Vinylidene carbonylation at a manganese-iron complex: A density functional study of mechanism

Elena A. Ivanova Shor, Vladimir A. Nasluzov, Aleksey M. Shor, Alla B. Antonova, Notker Rösch

Publikation: Beitrag in FachzeitschriftArtikelBegutachtung

10 Zitate (Scopus)


Treating the phenylvinyldene manganese complex Cp(CO)2MnC 1C2HPh, 1, with [Fe(CO)4 yields the binuclear μ-vinylidene complex Cp(CO)2MnFe(μ-C1C 2HPh)(CO)4, 2, that further isomerizes to the carbonylated product η4-[Cp(CO)2MnC1(CO)C 2HPhFe(CO)3, 3. In a computational study of the mechanism using a hybrid density functional method, we considered two stereoisomers for species 2 and 3 where the phenyl group at center C2 is oriented in cis (E form) or trans (Z form) fashion to the Cp(CO)2Mn unit. Isomers 2E and 2Z were calculated to be degenerate whereas the experimentally detected species 3E is 8 kcal/mol more stable than its isomer 3Z. The two-step pathway 1 → 2Z → 3E was calculated to be the lowest-energy route with the highest activation barrier at 12 kcal/mol. The activation energy of the alternative single-step pathway 1 → 3E is 19 kcal/mol. We rationalized the stabilization of the ground state of 3E and the transition states leading to or starting from isomer 2Z as conjugation effect between the Mn-CC metallaallene fragment and the co-planar phenyl ring.

Seiten (von - bis)3445-3453
FachzeitschriftJournal of Organometallic Chemistry
PublikationsstatusVeröffentlicht - 1 Nov. 2011


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