128 results about "Rhodamine" patented technology

The invention discloses an ether chain modified rhodamine fluorescent dye, an ether chain modified rhodamine fluorescent dye probe and a preparation method and application thereof, through modification of an ether chain, the water solubility of the rhodamine dye is improved, the aggregation quenching effect is reduced, meanwhile, the intramolecular torsional charge transfer (TICT) is reduced through the electron withdrawing effect of oxygen atoms, and the fluorescence sensitivity is improved. Finally, the quantum yield of the rhodamine dye is greatly improved. The quantum yield of ether chain modified oxygen rhodamine water is increased from 0.31 to 0.70, and the quantum yield of silicon-based rhodamine water is increased from 0.19 to 0.41. The rhodamine dye disclosed by the invention has the characteristics of high brightness, easiness in functional derivation and the like, and has application prospects in the fields of fluorescent probes, fluorescent labels, super-resolution fluorescence imaging and the like.

The structural formula of the oxygen-rhodamine near-infrared fluorescent dye is shown as a formula (a) or a formula (b), and R1 and R2 are respectively selected from hydrogen, alkyl or alkenyl; r3 and R4 are respectively selected from hydrogen, alkyl and alkenyl; r5-R9 are respectively selected from hydrogen, alkyl, methoxyl, ethyoxyl, halogen, carboxyl, sulfonic acid group, ethylene glycol group, hydroxyl or amino, and N is an integer greater than or equal to 0. The invention also discloses a preparation method and application of the fluorescent dye. The compound is novel in structure, excellent in performance, simple in preparation method and good in product application prospect.

The invention relates to an amorphous bismuth molybdate photocatalytic material as well as a preparation method and application thereof, and belongs to the technical field of photocatalytic materials. The preparation method of the amorphous bismuth molybdate photocatalytic material comprises the following steps: (1) dissolving Bi (NO3) 3.5 H2O in an HAC solution, uniformly mixing and stirring at room temperature, and marking as a solution A; dissolving Na2MoO4 in water, adding a water-soluble anionic polymer, uniformly stirring, and marking as a solution B; and (2) slowly dropwise adding the solution B into the solution A, carrying out a co-precipitation reaction under the conditions of normal temperature and normal pressure, after dropwise adding is completed, maintaining heating and stirring for a period of time, then carrying out normal-temperature stirring, and after stirring is completed, carrying out centrifugation, washing and drying to obtain the amorphous bismuth molybdate photocatalytic material A-Bi2MoO6. The modified amorphous A-Bi2MoO6 provided by the invention has a relatively large specific surface area and more mesoporous structures, so that the adsorption of rhodamine B is enhanced, and the adsorbed dye can be efficiently catalyzed and degraded under the action of illumination.

The application provides a cucurbituril fluorescent probe and a preparation method and application thereof, and a qualitative and quantitative detection method of melamine, and belongs to the field of substance detection. The application provides a cucurbituril fluorescent probe, which comprises cucurbit[8]uril (CB[8]) and rhodamine, and the rhodamine is included in the cavity of the cucurbit[8]uril. The application contains the rhodamine in the cavity of CB[8] through host-guest non-covalent interaction, and aims at detecting melamine; the probe has high sensitivity, simple operation and the characteristics of rapid detection.

The present application relates to the field of biological detection, and more particularly to compounds, probes, kits and their applications. The compounds provided by the present application include: modified rhodamine series fluorescent dyes and D-type amino acids, intermediate groups for regulating the luminescence properties of the dyes. Through the optimization of the dye part, we obtain a series of compounds that can be detected in different fluorescent color channels (400-820 nm).

The invention relates to a double-response visual fluorescent probe as well as a construction method and application thereof. According to the present invention, carboxyl activation is performed on rhodamine B, Eu < 3 + > fixes the carboxyl of TAT through bridging and chelation, the Rh B can be combined with EuTAT through the amide reaction due to the steric hindrance effect of the asymmetric amino group to obtain the spirolactam ring so as to obtain the switch fluorescent probe controlled by the spirolactam ring, and the synthesized EuTAT-Rh B compound has characteristics of pH responsiveness and low fluorescence background, according to pH-dependent morphological structure conversion and fluorescence signal conversion caused by conjugate system change induced by vanadate coordination, visual vanadate solution monitoring and synchronous morphological discrimination can be realized in ultraviolet and fluorescence dual channels, and a convenient, simplified and highly sensitive visual platform is provided for visual analysis of vanadate.

