| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 1 | 一种含氟有机物痕量不饱和杂质去除方法 | CN202111651467.9 | 2021-12-30 | CN114276213B | 2024-03-19 | 周井森; 张广第; 张学良; 张雪刚; 王宁; 李军; 孙立柱; 花永紧 |
| 该发明涉及提纯除杂技术领域，具体关于一种含氟有机物痕量不饱和杂质去除方法；本发明在一种钛硅负载加氢催化剂的催化下将含氟有机物中的痕量不饱和杂质加杂质加氢转化为饱和含氟有机杂质，显著改变杂质的沸点，使得杂质能通过精馏的方法除去；本发明属于催化加氢反应性转化杂质气体与精馏耦合方法，具有产品纯度高，杂质含量极低的优点。 | ||||||
| 2 | 治疗代谢综合征的组合物和方法 | CN201380030661.2 | 2013-02-03 | CN104603090A | 2015-05-06 | M·坎杜拉 |
| 本发明涉及式I的化合物或其可药用盐，以及其多晶型物、溶剂化物、对映异构体、立体异构体和水合物。包含有效量的式I的化合物的药物组合物以及治疗代谢综合征的方法可以被配制以用于口腔、颊部、直肠、局部、经皮、透粘膜、静脉内、肠胃外施药、糖浆或注射。这种组合物可以用于治疗高尿酸血症、痛风、血脂异常、肥胖、尿素循环障碍、高血糖症、胰岛素抵抗、糖尿病、尿崩症、1型糖尿病、2型糖尿病、微血管并发症、大血管并发症、血脂异常、糖尿病前期、肥胖、心律失常、心肌梗死、中风、神经病变、肾脏并发症、高甘油三酯血症、心血管并发症以及餐后高血糖症。 | ||||||
| 3 | 一种含氟有机物痕量不饱和杂质去除方法 | CN202111651467.9 | 2021-12-30 | CN114276213A | 2022-04-05 | 周井森; 张广第; 张学良; 张雪刚; 王宁; 李军; 孙立柱; 花永紧 |
| 该发明涉及提纯除杂技术领域，具体关于一种含氟有机物痕量不饱和杂质去除方法；本发明在一种钛硅负载加氢催化剂的催化下将含氟有机物中的痕量不饱和杂质加杂质加氢转化为饱和含氟有机杂质，显著改变杂质的沸点，使得杂质能通过精馏的方法除去；本发明属于催化加氢反应性转化杂质气体与精馏耦合方法，具有产品纯度高，杂质含量极低的优点。 | ||||||
| 4 | 全氟化碳类乳液 | CN201080017461.X | 2010-04-15 | CN102395548A | 2012-03-28 | 理查德·凯瑞; 德宝·P·汤普森; 格瑞·克劳森 |
| 本申请提供了一种乳液，它包含一定量的作为颗粒分散在连续液相中的全氟化碳液体，其特征在于，该分散的颗粒具有单峰粒径分布，以及乳液的应用。本申请也提供了一种生产全氟化碳乳液的方法，一种制备含有PFC乳液的药物产品的方法，以及验证一个批次的乳液用于药物使用的方法。 | ||||||
| 5 | 含氟化合物、含氟聚合物及其制备方法 | CN03819683.2 | 2003-08-21 | CN1286867C | 2006-11-29 | 儿玉俊一; 金子勇; 横小路修; 冈田伸治; 武部洋子; 川口泰秀 |
| 本发明提供了官能团浓度高、可获得充分的官能团特性、且Tg不会下降的含氟聚合物。该聚合物是具有通过式(1)CFR1＝CR2-Q-CR3＝CHR4-(1)表示的含官能团的含氟二烯的环化聚合而形成的单体单元的含氟聚合物。式中，R1～R4互相独立，表示氢原子、氟原子、碳原子数小于等于8的烷基或环状脂肪族烃基，其中至少1个为环状脂肪族烃基，烷基及环状脂肪族烃基中的氢原子可被氟原子、烷基或氟烷基取代；Q表示2价有机基团，该基团是具有通过酸可显现酸性基的嵌段化酸性基或可转变为该嵌段化酸性基的基团的有机基团。 | ||||||
| 6 | Electronic devices made with compositions and such compositions comprising the novel compounds | JP2006554290 | 2005-02-17 | JP2007525498A | 2007-09-06 | ダブロウフスキー アーサー; モーリス スミス エリック; エー．ヨハンソン ガリー; エム．ロッシ ジーン; ヘロン ノーマン; サバイナ ラドゥ ノラ; ピー．ジェントリー フレデリック |
| 本発明は、新規な化合物、ならびに新規なオリゴマーおよびポリマーを含む組成物、ならびにこれらの組成物を含有する少なくとも１つの層を含む電子デバイスに関する。 新規なオリゴマーおよびポリマーは、可溶化することができ、溶液中で使用して、電子デバイスを形成することができる。 これらの化合物は、モノマーとして機能することができ、そのようなモノマーからコポリマーを形成することができ、そのようなコポリマーは、化合物の複数の単位を、重合単位として含む。 | ||||||
| 7 | Extraction of halogenated hydrocarbon from aqueous solution using phosphine oxide on inert substrate as extractant | JP17947483 | 1983-09-29 | JPS5982989A | 1984-05-14 | JIYON HAABEI BURAITO; AJITO KUMAARU SHIYAUDOURI; KURISUTOSU SABIDESU |
| 8 | Preparation of derivative of dihalocyclopropane | JP5455978 | 1978-05-10 | JPS53141246A | 1978-12-08 | PIITERU ADORIAAN BUERUBURUUGE; BUIREMU TERUROUBU; PETORUSU ANTONIUSU KURAMERU |
| 9 | JPS538681B1 - | JP2500368 | 1968-04-16 | JPS538681B1 | 1978-03-31 | |
| 10 | Method of accelerating reactions | JP8211776 | 1976-07-09 | JPS537602A | 1978-01-24 | YOSHIMURA NORIAKI; TAMURA MASUHIKO |
| PURPOSE: To effectively accelerate org. ionic reactions which proceed in a heterogeneous system consisting of aq. and org. layers in the presence of an alkali salt or hydroxide, by the addition of a certain polyoxyalkylene diether. COPYRIGHT: (C)1978,JPO&Japio | ||||||
