The triplet state of a platinum acetylide chromophore examined by time-resolved infrared spectroscopy and density functional theory

To understand platinum acetylide molecular structure changes upon conversion to the triplet state, we measured time-resolved infrared (TRIR) spectra of the platinum acetylide complex trans-bis(tributylphosphine)bis(4-ethynyl-1-(2-phenylethynyl)benzene)platinum (abbreviated as PE2). We used density f...

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Published inChemical physics letters Vol. 400; no. 1; pp. 239 - 244
Main Authors Cooper, Thomas M., Blaudeau, Jean-Philippe, Hall, Benjamin C., Rogers, Joy E., McLean, Daniel G., Liu, Yonglin, Toscano, John P.
Format Journal Article
LanguageEnglish
Published Elsevier B.V 11.12.2004
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Summary:To understand platinum acetylide molecular structure changes upon conversion to the triplet state, we measured time-resolved infrared (TRIR) spectra of the platinum acetylide complex trans-bis(tributylphosphine)bis(4-ethynyl-1-(2-phenylethynyl)benzene)platinum (abbreviated as PE2). We used density functional theory (DFT) methods to calculate the geometry, molecular orbitals and vibrational spectra of the ground and lowest energy triplet state of PE2. Solutions of PE2 were excited upon ns pulsed laser excitation at 355 nm and TRIR spectra were collected. The TRIR data show cumulenic vibrations in the triplet state as well as evidence for photoproduct formation. The DFT results support the experimental data, suggesting PE2’s triplet state has quinone character.
ISSN:0009-2614
1873-4448
DOI:10.1016/j.cplett.2004.10.132