| 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 | Synthesis of elastomeric poly(carborane-siloxane-acetelyene)S | US12633854 | 2009-12-09 | US07923523B2 | 2011-04-12 | Teddy M Keller; Manoj K. Kolel-Veetil |
| A linear polymer comprising carborane, siloxane, and acetylene units, which may be cross-linked to a cured polymer and/or pyrolyzed to a ceramic. | ||||||
| 182 | POLYMERS CONTAINING BORANE OR CARBORANE CAGE COMPOUNDS AND RELATED APPLICATIONS | US12859658 | 2010-08-19 | US20110046253A1 | 2011-02-24 | Daniel E. Bowen, III; Eric A. Eastwood |
| Polymers comprising residues of borane and/or carborane cage compound monomers having at least one polyalkoxy silyl substituent. Such polymers can further comprise one or more reactive matrices and/or co-monomers covalently bound with the cage compound monomer residues. Methods of making and applications for using such polymers are also disclosed. | ||||||
| 183 | Polymeric, phosphorescent, organically semi-conductive emitter materials based on perarylated boranes, method for their production and use thereof | US10585182 | 2004-12-29 | US07858724B2 | 2010-12-28 | Andreas Kanitz; Wolfgang Rogler; Wolfgang Roth; Thomas Sonnabend; Jasmin Woerle |
| The invention relates to luminescent compounds with semi-conducting properties, as well as their production and their use in organic light-emitting diodes (OLEDs). The compounds are copolymers comprising a metal complex with a central atom from subgroup 8 of the periodic table of elements. | ||||||
| 184 | SYNTHESIS OF ELASTOMERIC POLY(CARBORANE-SILOXANE-ACETELYENE)S | US12633854 | 2009-12-09 | US20100173155A1 | 2010-07-08 | Teddy M. Keller; Manoj K. Kolel-Veetil |
| A linear polymer comprising carborane, siloxane, and acetylene units, which may be cross-linked to a cured polymer and/or pyrolyzed to a ceramic. | ||||||
| 185 | Alkoxylated alkyl phenols and the use thereof in fuels and lubricants | US10466396 | 2002-01-22 | US07435273B2 | 2008-10-14 | Arno Lange; Hans Peter Rath; Marc Walter |
| Alkoxylated alkylphenols which have at least one long-chain alkyl radical having at least one tertiary or quaternary carbon atom are prepared and are used as fuel or lubricant additives in fuel and lubricant compositions. | ||||||
| 186 | Low dielectric constant insulating material and semiconductor device using the material | US10809704 | 2004-03-26 | US07427443B2 | 2008-09-23 | Yuko Uchimaru; Masami Inoue |
| The use of a material possessing a six-member borazine ring consisting of at least boron and nitrogen elements in the form of a low dielectric constant insulating film in a hard mask, a Cu diffusion barrier layer and an etching stopper which are necessary when low dielectric constant interlayer insulating films and Cu wiring in the multilayer interconnection of an LSI allows the parasitic capacity between the multilayer wirings to be suppressed and enables the ULSI to produce a high-speed operation. | ||||||
| 187 | Synthesis of elastomeric poly(carborane-siloxane-acetelyene)s | US11164431 | 2005-11-22 | US07411030B2 | 2008-08-12 | Teddy Keller |
| A linear polymer comprising carborane, siloxane, and acetylene units, which may be cross-linked to a cured polymer and/or pyrolyzed to a ceramic. | ||||||
| 188 | Boron-containing compound, ion-conductive polymer and polyelectrolyte for electrochemical devices | US10717645 | 2003-11-21 | US07230057B2 | 2007-06-12 | Takefumi Okumura; Shin Nishimura; Norio Iwayasu; Shoichi Yokoyama; Takeshi Yabe |
| An object of the present invention is to provide a boron-containing compound capable of forming an ion-conductive polyelectrolyte having high ion-conductive properties, and a polymer of said compound. According to the present invention, there are provided a polymerizable boron-containing compound of (formula 1), a polymer thereof, a polymer of a compound of (formula 2) and a compound of (formula 3), and a polyelectrolyte for electrochemical device comprising either of these polymers and at least one electrolyte salt: | ||||||
