子分类：
| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 81 | Process for the production of thioacylhydrazones | US52458155 | 1955-07-26 | US2774757A | 1956-12-18 | ENGELBERT KUHLE; RICHARD WEGLER |
| 82 | Fluorescent schiff base conjugate Cu(II) chemosensors and methods thereof | US15082808 | 2016-03-28 | US09994713B2 | 2018-06-12 | Aasif Helal |
| Fluorescent Schiff base compounds comprising a xanthene dye based moiety and an alkyl imidazole moiety. Methods of assessing these fluorescent Schiff base compounds as fluorescent probes for metal ions in Cu2+ chemosensing applications, methods of preparing the fluorescent Schiff base compounds and methods of detecting Cu2+ ions with the same are also provided. | ||||||
| 83 | AIE LUMINOGENS FOR VISUALIZATION AND TREATMENT OF CANCER | US15737187 | 2016-06-24 | US20180156811A1 | 2018-06-07 | Benzhong TANG; Engui ZHAO; Chen GUI; Meijuan JIANG; Haiqin DENG; Wai Tung LEUNG; Zhiming WANG; Yueyue ZHAO; Tsz Kin KWOK; Lucia VIGLIANTI; Ni XIE |
| The present subject matter relates to ATE luminogens for visualization and treatment of cancer, particularly AIE luminogenic probes for cancer cell visualization and discrimination, lysosome-targeting AIEgens for imaging and autophagy visualization, highly fluorescent AIE-active theranostic agents for monitoring drug distribution and having anti-tumor activity to specific cancer cells, probes comprising AIE luminogens for cancer cell imaging and staining, AIE luminogens having clusteroluminogenic features and applications thereof, and methods of preparing thereof. | ||||||
| 84 | FLUORESCENT SCHIFF BASE CONJUGATE CU(II) CHEMOSENSORS AND METHODS THEREOF | US15082808 | 2016-03-28 | US20170276607A1 | 2017-09-28 | Aasif HELAL |
| Fluorescent Schiff base compounds comprising a xanthene dye based moiety and an alkyl imidazole moiety. Methods of assessing these fluorescent Schiff base compounds as fluorescent probes for metal ions in Cu2+ chemosensing applications, methods of preparing the fluorescent Schiff base compounds and methods of detecting Cu2+ ions with the same are also provided. | ||||||
| 85 | INK SET AND THERMAL TRANSFER RECORDING SHEET | US15130695 | 2016-04-15 | US20160303882A1 | 2016-10-20 | Koromo Shirota; Taichi Shintou; Masao Nakano |
| An ink set contains a first ink containing a compound in which a pyrazolone ring and a thiazole ring are bonded and a second ink containing a compound in which a pyrazolone ring and a pyridinedione ring are bonded. A thermal transfer recording sheet has a first ink layer containing a compound in which a pyrazolone ring and a thiazole ring are bonded and a second ink layer containing a compound in which a pyrazolone ring and a pyridinedione ring are bonded. | ||||||
| 86 | ORGANIC DYES COMPRISING A HYDRAZONE MOIETY AND THEIR USE IN DYE-SENSITIZED SOLAR CELLS | US14992761 | 2016-01-11 | US20160126022A1 | 2016-05-05 | Ingmar Bruder; Robert Send; Simona Urnikaite; Tadas Malinauskas; Maryte Daskeviciene; Vytautas Getautis |
| The present invention relates to compounds of general formula I wherein R100 and R200 are each independently hydrogen, C1-C10-alkyl which in case of C2-alkyl may be interrupted by one and in case of C3-C10-alkyl by one or two non-adjacent oxygen atoms, C5-C7-cycloalkyl, aryl, aryl-C1-C10-alkyl or aryloxy-C1-C10-alkyl, D is an m-valent (m=1, 2 or 3) donor moiety which comprises at least one carbon-carbon or carbon-heteroatom double bond and/or at least one unfused or fused carbo- or heterocyclic ring, A is an acceptor moiety which comprises at least one carbon-carbon or carbon-heteroatom double bond and/or at least one unfused or fused carbo- or heterocyclic ring, and the donor moiety D and the acceptor moiety A are π-conjugated to one another.Furthermore, the present invention relates to the use of compounds of formula I for producing dye-sensitized solar cells and to dye-sensitized solar cells comprising compounds of formula I. | ||||||
