| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 121 | Ceramic material with boron nitride as base, polymer with boron and nitrogen as base, which can especially be used for the manufacture of the same and its manufacture | JP22488988 | 1988-09-09 | JPH01129033A | 1989-05-22 | JIERAARU MINIYANI; JIYANJIYATSUKU RUBURAN |
| PURPOSE: To manufacture the polymers of various forms, in which a material with BN as a base can be obtained with high weight yield at the time of thermal decomposition by an efficient and economic method that is easily executed by reacting the mixture of trihalogeno borane and specified cyclic compound with compound containing an NH 2 group. CONSTITUTION: Polymers with B and N as the base are manufactured by allowing react the mixture of (A) trihalogeno borane (example: trichloroborane) and the cyclic compound [compound of a formula II ((n) is 2-20) is preferable] constituted of the repetitive unit of (B) a formula I (A is halogen; R is H, hydrocarbon group, organosilyl or hydrogenoorganosilyl) to react with (C) the compound (example: ammonia, methyl amine, etc., containing at least one NH 2 group. With the method, the polymers where the material with BN as the base at the time of thermal decomposition is obtained with high weight yield can easily, efficiently and economically be manufactured in the various forms (thread, fiber, moldings, sheet and the like) so that it can easily be executed. COPYRIGHT: (C)1989,JPO | ||||||
| 122 | Novel composition based on boron nitride | JP22489188 | 1988-09-09 | JPH01111775A | 1989-04-28 | JIERAARU MINIYANI; JIYANJIYATSUKU RUBURAN |
| PURPOSE: To produce the subject composition excellent in compatibility with a silicon-containing compd. by pyrolitically decomposing a specified organometallic precursor in an ammonia atmosphere. CONSTITUTION: A mixture mixing trihalogenoboron (e.g. trichloroboron) and a compd. expressed by formula I (X is halogen, R 1 and R 2 are each silyl) in a molar ratio of more than 1 and the compd. expressed by formula II (R 3 is H, alkyl, cycloalkyl, aryl, alkylaryl, arylalkyl, alkenyl, alkynyl, organosilyl and hydrogenoorganosilyl) and having at least one NH 2 group is subjected to a coaminolysis reaction in bulk or in an anhydrous org. solvent (e.g. hexane) to obtain the organometallic precursor. Then the precursor is pyrolitically decomposed at 1,000-2,000°C in the ammonia atmosphere to obtain the composition in which at least 80% Si incorporated in a ceramic material is allowed to exist at an outer layer part of in order of 200 Å and based on BN. COPYRIGHT: (C)1989,JPO | ||||||
| 123 | Preceramic polymer of boron nitride | JP3170488 | 1988-02-13 | JPS6487A | 1989-01-05 | KAAJIIMIERAA JIEI ERU PAACHIYO; RAINHORUTO HAA KURATSUTSUAA; DEIBUITSUDO EICHI HARISU; BUIRUFURIITO KUROUN SHIYUMITSU |
| PURPOSE: To obtain a preceramic polymer of boron nitride thermally convertible into pure boron nitride ceramic by allowing chloroborazine to react with disilazine under specified conditions. CONSTITUTION: Chloroborazine is allowed to react with disilazine in an org. solvent mixture contg. an arom. component and a nonpolar aliphatic component at a temp. between the solidifying point of the mixture and 0°C for a sufficiently long time to form a polymer soln. in an inert gaseous atmosphere. A precipitate is then removed from the resultant polymer soln. and the solvents are removed to obtain the objective preceramic polymer of boron nitride represented by the formula [where R is methyl, ethyl, propyl or butyl and (x) is a positive integer]. COPYRIGHT: (C)1989,JPO | ||||||
