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44 results about "Cyanomethylidyne" patented technology

Cyanomethylidyne; dicyanomethylene; from MeSH. Depositor-Supplied Synonyms. Chemical names and identifiers provided by individual data contributors and associated to PubChem Substance records. Synonyms of Substances corresponding to a PubChem Compound record are combined.

Imaging members

A member including, for example, a supporting layer and a single photogenerating layer, the photogenerating layer comprising particles including hydroxygallium phthalocyanine phthalocyanine Type V, x polymorph metal free phthalocyanine, or chlorogallium phthalocyanine dispersed in a matrix comprising an arylamine hole transporter and an electron transporter selected from the group consisting of N,N'bis(1,2-dimethylpropyl)-1,4,5,8-naphthalenetetracarboxylic diimide, 1,1'-dioxo-2-(4-methylphenyl)-6-phenyl-4-(dicyanomethylidene)thiopyran, and a quinone selected from the group consisting of carboxybenzylhaphthaquinone, and tetra (t-butyl) diphenoquinone, and mixtures thereof, and submicrometer size polytetrafluroethylene particles, and a film forming binder.
Owner:XEROX CORP

Binaphthol-based aggregation-induced light-emitting chiral fluorescent material

InactiveCN105154068AImprove solubilityAberrant aggregation-induced quenching of CD signalsCarboxylic acid nitrile preparationOrganic compound preparationSolubilityOrganic solvent
The invention discloses a binaphthol-based aggregation-induced light-emitting chiral fluorescent material. The fluorescent material is prepared through simple condensation reaction carried out by taking chiral binaphthol with any structure as a framework and dicyanomethylidene as an electron acceptor. The fluorescent material disclosed by the invention has favorable solubility in a common organic solvent, is hardly dissolved into water, not only has aggregation-induced light-emitting property, but also shows an abnormal aggregation-induced CD signal quenching phenomenon so as to provide a new approach for constructing a binaphthol-based chiral sensor.
Owner:SHAANXI NORMAL UNIV

Preparation method of baricitinib

The invention discloses a preparation method of baricitinib. The method comprises the following steps: performing a substitution reaction on 4-chloro-7H-pyrrolo[2,3-d]pyrimidine (II) serving as a raw material and benzene sulfonyl chloride in the presence of an alkali to obtain an intermediate III; then, performing a Suzuki coupling reaction on the intermediate III and 4-pyrazole-4-boronic acid pinacol ester in the presence of a palladium catalytic system and an alkali to obtain an intermediate V; then performing a Michael addition reaction on the intermediate V and 3-(cyanomethylene)azetidine-1-tert-butyl formate in the presence of a catalyst to obtain an intermediate VII; then removing Boc protection from the intermediate VII under the action of hydrochloric acid to obtain an intermediate VIII; then performing a sulfoamidate reaction on the intermediate VIII and ethyl sulfonyl chloride in an organic solvent in the presence of an alkali to obtain an intermediate IX; lastly, removing benzenesulfonyl protection from the intermediate IX under the action of tetramethylammonium fluoride or tetrabutylammonium fluoride or a trihydrate of the tetramethylammonium fluoride or the tetrabutylammonium fluoride to obtain baricitinib (I). Compared with the prior art, the method has the advantages of adoption of readily-available raw materials, low cost, high product yield and easiness for industrial production.
Owner:NANJING YOKO PHARMA +2

Dicyanomethylene-4H-pyran derivatives as well as preparation method and application thereof

The invention particularly relates to dicyanomethylene-4H-pyran derivatives as well as a preparation method and an application thereof. The preparation method of the dicyanomethylene-4H-pyran derivatives comprises the following steps: (1) 2,6-dimethyl-4H-pyran-4-one 1 as a starting material is subjected to an addition-elimination reaction with malononitrile, and an intermediate 2 is obtained; (2) the intermediate 2 is subjected to an addition-elimination reaction with indolal with different alkyl chains, and the dicyanomethylene-4H-pyran derivatives are obtained. Indole structural units with different alkyl groups and dicyanomethylene-4H-pyran structural units are introduced into the field of organic solid luminescent materials, novel piezoluminescence color change materials are developed, and the derivatives play an important role in the field of photoelectricity. The provided method adopts a simple synthesis process, purification is easy, and the synthesized piezoluminescence materials are quite applicable to various fields of preparation of pressure sensors, anti-counterfeiting trademarks and the like and have good scientific research value and industrialized application potential.
Owner:WENZHOU UNIVERSITY

Substituted 1,2,3-triylidenetris(cyanomethanylylidene)) cyclopropanes for vte, electronic devices and semiconducting materials using them

