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Synthesis and Applications of RuCl2(CHR‘)(PR3)2: The Influence of the Alkylidene Moiety on Metathesis Activity

Schwab, Peter, Grubbs, Robert H., Ziller, Joseph W.·1996·Journal of the American Chemical Society

Abstract

The reactions of RuCl 2 (PPh 3 ) 3 with a number of diazoalkanes were surveyed, and alkylidene transfer to give RuCl 2 ( CHR)(PPh 3 ) 2 (R = Me ( 1 ), Et ( 2 )) and RuCl 2 ( CH- p -C 6 H 4 X)(PPh 3 ) 2 (X = H ( 3 ), NMe 2 ( 4 ), OMe ( 5 ), Me ( 6 ), F ( 7 ), Cl ( 8 ), NO 2 ( 9 )) was observed for alkyl diazoalkanes RCHN 2 and various para -substituted aryl diazoalkanes p -C 6 H 4 XCHN 2 . Kinetic studies on the living ring-opening metathesis polymerization (ROMP) of norbornene using complexes 3 − 9 as catalysts have shown that initiation is in all cases faster than propagation ( k i / k p = 9 for 3 ) and that the electronic effect of X on the metathesis activity of 3 − 9 is relatively small. Phosphine exchange in 3 − 9 with tricyclohexylphosphine leads to RuCl 2 ( CH- p -C 6 H 4 X)(PCy 3 ) 2 10 − 16, which are efficient catalysts for ROMP of cyclooctene (PDI = 1.51−1.63) and 1,5-cyclooctadiene (PDI = 1.56−1.67). The crystal structure of RuCl 2 ( CH- p -C 6 H 4 Cl)(PCy 3 ) 2 ( 15 ) indicated a distorted square-pyramidal geometry, in which the two phosphines are trans to each other, and the alkylidene unit lies in the Cl−Ru−Cl plane. The benzylidenes RuCl 2 ( CHPh)(PR 3 ) 2 (R = Cy (cyclohexyl) ( 10 ), Cp (cyclopentyl) ( 17 ), i -Pr ( 18 )) are quantitatively available via one-pot synthesis with RuCl 2 (PPh 3 ) 3, PhCHN 2, and PR 3 as reaction components. 10 is an efficient catalyst for metathesis of acyclic olefins: On reaction with excess ethylene, the methylidene complex RuCl 2 ( CH 2 )(PCy 3 ) 2 ( 19 ) is formed quantitatively, and various alkylidene compounds RuCl 2 ( CHR)(PCy 3 ) 3 (R = Me ( 20 ), Et ( 21 ), n -Bu ( 22 )) are isolated as the kinetic products from the reaction of 10 with an excess of the corresponding terminal or disubstituted olefins. Metathesis of conjugated and cumulated olefins with 10 results in the formation of vinylalkylidene and vinylidene complexes, as shown by the synthesis of RuCl 2 ( CHCH CH 2 )(PCy 3 ) 2 ( 23 ) and RuCl 2 ( C CH 2 )(PCy 3 ) 2 ( 24 ) from 1,3-butadiene or 1,2-propadiene, respectively. Also, functional groups such as −OAc, −Cl, and −OH can be introduced into the alkylidene moiety via cross metathesis with the appropriate alkene.

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Metadata

Authors
Schwab, P., Grubbs, R. H., & Ziller, J. W.
Venue
Journal of the American Chemical Society
Published
1996-01-01
Volume
118
Issue
1
Pages
100-110
ISSN
  • 0002-7863 (ISSN-L)
  • 1520-5126
OpenAlex
W1981287002
Cited by
2,117
References
6
FWCI
79.57
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Synthesis and Applications of RuCl2(CHR‘)(PR3)2: The Influence of the Alkylidene Moiety on Metathesis Activity. https://app.cochat.ai/papers/10.1021/ja952676d
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Schwab, P., Grubbs, R. H., & Ziller, J. W. (1996). Synthesis and Applications of RuCl2(CHR‘)(PR3)2: The Influence of the Alkylidene Moiety on Metathesis Activity. Journal of the American Chemical Society. https://doi.org/10.1021/ja952676d

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