[2 + 2 + 2] cyclotrimerisation as a convenient route to 6N-doped nanographenes: a synthetic introduction to hexaazasuperbenzenes-Reference-Cited by-同舟云学术

[2 + 2 + 2] cyclotrimerisation as a convenient route to 6N-doped nanographenes: a synthetic introduction to hexaazasuperbenzenes

Published:2017 Issue:39 Volume:7 Page:24163-24167
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Wijesinghe Lankani P.¹²³⁴^ORCID,Perera Sarath D.¹²³⁴⁵,Larkin Eugene¹²³⁴,Ó Máille Gearóid M.¹²³⁴,Conway-Kenny Robert¹²³⁴^ORCID,Lankage Buddhie S.¹²³⁴,Wang Longsheng¹²³⁴^ORCID,Draper Sylvia M.¹²³⁴^ORCID

Affiliation:

1. School of Chemistry

2. Trinity College

3. Dublin, D2

4. Ireland

5. Chemistry Department

Abstract

Novel, fully and 5/6^th partially-fused, hexaazasuperbenzenes are obtained using a variety of oxidative cyclodehydrogenation conditions. Their spectroscopic properties are compared.

Funder

Science Foundation Ireland

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/RA/C7RA02648J

Reference34 articles.

1. Heterosuperbenzenes: A New Family of Nitrogen-Functionalized, Graphitic Molecules

2. Terpyridine-fused polyaromatic hydrocarbons generated via cyclodehydrogenation and used as ligands in Ru(ii) complexes

3. Annularly Fused Hexapyrrolohexaazacoronenes: An Extended π System with Multiple Interior Nitrogen Atoms Displays Stable Oxidation States