@article { ISI:000355382500001,
	title = {Amidate-Ligated Complexes of Rhodium(I): A Showcase of Coordination Flexibility},
	journal = {ORGANOMETALLICS},
	volume = {34},
	number = {10},
	year = {2015},
	month = {MAY 25},
	pages = {1783-1786},
	abstract = {Reaction of the amidate ligand salts Na{[}N(Dipp)C(O)R] (R = Ph (1a), tBu (1b); Dipp = 2,6-diisopropylphenyl) with {[}Rh(NBD)-Cl](2) (NBD = norbomadiene) proceeds to give the dirhodium(I) complexes {[}Rh-2\{mu(2)-N,O-N(Dipp)C(O)R\}(2)(NBD)(2)] (R = Ph (2a), tBu (2b)) with variable coordination behavior. For complex 2b, a monomer-dimer equilibrium with the mononuclear complex {[}Rh\{kappa(2)-N,O-N(Dipp)-C(O)tBu\}(NBD)] (3b) was established for the first time. Precursors 2a,b were treated with PPh3 and PCy3, giving the distorted-square-planar kappa(2)-N,O amidates {[}Rh-\{kappa(2)-N,O-N(Dipp)C(O)R\}(PPh3)(2)] (R = Ph (4a), tBu (4b)) or the kappa(1)-O complexes {[}Rh\{kappa(1)-O-N(Dipp)C(O)R\}(NBD)(PCy3)] (R = Ph (5a), tBu (5b)). Initial reactivity screening showed that complex 4b undergoes O-2 activation, providing Ph3P=O; via the transient peroxo complex 6b, which was characterized in the solution phase. The kappa(2)-N,O amidate coordination in 6b has been conclusively established by diagnostic C-13\{H-1\} NMR spectroscopy.},
	issn = {0276-7333},
	doi = {10.1021/om501209c},
	author = {Drover, Marcus W. and Schafer, Laurel L. and Love, Jennifer A.}
}
