Site of Bond Breaking in mer-(Dihapto-[60]fullerene) (Dihapto-1,2-Bis-(DiphenyIphosphino)ethane Tricarbonyl Tungsten(0)

Verfasser / Beitragende:
[Yessenia Ocasio-Delgadof, Luis A. Rivera-Riveraf, Gisela Crespo-Romanf, Jose E. Cortes-Figueroa]
Ort, Verlag, Jahr:
2003
Enthalten in:
BioInorganic Reaction Mechanisms, 5/1(2003-01-01), 13-20
Format:
Artikel (online)
ID: 378871099
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024 7 0 |a 10.1515/irm-2003-0102  |2 doi 
035 |a (NATIONALLICENCE)gruyter-10.1515/irm-2003-0102 
245 0 0 |a Site of Bond Breaking in mer-(Dihapto-[60]fullerene) (Dihapto-1,2-Bis-(DiphenyIphosphino)ethane Tricarbonyl Tungsten(0)  |h [Elektronische Daten]  |c [Yessenia Ocasio-Delgadof, Luis A. Rivera-Riveraf, Gisela Crespo-Romanf, Jose E. Cortes-Figueroa] 
520 3 |a Piperidine (pip) displaces l,2-bis(diphenylphosphino)ethane (dppe) from mer-(η2-C60)(η2-dppe)W(CO)3 to produce mer*-(η2-C60)(η1-ρίρ)2\ν(ΟΟ)3. The reactions are first order and second order with respect to the molar concentrations of m£r-(r|2-C60)(r|2-dppe)W(CO)3 and pip, respectively. The proposed mechanism, based on the rate law and on the activation parameters, involves an initial pip-assisted ringopening of the dppe ligand to produce the electronically-saturated intermediate fac (η2-C60)(η'-ρίρ) (n1-dppe)W(CO)3. This mechanism differs from previously proposed mechanisms for the ligand exchange reactions of closely-related complexes such as/fac-(η1-L)(η2-dppe)W(CO)3 (L = CO, piperidine, pyridine) and is contrary to the known cis labilizing property of dppe. These results suggest that [60]fullerene has a strong steric influence on the inorganic moiety of the complex and on its chemical behavior. 
540 |a © 2014 by Walter de Gruyter Berlin/Boston 
690 7 |a [60]fullerene  |2 nationallicence 
690 7 |a Metal Carbonyls  |2 nationallicence 
690 7 |a Transition Metals  |2 nationallicence 
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700 1 |a Crespo-Romanf  |D Gisela  |4 aut 
700 1 |a Cortes-Figueroa  |D Jose E.  |4 aut 
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