinum(II) complexes. Summary of the Invention

[0006] The purpose of this invention is to provide a tetradentate cyclic platinum(II) complex based on the structure of 1,1,4,4-tetramethyl-1,2,3,4-tetrahydronaphthalene and its derivatives, and its applications. This invention increases steric hindrance by introducing 1,1,4,4-tetramethyl-1,2,3,4-tetrahydronaphthalene and its derivatives, thus avoiding redshift or luminescence quenching caused by molecular aggregation. Deuteration around the cyclic metal ligand improves material stability, giving the phosphorescent material of this invention excellent chemical and thermal stability, making it easy to fabricate vapor-deposited OLED devices. Organic electroluminescent devices fabricated using the compounds of this invention as the emitting layer show significant improvements in current efficiency and lifetime, and have great application prospects in the fields of OLED displays and lighting.

[0007] The objective of this invention is achieved through the following technical solutions;

[0008] In many embodiments, the present invention provides a four-toothed ring platinum(II) complex having the general structure shown in formula (I):

[0009] In formula (I), A is a cycloalkane group; R a R b R c R d R e R f R g Each can be independently represented as monosubstituted, disubstituted, trisubstituted, tetrasubstituted, or pentasubstituted; R a -R g Each can be independently represented as hydrogen, deuterium, C1–C30 alkyl, C1–C30 deuterated alkyl, C3–C30 cycloalkyl, substituted or unsubstituted C6–C60 aryl; when substituted, the substituent can be selected from one or more of deuterium, C1–C14 alkyl, C6–C60 aryl; the hydrogen atom in formula (I) can be partially or completely substituted with deuterium.

[0010] Preferably, the R described in formula (I) a R b R c R d R e R f R g At least one hydrogen atom is replaced by deuterium.

[0011] In many implementations, R f It may be selected from one or a combination of methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, sec-pentyl, tert-pentyl, n-hexyl, isohexyl, sec-hexyl, tert-hexyl, n-heptyl, isoheptyl, sec-heptyl, tert-heptyl, n-octyl, isooctyl, sec-octyl, tert-octyl, n-nonyl, isononyl, sec-nonyl, tert-nonyl, n-decyl, isodel, sec-decyl, tert-decyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, adamantyl, phenyl, indene, and tert-butyl-substituted phenyl groups.

[0012] Furthermore, the R d It may be selected from one or a combination of hydrogen, deuterium, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, sec-pentyl, tert-pentyl, n-hexyl, isohexyl, sec-hexyl, tert-hexyl, n-heptyl, isoheptyl, sec-heptyl, tert-heptyl, n-octyl, isooctyl, sec-octyl, tert-octyl, n-nonyl, isononyl, sec-nonyl, tert-nonyl, n-decyl, isodel, sec-decyl, tert-decyl, adamantyl, C1-C10 alkyl-substituted or unsubstituted phenyl groups.

[0013] In many embodiments, the platinum(II) complex has the general formula structure shown in formula (Ii) or formula (I-ii):

[0014] In many embodiments, the platinum(II) complex is selected from any of the following chemical structures: where "D" represents deuterium:

[0015] In many embodiments, the present invention also provides the use of platinum(II) complex guest phosphorescent materials having the structure shown in formula (I) above in the fabrication of electronic devices.

[0016] Furthermore, the electronic device includes one or more of the following: organic electroluminescent device, organic optoelectronic device, organic integrated circuit, organic field-effect transistor, organic thin-film transistor, organic light-emitting transistor, organic solar cell, organic optical detector, organic photoreceptor, organic field quenching device, luminescent electrochemical cell, or organic laser diode.

[0017] In many embodiments, the present invention provides an organic electroluminescent device comprising: a cathode, an anode, and an organic functional layer therebetween, the organic functional layer comprising a platinum(II) complex guest phosphorescent material having the structure shown in formula (I) above.

[0018] Preferably, the organic functional layer includes a light-emitting layer, which contains a platinum(II) complex guest phosphorescent material having the structure shown in Formula (I) above.

[0019] More preferably, the light-emitting layer further comprises a fluorescent dopant material; the fluorescent dopant material is preferably a boron-containing organic luminescent material, and more preferably a boron-containing compound.

[0020] In many embodiments, the present invention also provides an organic optoelectronic device comprising: a substrate layer; a first electrode on the substrate; an organic light-emitting functional layer on the first electrode; and a second electrode on the organic light-emitting functional layer; wherein the organic light-emitting functional layer comprises a platinum(II) complex guest phosphorescent material having the structure shown in formula (I) above. For example, the platinum(II) complex can be included as a luminescent material in the organic light-emitting functional layer.

[0021] Furthermore, the organic light-emitting functional layer also contains any one or more fluorescent doping materials, wherein the fluorescent doping material is preferably a boron-containing organic luminescent material, and more preferably a phosphorus-sensitive boron-containing compound.

[0022] In this invention, organic optoelectronic devices can be fabricated by depositing metals or conductive oxides and their alloys onto a substrate using methods such as sputtering, electron beam evaporation, and vacuum deposition to form the anode. A hole injection layer, hole transport layer, light-emitting layer, air-blocking layer, and electron transport layer are then sequentially deposited onto the surface of the anode, followed by the deposition of the cathode. Alternatively, organic electroluminescent devices can be fabricated by depositing the cathode, organic functional layer, and anode onto a substrate in that order. The organic functional layer can include a multilayer structure comprising a hole injection layer, a hole transport layer, a light-emitting layer, a hole-blocking layer, and an electron transport layer. In this invention, the organic functional layer is prepared using polymer materials via solvent engineering (spin-coating, tape-casting, doctor-blading, screen-printing, inkjet printing, or thermal imaging, etc.) instead of evaporation methods, which can reduce the number of device layers.

[0023] The present invention also provides a composition comprising a platinum(II) complex guest phosphorescent material having the structure shown in formula (I) as described above. Preferably, the composition further comprises a fluorescent dopant material, which is preferably a boron-containing organic luminescent material, and more preferably a phosphorescently sensitizable boron-containing compound.

[0024] The present invention also provides a formulation comprising a platinum(II) complex guest phosphorescent material having the structure shown in formula (I) as described above and at least one solvent. The solvent is not particularly limited and may be any solvent well known to those skilled in the art.

[0025] The present invention also provides a display or lighting device comprising one or more of the organic electroluminescent devices or organic optoelectronic devices as described above.

[0026] Preferably, the organic electroluminescent device of the present invention is any one of organic photovoltaic devices, organic light-emitting devices (OLEDs), organic solar cells (OSCs), electronic paper (e-paper), organic photosensitive materials (OPCs), organic thin-film transistors (OTFTs), organic memory elements, lighting and display devices.

[0027] The materials used in the organic electroluminescent devices according to the present invention can be classified as top-emitting, low-emitting, or bifacial-emitting.

[0028] The compounds of the organic electroluminescent devices according to embodiments of the present invention can be applied to electroluminescent devices such as organic solar cells, OLEDs for lighting, flexible OLEDs, organic photosensitive materials, and organic thin-film transistors, based on similar principles to those of organic light-emitting devices.

[0029] Compared with the prior art, the beneficial effects of the present invention are:

[0030] (1) By introducing rigid 5,5,8,8-tetramethyl-2-phenyl-5,6,7,8-tetrahydronaphthyl groups, the steric hindrance is increased, the distance between molecules is expanded, and the red shift or luminescence quenching caused by molecular aggregation is avoided.

[0031] (2) Deuteration around the cyclic metal ligand can improve the stability of CH bonds, thereby giving the phosphorescent materials shown in formula (I) and formula (II) good chemical and thermal stability, making it easy to prepare vapor-deposited OLED devices;

[0032] (3) When the phosphorescent material provided by the present invention is used as the light-emitting layer material to make an organic electroluminescent device, it has a more superior performance improvement; the energy transfer between the host and the guest is more efficient, and there is a significant improvement in current efficiency and lifetime; and the use of phosphorus photosensitive boron-containing compound system can further improve the light color purity of the device. Attached Figure Description

[0033] Figure 1 shows the spectrum of some of the complexes in dichloromethane solution at room temperature. Detailed Implementation

[0034] As used in this invention, the terms "optional" or "optionally" mean that the event or situation described below may or may not occur, and the description includes both the case where the event or situation occurs and the case where it does not occur.

