1952
DOI: 10.1021/ja01135a022
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The Absorption Spectra of Benzoic Acid and Esters

Abstract: The absorption spectra of benzoic acid and some of its simple esters have been determined in various concentrations in polar and non-polar solvents. Changes in solvents and concentrations affect the fine structure of the curves more than the wave lengths and intensities of the maxima and the conclusions are therefore based primarily on variations in fine structure.The spectral changes are discussed in terms of dimerization, bonding with the solvent and ionization.

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Cited by 37 publications
(16 citation statements)
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“…The absorption spectra of p-TPh and p-QPh in chloroform show maxima in accord with data given in the literature (44,61,62). These maxima allow us to calculate the excitation energies AE' related to isolated molecules; they are 4.…”
Section: Mark and Helfrichsupporting
confidence: 89%
“…The absorption spectra of p-TPh and p-QPh in chloroform show maxima in accord with data given in the literature (44,61,62). These maxima allow us to calculate the excitation energies AE' related to isolated molecules; they are 4.…”
Section: Mark and Helfrichsupporting
confidence: 89%
“…23 The absorption peak of HfBA nanoparticles is slightly shifted to 285 nm, consistent with the C-band position of benzoic acid. 24 Nevertheless all three hybrid nanoparticles showed significant and similar UV absorption at 254 nm, the wavelength of the UV lamp source used in the follow up experiments.…”
Section: Methodsmentioning
confidence: 88%
“…Based on the currently available data on the structure of melanoidins, their spectra in the first approximation should be the additive sum of the absorptions of many chromophore systems. The bands at 205 and 270 nm were B-band and C-band caused by A 1g ’→B 1u ’ and A 1g ’→B 2u ’ transitions, respectively [ 73 ], and the redshift of the spectrum compared to that of benzene was due to the influence of substituents, such as hydroxyls, alkyls, etc. [ 74 ].…”
Section: Resultsmentioning
confidence: 99%