1999
DOI: 10.1016/s0022-2860(99)00063-0
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IR study of the dimerization and the proton acceptor ability of N - tertio -butoxycarbonyl- l -phenylalanine

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Cited by 4 publications
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“…Either if there was a random orientation of the molecule at the surface or a defined adsorption (aromatic ring parallel or perpendicular orientation), the phenol or hydroquinone molecule produces quinone derivates in acid solution at a smooth or a rough platinum surface [46][47][48]. Moreover, different authors have conducted FTIR spectral measurements on phenol complexes with amino acids [49] and betaines [50] to prove the formation of dimers through the characteristic bands of the phenolic group. We have check for these signals conducting in situ FTIR spectra of hydroquinone ( Fig.…”
Section: Products Assignmentmentioning
confidence: 99%
“…Either if there was a random orientation of the molecule at the surface or a defined adsorption (aromatic ring parallel or perpendicular orientation), the phenol or hydroquinone molecule produces quinone derivates in acid solution at a smooth or a rough platinum surface [46][47][48]. Moreover, different authors have conducted FTIR spectral measurements on phenol complexes with amino acids [49] and betaines [50] to prove the formation of dimers through the characteristic bands of the phenolic group. We have check for these signals conducting in situ FTIR spectra of hydroquinone ( Fig.…”
Section: Products Assignmentmentioning
confidence: 99%