Rotational Spectra of Two Hydrogen-Bonded Methyl Salicylate Monohydrates: Relative Stability and Tunneling Motions
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- 作者：Supriya Ghosh ; Javix Thomas ; Wenyuan Huang ; Yunjie Xu ; Wolfgang J盲ger
- 刊名：The Journal of Physical Chemistry Letters
- 出版年：2015
- 出版时间：August 20, 2015
- 年：2015
- 卷：6
- 期：16
- 页码：3126-3131
- 全文大小：289K
- ISSN：1948-7185
文摘
The mechanism for the dual fluorescence of methyl salicylate (MS) is a long-standing research topic. Two distinctly different hydrogen-bonded MS鈥搘ater complexes, one with the carbonyl O and the other with the hydroxy O serving as the hydrogen-bond acceptor, were detected using chirped pulse and cavity-based Fourier transform microwave spectroscopy and found to be of comparable stability. This observation provides direct experimental evidence for the previously undetected hydroxy O-bonded isomer, supporting the recently proposed new mechanism for the dual fluorescence of MS in protic solvents. An interesting interplay between the methyl internal rotation and water tunneling motions was also investigated. The existence of an unconventional O路路路H鈥揅 hydrogen-bond was verified using the atoms-in-molecules theory. Thorough searches for the elusive ketoA, a higher energy form of MS, were unsuccessful. This result supports recent theoretical reports that only one MS species exists in the ground state.