Continuous Tuning of Intersystem Crossing Times in Rose Bengal Water/Methanol Solutions

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Authors

  • Onno Strolka
  • Pascal Rauthe
  • Tim Muschik
  • Philipp Frech
  • André Niebur
  • Andreas N. Unterreiner
  • Jannika Lauth

External Research Organisations

  • University of Tübingen
  • Karlsruhe Institute of Technology (KIT)
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Details

Original languageEnglish
Pages (from-to)12189-12196
Number of pages8
JournalJournal of Physical Chemistry B
Volume128
Issue number49
Early online date26 Nov 2024
Publication statusPublished - 12 Dec 2024

Abstract

We use femtosecond transient broadband absorption spectroscopy (TAS) to characterize Rose Bengal in water/methanol solutions and reveal a continuous tunability of intersystem crossing (ISC) times by changing the mole fraction of the solvents. We find that the transients of excited state absorptions (ESAs) in Rose Bengal at ∼430 nm can be attributed to transitions from the singlet state S1, with decay times of 74 ps via ISC in pure water and up to 405 ps in pure methanol. TA measurements at near-infrared wavelengths, on the other hand, reveal the rise of an ESA at ∼1080 nm from the triplet state T1 with time constants of 68 and 491 ps in pure water and methanol, respectively, strongly supporting the associated UV-vis TAS data. Solvent mixtures show a quasi-linear rise of the ISC times with increasing mole fractions of methanol and indicate that Rose Bengal in varying solvent mixtures can be used as a model system to study their influence on excited state photophysics.

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Cite this

Continuous Tuning of Intersystem Crossing Times in Rose Bengal Water/Methanol Solutions. / Strolka, Onno; Rauthe, Pascal; Muschik, Tim et al.
In: Journal of Physical Chemistry B, Vol. 128, No. 49, 12.12.2024, p. 12189-12196.

Research output: Contribution to journalArticleResearchpeer review

Strolka, O, Rauthe, P, Muschik, T, Frech, P, Niebur, A, Unterreiner, AN & Lauth, J 2024, 'Continuous Tuning of Intersystem Crossing Times in Rose Bengal Water/Methanol Solutions', Journal of Physical Chemistry B, vol. 128, no. 49, pp. 12189-12196. https://doi.org/10.1021/acs.jpcb.4c07449
Strolka, O., Rauthe, P., Muschik, T., Frech, P., Niebur, A., Unterreiner, A. N., & Lauth, J. (2024). Continuous Tuning of Intersystem Crossing Times in Rose Bengal Water/Methanol Solutions. Journal of Physical Chemistry B, 128(49), 12189-12196. https://doi.org/10.1021/acs.jpcb.4c07449
Strolka O, Rauthe P, Muschik T, Frech P, Niebur A, Unterreiner AN et al. Continuous Tuning of Intersystem Crossing Times in Rose Bengal Water/Methanol Solutions. Journal of Physical Chemistry B. 2024 Dec 12;128(49):12189-12196. Epub 2024 Nov 26. doi: 10.1021/acs.jpcb.4c07449
Strolka, Onno ; Rauthe, Pascal ; Muschik, Tim et al. / Continuous Tuning of Intersystem Crossing Times in Rose Bengal Water/Methanol Solutions. In: Journal of Physical Chemistry B. 2024 ; Vol. 128, No. 49. pp. 12189-12196.
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AU - Strolka, Onno

AU - Rauthe, Pascal

AU - Muschik, Tim

AU - Frech, Philipp

AU - Niebur, André

AU - Unterreiner, Andreas N.

AU - Lauth, Jannika

N1 - Publisher Copyright: © 2024 The Authors. Published by American Chemical Society.

PY - 2024/12/12

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N2 - We use femtosecond transient broadband absorption spectroscopy (TAS) to characterize Rose Bengal in water/methanol solutions and reveal a continuous tunability of intersystem crossing (ISC) times by changing the mole fraction of the solvents. We find that the transients of excited state absorptions (ESAs) in Rose Bengal at ∼430 nm can be attributed to transitions from the singlet state S1, with decay times of 74 ps via ISC in pure water and up to 405 ps in pure methanol. TA measurements at near-infrared wavelengths, on the other hand, reveal the rise of an ESA at ∼1080 nm from the triplet state T1 with time constants of 68 and 491 ps in pure water and methanol, respectively, strongly supporting the associated UV-vis TAS data. Solvent mixtures show a quasi-linear rise of the ISC times with increasing mole fractions of methanol and indicate that Rose Bengal in varying solvent mixtures can be used as a model system to study their influence on excited state photophysics.

AB - We use femtosecond transient broadband absorption spectroscopy (TAS) to characterize Rose Bengal in water/methanol solutions and reveal a continuous tunability of intersystem crossing (ISC) times by changing the mole fraction of the solvents. We find that the transients of excited state absorptions (ESAs) in Rose Bengal at ∼430 nm can be attributed to transitions from the singlet state S1, with decay times of 74 ps via ISC in pure water and up to 405 ps in pure methanol. TA measurements at near-infrared wavelengths, on the other hand, reveal the rise of an ESA at ∼1080 nm from the triplet state T1 with time constants of 68 and 491 ps in pure water and methanol, respectively, strongly supporting the associated UV-vis TAS data. Solvent mixtures show a quasi-linear rise of the ISC times with increasing mole fractions of methanol and indicate that Rose Bengal in varying solvent mixtures can be used as a model system to study their influence on excited state photophysics.

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