Fluxional σ-bonds of 2,5,8-tri-tert-butyl-1,3-diazaphenalenyl dimers: stepwise [3,3], [5,5] and [7,7] sigmatropic rearrangements viaπ-dimer intermediates-Reference-Cited by-同舟云学术

Fluxional σ-bonds of 2,5,8-tri-tert-butyl-1,3-diazaphenalenyl dimers: stepwise [3,3], [5,5] and [7,7] sigmatropic rearrangements viaπ-dimer intermediates

Published:2010 Issue:19 Volume:12 Page:5084
ISSN:1463-9076
Container-title:Physical Chemistry Chemical Physics
language:en
Short-container-title:Phys. Chem. Chem. Phys.

Author:

Tian Yong-Hui,Huang Jingsong,Kertesz Miklos

Publisher

Royal Society of Chemistry (RSC)

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

Link

http://pubs.rsc.org/en/content/articlepdf/2010/CP/B925259B

Reference56 articles.

1. Notiz über das ESR.-Spektrum des Phenalenyl-Radikals

2. Stable π-electron systems and new aromatic structures

3. Synthesis, Characterization, and Coordination Chemistry of the 2-Azaphenalenyl Radical

4. Steric Modulations in the Reversible Dimerizations of Phenalenyl Radicals via Unusually Weak Carbon-Centered π- and σ-Bonds

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