112533-44-5Relevant articles and documents
Transition-Metal Silyl Complexes. 37.1 Reaction of Anionic Silyl, Germyl, and Stannyl Complexes [(η5-C5H4Me)(CO)2MnER 3]- (E = Si, Ge, Sn) with Geminal Organic Dihalides: A Novel Route for the Preparation of Carbene Complexes
Kirchg?ssner, Uwe,Piana, Hermann,Schubert, Ulrich
, p. 2228 - 2232 (2007/10/02)
The anionic complexes Na[MeCp(CO)2MnER3] (E = Si, Ge, Sn) (MeCp = η5-C5H4Me), obtained by deprotonation of the corresponding hydrido complexes MeCp(CO)2Mn(H)ER3, react with 3,3-dichlorocyclopropenes to give the cyclopropenylidene complexes MeCp(CO)2Mn=C-CR=CR (2) by NaCl and R3ECl elimination. Aminocarbene complexes MeCp(CO)2Mn=C(NR2)R′ (5), including the N-methylpyridinylidene complex MeCp(CO)2Mn=CN(Me)CHCHCHCH (5h) and a thiazolinylidene derivative, MeCp(CO)2Mn=CN(Me)C(Me)CHS (5i), were alalogously prepared from [MeCp(CO)2MnSiMePh2]- and [R2N=C(R′)Cl]+. In these reactions, the anionic complexes Na[MeCp(CO)2MnER3] act as preparative equivalents to the dianionic complex MeCp(CO)2Mn2-. The X-ray structure analysis of 5i is reported (Mn-C(carbene) 197.0 (3) pm): monoclinic, space group P21/c (Z = 4), a = 736.4 (1) pm, b = 1418.4 (3) pm, c = 1304.6 (1) pm, β = 95.58 (1)°.