| 124 | Production of inorganic fiber containing silicon, carbon, boron and nitrogen | JP24803083 | 1983-12-27 | JPS60139820A | 1985-07-24 | TAKAMIZAWA MINORU; KOBAYASHI YASUSHI; HAYASHIDA AKIRA; TAKEDA YOSHIFUMI |
| PURPOSE: To obtain the titled fibers having high heat resistance and strength, by mixing an organosilicon compound with an organoboron compound having specific structures in a specific composition, decomposing and polycondensing the resultant mixture in an inert atmosphere, preparing a spinning solution, spinning the resultant solution, infusibilizing the resultant fibers, and firing the infusibilized fibers in sequence. CONSTITUTION: One or more of organisilicon compounds having one or more unit formulas expressed by formula I (R 1 is H, methyl, ethyl, vinyl or phenyl), formula II and formula III are mixed with one or more organoboron compounds expressed by formula IV [R 2 is monofunctional hydrocarbon or expressed by formula V (n is an integer; R 4 is monofunctional hydrocarbon), etc.; R 3 is monofunctional hydrocarbon] within 2:1W200:1mol ratio range between Si and B, and the resultant mixture is decomposed thermally and polycondensed under heating at 250W500°C in an inert atmosphere to give an organometallic polymer having 1,000W50,000 number-average molecular weight and Si, C, B and N as main skeleton. A spinning solution of the resultant copolymer is prepared and spun into fibers, which are then infusibilized under (no) tension and fired at 900W1,800°C in an inert gas atmosphere to afford the aimed fibers. COPYRIGHT: (C)1985,JPO&Japio | ||||||
| 125 | JPS5733288B2 - | JP10524179 | 1979-08-17 | JPS5733288B2 | 1982-07-16 | |
| 126 | Preparation of imide prepolymer | JP10524179 | 1979-08-17 | JPS5628215A | 1981-03-19 | TAKAHASHI AKIO; ITOU YUTAKA; SHIMAZAKI TAKESHI; WAJIMA MOTOYO; MORISHITA YASUSADA; MIZUNO YUTAKA; YOKOZAWA SHIYUNYA; TSUKANISHI KENJI |
| PURPOSE: To prepare an imide prepolymer soluble in a low-boiling general-purpose organic solvent, and therefore having excellent processability, free from adverse effect of the residual solvent after curing, and having excellent heat stability, by reacting an epoxy compound with a solution of the reaction product of a bisimide and a diamine. CONSTITUTION: (A) A bisimide expressed by the formula (R 1 is a divalent organic group having a C-C double bond; R 2 is ≥2C divalent organic group) is thermally reacted with (B) a diamine of formula H 2N-R 3-NH 2 (R 3 is ≥2C divalent organic group) in an organic solvent having a boiling point of 100W170°C at the ordinary pressure (e.g. 2-methoxyethanol), and the solution of the reaction product is thermally reacted with (C) an epoxy compound having two or more groups. Preferably the molar ratio A:B is 1:0.1W1 and the amount of (C) is 15W70wt% on the basis of that of (A)+(B)+(C). USE: Impregnating varnishes for production of insulating sheets. COPYRIGHT: (C)1981,JPO&Japio | ||||||
| 127 | Process for making ceramic sintered body | JP890078 | 1978-01-31 | JPS54102311A | 1979-08-11 | YAJIMA SEISHI; OKAMURA KIYOTO; NIKUDO NORIYOSHI |
| 128 | BORON-CONTAINING PI-ELECTRON MATERIALS INCORPORATING FORMALLY AROMATIC AND NEUTRAL BOREPIN RINGS | PCT/US2011031742 | 2011-04-08 | WO2011127383A3 | 2012-02-23 | TOVAR JOHN DAYTON; CARUSO JR ANTHONY |
| The synthesis, functionalization and characterization of borepin-based extended pi-electron molecules is disclosed. Bulky substituents shielded the vacant boron p-orbitals thus allowing synthetic manipulation and purification under ambient lab conditions. The presently disclosed borepin-containing compounds displayed reversible cathodic electrochemistry and can be viewed as n-type analogues to bent acene hydrocarbons. | ||||||
