50870-64-9Relevant academic research and scientific papers
Silanol Compound, Composition, and Method for Producing Silanol Compound
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Paragraph 0160, (2017/07/14)
The purpose of the present invention is to provide silanol compounds that can be used as raw materials of siloxane compounds and the like, and a composition of the silanol compounds, as well as to provide a production method that makes it possible to produce silanol compounds at excellent yield. A composition comprising 5 mass % to 100 mass % of a silanol compound represented by Formulas (A) to (C) can be prepared by devising to produce silanol compounds under water-free conditions, to produce silanol compounds in a solvent having the effect of suppressing the condensation of silanol compounds, and to perform other such processes, the composition being able to be used as a raw material or the like of siloxane compounds because the silanol compounds can be stably present in the resulting composition.
Iron-Catalyzed Silylation of Alcohols by Transfer Hydrosilylation with Silyl Formates
Godou, Timothé,Chauvier, Clément,Thuéry, Pierre,Cantat, Thibault
supporting information, p. 2473 - 2477 (2017/10/26)
An iron catalyst is shown for the first time to promote transfer hydrosilylation with silyl formates and is utilized for the silylation of alcohols. Attractive features of this protocol include the use of an earth-abundant transition-metal catalyst, mild reaction conditions, and the release of gases as the only byproducts (H 2 and CO 2).
Siloxane bond formation by heterofunctional condensation of alkoxysilane and halogenosilane. Application to the preparation of copoly(tetramethyl-p-silphenylenesiloxane-dimethylsiloxane)
Corriu, R.J.P.,Leclercq, D.,Mutin, P.H.,Samson, H.,Vioux, A.
, p. 43 - 50 (2007/10/02)
Siloxane linkages are formed non-hydrolytically by the reaction of dihalogenosilanes with either dibenzylether, or dibenzyloxysilanes and dibenzhydryloxysilanes.The heterocondensation reaction is activated in the presence of NaI (in acetonitrile) or fluoride anions.This offers an alternative copolymerization route to the usual dehydrocondensation of SiOH-terminated species.Thus, the title copolymer was prepared by reaction of equimolar amounts of Me2Si(OCHPh2)2 and 1,4-bis(chlorodimethylsilyl)benzene at 100 deg C.The 29Si NMR spectrum supports a quasi-random sequence in the copolymer.Thermal stability is similar to that reported for an alternating microstructure, as inferred from thermogravimetric analysis. Key words: Siloxane; Polymer
O-SILYLATED KETENE ACETAL CHEMISTRY; DIVINYLOXYSILANE DERIVATIVES AS NOVEL AND USEFUL BIFUNCTIONAL PROTECTING AGENTS FOR H-ACIDIC MATERIALS
Kita, Yasuyuki,Yasuda, Hitoshi,Sugiyama, Yoshie,Fukata, Fumio,Haruta, Jun-ichi,Yasumitsu, Tamura
, p. 1273 - 1276 (2007/10/02)
Novel reagents, bis(1-methoxy-2-methyl-1-propenyloxy)silanes (2a-d) have been shown to be very useful bifunctional protecting agents for various types of H-acidic materials, such as diols, dithiols, diacids and their combined materials.The reaction proceeds rapidly under mild conditions to give the corresponding silylene derivatives in almost quantitative yields.