According to the method, melamine and urea are used as carbon and nitrogen sources, hollow tubular phosphorus-doped carbon nitride is constructed by adopting a sodium polyphosphate-assisted hydrothermal-thermal polymerization method, molybdenum disulfide is loaded on the surface of P-TCN in a hydrothermal in-situ growth mode, and the hollow tubular phosphorus-doped heterojunction photocatalyst is obtained. The hollow tubular phosphorus-doped heterojunction photocatalyst P-TCN / MoS2 is prepared; the catalyst disclosed by the invention shows excellent degradation performance on ciprofloxacin, levofloxacin, rhodamine B and methylene blue under an illumination condition. The catalyst disclosed by the invention is simple in preparation method, low in cost and easily available in raw materials, and has a wide application prospect in the field of photocatalytic treatment of antibiotic and dye wastewater.

The invention discloses a preparation method and application of a bimetallic nano-enzyme induced MOFs (at) CDs material, and the preparation method at least comprises the following steps: I, dissolving FeCl3, CoCl2 and 2-aminoterephthalic acid in N, N '-dimethylformamide to form a mixed solution I, and carrying out a reaction I to obtain a bimetallic MOFs material; step II, mixing tricarballylic acid and m-phenylenediamine, and carrying out a reaction II to obtain carbon dot powder; step III, dissolving the carbon dot powder obtained in the step II in methanol, and adding rhodamine B dye to obtain a CDs material; and IV, dissolving the bimetallic MOFs material obtained in the step I and the CDs material obtained in the step III in water, stirring, and drying to obtain the MOFs (at) CDs material. The synthesized nano-enzyme is simple to prepare and high in catalytic activity, the carbon dot material is encapsulated into the MOFs material, the fluorescence characteristic of the MOFs material is enhanced, and the carbon dot material is combined with o-phenylenediamine to be used for detecting H2O2.

The present application relates to a kind of electron donor (alpha-trithiophene) modified rhodamine dye, its synthesis method and application.The dye has strong absorption of 500-600 nm, can emit efficiently in 550-700 nm band, suitable for deep tissue imaging.The structure endows mitochondria targeting ability, can be used as biomarker probe to realize subcellular organelle accurate positioning;Meanwhile, under light, it can efficiently produce reactive oxygen species through type I mechanism, suitable for the photodynamic regulation and biosensing for non-disease diagnosis and treatment purposes.In addition, the dye can also be used as organic photocatalyst for environmental or energy-related photocatalytic reaction.The present application provides a new choice for multi-scene optoelectronic functional materials.

The invention discloses a preparation method of a BiOBr / LaNiO3 nanofiber composite photocatalyst, which is characterized in that a perovskite material LaNiO3 prepared by electrostatic spinning is used as a carrier, and BiOBr is loaded on the fiber surface by a solvothermal method to form a heterojunction structure. According to the composite material, separation of photon-generated carriers is promoted through heterojunction of BiOBr and LaNiO3 nanofibers, and the catalytic activity under visible light is remarkably improved. The invention further discloses application of the prepared BiOBr / LaNiO3 nanofiber composite photocatalyst in degradation of rhodamine B. The degradation efficiency of the BiOBr / LaNiO3 nanofiber composite photocatalyst on rhodamine B can reach 93% within 90 min, and after four times of circulation, the composite material shows good circulation stability. The method has the advantages of being low in cost, high in stability, environmentally friendly and the like, and a green solution is provided for organic dye pollution control.

