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Synthesis and crystal structure investigation of pyridine-2-(3′-mercaptopropanoic acid)-N -oxide
✍ Scribed by R. Ramasubramanian; S. Kumaresan; R. Thomas; A. David Stephen; P. Kumaradhas
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 190 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0232-1300
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✦ Synopsis
Abstract
Pyridine‐2‐(3′‐mercaptopropanoic acid)‐N ‐oxide (I), is a higher homologue of 1‐oxopyridinium‐2‐thioacetic acid (II) [1]. It crystallizes in monoclinic space group P2~1~ with a = 9.2168(2) Å, b = 4.1423(2) Å, c = 11.3904(4) Å, β = 98.65(2)°, V = 429.93(3) Å^3^ and Z = 2. The least‐squares refinement gave residual index R = 0.024 for 1070 observed reflections. The introduction of an additional methylene group in (II) causes a flip in the carboxylic acid group of (I) that facilitates the molecules to align infinite antiparallel chains through strong C–H···O interactions. The molecules are interlinked by O–H···O hydrogen bonding across the chains and forming an infinite screw chain along y‐direction. The molecular packing is stabilized by O–H···O and C–H···O hydrogen bonding and π‐π electron interactions. This is an important facet of the crystal packing. (© 2007 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)
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## Abstract A new complex of Zinc(II) and guanidinium pyridine–2,6–dicarboxylate proton transfer compound, (GnH)~2~ (pydc), was synthesized and characterized using IR, ^1^H NMR and ^13^C NMR spectroscopy and single crystal X–ray diffraction. The chemical formula and space group of the resulting com