Triplet excited state in platinum-acetylide oligomers: Triplet localization and effects of conformation


GLUSAC K., Kose M. E. , JIANG H., SCHANZE K. S.

JOURNAL OF PHYSICAL CHEMISTRY B, cilt.111, ss.929-940, 2007 (SCI İndekslerine Giren Dergi)

  • Cilt numarası: 111 Konu: 5
  • Basım Tarihi: 2007
  • Doi Numarası: 10.1021/jp065892p
  • Dergi Adı: JOURNAL OF PHYSICAL CHEMISTRY B
  • Sayfa Sayısı: ss.929-940

Özet

An experimental and theoretical investigation was carried out on a series of platinum-acetylide oligomers of the general structure Ph-CC-[PtL2-CC-(1,4-Ph)-CC-](n)-PtL2-CC-Ph (where n = 1, 2, 3, 4, 6; Ph = phenyl, 1,4-Ph = 1,4-phenylene; L = P(n-Bu)(3), and the geometry at Pt = trans). The objective of this work is to understand the geometry and electronic structure of the ground and triplet excited states of Pt-acetylide oligomers. The experiments carried out include temperature-dependent absorption and photoluminescence spectroscopy (80-298 K range) and ambient temperature transient absorption spectroscopy. Density functional theory (DFT) and time-dependent density functional theory (TD-DFT) calculations were carried out on several of the oligomers using the hybrid Becke's three-parameter functional with the B3LYP correlation functional and the SDD basis set. The combined experimental and theoretical results provide very clear evidence that the triplet excited state is localized on a chromophore consisting approximately of a single -[PtL2-CC-(1,4-Ph)-CC-PtL2]- repeat unit. DFT calculations indicate that in the ground state conformers that differ in the (rotational) orientation of the 1,4-phenylenes with respect to the plane defined by the PtL2(C)(2) units (twisted = t and planar = p) are very close in energy (difference of < 1 kcal center dot mol(-1)). By contrast, in the triplet excited state, the p conformer is 3 kcal center dot mol(-1) lower in energy than the t conformer. The torsional geometry change in the triplet state is reflected in the low-temperature phosphorescence spectra of the short oligomers, where separate emission bands are seen from the t and p conformers.