Supersilyliertes Ethen trans- ( t Bu
3Si)HC=CH(Si t Bu
3) und Ethin ( t Bu
3Si)C
≡C(Si t Bu
3)
Supersilylated Ethenetrans-(tBu3Si)HC=CH(SitBu3) and Ethyne (tBu3Si)C≡≡≡C(SitBu3) Hannes Vitzea, Ulrich Wietelmannb, Alexander Mursob, Michael Boltea, Matthias Wagnera und Hans-Wolfram Lernera
aInstitut f¨ur Anorganische Chemie, Goethe-Universit¨at Frankfurt am Main, Max-von-Laue-Straße 7, 60438 Frankfurt am Main, Germany
bR&D Lithium Division Chemetall GmbH, Trakehner Str. 3, 60487 Frankfurt am Main, Germany Reprint requests to Dr. Hans-Wolfram Lerner. Fax: ++49-69-79829260.
E-mail: lerner@chemie.uni-frankfurt.de
Z. Naturforsch.2009,64b,223 – 228; received October 31, 2008
The supersilylated ethene trans-(tBu3Si)HC=CH(SitBu3) (triclinic, P¯1) is accessible from the reaction of tBu3SiCHBr2 with nBuLi at −78 ◦C in THF or Et2O. The reaction of Li(H2NCH2CH2NH2)C≡CH with tBu3SiBr leads to the formation of (tBu3Si)C≡CH and (tBu3Si)C≡C(SitBu3). X-Ray quality crystals of (tBu3Si)C≡C(SitBu3) (triclinic,P¯1) were obtained by recrystallization from hexane. In contrast to the structures of the disilanetBu3Si-SitBu3 and the disiloxanetBu3Si–O–SitBu3, the sterically crowded ethenetrans-(tBu3Si)HC=CH(SitBu3) and ethyne (tBu3Si)C≡C(SitBu3) feature dihedral angles of 60◦in the solid-state structures.
Key words:Ethene, Ethyne, Supersilyl, Carbene, Crystal Structure Analysis