Terpyridine isomerism as a tool for tuning red-to-NIR emissive properties in heteronuclear gold(I)-thallium(I) complexes.
David RoyoSonia MorenoMaría Rodríguez-CastilloMiguel MongeM Elena OlmosFedor Ivanovich ZubkovAnastasia A ProninaGhodrat MahmoudiJosé María López-de-LuzuriagaPublished in: Dalton transactions (Cambridge, England : 2003) (2024)
The polymeric linear chain [AuTl(C 6 Cl 5 ) 2 ] n reacts with three terpyridine-type ligands substituted with thiophene groups containing N-donor centres in different relative positions (L1, L2 and L3), leading to the Au(I)/Tl(I) complexes [AuTl(C 6 Cl 5 ) 2 (L1)] n (1), [{AuTl(C 6 Cl 5 ) 2 } 2 (L2)] n (2) and [AuTl(C 6 Cl 5 ) 2 (L3)] n (3). X-Ray diffraction studies reveal that L1 acts as a chelate, while L2 and L3 act as bridging ligands, resulting in different coordination indexes for the thallium(I) centre. These structural differences strongly influence their optical properties, and while compounds 2 and 3 emit near the limit of the visible range, complex 1 emits in the infrared region. DFT calculations have also been carried out in order to determine the origin of the electronic transitions responsible for their optical properties.