The invention discloses a preparation method and application of a metal-organic dye adsorbent based on sulfonyl calixarene, Ni (II) is used as a metal node, and the metal-organic dye adsorbent is prepared through a solvothermal directional assembly strategy by utilizing the synergistic coordination effect of a dicarboxylic acid ligand 4, 4 '-dithiobisbenzoic acid and p-tert-butylsulfonyl calix [4] arene (H4TBSC). The sulfonyl calixarene-based structure metal-organic dye adsorbent with definite inner and outer cavity partitions is successfully constructed. The adsorption material comprises a central large cavity and two symmetrically distributed peripheral cavities, and the special structure enables the adsorption material to show excellent selective adsorption performance on Congo red (CR) dye molecules. And efficient separation of a Congo red / rhodamine B (RhB) mixed system can be realized through a molecular size screening effect. The invention provides a new thought and method for developing a multifunctional supramolecular adsorption material based on dynamic coordination engineering, and has a wide application prospect in the fields of dye separation and wastewater treatment.

The application relates to the technical field of complex nanomaterials, in particular to a preparation method of an indium complex nanomaterial, the obtained material and application thereof. The application discloses a preparation method of an indium complex nanomaterial, which comprises the following steps: adding inorganic indium salt and 5-bromoisophthalic acid into N,N-dimethylformamide to obtain a transparent reaction liquid; carrying out a solvothermal reaction on the reaction liquid in a reaction kettle; cooling the reaction kettle after the solvothermal reaction, and separating to obtain a solid crude product; washing the solid crude product, drying, and obtaining the indium complex nanomaterial. The application also discloses the indium complex nanomaterial prepared by the above preparation method and application of the indium complex nanomaterial in adsorption of organic dye wastewater. The indium complex nanomaterial prepared by the application has excellent adsorption performance on Congo red dye in a water environment, and also has certain adsorption performance on rhodamine B and methyl orange, and has relatively high practical application value in treatment of organic dye wastewater containing Congo red dye.

The application belongs to the technical field of fluorescent probe, and particularly relates to a near-infrared selenium rhodamine photodynamic photosensitizer as well as a preparation method and application thereof. In order to provide a selenium rhodamine photosensitizer with an excitation light wavelength in a near-infrared region, a selenium rhodamine dye is used as a parent chromophore and an electron acceptor, anthracene is used as an electron donor, and a non-heavy atom photodynamic photosensitizer AN-SeR is designed and synthesized. The photosensitizer exists in a monomer and a J-aggregate in an aqueous solution. The J-aggregate can not only improve the singlet oxygen quantum yield by reducing the energy level gap between the singlet state and the triplet state, but also more importantly expand the excitation light wavelength of AN-SeR from the visible region to the near-infrared region which is more suitable for biological application. Under near-infrared light (650 nm) irradiation, the half lethal concentration of AN-SeR to cancer cells is 0.052 muM, and AN-SeR has potential biological application value.

This invention discloses a GSH-functionalized carbon dots / rhodamine B ratiometric fluorescence system, its construction method, and its application in nitrite detection. GSH-CDs are synthesized via a one-step hydrothermal method by mixing citric acid, o-phenylenediamine, glutathione, and hydrochloric acid in water. Unreacted precursors and small molecules are removed by purification, and the GSH-CDs are obtained by freeze-drying. The ratiometric fluorescence system is constructed by mixing rhodamine B, GSH-CDs, and an acidic buffer solution. The fluorescence intensity ratio F of GSH-CDs to rhodamine B is established. 460 / F 590 With nitrite (NO2) ‑ A calibration curve between concentrations was obtained, and the NO2 in the actual sample was experimentally detected using the spiked recovery method. ‑ Content. Under acidic conditions, with NO2... ‑ With increasing concentration, the GSH-CDs / RhB fluorescence intensity ratio (I 460 / I 590 Significant changes occurred, with the fluorescence intensity ratio compared to NO2. ‑ There is a good linear relationship between concentrations. Compared with the detection platform based on GSH-CDs, the ratio fluorescence system provided by this invention has a lower detection limit and significantly higher sensitivity.

The invention discloses a baijiu detection method based on a colorimetric and fluorescent dual-signal sensing array, and relates to the technical field of substance detection and analysis. According to the detection method, the principle that rhodamine B and rhodamine 6G have remarkable ultraviolet-visible spectrums and fluorescence characteristic peaks, and rhodamine B and rhodamine 6G can be accelerated to be catalytically degraded by MnONSs under the acidic condition is utilized, so that optical signals (colorimetric-fluorescence double signals) of rhodamine B and rhodamine 6G can be adjusted by adjusting the catalytic action of MnONSs; according to the method, a colorimetric and fluorescent dual-signal sensing array is constructed, then the dual-signal sensing array is utilized to form characteristic fingerprints of various Baijiu samples, rapid and accurate detection of Baijiu is achieved, and the method is few in types of detection materials, simple and convenient to operate and more suitable for large-scale popularization and application.

