Academic Journal
Unraveling the Ultrafast Photochemical Dynamics of Nitrobenzene in Aqueous Solution
| العنوان: | Unraveling the Ultrafast Photochemical Dynamics of Nitrobenzene in Aqueous Solution |
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| المؤلفون: | Lau, Nicholas, Ghosh, Deborin, Bourne-Worster, Susannah L, Kumar, Rhea, Whitaker, William, Heitland, Jonas, Davies, Julia, Karras, Gabriel, Clark, Ian, Greetham, Gregory M., Worth, Graham, Orr-Ewing, Andrew J, Fielding, Helen |
| المصدر: | Lau , N , Ghosh , D , Bourne-Worster , S L , Kumar , R , Whitaker , W , Heitland , J , Davies , J , Karras , G , Clark , I , Greetham , G M , Worth , G , Orr-Ewing , A J & Fielding , H 2024 , ' Unraveling the Ultrafast Photochemical Dynamics of Nitrobenzene in Aqueous Solution ' , Journal of the American Chemical Society , vol. 146 , no. 15 , pp. 10407-10417 . https://doi.org/10.1021/jacs.3c13826 |
| سنة النشر: | 2024 |
| المجموعة: | University of Bristol: Bristol Reserach |
| الوصف: | Nitroaromatic compounds are major constituents of the brown carbon aerosol particles in the troposphere that absorb near-ultraviolet (UV) and visible solar radiation and have a profound effect on the Earth’s climate. The primary sources of brown carbon include biomass burning, forest fires and residential burning of biofuels, and an important secondary source is photochemistry in aqueous cloud and fog droplets. Nitrobenzene is the smallest nitroaromatic molecule and a model for the photochemical behaviour of larger nitroaromatic compounds. Despite the obvious importance of its droplet photochemistry to the atmospheric environment, there have not been any detailed studies of the ultrafast photochemical dynamics of nitrobenzene in aqueous solution. Here, we combine femtosecond transient absorption spectroscopy, time-resolved infrared spectroscopy, and quantum chemistry calculations, to investigate the primary steps following the near-UV (λ ≥ 340 nm) photoexcitation of aqueous nitrobenzene. To understand the role of the surrounding water molecules on the photochemical dynamics of nitrobenzene, we compare the results of these investigations with analogous measurements in solutions of methanol, acetonitrile, and cyclohexane. We find that vibrational energy transfer to the aqueous environment quenches internal excitation and therefore, unlike the gas phase, we do not observe any evidence for formation of photoproducts on timescales up to 500 ns. We also find that hydrogen-bonding between nitrobenzene and surrounding water molecules slows the S 1 /S 0 internal conversion process. |
| نوع الوثيقة: | article in journal/newspaper |
| اللغة: | English |
| DOI: | 10.1021/jacs.3c13826 |
| الاتاحة: | https://hdl.handle.net/1983/17d9fc9a-d150-4b24-adf5-44d9fd72d93f https://research-information.bris.ac.uk/en/publications/17d9fc9a-d150-4b24-adf5-44d9fd72d93f https://doi.org/10.1021/jacs.3c13826 |
| Rights: | info:eu-repo/semantics/openAccess |
| رقم الانضمام: | edsbas.DFA9F16A |
| قاعدة البيانات: | BASE |
| DOI: | 10.1021/jacs.3c13826 |
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