Contrasting ring-opening propensities in UV-excited α-pyrone and coumarin. Issue 4 (24th December 2015)
- Record Type:
- Journal Article
- Title:
- Contrasting ring-opening propensities in UV-excited α-pyrone and coumarin. Issue 4 (24th December 2015)
- Main Title:
- Contrasting ring-opening propensities in UV-excited α-pyrone and coumarin
- Authors:
- Murdock, Daniel
Ingle, Rebecca A.
Sazanovich, Igor V.
Clark, Ian P.
Harabuchi, Yu
Taketsugu, Tetsuya
Maeda, Satoshi
Orr-Ewing, Andrew J.
Ashfold, Michael N. R. - Abstract:
- Abstract : Ring-opening quantum yields following UV-photoexcitation of coumarin and α-pyrone are influenced by the dynamics through, rather than just the geometries of, conical intersections. Abstract : The photoisomerisation dynamics following excitation to the S1 electronic state of two structurally related heterocyclic molecules, α-pyrone and coumarin, in acetonitrile solution have been probed by time-resolved vibrational absorption spectroscopy. Following irradiation at 310 nm, α-pyrone relaxes rapidly from its initially excited state, with a quantum yield for parent molecule reformation of 68%. Probing the antisymmetric ketene stretch region between 2100 cm −1 and 2150 cm −1 confirms the presence of at least two isomeric ring-opened photoproducts, which are formed highly vibrationally excited and relax on a picosecond timescale. Following vibrational cooling, a secondary, thermally driven, isomerisation is observed with a 1.8(1) ns time constant. In contrast, coumarin reforms the parent molecule with essentially 100% efficiency following excitation at 330 nm. The conical intersections driving the non-radiative relaxation of α-pyrone have been investigated using an automated search algorithm. The two lowest energy conical intersections possess remarkably similar structures to the two energetically accessible conical intersections reported previously for coumarin, suggesting that the differing photochemistry is the result of dynamical effects occurring after passageAbstract : Ring-opening quantum yields following UV-photoexcitation of coumarin and α-pyrone are influenced by the dynamics through, rather than just the geometries of, conical intersections. Abstract : The photoisomerisation dynamics following excitation to the S1 electronic state of two structurally related heterocyclic molecules, α-pyrone and coumarin, in acetonitrile solution have been probed by time-resolved vibrational absorption spectroscopy. Following irradiation at 310 nm, α-pyrone relaxes rapidly from its initially excited state, with a quantum yield for parent molecule reformation of 68%. Probing the antisymmetric ketene stretch region between 2100 cm −1 and 2150 cm −1 confirms the presence of at least two isomeric ring-opened photoproducts, which are formed highly vibrationally excited and relax on a picosecond timescale. Following vibrational cooling, a secondary, thermally driven, isomerisation is observed with a 1.8(1) ns time constant. In contrast, coumarin reforms the parent molecule with essentially 100% efficiency following excitation at 330 nm. The conical intersections driving the non-radiative relaxation of α-pyrone have been investigated using an automated search algorithm. The two lowest energy conical intersections possess remarkably similar structures to the two energetically accessible conical intersections reported previously for coumarin, suggesting that the differing photochemistry is the result of dynamical effects occurring after passage through these intersections. … (more)
- Is Part Of:
- Physical chemistry chemical physics. Volume 18:Issue 4(2016)
- Journal:
- Physical chemistry chemical physics
- Issue:
- Volume 18:Issue 4(2016)
- Issue Display:
- Volume 18, Issue 4 (2016)
- Year:
- 2016
- Volume:
- 18
- Issue:
- 4
- Issue Sort Value:
- 2016-0018-0004-0000
- Page Start:
- 2629
- Page End:
- 2638
- Publication Date:
- 2015-12-24
- Subjects:
- Chemistry, Physical and theoretical -- Periodicals
541.3 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/cp#!issueid=cp016040&type=current&issnprint=1463-9076 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c5cp06597f ↗
- Languages:
- English
- ISSNs:
- 1463-9076
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6475.306000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 5081.xml