含时密度泛函理论
化学
二聚体
密度泛函理论
荧光
光化学
发光
乙腈
聚集诱导发射
计算化学
有机化学
光电子学
物理
量子力学
作者
Carla Cunha,Andrea Pinto,Adelino M. Galvão,Laura Rodrı́guez,J. Sérgio Seixas de Melo
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2022-04-27
卷期号:61 (18): 6964-6976
被引量:11
标识
DOI:10.1021/acs.inorgchem.2c00366
摘要
Aggregation-induced emission (AIE) has gained a remarkable amount of interest in the past 20 years, but the majority of the studies are based on organic structures. Herein, three dinuclear gold(I) complexes, with the general formula [PPh2XPPh2-Au2-Coum2], where the Au(I) atom is linked to three different diphosphanes [PPh2XPPh2; DPPM for X = CH2 (1.1), DPPP for X = (CH2)3 (1.2), and DPPA for X = C≡C (1.3)] and the propynyloxycoumarin precursor (1, 4-methyl-substituted coumarin), have been synthesized. The compounds present AIE characteristics, AIEgens, with high luminescence quantum yields in the solid state when they are compared to dilute solutions. Photophysical studies (steady-state and time-resolved fluorescence) were obtained, with AIE being observed with the three gold(I) complexes in acetonitrile/water mixtures. This was further corroborated with dynamic light scattering measurements. Time-dependent density functional theory (TDDFT) electronic calculations show that the compounds have different syn and anti conformations (relative to the coumarin core) with 1.1 syn and 1.2 and 1.3 both anti. From time-resolved fluorescence experiments, the augment in the contribution of the longer decay component is found to be associated with the emission of the aggregate (AIE effect) and its nature (involving a dimer) rationalized from TDDFT electronic calculations.
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