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从热可调合成到气相和溶液中苯基亚甲亚胺光谱学的历程

A Journey from Thermally Tunable Synthesis to Spectroscopy of Phenylmethanimine in Gas Phase and Solution.

作者信息

Melli Alessio, Potenti Simone, Melosso Mattia, Herbers Sven, Spada Lorenzo, Gualandi Andrea, Lengsfeld Kevin G, Dore Luca, Buschmann Philipp, Cozzi Pier Giorgio, Grabow Jens-Uwe, Barone Vincenzo, Puzzarini Cristina

机构信息

Scuola Normale Superiore, Piazza dei Cavalieri 7, 56126, Pisa, Italy.

Dipartimento di Chimica "Giacomo Ciamician", Universitá di Bologna, Via Selmi 2, 40126, Bologna, Italy.

出版信息

Chemistry. 2020 Nov 20;26(65):15016-15022. doi: 10.1002/chem.202003270. Epub 2020 Oct 15.

DOI:10.1002/chem.202003270
PMID:32717136
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7756512/
Abstract

Phenylmethanimine is an aromatic imine with a twofold relevance in chemistry: organic synthesis and astrochemistry. To tackle both aspects, a multidisciplinary strategy has been exploited and a new, easily accessible synthetic approach to generate stable imine-intermediates in the gas phase and in solution has been introduced. The combination of this formation pathway, based on the thermal decomposition of hydrobenzamide, with a state-of-the-art computational characterization of phenylmethanimine laid the foundation for its first laboratory observation by means of rotational electric resonance spectroscopy. Both E and Z isomers have been accurately characterized, thus providing a reliable basis to guide future astronomical observations. A further characterization has been carried out by nuclear magnetic resonance spectroscopy, showing the feasibility of this synthetic approach in solution. The temperature dependence as well as possible mechanisms of the thermolysis process have been examined.

摘要

苯甲亚胺是一种在化学领域具有双重重要性的芳香亚胺

有机合成和天体化学。为了应对这两个方面,人们采用了多学科策略,并引入了一种新的、易于实现的合成方法,以在气相和溶液中生成稳定的亚胺中间体。这种基于氢苯甲酰胺热分解的生成途径与苯甲亚胺的先进计算表征相结合,为通过旋转电共振光谱首次在实验室中观测到它奠定了基础。E和Z异构体均已得到精确表征,从而为指导未来的天文观测提供了可靠依据。通过核磁共振光谱进行了进一步表征,证明了这种合成方法在溶液中的可行性。研究了热解过程的温度依赖性以及可能的机理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/168f/7756512/4d4fc2a90b09/CHEM-26-15016-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/168f/7756512/80140b3ad188/CHEM-26-15016-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/168f/7756512/197a2cee7f4c/CHEM-26-15016-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/168f/7756512/929bf059a93e/CHEM-26-15016-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/168f/7756512/fcd303264d5c/CHEM-26-15016-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/168f/7756512/4d4fc2a90b09/CHEM-26-15016-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/168f/7756512/80140b3ad188/CHEM-26-15016-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/168f/7756512/197a2cee7f4c/CHEM-26-15016-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/168f/7756512/929bf059a93e/CHEM-26-15016-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/168f/7756512/fcd303264d5c/CHEM-26-15016-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/168f/7756512/4d4fc2a90b09/CHEM-26-15016-g005.jpg

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