[0035] The term "substituted" as used in this invention is intended to encompass all permissible substituents of organic compounds. In a broad sense, permissible substituents include acyclic and cyclic, branched and unbranched, carbocyclic and heterocyclic, and aromatic and non-aromatic substituents of organic compounds. Illustrative substituents include, for example, those described below. For a suitable organic compound, permissible substituents may be one or more, the same or different. For the purposes of this invention, heteroatoms (e.g., nitrogen) can have hydrogen substituents and / or any permissible substituent of the organic compound described herein, satisfying the valence bond of that heteroatom. This disclosure is not intended to limit in any way to permissible substituents of organic compounds. Similarly, the terms "substituted" or "substituted with" imply that such substitution conforms to the permissible valence bond of the substituted atom and the substituent, and that the substitution results in a stable compound (e.g., a compound that does not spontaneously undergo transformations (e.g., by rearrangement, cyclization, elimination, etc.)). It is also expected that, in some respects, unless explicitly stated otherwise, individual substituents can be further optionally substituted (i.e., further substituted or unsubstituted).

[0036] When defining various terms, R a -R g In this invention, the general symbols are used to denote various specific substituents. These symbols can be any substituent, not limited to those disclosed in this invention, and while they may be defined as certain substituents in one case, they may be defined as other substituents in other cases.

[0037] As used in this invention, the term "alkyl" refers to a branched or unbranched saturated hydrocarbon group with 1 to 30 carbon atoms. Preferred alkyl groups are alkyl groups containing 1 to 24 carbon atoms, more preferably 1 to 9 carbon atoms. Examples include methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, sec-pentyl, neopentyl, hexyl, heptyl, semi-alkyl, nonyl, decyl, dodecyl, tetradecyl, hexadecyl, eicosyl, tetracosyl, etc. The alkyl group may be cyclic or acyclic. It may be branched or unbranched. It may also be substituted or unsubstituted. For example, the alkyl group may be substituted with one or more groups, including but not limited to the optionally substituted alkyl, cycloalkyl, alkoxy, amino, halogen, hydroxyl, nitro, silyl, sulfoxo, or mercapto groups described in this invention.

[0038] Throughout this specification, "alkyl" is generally used to refer to both unsubstituted and substituted alkyl groups; however, substituted alkyl groups are also specifically referred to in this invention by identifying the specific substituents on the alkyl group. For example, the terms "halogenated alkyl" or "halogenated alkyl" specifically refer to an alkyl group substituted with one or more halogens (e.g., fluorine, chlorine, bromine, or iodine). The term "deuterated alkyl" specifically refers to an alkyl group substituted with one or more deuterium atoms. The alkyl term "alkoxyalkyl" specifically refers to an alkyl group substituted with one or more alkoxy groups, as described below. The term "alkylamino" specifically refers to an alkyl group substituted with one or more amino groups, as described below, etc. When "alkyl" is used in one context and a specific term such as "alkyl alcohol" is used in another context, it does not imply that the term "alkyl" does not simultaneously refer to the specific term such as "alkyl alcohol," etc.

[0039] This practice is also applied to other groups described in this invention. That is, when a term such as "cycloalkyl" refers to both an unsubstituted and a substituted cycloalkyl portion, the substituted portion may be specifically identified separately in this invention; for example, a specifically substituted cycloalkyl may be referred to as, for example, "alkylcycloalkyl". Similarly, a substituted alkoxy may be specifically referred to as, for example, "halogenated alkoxy", and a specifically substituted alkenyl may be, for example, "enol", etc. Likewise, the practice of using the general term such as "cycloalkyl" and the specific term such as "alkylcycloalkyl" is not intended to imply that the general term does not simultaneously include the specific term.

[0040] As used in this invention, the term "cycloalkyl" refers to a non-aromatic carbon-based ring consisting of at least three carbon atoms. Examples of cycloalkyl groups include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclononyl, adamantyl, etc. The term "heterocyclic alkyl" is a class of cycloalkyl groups as defined above and is included in the meaning of the term "cycloalkyl," wherein at least one ring carbon atom is substituted by a heteroatom, such as, but not limited to, nitrogen, oxygen, sulfur, or phosphorus. The cycloalkyl and heterocyclic alkyl groups may be substituted or unsubstituted. The cycloalkyl and heterocyclic alkyl groups may be substituted with one or more groups, including but not limited to alkyl, cycloalkyl, alkoxy, amino, halogen, hydroxyl, nitro, silyl, sulfo-oxo, or mercapto groups as described in this invention.

[0041] As used in this invention, the term "aryl" refers to any carbon-based aromatic group containing 6 to 60 carbon atoms, preferably aryl groups containing 6 to 30 carbon atoms, more preferably 6 to 18 carbon atoms. The carbon-based aromatic groups include, but are not limited to, phenyl, naphthyl, phenyl, biphenyl, phenoxyphenyl, anthracene, phenanthrene, etc. The term "aryl" also includes "heteroaryl," which is defined as a group containing an aromatic group having at least one heteroatom introduced into the ring of the aromatic group. Examples of heteroatoms include, but are not limited to, nitrogen, oxygen, sulfur, and phosphorus. Aryl groups may be substituted or unsubstituted. Aryl groups may be substituted with one or more groups, including, but not limited to, the alkyl, cycloalkyl, alkoxy, alkenyl, cycloalkenyl, alkynyl, cycloalkynyl, aryl, heteroaryl, aldehyde, amino, carboxyl, ester, halogen, hydroxyl, carbonyl, azide, nitro, silyl, sulfo-oxo, or mercapto groups described in this invention. The term "biaryl" refers to a specific type of aryl group and is included in the definition of "aryl". A biaryl group is two aryl groups that are bonded together by a fused ring structure, as in naphthalene, or two aryl groups that are linked by one or more carbon-carbon bonds, as in biphenyl.

[0042] This document discloses compounds or complexes containing platinum. The terms "compound" and "complex" are used interchangeably in this invention. Additionally, the compounds disclosed herein have a neutral charge.

[0043] The compounds disclosed herein are applicable to a wide variety of optical and electro-optic devices, including but not limited to light-absorbing devices such as solar and photosensitive devices, organic light-emitting diodes, light-emitting devices or devices capable of both light absorption and emission, and as markers for biological applications.

[0044] As stated above, the disclosed compounds are platinum complexes. Furthermore, the compounds disclosed herein can be used as host materials for OLED applications, such as full-color displays.

[0045] The compounds disclosed herein can be used in a variety of applications. As luminescent materials, these compounds can be used in organic light-emitting diodes (OLEDs), light-emitting devices and displays, and other light-emitting devices.

[0046] In addition, compared with traditional materials, the compounds in this invention can improve luminous efficiency and device operating time when used in light-emitting devices (such as OLEDs).

[0047] The compounds of the present invention can be prepared using a variety of methods, including but not limited to those described in the examples provided herein.

[0048] The compounds disclosed in the embodiments of the present invention are applicable to a wide variety of optical and electro-optic devices, including but not limited to light-absorbing devices such as solar cells and photosensors, organic light-emitting diodes (OLEDs), light-emitting devices or devices that have both light absorption and light emission capabilities, and markers for use in biological applications.

[0049] The compounds provided by embodiments of the present invention can be used in a light-emitting device such as an OLED, the device comprising at least one cathode, at least one anode, and at least one light-emitting layer, wherein at least one of the light-emitting layers comprises a platinum(II) complex guest phosphorescent material with the structure shown in formula (I). Specifically, the light-emitting device may include an anode, a hole transport layer, a light-emitting layer, an electron transport layer, and a cathode, which are sequentially deposited. The hole transport layer, the light-emitting layer, and the electron transport layer are all organic layers, and the anode and cathode are electrically connected.

[0050] It should be noted that the general instructions above and the detailed instructions below are merely illustrative and explanatory, and are not restrictive.

[0051] This disclosure can be more readily understood by referring to the following detailed description and the embodiments contained therein.

[0052] Before disclosing and describing the compounds, devices, and / or methods of the present invention, it should be understood that they are not limited to specific synthetic methods (otherwise indicated) or specific reagents (otherwise indicated), as these are, of course, subject to variation. It should also be understood that the terminology used in this invention is for descriptive purposes only and is not intended to be limiting. While any methods and materials similar to or equivalent to those described in this invention may be used in this practice or experiment, exemplary methods and materials are described below.

[0053] Synthesis Examples

[0054] The examples of compound synthesis, composition, devices, or methods below are intended to provide a general approach to the industry and are not intended to limit the scope of this patent. While we strive for accuracy in the data (quantities, temperatures, etc.) mentioned in the patent, some errors may still exist. Unless otherwise specified, weighings are performed separately, temperatures are in °C or room temperature, and pressures are close to atmospheric pressure.

