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Activation of SiH, BH, and PH Bonds at a Single Nonmetal Center
Author(s) -
Frey Guido D.,
Masuda Jason D.,
Donnadieu Bruno,
Bertrand Guy
Publication year - 2010
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.201005698
Subject(s) - electrophile , nonmetal , boranes , chemistry , nucleophile , silanes , cleavage (geology) , bond cleavage , medicinal chemistry , transition metal , stereochemistry , boron , catalysis , metal , organic chemistry , materials science , silane , composite material , fracture (geology)
Carbenes more than measure up : Singlet stable carbenes compete with transition metals in the activation of enthalpically strong bonds, as shown by the cleavage of the EH bonds of silanes, boranes, and phosphanes (see scheme). However, in contrast with the electrophilic mode of activation observed with metals, carbenes act as nucleophiles towards these substrates. Dipp=2,6‐diisopropylphenyl.

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