Academic Journal
Direct Observation of Polaritonic Chemistry by Nuclear Magnetic Resonance Spectroscopy
العنوان: | Direct Observation of Polaritonic Chemistry by Nuclear Magnetic Resonance Spectroscopy |
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المؤلفون: | Patrahau, B., Piejko, M., Mayer, R. J., Antheaume, C., Sangchai, T., Ragazzon, G., Jayachandran, A., Devaux, E., Genet, C., Moran, J., Ebbesen, T. W. |
المساهمون: | Agence Nationale de la Recherche, European Research Council |
المصدر: | Angewandte Chemie ; volume 136, issue 23 ; ISSN 0044-8249 1521-3757 |
بيانات النشر: | Wiley |
سنة النشر: | 2024 |
المجموعة: | Wiley Online Library (Open Access Articles via Crossref) |
الوصف: | Polaritonic chemistry is emerging as a powerful approach to modifying the properties and reactivity of molecules and materials. However, probing how the electronics and dynamics of molecular systems change under strong coupling has been challenging due to the narrow range of spectroscopic techniques that can be applied in situ. Here we develop microfluidic optical cavities for vibrational strong coupling (VSC) that are compatible with nuclear magnetic resonance (NMR) spectroscopy using standard liquid NMR tubes. VSC is shown to influence the equilibrium between two conformations of a molecular balance sensitive to London dispersion forces, revealing an apparent change in the equilibrium constant under VSC. In all compounds studied, VSC does not induce detectable changes in chemical shifts, J‐couplings, or spin‐lattice relaxation times. This unexpected finding indicates that VSC does not substantially affect molecular electron density distributions, and in turn has profound implications for the possible mechanisms at play in polaritonic chemistry under VSC and suggests that the emergence of collective behavior is critical. |
نوع الوثيقة: | article in journal/newspaper |
اللغة: | English |
DOI: | 10.1002/ange.202401368 |
الاتاحة: | http://dx.doi.org/10.1002/ange.202401368 https://onlinelibrary.wiley.com/doi/pdf/10.1002/ange.202401368 |
Rights: | http://creativecommons.org/licenses/by-nc-nd/4.0/ |
رقم الانضمام: | edsbas.B9A281A0 |
قاعدة البيانات: | BASE |
DOI: | 10.1002/ange.202401368 |
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