From a 1,2-azaborinine to large BN-PAHs via electrophilic cyclization: synthesis, characterization and promising optical properties-Reference-Cited by-同舟云学术

From a 1,2-azaborinine to large BN-PAHs via electrophilic cyclization: synthesis, characterization and promising optical properties

Published:2021 Issue:1 Volume:8 Page:10-17
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Appiarius Yannik¹²³⁴⁵^ORCID,Stauch Tim⁵³⁴¹⁶^ORCID,Lork Enno¹⁶³⁴¹^ORCID,Rusch Pascal⁷³⁴⁸⁹,Bigall Nadja C.⁷³⁴⁸⁹^ORCID,Staubitz Anne¹²³⁴⁵^ORCID

Affiliation:

1. University of Bremen

2. Institute for Analytical and Organic Chemistry

3. D-28359 Bremen

4. Germany

5. MAPEX Center for Materials and Processes

6. Institute for Physical and Theoretical Chemistry

7. Bremen Center for Computational Materials Science

8. Leibniz University Hannover

9. Institute for Physical Chemistry and Electrochemistry

Abstract

A synthetic approach towards boron-nitrogen substituted polycyclic aromatic hydrocarbons (BN-PAHs) via electrophilic cyclization is described and it is shown that the variation of the rings' connectivity may tune the emission wavelengths effectively.

Funder

Deutsche Forschungsgemeinschaft

Horizon 2020

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/QO/D0QO00723D

Reference73 articles.

1. A Synthesis of Aromatic Five- and Six-Membered B−N Heterocycles via Ring Closing Metathesis

2. Recent Advances in Azaborine Chemistry