Tri-s-triazine and Its Nitrogen Isoelectronic Equivalents: An ab Initio Study-Reference-Cited by-同舟云学术

Tri-s-triazine and Its Nitrogen Isoelectronic Equivalents: An ab Initio Study

Published:2004-12-01 Issue:52 Volume:108 Page:11721-11727
ISSN:1089-5639
Container-title:The Journal of Physical Chemistry A
language:en
Short-container-title:J. Phys. Chem. A

Author:

Zheng Wenxu¹,Wong Ning-Bew¹,Li Wai-Kee¹,Tian Anmin¹

Affiliation:

1. Faculty of Chemistry, Sichuan University, Chengdu, Sichuan 610064, People's Republic of China, and Department of Biology and Chemistry, City University of Hong Kong, Kowloon, and Department of Chemistry, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong

Publisher

American Chemical Society (ACS)

Subject

Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jp046909b

Reference47 articles.

1. Theoretical Prediction of 2,4,6-Trinitro-1,3,5-triazine (TNTA). A New, Powerful, High-Energy Density Material?

2. A Simple Molecular Orbital Method for Discussing the Electronic Structures of Stereoisomers—The Theoretical Method and ESR Hyper fine Splittings of the Terephthalaldehyde Anion

3. Rotational modulation of fluorescence decay and quantum beats in expansion‐cooled azabenzenes: Small molecule behavior of rotationally cold s‐triazine in the lower vibronic levels of the Ã 1E″ state

4. Observation of high vibrational excitation in HCN molecules produced from 193 nm photolysis of 1,3,5‐triazine

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