Browse by author
Lookup NU author(s): Professor William Clegg, Gary Nichol
This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0).
A survey of the trends in metal-ligand coordination and hydrogen bonding has been carried out on complexes of singly deprotonated cyanuric acid CY− and alkaline earth metals, synthesised from aqueous solution and characterised by X-ray crystallography. Involvement of cyanurate in the metal coordination increases from Mg through Ca and Sr to Ba relative to coordination by water, in parallel with the increasing ionic radius and coordination number. The incidence of bridging of metal centres by both water and cyanurate also increases in this series. The Mg complex [Mg(H2O)6][CY]2·2H2O contains hexaaqua-coordinated cations, uncoordinated CY− anions, and additional water molecules. Ca and Sr complexes {[Ca(CY)(H2O)3][CY]}∞ and {[Sr(CY)2(H2O)4]}∞ feature polymeric chains of coordinated metal ions, the Ca complex with uncoordinated anions and the Sr complex with all potential ligands coordinated. The Ba complex {[Ba(CY)2(H2O)2]}∞ has a two-dimensional coordination network. Extensive hydrogen bonding plays a key role in generating a three-dimensional network in all four structures. The competition between cyanurate and water for coordination to the alkaline earth metal cations, and that between coordination and hydrogen bonding propensities of the cyanurate anion, appear to be finely balanced, with the structural outcomes depending on the relative sizes and degrees of hardness of the four cations of the group.
Author(s): Clegg W, Nichol GS
Publication type: Article
Publication status: Published
Journal: Crystals
Year: 2024
Volume: 14
Issue: 1
Online publication date: 22/01/2024
Acceptance date: 16/01/2024
Date deposited: 16/01/2024
ISSN (electronic): 2073-4352
Publisher: MDPI
URL: https://doi.org/10.3390/cryst14010098
DOI: 10.3390/cryst14010098
Data Access Statement: Processed X-ray diffraction data are available as part of the information deposited at the Cambridge Crystallographic Data Centre. These may also be obtained from the author (W.C.) on request.
Altmetrics provided by Altmetric
