JOURNAL ARTICLE
Structural and supramolecular insights into crystalline multicomponent systems of 2,4‐diamino‐6‐phenyl‐1,3,5‐triazine with various carboxylic acids.
Published In: Acta Crystallographica Section C: Structural Chemistry, 2025, v. 81, n. 4. P. 212 1 of 3
Database: Academic Search Ultimate 2 of 3
Authored By: Nidhishree, Murugan; Gomathi, Sundaramoorthy; Nirmalram, Jeyaraman Selvaraj; Yasien, Sayed; Ramesh, Pandian 3 of 3
Abstract
Three multicomponent systems, namely, 2,4‐diamino‐6‐phenyl‐1,3,5‐triazine–nicotinic acid (DAPT–NA), C9H9N5·C6H5NO2, (I), 2,4‐diamino‐6‐phenyl‐1,3,5‐triazin‐1‐ium hydrogen malonate (DAPT–MMA), C9H10N5+·C3H3O4−, (II), and 2,4‐diamino‐6‐phenyl‐1,3,5‐triazin‐1‐ium hydrogen (+)‐dibenzoyl‐d‐tartarate (DAPT–DBTA), C9H10N5+·C18H13O8−, (III), have been synthesized and characterized via single‐crystal X‐ray diffraction, and their supramolecular interactions have been analysed. The formation of cocrystal (I) and salts (II) and (III) was confirmed through the widening of the C—N—C bond angle of the triazine moiety of 2,4‐diamino‐6‐phenyl‐1,3,5‐triazine and the difference in the C—O bond distances between the carboxyl and carboxylate groups of the respective carboxylic acids. Cocrystal (I) and salt (II) form robust homomeric and heteromeric R22(8) ring motifs through primary acid–base interactions and complementary base pairing. In cocrystal (I), the complementary base pair exists as wave‐like supramolecular strands, whereas in salt (II), it exists as a discrete pair. Salt (II) exhibits DDDAAD sextuple and DADA quadruple hydrogen‐bonded arrays (D is donor and A is acceptor) through acid–base interactions and generates a supramolecular rosette‐like architecture. In salt (III), the presence of carboxyl–carboxylate interactions and acid–base interactions led to the development of a supramolecular sheet and tunnel‐like architecture. Cocrystal (I) and salt (III) are stabilized through offset aromatic π–π stacking interactions and C—H...π interactions, and salts (II) and (III) are stabilized via weak carbonyl–π and C—H...O hydrogen bonds. Macrocyclic R1212(64) and R33(24) motifs are present in salts (II) and (III), respectively. Hirshfeld surface analysis of (I)–(III) reinforces the fact that N...H/H...N, O...H/H...O and C...H/H...C interactions contribute to the crystal packing and stability. [ABSTRACT FROM AUTHOR]
Additional Information
- Source:Acta Crystallographica Section C: Structural Chemistry. 2025/04, Vol. 81, Issue 4, p212
- Document Type:Article
- Subject Area:Chemistry
- Publication Date:2025
- ISSN:2053-2296
- DOI:10.1107/S2053229625001962
- Accession Number:184274178
- Copyright Statement:Copyright of Acta Crystallographica Section C: Structural Chemistry is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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