1080-42-8Relevant articles and documents
Synthesis of Bis(pentafluoroethyl)germanes
Pelzer, Stefanie,Neumann, Beate,Stammler, Hans-Georg,Ignat'ev, Nikolai,Hoge, Berthold
, p. 4758 - 4763 (2016/04/05)
The chemistry of bis(pentafluoroethyl)germanes (C2F5)2GeX2 is presented. The synthesis of such species requires Br2GePh2, wherein the phenyl substituents function as suitable protecting groups. After treatment with two equivalents of LiC2F5, (C2F5)2GePh2 is produced. The replacement of the phenyl rings is smoothly effected by gaseous HBr or HCl in the presence of a Lewis acidic catalyst. The trigermoxane [(C2F5)2GeO]3 results from the reaction of (C2F5)2GeBr2 with Ag2CO3. Its crystalline 1,10-phenanthroline adduct was fully characterised by X-ray diffraction. The combination of (C2F5)2GeBr2 with Bu3SnH gave rise to the formation of (C2F5)2GeH2.
Microwave-assisted Lewis acid catalysis: Application to the synthesis of alkyl- or arylhalogermanes
Laurent, Régis,Laporterie, André,Dubac, Jacques,Berlan, Jacques
, p. 2493 - 2495 (2008/10/08)
Under microwave irradiation, alkyl- or arylhalogermanes RnGeX4-n (R = Et, Bu, Ph; X = Cl, Br) are obtained by redistribution reactions of R4Ge with GeX4. These experimental conditions permit the synthesis of such compounds in good yield in a few minutes at atmospheric pressure. The direct Friedel-Crafts germylation of benzene and toluene by germanium tetrachloride also has been performed, but yields were low.
SYNTHESE DE COMPOSES A LIAISON MIVB-MERCURE. PRECURSEURS D'ESPECES MONOVALENTES (GERMYNES), ET BIVALENTES (GERMYLENES), DE RADICAUX CENTROMETALLES ET D'INTERMEDIAIRES
Riviere, P.,Castel, A.,Satge, J.
, p. 351 - 367 (2007/10/02)
Polynuclear germyl-mercury compounds are obtained from the reaction of organohydrogermanes PhnGeH4-n or digermanes Ph2nGe2H4-n (n = 1, 2) with dialkylmercury R2Hg.Di- or tri-mercurated geminal polygermates thus synthesized generally present a low stability and undergo thermal- or photodecompositions leading to the corresponding monovalent (germynes), divalent (germylenes) or, trivalent (germanium centered radicals) species and also to intermediate biradicals which could be considered as limit forms of germanium doubly-bonded compounds .Such intermediates have been chemically and spectroscopically characterized.Extension of these reactions to the silicon analogs met with difficulties, and thus previously observed differences between silicon and germanium chemistry were confirmed.