Anion Radicals of Di-trans-[12]annulene and Heptalene in a One-Pot Synthesis from a Common Fire Retardant
Author:
Affiliation:
1. Department of Chemistry, Illinois State University, Normal, Illinois 61790-4160
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol0362921
Reference15 articles.
1. Antiaromaticity in Monocyclic Conjugated Carbon Rings
2. The Cyclooctatriene-η2-ynyl Potassium Zwitterionic Radical: Evidence for a Potassium Organometallic
3. The Electron as a Protecting Group. 2. Generation of Benzocyclobutadiene Radical Anion in the Gas Phase and an Experimental Determination of the Heat of Formation of Benzocyclobutadiene
4. The Electron as a Protecting Group. 3. Generation of Acenaphthyne Radical Anion and the Determination of the Heat of Formation of a Strained Cycloalkyne
5. [12]Annulene
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1. Antiaromaticity-promoted radical anion stability in α-vinyl heterocyclics;Organic Chemistry Frontiers;2022
2. The Geometry and Electronic Topology of Higher-Order Charged Möbius Annulenes;The Journal of Physical Chemistry A;2009-07-28
3. [12]Annulene Radical Anions Revisited: Evaluation of Structure Assignments Based on Computed Energetic and Electron Spin Resonance Data;The Journal of Organic Chemistry;2008-10-22
4. Nature of Organic Ion-Radicals and Their Ground-State Electronic Structure;Ion-Radical Organic Chemistry;2008-10-20
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