The application relates to the technical field of metal ion detection, in particular to a fluorescent probe for early metal corrosion detection and a preparation method thereof. 35 H 33 N5O3.The application successfully develops a fluorescent small molecule Rhe-M sensitive to Fe 3+ response, which can be used as a fluorescent probe molecule capable of recognizing early corrosion sites of carbon steel, is applied to a surface layer of the carbon steel, and through irradiation of an ultraviolet lamp, corrosion sites and area sizes on the surface of the carbon steel can be directly observed; the method is simple in operation, sensitive in reaction, low in cost, strong in specific recognition ability, and is a high-efficiency method capable of detecting early metal corrosion sites.

The application provides a rhodamine bacterial lipid droplet membrane fluorescent dye and synthesis and application thereof. The fluorescent dye is based on the affinity of a long carbon chain connected to a nitrogen atom of rhodamine to lipids, the affinity of a positively charged open-loop rhodamine to a negative potential lipid membrane, and the enhancement of a benzene ring to TICT to reduce the background of non-lipid droplet membrane sites. A dye (C4, C6, C8) capable of positioning on a bacterial lipid droplet membrane is designed and synthesized, and the structural formula is shown in formula (1), wherein n is 2, 4 or 6. The dye realizes the lipid droplet membrane imaging of Bacillus cereus, Rhodococcus opacus , Rhodococcus jostii RHA1.

This invention discloses a small-molecule pyroptosis inducer for tumor cells. It utilizes an N,N-diethylimine group as an electron acceptor (A), a rhodamine scaffold as a π-conjugated system, thiophene and triphenylamine groups as the first electron donor (D1) and second electron donor (D2), respectively, and a rotatable vinyl and C-C single bond to increase intramolecular motion, forming a novel A-π-D1-D2 type small-molecule pyroptosis inducer, Rd-TTPA, with enhanced D-A structure and intramolecular motion. This small-molecule pyroptosis inducer can efficiently target tumor cell mitochondria, inducing pyroptosis through ultrasound-mediated reactive oxygen species production. It can serve as an enhanced sonodynamic deep tumor therapeutic agent guided by near-infrared II (NIR-II) fluorescence imaging.

The application discloses a CuS / Cu3(MoO4)2(OH)2 composite and a preparation method and application thereof. The CuS / Cu3(MoO4)2(OH)2 composite material is prepared by using CuCl2, Na2MoO4 and Na2S as raw materials and adopting a hydrothermal method. The CuS / Cu3(MoO4)2(OH)2 composite acoustic catalyst provided by the application can be used for ultrasonic catalytic degradation of organic pollutants in cooperation with H2O2. When the ultrasonic power is 500 W and the ultrasonic time is 30 min, the degradation rates of acid orange 7, tetracycline, rhodamine B, congo red, methylene blue and basic red 2 in water can reach 89.6(±5.78)%, 92.91(±0.36)%, 96.93(±0.16)%, 97.73(±0.61)%, 98.53(±0.37)% and 99.87(±0.18)%, respectively.

The application relates to preparation and application of a dye-functionalized rare earth metal organic framework material capable of recognizing sulfur ions: S1, selecting raw materials, terbium nitrate, pyrazine tetramethanic acid, potassium hydroxide and rhodamine B; S2, dissolving the pyrazine tetramethanic acid in distilled water and stirring; S3, adding the Tb(NO3)3.6H2O methanol solution obtained in S2 into the solution, and stirring; S4, adding the KOH solution into the solution obtained in S3, and stirring; S5, standing, centrifugally collecting the white precipitate, and drying after washing to obtain the white rare earth metal organic framework material; S6, immersing the sample in different concentrations of rhodamine B dyes for treatment; S7, collecting the purple red precipitate in S6, and drying to obtain the dye-functionalized rare earth metal organic framework material; and S8, using the obtained dye-functionalized rare earth metal organic framework material for sulfur ion detection. The preparation of the dye-coated rare earth metal organic framework is that the rare earth metal organic framework is coated with different concentrations of rhodamine B dyes, can be used as a ratio type fluorescent probe, and can more sensitively and accurately recognize and detect sulfur ions.

