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Lah, Nina; Šegedin, Primož; Leban, I.

doi:10.1023/a:1015824209616

Cited by 16 publications

(24 citation statements)

References 6 publications

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“…For applications of pyridinium compounds, see: Akkurt et al (2005); Navarro Ranninger et al (1985); Krizanovic et al (1993); Luque et al (1997); Qin et al (1999); Yip et al (1999); Lah et al (2002); Ren et al (2002); Rivas et al (2003); Luque et al (1997);Jin et al (2000); Albrecht et al (2003). For related structures, see: ; Quah et al (2010).…”

Section: Related Literaturementioning

confidence: 99%

“…There are numerous examples of 2-amino-substituted pyridine compounds in which the 2-aminopyridines act as neutral ligands (Navarro Ranninger et al, 1985;Krizanovic et al, 1993;Luque et al, 1997;Qin et al, 1999;Yip et al, 1999;Lah et al, 2002;Ren et al, 2002;Rivas et al, 2003) or as protonated cations (Luque et al, 1997;Jin et al, 2000;Albrecht et al, 2003). We have been interested in hydrogen-bonded systems formed by 2-aminopyridines and carboxylic acids that generate molecular assemblies Quah et al, 2010).…”

Section: Related Literaturementioning

confidence: 99%

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2-Amino-5-bromopyridinium 3-carboxy-4-hydroxybenzenesulfonate

Hemamalini

Fun

2010

Acta Cryst E

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The asymmetric unit of the title salt, C5H6BrN2 +·C7H5O6S−, contains two independent 2-amino-5-bromopyridinium cations and two independent 3-carboxy-4-hydroxybenzenesulfonate anions. The hydroxy and carboxyl groups of the anions are involved in intramolecular O—H⋯O hydrogen bonds, which generate S(6) ring motifs. In the crystal structure, the ions are linked by N—H⋯O and O—H⋯O hydrogen bonds into a two-dimensional network parallel to (110). Adjacent networks are linked via C—H⋯O hydrogen bonds.

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Section: Related Literaturementioning

confidence: 99%

Section: Related Literaturementioning

confidence: 99%

2-Amino-5-bromopyridinium 3-carboxy-4-hydroxybenzenesulfonate

Hemamalini

Fun

2010

Acta Cryst E

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“…There are numerous examples of 2-amino-substituted pyridine compounds in which the 2-aminopyridines act as ligands (Ranninger et al, 1985;Krizanovic et al, 1993;Luque et al, 1997;Qin et al, 1999;Yip et al, 1999;Lah et al, 2002;Ren et al, 2002;Rivas et al, 2003) or as protonated cations (Luque et al, 1997;Jin et al, 2000Jin et al, , 2001Jin et al, , 2002Jin et al, , 2005Albrecht et al, 2003). All of these studies provide important references to further research into 2-aminopyridines.…”

Section: Commentmentioning

confidence: 99%

2-Amino-5-methylpyridinium (2-amino-5-methylpyridine)trichlorozincate(II)

Jin

et al. 2005

Acta Crystallogr C

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The title compound, (C6H9N2)[ZnCl3(C6H8N2)], consists of one 2-amino-5-methylpyridinium cation and one (2-amino-5-methylpyridine)trichlorozincate(II) anion, which are held together by N-H...Cl hydrogen bonds and pi-pi interactions. The cation and the pyridine ligand show similar geometric features, except for the N-C bond lengths. Molecules of the title compound are connected by N-H...Cl hydrogen bonds to form chiral chains; these chains are associated further by C-H...Cl hydrogen bonds to form layers, which are in turn linked by pi-pi interactions.

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“…The next study by Lah et al [74] discussed copper(II) carboxylate complexes of 2-aminopyridine. Since this heterocycle is an ambidentate ligand, we may also consider its complexes as derivatives of 1H-pyridin-2-imine as well.…”

Section: Introductionmentioning

confidence: 98%