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72 results about "Naphthalocyanine" patented technology

Naphthalocyanine is a cross-shaped organic molecule consisting of 48 carbon, 8 nitrogen and 26 hydrogen atoms, it is a derivative of phthalocyanine. IBM Research labs used it for developing single-molecule logic switches and visualizing charge distribution in a single molecule.

Novel Fluorinated silicon (IV) phthalocyanines and naphthalocyanines for electrophoretic, magnetophoretic or electromagnetophoretic display

This invention relates to stable colorants of high extinction coefficient and high solubility or dispersibility for an electrophoretic, magnetophoretic or electromagnetophoretic display. More particularly, it relates to stable colorants for a microcup-based electrophoretic or electromagnetophoretic display the cells of which are filled with charged and / or magnetic particles dispersed in a halogenated, preferably a fluorinated, solvent. The use of the stable colorants allows the display to be of superior contrast ratio and longevity, and suitable for high-quality imagery applications.
Owner:SIPIX IMAGING INC

Ink formulations comprising gallium naphthalocyanines

There is provided an aqueous formulation comprising an IR-absorbing naphthalocyanine dye of formula (II):or a salt form thereof, wherein:M is Ga(A1);A1 is an axial ligand selected from —OH, halogen, —OR3, —OC(O)R4 or —O(CH2CH2O)eRe wherein e is an integer from 2 to 10 and Re is H, C1-8 alkyl or C(O)C1-8 alkyl;R1 and R2 may be the same or different and are selected from hydrogen or C1-12 alkoxy;R3 is selected from C1-12 alkyl, C5-12 aryl, C5-12 arylalkyl or Si(Rx)(Ry)(Rz);R4 is selected from C1-12 alkyl, C5-12 aryl or C5-12 arylalkyl; andRx, Ry and Rz may be the same or different and are selected from C1-12 alkyl, C5-12 aryl, C5-12 arylalkyl, C1-12 alkoxy, C5-12 aryloxy or C5-12 arylalkoxy;The formulation has a pH in the range of 3.5 to 7 and is particularly suitable for use as an IR-absorbing inkjet ink, providing compatibility with known CMYK inks together with an optimally red-shifted λmax.
Owner:BASF AG

Compositions, systems, and methods for imaging

A composition, method, and system for recording an image. The system includes an imaging material in which radiation energy is absorbed by an antenna material. The antenna material may be chosen from the group consisting of phthalocyanines and naphthalocyanines.
Owner:HEWLETT PACKARD DEV CO LP

Flame retardant compositions for flammable plastics and flame retarded plastic compositions containing the same

A flame retardant composition for rendering flammable plastics flame retardant is provided. The composition comprises a brominated flame retardant, a free-radical generator selected from 2,3-dimethyl-2,3-diphenylbutane or its homologs, and a phthalocyanine or naphthalocyanine complex with a metal of groups 7 to group 10 of the IUPAC periodic chart. The quantity of the brominated flame retardant may be saved when incorporating into flammable plastic materials in conjunct with the free-radical generator and the phathalocyanine or naphthalocyanine complex of the above type.
Owner:DAI ICHI KOGYO SEIYAKU CO LTD

Solar control laminates

Provided is a solar control composition comprising an infrared absorbing phthalocyanine, naphthalocyanine or rylene compound and an ethylene acid copolymer or an ionomer of an ethylene acid copolymer. Further provided are solar control laminates comprising the solar control composition of the invention.
Owner:DOW GLOBAL TECH LLC

Gallium naphthalocyanine salts for use as improved infrared dyes

There is provided an IR-absorbing naphthalocyanine dye of formula (I):whereinM is Ga(A1);A1 is an axial ligand selected from —OH, halogen, —OR3, —OC(O)R4 or —O(CH2CH2O)eRe wherein e is an integer from 2 to 10 and Re is H, C1-8 alkyl or C(O)C1-8 alkyl;R1 and R2 may be the same or different and are selected from hydrogen or C1-12 alkoxy;R3 is selected from C1-12 alkyl, C5-12 aryl, C5-12 arylalkyl or Si(Rx)(Ry)(Rz);R4 is selected from C1-12 alkyl, C5-12 aryl or C5-12 arylalkyl;Rx, Ry and Rz may be the same or different and are selected from C1-12 alkyl, C5-12 aryl, C5-12 arylalkyl, C1-12 alkoxy, C5-12 aryloxy or C5-12 arylalkoxy; andeach B is independently selected from a base, wherein BH+ has a pKa of between 4 and 9.The dye is particularly suitable for use in IR-absorbing inkjet inks, providing compatibility with known CMYK inks together with an optimally red-shifted λmax.
Owner:BASF AG

