| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 181 | COLORING COMPOSITION, FILM, OPTICAL FILTER, SOLID-STATE IMAGING ELEMENT, AND IMAGE DISPLAY DEVICE | PCT/JP2022009249 | 2022-03-03 | WO2022202204A1 | 2022-09-29 | OOTA KAZUYA |
| Provided is a coloring composition capable of forming a film having excellent moisture resistance. Also provided are a film, an optical filter, a solid-state imaging element and an image display device, each using the coloring composition. The coloring composition comprises a colorant and a resin. The colorant contains Color Index Pigment Yellow 155 and the content of Color Index Pigment Yellow 155 in the total solid content of the coloring composition is 16 mass% or more. | ||||||
| 182 | COLORING COMPOSITION, FILM, OPTICAL FILTER, SOLID-STATE IMAGING ELEMENT, IMAGE DISPLAY DEVICE, AND COMPOUND | PCT/JP2021018694 | 2021-05-18 | WO2022009526A1 | 2022-01-13 | KANEKO YUSHI; TSURUTA TAKUYA; YASUHARA YUICHI; TAKISHITA HIROTAKA |
| Provided are a coloring composition capable of forming pixels having exceptional developer resistance, a film in which the coloring composition is used, an optical filter, a solid-state imaging element, an image display device, and a compound. The coloring composition includes at least one compound S selected from a compound S-1 represented by formula (1) and a compound S-2 in which the above compound S-1 is coordinated to a metal atom, a pigment, a resin P, and a solvent. The resin P includes at least one selected from graft resin P-1 having a specific graft chain, a block copolymer P-2 including a specific structure, and a resin P-3 in which at least one end of a polymer chain including a specific structure is blocked by an acid group. | ||||||
| 183 | DYE, AND HAIR DYE | PCT/JP2021008012 | 2021-03-02 | WO2021261019A1 | 2021-12-30 | AMAYA MINAKO; SAITO TAKUYA; IWASE SOSUKE; JOKO KYOHEI |
| Provided are: a dye comprising at least one selected from the group consisting of a compound represented by formula (1), a compound represented by formula (2), a compound represented by formula (3), and salts thereof; and a hair dye including such dye. | ||||||
| 184 | 着色組成物、膜、光学フィルタ、固体撮像素子及び画像表示装置 | PCT/JP2021/009402 | 2021-03-10 | WO2021215133A1 | 2021-10-28 | 金子 祐士; 鶴田 拓也; 瀧下 大貴 |
耐熱性に優れ、かつ、欠陥の発生が抑制された膜を製造できる着色組成物、着色組成物を用いた膜、光学フィルタ、固体撮像素子及び画像表示装置を提供する。着色組成物は、式（１）で表される化合物Ｓ－１、および、金属原子に前述の化合物Ｓ－１が配位している化合物Ｓ－２から選ばれる少なくとも１種の化合物Ｓと、顔料と、樹脂と、溶剤と、を含む。 |
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| 185 | 着色組成物、膜、赤色画素、カラーフィルタ、固体撮像素子、画像表示装置およびキット | PCT/JP2021/005565 | 2021-02-15 | WO2021166858A1 | 2021-08-26 | 尾田 和也; 森 全弘; 出井 宏明; 中村 翔一; 本橋 拓貴; 北島 峻輔 |
カラーインデックスピグメントレッド２７２を含む顔料と、硬化性化合物と、溶剤とを含む着色組成物であって、着色組成物の全固形分中における顔料の含有量が３０質量％以上である、着色組成物。膜、赤色画素、カラーフィルタ、固体撮像素子、画像表示装置およびキット。 |
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| 186 | 着色組成物、膜、赤色画素、カラーフィルタ、固体撮像素子、画像表示装置およびキット | PCT/JP2021/005563 | 2021-02-15 | WO2021166856A1 | 2021-08-26 | 中村 翔一; 尾田 和也; 森 全弘; 出井 宏明; 本橋 拓貴 |
