Two cobalt(II) supramolecular isomers based on N,N'-bis(pyridin-3-yl)oxalamide induced by the molecular orientation of lattice DMF molecules

Acta Crystallogr C Struct Chem. 2016 Feb;72(Pt 2):170-3. doi: 10.1107/S205322961600156X. Epub 2016 Jan 29.

Abstract

Supramolecular isomerism for coordination networks refers to the existence of different architectures having the same building blocks and identical stoichiometries. For a given building block, different arrangements can lead to the formation of a series of supramolecular isomers. Two one-dimensional Co(II) coordination polymers based on N,N'-bis(pyridin-3-yl)oxalamide (BPO), both catena-poly[[[dichloridocobalt(II)]-bis[μ-N,N'-bis(pyridin-3-yl)oxalamide-κ(2)N:N']] dimethylformamide disolvate], {[CoCl2(C12H10N4O2)2]·2C3H7NO}n, have been assembled by the solvothermal method. Single-crystal X-ray diffraction analyses reveal that the two compounds are supramolecular isomers, the isomerism being induced by the orientation of the dimethylformamide (DMF) molecules in the crystal lattice.

Keywords: BPO; N,N′-bis(pyridin-3-yl)oxalamide; cobalt(II); crystal structure; one-dimensional coordination polymers; supramolecular isomerism.

Publication types

  • Research Support, Non-U.S. Gov't