Understanding halogen-substituent assistance in H-atom abstraction-based reactions of CHCl•−with CH4 − nXn(X = H, F, Cl;n= 0-3)-Reference-Cited by-同舟云学术

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Understanding halogen-substituent assistance in H-atom abstraction-based reactions of CHCl•−with CH4 − nXn(X = H, F, Cl;n= 0-3)

Published:2014-01-13 Issue:5 Volume:27 Page:392-400
ISSN:0894-3230
Container-title:Journal of Physical Organic Chemistry
language:en
Short-container-title:J. Phys. Org. Chem.

Author:

Junxi Liang¹,Yu Li¹,Qiang Zhang²,Zhiyuan Geng³

Affiliation:

1. College of Chemical Engineering; Northwest University for Nationalities; Lanzhou Gansu 730030 China

2. Institute of Arid Meteorology; CMA; Key laboratory of Arid Climatic Change and Reducing Disaster of Gansu Province; Key Open Laboratory of Arid Climatic Change and Disaster Reduction of CMA; Lanzhou 730020 China

3. Gansu Key Laboratory of Polymer Materials, College of Chemistry and Chemical Engineering, Key Laboratory of Eco-environment-related Polymer Materials; Ministry of Education; Northwest Normal University; Lanzhou Gansu 730070 China

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference40 articles.

1. Formation and chemistry of radical anions in the gas phase

2. Halomethylenes: effects of halogen substitution on absolute heats of formation

3. Heats of Formation of Monohalo Carbenes. Stability and Reactivity of CHX.bul.- (X = F, Cl, Br, and I) Radical Anions

4. Reactivity of mono-halogen carbene radical anions (CHX–˙; X = F, Cl and Br) and the corresponding carbanions (CH2X–; X = Cl and Br) in the gas phase

5. Thermochemical properties of halogen-substituted methanes, methyl radicals, and carbenes in the gas phase

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