BN Heterosuperbenzenes: Synthesis and Properties

Replacement of CC unit with its isoelectronic BN unit in aromatics provides a new class of molecules with appealing properties, which have attracted great attention recently. In this Concept, we focus on BN‐substituted polycyclic aromatics with fused structures, and review their synthesis, photoph...

Full description

Saved in:
Bibliographic Details
Published inChemistry : a European journal Vol. 21; no. 9; pp. 3528 - 3539
Main Authors Wang, Xiao-Ye, Wang, Jie-Yu, Pei, Jian
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 23.02.2015
WILEY‐VCH Verlag
Wiley Subscription Services, Inc
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Replacement of CC unit with its isoelectronic BN unit in aromatics provides a new class of molecules with appealing properties, which have attracted great attention recently. In this Concept, we focus on BN‐substituted polycyclic aromatics with fused structures, and review their synthesis, photophysical, and redox properties, as well as their applications in organic electronics. We also present challenging synthetic targets, large BN‐ substituted polycyclic aromatics, such as regioregular BN heterosuperbenzenes, which can be viewed as BN‐doped nanographenes. Finally, we propose an atomically precise bottom‐up synthesis of structurally well‐defined BN‐doped graphenes. A new super hero! BN substitution in aromatic systems could provide a new family of interesting compounds. In this Concept, the development of BN‐substituted polycyclic aromatics is reported, and their synthesis, properties and electronic applications are summarized. From monocyclic BN‐substituted benzene to polycyclic BN heteroaromatics (like BN heterosuperbenzene), the possible ways to structurally well‐defined BN‐doped graphenes are proposed.
Bibliography:National Natural Science Foundation of China
istex:01767991AA18539CD188B34CAB1803A2F7162285
ArticleID:CHEM201405627
ark:/67375/WNG-Z7Z8PB80-5
Major State Basic Research Development Program - No. 2013CB933501
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ISSN:0947-6539
1521-3765
1521-3765
DOI:10.1002/chem.201405627