DFT Calculations on the Effects of Para Substituents on the Energy Differences between Singlet and Triplet States of 2,2-Difluoro-1,3-diphenylcyclopentane-1,3-diyls-Reference-Cited by-同舟云学术

DFT Calculations on the Effects of Para Substituents on the Energy Differences between Singlet and Triplet States of 2,2-Difluoro-1,3-diphenylcyclopentane-1,3-diyls

Published:2003-09-25 Issue:42 Volume:125 Page:12823-12828
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Zhang Daisy Y.¹,Hrovat David A.¹,Abe Manabu¹,Borden Weston Thatcher¹

Affiliation:

1. Contribution from the Department of Chemistry and Biochemistry, Seattle Pacific University, Seattle, Washington 98119-1997, Department of Materials Chemistry & Frontier Research Center, Graduate School of Engineering, Osaka University, Suita 565-0871, Osaka, Japan, and Department of Chemistry, Box 351700, University of Washington, Seattle, Washington 98195-1700

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja0355067

Reference31 articles.

1. Electron spin resonance study of matrix isolated 1,3-cyclopentadiyl, a localized 1,3-carbon biradical

2. Electron spin resonance and CIDNP studies on 1,3-cyclopentadiyls. A localized 1,3 carbon biradical system with a triplet ground state. Tunneling in carbon-carbon bond formation

3. 1,3-Diphenyl-1,3-cyclopentanediyl: A remarkably stable localized biradical

4. UV-laser photochemistry of azoalkanes: surprising effects of phenyl substitution on the lifetimes of 1,3-cyclopentanediyl and 1,4-cyclohexanediyl triplet diradicals

5. Diphenylbicyclo[2.1.0]pentane. A persistent hydrocarbon with a very weak carbon-carbon bond

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