[0055] The examples below provide methods for preparing novel compounds, but the preparation of such compounds is not limited to these methods. In this field of expertise, since the compounds protected in this patent are easily modified and prepared, their preparation can be carried out using the methods listed below or other methods. The examples below are merely illustrative and are not intended to limit the scope of protection of this patent. Temperature, catalyst, concentration, reactants, and reaction process can all be varied to select different conditions for preparing the compounds with different reactants.

[0056] HPLC-MS was performed on an Agilent 6210TOF LC / MS mass spectrometer; HRMS spectra were performed on an Agilent 6210TOF LC / MS liquid chromatography-time-of-flight mass spectrometer.

[0057] Synthetic route

[0058] Example 1: The synthetic route for the tetradentate cyclic platinum(II) complex Pt1 is as follows:

[0059] Synthesis of the intermediate chiral 1-OMe: Cl (1.2 equivalents), Cz-OMe (1.0 equivalent), Pd2(dba)3 (3 mol%), SPhos (12 mol%), and sodium tert-butoxide (2.0 equivalents) were added sequentially to a reaction flask. Nitrogen gas was purged three times, and toluene (25 mL) was added. The reaction mixture was stirred at 110 °C for 42 hours, and the solvent was removed by vacuum distillation. The mixture was purified by silica gel column chromatography with petroleum ether / ethyl acetate as eluent (50-10:1) to give 930 mg of 1-OMe as a yellow solid (90% yield).

[0060] Synthesis of the intermediate chiral 1-OH: 1-OMe (1.0 equivalent), hydrobromic acid (48%) (9 mL), and acetic acid (6 mL) were added sequentially to a reaction flask. The mixture was stirred at 120 °C for 16 hours and then cooled to room temperature. The solution was neutralized with aqueous NaHCO3, extracted with dichloromethane, dried over anhydrous sodium sulfate, filtered, and the solvent was removed by vacuum distillation. The product 1-OH was obtained by slurrying with petroleum ether / ethyl acetate, yielding 800 mg of a white solid (90% yield).

[0061] Synthesis of the intermediate chiral D-Cl: 1-OH (1.0 equivalent), 1-bromo-3-tert-butyl-5-chlorobenzene (1.2 equivalent), cuprous iodide (10 mol%), 2-pyridinecarboxylic acid (20 mol%), and potassium phosphate (2.0 equivalent) were added sequentially to a reaction flask. The mixture was purged with nitrogen three times, and then dimethyl sulfoxide (40 mL) was added. The reaction mixture was stirred at 100 °C for 26 hours. The mixture was diluted with water, extracted three times with ethyl acetate, washed once with brine, dried over anhydrous sodium sulfate, filtered, and the solvent was removed by vacuum distillation. The solution was purified by silica gel column chromatography with an eluent ratio of petroleum ether / ethyl acetate of 20:1–10:1, yielding 549 mg of a white solid (81% yield). MS: m / z 428.16 (M+H) + .

[0062] Synthesis of intermediate (1-1): TMNP-Br (10.00 g, 35.4 mmol, 1.0 equivalent), DtBu-Bpin (10.79 g, 35.43 mmol, 1.3 equivalent), tetrakis(triphenylphosphine)palladium (1.02 g, 0.88 mmol, 2 mol%), and potassium carbonate (12.12 g, 87.70 mmol, 2.0 equivalent) were added to a three-necked flask equipped with a magnetic stirrer. The mixture was then purged with nitrogen three times. Under nitrogen protection, ethylene glycol dimethyl ether (75 mL) and water (15 mL) were added. The reaction was carried out in an oil bath at 100 °C for 23 hours, then cooled to room temperature. The mixture was extracted with ethyl acetate, washed with water, dried over sodium sulfate, and the solvent was removed by vacuum distillation. The crude product was separated and filtered by silica gel column chromatography. Eluent: petroleum ether / ethyl acetate = 20:1, yielding 13.16 g of a red solid, 95% yield. MS: m / z 391.32 (M+H) + .

[0063] Synthesis of intermediates (1-2): 1-1 (15.07 g, 38.50 mmol, 1.0 equivalent), Br-NO2 (8.56 g, 42.35 mmol, 1.1 equivalent), tris(dibenzylacetone) dipalladium (531 mg, 0.58 mmol, 1.5 mol%), 2-biscyclohexylphosphine-2',6'-dimethoxy-1,1'-diphenyl (SPhos) (474 ​​mg, 1.16 mmol, 3 mol%), and cesium carbonate (25.09 g, 77.00 mmol, 2.0 equivalent) were added to a three-necked flask equipped with a magnetic stirrer. The mixture was then purged with nitrogen three times, and toluene (180 mL) was added under nitrogen protection. The reaction was carried out in an oil bath at 100 °C for 18 hours, then cooled to room temperature. The mixture was extracted with ethyl acetate, washed with water, dried over sodium sulfate, and the solvent was removed by vacuum distillation. The crude product was then separated and filtered using a silica gel column chromatography. Petroleum ether / ethyl acetate ratio of 20:1 yielded 18.54 g of a deep red solid, 94% yield. MS: m / z 512.34 (M+H) + .

[0064] Synthesis of intermediates (1-3): 1-2 (18.50 g, 36.11 mmol, 1.0 equivalent) and palladium on carbon (3.82 mg, 1.62 mmol, 4.5 mol%) were added to a three-necked flask equipped with a magnetic stirrer. The mixture was then purged with nitrogen three times. Ethanol (30 mL) and ethyl acetate (30 mL) were added under nitrogen protection, followed by purging with hydrogen three times. The reaction was carried out in an oil bath at 45 °C for 46 hours under a hydrogen atmosphere. After cooling to room temperature, the solvent was removed by vacuum distillation, yielding 16.89 g of a gray solid (97% yield). MS: m / z 482.37 (M+H) + .

[0065] Synthesis of intermediates (1-4): 1-3 (8.34 g, 17.28 mmol, 1.0 equivalence), D-Cl (8.00 g, 18.74 mmol, 2.0 equivalence), tris(dibenzylacetone)palladium (476 mg, 0.52 mmol, 3 mol%), 2-(di-tert-butylphosphine)biphenyl (John Phos) (310 mg, 1.04 mmol, 6 mol%), and sodium tert-butoxide (3.60 g, 37.84 mmol, 2.0 equivalence) were added to a three-necked flask equipped with a magnetic stirrer. The mixture was purged with nitrogen three times, and toluene (70 mL) was added under nitrogen protection. The reaction was carried out in an oil bath at 85 °C for 34 hours, then cooled to room temperature. The mixture was filtered, and the solvent was removed by vacuum distillation. The crude product was separated by silica gel column chromatography with petroleum ether / ethyl acetate as eluent (25:1) to give 12.83 g of a gray solid, yield 85%. MS: m / z 873.54 (M+H) + .

[0066] Synthesis of ligand L1: 1-4 (13.1 g, 15.00 mmol, 1.0 equivalent) and ammonium hexafluorophosphate (4.90 g, 30.00 mmol, 2.0 equivalent) were added to a three-necked flask equipped with a magnetic stirrer. The mixture was purged with nitrogen three times. Triethyl orthoformate (36 mL) was added under nitrogen protection. The reaction was carried out in an oil bath at 75 °C for 1 hour, then cooled to room temperature. The solvent was removed by vacuum distillation. Separation was performed by silica gel column chromatography with dichloromethane / methanol as the eluent (100:1-50:1), yielding 14.74 g of a purple-red solid (94% yield). MS: m / z 1045.53 (M+H) + .

