Binding Features of {M(3d)(cbdc)2 } Blocks (M(3d)=VIV O, CuII ; cbdc2- =Dianion of Cyclobutane-1,1-Dicarboxylic Acid) in Formation of Heterometallic Structures with d-Metal Cations
Compounds containing bis‐chelate dianionic blocks {M(3d)(cbdc)2}2– (M(3d)=VIVO, CuII) with cations VO2+ and Cu2+ chelated by two anions of dicarboxylic acid have been prepared as crystals when aqueous solutions of vanadyl sulfate VOSO4⋅3H2O or copper sulfate CuSO4⋅5H2O have been allowed to react with sulfates of d‐metals (MnII, CoII, NiII, ZnII, and CdII) and barium salt of cyclobutane‐1,1‐dicarboxylic acid (H2cbdc=C4H6(CO2H)2) in the 1:1:2 ratio. The nature of the M(3d) metal center has been found to influence on the structure of the heterometallic compounds formed. 1D polymers [M(VO)(cbdc)2(EtOH)2(H2O)3]n (M=Mn (1), Co (2), Ni (3)), molecular dinuclear complex [Zn(VO)(cbdc)2(H2O)5]⋅H2O (4), and 1D polymer {[Cd(VO)(cbdc)2(H2O)5]⋅H2O}n (5) are formed when M(3d)=VIVO, whereas in the case of the bis‐chelate block with the CuII atom, ionic compounds [M(H2O)6][Cu(cbdc)2(H2O)] (M=Mn (6), Co (7), Ni (8), Zn (9)) and 2D polymer {[CdCu(cbdc)2(H2O)2]⋅2H2O}n have been synthesized. The isolation of paramagnetic centers in compounds 1–10 is confirmed by magnetic measurements and EPR spectroscopy.
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