Abstract
Three novel bismuth-organic compounds, with the general formula [Bi(2)(HPDC)(2)(PDC)(2)]·(arene)·2H(2)O (H(2)PDC = 2,6-pyridinedicarboxylic acid; arene = pyrene, naphthalene, and azulene), that consist of neutral dinuclear Bi-pyridinedicarboxylate complexes and outer coordination sphere arene molecules were synthesized and structurally characterized. The structures of all three phases exhibit strong π-π stacking interactions between the Bi-bound PDC/HPDC and outer sphere organic molecules; these interactions effectively sandwich the arene molecules between bismuth complexes and thereby prevent molecular vibrations. Upon UV irradiation, the compounds containing pyrene and naphthalene displayed red and green emission, respectively, with quantum yields of 1.3(2) and 30.8(4)%. The emission was found to originate from the T(1) → S(0) transition of the corresponding arene and result in phosphorescence characteristic of the arene employed. By comparison, the azulene-containing compound displayed very weak blue-purple phosphorescence of unknown origin and is a rare example of T(2) → S(0) emission from azulene. The pyrene- and naphthalene-containing compounds both display radioluminescence, with intensities of 11 and 38% relative to bismuth germanate, respectively. Collectively, these results provide further insights into the structure-property relationships that underpin luminescence from Bi-based materials and highlight the utility of Bi-organic molecules in the realization of organic emission.