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Spectroscopic and computational studies of a μ-η2: η2-disulfido-bridged dinickel(II) species, [{(PhTt tBu)Ni}2(μ- η2: η2-S2)]: Comparison of side-on disulfido and peroxo bonding in (NiII) 2 and (CuII)2 species

Title
Spectroscopic and computational studies of a μ-η2: η2-disulfido-bridged dinickel(II) species, [{(PhTt tBu)Ni}2(μ- η2: η2-S2)]: Comparison of side-on disulfido and peroxo bonding in (NiII) 2 and (CuII)2 species
Authors
Van Heuvelen K.M.Cho J.Riordan C.G.Brunold T.C.
Ewha Authors
조재흥
Issue Date
2010
Journal Title
Inorganic Chemistry
ISSN
0020-1669JCR Link
Citation
vol. 49, no. 7, pp. 3113 - 3120
Indexed
SCI; SCIE; SCOPUS scopus
Abstract
In this study, a combined spectroscopic and computational approach has been employed to generate a detailed description of the electronic structure of a binuclear side-on disulfido (Ni")2 complex, [{(PhTt tBu Ni)2(μ-η2 :η2-S 2)] (1, where PhTttBu = phenyltris[(tert-birtylthto) methyl]borate). The disulfido-to-Ni" charge-transfer transitions that dominate the electronic absorption spectrum have been assigned on the basis of time-dependent density functional theory (DFT) calculations. Resonance Raman spectroscopic studies of 1 have revealed that the S-S stretching mode occurs at 446 cm-1, indicating that the S-S bond is weaker in 1 than in the analogous μ-η2:η;2-S2 dicopper species. DFT computational data indicate that the steric bulk of PhTt,tBu stabilize the side-on core enough to prevent its conversion to the electronically preferred bis(/i-sulfido) (NiIII)2 structure. Hence, 1 provides an interesting contrast to its O2-derived analogue, [((PhTt tBu)2(μ-O)2], which was shown previously to assume a bis(μ-O) (NiIII)2 "diamond core". By a comparison of 1 to analogous disuffidodicopper and peroxodinickel species, new insight has been obtained into the roles that the metal centers, bridging ligands, and supporting ligands play in determining the core structures and electronic properties of these dimers. © 2010 American Chemical Society.
DOI
10.1021/ic901731b
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자연과학대학 > 화학·나노과학전공 > Journal papers
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