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Articles

Spectroscopic, structural and computational studies of thiophenolato bridged dirhenium(III,III) complexes

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Pages 2829-2842 | Received 28 Jun 2022, Accepted 16 Oct 2022, Published online: 11 Nov 2022
 

Abstract

Thiophenol (HLH), 4-methylthiophenol (HLMe) and 4-chlorothiophenol (HLCl) react with dirhenium(III,II) complex [Re2(µ-O2CCH3)Cl4(µ-dppm)2] (1) (dppm = Ph2PCH2PPh2) in refluxing dry toluene to afford the diamagnetic Re26+ complexes of the type [Re2(μ-LR)2Cl4(μ-dppm)2] (2(LR)) [LR = C6H5S, p-MeC6H4S and p-ClC6H4S]. These are the first examples of thiophenolato bridged dirhenium complexes with a Re26+ core containing dppm ligand. The spectral properties of the complexes are reported. In the electrochemical experiment, the type 2(LR) complexes show one quasi-reversible one-electron oxidation and one-electron reduction waves. The identity of 2(LMe) has been established by single-crystal X-ray structure determination (Re–Re distance = 2.6178(5) Å) and is shown to have an edge-shared bi-octahedral structure. DFT analysis shows that the highest occupied molecular orbitals are mainly composed of metal δ-based orbitals whereas the lowest unoccupied molecular orbitals are metal π*-based orbitals and the electronic ground state for the 2(LR) complexes is σ2π2δ*2δ2. Time-dependent DFT (TD-DFT) analysis shows that the sharp peak at 455 nm in the experimental UV-vis spectrum is mainly due to the [Cl(π)]→[Re2(π*)] transition.

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Disclosure statement

No potential conflict of interest was reported by the authors.

Additional information

Funding

Financial support from the Department of Science and Technology, Government of India (No. SR/S1/IC-65/2010) and the Council of Scientific & Industrial Research, New Delhi, India (No. 01(2898)/17/EMR-II) are gratefully acknowledged, University of Kalyani for infrastructural facilities. The support of DST-FIST to the Department of Chemistry and DST-PURSE to the University of Kalyani are acknowledged. J. Chowdhury thanks CSIR, India for the pre-doctoral fellowships.

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