[0067] Synthesis of Pt1: L1 (12.86 g, 12.30 mmol, 1.0 equivalent), (1,5-cyclooctadiene)diplatinum chloride (4.60 g, 12.30 mmol, 1.0 equivalent), and sodium acetate (3.02 g, 36.90 mmol, 3.0 equivalent) were added to a three-necked flask equipped with a magnetic stirrer. The mixture was purged with nitrogen three times. N,N-dimethylformamide (460 mL) was added under nitrogen protection, and the mixture was bubbled with nitrogen for 30 min to remove oxygen. The reaction was carried out in an oil bath at 120 °C for 26 h. After cooling to room temperature, the solvent was removed by vacuum distillation. The crude product was separated by silica gel column chromatography with petroleum ether / dichloromethane as eluent (3:1-1:1) to give 4.43 g of a yellow solid, yield 33%. MS: m / z 1092.51 (M+H) +

[0068] Example 2: The synthetic route for the tetradentate cyclic platinum(II) complex Pt76 is as follows:

[0069] Synthesis of intermediate (2-1): DBr-Cl (14.00 g, 51.78 mmol, 1.0 equivalent), DtBu-Bpin (29.10 g, 124.30 mmol, 2.4 equivalent), tetrakis(triphenylphosphine)palladium (1.79 g, 1.55 mmol, 3 mol%), and potassium carbonate (28.67 g, 207.12 mmol, 4.0 equivalent) were added to a three-necked flask equipped with a magnetic stirrer. The mixture was then purged with nitrogen three times. Under nitrogen protection, ethylene glycol dimethyl ether (140 mL) and water (40 mL) were added. The reaction was carried out in a 90°C oil bath for 16 hours, then cooled to room temperature. The mixture was extracted with ethyl acetate, washed with water, dried over sodium sulfate, and the solvent was removed by vacuum distillation. The crude product was separated and filtered by silica gel column chromatography. Eluent: petroleum ether, yielding 23.00 g of a white solid, 91% yield. MS: m / z 488.33 (M+H) + .

[0070] Synthesis of intermediate (2-2): 2-1 (22.50 g, 46.08 mmol, 1.0 equivalent), D-Bpin (17.55 g, 69.11 mmol, 1.5 equivalent), tris(dibenzylacetone)palladium (844 mg, 0.92 mmol, 2 mol%), 2-bicyclohexylphosphine-2',4',6'-triisopropylbiphenyl (XPhos) (879 mg, 1.84 mmol, 4 mol%), and potassium acetate (13.57 g, 138.24 mmol, 3.0 equivalent) were added to a three-necked flask equipped with a magnetic stirrer. The mixture was purged with nitrogen three times, and 1,4-dioxane (200 mL) was added under nitrogen protection. The reaction was carried out in an oil bath at 100°C for 14 hours, then cooled to room temperature. The mixture was filtered, and the solvent was removed by vacuum distillation. The crude product was then separated by silica gel column chromatography with petroleum ether / ethyl acetate at a ratio of 30:1 to 20:1, yielding 21.96 g of a white solid (82% yield). MS: m / z 580.45 (M+H) + .

[0071] Synthesis of intermediates (2-3): TMNP-Br (6.17 g, 20.67 mmol, 1.0 equivalent), 3-2 (12.00 g, 20.67 mmol, 1.0 equivalent), tetraphenylphosphine palladium (717 mg, 0.62 mmol, 3 mol%), and potassium carbonate (5.71 g, 41.34 mmol, 2.0 equivalent) were added to a three-necked flask equipped with a magnetic stirrer. The mixture was then purged with nitrogen three times. Under nitrogen protection, ethylene glycol dimethyl ether (100 mL) and water (20 mL) were added. The reaction was carried out in an oil bath at 90 °C for 45 hours, then cooled to room temperature. The mixture was extracted with ethyl acetate, washed with water, dried over sodium sulfate, and the solvent was removed by vacuum distillation. The crude product was separated and filtered by silica gel column chromatography. Eluent: petroleum ether, yielding 12.47 g of a white solid, 92% yield. MS: m / z 655.52 (M+H) + .

[0072] Synthesis of intermediates (2-4): Br-NO2 (4.07 g, 20.14 mmol, 1.1 equivalents), 2-3 (12.00 g, 18.31 mmol, 1.0 equivalents), tris(benzylacetone)palladium (502 mg, 0.55 mmol, 3 mol%), 2-biscyclohexylphosphine-2',6'-dimethoxy-1,1'-diphenyl (SPhos) (900 mg, 2.19 mmol, 12 mol%), and cesium carbonate (11.90 g, 36.54 mmol, 2.0 equivalents) were added to a three-necked flask equipped with a magnetic stirrer. The flask was then purged with nitrogen three times, and toluene (90 mL) was added under nitrogen protection. The reaction was carried out in an oil bath at 110°C for 52 hours, then cooled to room temperature. The mixture was filtered, and the solvent was removed by vacuum distillation. The crude product was then separated by silica gel column chromatography with petroleum ether / ethyl acetate as the eluent (30:1), yielding 14.22 g of a yellow solid (91% yield). MS: m / z 776.53 (M+H) + .

[0073] Synthesis of intermediates (2-5): 2-4 (10.87 g, 14.00 mmol, 1.0 equivalent) and stannous chloride (10.62 g, 56.00 mmol, 4.0 equivalent) were added to a three-necked flask equipped with a magnetic stirrer. The mixture was then purged with nitrogen three times. Ethanol (60 mL) and ethyl acetate (60 mL) were added under nitrogen protection. The reaction was carried out in an oil bath at 45 °C for 48 hours. After cooling to room temperature, the solvent was removed by vacuum distillation, yielding 9.51 g of a gray solid (91% yield). MS: m / z 746.55 (M+H) + .

[0074] Synthesis of intermediates (2-6): 2-5 (8.40 g, 11.25 mmol, 1.0 equivalent), D-Cl (5.05 g, 11.82 mmol, 1.05 equivalent), tris(dibenzylacetone)palladium (155 mg, 0.17 mmol, 1.5 mol%), 2-(di-tert-butylphosphine)biphenyl (John Phos) (101 mg, 0.34 mmol, 3 mol%), and sodium tert-butoxide (2.16 g, 22.50 mmol, 2.0 equivalent) were added to a three-necked flask equipped with a magnetic stirrer. The mixture was purged with nitrogen three times, and toluene (30 mL) was added under nitrogen protection. The reaction was carried out in an oil bath at 100 °C for 52 hours, then cooled to room temperature. The mixture was filtered, and the solvent was removed by vacuum distillation. The crude product was separated by silica gel column chromatography with petroleum ether / ethyl acetate as the eluent (30:1) to give 9.60 g of a brown solid, yield 75%. MS: m / z 1137.75 (M+H) + .

[0075] Synthesis of ligand L76: 2-6 (9.45 g, 8.31 mmol, 1.0 equivalent) and ammonium hexafluorophosphate (2.70 g, 16.61 mmol, 2.0 equivalent) were added to a three-necked flask equipped with a magnetic stirrer. The mixture was purged with nitrogen three times. Under nitrogen protection, triethyl orthoformate (20 mL) was added. The reaction was carried out in an oil bath at 75 °C for 1 hour, then cooled to room temperature. The solvent was removed by vacuum distillation. Separation was performed by silica gel column chromatography with dichloro / ethyl acetate as the eluent (10:1), yielding 6.45 g of a brown solid (60% yield). MS: m / z 1293.70 (M+H) + .

[0076] Synthesis of Pt76: L76 (6.05 g, 4.68 mmol, 1.0 equivalent), (1,5-cyclooctadiene)platinum dichloride (1.75 g, 4.68 mmol, 1.0 equivalent), and sodium acetate (1.15 g, 14.04 mmol, 3.0 equivalent) were added to a sealed tube equipped with a magnetic stirrer. Nitrogen was purged three times. Diethylene glycol dimethyl ether (200 mL) was added under nitrogen protection, and the mixture was bubbled with nitrogen for 30 min to remove oxygen. The reaction was carried out in an oil bath at 120 °C for 24 hours. After cooling to room temperature, the solvent was removed by vacuum distillation. The crude product was separated by silica gel column chromatography with petroleum ether / dichloromethane as eluent at a ratio of 2:1 to 1:1, yielding 2.20 g of a yellow solid (35% yield). MS: m / z 1342.66 (M+H) + .

[0077] Example 3: Tetradentate ring platinum(II) complex Pt221

[0078] Synthesis of intermediate (3-1): TMID-Br (9.50 g, 35.40 mmol, 1.0 equivalent), DtBu-B(OH)₂ (10.79 g, 35.43 mmol, 1.3 equivalent), tetrakis(triphenylphosphine)palladium (1.02 g, 0.88 mmol, 2 mol%), and potassium carbonate (12.12 g, 87.70 mmol, 2.0 equivalent) were added to a three-necked flask equipped with a magnetic stirrer. The mixture was then purged with nitrogen three times. Under nitrogen protection, ethylene glycol dimethyl ether (75 mL) and water (15 mL) were added. The reaction was carried out in an oil bath at 100 °C for 23 hours, then cooled to room temperature. The mixture was extracted with ethyl acetate, washed with water, dried over sodium sulfate, and the solvent was removed by vacuum distillation. The crude product was separated and filtered by silica gel column chromatography. Eluent: petroleum ether / ethyl acetate = 20:1, yielding 12.82 g of a red solid, 96% yield. MS: m / z 377.33 (M+H) + .

