Abstract
The reactions of transition metal macrocyclic complexes [ML](ClO4)2 (L = 5,5,7,12,12,14-hexamethyl-1,4,8,11-tetraazacyclotetradecane, M = Ni, Cu) with NH4VO3 under hydrothermal conditions gave two coordination polymers, namely [NiL]2[V6O17] and [CuL]2[V6O17]. Single-crystal X-ray diffraction analyses indicated that the central Ni(II)/Cu(II) atom displays a distorted six-coordinate octahedral coordination geometry by coordination with four nitrogen atoms of L, and two oxygen atoms of [VO4] tetrahedrons. Compounds [NiL]2[V6O17] and [CuL]2[V6O17] show three-dimensional structures, which are constructed through the connections of dodecanuclear [V12O32]4− rings with [NiL]2+ in [NiL]2[V6O17], and [V8O22] 4n−n chains with [CuL]2+ in [CuL]2[V6O17], respectively, generating one-dimensional channels.
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Acknowledgments
This work was financially supported by the Science and Technology Planning Project of Hunan Province (2012FJ3050, 2012NK3067), the Construct Program of the Key Discipline in Hunan Province (2011-76), and the Science and Technology Innovative Research Team in Higher Educational Institutions of Hunan Province (2012-318).
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Ou, GC., Yuan, XY. & Li, ZZ. Synthesis and crystal structures of two three-dimensional vanadium polyoxoanion-bridged macrocyclic metal complexes. Transition Met Chem 37, 705–711 (2012). https://doi.org/10.1007/s11243-012-9641-0
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DOI: https://doi.org/10.1007/s11243-012-9641-0