Triazole-directed hydrogen-bonded structures of cationic iridium(III) complexes

J.M. Rawson, L. Donato, E. Zysman-Colman

Research output: Contribution to journalArticlepeer-review

7 Citations (Scopus)
1 Downloads (Pure)


Despite the differing size of the Cl and PF6 counter-ions, the structures of the heteroleptic iridium(III) complexes, [Ir(dFphtl)2(btl)]Cl, [1]Cl, and [Ir(dFphtl)2(btl)]PF6, [1]PF6, (where dFphtl = 1-benzyl-4-(2,4-difluorophenyl)-1H-1,2,3-triazole and btl = 1,1′-dibenzyl-4,4′-bi-1H-1,2,3-triazolyl) are found to exhibit similar morphologies in which both structures adopt hydrogen-bonded networks driven by the hydrogen-bond donor and acceptor demands of the triazole functional group. The triazole thus can be used as a supramolecular synthon to control the internuclear distance in the solid-state.

Original languageEnglish
Pages (from-to)8531-8536
Number of pages6
Issue number36
Early online date22 Jul 2014
Publication statusPublished - 28 Sept 2014


Dive into the research topics of 'Triazole-directed hydrogen-bonded structures of cationic iridium(III) complexes'. Together they form a unique fingerprint.

Cite this