专利号:US-7576169-B2 优先权日:2003-10-23 标 题:Facile synthesis of polyhedral silsesquioxane anions and use thereof 发明人:HASEGAWA ISAO; LAINE RICHARD M; ASUNCION MICHAEL Z; TAKAMURA NORIHIRO 权利人:UNIV MICHIGAN 摘要:Polyhedral silsesquioxane anions are economically prepared by reaction of a silica source derived from combusted organic material with a quaternary ammonium hydroxide compound. Reaction of the resulting anions with chlorosilanes may be effected in near stoichiometric fashion in organic solvent containing reactive quantities of organic acids such as formic acid. The functional groups on the resulting functionalized silsesquioxanes may be substituted for other functional groups by reaction with di- or polysiloxanes in the presence of a synthetic ion exchange resin.
专利号:US-6136926-A 优先权日:1996-07-22 标 题 :Cross-linkable, olefinic polymers and methods for their synthesis 发明人:RAETZSCH MANFRED; HESSE ACHIM; BUCKA HARMUT; LEISTNER DIRK; IVANCHEV SERGEJ; HEIKIN SAUL; MESH ALLA; PUKSCHANSKI MOISEJ 权利人:BOREALIS GMBH 摘要:Cross-linkable, olefinic polymers synthesized from mixtures of olefinic polymers and ethylenically unsaturated organosilane compounds, which can be grafted, by a 2-step method using thermally decomposing free radical-forming agents by heating the mixtures to a temperature of 30 DEG to 110 DEG C. below the softening temperature or the crystallite melting point of the olefinic polymers used and subsequently heating the mixtures to a reaction temperature of 10 DEG to 60 DEG C. below the softening temperature or the crystallite melting point of the olefinic polymers used. In the alternative, they can be grafted by a method involving the action of ionizing radiation with simultaneous absorption of organosilane compounds and the action of radiation. The method is suitable for producing films, sheets, fibers, panels, coatings, pipes, hollow objects, foamed materials and molded articles.
专利号:US-2005142054-A1 优先权日:2003-10-23 标 题 :Facile synthesis of polyhedral silsesquioxane anions and use thereof
专利号:US-11767388-B1 优先权日:2019-09-18 标 题 :Silicon-functionalized rubber 发明人:ENSIGN SETH CODY; VIELHABER MARGARET FLOOK; JOHNGRASS JENA LYNN; MA LIQING 权利人:GOODYEAR TIRE & RUBBER 摘要:The compatibility between silica fillers and synthetic rubbers which are synthesized utilizing lanthanide-based catalyst systems, such as neodymium catalyst systems can be improved by terminating the polymerization with a vinyl silane terminating agent. In doing so the vinyl silane is allowed to react with the polymer chain ends of the neodymium rubber to functionalize the chain ends of the polymer chains with silicon containing groups. This results in the rubber having better characteristics for utilization in tire rubber formulations, such a tire tread formulations, that exhibit improved wear characteristics and lower rolling resistance. The process for the synthesis of such functionalized polydiene rubber comprises (1) polymerizing a diene monomer in the presence of a lanthanide-based catalyst system, and (2) terminating the polymerization with a vinyl silane terminator. The functionalized polydiene rubber composition made by this method is comprised of a polydiene rubber which is functionalized at its chain ends with a silicon containing group.
专利号:WO-2005039744-A2 优先权日:2003-10-23 标 题 :Facile synthesis of polyhedral silsesquioxane anions and use thereof
专利号:EP-1675671-A2 优先权日:2003-10-23 标题 :Facile synthesis of polyhedral silsesquioxane anions and use thereof
参考标题:Synthesis Of C-Glycosides Via Radical Cyclization Reactions With A Vinylsilyl Tether. Control Of The Reaction Course By A Change In The Conformation Of The Pyranose Ring Due To Steric Repulsion Between Adjacent Bulky Protecting Groups 作者:Yumi Yahiro,Satoshi Ichikawa,Satoshi Shuto,Akira Matsuda |发布日期:1999.7 摘要:And 1β-Postions Of D-Glucose And D-Mannose, Respectively, Via A Radical Cyclization Reaction With Vinylsilyl Group As A Temporary Connecting Tether, Was Developed. The Radical Cyclization Of D-Glucose Substrates Was Effectively Facilitated By A Change In The Conformation Of The Pyranose Ring Into A 1C4-Form Due To Steric Repulsion Between Adjacent Bulky Tbs-Protecting Groups.