27607-78-9Relevant articles and documents
Exploring structural trends for complexes of Me2E(OSO 2CF3)2 (E = Si, Ge, Sn) with pyridine derivatives
Robertson, Alasdair P. M.,Friedmann, Jordan N.,Jenkins, Hilary A.,Burford, Neil
, p. 7979 - 7981 (2014)
The coordination of Me2E(OTf)2 (E = Si, Ge, Sn) acceptors by dmap or 2,2′-bipy furnishes two series of complexes which exhibit distinct structural trends that correlate with the covalent radii of the tetrael elements, and which contrast complexes of these ligands with EX 4 (X = Cl or Br). the Partner Organisations 2014.
Hydrosilane Synthesis by Catalytic Hydrogenolysis of Chlorosilanes and Silyl Triflates
Glüer, Arne,Schweizer, Julia I.,Karaca, Uhut S.,Würtele, Christian,Diefenbach, Martin,Holthausen, Max C.,Schneider, Sven
, p. 13822 - 13828 (2018/10/24)
Hydrogenolysis of the chlorosilanes and silyl triflates (triflate = trifluoromethanesulfonate, OTf-) Me3-nSiX1+n (X = Cl, OTf; n = 0, 1) to hydrosilanes at mild conditions (4 bar of H2, room temperature) is reported using low loadings (1 mol %) of the bifunctional catalyst [Ru(H)2CO(HPNPiPr)] (HPNPiPr = HN(CH2CH2P(iPr)2)2). Endergonic chlorosilane hydrogenolysis can be driven by chloride removal, e.g., with NaBArF4 [BArF4- = B(C6H3-3,5-(CF3)2)4-]. Alternatively, conversion to silyl triflates enables facile hydrogenolysis with NEt3 as the base, giving Me3SiH, Me2SiH2, and Me2SiHOTf, respectively, in high yields. An outer-sphere mechanism for silyl triflate hydrogenolysis is supported by density functional theory computations. These protocols provide key steps for synthesis of the valuable hydrochlorosilane Me2SiClH, which can also be directly obtained in yields of over 50% by hydrogenolysis of chlorosilane/silyl triflate mixtures.
Procatalyst Composition with Silyl Glutarate and Method
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Page/Page column 11, (2010/11/03)
Disclosed are procatalyst compositions having an internal electron donor which includes a silyl glutarate and optionally an electron donor component. Ziegler-Natta catalyst compositions containing the present procatalyst compositions exhibit strong activity and produce propylene-based olefins with high isotacticity.