A molecular modeling study of the changes of some steric properties of the precatalysts during the olefin metathesis reaction
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Marx, Frans T.I.
Jordaan, Johan H.L.
Lachmann, Gerhard
Vosloo, Hermanus C.M.
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Wiley
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Abstract
The productive self-metathesis of 1-octene with a series of new
phosphine ligated Grubbs-type precatalysts was studied. The
resulting structures were used to compare some steric properties
of the new precatalysts with those of well-known precatalysts.
The possibility of α-CC agnostic stabilization as well as the
ability of the ligands to shield the metal was studied. A comparison
of the obtained data, pointed to the unlikelihood that α-
CC agostic stabilization is a major contribution to the stabilization
of the various metallacyclobutane rings. The similarity in
the ability of the ligands to shield the metal also raised questions
about the comparison of experimentally observed trends
with those obtained theoretically
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Additional supporting information may be found in the
online version of this article: http://onlinelibrary.wiley.com/journal/10.1002/%28ISSN%291096-987X
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Marx, F.T.I. et al. 2014. A molecular modeling study of the changes of some steric properties of the precatalysts during the olefin metathesis reaction. Journal of computational chemistry, 35(19):1457-1463. [https://doi.org/10.1002/jcc.23641]