[0079] Synthesis of intermediate (3-2): 3-1 (14.53 g, 38.50 mmol, 1.0 equivalent), Br-NO2 (8.56 g, 42.35 mmol, 1.1 equivalent), tris(dibenzylacetone) dipalladium (531 mg, 0.58 mmol, 1.5 mol%), 2-biscyclohexylphosphine-2',6'-dimethoxy-1,1'-diphenyl (SPhos) (474 ​​mg, 1.16 mmol, 3 mol%), and cesium carbonate (25.09 g, 77.00 mmol, 2.0 equivalent) were added to a three-necked flask equipped with a magnetic stirrer. The mixture was then purged with nitrogen three times, and toluene (180 mL) was added under nitrogen protection. The reaction was carried out in an oil bath at 100 °C for 18 hours, then cooled to room temperature. The mixture was extracted with ethyl acetate, washed with water, dried over sodium sulfate, and the solvent was removed by vacuum distillation. The crude product was then separated and filtered using a silica gel column chromatography. Petroleum ether / ethyl acetate ratio of 20:1 yielded 17.65 g of a deep red solid, 92% yield. MS: m / z 498.30 (M+H) + .

[0080] Synthesis of intermediate (3-3): 3-2 (17.44 g, 35.00 mmol, 1.0 equivalent) and palladium on carbon (3.71 mg, 1.58 mmol, 4.5 mol%) were added to a three-necked flask equipped with a magnetic stirrer. The mixture was then purged with nitrogen three times. Ethanol (30 mL) and ethyl acetate (30 mL) were added under nitrogen protection, followed by purging with hydrogen three times. The reaction was carried out in an oil bath at 45 °C for 46 hours under a hydrogen atmosphere. After cooling to room temperature, the solvent was removed by vacuum distillation, yielding 15.57 g of a gray solid (95% yield). MS: m / z 468.35 (M+H) + .

[0081] Synthesis of intermediates (3-4): 3-3 (8.10 g, 17.28 mmol, 1.0 equivalent), D-Cl (8.00 g, 18.74 mmol, 2.0 equivalent), tris(dibenzylacetone)palladium (476 mg, 0.52 mmol, 3 mol%), 2-(di-tert-butylphosphine)biphenyl (John Phos) (310 mg, 1.04 mmol, 6 mol%), and sodium tert-butoxide (3.60 g, 37.84 mmol, 2.0 equivalent) were added to a three-necked flask equipped with a magnetic stirrer. The mixture was purged with nitrogen three times, and toluene (70 mL) was added under nitrogen protection. The reaction was carried out in an oil bath at 85 °C for 34 hours, then cooled to room temperature. The mixture was filtered, and the solvent was removed by vacuum distillation. The crude product was separated by silica gel column chromatography with petroleum ether / ethyl acetate as eluent (25:1) to give 12.77 g of a gray solid, yield 86%. MS: m / z 859.54 (M+H) + .

[0082] Synthesis of ligand L221: 3-4 (12.89 g, 15.00 mmol, 1.0 equivalent) and ammonium hexafluorophosphate (4.90 g, 30.00 mmol, 2.0 equivalent) were added to a three-necked flask equipped with a magnetic stirrer. The mixture was purged with nitrogen three times. Triethyl orthoformate (36 mL) was added under nitrogen protection. The reaction was carried out in an oil bath at 75 °C for 1 hour, then cooled to room temperature. The solvent was removed by vacuum distillation. Separation was performed by silica gel column chromatography with dichloromethane / methanol as the eluent (100:1-50:1), yielding 14.74 g of a purple-red solid (94% yield). MS: m / z 1045.53 (M+H) + .

[0083] Synthesis of Pt221: L221 (12.86 g, 12.30 mmol, 1.0 equivalent), (1,5-cyclooctadiene)platinum dichloride (4.60 g, 12.30 mmol, 1.0 equivalent), and sodium acetate (3.02 g, 36.90 mmol, 3.0 equivalent) were added to a three-necked flask equipped with a magnetic stirrer. Nitrogen was purged three times. N,N-dimethylformamide (460 mL) was added under nitrogen protection, and the mixture was bubbled with nitrogen for 30 min to remove oxygen. The reaction was carried out in an oil bath at 120 °C for 26 h. After cooling to room temperature, the solvent was removed by vacuum distillation. The crude product was separated by silica gel column chromatography with petroleum ether / dichloromethane as eluent (3:1-1:1) to give 4.51 g of a yellow solid (34% yield). MS: m / z 1079.48 (M+H) + .

[0084] Example 4: Tetradentate ring platinum(II) complex Pt441

[0085] Synthesis of intermediate (4-1): mBr-NO2 (1.0 equivalent), Bpin (1.0 equivalent), tetrakis(triphenylphosphine)palladium (2 mol%), and potassium carbonate (2.0 equivalent) were added to a three-necked flask equipped with a magnetic stirrer. The mixture was then purged with nitrogen three times. Under nitrogen protection, ethylene glycol dimethyl ether (75 mL) and water (15 mL) were added. The reaction was carried out in an oil bath at 100 °C for 23 hours, then cooled to room temperature. The mixture was extracted with ethyl acetate, washed with water, dried over sodium sulfate, and the solvent was removed by vacuum distillation. The crude product was separated and filtered using a silica gel column chromatography. The eluent was petroleum ether / ethyl acetate = 20:1, yielding 7.20 g of a yellow solid (90% yield). MS: m / z 421.30 (M+H) + .

[0086] Synthesis of intermediate (4-2): 4-1 (1.0 equivalent) and palladium on carbon (4.5 mol%) were added to a three-necked flask equipped with a magnetic stirrer. The mixture was then purged with nitrogen three times. Ethanol (80 mL) and ethyl acetate (80 mL) were added under nitrogen protection, followed by purging with hydrogen three times. The reaction was carried out in an oil bath at 45 °C for 17 hours under a hydrogen atmosphere. After cooling to room temperature, the solvent was removed by vacuum distillation, yielding 14.1 g of a white solid, 82% yield. MS: m / z 391.32 (M+H) + .

[0087] Synthesis of intermediate (4-3): 4-2 (1.0 equivalent), Br-NO2 (1.0 equivalent), tris(dibenzylacetone) dipalladium (3 mol%), 2-dicyclohexylphosphine-2',6'-dimethoxy-1,1'-diphenyl (SPhos) (3 mol%), and cesium carbonate (2.0 equivalent) were added to a three-necked flask equipped with a magnetic stirrer. The mixture was then purged with nitrogen three times, and toluene (40 mL) was added under nitrogen protection. The reaction was carried out in an oil bath at 100 °C for 17 hours, then cooled to room temperature. The mixture was extracted with ethyl acetate, washed with water, dried over sodium sulfate, and the solvent was removed by vacuum distillation. The crude product was separated and filtered using a silica gel column chromatography. Petroleum ether / ethyl acetate ratio of 20:1 yielded 4.70 g of a red solid, 90% yield. MS: m / z 512.34 (M+H) + .

[0088] Synthesis of intermediate (4-4): 4-3 (1.0 equivalent) and palladium on carbon (4.5 mol%) were added to a three-necked flask equipped with a magnetic stirrer. Nitrogen was then purged three times. Ethanol (30 mL) and ethyl acetate (30 mL) were added under nitrogen protection, followed by three purgings with hydrogen. The reaction was carried out in an oil bath at 45 °C for 17 hours under a hydrogen atmosphere. After cooling to room temperature, the solvent was removed by vacuum distillation, yielding 3.70 g of a white solid, 84% yield. MS: m / z 482.36 (M+H) + .

[0089] Synthesis of intermediate (4-5): 4-4 (1.0 equivalent), Cl (1.05 equivalent), tris(dibenzylacetone)palladium (3 mol%), 2-(di-tert-butylphosphine)biphenyl (JohnPhos) (6 mol%), and sodium tert-butoxide (2.0 equivalent) were added to a three-necked flask equipped with a magnetic stirrer. The mixture was purged with nitrogen three times, and toluene (20 mL) was added under nitrogen protection. The reaction was carried out in an oil bath at 85°C for 7 hours, then cooled to room temperature. The mixture was filtered, and the solvent was removed by vacuum distillation. The crude product was separated by silica gel column chromatography with petroleum ether / ethyl acetate as the eluent at a ratio of 40:1, yielding 5.86 g of a green solid (85% yield). MS: 872.54 m / z (M+H) + .

