Journal
INORGANICA CHIMICA ACTA
Volume 514, Issue -, Pages -Publisher
ELSEVIER SCIENCE SA
DOI: 10.1016/j.ica.2020.120033
Keywords
N-heterocyclic carbene; Copper; X-ray crystallography; Coordination
Categories
Funding
- Southeastern Conference (SEC) Visiting Faculty Travel Grant Program
- National Science Foundation [CHE-1855641]
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N-Heterocyclic Carbene (NHC) ligands play a crucial role in synthesizing novel metal and main group-containing compounds. This study focuses on the coordination chemistry of CS2 and PhNCS derivatives of the sterically encumbering 1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene (IPr).
N-Heterocyclic Carbene (NHC) ligands have been instrumental in the synthesis of novel metal and main group-containing compounds, as well as their subsequent reactivity. Here, the coordination chemistry of CS2 and PhNCS derivatives of the sterically encumbering 1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene (IPr) are studied. The reaction of IPr center dot CS2 with Cu(I) and Ag(I) salts results in the isolation of dinuclear complexes, [(IPr center dot CS2)(2)M-2(THF)(n)][X](2), M = Cu, X = PF6, n = 4; M = Ag, X = OTf, n = 2. The 1:1 stoichiometric reaction of IPr center dot PhNCS with CuI results in to the formation of ([IPr center dot PhNCS)(2)Cul[CuI2]. All complexes were characterized by H-1, C-13, and IR spectroscopy and their solid-state structures determined by X-ray crystallography.
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