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A selenium-bonded oxorhenium(V) complex: solvothermal synthesis, structural characterization, and electrochemical behavior

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Abstract

The solvothermal reaction of [ReOCl3(PPh3)2] with 2,2′-seleno-bis(4,6-di-tert-butylphenol) (H2L1) in ethanol at 95 °C resulted in an oxorhenium(V) complex of formulation [ReO(L1)(L2)] due to the in situ formation of 2-selenochloromethyl-4,6-di-tert-butylphenolate (L2) through the cleavage of one C–Se bond of H2L1. The mononuclear oxorhenium(V) complex was characterized by physicochemical and spectroscopic methods along with detailed structural analysis by single crystal X-ray crystallography. Electrochemical studies revealed a one-electron equivalent quasi-reversible voltammogram for the ReO(V)/ReO(VI) redox couple at 1.28 V (versus SCE) with no cathodic response for ReO(V) → ReO(IV) reduction.

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Acknowledgments

Financial support from UGC-DAE-CSR, Kolkata, India, is gratefully acknowledged. E. Zangrando thanks MIUR-Rome, PRIN No 2007HMTJWP_002 for financial support.

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Correspondence to Pabitra Chattopadhyay.

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Das, B., Chakraborty, R., Sarkar, S. et al. A selenium-bonded oxorhenium(V) complex: solvothermal synthesis, structural characterization, and electrochemical behavior. Transition Met Chem 36, 663–667 (2011). https://doi.org/10.1007/s11243-011-9516-9

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  • DOI: https://doi.org/10.1007/s11243-011-9516-9

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