顔料を含む色材と、樹脂と、溶剤とを含む着色組成物であって、上記顔料は、カラーインデックスピグメントレッド２７２を含み、上記樹脂は、芳香族カルボキシル基を有する樹脂を含む、着色組成物。膜、赤色画素、カラーフィルタ、固体撮像素子、画像表示装置およびキット。 |
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| 187 | 着色組成物、膜、光学フィルタ、固体撮像素子及び画像表示装置 | PCT/JP2021/003442 | 2021-02-01 | WO2021157501A1 | 2021-08-12 | 瀧下 大貴; 出井 宏明; 田口 貴規 |
黄色着色剤を含む着色剤と、樹脂と、溶剤とを含む着色組成物であって、着色剤中における黄色着色剤の含有量が３０質量％以上であり、黄色着色剤は、アゾメチン金属錯体を１５質量％以上含む、着色組成物。前述の着色組成物を用いた膜、光学フィルタ、固体撮像素子及び画像表示装置。 |
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| 188 | UTILISATION DE COMPOSÉS FLUOROPHORES DE TYPE AZA-BODIPY COMME AGENTS DE CONTRASTE DANS L'INFRAROUGE TRÈS LOINTAIN | PCT/EP2020/071865 | 2020-08-04 | WO2021023731A1 | 2021-02-11 | SANCEY, Lucie; GOZE, Christine; BODIO, Even; BUSSER, Benoît; PLIQUETT, Jacques; GODARD, Amélie; KALOT, Ghadir; JOSSERAND, Véronique; LE GUEVEL, Xavier; COLL, Jean-Luc; DENAT, Franck |
La présente invention se rapporte à l'utilisation comme agent de contraste, dans la fenêtre optique allant de 1000 à 1700 nm, d'un composé fluorophore aza-BODIPY. L'invention se rapporte aussi à l'utilisation comme agent de contraste d'une composition comprenant ledit composé fluorophore et un excipient pharmaceutiquement acceptable et/ou un solvant, à un kit comprenant un système d'injection et ledit fluorophore ou ladite composition et aussi à une méthode d'identification d'une cible biologique (telle qu'une cellule saine ou tumorale, une protéine, de l'ADN, ARN par exemple). |
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| 189 | 化合物、インク、カラーフィルター用レジスト組成物、カラーフィルター、感熱転写記録用シート、及びトナー | PCT/JP2019/028485 | 2019-07-19 | WO2020026855A1 | 2020-02-06 | 新藤 太一; 城田 衣; 早川 愛; 三東 剛 |
本件で規定するアゾメチン化合物は、高彩度を示し、耐光性に優れた化合物である。 |
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| 190 | OXIDATIVE DYE COUPLERS WITH NOVEL AUXOCHROME SUBSTITUENTS AND AZOMETHINE DYES AND LEUCO FORMS THEREOF | PCT/US2018/045751 | 2018-08-08 | WO2019032671A1 | 2019-02-14 | MURPHY, Bryan P.; GUIRU, Zhang |
The present invention concerns an auxochrome substituent for an oxidative dye coupler. The auxochrome substituent enables ready developer reaction with the coupler to form azomethine and leuco dyes. Manipulation of the auxochrome substituent enables a bathochromic or hypsochromic shift of the light absorbance by the azomethine dye formed with the auxochrome substituted coupler. |
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| 191 | SYNTHESIS OF A THIOSULFONIC ACID BY A STEP OF PERIODATE MEDIATED OXIDATIVE COUPLING OF A THIOSULFONIC ACID WITH AN ANILINE | PCT/EP2017/084111 | 2017-12-21 | WO2018115292A1 | 2018-06-28 | SINCLAIR, James Peter; NICOLL, Sarah Louise; STOREY, John Mervyn David; LARCH, Christopher Paul |
The present invention pertains generally to the field of chemical synthesis, and more particularly to methods for the chemical synthesis of a thiosulfonic acid of Formula (1) by a step of periodate mediated oxidative coupling of a thiosulfonic acid of Formula (2) with an aniline of Formula (3), as described herein. The present invention also relates to such methods which incorporate one or more additional (subsequent and/or preceding) steps, for example, to prepare compounds of Formula (5) from compounds of Formula (1); to prepare compounds of Formula (6) from compounds of Formula (5); and to prepare compounds of Formula (2) from compounds of Formula (4), as described herein. |