Synthetically expedient water-dispersible IR dyes having improved lightfastness

The present invention provides an IR-absorbing naphthalocyanine dye of formula (I): wherein M is selected from Ga(A1); A1 is an axial ligand selected from —OH, halogen (preferably Cl), —OR3, a hydrophilic ligand and / or a ligand suitable for reducing cofacial interactions; R1 and R2 may be the same or different and are selected from hydrogen or C1-12 alkoxy (preferably C1-6 alkoxy); R3 is selected from C1-12 alkyl, C5-12 aryl, C5-12 arylalkyl or Si(Rx)(Ry)(Rz); and Rx, Ry and Rz may be the same or different and are selected from C1-12 alkyl, C5-12 aryl, C5-12 arylalkyl, C1-12 alkoxy, C5-12 aryloxy or C5-12 arylalkoxy; W is a hydrophilic group; n1 is 0, 1, 2 or 3; n2 is 0, 1, 2 or 3; n3 is 0, 1, 2 or 3; n4 is 0, 1, 2 or 3; provided that at least one of n1, n2, n3 or n4 is greater than 0. Dyes of this type are especially suitable for use in netpage and Hyperlabel™ systems.
Owner:BASF AG

Method of preparing naphthalocyanines

A method of preparing a naphthalocyanine is provided. The method comprises the steps of: (i) providing a tetrahydronaphthalic anhydride; (ii) converting said tetrahydronaphthalic anhydride to a benzisoindolenine; and (iii) macrocyclizing said benzisoindolenine to form a naphthalocyanine.
Owner:BASF AG

Inkjet lnks for printing coded data comprising naphthalocyanine dyes

The present invention provides an inkjet ink comprising an IR-absorbing naphthalocyanine dye of formula (I): wherein M is selected from Si(A1)(A2), Ge(A1)(A2), Ga(A1), Mg, Al(A1), TiO, Ti(A1)(A2), ZrO, Zr(A1)(A2), VO, V(A1)(A2), Mn, Mn(A1), Fe, Fe(A1), Co, Ni, Cu, Zn, Sn, Sn(A1)(A2), Pb, Pb(A1)(A2), Pd and Pt; A1 and A2 are axial ligands, which may be the same or different, and are selected from —OH, halogen or —OR3; R1 and R2 are selected from H or C1-12 alkoxy; R3 is selected from C1-12 alkyl, C5-12 aryl, C5-12 arylalkyl or Si(Rx)(Ry)(Rz); and Rx, Ry and Rz may be the same or different and are selected from C1-12 alkyl, C5-12 aryl, C5-12 arylalkyl, C1-12 alkoxy, C5-12 aryloxy or C5-12 arylalkoxy; W is selected from a sulfonic acid group (including salts thereof) or a sulfonamide group; n1 is 0, 1, 2 or 3; n2 is 0, 1, 2 or 3; n3 is 0, 1, 2 or 3; n4 is 0, 1, 2 or 3; provided that at least one of n1, n2, n3 or n4 is greater than 0. Inks of this type are especially suitable for use in netpage and Hyperlabel systems.
Owner:BASF SE

Inkjet ink comprising gallium naphthalocyanine dye

There is provided an inkjet ink comprising an IR-absorbing dye of formula (I): wherein M is Ga(A1); A1 is an axial ligand selected from —OH, halogen, —OR3, —OC(O)R4, a hydrophilic ligand and / or a ligand suitable for reducing cofacial interactions; R1 and R2 may be the same or different and are selected from hydrogen or C1-12 alkoxy; R3 is selected from C1-12 alkyl, C5-12 aryl, C5-12 arylalkyl or Si(Rx)(Ry)(Rz); and R4 is selected from C1-12 alkyl, C5-12 aryl or C5-12 arylalkyl Rx, Ry and Rz may be the same or different and are selected from C1-12 alkyl, C5-12 aryl, C5-12 arylalkyl, C1-12 alkoxy, C5-12 aryloxy or C5-12 arylalkoxy; W is a hydrophilic group, each W group being independently selected from a substituent comprising a sulfonic acid group (including salts thereof), or a substituent comprising a sulfonamide group; n1 is 0, 1, 2 or 3; n2 is 0, 2, or 3; n3 is 0, 1, 2 or 3; n4 is 0, 1, 2 or 3; provided that at least one of n1, n2, n3 or n4 is greater than 0. Such inks are suitable for use in netpage, Hyperlabel and other applications.
Owner:BASF AG

