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Dinitrogen chemistry from trigonally coordinated iron and cobalt platforms

Betley, Theodore A. and Peters, Jonas C. (2004) Dinitrogen chemistry from trigonally coordinated iron and cobalt platforms. Abstracts of Papers of the American Chemical Society, 227 . INOR 506. ISSN 0065-7727. https://resolver.caltech.edu/CaltechAUTHORS:20140728-135836434

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Abstract

The chemistry of low-valent iron and cobalt has been slow to develop, due largely in part to a lack of ligand scaffolds that can stabilize these species. Using the anionic tris(phosphino)borate ligand, [PhB(CH_2PiPr_2)_3]-, we have stabilized reactive complexes of the type [P_3M-L] where L can be varied from weakly-donating π-acidic ligands (e.g. N_2), to strongly π-basic ligands where multiple bonding occurs between the metal and L (e.g. NR ^2-). In addition to stabilizing a broad range of ligand types in a variety of oxidation states, the [P_3M] template has been shown to mediate the coordination and activation of dinitrogen on both iron and cobalt. The reaction chemistry of the [P_3M-L] scaffolds will be presented in addition to synthetic strategies targeting high-valent species (M^(IV), L=N ^3-).


Item Type:Article
ORCID:
AuthorORCID
Peters, Jonas C.0000-0002-6610-4414
Additional Information:© 2004 American Chemical Society.
Record Number:CaltechAUTHORS:20140728-135836434
Persistent URL:https://resolver.caltech.edu/CaltechAUTHORS:20140728-135836434
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:47529
Collection:CaltechAUTHORS
Deposited By: Tony Diaz
Deposited On:29 Jul 2014 18:34
Last Modified:26 Nov 2019 11:15

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