Title of article :
Mono(cyclooctatetraenyl)samarium Complexes: the Return of the Normally "Inaccessible" Bis(trimethylsilyl)amido Derivative
Author/Authors :
Visseaux، M. نويسنده , , Dormond، A. نويسنده , , Barbier-Baudry، D. نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 1999
Abstract :
Photolytically-induced reactions of chromyl chloride with acetylene and but-2-yne (dimethylacetylene) in low-temperature argon matrices yield end-on ketene and dimethylketene complexes of O=CrCl2, respectively. The product formation probably results from an electrophilic attack of a Cr=O linkage on the C=C triple bonds, leading to radical-like transition states or intermediates, which subsequently rearrange through 1,2-H or 1,2-methyl shifts. Consequently, allene is attacked at its central carbon and the allyl radical thus generated undergoes subsequent ring-closure to give a cyclopropanone complex of O=CrCl2.
Keywords :
Samarium , Bis(trimethylsilyl)amido , Early organolanthanides , Cyclooctatetraenyl , Lanthanides
Journal title :
EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
Journal title :
EUROPEAN JOURNAL OF INORGANIC CHEMISTRY