Substituent Effects on the Energies of the Electronic Transitions of Geminally Diphenyl-Substituted Trimethylenemethane (TMM) Radical Cations. Experimental and Theoretical Evidence for a Twisted Molecular and Localized Electronic Structure-Reference-Cited by-同舟云学术

Substituent Effects on the Energies of the Electronic Transitions of Geminally Diphenyl-Substituted Trimethylenemethane (TMM) Radical Cations. Experimental and Theoretical Evidence for a Twisted Molecular and Localized Electronic Structure

Published:2007-05-01 Issue:20 Volume:111 Page:4436-4442
ISSN:1089-5639
Container-title:The Journal of Physical Chemistry A
language:en
Short-container-title:J. Phys. Chem. A

Author:

Namai Hayato¹,Ikeda Hiroshi¹,Kato Nobuyuki¹,Mizuno Kazuhiko¹

Affiliation:

1. Department of Chemistry, Graduate School of Science, Tohoku University, Sendai 980-8578, Japan, and Department of Applied Chemistry, Graduate School of Engineering, Osaka Prefecture University, Sakai, Osaka 599-8531, Japan

Publisher

American Chemical Society (ACS)

Subject

Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jp068308l

Reference34 articles.

1. Trimethylenemethane

2. [3+2] Cycloaddition Approaches to Five-Membered Rings via Trimethylenemethane and Its Equivalents [New Synthetic Methods (55)]

3. Diyl Trapping and Electroreductive Cyclization Reactions

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