Keto-enol tautomerism in asymmetric Schiff bases derived from p-phenylenediamine

Journal of Molecular Structure

Volumn 984, Issue 1-3, 2010, Pages 232-239

  Užarević, Krunoslav ^a   Rubčić, Mirta ^a   Stilinović, Vladimir ^a   Kaitner, Branko ^a   Cindrić, Marina ^a  

^a UNIVERSITY OF ZAGREB   (Croatia)

Author keywords

Asymmetric Schiff bases; Crystal engineering; Dehydroacetic acid; Keto enol tautomerism; Resonance assisted hydrogen bond

Indexed keywords

AMINO GROUP; DEHYDROACETIC ACID; ELEMENTAL ANALYSIS; IR AND NMR SPECTROSCOPY; KETO-ENOL TAUTOMERISM; P-PHENYLENE DIAMINES; POWDER X RAY DIFFRACTION; RESONANCE-ASSISTED HYDROGEN BOND; SALICYLALDEHYDE; SCHIFF BASIS; SCHIFF-BASE; SINGLE CRYSTAL X-RAY CRYSTALLOGRAPHY; SPECTROSCOPIC STUDIES; STRONG RESONANCE; TAUTOMERIC FORMS; THERMAL METHODS;

ALDEHYDES; COMPLEXATION; CRYSTAL ENGINEERING; FUNCTIONAL GROUPS; HYDROGEN; NUCLEAR MAGNETIC RESONANCE; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; RESONANCE; SINGLE CRYSTALS; SPECTROSCOPIC ANALYSIS; SYNTHESIS (CHEMICAL); X RAY CRYSTALLOGRAPHY; X RAY DIFFRACTION; X RAY DIFFRACTION ANALYSIS;

HYDROGEN BONDS;

EID: 78649325615     PISSN: 00222860     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molstruc.2010.09.034     Document Type: Article

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