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Heterolytic Dihydrogen Activation by a Frustrated Carbene–Borane Lewis Pair

Holschumacher, Dirk, Bannenberg, Thomas, Hrib, Cristian G., Jones, Peter G., Tamm, Matthias·2008·Angewandte Chemie International Edition

Abstract

Relief from frustration: The sterically demanding carbene 1,3-di-tert-butylimidazolin-2-ylidene and B(C6F5)3, a “frustrated” Lewis pair, is a viable system for the activation of CO, HH, and CH bonds. However, slow rearrangement to an abnormal carbene–borane adduct allows the irreversible formation of a strong BC bond and enables this system to circumvent frustration at the expense of its activity.

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Metadata

Authors
Holschumacher, D., Bannenberg, T., Hrib, C. G., Jones, P. G., & Tamm, M.
Venue
Angewandte Chemie International Edition
Publisher
Wiley
Published
2008-09-09
Volume
47
Issue
39
Pages
7428-7432
ISSN
  • 1433-7851 (ISSN-L)
  • 1521-3773
OpenAlex
W2115378983
Cited by
393
References
0
FWCI
22.61
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Heterolytic Dihydrogen Activation by a Frustrated Carbene–Borane Lewis Pair. https://app.cochat.ai/papers/10.1002/anie.200802705
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Holschumacher, D., Bannenberg, T., Hrib, C. G., Jones, P. G., & Tamm, M. (2008). Heterolytic Dihydrogen Activation by a Frustrated Carbene–Borane Lewis Pair. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.200802705

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