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Synthesis and characterization of three co-crystals of bis(benzimidazole) derivatives with aromatic dicarboxylic acids.

Authors :
Wu, Shang-Zhuo
Yu, Qiang
Li, Yue-Hua
Cui, Guang-Hua
Source :
Research on Chemical Intermediates; Feb2021, Vol. 47 Issue 2, p835-851, 17p
Publication Year :
2021

Abstract

Combination of three aromatic carboxylic acids (5-nitroisophthalic acid (H<subscript>2</subscript>nip), 2,6-naphthalenedicarboxylic acid (H<subscript>2</subscript>ndc), tetrabromoterephthalic acid (H<subscript>2</subscript>tbta)) and flexible bis(benzimidazole) derivatives (1,6-bis(2-methylbenzimidazol-1-yl)hexane (L1), 1,2-bis(2-methylbenzimidazol-1-ylmethyl)benzene (L2), 1,4-bis(2-methylbenzimidazol-1-yl)butane (L3)), three co-crystals [(H<subscript>2</subscript>L1)<superscript>2+</superscript>·2(Hnip)<superscript>−</superscript>·H<subscript>2</subscript>O] (1), [(L2)·(H<subscript>2</subscript>ndc)] (2) and [(H<subscript>2</subscript>L3)<superscript>2+</superscript>·(tbta)<superscript>2−</superscript>] (3) were synthesized hydrothermally. Single-crystal X-ray diffraction, elemental analysis and IR spectra are employed to characterize 1, 2 and 3. The 2D fingerprint plots and Hirshfeld surfaces of 1, 2 and 3 indicate that the 3D supramolecular network for 1 was generated by N–H···O, O–H···O, C–H··O hydrogen bonds and π−π interactions, the 2D sheet for 2 was produced by O–H···N hydrogen bonds and π−π interactions, and C–H···O hydrogen bonds make structures more stable. For 3, the 2D supramolecular layer was yielded by N–H···O, C–H···O hydrogen bond interactions. Furthermore, thermogravimetric analyses and photoluminescence properties of three compounds were presented. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09226168
Volume :
47
Issue :
2
Database :
Complementary Index
Journal :
Research on Chemical Intermediates
Publication Type :
Academic Journal
Accession number :
148753784
Full Text :
https://doi.org/10.1007/s11164-020-04300-x