Ink comprising gallium naphthalocyanine dye

An ink comprising an IR-absorbing naphthalocyanine dye of formula (I) is described: Wherein M is Ga(A1); A1 is an axial ligand selected from —OH, halogen, —OR3, —OC(O)R4; R1 and R2 may be the same or different and are selected from hydrogen or C1-12 alkoxy; R3 is selected from C1-12 alkyl, C5-12 aryl, C5-12 arylalkyl or Si(Rx)(Ry)(Rz); and R4 is selected from C1-12 alkyl, C5-12 aryl or C5-12 arylalkyl Rx, Ry and Rz may be the same or different and are selected from C1-12 alkyl, C5-12 aryl, C5-12 arylalkyl, C1-12 alkoxy, C5-12 aryloxy or C5-12 arylalkoxy; and W is a sulfonic acid group, including salts thereof.
Owner:BASF AG

Solar control laminates

Provided is a solar control composition comprising an infrared absorbing phthalocyanine compound or naphthalocyanine compound and a resin having a modulus from 20,000 psi (138 MPa) to 1000 psi (7 MPa) and solar control laminates comprising the solar control composition of the invention.
Owner:EI DU PONT DE NEMOURS & CO

Naphthalocyanine dye and ink containing the same

The present disclosure includes naphthalocyanine dyes or fused naphthalocyanine dyes represented by one of the general structures I to XV; inkjet ink formulations including the naphthalocyanine dyes; and a detection system (300) including the dyes.
Owner:HEWLETT PACKARD DEV CO LP

Organic semiconducting material, and film, organic electronic device and infrared dye composition each including said material

An organic semiconducting material comprises a naphthalocyanine derivative represented by formula (1);wherein M represents Si, Ge or Sn, R1 to R3 represent substituents other than a hydrogen atom except that all of R1 to R3 are identical straight-chain alkyl groups, and R4 to R27 each independently represents a hydrogen atom or a substituent.
Owner:FUJIFILM CORP

Solid naphthalocyanine device with optical limiting properties

ActiveCN101561614AOvercoming fragileOvercome the defect of poor laser resistanceNon-linear opticsInorganic compoundElectron
The invention relates to a solid naphthalocyanine device with excellent optical limiting properties. The device is made by the following steps: adding tetraethoxysilane, diglycidyl ether propyltrimethoxy siloxane, analytically pure ethanol and acidic aqueous solution to a reactor; stirring in an enclosed reactor for 2-3h, then opening the reactor and continuing stirring for 1-2h; adding a naphthalocyanine solution and stirring to cause the mixture to become viscous; transferring the viscous mixture to a mould, and taking out after drying to obtain the novel solid naphthalocyanine device with optical limiting properties. The device is made by an organosilicon modification method combined with doped inorganic salt, and by doping naphthalocyanine with a larger pi electron conjugated system to form a continuous random network system with bonded chemical bonds of organic components and inorganic components instead of physical hybrid. The device has good laser resistance and excellent optical limiting properties.
Owner:INST OF CHEM CHINESE ACAD OF SCI

Solar control laminates

Provided is a solar control composition comprising an infrared absorbing phthalocyanine compound or naphthalocyanine compound and a resin having a modulus from 20,000 psi (138 MPa) to 1000 psi (7 MPa) and solar control laminates comprising the solar control composition of the invention.
Owner:WALL JASON S +4

Particles and contrast agent including the same for optical imaging

A particle includes a copolymer of lactic acid and glycolic acid, and at least one compound selected from silicon naphthalocyanine and derivatives of silicon naphthalocyanine, in which the particle has a particle size of 10 nm or more and less than 1000 nm.
Owner:CANON KK

Synthetically expedient water-dispersible IR dyes

The present invention provides an IR-absorbing naphthalocyanine dye of formula (I): wherein M is selected from Si(A1)(A2), Ge(A1)(A2), Ga(A1), Mg, Al(A1), TiO, Ti(A1)(A2), ZrO, Zr(A1)(A2), VO, V(A1)(A2), Mn, Mn(A1), Fe, Fe(A1), Co, Ni, Cu, Zn, Sn, Sn(A1)(A2), Pb, Pb(A1)(A2), Pd and Pt; A1 and A2 are axial ligands, which may be the same or different, and are selected from —OH, halogen, —OR3, a hydrophilic ligand and / or a ligand suitable for reducing cofacial interactions; R1 and R2 are selected from H or C1-12alkoxy; R3 is selected from C1-12alkyl, C5-12aryl, C5-12arylalkyl or Si(Rx)(Ry)(Rz); and Rx, Ry and Rz may be the same or different and are selected from C1-12alkyl, C5-12aryl, C5-12arylalkyl, C1-12alkoxy, C5-12aryloxy or C5-12arylalkoxy; W is a hydrophilic group; n1 is 0, 1, 2 or 3; n2 is 0, 1, 2 or 3; n3 is 0, 1, 2 or 3; n4 is 0, 1, 2 or 3; provided that at least one of n1, n2, n3 or n4 is greater than 0. Dyes of this type are especially suitable for use in netpage and Hyperlabel systems.
Owner:BASF AG