| 189 | Solid polymeric electrolytes for lithium batteries | US11371861 | 2006-03-07 | US20060189776A1 | 2006-08-24 | Charles Angell; Wu Xu; Xiaoguang Sun |
| Novel conductive polyanionic polymers and methods for their preparation are provided. The polyanionic polymers comprise repeating units of weakly-coordinating anionic groups chemically linked to polymer chains. The polymer chains in turn comprise repeating spacer groups. Spacer groups can be chosen to be of length and structure to impart desired electrochemical and physical properties to the polymers. Preferred embodiments are prepared from precursor polymers comprising the Lewis acid borate tri-coordinated to a selected ligand and repeating spacer groups to form repeating polymer chain units. These precursor polymers are reacted with a chosen Lewis base to form a polyanionic polymer comprising weakly coordinating anionic groups spaced at chosen intervals along the polymer chain. The polyanionic polymers exhibit high conductivity and physical properties which make them suitable as solid polymeric electrolytes in lithium batteries, especially secondary lithium batteries. | ||||||
| 190 | Aryl boronate functionalized polymers for treating obesity | US11342129 | 2006-01-27 | US20060128663A1 | 2006-06-15 | Stephen Holmes-Farley; W. Mandeville; Pradeep Dhal; Chad Huval; Xinhua Li; Steven Polomoscanik |
| 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 aryl 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. | ||||||
| 191 | Synthesis of elastomeric poly(carborane-siloxane-acetylene)s | US10456216 | 2003-06-06 | US06967233B2 | 2005-11-22 | Teddy M. Keller |
| A linear polymer comprising carborane, siloxane, and acetylene units, which may be cross-linked to a cured polymer and/or pyrolyzed to a ceramic. | ||||||
| 192 | Polydioxaborines | US10235182 | 2002-09-03 | US06916894B2 | 2005-07-12 | J. Kevin Cammack; Seth R. Marder; Bernard Kippelen |
| Novel polydioxaborines are prepared by polymerizing novel monomers that contain a dioxaborine group. Polydioxaborines are readily soluble, excellent film formers, and have semiconducting properties useful in various applications. | ||||||
| 193 | SYNTHESIS OF ELASTOMERIC POLY(CARBORANE-SILOXANE-ACETELYENE)S | US10456216 | 2003-06-06 | US20050148750A1 | 2005-07-07 | Teddy Keller |
| A linear polymer comprising carborane, siloxane, and acetylene units, which may be cross-linked to a cured polymer and/or pyrolyzed to a ceramic. | ||||||
| 194 | Boron-containing compound, ion-conductive polymer and polyelectrolyte for electrochemical devices | US10717645 | 2003-11-21 | US20040147697A1 | 2004-07-29 | Takefumi Okumura; Shin Nishimura; Norio Iwayasu; Shoichi Yokoyama; Takeshi Yabe |
| An object of the present invention is to provide a boron-containing compound capable of forming an ion-conductive polyelectrolyte having high ion-conductive properties, and a polymer of said compound. According to the present invention, there are provided a polymerizable boron-containing compound of (formula 1), a polymer thereof, a polymer of a compound of (formula 2) and a compound of (formula 3), and a polyelectrolyte for electrochemical device comprising either of these polymers and at least one electrolyte salt: 1 | ||||||
| 195 | Thermoset and ceramic containing silicon and boron | US10254938 | 2002-09-26 | US06767981B1 | 2004-07-27 | Teddy M. Keller; David Y. Son |
