Transient Raman snapshots of the twisted intramolecular charge transfer state
Optically triggered twisted intramolecular charge transfer (TICT) states in donor-acceptor chromophores form the molecular basis for designing bio-imaging probes that sense polarity, microviscosity or pH in vivo.[1] However, a lack of predictive understanding of the ‘twist’ localization has limited...
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| 格式: | Conference or Workshop Item |
| 語言: | English |
| 出版: |
2020
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| 在線閱讀: | https://hdl.handle.net/10356/144221 |
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| 機構: | Nanyang Technological University |
| 語言: | English |
| 總結: | Optically triggered twisted intramolecular charge transfer (TICT) states in donor-acceptor chromophores form the molecular basis for designing bio-imaging probes that sense polarity, microviscosity or pH in vivo.[1] However, a lack of predictive understanding of the ‘twist’ localization has limited rational structure-function correlations for TICT-based dyes. Time-resolved absorption and emission spectroscopy traditionally used to address this problem, could never unequivoally identify the twist location.[2] Here, using femtosecond stimulated Raman spectroscopy, we reveal distinct Raman signature of the TICT state for stilbazolium-class of mitochondrial staining dye for the first time. |
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