[0090] Synthesis of ligand L441: 4-5 μL (1.0 equivalent) of ammonium hexafluorophosphate (2.0 equivalent) was added to a three-necked flask equipped with a magnetic stirrer. The mixture was purged with nitrogen three times. Under nitrogen protection, 20 mL of triethyl orthoformate was added. The reaction was carried out in an oil bath at 75°C for 1 hour, then cooled to room temperature. The solvent was removed by vacuum distillation. Separation was performed by silica gel column chromatography with dichloromethane / methanol as the eluent (100:1), yielding 6.25 g of a red solid (91% yield). MS: m / z 883.52 (M+H) + .

[0091] Synthesis of Pt441: L1 (1.0 equivalent), (1,5-cyclooctadiene)diplatinum chloride (1.0 equivalent), and sodium acetate (3.0 equivalent) were added to a three-necked flask equipped with a magnetic stirrer. The mixture was purged with nitrogen three times. Under nitrogen protection, N,N-dimethylformamide (460 mL) was added, and the mixture was bubbled with nitrogen for 30 min to remove oxygen. The reaction was carried out in an oil bath at 120 °C for 24 hours. After cooling to room temperature, the solvent was removed by vacuum distillation. The crude product was separated by silica gel column chromatography with petroleum ether / dichloromethane as the eluent (3:1), yielding 3.60 g of a yellow solid (31% yield). MS: m / z 1076.49 (M+H) + .

[0092] Example 5: Tetradentate ring platinum(II) complex Pt4

[0093] The synthetic complex Pt4 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursors in the examples. The final product was a yellow solid, 100 mg, with a yield of 43%. MS: m / z 1078.48 (M+H) + .

[0094] Example 6: Tetradentate ring platinum(II) complex Pt5

[0095] The synthetic complex Pt5 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursors in the examples. The final yield was 104 mg of a yellow solid, with a yield of 32%. MS: m / z 1082.51 (M+H) + .

[0096] Example 7: Tetradentate ring platinum(II) complex Pt6

[0097] The synthetic complex Pt6 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursors in the examples. The final product was a yellow solid, 98 mg, with a yield of 43%. MS: m / z 1079.50 (M+H) + .

[0098] Example 8: Tetradentate ring platinum(II) complex Pt9

[0099] The synthetic complex Pt9 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursors in the examples. The final yield was 128 mg of a yellow solid, with a yield of 50%. MS: m / z 1081.37 (M+H) + .

[0100] Example 9: Tetradentate ring platinum(II) complex Pt11

[0101] The synthetic complex Pt11 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursors in the examples. The final yield was 124 mg of a yellow solid, with a yield of 45%. MS: m / z 1049.28 (M+H) + .

[0102] Example 10: Tetradentate ring platinum(II) complex Pt12

[0103] The synthetic complex Pt12 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursors in the examples. The final yield was 115 mg of a yellow solid, with a yield of 38%. MS: m / z 1026.42 (M+H) + .

[0104] Example 11: Tetradentate ring platinum(II) complex Pt16

[0105] The synthetic complex Pt16 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursors in the examples. The final yield was 134 mg of a yellow solid, with a yield of 39%. MS: m / z 1079.52 (M+H) + .

[0106] Example 12: Tetradentate ring platinum(II) complex Pt22

[0107] The synthetic complex Pt22 was prepared using the same synthesis method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursors in the examples. The final yield was 137 mg of a yellow solid, with a yield of 43%. MS: m / z 1098.65 (M+H) + .

[0108] Example 13: Tetradentate ring platinum(II) complex Pt24

[0109] The synthetic complex Pt24 was prepared using the same synthesis method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursors in the examples. The final yield was 121 mg of a yellow solid, with a yield of 28%. MS: m / z 1112.56 (M+H) + .

[0110] Example 14: Tetradentate ring platinum(II) complex Pt27

[0111] The synthetic complex Pt27 was prepared using the same synthesis method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursors in the examples. The final yield was 128 mg of a yellow solid, with a yield of 40%. MS: m / z 1157.46 (M+H) + .

[0112] Example 15: Tetradentate ring platinum(II) complex Pt30

[0113] The synthetic complex Pt30 was prepared using the same synthesis method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursors in the examples. The final yield was 128 mg of a yellow solid, with a yield of 36%. MS: m / z 1052.30 (M+H) + .

[0114] Example 16: Tetradentate ring platinum(II) complex Pt31

[0115] The synthetic complex Pt31 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursors in the examples. The final yield was 136 mg of a yellow solid, with a yield of 44%. MS: m / z 1116.40 (M+H) + .

[0116] Example 17: Tetradentate ring platinum(II) complex Pt32

[0117] The synthetic complex Pt32 was prepared according to the synthesis method of the complexes in Examples 1-3, with the only difference being the replacement of the corresponding fragment ligand raw materials in the examples. The final yield was 114 mg of a yellow solid, with a yield of 27%. MS: m / z 1127.49 (M+H) + .

[0118] Example 18: Tetradentate ring platinum(II) complex Pt34

[0119] The synthetic complex Pt34 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursors in the examples. The final yield was 132 mg of a yellow solid, with a yield of 36%. MS: m / z 1343.67 (M+H)+ .

[0120] Example 19: Tetradentate ring platinum(II) complex Pt36

[0121] The synthetic complex Pt36 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursors in the examples. The final yield was 111 mg of a yellow solid, with a yield of 38%. MS: m / z 1023.46 (M+H) + .

[0122] Example 20: Tetradentate ring platinum(II) complex Pt41

[0123] The synthetic complex Pt41 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursors in the examples. The final yield was 126 mg of a yellow solid, with a yield of 42%. MS: m / z 1133.52 (M+H) + .

[0124] Example 21: Tetradentate ring platinum(II) complex Pt42

[0125] The synthetic complex Pt42 was prepared using the same synthesis method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursors in the examples. The final yield was 143 mg of a yellow solid, with a yield of 46%. MS: m / z 1136.55 (M+H) + .

[0126] Example 22: Tetradentate ring platinum(II) complex Pt49

[0127] The synthetic complex Pt49 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the substitution of the corresponding ligand precursor in the examples. The final yield was 140 mg of a yellow solid, with a yield of 49%. MS: m / z 1142.63 (M+H) + .

[0128] Example 23: Tetradentate ring platinum(II) complex Pt51

[0129] The synthetic complex Pt51 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursors in the examples. The final yield was 148 mg of a yellow solid, with a yield of 48%. MS: m / z 1085.48 (M+H) + .

[0130] Example 24: Tetradentate ring platinum(II) complex Pt57

[0131] The synthetic complex Pt57 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the substitution of the corresponding ligand precursor in the examples. The final yield was 123 mg of a yellow solid, with a yield of 42%. MS: m / z 1293.67 (M+H) + .

[0132] Example 25: Tetradentate ring platinum(II) complex Pt59

[0133] The synthetic complex Pt59 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the substitution of the ligand precursor for the corresponding fragment in the examples. The final yield was 106 mg of a yellow solid, with a yield of 46%. MS: m / z 1255.56 (M+H) + .

[0134] Example 26: Tetradentate ring platinum(II) complex Pt60

[0135] The synthetic complex Pt60 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursors in the examples. The final yield was 126 mg of a yellow solid, with a yield of 45%. MS: m / z 1186.56 (M+H) + .

[0136] Example 27: Tetradentate ring platinum(II) complex Pt113

[0137] The synthetic complex Pt113 was prepared according to the synthesis method of the complexes in Examples 1-3, with the only difference being the replacement of the corresponding fragment ligand raw materials in the examples. A total of 137 mg of yellow solid was obtained, with a yield of 33%. MS: m / z 1231.56 (M+H) + .

[0138] Example 28: Tetradentate ring platinum(II) complex Pt127

[0139] The synthetic complex Pt127 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursors in the examples. The final yield was 142 mg of a yellow solid, with a yield of 35%. MS: m / z 1093.51 (M+H) + .

[0140] Example 29: Tetradentate ring platinum(II) complex Pt133

[0141] The synthetic complex Pt133 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursors in the examples. The final yield was 139 mg of a yellow solid, with a yield of 32%. MS: m / z 1275.59 (M+H) + .

[0142] Example 30: Tetradentate ring platinum(II) complex Pt175

[0143] The synthetic complex Pt175 was prepared according to the synthesis methods described in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursors in the examples. A total of 133 mg of yellow solid was obtained, with a yield of 30%. MS: m / z 1198.57 (M+H) + .