| A thermoset polymer has a repeating unit comprising at least one crosslinking group having at least one unsaturated carbon-carbon bond and at least two crosslinking bonds, at least one borate group, at least one silyl group and/or at least one siloxyl group. The thermoset polymer of the present invention may be prepared by reacting a first compound having at least one alkynyl group, and at least one group selected from silyl groups and siloxyl groups, with a second compound selected from boric acid, hydrocarbon boronic acid, hydrocarbon borate, and pyroboric acid under reaction conditions sufficient to crosslink a sufficient number of alkyne bonds to form the thermoset polymer. The thermoset polymer of the present invention possesses both the processability of an organic polymer and the thermal and oxidative stability of an inorganic polymer. The thermoset polymer of the present invention may be further processed into a ceramic material by pyrolysis. | ||||||
| 196 | THERMOSET AND CERAMIC CONTAINING SILICON AND BORON | US10254938 | 2002-09-26 | US20040132945A1 | 2004-07-08 | Teddy M. Keller; David Y. Son |
| A thermoset polymer has a repeating unit comprising at least one crosslinking group having at least one unsaturated carbon-carbon bond and at least two crosslinking bonds, at least one borate group, at least one silyl group and/or at least one siloxyl group. The thermoset polymer of the present invention may be prepared by reacting a first compound having at least one alkynyl group, and at least one group selected from silyl groups and siloxyl groups, with a second compound selected from boric acid, hydrocarbon boronic acid, hydrocarbon borate, and pyroboric acid under reaction conditions sufficient to crosslink a sufficient number of alkyne bonds to form the thermoset polymer. The thermoset polymer of the present invention possesses both the processability of an organic polymer and the thermal and oxidative stability of an inorganic polymer. The thermoset polymer of the present invention may be further processed into a ceramic material by pyrolysis. | ||||||
| 197 | Alkoxylated alkyl phenols and the use thereof in fuels and lubricants | US10466396 | 2003-07-16 | US20040077507A1 | 2004-04-22 | Arno Lange; Hans Peter Rath; Marc Walter |
| Alkoxylated alkylphenols which have at least one long-chain alkyl radical having at least one tertiary or quaternary carbon atom are prepared and are used as fuel or lubricant additives in fuel and lubricant compositions. | ||||||
| 198 | Polydioxaborines | US10235182 | 2002-09-03 | US20030220500A1 | 2003-11-27 | J. Kevin Cammack; Seth R. Marder; Bernard Kippelen |
| Novel polydioxaborines are prepared by polymerizing novel monomers that contain a dioxaborine group. Polydioxaborines are readily soluble, excellent film formers, and have semiconducting properties useful in various applications. | ||||||
| 199 | Process for manufacturing boron nitride fibres and resulting fibres | US10346121 | 2003-01-17 | US20030180206A1 | 2003-09-25 | Philippe Miele; Berangere Toury; David Cornu; Samuel Bernard; Marie-Paule Berthet; Loic Rousseau; Guy Beauhaire |
| The present invention concerns high performance boron nitride fibres and a process for manufacturing said fibres. The present invention uses a borylborazine precursor of the following formula (I):null(NHR)2B(NR)null3B3N3H3nullnull(I)in which R represents a hydrogen atom or an alkyl, cycloalkyl or aryl group, said group comprising from 1 to 30 carbon atoms. | ||||||
| 200 | Heat resistant insulated wire and method of preparing the same | US293052 | 1994-08-19 | US5431954A | 1995-07-11 | Shinji Inazawa; Kouichi Yamada |
| Disclosed herein are a heat resistant insulated wire which is not decomposed but maintains insulativity under a high temperature with excellent adhesion of a coating film, and a method of preparing the same. The heat resistant insulated wire includes a base material consisting of an electrical conductor, and an insulating layer provided on its surface. The insulating layer is obtained by heating a second polymer, in which main chains expressed in a chemical formula --[Si(R.sub.1).sub.2 --N(R.sub.2)].sub.n -- are cross-linked with each other by chloroborazine through side chains containing trialkylsilyl radicals at a temperature of at least about 300.degree. C. and not more than 500.degree. C. | ||||||
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