Polymorphism control in the mechanochemical and solution-based synthesis of a thermochromic Schiff base. Issue 41 (25th September 2015)

• Record Type: Journal Article
• Authors: Zbačnik, Marija; Nogalo, Ivana; Cinčić, Dominik; Kaitner, Branko
• Is Part Of: CrystEngComm. Volume 17:Issue 41(2015)
• Page Start: 7870
• Page End: 7877
• Publication Date: 2015-09-25
• Subjects: Crystals -- Periodicals; Crystal growth -- Periodicals; Crystallography -- Periodicals; Cristaux -- Périodiques; Cristaux -- Croissance -- Périodiques; Cristallographie -- Périodiques; 548
• DOI: 10.1039/c5ce01445j
• Languages: English
• ISSNs: 1466-8033

Abstract

Abstract : Three crystal forms of a thermochromic Schiff base derived from o -vanillin and 3-aminoacetophenone were obtained by conventional solution-based methods. Two polymorphs out of three were synthesized by mechanochemical syntheses, under solvent-free conditions. Abstract : Three crystal forms of a thermochromic Schiff base, namely 1-{3-[(2-hydroxy-3-methoxy-benzylidene)-amino]-phenyl}-ethanone, derived from o -vanillin and 3-aminoacetophenone, were obtained by conventional solution-based methods. Two out of the three polymorphs were synthesized by mechanochemical syntheses, under solvent-free conditions. Herein, we report a study of the dependence of the composition of solvent, the crystallization temperature and impurities on the outcome of the synthesis of Schiff base polymorphs. We report the important role of seed crystals in directing the supramolecular organization of the product of a covalent solvent-free reaction towards the intended polymorphic outcome as well. All obtained polymorphs were investigated by means of thermal analysis, single crystal X-ray diffraction, ex situ and in situ powder X-ray diffraction and IR spectroscopy. The polymorphs display interesting and remarkably different molecular packing arrangements governed by C–H⋯O interactions leading to two-dimensional networks in formsI andIII, and a three-dimensional networks in formII .