TY - JOUR
T1 - Co-trimerization of benzonitriles with guanidine hydrochloride
T2 - synthesis of 2-bromo-4,6-diaryl-1,3,5-triazine derivatives bearing electron-withdrawing groups
AU - Chitose, Youhei
AU - Tamura, Yuika
AU - Tsuchiya, Yoichi
AU - Adachi, Chihaya
N1 - Publisher Copyright:
© The Author(s) 2024. Published by Oxford University Press on behalf of the Chemical Society of Japan. All rights reserved.
PY - 2024/4
Y1 - 2024/4
N2 - In recent decades, various types of aryl-substituted 1,3,5-triazine derivatives have been applied in many research fields, including biomedical chemistry, non-linear optics, and organic electronics. However, the substituent scope for 4,6-diaryl-1,3,5-triazines (DAr-TRZs) remains limited. Here, we present our work on the synthesis of 2-amino- and 2-bromo-DAr-TRZ derivatives bearing electron-withdrawing groups on the aryl rings. Our synthetic methods successfully provided trifluoromethyl-, nitrile-, and nitro-substituted DAr-TRZs. These will expand the structural diversity of conventional triazine-based functional materials.
AB - In recent decades, various types of aryl-substituted 1,3,5-triazine derivatives have been applied in many research fields, including biomedical chemistry, non-linear optics, and organic electronics. However, the substituent scope for 4,6-diaryl-1,3,5-triazines (DAr-TRZs) remains limited. Here, we present our work on the synthesis of 2-amino- and 2-bromo-DAr-TRZ derivatives bearing electron-withdrawing groups on the aryl rings. Our synthetic methods successfully provided trifluoromethyl-, nitrile-, and nitro-substituted DAr-TRZs. These will expand the structural diversity of conventional triazine-based functional materials.
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U2 - 10.1093/chemle/upae059
DO - 10.1093/chemle/upae059
M3 - Article
AN - SCOPUS:85191959008
SN - 0366-7022
VL - 53
JO - Chemistry Letters
JF - Chemistry Letters
IS - 4
M1 - upae059
ER -