4.7 Article

A Copper(II) Thiolate from Reductive Cleavage of an S-Nitrosothiol

Journal

INORGANIC CHEMISTRY
Volume 51, Issue 16, Pages 8658-8660

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ic301356h

Keywords

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Funding

  1. NSF [CHE-0957606, CHE-0840453]
  2. DFG [SFB-583]
  3. Division Of Chemistry
  4. Direct For Mathematical & Physical Scien [0957606] Funding Source: National Science Foundation

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S-Nitrosothiols RSNO represent circulating reservoirs of nitric oxide activity in the plasma and play intricate roles in protein function control in health and disease. While nitric oxide has been shown to reductively nitrosylate copper(II) centers to form copper(I) complexes and ENO species (E = R2N, RO), well-characterized examples of the reverse reaction are rare. Employing the copper(I) beta-diketiminate [Me2NN]Cu, we illustrate a clear example in which an RS NO bond is cleaved to release NO g with formation of a discrete copper(II) thiolate. The addition of Ph3CSNO to [Me2NN]Cu generates the three-coordinate copper(H) thiolate [Me2NN]CuSCPh3, which is unstable toward free NO.

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