Inorg. Chem., 46 (18), 7536 -7544, 2007. 10.1021/ic700878y S0020-1669(70)00878-9
Web Release Date: August 8, 2007

Copyright © 2007 American Chemical Society

An Experimental and Computational Study of Sulfur-Modified Nucleophilicity in a Dianionic NiN2S2 Complex

Kayla N. Green, Scott M. Brothers, Roxanne M. Jenkins, Cody E. Carson, Craig A. Grapperhaus, and Marcetta Y. Darensbourg*

Department of Chemistry, Texas A&M University, College Station, Texas 77845, and Department of Chemistry, University of Louisville, Louisville, Kentucky 40292

Received May 7, 2007

Abstract:

The dianionic NiN2S2 complex, Ni(ema)2-, ema = N,N'-ethylenebis-2-mercaptoacetamide, known as a reasonable model of the tripeptide complex Ni(CGC)2- (C = cysteine; G = glycine) with respect to the two carboxyamido nitrogens and cis-dithiolates in a (N2S2)4- ligand scaffold as found in acetyl CoA synthase, has been explored for S-based reactivity toward oxygenation and alkylation. The isolation and structural characterization of a sulfinato species, [Et4N]2[Ni(ema)·O2], prepared through a unique direct reaction of molecular O2 with crystalline [Et4N]2[Ni(ema)] is described. Reaction of [Et4N]2[Ni(ema)] with Br(CH2)3Br yields a neutral N2S2 macrocyclic complex shown by DFT computations and electrostatic-potential mapping to be opposite in electron distribution from the neutral NiN2S2 complexes in which the anionic charge is localized on sulfur.


Download the full text: PDF | HTML