📜Hexaphenylstannol置于cl2体系中,用 四氯化碳 用作溶剂,化学反应生成二苯基二氯化锡 参考文献:Synthesis Of Tetraphenylstannacyclopentadienes (Stannoles). 2. Derivatives And Adducts Of 1,1-Dihalo-2,3,4,5-Tetraphenylstannoles 标题:Synthesis Of Tetraphenylstannacyclopentadienes (Stannoles). 2. Derivatives And Adducts Of 1,1-Dihalo-2,3,4,5-Tetraphenylstannoles 摘要: Doi:10.1021/ic50224A060
专利号:US-2024368099-A1 优先权日:2022-01-18 标 题:Methods for the synthesis of di(hydroxymethyl)tetrahydrofuran and its application in polyesters and polyurethanes 发明人:SPIEGELBERG BRIAN; BRANDT ADRIAN; BECK HORST; KUX ALEXANDER; TIN SERGEY; DE VRIES JOHANNES GERARDUS 权利人:HENKEL AG & CO KGAA 摘要:The present invention relates to the synthesis of di(hydroxymethyl)tetrahydrofuran (DHMTHF) and the preparation of trans-enriched mixtures of DHMTHF. The invention further refers to polyester polyols which are obtained by reaction of cis/trans DHMTHF mixtures with a dicarboxylic acid. The invention further relates to polyurethanes and compositions containing a polyester polyol comprising DHMTHF, in particular to such polyurethane-containing (adhesive) compositions.
专利号:US-10294336-B2 优先权日:2014-11-27 标题 :Synthesis of polymer polyols in unsaturated polyols, polymer polyols and their use 发明人:KOENIG CHRISTIAN; EMGE ANDREAS; OTERO MARTINEZ IRAN 权利人:BASF SE 摘要:The present invention relates to the synthesis of polymer polyols in unsaturated polyols as liquid phase, polymer polyols and their use.
专利号:US-5502126-A 优先权日:1993-06-17 标 题 :Process for the synthesis of isoprene butadiene rubber 发明人:BELL ANTHONY J; MATRANA BARRY A; HALASA ADEL F 权利人:GOODYEAR TIRE & RUBBER 摘要:The subject invention relates to a technique for synthesizing rubbery non-tapered, random, copolymers of 1,3-butadiene and isoprene. These rubbery copolymers exhibit an excellent combination of properties for utilization in tire sidewall rubber compounds for truck tires. By utilizing these isoprene-butadiene rubbers in tire sidewalls, tires having improved cut growth resistance can be built without sacrificing rolling resistance. Such rubbers can also be employed in tire tread compounds to improve tread wear characteristics and decrease rolling resistance without sacrificing traction characteristics. This invention more specifically discloses a process for the synthesis of isoprene-butadiene rubbers which comprises copolymerizing isoprene monomer and 1,3-butadiene monomer in an organic solvent in the presence of a catalyst system which is made by the sequential steps of (1) mixing (a) an organoaluminum hydride, (b) a member selected from the group consisting of aliphatic alcohols, cycloaliphatic alcohols, aliphatic thiols, cycloaliphatic thiols, trialkyl silanols, and triaryl silanols, and (c) optionally, 1,3-butadiene in an organic solvent to produce a modified organoaluminum catalyst component; (2) adding an organometallic compound which contains a metal from Group III-B of the Periodic System to the modified organoaluminum catalyst component to produce a Group III-B metal containing catalyst component; and (3) adding a compound which contains at least one labile halogen atom to the Group III-B metal containing catalyst component.