| 11 | Satsudani satsuchukagobutsusoseibutsu | JP10200275 | 1975-08-22 | JPS5148428A | 1976-04-26 | MAIKERU REIMONDO GUREEBUSU RII; AREKISANDAA BOORINGOORU PENROO |
| 12 | HPMA POLYMER PLATINUM CHELATES | PCT/US2011/036682 | 2011-05-16 | WO2011146408A1 | 2011-11-24 | SOOD, Paul; UMMANENI, N. Rao; THURMOND, Bruce; ZARZYCKI, Richard |
Polymeric platinum amidomalonate complexes, where the platinum is in +2 or +4 oxidation state, and where the complexes optionally contain tumor seeking groups, are useful in the treatment of cancer. |
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| 13 | SYNTHESIS OF (DIBROMOCYCLOBUTA) AROMATIC COMPOUNDS | PCT/US0218251 | 2002-06-12 | WO02102810A8 | 2004-02-12 | STANGER AMNON |
| A method for the synthesis of cyclobuta aromatic compounds by cyclizing two ortho dibromoalkyl substituents is described. Using a mediator, such as nickel metal, and continuous removal of product from contact with the mediator, high product yields are achieved. A method for bromination of ortho alkyl substituents of aromatic compounds is also described. | ||||||
| 14 | New triaryl amine compounds and methods of manufacturing the | JP2006554290 | 2005-02-17 | JP4820762B2 | 2011-11-24 | ダブロウフスキー アーサー; モーリス スミス エリック; エー．ヨハンソン ガリー; エム．ロッシ ジーン; ヘロン ノーマン; サバイナ ラドゥ ノラ; ピー．ジェントリー フレデリック |
| 15 | Composition containing new compound, and electronic device manufactured from such composition | JP2011074540 | 2011-03-30 | JP2011173893A | 2011-09-08 | HERRON NORMAN; JOHANSSON GARY A; RADU NORA SABINA; SMITH ERIC MAURICE; DABROWSKI ARTHUR; GENTRY FREDERICK P; ROSSI GENE M |
| PROBLEM TO BE SOLVED: To provide a new compound useful as a hole transport material in manufacture of an electronic device. SOLUTION: The invention relates to a new compound, a composition containing a new oligomer and polymer, and an electronic device including at least one layer containing the composition. The new oligomer and polymer can be solubilized and can be used in a solution to form the electronic device. The compounds can function as a monomer, and a copolymer can be formed from such a monomer, such a copolymer containing a plurality of units of the compound as a polymerization unit. COPYRIGHT: (C)2011,JPO&INPIT | ||||||
| 16 | Cyclohexylbenzene derivative, its production, liquid crystal composition containing the same and liquid crystal element | JP11628996 | 1996-05-10 | JPH09301897A | 1997-11-25 | FUJIMOTO YUKARI; MIYAMOTO YASUNOBU; MINAMII MASAYOSHI |
| PROBLEM TO BE SOLVED: To obtain the subject low-viscosity compound having relatively broad liquid crystal phase and useful as a component of a liquid crystal composition. SOLUTION: This new compound is shown by formula I [R 1 is H, F, cyano or R 3(O) m; R 3 is a (F-substituted) 1-12C alkyl, alkenyl, etc.; A 1 and A 2 are each a group of formula II, at least one of them being cyclohexylene or cyclohexelene; (n) is 1-4; (m), (p) and (q) are each 0 or 1; X 1 to X 4 are each CH, CF or N; R 2 is a (F-substituted) 1-12C alkyl or 2-12C alkoxyalkyl], e.g. 1-[(4-trans-propylcyclohexyl) cyclohexyl]-4-(1-(E)-pentenyl)benzene. This compound of formula I is obtained by reaction of a compound of formula III [D is a halogen or OSO 2R'; R' is a (F-substituted) lower alkyl or (substituted)phenyl] with a boron compound of the formula (R 4) 2B-CH=CH-R 2 (R 4 is OH, an alkyl or alkoxy) in the presence of a Pd catalyst and a base. COPYRIGHT: (C)1997,JPO | ||||||
