Dataset Information

X-ray absorption spectroscopic and computational investigation of a possible S···S interaction in the [Cu3S2]3+ core.

ABSTRACT: The electronic structure of the [Cu(3)S(2)](3+) core of [(LCu)(3)(S)(2)](3+) (L = N,N,N',N'-tetramethyl-2R,3R-cyclohexanediamine) is investigated using a combination of Cu and S K-edge X-ray absorption spectroscopy and calculations at the density functional and multireference second-order perturbation levels of theory. The results show that the [Cu(3)S(2)](3+) core is best described as having all copper centers close to but more oxidized than Cu(2+), while the charge on the S(2) fragment is between that of a sulfide (S(2-)) and a subsulfide (S(2)(3-)) species. The [Cu(3)S(2)](3+) core thus is different from a previously described, analogous [Cu(3)O(2)](3+) core, which has a localized [(Cu(3+)Cu(2+)Cu(2+))(O(2-))(2)](3+) electronic structure. The difference in electronic structure between the two analogues is attributed to increased covalent overlap between the Cu 3d and S 3p orbitals and the increased radial distribution function of the S 3p orbital (relative to O 2p). These features result in donation of electron density from the S-S ?* to the Cu and result in some bonding interaction between the two S atoms at ~2.69 Å in [Cu(3)S(2)](3+), stabilizing a delocalized S = 1 ground state.

SUBMITTER: Sarangi R

PROVIDER: S-EPMC3202975 | biostudies-literature | 2011 Nov

REPOSITORIES: biostudies-literature

ACCESS DATA

Publications

X-ray absorption spectroscopic and computational investigation of a possible S···S interaction in the [Cu3S2]3+ core.

Sarangi Ritimukta R Yang Lei L Winikoff Stuart G SG Gagliardi Laura L Cramer Christopher J CJ Tolman William B WB Solomon Edward I EI

Journal of the American Chemical Society 20111006 43

The electronic structure of the [Cu(3)S(2)](3+) core of [(LCu)(3)(S)(2)](3+) (L = N,N,N',N'-tetramethyl-2R,3R-cyclohexanediamine) is investigated using a combination of Cu and S K-edge X-ray absorption spectroscopy and calculations at the density functional and multireference second-order perturbation levels of theory. The results show that the [Cu(3)S(2)](3+) core is best described as having all copper centers close to but more oxidized than Cu(2+), while the charge on the S(2) fragment is betw ...[more]

PMID: 21923178

Similar Datasets

Project description:Six-coordinate MnIII complexes are typically high-spin (S = 2), however, the scorpionate ligand, both in its traditional, hydridotris(pyrazolyl)borate form, Tp- and Tp*- (the latter with 3,5-dimethylpyrazole substituents) and in an aryltris(carbene)borate (i.e., N-heterocyclic carbene, NHC) form, [Ph(MeIm)3B]-, (MeIm = 3-methylimidazole) lead to formation of bis(scorpionate) complexes of MnIII with spin triplet ground states; three of which were investigated herein: [Tp2Mn]SbF6 (1SBF6), [Tp*2Mn]SbF6 (2SBF6), and [{Ph(MeIm)3B}2Mn]CF3SO3 (3CF3SO3). These trigonally symmetric complexes were studied experimentally by magnetic circular dichroism (MCD) spectroscopy (the propensity of 3 to oxidize to MnIV precluded collection of useful MCD data) including variable temperatures and fields (VTVH-MCD) and computationally by ab initio CASSCF/NEVPT2 methods. These combined experimental and theoretical techniques establish the 3A2g electronic ground state for the three complexes, and provide information on the energy of the "conventional" high-spin excited state (5Eg) and other, triplet excited states. These results show the electronic effect of pyrazole ring substituents in comparing 1 and 2. The tunability of the scorpionate ligand, even by perhaps the simplest change (from pyrazole in 1 to 3,5-dimethylpyrazole in 2) is quantitatively manifested through perturbations in ligand-field excited-state energies that impact ground-state zero-field splittings. The comparison with the NHC donor is much more dramatic. In 3, the stronger ?-donor properties of the NHC lead to a quantitatively different electronic structure, so that the lowest lying spin triplet excited state, 3Eg, is much closer in energy to the ground state than in 1 or 2. The zero-field splitting (zfs) parameters of the three complexes were calculated and in the case of 1 and 2 compare closely to experiment (lower by < 10%, < 2 cm-1 in absolute terms); for 3 the large magnitude zfs is reproduced, although there is ambiguity about its sign. The comprehensive picture obtained for these bis(scorpionate) MnIII complexes provides quantitative insight into the role played by the scorpionate ligand in stabilizing unusual electronic structures.

Dataset Information

X-ray absorption spectroscopic and computational investigation of a possible S···S interaction in the [Cu3S2]3+ core.

Publications

X-ray absorption spectroscopic and computational investigation of a possible S···S interaction in the [Cu3S2]3+ core.

Similar Datasets

OmicsDI is part of the ELIXIR infrastructure

Tweets