专利号:US-6924375-B2 优先权日:2003-09-03 标题:Facile synthesis of 1,9-diacyldipyrromethanes 发明人:LINDSEY JONATHAN S; TAMARU SHUN-ICHI; YU LIANHE 权利人:UNIV NORTH CAROLINA STATE 摘要:The present invention provides a method of making a metal complex. The method comprises the steps of: (a) acylating a dipyrromethane or a 1-monoacyldipyrromethane to form a mixed reaction product comprising a 1,9-diacyidipyrromethane; (b) combining the reaction product with a compound of the formula R 2 MX 2 in the presence of a base, where R is alkyl or aryl, M is Sn, Si, Ge, or Pb (preferably Sn), and X is halo, OAc, acac, or OTf, to form a product comprising a metal complex of the formula DMR 2 in the mixed reaction product, wherein D is a 1,9-diacyldipyrromethane; and then (c) separating the metal complex from the mixed reaction product. The method may be utilized for the convenient synthesis and separation of 1,9-diacyldipyrromethanes. Metal complex intermediates useful in such methods are also described.
专利号:WO-0034353-A9 优先权日:1998-11-12 标题 :Method for the synthesis of thermoplastic elastomers in non-halogenated solvents 发明人:SANDERSON ANDREW J; EDWARDS WAYNE 权利人:CORDANT TECH INC; SANDERSON ANDREW J; EDWARDS WAYNE 摘要:A method of preparing a thermoplastic elastomer having A blocks which are crystalline at temperatures below about 75 °C and B blocks which are amorphous at temperatures above about -20 °C is disclosed. The A blocks are derived from oxetane derivatives and/or tetrahydrofuran derivatives. The B blocks are derived from oxetanes, tetrahydrofuran, oxiranes, and derivatives thereof. The A blocks and B blocks are dissolved into solution containing a non-halogenated solvent, preferably tetrahydrofuran. The dissolved A blocks and B blocks are dried of water by azeotropic distillation of the non-halogenated solvent. Next, the dried A blocks and the dried B-blocks are end-capped with a diisocyanate having one isocyanate moiety substantially more reactive with the terminal groups of the blocks than the other isocyanate moiety, whereby the more reactive isocyanate moiety is capable of reacting with the terminal groups of the blocks, leaving the less reactive isocyanate moiety free and unreacted. The end-capped A blocks and the end-capped B blocks are linked together with a linking compound having two isocyanate-reactive groups which are sufficiently unhindered to react with the free and unreacted isocyanate moieties of the end-capped polymers.
专利号:US-6997997-B1 优先权日:1998-11-12 标 题 :Method for the synthesis of energetic thermoplastic elastomers in non-halogenated solvents 发明人:SANDERSON ANDREW J; EDWARDS WAYNE W 权利人:ALLIANT TECHSYSTEMS INC 摘要:A method is provided for preparing thermoplastic elastomers. A blocks of the thermoplastic elastomers are crystalline at temperatures below about 60° C. and are derived from oxetane derivatives and/or tetrahydrofuran derivatives. B blocks of the thermoplastic elastomer are amorphous above about −20° C. and are derived from oxetanes, tetrahydrofuran, oxiranes, and derivatives thereof. According to this method, the A and B blocks are dissolved into solution containing a non-halogenated solvent, preferably tetrahydrofuran, then dried by azeotropic distillation. The dried blocks are end-capped with a diisocyanate, preferably a diisocyanate having one isocyanate moiety substantially more reactive with the terminal groups of the blocks than the other isocyanate moiety of the diisocyanate. The end-capped blocks are then linked together with a linking compound.
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合成参考文献
摘要:Ramirez y Medina, I.-M.; Kipke, W.; Makow, J.; Staubitz, A., Science of Synthesis Knowledge Updates, (2020) 2, 43. 摘要:Hlina, J. A., Science of Synthesis Knowledge Updates, (2021) 1, 108. 摘要:Hlina, J. A., Science of Synthesis Knowledge Updates, (2021) 1, 103. 摘要:Ramirez y Medina, I.-M.; Kipke, W.; Makow, J.; Staubitz, A., Science of Synthesis Knowledge Updates, (2020) 2, 46. 摘要:Ramirez y Medina, I.-M.; Kipke, W.; Makow, J.; Staubitz, A., Science of Synthesis Knowledge Updates, (2020) 2, 35.