Issue 43, 2008

A total loss of innocence: double ortho-metallation of bis(triphenylphosphano)iminium cation, [N(PPh3)2]+, by tris(η-naphthalene)tantalate(1−)

Abstract

For the first time [N(PPh3)2]+, or [PPN]+, has been shown to undergo an irreversible reaction with a transition metal complex under ambient conditions and affords a product containing a unique structural motif in which two phenyl groups on onePPh3 substituent of [PPN]+ are ortho-metallated, while the third phenyl ring is hydrogenated to provide a tantalum bound 1,3-cyclohexadiene group.

Graphical abstract: A total loss of innocence: double ortho-metallation of bis(triphenylphosphano)iminium cation, [N(PPh3)2]+, by tris(η-naphthalene)tantalate(1−)

Supplementary files

Article information

Article type
Communication
Submitted
03 Jul 2008
Accepted
12 Sep 2008
First published
01 Oct 2008

Chem. Commun., 2008, 5642-5644

A total loss of innocence: double ortho-metallation of bis(triphenylphosphano)iminium cation, [N(PPh3)2]+, by tris(η-naphthalene)tantalate(1−)

V. J. Sussman and J. E. Ellis, Chem. Commun., 2008, 5642 DOI: 10.1039/B811320C

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