Triazole-directed hydrogen-bonded structures of cationic iridium(III) complexes
MetadataShow full item record
Altmetrics Handle Statistics
Altmetrics DOI Statistics
Despite the differing size of the Cl− and PF6− counter-ions, the structures of the heteroleptic iridium(III) complexes, [Ir(dFphtl)2(btl)]Cl, Cl, and [Ir(dFphtl)2(btl)]PF6, 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.
Rawson , J M , Donato , L & Zysman-Colman , E 2014 , ' Triazole-directed hydrogen-bonded structures of cationic iridium(III) complexes ' , CrystEngComm , vol. 16 , no. 36 , pp. 8531-8536 . https://doi.org/10.1039/c4ce00980k
© Royal Society of Chemistry 2014. This work is made available online in accordance with the publisher’s policies. This is the author created, accepted version manuscript following peer review and may differ slightly from the final published version. The final published version of this work is available at http://dx.doi.org/10.1039/C4CE00980K