[Ru(HNO)('py(bu)S4')], the first HNO complex resulting from hydride addition to a NO complex ('pybuS4'2-=2,6-Bis(2-mercapto-3,5-di-tert-butylphenylthio)dime thylpyridine(2-1))

D Sellmann; T Gottschalk-Gaudig; D Häussinger; F W Heinemann; B A Hess

doi:10.1002/1521-3765(20010518)7:10<2099::aid-chem2099>3.0.co;2-a

[Ru(HNO)('py(bu)S4')], the first HNO complex resulting from hydride addition to a NO complex ('pybuS4'2-=2,6-Bis(2-mercapto-3,5-di-tert-butylphenylthio)dime thylpyridine(2-1))

Chemistry. 2001 May 18;7(10):2099-103. doi: 10.1002/1521-3765(20010518)7:10<2099::aid-chem2099>3.0.co;2-a.

Authors

D Sellmann¹, T Gottschalk-Gaudig, D Häussinger, F W Heinemann, B A Hess

Affiliation

¹ Institut für Anorganische Chemie der Universität Erlangen-Nürnberg, Germany. sellmann@anorganik.chemie.uni.erlangen.de

PMID: 11411982
DOI: 10.1002/1521-3765(20010518)7:10<2099::aid-chem2099>3.0.co;2-a

Abstract

Treatment of the nitrosyl complex [Ru(NO)('pybuS4')]Br (1a) with NaBH4 in CH3OH yielded [Ru(HNO)('pybuS4')](2), which could be completely characterized. The X-ray structure determination of 2 confirmed the N coordination of the HNO ligand. Density functional theory calculations enabled us to assign the nu(NO) IR band of 2, which appears in KBr at 1358cm(-1) and in THF at 1378 cm(-1). The unprecedented hydride addition to nitrosyl complexes yielding HNO complexes fills a white spot on the map of chemical reactions, represents the as yet unknown counterpart to the well-established formyl complex formation from CO complexes and hydrides, and distinctly differs from the formation reaction of [Os(HNO)(CO)Cl2(PPh3)2], the only other HNO complex characterized structurally. The HNO complex 2 is oxidized stepwise by [Cp2Fe]PF6 in the presence of NEt3 and directly by Bronsted acids to give [Ru(NO)('pybuS4')]+ in 2e- oxidations. H+/D+ exchange indicates acidity of the HNO proton.