Thermal Transformation of Ring-Opened [2+2] C60 Dimer into a Wide-Bridged C120 Isomer. A Computational Evaluation of Fulvalene-Naphthalene Rearrangements-Reference-Cited by-同舟云学术

Thermal Transformation of Ring-Opened [2+2] C60 Dimer into a Wide-Bridged C120 Isomer. A Computational Evaluation of Fulvalene-Naphthalene Rearrangements

Published:1996-09 Issue:5 Volume:4 Page:819-834
ISSN:1064-122X
Container-title:Fullerene Science and Technology
language:en
Short-container-title:Fullerene Science and Technology

Author:

Honda Kazuhiko¹,[Obar]sawa Eiji¹,Slanina Zdenek²,Matsumoto Takatoshi¹

Affiliation:

1. a Computational Chemistry Group, Department of Knowledge-Based Information Engineering , Toyohashi University of Technology , Toyohashi, 441, Japan

2. b Department of Chemistry , National Chung-Cheng University , 160, San-Hsing, Ming-Hsiung, Chia-yi 621, Taiwan ROC

Publisher

Informa UK Limited

Subject

General Chemical Engineering

Link

https://www.tandfonline.com/doi/pdf/10.1080/10641229608001145

Reference8 articles.

1. Doubly Bonded C60Dimers and Congeners: Computational Studies of Structures, Bond Energies and Transformations

2. Theoretical studies of icosahedral C60 and some related species

3. Pyracylene rearrangement classes of fullerene isomers

4. Role of sp3 carbon and 7-membered rings in fullerene annealing and fragmentation

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