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Polymorphism in pyridine-2,6-dicarboxylic acid: Competition between “robust” synthons†
Abstract
A new polymorph of anhydrous pyridine-2,6-dicarboxylic (dipicolinic) acid in which salt formation is favoured over
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Supplementary files
- Crystal structure data CIF (34K)
- Tables of fractional atomic co-ordinates, selected inter-atomic distances, bond and torsion angles, and anisotropic temperature factors for compounds 4a, 4b and 6 together with additional figures showing Ortep plots and the numbering scheme used for the structure solutions. Diagrams containing full atomic numbering schemes of 4a, 4b, 6 and the revised dipicolinic acid mono-hydrate 4 are available also enlarged versions of Figs. 8, 9 and 11 PDF (2035K)
- Crystal structure data TXT (34K)
Additions and corrections
Article information
- Article type
- Communication
- Submitted
- 21 Nov 2005
- Accepted
- 25 Jan 2006
- First published
- 22 Feb 2006
CrystEngComm, 2006,8, 123-128
Permissions
Polymorphism in pyridine-2,6-dicarboxylic acid : Competition between “robust” synthons
M. C. Grossel, A. N. Dwyer, M. B. Hursthouse and J. B. Orton, CrystEngComm, 2006, 8, 123 DOI: 10.1039/B516387K
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