Self-assembly in solvates of 2,4-diamino-6-(4-methyl- phenyl)-1,3,5-triazine and in its molecular adducts with some aliphatic dicarboxylic acids

被引:2
作者
Nandy, Purnendu [1 ]
Nayak, Amrita [1 ]
Biswas, Sharmita Nandy [1 ]
Pedireddi, V. R. [1 ]
机构
[1] Indian Inst Technol Bhubaneswar, Sch Basic Sci, Solid State & Supramol Struct Chem Lab, Bhubaneswar 751007, Orissa, India
关键词
2,4-Diamino-6-(4-methylphenyl)-1,3,5-triazine; Aliphatic dicarboxylic acids; Single crystal X-ray diffraction; Hydrogen bond; 3D; COCRYSTALLIZATION; CRYSTAL-STRUCTURES; MELAMINE; ORGANIZATION; RECOGNITION; COMPLEXES; CYTOSINE; ADENINE; DESIGN; 2D;
D O I
10.1016/j.molstruc.2015.11.083
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Solid state structures of 2,4-diamino-6-(4-methylpheny1)-1,3,5-triazine, 1, in the form of methanol and dimethylsulfoxide (DMSO) solvates, as well as supramolecular assemblies of 1 with various aliphatic dicarboxylic acids, oxalic (a), malonic (b), succinic (c), glutaric (d) and adipic (e) have been reported. Analysis of the assemblies has been carried out by single crystal X-ray diffraction and thermal methods. Triazine 1 yields anhydrous molecular adducts with acids a-d, upon co-crystallization either from CH3OH and DMSO solvents. However acid e gives anhydrous adduct from DMSO solvent, while it gives a methanol adduct from CH3OH. Structure determination reveals that molecular adducts 1a, 1d and 1e are in a 2:1 ratio of 1 and the corresponding acid. However the ratio is 1:1, in 1b, perhaps due to the involvement of one of the acid groups in the intramolecular hydrogen bonding and in adduct 1c the ratio observed is 3:2. Structural features in all these assemblies have been rationalised in terms of various recognition patterns formed between the acceptor and donor groups. A noteworthy feature is that -COOH groups in acid a establish interaction with 1 through amino groups, while such interactions are observed to be through hetero -N atoms in case of the acids b-e. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:717 / 726
页数:10
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