[0144] Example 31: Tetradentate ring platinum(II) complex Pt181

[0145] The synthetic complex Pt181 was prepared according to the synthesis method of the complexes in Examples 1-3, with the only difference being the replacement of the corresponding fragment ligand raw materials in the examples. A total of 129 mg of yellow solid was obtained, with a yield of 32%. MS: m / z 1291.67 (M+H) + .

[0146] Example 32: Tetradentate ring platinum(II) complex Pt187

[0147] The synthetic complex Pt187 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursors in the examples. The final yield was 143 mg of a yellow solid, with a yield of 37%. MS: m / z 1370.71 (M+H) + .

[0148] Example 33: Tetradentate ring platinum(II) complex Pt2O3

[0149] The synthetic complex Pt2O3 was prepared according to the synthesis method of the complexes in Examples 1-3, with the only difference being the replacement of the corresponding fragments of the ligand raw materials in the examples. A total of 132 mg of yellow solid was obtained, with a yield of 31%. MS: m / z 1127.58 (M+H) + .

[0150] Example 34: Tetradentate ring platinum(II) complex Pt2O7

[0151] The synthetic complex Pt2O7 was prepared according to the synthesis method of the complexes in Examples 1-3, with the only difference being the replacement of the corresponding fragment ligand raw materials in the examples. A total of 129 mg of yellow solid was obtained, with a yield of 30%. MS: m / z 1328.66 (M+H) + .

[0152] Example 35: Tetradentate ring platinum(II) complex Pt216

[0153] The synthetic complex Pt216 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the substitution of the corresponding ligand precursor in the examples. The final yield was 143 mg of a yellow solid, with a yield of 40%. MS: m / z 1297.62 (M+H) + .

[0154] Example 36: Tetradentate ring platinum(II) complex Pt222

[0155] The synthetic complex Pt222 was prepared according to the synthesis method of the complexes in Examples 1-3, with the only difference being the replacement of the corresponding fragment ligand raw materials in the examples. A total of 132 mg of yellow solid was obtained, with a yield of 41%. MS: m / z 1066.46 (M+H) + .

[0156] Example 37: Tetradentate ring platinum(II) complex Pt223

[0157] The synthetic complex Pt223 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursors in the examples. The final yield was 128 mg of a yellow solid, with a yield of 40%. MS: m / z 1064.50 (M+H) + .

[0158] Example 38: Tetradentate ring platinum(II) complex Pt225

[0159] The synthetic complex Pt225 was prepared according to the synthesis method of the complexes in Examples 1-3, with the only difference being the replacement of the corresponding fragment ligand raw materials in the examples. The final yield was 102 mg of a yellow solid, with a yield of 32%. MS: m / z 1068.52 (M+H) + .

[0160] Example 39: Tetradentate ring platinum(II) complex Pt228

[0161] The synthetic complex Pt228 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursors in the examples. The final yield was 138 mg of a yellow solid, with a yield of 47%. MS: m / z 1074.58 (M+H) + .

[0162] Example 40: Tetradentate ring platinum(II) complex Pt234

[0163] The synthetic complex Pt234 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursors in the examples. The final yield was 117 mg of a yellow solid, with a yield of 35%. MS: m / z 1083.60 (M+H) + .

[0164] Example 41: Tetradentate ring platinum(II) complex Pt237

[0165] The synthetic complex Pt237 was prepared according to the synthesis method of the complexes in Examples 1-3, with the only difference being the replacement of the corresponding fragment ligand raw materials in the examples. A total of 115 mg of yellow solid was obtained, with a yield of 33%. MS: m / z 1145.55 (M+H) + .

[0166] Example 42: Tetradentate ring platinum(II) complex Pt242

[0167] The synthetic complex Pt242 was prepared according to the synthesis method of the complexes in Examples 1-3, with the only difference being the replacement of the corresponding fragment ligand raw materials in the examples. A total of 112 mg of yellow solid was obtained, with a yield of 38%. MS: m / z 1083.62 (M+H) + .

[0168] Example 43: Tetradentate ring platinum(II) complex Pt251

[0169] The synthetic complex Pt251 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursors in the examples. The final yield was 135 mg of a yellow solid, with a yield of 35%. MS: m / z 1104.43 (M+H) + .

[0170] Example 44: Tetradentate ring platinum(II) complex Pt260

[0171] The synthetic complex Pt260 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursors in the examples. The final yield was 122 mg of a yellow solid, with a yield of 45%. MS: m / z 1147.71 (M+H) + .

[0172] Example 45: Tetradentate ring platinum(II) complex Pt261

[0173] The synthetic complex Pt261 was prepared according to the synthesis method of the complexes in Examples 1-3, with the only difference being the replacement of the corresponding fragment ligand raw materials in the examples. The final yield was 125 mg of a yellow solid, with a yield of 34%. MS: m / z 1118.52 (M+H) + .

[0174] Example 46: Tetradentate ring platinum(II) complex Pt269

[0175] The synthetic complex Pt269 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursor in the examples. The final yield was 123 mg of a yellow solid, with a yield of 37%. MS: m / z 1129.60 (M+H) + .

[0176] Example 47: Tetradentate ring platinum(II) complex Pt278

[0177] The synthetic complex Pt278 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursors in the examples. The final yield was 131 mg of a yellow solid, with a yield of 40%. MS: m / z 1298.62 (M+H) + .

[0178] Example 48: Tetradentate ring platinum(II) complex Pt296

[0179] The synthetic complex Pt296 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursors in the examples. The final yield was 163 mg of a yellow solid, with a yield of 58%. MS: m / z 1327.66 (M+H) + .

[0180] Example 49: Tetradentate ring platinum(II) complex Pt300

[0181] The synthetic complex Pt300 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursors in the examples. The final yield was 121 mg of a yellow solid, with a yield of 41%. MS: m / z 1334.71 (M+H) + .

[0182] Example 50: Tetradentate ring platinum(II) complex Pt319

[0183] The synthetic complex Pt319 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the substitution of the corresponding ligand precursor in the examples. The final yield was 131 mg of a yellow solid, with a yield of 36%. MS: m / z 1121.54 (M+H) + .

[0184] Example 51: Tetradentate ring platinum(II) complex Pt334

[0185] The synthetic complex Pt334 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursors in the examples. The final yield was 111 mg of a yellow solid, with a yield of 35%. MS: m / z 1330.64 (M+H) + .

[0186] Example 52: Tetradentate ring platinum(II) complex Pt369

[0187] The synthetic complex Pt369 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursor in the examples. The final yield was 122 mg of a yellow solid, with a yield of 29%. MS: m / z 1089.45 (M+H) + .

[0188] Example 53: Tetradentate ring platinum(II) complex Pt379

[0189] The synthetic complex Pt379 was prepared using the same synthesis method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursor in the examples. The final yield was 131 mg of a yellow solid, with a yield of 42%. MS: m / z 1332.69 (M+H) + .

[0190] Example 54: Tetradentate ring platinum(II) complex Pt399

[0191] The synthetic complex Pt399 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursors in the examples. The final yield was 117 mg of a yellow solid, with a yield of 31%. MS: m / z 1167.53 (M+H) + .

[0192] Example 55: Tetradentate ring platinum(II) complex Pt415

[0193] The synthetic complex Pt415 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursors in the examples. The final yield was 131 mg of a yellow solid, with a yield of 34%. MS: m / z 1176.60 (M+H) + .

[0194] Example 56: Tetradentate ring platinum(II) complex Pt428

[0195] The synthetic complex Pt428 was prepared using the same synthetic method as in Examples 1-3, with the only difference being the replacement of the corresponding ligand precursors in the examples. The final yield was 127 mg of a yellow solid, with a yield of 34%. MS: m / z 1127.56 (M+H) + .

[0196] Example 57: Tetradentate ring platinum(II) complex Pt441

[0197] The synthetic complex Pt442 was prepared according to the synthesis method of the complexes in Examples 1-3, with the only difference being the replacement of the corresponding fragment ligand raw materials in the examples. A total of 119 mg of yellow solid was obtained, with a yield of 30%. MS: m / z 1076.50 (M+H) + .

[0198] Example 58: Tetradentate ring platinum(II) complex Pt442

[0199] The synthetic complex Pt442 was prepared according to the synthesis method of the complexes in Examples 1-3, with the only difference being the replacement of the corresponding fragment ligand raw materials in the examples. A total of 121 mg of yellow solid was obtained, with a yield of 32%. MS: m / z 1074.45 (M+H) + .

