Gas phase formation of phenalene via 10π-aromatic, resonantly stabilized free radical intermediates-Reference-Cited by-同舟云学术

Gas phase formation of phenalene via 10π-aromatic, resonantly stabilized free radical intermediates

Published:2020 Issue:27 Volume:22 Page:15381-15388
ISSN:1463-9076
Container-title:Physical Chemistry Chemical Physics
language:en
Short-container-title:Phys. Chem. Chem. Phys.

Author:

Zhao Long¹²³⁴^ORCID,Kaiser Ralf I.¹²³⁴^ORCID,Lu Wenchao⁵⁶⁷⁴,Ahmed Musahid⁵⁶⁷⁴^ORCID,Oleinikov Artem D.⁸⁹¹⁰¹¹¹²,Azyazov Valeriy N.⁸⁹¹⁰¹¹¹²,Mebel Alexander M.⁸⁹¹⁰¹¹¹³^ORCID,Howlader A. Hasan¹³¹⁴¹⁵⁴^ORCID,Wnuk Stanislaw F.¹³¹⁴¹⁵⁴

Affiliation:

1. Department of Chemistry

2. University of Hawaii at Manoa

3. Honolulu

4. USA

5. Chemical Sciences Division

6. Lawrence Berkeley National Laboratory

7. Berkeley

8. Department of Physics

9. Samara National Research University

10. Samara 443086

11. Russian Federation

12. Lebedev Physical Institute

13. Department of Chemistry and Biochemistry

14. Florida International University

15. Miami

Abstract

1H-Phenalene can be synthesized via the reaction of the 1-naphthyl radical with methylacetylene and allene under high temperature conditions prevalent in carbon-rich circumstellar environments and combustion systems.

Funder

Basic Energy Sciences

Ministry of Education and Science of the Russian Federation

Publisher

Royal Society of Chemistry (RSC)

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

Link

http://pubs.rsc.org/en/content/articlepdf/2020/CP/D0CP02216K

Reference54 articles.

1. Über Perinaphthinden

2. Intermolecular π-to-π Bonding between Stacked Aromatic Dyads. Experimental and Theoretical Binding Energies and Near-IR Optical Transitions for Phenalenyl Radical/Radical versus Radical/Cation Dimerizations