| 129 | ALKOXYLATED ALKYL PHENOLS AND THE USE THEREOF IN FUELS AND LUBRICANTS | PCT/EP0200599 | 2002-01-22 | WO02059237A3 | 2003-04-24 | LANGE ARNO; RATH HANS PETER; WALTER MARC |
| The invention relates to the use of alkoxylated alkyl phenols comprising at least one long-chained alkyl radical having at least one tertiary or quaternary carbon atom, as fuel additives or lubricant additives, in addition to novel alkoxylated polyalkenyl phenols. The invention also relates to a method for the production of the same and the use thereof as constituents in fuel and lubricant compositions. | ||||||
| 130 | ELECTROLYTIC SALTS FOR LITHIUM BATTERIES | PCT/US0119359 | 2001-06-18 | WO0199209A3 | 2002-05-23 | ANGELL CHARLES A; XU WU |
| Orthoborate salts suitable for use as electrolytes in lithium batteries and methods for making the electrolyte salts are provided. The electrolytic salts have one of the formulae (I). In this formula anionic orthoborate groups are capped with two bidentate chelating groups, Y1 and Y2. Certain preferred chelating groups are dibasic acid residues, most preferably oxalyl, malonyl and succinyl, disulfonic acid residues, sulfoacetic acid residues and halo-substituted alkylenes. The salts are soluble in non-aqueous solvents and polymeric gels and are useful components of lithium batteries in electrochemical devices. | ||||||
| 131 | MULTI-ARM POLYMERIC ALKANOATE CONJUGATES | EP09789119.6 | 2009-08-11 | EP2331140B1 | 2018-07-04 | KOZLOWSKI, Antoni; MCMANUS, Samuel P.; RIGGS-SAUTHIER, Jennifer; SHEN, Xiaoming; ZHANG, Wen |
| Among other aspects, provided herein are multi-armed polymer conjugates comprising an alkanoate-linker, compositions comprising such conjugates, and related methods of making and administering the same. Methods of treatment employing such conjugates and related uses are also provided. The conjugates are prepared with high drug loading efficiencies. | ||||||
| 132 | ORGANISCHE ELEKTROLUMINESZENZVORRICHTUNG UND IN DEREN HERSTELLUNG VERWENDETE BORONSÄURE- UND BORINSÄURE-DERIVATE | EP06724095.2 | 2006-04-06 | EP1888706B1 | 2017-03-01 | STOESSEL, Philipp; BREUNING, Esther; BUESING, Arne; PARHAM, Amir; HEIL, Holger; VESTWEBER, Horst |
| 133 | NANOPARTICLES STABILIZED WITH NITROPHENYLBORONIC ACID COMPOSITIONS | EP13876452.7 | 2013-03-01 | EP2961788A1 | 2016-01-06 | DAVIS, Mark, E.; HAN, Han |
| Described herein are carrier nanoparticles comprising a polymer containing a polyol coupled to a polymer containing a boronic acid, configured to present the polymer containing a boronic acid to an environment external to the nanoparticle. Targeted versions of the described nanoparticles are also described, as are related compositions, methods and systems. | ||||||
| 134 | POLYETHERIMIDES, METHODS OF MANUFACTURE, AND ARTICLES FORMED THEREFROM | EP12813574.6 | 2012-10-26 | EP2771385A1 | 2014-09-03 | HARALUR, Gurulingamurthy M.; KUHLMAN, Matthew |
| A polyetherimide composition comprising a polyetherimide manufactured by reaction of an alkali metal salt of a dihydroxy aromatic compound with a bis(halophthalimide) composition comprising, based on the weight of the bis(halophthalimide) composition, at least 15 wt. % of a 3,3′-bis(halophthalimide) of the formula from more than 17 wt. % to less than 85 wt. % of a 4,3′-bis(halophthalimide) of the formula from more than 0 to less than 27 wt. % of a 4,4′-bis(halophthalimide) of the formula | ||||||
| 135 | Boron-containing compound, ion-conductive polymer and polyelectrolyte for electrochemical devices | EP03026140.8 | 2003-11-13 | EP1422781B1 | 2009-08-19 | Okumura, Takefumi, Hitachi, Ltd.; Nishimura, Shin, Hitachi, Ltd.; Iwayasu, Norio, Hitachi, Ltd.; Yokoyama, Shoichi; Yabe, Takeshi |