[0200] Photophysical properties:

[0201] Figure 1 shows the spectra of some representative complexes and the comparative compound R1 in dichloromethane solution at room temperature. The structure of R1 is as follows:

[0202] As shown in Figure 1, the cycloplatinum(II) complex of this invention exhibits a significantly lower shoulder peak in dichloromethane solution at room temperature compared to the comparative compound R1, which improves the color purity of the emitted color. Furthermore, the phosphorescent material of the platinum metal complex in this application emits light in the blue emission region of 455-460 nm; its full width at half maximum (FWHM) is small, mostly at 25 nm or less, indicating high color purity; its quantum efficiency in polymethyl methacrylate (PMMA) is high, mostly above 90%, and even reaching 95% or more; the deuteration of the ligand periphery ensures improved material stability while having almost no impact on the emission wavelength and FWHM; in addition, fine adjustment of the emission wavelength can be achieved by controlling the peripheral substituents.

[0203] Fabrication of OLED devices:

[0204] An OLED device is fabricated by depositing p-doped material onto the surface or anode of an ITO glass with a light-emitting area of ​​2 mm × 2 mm, or by co-evaporating p-doped material with hole injection material at a concentration of 1% to 50% to form a 5-100 nm hole injection layer (HIL) and a 5-200 nm hole transport layer (HTL). Subsequently, a 10-100 nm light-emitting layer (EML) (which may contain the compound described in this invention) is formed on the hole transport layer, followed by a 20-200 nm electron transport layer (ETL) and a 50-200 nm cathode. If necessary, an electron blocking layer (EBL) is added between the HTL and EML layers, and an electron injection layer (EIL) is added between the ETL and the cathode. The OLED is then tested using standard methods. Unless otherwise specified, the device materials involved in this invention can be obtained using known synthesis methods.

[0205] In a preferred embodiment, the structure of the device Example 1 provided by the present invention is: ITO / P-4 (10nm) / HT1 (60nm) / HTH-85 (5nm) / platinum (II) complex:HTH-85:ETH-45 (25nm) (Pt1:HTH-85:ETH-45 mass ratio is 10:60:30) / ETH-5 (5nm) / ET-14 (40nm) / LiQ (1nm) / Al (100nm).

[0206] Device Examples 2-30 and Comparative Example 1 were fabricated using structures similar to those in Device Example 1, the only difference being that the Pt1 in Device Example 1 was replaced with the platinum(II) complex shown in Table 2. The luminescence properties of the comparative examples and each device example prepared above were tested using standard methods and are shown in Table 2. The device structural formulas involved are as follows: where P-4 is HATCN.

[0207] Table 1. Luminescence properties of some compounds after fabrication into devices

[0208] As shown in Table 1, compared with Comparative Example 1, Device Examples 1-30 prepared in this application exhibit excellent device performance in terms of driving voltage, current efficiency, and device lifetime. The performance improvement of each device example is based on the high chemical stability and better electron transport capability of the specific compound material of this invention. Furthermore, all devices prepared in this invention are deep blue light-emitting devices with CIEy values ​​less than 0.2. This demonstrates that using this material as a light-emitting layer material in electronic devices achieves higher current efficiency, device lifetime, and color purity while reducing the driving voltage. This indicates that the compound provided by this invention has certain commercial application value.

[0209] In a preferred embodiment, the structure of device example 31 provided by the present invention is as follows: ITO / P-4 (10nm) / HT1 (60nm) / HTH-85 (5nm) / platinum (II) complex: boron-containing compound: HTH-85:ETH-45 (25nm) (Pt1:BN1-8:HTH-85:ETH-45 mass ratio is 10:1:59:30) / ETH-5 (5nm) / ET-14 (40nm) / LiQ (1nm) / Al (100nm).

[0210] Device Examples 32-37 were fabricated using a structure similar to that of Device Example 31, the only difference being that the platinum(II) complex and boron-containing compound in Device Example 31 were replaced with platinum(II) complexes and boron-containing compounds as listed in Table 2. The device structural formulas are as follows, and the device structure and luminescence characteristic data are shown in Table 2.

[0211] Table 2. Device Structure and Luminescent Properties Data

[0212] As shown in Table 2, when the compounds of this invention are used as sensitizing materials, together with boron-containing compounds as luminescent materials in devices, the performance of each device is significantly improved. This further demonstrates that the compounds provided by this invention have certain commercial application value. Adding boron-containing compounds to sensitize the device structure can further reduce the CIEy value, thereby improving the purity of the emitted color.

[0213] The above description is only a preferred embodiment of the present invention, but the scope of protection of the present invention is not limited thereto. Any equivalent substitutions or modifications made by those skilled in the art within the scope of the technology disclosed in the present invention, based on the technical solution and inventive concept of the present invention, should be covered within the scope of protection of the present invention.

Claims

A tetradentate cyclic platinum(II) complex, characterized in that, It has the general formula structure shown in equation (I): In formula (I), A is a cycloalkane group; R a R b R c R d R e R f R g Each can be independently represented as monosubstituted, disubstituted, trisubstituted, tetrasubstituted, or pentasubstituted; R a -R g Each can be independently represented as hydrogen, deuterium, C1–C30 alkyl, C1–C30 deuterated alkyl, C3–C30 cycloalkyl, substituted or unsubstituted C6–C60 aryl; when substituted, the substituent can be selected from one or more of deuterium, C1–C14 alkyl, C6–C60 aryl; the hydrogen atom in formula (I) can be partially or completely substituted with deuterium. The tetradentate ring platinum(II) complex according to claim 1 is characterized in that, R f It may be selected from one or a combination of methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, sec-pentyl, tert-pentyl, n-hexyl, isohexyl, sec-hexyl, tert-hexyl, n-heptyl, isoheptyl, sec-heptyl, tert-heptyl, n-octyl, isooctyl, sec-octyl, tert-octyl, n-nonyl, isononyl, sec-nonyl, tert-nonyl, n-decyl, isodel, sec-decyl, tert-decyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, adamantyl, phenyl, indene, and tert-butyl-substituted phenyl groups. The tetradentate ring platinum(II) complex according to claim 1 is characterized in that, The R d It may be selected from one or a combination of hydrogen, deuterium, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, sec-pentyl, tert-pentyl, n-hexyl, isohexyl, sec-hexyl, tert-hexyl, n-heptyl, isoheptyl, sec-heptyl, tert-heptyl, n-octyl, isooctyl, sec-octyl, tert-octyl, n-nonyl, isononyl, sec-nonyl, tert-nonyl, n-decyl, isodel, sec-decyl, tert-decyl, adamantyl, C1-C10 alkyl-substituted or unsubstituted phenyl groups. The tetradentate ring platinum(II) complex according to claim 1 is characterized in that, The platinum(II) complex has the general formula structure shown in formula (Ii) or formula (I-ii): The tetradentate ring platinum(II) complex according to claim 1 is characterized in that, The platinum(II) complex is selected from any of the following chemical structures, where "D" represents deuterium: The use of the platinum(II) complex according to any one of claims 1-5 in the preparation of electronic devices. The application according to claim 6 is characterized in that, The electronic devices include one or more of the following: organic electroluminescent devices, organic optoelectronic devices, organic integrated circuits, organic field-effect transistors, organic thin-film transistors, organic light-emitting transistors, organic solar cells, organic optical detectors, organic photosensors, organic field quenching devices, luminescent electrochemical cells, or organic laser diodes. An organic electroluminescent device, characterized in that, The organic electroluminescent device comprises a cathode, an anode, and an organic functional layer between the two; the organic functional layer comprises the platinum(II) complex according to any one of claims 1-5. The organic electroluminescent device according to claim 8 is characterized in that, The organic functional layer further comprises a light-emitting layer, wherein the light-emitting layer contains the platinum(II) complex according to any one of claims 1-5. An organic optoelectronic device, characterized in that, The organic optoelectronic device comprises: a substrate layer; a first electrode on the substrate; an organic light-emitting functional layer on the first electrode; and a second electrode on the organic light-emitting functional layer; wherein the organic light-emitting functional layer comprises a platinum(II) complex as described in any one of claims 1-5. A composition, characterized in that, The composition comprises the platinum(II) complex according to any one of claims 1-5. A formulation, characterized in that, The formulation comprises the platinum(II) complex according to any one of claims 1-5. A display or lighting device, characterized in that, The device comprises one or more of the organic electroluminescent device of claim 8 or the organic optoelectronic device of claim 10.

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