17876-93-6Relevant academic research and scientific papers
Convenient and selective preparation of mono-alkoxyphenylsilanes from phenylsilane and alcohols
Gunji, Yasuhiko,Yamashita, Yoshihiro,Ikeno, Taketo,Yamada, Tohru
, p. 714 - 715 (2006)
The selective dehydrogenative coupling of phenylsilane and alcohols, including primary, secondary, and tertiary alcohols, was smoothly catalyzed by bis(hexafluoroacetylacetonato)-copper(II) complex to afford the corresponding mono-alkoxysilanes in good-to
Coexistence of Cu(ii) and Cu(i) in Cu ion-doped zeolitic imidazolate frameworks (ZIF-8) for the dehydrogenative coupling of silanes with alcohols
Dai, Yan,Xing, Peng,Cui, Xiaoqin,Li, Zhihong,Zhang, Xianming
, p. 16562 - 16568 (2019)
Recently, metal-ion-doped zeolitic imidazolate frameworks have gained considerable attention for their structure tailorability and potential catalytic applications. Herein, Cu ion-doped ZIF-8 nanocrystals were successfully prepared by the mechanical grind
Synthesis of nitrogen and sulfur co-doped hierarchical porous carbons and metal-free oxidative coupling of silanes with alcohols
Chen, Bingfeng,Li, Fengbo,Mei, Qingqing,Yang, Youdi,Liu, Huizhen,Yuan, Guoqing,Han, Buxing
supporting information, p. 13019 - 13022 (2017/12/15)
Hierarchically porous N and S co-doped carbon was prepared by using 2,5-dihydroxy-1,4-benzoquinone as the carbon source, thiourea as the N and S source, and SiO2 particles as the template. Using the material as the catalyst, oxidative coupling of silanes with alcohols was conducted for the first time under metal-free conditions.
Hydridosilylamido complexes of Ta and Mo isolobal with Berry's zirconocenes: Syntheses, β-Si-H agostic interactions, catalytic hydrosilylation, and insight into mechanism
McLeod, Nicolas A.,Kuzmina, Lyudmila G.,Korobkov, Ilia,Howard, Judith A. K.,Nikonov, Georgii I.
supporting information, p. 2554 - 2561 (2016/02/18)
The syntheses of novel Group 5 and Group 6 hydrosilylamido complexes of the type R(ArN)M{N(tBu)SiMe2-H}X (M = Ta, R = Cp; M = Mo, R = ArN; X = Cl, H, OBn, Me) are described. The various substituents in the X position seem to play the
