Abstract

AbstractThe polynuclear copper(II) complex [Cu2(Hdpa)2(μ‐ClDHBQ)(ClO4)2]n, 1 is bridged by ClDHBQ−2 (2,5‐dichloro‐3,6‐dihydroxy‐1,4‐benzoquinone dianionic) and 2,2′‐dipyridylamine (Hdpa). In the axial position, Cu is connected with the oxygen atom of ClO. The perchlorate anion may be envisaged as a monodentate O‐bound ligand. Through the bond bridge of O–Cu … O–Cl, the binuclear compound [Cu2(Hdpa)2(μ‐ClDHBQ)(ClO4)2] is strung together into a long chain compound. Tetrachlorocatechol underwent partial oxidation/hydrolysis/dechlorination processes to produce ClDHBQ−2.The other mononuclear complex [Cu(Hdpa)(TeCQ)](DMF), 2, in which tetrachloroquinone (TeCQ) was produced by oxidation of tetrachlorocatechol (TeCC), therefore complex 2 is in the quinone form.The magnetic susceptibility measurements show antiferromagnetic coupling with J = −11.9 cm−1, θ = 2.6 K, and g = 2.05 for complex 1. Complex 2 exhibits the typical paramagnetic behavior of s = 1/2.

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