1978
DOI: 10.1246/bcsj.51.2460
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Absorption and Fluorescence Spectra of Anthracenecarboxylic Acids. I. 9-Anthroic Acid and Formation of Excimer

Abstract: The absorption spectra of 9-anthroic acid (9-anthracenecarboxylic acid) in ethanol have been measured as a function of solute concentration. It was revealed that 9-anthroic acid forms a hydrogen-bonded dimer. The equilibrium constant for dimer formation was determined to be 6.6×104 mol−1 1 in ethanol at 298 K. The fluorescence spectra of 9-anthroic acid have been investigated as a function of concentration and temperature in various solvents. An excimer mechanism was proposed for a broad fluorescence of 9-anth… Show more

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Cited by 22 publications
(39 citation statements)
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“…[1][2][3][4] The effect of many solvents on the fluorescence of 9-ACA has also been examined. These include hydrophobic, hydrophilic, protic, and aprotic solvents.…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…[1][2][3][4] The effect of many solvents on the fluorescence of 9-ACA has also been examined. These include hydrophobic, hydrophilic, protic, and aprotic solvents.…”
Section: Introductionmentioning
confidence: 99%
“…These include hydrophobic, hydrophilic, protic, and aprotic solvents. 3 The fluorescence of other anthracene substitutions such as 9-COOCH 3 has also been studied 2 and compared with that of 9-ACA. Various environmental factors that have been examined include the effects of pH, concentration, temperature, and viscosity.…”
Section: Introductionmentioning
confidence: 99%
“…O grupo carboxilato do 9-AA assume uma configuração espacial perpendicular ao plano do anel antracênico na forma ionizada, tanto no estado eletrônico fundamental como no estado excitado, mantendo a mesma geometria [21,[24][25][26] . A banda não-estruturada do 9-AA pode ser atribuída à emissão da forma protonada do 9-AA [21][22][23] , uma vez que o grupo carboxilato adquire uma posição coplanar ao anel antracênico, fazendo com que ocorra uma mudança significativa da geometria da molécula no estado eletrônico excitado.…”
Section: Comportamento Gravimétrico Das Amostras Analisadasunclassified
“…In the molecule, the anthracene moiety is almost planar and the dihedral angle between the plane of the aromatic ring and the carboxylic group is 54.9°. In the crystalline structure, occurs the formation of cyclic dimers, through hydrogen bonds of type C@OÁ Á ÁH, according to studies due to Susuki and collaborators [14] and Swayambunathan et al [15].…”
Section: Introductionmentioning
confidence: 99%