This application discloses a fluorescent probe for labeling the outer membrane of Gram-negative bacteria, its preparation method, and its application. The fluorescent probe uses polymyxin (with its hydrophobic tail and two amino acid residue pairs removed) as a targeting group specifically targeting the outer membrane of Gram-negative bacteria. This structure can specifically bind to the lipopolysaccharide structure in the outer membrane, and is then linked to the fluorophore rhodamine, which has switching properties, to design and synthesize a fluorescent dye. This fluorescent probe, possessing fluorescent switching properties, can be applied to super-resolution imaging of the outer membrane of Gram-negative bacteria.

The application belongs to the technical field of laser, and relates to a method for manufacturing a PVA / dye flexible random laser based on an electrostatic spinning method. A mixed solution of PVA, ovalbumin, rhodamine dye and Au nano-particles is adopted, the sample size and the morphology of the spinning structure are controlled by controlling the voltage, the spraying distance and the needle tip size in the electrostatic spinning technology process, and then the wavelength and the mode of laser emission and other parameters are adjusted. The design is simple and intuitive, the method is flexible and convenient, the principle is reliable, and the method is easy to realize. The obtained flexible random laser is easy to be coupled with other photon devices, and the quantitative control of the laser property is easy to be realized.

The invention relates to the technical field of photocatalytic materials, and particularly discloses an efficient FRET-ISC synergistic composite photosensitive nano material based on aggregation-induced emission (AIE) matrix coating, a preparation method of the nano material and application of the nano material in photocatalytic degradation of organic pollutants. The material comprises an AIE characteristic matrix (such as tetraphenylethylene), an energy donor dye (such as coumarin 6) dispersed in the matrix and an energy acceptor dye (such as iodo-boron dipyrromethene) with a heavy atom effect, a donor emission spectrum and an acceptor absorption spectrum are overlapped, so that the synergistic effect of fluorescence resonance energy transfer and intersystem crossing (FRET-ISC) is realized, and the fluorescence intensity of the material is improved. The generation efficiency of singlet oxygen (1O2) is obviously improved. The material is prepared by adopting a microfluidic anti-solvent precipitation method, water-phase dispersed nano-particles (the particle size is 100-400 nm) are formed, the singlet oxygen quantum yield of the material reaches 0.75, the degradation rate constant (0.025 min <-1 >) of the material to rhodamine B is 4.3 times that of a single IBDP system, the degradation rate in 2 hours exceeds 90%, and the activity is kept above 80% after the material is recycled for 5 times. The invention solves the problems of aggregation quenching (ACQ) and narrow spectrum utilization of the traditional photosensitizer, has high stability, wide spectrum response and efficient catalytic ability, and is suitable for degrading organic pollutants (such as RhB, methylene blue and tetracycline) in a water phase.

The invention discloses a preparation method of a water-resistant biomass-based long-afterglow phosphorescent material as well as a product and application of the water-resistant biomass-based long-afterglow phosphorescent material, and belongs to the technical field of functional materials. The preparation method comprises the following steps: taking lignin (soluble components subjected to ethanol grading treatment) and urea as raw materials, dissolving the raw materials in deionized water according to a specific proportion, adjusting the pH value to be alkaline, and carrying out microwave heating to obtain the product. Rhodamine B is added to prepare the red afterglow material. The product shows blue, green and red afterglow under excitation of different ultraviolet lights, and has long afterglow life and excellent water resistance through a hydrogen bond network and a chemical crosslinking structure formed by cyanuric acid. The material is simple and convenient to prepare, low in cost and sustainable, can be applied to the fields of anti-counterfeiting identification, information encryption storage and the like, and can also be compounded with guar gum to be used for 3D printing functional components.