Water-soluble naphthalocyanine base compound, preparation method and application of compound as photosensitizer

The invention relates to a water-soluble naphthalocyanine base compound, a preparation method and an application of the compound as a photosensitizer. A structural formula of the compound is as Formula (I) as shown in the specification. The compound is a carboxylic acid base modified water-soluble naphthalocyanine metal complex, has a good singlet oxygen occurrence rate, low cell photophobic toxicity, and excellent phototoxicity under irradiation, and can serve as a near-infrared PDT (Photodynamic Therapy) photosensitizer. The invention also provides a preparation method of the compound. The preparation method is simple in technology and wide in application scope.
Owner:SHANDONG UNIV

Composition comprising photosensitive compound in polymeric nanoparticle, and method of using composition

Embodiments of a composition comprising a photosensitive compound and a polymer nanoparticle are disclosed herein. The composition may further comprise a targeting moiety. In some embodiments, the photosensitive compound is a phthalocyanine or phthalocyanine derivative, such as a naphthalocyanine. Upon irradiation with near infrared light, the composition may be used as a fluorescent imaging agentand / or as a phototherapeutic agent, such as for photodynamic and / or photothermal therapies. In certain embodiments, the composition is used to treat certain cancers.
Owner:THE STATE OF OREGON ACTING BY & THROUGH THE OREGON STATE BOARD OF HIGHER EDUCATION ON BEHALF OF OREGON STATE UNIV

Azobenzene phi-phi stacked graphene photoresponse material and preparation method thereof

ActiveCN102593360AFast Light Response CapabilityEasy to adjust electrical propertiesFinal product manufactureSolid-state devicesIndiumElectric properties
The invention discloses an azobenzene phi-phi stacked graphene photoresponse material and a preparation method thereof. The phoresponse material is produced by stacking azobenzene 5, 9, 14, 18, 23, 27, 32, 36- octabutoxy-2,3-copper naphthalocyanine. The preparation process comprises the following steps that: the well-prepared oxidized graphene solution is sprayed onto tin indium oxide glass to be thermally treated under the temperature of 120 DEG C, and then hydrazine solution with mass fraction of 80 percent is used for reducing the tin indium oxide glass coated with the oxidized graphene; and then the tin indium oxide glass coated with the reduced graphene is soaked in mixed solution of azobenzene and chloroform, which are uniformly dispersed to prepare the photoresponose material. The prepared azobenzene phi-phi stacked graphene photoresponse material has advantages of easiness in controlling optical properties and electric properties, fast photoelectric conversion speed, apparent photoelectric conversion, simple production process and the like.
Owner:TIANJIN UNIV

Photobleaching compositions effective on dingy fabric

Photosensitizing compounds suitable for use as laundry detergent photobleaches are disclosed. The disclosed compounds are phthalocyanine and naphthalocyanines comprising axial moieties selected for their hydrophobic character as measured by their ClogP. Also disclosed are methods for bleaching fabrics and methods for disinfecting hard surfaces.
Owner:CASE WESTERN RESERVE UNIV

Method of proving authenticity, signal conversion method, polymer welding method, method of producing lithographic printing plate, ink for printing, toner, and heat ray-shielding material, each using naphthalocyanine compound, and method of producing naphthalocyanine compound

InactiveUS20110311911A1Improve infrared absorption efficiencyHigh yieldOrganic chemistryReactive dyesHydrogen atomNaphthalocyanine
Disclosed is a method of proving the authenticity of goods or a support comprising using a compound represented by Formula (I).wherein, in Formula (I), each of R11 to R46 independently represents a hydrogen atom or a substituent group, wherein when a benzene ring is substituted with any of R11 to R46, any groups adjacent to each other among R11 to R46 may be bonded each other to form a ring; M represents a hydrogen atom, a metal ion, or a group containing a metal ion; and n represents 1 or 2. The infrared absorption efficiency is high and the deterioration in infrared absorption over time is ameliorated. The infrared absorption efficiency is high and the deterioration in infrared absorption over time is ameliorated.
Owner:FUJIFILM CORP
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