Stone-Wales Rearrangement Pathways from the Hinge-Opened [2+2] C60 Dimer to Ipr C120 Fullerenes. Vibrational Analysis of Intermediates-Reference-Cited by-同舟云学术

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Stone-Wales Rearrangement Pathways from the Hinge-Opened [2+2] C60 Dimer to Ipr C120 Fullerenes. Vibrational Analysis of Intermediates

Published:1998-03 Issue:2 Volume:6 Page:319-338
ISSN:1064-122X
Container-title:Fullerene Science and Technology
language:en
Short-container-title:Fullerene Science and Technology

Author:

Ueno Hiroshi¹,[Obar]sawa Shuichi²,[Obar]sawa Eiji¹,Takeuchi Kazuo²

Affiliation:

1. a Department of Knowledge-Based Information Engineering , Toyohashi University of Technology , Tempaku-cho, Toyohashi, Aichi, 441

2. b Applied Laser Chemistry Laboratory , Institute of Physical and Chemical Research (RIKEN) , 2-lHirosawa, Wako, Saitama, 351-01, Japan

Publisher

Informa UK Limited

Subject

General Chemical Engineering

Link

https://www.tandfonline.com/doi/pdf/10.1080/10641229809350204

Reference25 articles.

1. Nature of Cyclobutane Bonds in the Neutral [2+2] Dimer of C60

2. Table 1 of ref. 1

3. Synthesis and X-ray structure of dumb-bell-shaped C120

4. What is the lowest-energy isomer of the C60 dimer?

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

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