| 87 | POLYMERS, SUBSTRATES, METHODS FOR MAKING SUCH, AND DEVICES COMPRISING THE SAME | US14765982 | 2014-02-06 | US20160002391A1 | 2016-01-07 | Nicholas Brendan Duck |
| The present invention relates generally to substrates for making polymers and methods for making polymers. The present invention also relates generally to polymers and devices comprising the same. | ||||||
| 88 | ORGANIC LIGHT EMITTING DEVICE | US14330367 | 2014-07-14 | US20150123087A1 | 2015-05-07 | Mi Kyung Kim; Kwan Hee Lee; Chang Woong Chu; Jin Kook Lee; Sam Il Kho |
| A compound for an organic light emitting device is represented by Chemical Formula 1. An organic light emitting device includes a first electrode, a second electrode facing the first electrode and an organic layer between the first electrode and the second electrode, and the organic layer includes a compound represented by Chemical Formula 1. In the above Chemical Formula 1, Ar and L are the same as defined in the specification. | ||||||
| 89 | Reagents and methods for direct labeling of nucleotides | US13373959 | 2011-12-06 | US08916346B2 | 2014-12-23 | John J. Naleway; Ying Jiang; Ryan Link-Cole |
| The present invention provides systems and methods for production of activatable diazo-derivatives for use in labeling nucleotides. Labeling nucleotides is accomplished by contacting a stable hydrazide derivative of a detectable moiety with an activating polymer reagent which is used to directly label the nucleotide sample. Labeling occurs on the phosphate backbone of the nucleotide which does not perturb hybridization of the labeled nucleotide with its anti-sense strand. Since the method involves direct labeling, all types of nucleotides can be labeled without prior amplification or alteration. | ||||||
| 90 | Process for preparing structured organic films (SOFS) via a pre-SOF | US13748114 | 2013-01-23 | US08591997B2 | 2013-11-26 | Matthew A. Heuft; Adrien Pierre Cote |
| A processes for preparing structured organic film (SOF) comprising a plurality of segments and a plurality of linkers arranged as a covalent organic framework, wherein the structured organic film may be a multi-segment thick structured organic film. | ||||||
| 91 | Mixed solvent process for preparing structured organic films | US12716706 | 2010-03-03 | US08357432B2 | 2013-01-22 | Adrien Pierre Cote; Matthew A. Heuft; David M. Skinner; Jane Robinson Cowdery-Corvan |
| A mixed solvent process for preparing structured organic film comprising a plurality of segments and a plurality of linkers arranged as a covalent organic framework, wherein the structured organic film may be a multi-segment thick structured organic film. | ||||||
| 92 | STRUCTURED ORGANIC FILMS | US13315452 | 2011-12-09 | US20120082835A1 | 2012-04-05 | Matthew A. HEUFT; Adrien Pierre CÔTÉ; Kathy L. De Jong |
| A structured organic film comprising a plurality of segments and a plurality of linkers arranged as a covalent organic framework, wherein the structured organic film may be a multi-segment thick structured organic film. | ||||||
| 93 | STRUCTURED ORGANIC FILMS HAVING AN ADDED FUNCTIONALITY | US12716449 | 2010-03-03 | US20100228025A1 | 2010-09-09 | Adrien Pierre COTE; Matthew A. HEUFT |
| A structured organic film with an added functionality comprising a plurality of segments and a plurality of linkers arranged as a covalent organic framework, wherein the structured organic film may be a multi-segment thick structured organic film. | ||||||
| 94 | INDICATOR FOR ASSESSING BODY ODOR, PROCESS FOR PRODUCING THE SAME, BODY ODOR ASSESSMENT METHOD, METHOD OF ASSESSING EFFICACIOUSNESS OF DEODORANT AND KIT FOR CONVENIENTLY ASSESSING BODY ODOR | US12750090 | 2010-03-30 | US20100184122A1 | 2010-07-22 | Masayuki Yabuki; Yoshihiro Hasegawa; Masamoto Matsukane |
