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Two Supramolecular Isomers of Molecular Squares and 1D Helical Chains with Alternating Right- and Left-Handed Chirality

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journal contribution
posted on 03.10.2005, 00:00 by Long Jiang, Tong-Bu Lu, Xiao-Long Feng
The reaction of [Ni(α-rac-L)](ClO4)2 with K2[Ni(CN)4] gives a cyanide bridged [2+2] type of molecular square, {cis-[Ni(f-rac-L)][Ni(CN)4]}2 (1). By slightly changing the reaction conditions, the reaction of [Ni(α-rac-L)](ClO4)2 with KCN leads to a metastable compound, cis-[Ni(f-rac-L)(CN)2] (2), and an unexpected 1D helical chain, {cis-[Ni(f-rac-L)][Ni(CN)4]}n (3). In 3, the 1D helical chains are packed in an alternating right- and left-handed chirality due to the oppositely twisted arrangements of two adjacent [Ni(CN)4]2- anions. The metastable compound 2 can be converted to 3 in a CH3CN/CH3OH solution. Compounds 1 and 3 are classified as supramolecular isomers, and isomer 3 can be considered to be formed by the ring-opening polymerization of the square precursor 1. Magnetic susceptibility measurements of 1 and 3 show that the adjacent six-coordinated Ni(II) atoms are antiferromagnetically coupled through the bent −NC−Ni−CN− bridges of the diamagnetic [Ni(CN)4]2- anions, with g = 2.08 and J = −0.426 cm-1 for 1 and g = 2.08 and J = − 0.278 cm-1 for 3. The correlation between the structures and the J values is discussed.

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