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Título: | Different phosphorescent excited states of tetra- and octanuclear dendritic-like phosphine gold(i) thiolate complexes: Photophysical and theoretical studies |
Autor: | Fernández, Eduardo J.; Laguna, Antonio CSIC ORCID; López-de-Luzuriaga, José M. CSIC ORCID; Monge, Miguel; Sánchez-Forcada, Eva | Fecha de publicación: | 2011 | Editor: | Royal Society of Chemistry (UK) | Citación: | Dalton Transactions 40(13): 3287-3294 (2011) | Resumen: | The study of the photophysical properties of dendritic-like phosphinothiolate gold(I) complexes has been carried out. The studied complexes are two series of analogous compounds bearing 4 or 8 metal centers: the tetranuclear [Au4(S-C6H4-X)4{DAB-G0-(PPh2)4}] (X = F (3), MeO (4), Me (5) and NO2 (6)) and the octanuclear [Au8(S-C6H4-X)8{DAB-G1-(PPh2)8}] (X = F (9), MeO (10), Me (11) and NO2 (12)) complexes. All compounds are brightly luminescent in solid state at 77 K displaying lifetimes in the microsecond range. The correlation between the substituent in position four of the benzenethiolate ligand and the emission energy shows that the emissions arise from 3[pπ(S)→pσ(Au)] or from intra-ligand 3[π(S)→π*(C6H4X)] charge transfer transitions, depending on the substituents. Theoretical DFT-B3LYP, ONIOM (DFT-B3LYP/UFF) and ONIOM (MP2/UFF) calculations on mononuclear and dinuclear model systems permit evaluation of both the structural distortions upon excitation to the lowest triplet excited state T1 and the shape of the orbitals involved in the charge transfer transitions. These calculations also allow us to evaluate the influence of the substituent in position four of the benzenethiolate ligand and the presence of Au***Au interactions. | URI: | http://hdl.handle.net/10261/52579 | DOI: | 10.1039/C0DT01385D | Identificadores: | doi: 10.1039/C0DT01385D issn: 1477-9226 e-issn: 1477-9234 |
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