Issue 9, 2011

Synthesis and polymorphism of (4-ClpyH)2[CuCl4]: solid–gas and solid–solid reactions

Abstract

Reaction of blue crystalline solid trans-[CuCl2(4-Clpy)2] 1 (4-Clpy = 4-chloropyridine) with anhydrous HCl gas yields yellow crystalline salt (4-ClpyH)2[CuCl4] 2 with quantitative conversion. The reaction has been followed in situ by synchrotron powder X-ray diffraction using a specially designed gas-handling rig and demonstrates that the initial product is a C-centred monoclinic form of (4-ClpyH)2[CuCl4] (phase II), which then converts in the solid state to a primitive monoclinic form (phase I). The conversion has been quantified at each stage by mixed-phase Rietveld refinement of the powder diffraction data. The two polymorphic forms exhibit different patterns of N–H⋯Cl(Cu) hydrogen bonding and C–Cl⋯Cl(Cu) halogen bonding. Evidence from solution-phase crystallisations of 2 suggests that phase II is a kinetic product and phase I is the thermodynamic product. The salt 2 can also be prepared mechanochemically, by grinding for 2 min green-blue solid CuCl2·2H2O with white solid [4-ClpyH]Cl in a 1 : 2 stoichiometric ratio. The product was identified by powder diffraction as phase I of compound 2 in 97.5% yield, with the remaining material being compound 1.

Graphical abstract: Synthesis and polymorphism of (4-ClpyH)2[CuCl4]: solid–gas and solid–solid reactions

Supplementary files

Article information

Article type
Paper
Submitted
10 Sep 2010
Accepted
04 Nov 2010
First published
03 Dec 2010

CrystEngComm, 2011,13, 3189-3196

Synthesis and polymorphism of (4-ClpyH)2[CuCl4]: solid–gas and solid–solid reactions

I. J. Vitorica-Yrezabal, R. A. Sullivan, S. L. Purver, C. Curfs, C. C. Tang and L. Brammer, CrystEngComm, 2011, 13, 3189 DOI: 10.1039/C0CE00628A

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