Abstract

Four novel ion-pair complexes, [FClBzTPP]2[Cu(mnt)2](1), [DiClBzTPP]2[Cu(mnt)2](2), [FClBzTPP][Ni(mnt)2](3) and [DiClBzTPP][Ni(mnt)2](4), where [FClBzTPP]+=1-(2′-chloro-4′-flurobenzyl)triphenylphosphonium, [DiClBzTPP]+=1-(2′, 4′-chlorobenzyl)triphenylphosphonium and mnt2−=maleonitriledithiolate, have been prepared and characterized by elemental analyses, IR, UV, single crystal X-ray diffraction and magnetic measurements. Weak interactions such as F⋯F, Cl⋯Cl, and C–H⋯N, C–H⋯Cl, C–H⋯Cu observed in 1 and 2 consolidate 3D network structure. The Ni(III) ions of 3 and 4 form a 1D linear chain in a column of [Ni(mnt)2]− anions by intermolecular Ni⋯Ni and Ni⋯S or π⋯π weak interactions. The change of 4-substituted group in the benzyl ring from F to Cl atom results in the crystal system, space group, and the stacking and overlapping modes of [Ni(mnt)2]− anions in 3 and 4. Magnetic susceptibility measurements show that 1 and 2 at 20–300K exhibit weak ferromagnetic coupling with θ=4.21K and 1.80K, whereas while 3 and 4 show antiferromagnetic coupling with J=−36.42cm−1 and −55.78cm−1.

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