4.5 Article

Unusual η1 (S) coordination of dibenzothiophene to trinuclear acetylide clusters [(μ-H)M3(CO)9(CCSiMe3)] (M = Ru, Os).)

Journal

JOURNAL OF ORGANOMETALLIC CHEMISTRY
Volume 939, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jorganchem.2021.121766

Keywords

Trinuclear ruthenium clusters; Osmium clusters; Acetylide ligands; Dibenzo-and benzothiophene; Sulfur coordination

Funding

  1. Conacyt

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Acetylide derivatives react with dibenzothiophene to produce complexes characterized by NMR and X-ray crystal structures. The DBT and benzothiophene complexes show ligands coordinated to metal atoms in specific ways.
The acetylide derivatives [(mu-H)M-3(CO)(9)(CCSiMe3)] (M = Ru, Os) react with dibenzothiophene (DBT) in the presence of Me3NO to produce a DBT complex where the acetylide ligand remains coordinated without modifications and the DBT is coordinated eta(1) through the sulfur atom. Both complexes were characterized by NMR spectroscopy and X-ray crystal structures were determined. Benzothiophene was also made to react with the ruthenium complex producing a complex with similar spectroscopic data. The DBT structures show the ligand to be coordinated eta(1)(S) to one of the metal atoms. (C) 2021 Elsevier B.V. All rights reserved.

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