Determination of the highest occupied molecular orbital and conformational structures of morpholine based on its conformer-specific photoionization dynamics-Reference-Cited by-同舟云学术

Determination of the highest occupied molecular orbital and conformational structures of morpholine based on its conformer-specific photoionization dynamics

Published:2022 Issue:46 Volume:24 Page:28477-28485
ISSN:1463-9076
Container-title:Physical Chemistry Chemical Physics
language:en
Short-container-title:Phys. Chem. Chem. Phys.

Author:

Eom So Young¹,Lee Yu Ran²^ORCID,Park Sung Man¹^ORCID,Kwon Chan Ho¹^ORCID

Affiliation:

1. Department of Chemistry and Institute for Molecular Science and Fusion Technology, Kangwon National University, Chuncheon, 24341, Republic of Korea

2. Forensic Chemistry Division, National Forensic Service, Wonju, 26460, Republic of Korea

Abstract

Morpholine, a heterocycle composed of an ether and amine, is commonly used as a precursor in many organic synthesis processes because of the nucleophilicity induced by the lone-pair electrons of the nitrogen atom within its ring.

Funder

National Research Foundation of Korea

Kangwon National University

Publisher

Royal Society of Chemistry (RSC)

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

Link

http://pubs.rsc.org/en/content/articlepdf/2022/CP/D2CP04112J

Reference27 articles.

1. The conformer resolved ultraviolet photodissociation of morpholine

2. Antifungal agents: An overview. Part II

3. Application of a process friendly morpholine synthesis to (S,S)-Reboxetine

4. 610. Molecular polarisability. Application of the N–H and N–C link polarisabilities to the conformations of tertiary amines, piperidine, and morpholine

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