InactiveCN107207420AApplicable industrial scaleOrganic chemistrySolid-state devicesDopantAryl
The present invention relates to a process for preparation of an electrically doped semiconducting material comprising a [3]-radialene p-dopant or for preparation of an electronic device containing a layer comprising a [3]-radialene p-dopant, the process comprising the steps : (i) loading an evaporation source with the [3]-radialene p-dopant; and (ii) evaporating the [3]-radialene p-dopant at an elevated temperature and at a reduced pressure, wherein the [3]-radialene p-dopant is selected from compounds having a structure according to formula (I) wherein A1 and A2 are independently aryl- or heteroaryl- substituted cyanomethylidene groups, the aryl and / or heteroaryl is selected independently in A1 and A2 from 4-cyano-2,3,5,6-tetrafluorphenyl,2,3,5,6-tetrafluorpyridine-4-yl, 4-trifluormethyl-2,3,5,6-tetrafluorphenyl, 2,4-bis(trifluormethyl)-3,5,6-trifluorphenyl, 2,5-bis(trifluormethyl)-3,4,6-trifluorphenyl, 2,4,6-tris(trifluormethyl)-1,3-diazine-5-yl, 3,4-dicyano-2,5,6-trifluorphenyl, 2-cyano-3,5,6-trifluorpyridine-4-yl, 2-trifluormethyl-3,5,6-trifluorpyridine-4-yl, 2,5,6-trifluor-1,3-diazine-4-yl and 3-trifluormethyl-4-cyano-2,5,6-trifluophenyl), and at least one aryl or heteroaryl is 2,3,5,6-tetrafluorpirydine-4-yl, 2,4-bis(trifluormethyl)-3,5,6-trifluorphenyI, 2,5-bis(trifluormethyl)-3,4,6-trifluorphenyl, 2,4,6-tris(trifluormethyl)-1,3-diazine-5-yl, 3,4-dicyano-2,5,6-trifluorphenyl, 2-cyano-3,5,6-trifluorpyridine-4-yl, 2-trifluormethyl-3,5,6-trifluorphenyl, provided that the heteroaryl in both A1 and A2 cannot be 2,3,5,6-tetrafluorpyridine-4-yl at the same time, respective [3]-radialene compounds, and semiconducting materials and layer, and electronic devices comprising said compounds.
Owner:NOVALED GMBH

Substituted 1,2,3-Triylidenetris(cyanomethanylylidene) Cyclopropanes for VTE, Electronic Devices and Semiconducting Materials Using Them

The present invention relates to a process for preparation of an electrically doped semiconducting material comprising a [3]-radialene p-dopant or for preparation of an electronic device containing a layer comprising a [3]-radialene p-dopant, the process comprising the steps: (i) loading an evaporation source with the [3]-radialene p-dopant; and (ii) evaporating the [3]-radialene p-dopant at an elevated temperature and at a reduced pressure, wherein the [3]-radialene p-dopant is selected from compounds having a structure according to formula (I) wherein A1 and A2 are independently aryl- or heteroaryl-substituted cyanomethylidene groups, the aryl and/or heteroaryl is selected independently in A1 and A2 from 4-cyano-2,3,5,6-tetrafluorphenyl,2,3,5,6-tetrafluorpyridine-4-yl, 4-trifluormethyl-2,3,5,6-tetrafluorphenyl, 2,4-bis(trifluormethyl)-3,5,6-trifluorphenyl, 2,5-bis(trifluormethyl)-3,4,6-trifluorphenyl, 2,4,6-tris(trifluormethyl)-1,3-diazine-5-yl, 3,4-dicyano-2,5,6-trifluorphenyl, 2-cyano-3,5,6-trifluorpyridine-4-yl, 2-trifluormethyl-3,5,6-trifluorpyridine-4-yl, 2,5,6-trifluor-1,3-diazine-4-yl and 3-trifluormethyl-4-cyano-2,5,6-trifluophenyl), and at least one aryl or heteroaryl is 2,3,5,6-tetrafluorpirydine-4-yl, 2,4-bis(trifluormethyl)-3,5,6-trifluorphenyl, 2,5-bis(trifluormethyl)-3,4,6-trifluorphenyl, 2,4,6-tris(trifluormethyl)-1,3-diazine-5-yl, 3,4-dicyano-2,5,6-trifluorphenyl, 2-cyano-3,5,6-trifluorpyridine-4-yl, 2-trifluormethyl-3,5,6-trifluorphenyl, provided that the heteroaryl in both A1 and A2 cannot be 2,3,5,6-tetrafluorpyridine-4-yl at the same time, respective [3]-radialene compounds, and semiconducting materials and layer, and electronic devices comprising said compounds.
Owner:NOVALED GMBH