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| 192 | DIPHENYLAMINE SALAN CATALYST | PCT/US2013/069419 | 2013-11-11 | WO2014143202A1 | 2014-09-18 | HOLTCAMP, Matthew W; EVANS, Meagan E.; CANO, David A.; WHETMORE, Eric D.; DAY, Gregory S.; KOL, Moshe |
Catalysts comprising Salan ligands with bridged or unbridged diphenyl amine moieties. Also, catalyst systems comprising the catalyst and an activator; methods to prepare the ligands, catalysts and catalyst systems; processes to polymerize olefins using the catalysts and/or catalyst systems; and the olefin polymers prepared according to the processes. |
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| 193 | VINYL TERMINATED POLYETHYLENE WITH LONG CHAIN BRANCHING | PCT/US2013/046601 | 2013-06-19 | WO2014022012A1 | 2014-02-06 | GIESBRECHT, Garth R.; HOLTCAMP, Matthew W.; KOL, Moshe |
Vinyl terminated polyolefins with long chain branching produced with Salan catalysts having carbazole moieties |
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| 194 | COLORED COMPOSITION AND IMAGE DISPLAY STRUCTURE | PCT/JP2012084270 | 2012-12-26 | WO2013100170A3 | 2013-09-19 | KATO TAKASHI; ISHIWATA YASUHIRO; NAITO HIROYUKI |
| A colored composition includes: (A) a dye that is selected from the group consisting of a methine dye, an anthraquinone dye and an azomethine dye, and that is a mixture of stereoisomers; and (B) a non-polar solvent. | ||||||
| 195 | PARTICULAR AZOMETHINE DIRECT DYES, DYE COMPOSITION COMPRISING AT LEAST ONE SUCH COMPOUND, IMPLEMENTATION PROCESS THEREFORE AND USE THEREOF | PCT/EP2012/075103 | 2012-12-11 | WO2013087636A1 | 2013-06-20 | SABELLE, Stéphane; LEDUC, Madeleine |
The present invention relates to direct dyes of azomethine type of formula (I) below; and also to the use thereof for dyeing keratin fibres, in particular human keratin fibres such as the hair. The invention also relates to a composition for dyeing keratin fibres, comprising such direct dyes in a suitable dyeing medium. Similarly, a subject of the invention is a process for dyeing keratin fibres using the said dye composition, and also a device comprising the same. Finally, the present invention also relates to precursors of these direct dyes. |
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| 196 | アゾ化合物、該アゾ化合物を含有する顔料分散剤、顔料組成物、顔料分散体およびトナー | PCT/JP2011/004592 | 2011-08-16 | WO2012032717A1 | 2012-03-15 | 谷 泰; 広瀬 雅史; 豊田 隆之; 村井 康亮; 田中 正健; 河村 政志; 井上 圭; 長谷川 由紀 |
アゾ顔料の非水溶性溶剤に対する分散性を改善する色素化合物の提供。下記一般式（１）で表される色素化合物。Ｒ1は炭素原子数が１乃至６のアルキル基又はフェニル基を表す。Ｒ2乃至Ｒ6は水素原子又は一般式（２）で表わされる置換基を表す。Ｒ7乃至Ｒ11は水素原子、ＣＯＯＲ12基又はＣＯＮＲ13Ｒ14基を表す。Ｒ12乃至Ｒ14は水素原子、又は炭素原子数が１乃至３のアルキル基を表す。Ｐ1は、ポリマー成分を表し、Ｌ1は、炭素原子数が１乃至３のアルキレン基又は炭素原子数が６乃至１０のアリーレン基を表し、＊は、結合部位を表す。 |
