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Electrochemical studies on organometallic compounds XXXII. Pseudo-reversibility of the first reduction stage of Nb[η5-1,3-C5H3(SiMe3)2]2Cl2

✍ Scribed by H. Nabaoui; Y. Mugnier; A. Fakhr; E. Laviron; A. Antiñolo; F.A. Jalon; M. Fajardo; A. Otero


Publisher
Elsevier Science
Year
1989
Tongue
English
Weight
367 KB
Volume
375
Category
Article
ISSN
0022-328X

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## Abstract Reaction of [(η^5^‐C~5~H~5~)(CO)~2~M=P=C(SiMe~3~)~2~] [where M = Mo (2), W (5)] with the phosphaalkene __t__BuP=C(NMe~2~)~2~ (1a) afforded the η^3^‐1,2‐diphosphaallyl complexes [(η^5^‐C~5~H~5~)(CO)~2~M{η^3^‐__t__BuPPC(SiMe~3~)~2~}], [where M = Mo (3a); M = W (6)]. Similarly, 2 and CyP=C

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## Abstract The preparation of a family of dinuclear monocyclopentadienyl imidoniobium and ‐tantalum complexes was achieved by two different synthetic routes. The diimido complexes [{M(Cp′)Cl~2~}~2~(μ‐1,__i__‐NC~6~H~4~N)] [Cp′ = η^5^‐C~5~H~4~SiMe~3~, M = Nb, __i__ = 4 (1); Cp′ = η^5^‐C~5~H~4~SiMe~3