| A method of assessing body odor using as an index an indicator material comprising an alcohol compound having a mercapto group at the 3-position represented by the following formula (2) and/or a substance that is a derivative of an alcohol compound having a mercapto group at the 3-position, wherein an atom(s) or an atom group(s) is introduced to a mercapto group and/or a hydroxyl group of an alcohol compound having a mercapto group at the 3-position represented by the formula (2): | ||||||
| 95 | Mono- and bis-hydrazone pigments | US11209213 | 2005-08-23 | US07148335B2 | 2006-12-12 | Terence Chamberlain; Norman W. Smith; Donald T. DeRussy |
| Mono- and Bis-Azo/Hydrazone Pyrrole Pigments and Methods for preparing same. | ||||||
| 96 | Mono- and bis-hydrazone pigments | US11209213 | 2005-08-23 | US20050288495A1 | 2005-12-29 | Terence Chamberlain; Norman Smith; Donald DeRussy |
| Mono- and Bis-Azo/Hydrazone Pyrrole Pigments and Methods for preparing same. | ||||||
| 97 | Benzofuran-2-one | US09518464 | 2000-03-03 | US06872839B1 | 2005-03-29 | Leonhard Feiler; Thomas Ruch; Olof Wallquist; Peter Nesvadba |
| Benzofuran-2-ones, compositions comprising benzofuranones, processes for preparing them, and their use as colorants for high or low molecular mass organic material. | ||||||
| 98 | Hair dye composition | US09809077 | 2001-03-16 | US20010054206A1 | 2001-12-27 | Kenichi Matsunaga; Hajime Miyabe; Yukihiro Ohashi |
| Provided is a hair dye composition containing a direct dye (1) or (2). The hair dye composition has markedly high hair dyeing power, has less color fade over time and undergoes a smaller change in the color tone of the dye after storage. 1 nullR1, R2 and R3 are the same or different and each independently represents a C1-3 alkyl group and benzene ring A or B may contain a nondissociative substituentnull. | ||||||
| 99 | Dyes and dye-donor elements for use in thermal dye transfer | US447941 | 1995-05-23 | US5595574A | 1997-01-21 | Wilhelmus Janssens; Luc Vanmaele |
| Dye donor element for use according to thermal dye sublimation transfer comprising a support having thereon a dye layer comprising at least one heterocyclic hydrazono dye, wherein said dye corresponds to the general formula:A=N-N=Hetwherein A is a carbocyclic or heterocyclic coupler group or a cyclic reactive methylene system, which may carry at least one substituent, and Het is a heterocyclic nucleus, which may carry at least one substituent. | ||||||
| 100 | Hydrazide compounds useful as co-developers for black-and-white photothermographic elements | US520291 | 1995-08-28 | US5536622A | 1996-07-16 | Sharon M. Simpson; Lori S. Harring |
| Trityl hydrazides and formyl-phenyl hydrazines are useful as co-developers with hindered phenols in phothothermographic and thermographic elements. These co-developers have the formula:R.sup.1 --(C.dbd.O).sub.n --NHNH--R.sup.2R.sup.1 represents hydrogen and R.sup.2 represents an aryl or substituted aryl group; or,R.sup.1 represents hydrogen, alkyl and alkenyl groups of up to 20 carbon atoms; alkoxy, thioalkoxy, or amido groups of up to 20 carbon atoms; aryl, alkaryl, or aralkyl groups of up to 20 carbon atoms; aryloxy, thioaryloxy, or anilino groups of up to 20 carbon atoms; aliphatic or aromatic heterocyclic ring groups containing up to 6 ring atoms; carbocyclic ring groups comprising up to 6 ring carbon atoms; or fused ring or bridging groups comprising up to 14 ring atoms; and R.sup.2 represents a trityl group.The photothermographic and thermographic elements in the present invention may be used as a photomask in a process where there is a subsequent exposure of an ultraviolet or short wavelength visible radiation sensitive imageable medium. | ||||||
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