Quantum chemical studies of azoles 9. Tetrazole halogenation according to the elimination—addition scheme without preliminary formation of N-protonated azolium salts
- 作者: Belen’kii L.1, Subbotin A.1, Chuvylkin N.1
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隶属关系:
- N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
- 期: 卷 65, 编号 11 (2016)
- 页面: 2578-2582
- 栏目: Full Articles
- URL: https://journals.rcsi.science/1066-5285/article/view/239271
- DOI: https://doi.org/10.1007/s11172-016-1621-7
- ID: 239271
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详细
Thermodynamic characteristics of electrophilic substitution reactions of 1H-tetrazole and 2H-tetrazole proceeding by the elimination—addition scheme with F+, Cl+, and Br+ as model cations were compared using the results of DFT/B3LYP/6-31G(d,p) quantum chemical calculations carried out with inclusion of specific solvation effects. Possible reasons for lower reactivity (based on the results of calculations) of 2H-tetrazole compared to that of 1H-isomer are discussed.
作者简介
L. Belen’kii
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
编辑信件的主要联系方式.
Email: libel31@mail.ru
俄罗斯联邦, 47 Leninsky prosp., Moscow, 119991
A. Subbotin
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Email: libel31@mail.ru
俄罗斯联邦, 47 Leninsky prosp., Moscow, 119991
N. Chuvylkin
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Email: libel31@mail.ru
俄罗斯联邦, 47 Leninsky prosp., Moscow, 119991