TY - JOUR
T1 - 1,4-Azaborines
T2 - Origin, Modern Synthesis, and Applications as Optoelectronic Materials
AU - Shin, Inji
AU - Lim, Hee Nam
AU - Hong, Wan Pyo
N1 - Publisher Copyright:
© 2021 Georg Thieme Verlag. All rights reserved.
PY - 2021/2/1
Y1 - 2021/2/1
N2 - This short review summarizes the origins and recent progress in 1,4-azaborine research, focusing on synthetic methodologies. Academic laboratories have made significant efforts to generate boronnitrogen-containing heteroaromatic compounds that mimic arenes. 1,2-, 1,3-, and 1,4-Azaborine motifs have provided breakthrough molecules in applications ranging from medicines to materials. Owing to recent advances in polyaromatic 1,4-azaborine synthesis and applications in industry, the research field is currently undergoing a renaissance. Photo- and electroluminescent properties driven by distinct structural variations are key components in the design of novel 1,4-azaborine structures. In this review, seminal reports on the synthesis of simple 1,4-azaborines to complex π-extended structures are briefly highlighted together along with key optoelectronic properties. 1 Introduction 2 Non-Fused 1,4-Azaborines 3 Monobenzo-Fused 1,4-Azaborines 4 Dibenzo-Fused 1,4-Azaborines and Their Derivatives 5 Ladder-Type 1,4-Azaborines 6 Complex 1,4-Azaborines 7 Optoelectronic Properties of Key 1,4-Azaborines 8 Conclusion and Outlook.
AB - This short review summarizes the origins and recent progress in 1,4-azaborine research, focusing on synthetic methodologies. Academic laboratories have made significant efforts to generate boronnitrogen-containing heteroaromatic compounds that mimic arenes. 1,2-, 1,3-, and 1,4-Azaborine motifs have provided breakthrough molecules in applications ranging from medicines to materials. Owing to recent advances in polyaromatic 1,4-azaborine synthesis and applications in industry, the research field is currently undergoing a renaissance. Photo- and electroluminescent properties driven by distinct structural variations are key components in the design of novel 1,4-azaborine structures. In this review, seminal reports on the synthesis of simple 1,4-azaborines to complex π-extended structures are briefly highlighted together along with key optoelectronic properties. 1 Introduction 2 Non-Fused 1,4-Azaborines 3 Monobenzo-Fused 1,4-Azaborines 4 Dibenzo-Fused 1,4-Azaborines and Their Derivatives 5 Ladder-Type 1,4-Azaborines 6 Complex 1,4-Azaborines 7 Optoelectronic Properties of Key 1,4-Azaborines 8 Conclusion and Outlook.
KW - 1,4-azaborine
KW - B,N-doped
KW - C-H borylation
KW - nanographene
KW - organic light emitting diode
UR - http://www.scopus.com/inward/record.url?scp=85123199660&partnerID=8YFLogxK
U2 - 10.1055/s-0040-1719851
DO - 10.1055/s-0040-1719851
M3 - Review article
AN - SCOPUS:85123199660
SN - 0039-7881
VL - 54
SP - 570
EP - 588
JO - Synthesis (Germany)
JF - Synthesis (Germany)
IS - 3
ER -