ISSN:
0894-3230
Keywords:
Chemistry
;
Theoretical, Physical and Computational Chemistry
Source:
Wiley InterScience Backfile Collection 1832-2000
Topics:
Chemistry and Pharmacology
,
Physics
Notes:
Measurements were made in CCl4 of the formation constant KHB of the 1:1 hydrogen-bonded complexes between the reference donor 4-fluorophenol and the intramolecular hydrogen-bonded systems I (one lone pair on heteroatom Y, one intramolecular hydrogen bond: 8-hydroxyquinaldine and 2-(2-hydroxyphenyl)benzoxazole); II: (two lone pairs, two intramolecular hydrogen bonds: 2,2′-dihydroxybenzophenone and 1,8-dihydroxyanthrone) and III (two lone pairs, one intramolecular hydrogen bond: tropolone, salicylic acid derivatives and guaiacol). The pKHB values and the structural vibrational studies show that system I has a non-zero hydrogen-bond basicity which is due to the oxygen atom. In system II the non-zero basicity is explained by the two oxygens and the breaking of one intramolecular hydrogen bond. In the push-pull system III (e.g. tropolone), in spite of the great decrease of the basicity of the free lone pair by the intramolecular hydrogen bond (e.g. compared with tropone), Y remains the major site for intermolecular association. However in guaiacol, a non push-pull system III, the cooperativity effect makes the phenolic oxygen the major site.
Additional Material:
3 Ill.
Type of Medium:
Electronic Resource
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