序号 专利名 申请号 申请日 公开(公告)号 公开(公告)日 发明人
21 苯并咪唑颜料的纳米级颗粒 CN201010236603.3 2010-07-23 CN101962487A 2011-02-02 R·卡利尼; D·A·马凯夫
发明涉及苯并咪唑颜料的纳米级颗粒。纳米尺度颜料颗粒组合物包括有机苯并咪唑酮颜料和空间大体积稳定剂化合物,其中苯并咪唑酮颜料以非共价键方式与空间大体积稳定剂化合物结合,所述空间大体积稳定剂化合物为烷基化苯并咪唑酮化合物;和结合的稳定剂的存在限制颗粒增长和聚集的程度,获得纳米尺度颜料颗粒。
22 作为有机材料着色剂的苯并呋喃-2-类化合物 CN00804706.5 2000-03-02 CN1330645C 2007-08-08 L·菲勒; T·鲁赫; O·瓦尔奎斯特; P·尼斯瓦巴
发明涉及苯并呋喃-2-类化合物,含有苯并呋喃酮类化合物的组合物,其制备方法和其作为高或低分子量有机材料着色剂的用途。
23 양이온성 알킬아릴하이드라존 염료 및 이의 색소염기의 제조방법 KR1019810002283 1981-06-24 KR1019840001842B1 1984-10-22 로데리히라우에; 한스-페터귈타우
Cationic dyes (I; R1, R2 = H, alkyl, alkenyl, or aralkyl; R3, R4 = Me or Et; X = an anion; rings A and B and R may contain condensed rings) and their dye bases II were prepd. The dyes are useful for dyeing paper, prepd. from wood pulp, acrylic fibers, and other synthetic fibers. Thus, 12.3 g 4-anisidine and 17.3 g 1,3,3trimethyl- 2-methyleneindoline were dissolved in AcOH, cooled, treated with NaNO2, and stirred to give I ≮R1=R3=R4=Me, R2 = H, X = AcO, MeO at position 4 of the B ring), which dyed the paper a reddish-orange color.
24 양이온성 알킬아릴하이드라존 염료 및 이의 색소염기의 제조방법 KR1019810002283 1981-06-24 KR1019830006390A 1983-09-24 로데리히라우에; 한스-페터귈타우
내용없음
25 중합체, 이를 제조하기 위한 기재, 방법, 및 이를 포함하는 장치 KR1020157023889 2014-02-06 KR1020150119883A 2015-10-26 덕,니콜라스,브렌던
본발명은일반적으로중합체를제조하기위한기재및 중합체를제조하는방법에관한것이다. 본발명은또한일반적으로중합체및 이를포함하는장치에관한것이다.
26 하이드로존 잔기를 포함하는 유기 염료 및 염료-감응형 태양 전지에서의 이의 용도 KR1020157002873 2013-06-26 KR1020150036349A 2015-04-07 브루더인그마르; 센드로베르트; 우르니카이테시모나; 말리나우스카스타다스; 다스케비씨에네마리테; 게타우티스비타우타스
본발명은하기화학식 I의화합물, 염료-감응형태양전지의제조에서의용도, 및화학식 I의화합물을포함하는염료-감응형태양전지에관한것이다.
27 나노크기의 벤즈이미다졸론 안료 입자 KR1020100071662 2010-07-23 KR1020110010585A 2011-02-01 카를리니리나; 마케이프다렌
PURPOSE: A nano-sized alkylated benzimidazolone-containing pigment particle composition is provided to be useful for paint, coating, ink jet printing, coloring plastic and resin, optoelectronic imaging components, optical color filters, and photograph members and cosmetics. CONSTITUTION: A nanoscale pigment particle composition comprises: a benzimidazolone pigment; and a sterically bulky stabilizer compound associated non-covalently with the benzimidazolone pigment. The sterically bulky stabilizer compound comprises an alkylated-benzimidazolone compound. The presence of the associated stabilizer limits an extent of particle growth and aggregation, to afford nanoscale pigment particles.
28 나노크기의 벤즈이미다졸론 안료 입자 KR1020100071662 2010-07-23 KR101589930B1 2016-02-01 카를리니리나; 마케이프다렌
나노스케일의안료입자조성물은유기벤즈이미다졸론안료와입체적으로벌키한안정화제조성물을포함하는데, 상기벤즈이미다졸론안료는알킬화벤즈이미다졸론화합물인입체적으로벌키한안정화제화합물과비공유적으로회합되어있으며; 상기회합된안정화제의존재는입자성장및 집합의정도를제한하여나노스케일의안료입자를제공한다.
29 중합체, 이를 제조하기 위한 기재, 방법, 및 이를 포함하는 장치 KR1020157023893 2014-02-06 KR1020150123822A 2015-11-04 덕,니콜라스브렌던
본발명은일반적으로중합체를제조하기위한기재및 중합체를제조하는방법에관한것이다. 본발명은또한일반적으로중합체및 이를포함하는장치에관한것이다.
30 유기 발광 장치 KR1020130133708 2013-11-05 KR1020150052449A 2015-05-14 김미경; 이관희; 추창웅; 이진국; 고삼일
하기화학식 1로표시되는유기발광장치용화합물, 그리고제1 전극, 상기제1 전극과마주하는제2 전극, 및상기제1 전극과상기제2 전극사이에위치하는유기막을포함하고, 상기유기막은하기화학식 1로표현되는화합물을포함하는유기발광장치를제공한다. [화학식 1]상기화학식 1에서, Ar 및 L의정의는명세서내에기재한바와같다.
31 전자사진 광수용체 KR1019870001040 1987-02-06 KR1019940010124B1 1994-10-21 스즈끼데쯔미; 오노히또시; 안도오사무
내용 없음.
32 BENZOFURAN-2-ONES AS COLORANTS FOR ORGANIC MATERIALS PCT/EP0001808 2000-03-02 WO0053597B1 2001-02-22 FEILER LEONHARD; RUCH THOMAS; WALLQUIST OLOF; NESVADBA PETER
Benzofuran-2-ones, compositions comprising benzofuranones, processes for preparing them and their use as colorants for high or low molecular weight organic material.
33 ORGANIC DYES COMPRISING HYDRAZONE MOIETY AND USE IN DYE- SENSITIZED SOLAR CELLS THEREOF PCT/IB2013055252 2013-06-26 WO2014006544A3 2014-02-27 BRUDER INGMAR; SEND ROBERT; URNIKAITE SIMONA; MALINAUSKAS TADAS; DASKEVICIENE MARYTE; GETAUTIS VYTAUTAS
Provided are compounds of general formula (I), the use for producing dye-sensitized solar cells and dye-sensitized solar cells comprising ompounds of formula (I).
34 Method for making Schiff base US15917274 2018-03-09 US10106684B2 2018-10-23 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.
35 METHOD FOR MAKING SCHIFF BASE US15917274 2018-03-09 US20180194944A1 2018-07-12 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.
36 Organic dyes comprising a hydrazone moiety and their use in dye-sensitized solar cells US14992761 2016-01-11 US09831042B2 2017-11-28 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 nonadjacent 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.
37 Ink set and thermal transfer recording sheet US15130695 2016-04-15 US09701146B2 2017-07-11 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.
38 Organic light emitting device US14330367 2014-07-14 US09660201B2 2017-05-23 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.
39 Polymers, substrates, methods for making such, and devices comprising the same US14173269 2014-02-05 US09193819B2 2015-11-24 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.
40 REAGENTS AND METHODS FOR DIRECT LABELING OF NUCLEOTIDES US14544153 2014-12-03 US20150152476A1 2015-06-04 JOHN JOSEPH 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.
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