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Issue 4, 1999
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Hydrogen bonding properties and intermediate structure of N-(2-carboxyphenyl)salicylidenimine

Abstract

The hydrogen bonding properties, the nature of the tautomeric structure and dimerization of N-(2-carboxyphenyl)salicylidenimine 1 has been studied. The crystal and molecular structure of 1 has been determined by single-crystal X-ray diffraction analysis. This compound forms a dimer in the solid state, which is held together by two strong intermolecular O–H  · · ·  O bridges [O(1)  · · ·  O(2a) = 2.455(1) Å]. This dimeric structure is further stabilized by two intramolecular N–H  · · ·  O hydrogen bonds [N(1)  · · ·  O(1) = 2.654(1) and N(1)  · · ·  O(2) = 2.663(1) Å]. In this way, an eight-membered pseudocycle is created. However, in methanol or acetonitrile solution, no dimerization was observed according to 1H-NMR, IR and UV measurements. It was also found that this compound exists as an intermediate form between a phenol-imine and an o-quinoid structure. In addition, a derivative soluble in chloroform, 2-[2-hydroxy-5-(2-butyl)benzylideneamino]benzoic acid 3, was examined for comparison.

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Article information


J. Chem. Soc., Perkin Trans. 2, 1999, 807-812
Article type
Paper

Hydrogen bonding properties and intermediate structure of N-(2-carboxyphenyl)salicylidenimine

A. G. J. Ligtenbarg, R. Hage, A. Meetsma and B. L. Feringa, J. Chem. Soc., Perkin Trans. 2, 1999, 807
DOI: 10.1039/A809497G

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