993-52-2Relevant academic research and scientific papers
On the Role of the Solid-Gas Interface in the Thermolysis of Trimethylgermane and Trimethylstannane
Harrison, Philip G.,McManus, James,Podesta, David M.
, p. 291 - 293 (2007/10/02)
Metal film surfaces have a profound effect on the thermal decomposition of Me3MH (M = Ge and Sn), both of which unusually decompose by half-order kinetics at elevated temperature.
Electroreductive Synthesis of Polygermane and Germane-Silane Copolymer
Shono, Tatsuya,Kashimura, Shigenori,Murase, Hiroaki
, p. 896 - 897 (2007/10/02)
Formation of Ge-Ge and Ge-Si bonds has been achieved by electroreduction with an Mg electrode and this method has been successfully applied to the preparation of polygermane and germane-silane copolymer.
Photochemical Reactions of Vinyl-, Styryl- and Benzyl-Substituted Digermanes
Mochida, Kunio,Kikkawa, Haruhiko,Nakadaira, Yasuhiro
, p. 2772 - 2777 (2007/10/02)
Photochemical reactions of vinyl-, styryl- and benzyl-substituted digermanes by chemical trapping experiments.Photolysis of vinylpentamethyldigermane afforded 1-trimethyl-2-(pentamethyldigermyl)ethane as a major product, and styrylpentamethyldigermanes gave mainly styryltrimethylgermane.On the other hand, photolysis of benzyl-substituted digermanes (benzylpentamethyldigermane and 1,2-dibenzyltetramethyldigermane) gave hydrogermanes and hydrodigermanes as main products, respectively.These products were derived from germyl radicals generated by photoinduced homolysis of the germanium-germanium bond.In carbon tetra chloride (CCl4), these germyl radicals were converted to the corresponding chlorogermanes by abstraction of a chlorine atom.Germylene species were also to be evolved from such photolyses.
Photochemical reactions of aryl-substituted catenates of group 4B elements, PhMe2E-E'Me3 (E, E' = Si and Ge). Formation of a radical pair
Mochida, Kunio,Kikkawa, Haruhiko,Nakadaira, Yasuhiro
, p. 9 - 19 (2007/10/02)
Photochemical reactions of phenyl substituted catenates of group 4B elements, PhMe2E-E'Me3 (E, E' = Si and Ge) have been investigated by chemical trapping experiments and laser flash-photolysis.On irradiation, the phenylated group 4B catenate undergoes E-E' bond homolysis to give a pair of radicals (PhMe2E. and Me3E'.).In CCl4, these radicals are converted to the corresponding chlorides by abstraction of a chlorine atom.In a nonhalogenated solvent, the radical pair couples at the ipso-position of the phenyl group of the pairing radical (PhMe2E.) to yield the cor responding diradical.This undergoes either elimination of a divalent species (Me2E:) with concomitant formation of trimethylphenyl group 4B element PhMe3E') or intramolecular 1,2-group 4B element migration to yield group 4B metal-carbon double bonded species.The radical escapes from the solvent cage coupled to the metal atom of the radical to yield the dimetallic product.The reaction path observed is highly dependent on the nature of the group 4B element comprising the phenyl substituted catenate.
Photochemistry of aryl-substituted trigermanes. Generation and mechanism of formation of germylenes
Mochida, Kunio,Yoneda, Isao,Wakasa, Masanobu
, p. 53 - 62 (2007/10/02)
Photochemical reactions of aryl-substituted trigermanes have studied by trapping experiments, matrix isolation, and laser flash-photolysis techniques.Photolysis of the phenylated trigermanes involved both the simple extrusion of germylenes and the formati
Photochemistry of aryl-substituted trigermanes
Wakasa, Masanobu,Yoneda, Isao,Mochida, Kunio
, p. C1 - C5 (2007/10/02)
The photolysis of phenyl-substituted trigermanes affords digermanes and germenylenes.Trapping experiments, matrix isolation, and laser-photolysis studies indicate that the photoreaction of these compounds involves both the extrusion of germylenes and the
Photochemistry of Phenylpentamethyldigermane
Mochida, Kunio,Kikkawa, Haruhiko,Nakadaira, Yasuhiro
, p. 1089 - 1092 (2007/10/02)
Photolysis of phenylpentamethyldigermane afforded hydrogermanes and digermanes, as main products.These are derived from two germyl radicals generated by photo-induced homolysis of the germanium-germanium bond.Dimethylgermylene is shown to be evolved also
Reactions of Trialkylstannane Anions R3Sn- with Arylstannanes ArSnR'3
Mochida, Kunio
, p. 3299 - 3306 (2007/10/02)
The reactions of trialkylstannane anions R3Sn- with arylstannanes ArSnR'3 have been investigated; trialkylstannane anions with arylstannanes at 50 deg C gave substitution products ArSnR3 in good yields.Most of these substitution products are diverted to r