| 17 | Fluorination of cyclic organic compound | JP571588 | 1988-01-16 | JPH01186828A | 1989-07-26 | NISHIMURA MASAKATSU; OKADA NAOYA; TOKUNAGA SHINJI |
| PURPOSE: To effect efficient perfluorination by partial fluorination of a cyclic organic compound in contact with a high-valency metal fluoride efficiently at a lower temperature than in the conventional process, followed by reaction with a fluorine gas at a relatively high temperature. CONSTITUTION: A cyclic organic compound, preferably pentalene, naphthalene, 1,2,3,4-tetrahydronaphthalene, decalin is brought into contact with a high-valency metal fluoride such as CoF 3, MnF 3, potassium tetrafluorocobaltate, at 200W300°C to effect partial fluorination. Then, the product is allowed to react with a fluorine gas at 110W180°C, preferably 120W150°C to give a perfluorinated cyclic organic compound. The fluorination is preferably carried out in a liquid phase using the perfluorinated product corresponding to the starting substance as the liquid medium for high yield production. The product is used as a heat medium for vapor-phase soldering and a lubricant in the semiconductor production. COPYRIGHT: (C)1989,JPO&Japio | ||||||
| 18 | JPS5827775B2 - | JP8211776 | 1976-07-09 | JPS5827775B2 | 1983-06-11 | YOSHIMURA NORIAKI; TAMURA MASUHIKO |
| 19 | Preparation of organic halogen compound | JP16044577 | 1977-12-29 | JPS5492902A | 1979-07-23 | KUMADA MAKOTO; TAMAO KOUHEI |
| PURPOSE: To prepare an organic halogen compound useful as a raw material of fine chemicals, especially a raw material for the syntheses of medicines, efficiently by the halogenation of an easily available hexacoordinate Si compound. CONSTITUTION: Organic halides are prepared by halogenating Si compounds of K 2 [RSiF 5] (R is substituted or unsubstituted monovalent hydrocarbon residue), e.g. K 2[n-C 8H 17SiF 5]. K 2[n-C 12H 25SiF 5], etc., at -30 -100°C in the presence or absence of a solvent, using halogen, such as C1 or Br, or a hlogenating agent such as N- bromosuccinic imide. The molar ratio of the halogen, etc. to the Si compound is 1 2 to 1. COPYRIGHT: (C)1979,JPO&Japio | ||||||
| 20 | Method of accelerating base-catalyzed, ionic, organic reactions | JP8211876 | 1976-07-09 | JPS537603A | 1978-01-24 | YOSHIMURA NORIAKI; TAMURA MASUHIKO |
| PURPOSE: To effectively and economically accelerate org. ionic reactions which proceed in on org. liquid in the presence of a basic alkali metal compound as catalyst, by the addition of a certain polyoxyalkylene derivative. COPYRIGHT: (C)1978,JPO&Japio | ||||||
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