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| 197 | AZOMETHINE DIRECT DYES OR REDUCED PRECURSORS OF THESE DYES OBTAINED FROM SECONDARY, N-ALKYLAMINATED PARA-PHENYLENEDIAMINES, METHOD OF HAIR DYEING USING THESE DYES | PCT/EP2010/058189 | 2010-06-10 | WO2010142777A1 | 2010-12-16 | SABELLE, Stéphane; LEDUC, Madeleine; METAIS, Eric |
The invention relates to the dyeing of keratin fibres using azomethine direct dyes or reduced precursors of azomethine direct dyes obtained from secondary, N-alkylaminated para-phenylenediamines. The subject of the present application is direct dyes derived from 2-[{2-[(4-aminophenyl) amino] ethyl}(2-hydroxyethyl) amino]ethanol, a dye composition comprising the direct dyes, a method for dyeing keratin fibres using the direct dyes and the use of these dyes for dyeing keratin fibres. This composition makes it possible to obtain a particularly stable and persistent colouring. |
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| 198 | 新規アゾメチン化合物およびそのアゾメチン化合物色素を用いた熱転写シート | PCT/JP2010/055903 | 2010-03-31 | WO2010114038A1 | 2010-10-07 | 真田 知幸; 小高 都明; 長谷川 裕之; 天野 寛子 |
カップリング反応を良好に行うことができるとともに、得られるアゾメチン化合物の製造コストも大幅に低減できる、１Ｈ－ピラゾロ〔１，５－ｂ〕〔１，２，４〕トリアゾール環に窒素原子を介してピリジン環を結合させたアゾメチン化合物を提供する。下記式（M-I）で表されるアゾメチン化合物とする。 （式中、Ｒ１は、フェニル基またはナフチル基であるが、該フェニル基またはナフチル基は、アルキル基もしくはハロゲンにより置換されていてもよく、Ｒ２およびＲ３は、それぞれ独立して、炭素数Ｃ２～４のアルキル基を示す。） |
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| 199 | 染毛用染料及び染毛用組成物 | PCT/JP2008/056407 | 2008-03-31 | WO2009041095A1 | 2009-04-02 | 山口 昌彦; 入佐 史郎; 高橋 英治; 吉川 勝正 |
下記一般式（Ｉ）で表される化合物からなる染毛用染料。 ［式中、Ｒ１及びＲ２は、それぞれ独立に、水素原子又は直鎖若しくは分岐の炭素数１～５のアルキル基、Ａｎ－は無機陰イオン、有機陰イオン又は錯塩陰イオン、をそれぞれ示す。］ |
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| 200 | 架橋型シアニン化合物及び該化合物を用いた光学記録材料 | PCT/JP2007/063704 | 2007-07-10 | WO2008010433A1 | 2008-01-24 | 柳澤 智史 |
| Cyanine compounds represented by the general formula (I): (I) wherein R1 and R2 are each independently hydrogen, hydroxy, halogeno, nitro, cyano, an organic group having 1 to 30 carbon atoms, or a group represented by the general formula (II), (II') or (III); R3 and R4 are each independently hydrogen, an organic group having 1 to 30 carbon atoms, or a substituent represented by the general formula (III); R1 and R2 may be united to form a ring structure; R3 and R4 may be united to form a heterocycle; N-R3 together with the adjacent methylene group of the polymethylene chain may form a heterocycle; X is oxygen, sulfur, selenium, -CR5R6-, -NH- or -NYj-; R5 and R6 are each independently an organic group having 1 to 30 carbon atoms or a substituent represented by the general formula (II), (II') or (III), or alternatively R5 and R6 may be united to form a ring structure; Yj is an organic group having 1 to 30 carbon atoms or a group represented by the general formula (III); Z0 is an organic group having 1 to 10 carbon atoms; n is 1 or 2; r is 2 to 8; Anq- is a q-valent anion; q is 1 or 2; and p is a coefficient making the charge neutral. | ||||||
