Monoaryloxide Pyrrolide (MAP) Imido Alkylidene Complexes of Molybdenum and Tungsten That Contain 2,6-Bis(2,5-R[subscript 2]-pyrrolyl)phenoxide (R = i-Pr, Ph) Ligands and an Unsubstituted Metallacyclobutane on Its Way to Losing Ethylene
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Reithofer_2013-Monoaryloxide pyrrolide.pdf
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Author(s) • • •
Reithofer, Michael R.
Dobereiner, Graham E.
Schrock, Richard Royce
Muller, Peter
Date Issued
May 2013
Journal
Organometallics
Publisher
American Chemical Society (ACS)
Citation
Reithofer, Michael R., Graham E. Dobereiner, Richard R. Schrock, and Peter Müller. “Monoaryloxide Pyrrolide (MAP) Imido Alkylidene Complexes of Molybdenum and Tungsten That Contain 2,6-Bis(2,5-R2-pyrrolyl)phenoxide (R = i-Pr, Ph) Ligands and an Unsubstituted Metallacyclobutane on Its Way to Losing Ethylene.” Organometallics 32, no. 9 (May 13, 2013): 2489-2492. © 2013 American Chemical Society
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Final published version
Abstract
We report the synthesis of Mo and W MAP complexes that contain O-2,6-(2,5-R[subscript 2]-pyrrolyl)[subscript 2]C[subscript 6]H[subscript 3] (2,6-dipyrrolylphenoxide or ODPP[superscript R]) ligands in which R = i-Pr, Ph. W(NAr)(CH-t-Bu)(Pyr)(ODPP[superscript Ph]) (4a; Ar = 2,6-disopropylphenyl, Pyr = pyrrolide) reacts readily with ethylene to yield a metallacyclobutane complex, W(NAr)(C[subscript 3]H[subscript 6])(Pyr)(ODPP[superscript Ph]) (5). The structure of 5 in the solid state shows that it is approximately a square pyramid with the WC[subscript 4] ring spanning apical and basal positions. This SP′ structure, which has never been observed as an actual intermediate, must now be regarded as an integral feature of the metathesis reaction.
MIT Department
Massachusetts Institute of Technology. Department of Chemistry
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DOI of Published Version
https://doi.org/10.1021/om400114h