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Sulfur transfer reactions of a zinc tetrasulfanido complex.
Ballesteros Ii, Moises; Tsui, Emily Y.
Affiliation
  • Ballesteros Ii M; Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, Indiana 46556, USA. etsui@nd.edu.
Dalton Trans ; 49(45): 16305-16311, 2020 Nov 25.
Article in En | MEDLINE | ID: mdl-32427258
ABSTRACT
A zinc tetrasulfanido complex supported by a bis(carboxamide)pyridine ligand framework has been synthesized by the insertion of elemental sulfur into the zinc-S(thiolate) bond of a zinc dithiolate complex ([LZn]2-). This paper reports on sulfur transfer reactions of this polysulfanido complex ([1]2-) and compares this behavior to known reactions of metal polysulfido complexes. Complex [1]2- was demonstrated to be in exchange with [LZn]2- and free elemental sulfur in solution. Although triphenylphosphine abstracts sulfur from [1]2- to form [LZn]2-, complex [LZn]2- can abstract sulfur from the zinc polysulfido complex (TMEDA)ZnS6 (TMEDA = N,N,N',N'-tetramethylethylenediamine). The tetrasulfanido complex [1]2- can also transfer sulfur to dimethyl acetylenedicarboxylate to form a zinc dithiolene complex. These studies demonstrate that the zinc complex with a tetrasulfanido moiety can undergo similar reactions as metal complexes with purely inorganic polysulfido groups, although the final metal-containing products are different.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Dalton Trans Journal subject: QUIMICA Year: 2020 Document type: Article Affiliation country: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Dalton Trans Journal subject: QUIMICA Year: 2020 Document type: Article Affiliation country: Estados Unidos