The invention discloses a fluorescent material and a preparation method and application thereof, and the preparation method of the fluorescent material specifically comprises the following steps: S1, dissolving 4-aminotetraphenyl ethylene and rhodamine aldehyde derivatives in ethanol; s2, heating to 50-90 DEG C, and carrying out reflux reaction for 10-20 hours; after the reaction is finished, filtering to obtain residues; s3, recrystallizing the residues to obtain the reddish brown fluorescent material.The defects in the prior art are overcome, a fluorescent material probe of a novel structure is prepared, and the preparation method of the fluorescent material is simple and low in cost; and the prepared fluorescent material probe can realize ratio type detection of tin ions, and is good in selectivity and low in detection limit.

This invention belongs to the field of nanofiltration membrane technology, and particularly relates to a polyamide nanofiltration membrane, its preparation method, and its application. The polyamide nanofiltration membrane provided by this invention includes an ultrafiltration membrane and a polyamide selective layer attached to the ultrafiltration membrane. The polyamide selective layer is formed by a polycondensation reaction of a fully amino columnar aromatic hydrocarbon [5] and 1,3,5-benzenetricarboxyl chloride. The polyamide nanofiltration membrane of this invention can separate organic micropollutants such as Congo red, Rhodamine B, methylene blue, and methyl orange dyes, with a rejection rate of more than 95%. It also has good separation performance for some inorganic salts, with a rejection rate of more than 50%. The polyamide nanofiltration membrane of this invention can adapt to some harsh acid and alkali environments while maintaining excellent rejection performance. The polyamide nanofiltration membrane provided by this invention also has excellent antifouling performance.

The invention discloses a green hydro-thermal synthesis method of a functionalized silver nano-material, and the preparation method comprises a preparation method of a functionalized silver nano-colloid prepared from a sorbus pohuashanensis fruit extract and a preparation method of functionalized nano-silver solid powder. The invention discloses the green hydro-thermal synthesis method of the functionalized silver nano-material. The spherical nano-silver can stably suspend in a colloidal solution, and the material has the bacteriostatic effect (escherichia coli, staphylococcus aureus and candida albicans) and the effect of rapidly removing methylene blue and rhodamine B dye in water. The nano-silver material is spherical, the particle size of the nano-silver material ranges from 14 nm to 70 nm, and the average particle size of the nano-silver material is 36 nm. The sorbus pohuashanensis fruit extract attached and modified in the nano material accounts for nearly 7.0% of the total mass of the nano material. The green hydrothermal synthesis method is high in safety coefficient, convenient and rapid in operation process, small in pollution or free of pollution and high in repeatability, and the method has application and development potential.

The application discloses a preparation method of full-color laser carbon dots based on rhodamine B derivation, which comprises the following steps: ultrasonic dispersion of rhodamine B in a liquid solvent, continuous heating in an autoclave, and preparation of green, yellow, red and near-infrared light carbon dots after filtration, elution, purification and freeze-drying; when rhodamine B is mixed with NaOH or KOH solid, heating is carried out in a beaker to prepare blue light carbon dots; in the application, rhodamine B is used as a precursor, and the carbon dots are synthesized by a solvothermal method; the excellent gain performance of rhodamine B is expanded from orange and red to the whole visible light and near-infrared light region; even the emission effect can be enhanced through cross-linking; the gain performance of the carbon dots is higher than that of rhodamine B, and the carbon dots have higher fluorescence quantum yield, higher radiation transition rate, lower laser threshold and more excellent laser stability.

This invention relates to the field of optical sensing and imaging detection technology, specifically to a triphenylene-oxanthracene derivative, its preparation method, and a fluorescent probe for viscosity detection. The triphenylene-oxanthracene derivative has the general formula shown in Formula I. Compared to Rhodamine B, the synthesized triphenylene-oxanthracene derivative exhibits a larger Stokes shift. Furthermore, the fluorescence intensity of the triphenylene-oxanthracene derivative increases with increasing cell viscosity. In addition, the triphenylene-oxanthracene derivative can be further used to detect mitochondrial viscosity, exhibiting good mitochondrial targeting. In summary, the probe improves the Stokes shift, has a wide optical response pH range, and possesses excellent mitochondrial targeting.