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醇 - 氮配合物中的协同作用:通过狭缝射流膨胀理解低温基质

Cooperativity in Alcohol-Nitrogen Complexes: Understanding Cryomatrices through Slit Jet Expansions.

作者信息

Oswald Sönke, Wallrabe Mareike, Suhm Martin A

机构信息

Institut für Physikalische Chemie, Georg-August-Universität Göttingen , Tammannstraße 6, 37077 Göttingen, Germany.

出版信息

J Phys Chem A. 2017 May 11;121(18):3411-3422. doi: 10.1021/acs.jpca.7b01265. Epub 2017 Apr 26.

Abstract

FTIR spectroscopy of supersonic expansions is used to characterize alcohol dimers with one, two, and several nitrogen molecules attached to them. The nitrogen coating causes progressive spectral downshifts of the OH stretching fundamentals which are related to and explain matrix isolation shifts. Comparison of methanol, tert-butyl alcohol and ethanol as well as deuteration of methanol assist in the assignment. Alcohol monomers and trimers are significantly more resistant to nitrogen coating due to a lack of cooperativity and dangling bonds, respectively. In the case of ethanol, the role of conformational isomerism and combination bands is further elucidated. The experimental findings help rationalize the anomalously small OH stretching dimerization shift of methanol in the gas phase, in comparison to that of tert-butyl alcohol.

摘要

超音速膨胀的傅里叶变换红外光谱用于表征附着有一个、两个和几个氮分子的醇二聚体。氮涂层导致OH伸缩基频的光谱逐渐下移,这与基质隔离位移相关并能解释该位移。甲醇、叔丁醇和乙醇的比较以及甲醇的氘代有助于进行归属。由于缺乏协同作用和分别存在悬键,醇单体和三聚体对氮涂层的抗性明显更强。对于乙醇,进一步阐明了构象异构和组合带的作用。实验结果有助于解释与叔丁醇相比,甲醇在气相中异常小的OH伸缩二聚化位移。

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