Colorimetric-fluorescent probe for detecting hypochlorite radical, preparation method and application thereof

The invention provides a colorimetric-fluorescent probe for detecting hypochlorite radical, a preparation method and application thereof. Aldehyde aniline and a 2-(3-cyano-4, 5, 5-trimethylfuran-2(5H)-acyl)acrylonitrile electron-withdrawing group are subjected to Knoevenagel condensation, thus obtaining the colorimetric-fluorescent probe (E)-((4-(2-(4-cyano-5-(dicyanomethylene)-2, 2-dimethyl-2, 5-dihydrofuran-3-yl)vinyl)phenyl)azanediyl)bis(ethane-2, 1-diyl)diacrylate. The response group of the probe to hypochlorite radical is C=C double bond, in a mixed solution of an organic solvent and water, the single probe has a fluorescence emission peak position at 632nm and an ultraviolet absorption peak position at 544nm, and when used for detecting hypochlorite radical, the probe shows obvious fluorescence quenching and fading response, the response speed is high, and real-time detection of hypochlorite radical can be realized; the detection sensitivity is high, and the detection limit is aslow as 0.19microM; and the probe can accurately determine the content of hypochlorite radical in a water sample and non-standard explosive raw material in the environment.
Owner:XINJIANG TECHN INST OF PHYSICS & CHEM CHINESE ACAD OF SCI

Non-fullerene electron acceptor material and preparation method and application thereof

ActiveCN113336777AThe synthesis process is mature and easy to controlHigh synthetic yieldSilicon organic compoundsFinal product manufactureSolar batteryPolymer chemistry
The invention discloses a non-fullerene electron acceptor material and a preparation method and application thereof. The star-shaped non-fullerene electron acceptor material is obtained by taking an electron donating structure as a central core unit and a five-membered fused ring as an arm unit, and blocking a terminal group by using electron withdrawing groups such as 3-(dicyanomethylene) indanone and derivatives thereof. The material not only maintains the advantages of a linear non-fullerene electron acceptor material, but also has high electron mobility and isotropic charge transfer characteristics of a fullerene electron acceptor material, and the multidimensional geometric structure of the material is beneficial to intramolecular charge transfer, so that the energy gap is reduced and the absorption range is expanded, and the star-shaped multi-dimensional structure can effectively inhibit excessive aggregation and is beneficial to exciton dissociation. The material can be used as an electron acceptor material of an active layer to be widely applied to preparation of organic solar cells, and excellent material film stability and excellent photoelectric conversion characteristics can be obtained.
Owner:NANJING UNIV OF POSTS & TELECOMM

Nonlinear optical materials and nonlinear optical device using the same

There is provided an organic nonlinear optical material including a polymer binder and a compound represented by the following Formula (I):wherein, in Formula (I),R1 and R2 each independently represent a substituted or unsubstituted alkyl group or a substituted or unsubstituted aryl group;R3 represents a hydrogen atom, a substituted or unsubstituted alkyl group, or a substituted or unsubstituted aryl group; andL represents a divalent linking group connecting a nitrogen atom and an oxopyrroline ring having a dicyanomethylidene group in a π-conjugated system containing an azo group (—N═N—).
Owner:FUJIFILM CORP

Near-infrared fluorescent compound for specific detection of hydrazine and preparation method of near-infrared fluorescent compound

The invention discloses a novel near-infrared fluorescent compound for specific detection of hydrazine, wherein the near-infrared fluorescent compound is (E)-2-(2-(3-(dicyanomethylene)-5,5-dimethylcyclohexyl-1-ene-1-yl)vinyl)-5-(diethylamino)phenyl 4-bromobutyric acid and is capable of specifically detecting hydrazine in an organism. The near-infrared fluorescent compound is simple in preparationprocess, readily available in raw materials, low in cost and stable in structure, has relatively good cell membrane permeability and relatively low cytotoxicity, can enter living cells and animal tissues and react with exogenous hydrazine to generate strong red fluorescence which can be distinguished by naked eyes; ultraviolet absorption and fluorescence spectrophotometry analysis shows that the near-infrared fluorescent compound has excellent selectivity to hydrazine under various interferents and has quite strong anti-interference capability to common biomolecules; the novel near-infrared fluorescent compound not only can selectively recognize exogenous hydrazine, but also can quantitatively detect hydrazine with high sensitivity in the growth environment of various living cells, and issuccessfully applied to imaging of living cells and zebra fishes.
Owner:ANHUI AGRICULTURAL UNIVERSITY
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