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The synthesis, characterisation and reactivity of two isostructural anionic magnesium and calcium complexes is reported. By X-ray and neutron diffraction techniques, the anionic hydrides are shown to exist as dimers, held together by a range of interactions between the two anions and two bridging potassium cations. Unlike the vast proportion of previously reported dimeric group 2 hydrides, which have hydrides that bridge two group 2 centres, here the hydrides are shown to be "terminal", but stabilised by interactions with the potassium cations.

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The novel mono-silyl [(RSi)AlX], di-silyl [(RSi)AlX], tri-silyl (RSi)Al·EtO, and -ate-complex [(RSi)Al]·Li(EtO) have been synthesized by reaction of AlX (X = Cl, Br) with silyl lithium reagents (BuMeSiLi, EtSiLi) in EtO. Treatment of these compounds with MeN yields the corresponding amine-coordinated silyl aluminum complexes (RSi)AlX·NMe, (RSi)AlX·NMe, and (RSi)Al·NMe. An intramolecular amine-coordinated mono-silyl aluminum complex MeN(CH)(BuMeSi)SiAlCl was prepared by the reaction of MeN(CH)(BuMeSi)SiLi with AlCl in EtO.

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The gapless feature and air instability greatly hinder the applications of silicene in nanoelectronics. We theoretically design an oxidized derivative of silicene (named silicether) assembled by disilyl ether molecules. Silicether has an indirect band gap of 1.

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Synthesis of Urea Derivatives from CO and Silylamines.

Angew Chem Int Ed Engl

April 2019

Department of Chemistry, University of Toronto, 80 St. George St., Toronto, Ontario, M5S3H6, Canada.

A series of thirty-three N,N'-diaryl, dialkyl, and alkyl-aryl ureas have been prepared in pyridine or toluene by reaction of silylamines with CO . This protocol is shown to provide facile access to C-labeled ureas, as well as chiral and macrocyclic ureas. These reactions proceed through initial generation of the corresponding silylcarbamates, which subsequently react with silylamine under thermal conditions to afford the thermodynamically favored urea and disilyl ether.

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This contribution presents evidence for new pathways manifested in the reactions of the phenylhydrosilanes PhnSiH4-n with the pincer complexes (POCsp(2)OP)Ni(OSiMe3), 1-OSiMe3, and (POCsp(3)OP)Ni(OSiMe3), 2-OSiMe3 (POCsp(2)OP = 2,6-(i-Pr2PO)2C6H3; POCsp(3)OP = (i-Pr2POCH2)2CH). Excess PhSiH3 or Ph2SiH2 reacted with 1-OSiMe3 to eliminate the disilyl ethers Ph(n)H(3-n)SiOSiMe3 (n = 1 or 2) and generate the nickel hydride species 1-H. Subsequent reaction of the latter with more substrate formed corresponding nickel silyl species 1-SiPhH2 or 1-SiPh2H and generated multiple Si-containing products, including disilanes and redistribution products.

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