| 136 | ORGANISCHE ELEKTROLUMINESZENZVORRICHTUNG UND IN DEREN HERSTELLUNG VERWENDETE BORONSÄURE- UND BORINSÄURE-DERIVATE | EP06724095.2 | 2006-04-06 | EP1888706A1 | 2008-02-20 | STOESSEL, Philipp; BREUNING, Esther; BUESING, Arne; PARHAM, Amir; HEIL, Holger; VESTWEBER, Horst |
| The invention relates to the application of aromatic boric acid or borinic acid derivatives in organic electronic devices in particular electroluminescent devices. | ||||||
| 137 | NICHT KONJUGIERTE POLYMERE PERARYLIERTE BORANE, DEREN VERWENDUNG ALS ORGANISCH HALBLEITENDE EMITTER UND/ODER TRANSPORTMATERIALIEN, VERFAHREN ZU DEREN HERSTELLUNG UND ANWENDUNGEN DAVON | EP04731627.8 | 2004-05-07 | EP1620492A1 | 2006-02-01 | KANITZ, Andreas; ROGLER, Wolfgang; WOERLE, Jasmin |
| The invention concerns non-conjugated luminophor compounds having semiconductor properties, as well as their production and their use in organic light-emitting diodes, organic solar cells, organic photodetectors and organic field effect transistors. Said luminophors are co-polyarylboranes of type K which are transformed, only when a suitable electric field is applied and/or when substituted by the aryl R substituent donor, into a type of structure which acts like a conjugated polymer. The symbols are as defined in Claim 1. | ||||||
| 138 | Ion-conductive polymeric compound, polymeric electrolyte and electric device | EP04002947.2 | 2000-08-28 | EP1428850A1 | 2004-06-16 | Nishiura, Masahito; Kono, Michiyuki; Watanabe, Masayoshi |
The present invention relates to a novel ion-conductive polymeric compound characterized in that at least one boron atom is present in a polymeric structure, to a polymeric electrolyte and to an electric device using the same. |
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| 139 | ARYL BORONATE FUNCTIONALIZED POLYMERS FOR TREATING OBESITY | EP02748036.7 | 2002-07-01 | EP1404686A1 | 2004-04-07 | HOLMES-FARLEY, Stephen, Randall; MANDEVILLE, Harry, W., III; DHAL, Pradeep, K.; HUVAL, Chad Cori; LI, Xinhua; POLOMOSCANIK, Steven, C. |
| Disclosed are polymers comprising one or more phenyl boronate ester, boronamide or boronate thioester groups. The phenyl boronate ester, boronamide and boronate thioester groups are represented by one of the following structural formulas: Ar in Structural Formulas (I) and (II) is substituted or unsubstituted; and each Z is O-, NH-or -S- and is independently selected. Pharmaceutically acceptable salts of the polymer are also included. The arly boronate ester, boronamide or boronate thioester can be cleaved to release the corresponding aryl boronic acid. Also disclosed are pharmaceutical compositions comprising the polymers of the present invention and a pharmaceutically acceptable carrier or diluent; and methods of treating a subject for obesity with the polymers of the present invention. | ||||||
| 140 | ALKOXYLIERTE ALKYLPHENOLE UND DEREN VERWENDUNG IN KRAFT- UND SCHMIERSTOFFEN | EP02702298.7 | 2002-01-22 | EP1356012A2 | 2003-10-29 | LANGE, Arno; RATH, Hans, Peter; WALTER, Marc |
| The invention relates to the use of alkoxylated alkyl phenols comprising at least one long-chained alkyl radical having at least one tertiary or quaternary carbon atom, as fuel additives or lubricant additives, in addition to novel alkoxylated polyalkenyl phenols. The invention also relates to a method for the production of the same and the use thereof as constituents in fuel and lubricant compositions. | ||||||
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