Structural landscape studies of aminopyridinium hypodiphosphates: dehydration and polymorphism in 4-aminopyridinium salts†

IF 2.6 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
CrystEngComm Pub Date : 2024-11-19 DOI:10.1039/D4CE01048E
Daria Budzikur-Maciąg, Vasyl Kinzhybalo and Katarzyna Ślepokura
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引用次数: 0

Abstract

A series of 4-aminopyridinium (4ap) hypodiphosphates has been synthesized and characterized by variable temperature (VT) optical microscopy, thermogravimetry (TGA-DSC) and X-ray diffraction techniques (SC-XRD, PXRD, VT μ-PXRD). Anhydrous salts (4apH)(H3P2O6) (2) and (4apH)2(H2P2O6) in monoclinic (C2/c) (4), orthorhombic (P212121) (5) and another monoclinic (Cc) (6) polymorphic modifications were obtained by single crystal-to-powder dehydrations of the hydrates: ionic co-crystal (4apH)2(H2P2O6)·H4P2O6·2H2O (1) and salt (4apH)2(H2P2O6)·2H2O (3), respectively. Compound (2) was the only anhydrous form which was also obtained by a typical solution-crystallization. Destructive dehydrations strongly affected hypodiphosphate substructures, generating new structural motifs (both in PP–PP and ap–PP interactions) and new crystal architectures, thus revealing the structural diversity in organic hypodiphosphates. Dehydration gave rise to new properties, as non-centrosymmetric and polar anhydrous structures, (5) and (6) respectively, were obtained from centrosymmetric hydrate (3).

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来源期刊
CrystEngComm
CrystEngComm 化学-化学综合
CiteScore
5.50
自引率
9.70%
发文量
747
审稿时长
1.7 months
期刊介绍: Design and understanding of solid-state and crystalline materials
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