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- W2950962425 abstract "Abstract Time-resolved resonance Raman spectra of the lowest excited triplet state T 1 , the radical cation R + and the radical anion R − of 1,4-diphenylbutadiyne (DPB) have been measured. It has been shown that the CC symmetric stretch exhibits low-frequency shifts in the order, S o (2219 cm −1 ), R + (2156 cm −1 ), R − (2108 cm −1 ), and T 1 (1999 cm −1 ), indicating that the CC triple bond weakens in this sequence. However, the frequency shifts are not as large as those observed for diphenylacetylene (DPA), suggesting that in the case of DPB the unpaired electron (spin density) is distributed over the two CC triple bonds of the conjugated system, which makes the weakening of the CC bonds of DPB much less than that of DPA. It has also been shown that like DPA, the ionization of DPB to generate R + can occur biphotonically through the T 1 state." @default.
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- W2950962425 date "2010-08-19" @default.
- W2950962425 modified "2023-09-26" @default.
- W2950962425 title "ChemInform Abstract: Structures and Dynamics of the Lowest Excited Triplet State, Radical Cation and Radical Anion of 1,4-Diphenylbutadiyne: Time-Resolved Resonance Raman Study." @default.
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- W2950962425 doi "https://doi.org/10.1002/chin.199411035" @default.
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