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Dithiolate and Catecholate Binding of Copper by the OO∼SS Bifunctional Ligand: Regioselectivity and Regioisomeric Transformations
Author(s) -
Kuropatov Viacheslav A.,
Cherkasova Anna V.,
Martyanov Konstantin A.,
Cherkasov Anton V.,
Starikov Andrey G.,
Cherkasov Vladimir K.
Publication year - 2021
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.202100517
Subject(s) - chemistry , bifunctional , regioselectivity , copper , ligand (biochemistry) , electron paramagnetic resonance , ring (chemistry) , quinone , adduct , bipyridine , ring size , metal , stereochemistry , crystallography , catalysis , organic chemistry , crystal structure , biochemistry , physics , receptor , nuclear magnetic resonance
o‐Quinone bearing annulated dithiete ring ( DitQ ) provides a unique opportunity for comparison of properties of benzodithiolene and benzodioxolene coordination sites. The majority of Pd, Pt or alkali metal containing metallofragments are regioselectively bound either by dithiolene or dioxolene site of the DitQ , whereas Cu(II) adducts with phenanthroline or bipyridine display equilibrium between catecholate and dithiolate forms. To the best of our knowledge this is a rare example of equilibrium between regioisomeric coordination compounds. We determined the energetic parameters of this equilibrium from temperature‐dependent electron paramagnetic resonance measurements. Unambiguous dithiolate binding mode for DitQ was found in case of trinuclear Cu(I)−Cu(II)−Cu(I) species where a formal oxidation state of copper is +1 1 / 3 .