1990
DOI: 10.1016/0021-9797(90)90336-m
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X-ray photoelectron and infrared spectroscopy of glycine adsorbed upon copper

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Cited by 47 publications
(47 citation statements)
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“…The second one, at 286.2 ± 0.1 eV, is assigned to carbon in C-N and C-S bonds, the third one at 287.7 ± 0.1 eV to carbon of amide functions and the highest BE peak, at 289.1 ± 0.1 eV to carbon of COOH function of the acidic or carboxylate groups for the basic or zwiterrionic form of GSH. [5,15,16] The N 1s peak presents two contributions for both the acidic and zwiterrionic forms, at 399.7 ± 0.1 and 401.3 ± 0.1 eV respectively, attributed to nitrogen of amide groups and NH 3 + [2,17] ; note that the intensity ratio NH 3 + /O C-NH = 1/2 is in agreement with the molecular formula of GSH. For the anionic form, there is only one contribution at 399.7 ± 0.1 eV assigned to nitrogen in NH 2 and in the amide functions (O C-NH).…”
Section: Xps Analysissupporting
confidence: 65%
“…The second one, at 286.2 ± 0.1 eV, is assigned to carbon in C-N and C-S bonds, the third one at 287.7 ± 0.1 eV to carbon of amide functions and the highest BE peak, at 289.1 ± 0.1 eV to carbon of COOH function of the acidic or carboxylate groups for the basic or zwiterrionic form of GSH. [5,15,16] The N 1s peak presents two contributions for both the acidic and zwiterrionic forms, at 399.7 ± 0.1 and 401.3 ± 0.1 eV respectively, attributed to nitrogen of amide groups and NH 3 + [2,17] ; note that the intensity ratio NH 3 + /O C-NH = 1/2 is in agreement with the molecular formula of GSH. For the anionic form, there is only one contribution at 399.7 ± 0.1 eV assigned to nitrogen in NH 2 and in the amide functions (O C-NH).…”
Section: Xps Analysissupporting
confidence: 65%
“…To confirm the obtained absorption data and perform band assignments, the glycine spectra were compared with spectra of glycine in KBr pellets as measured by Ihs et al (1990), Uvdal et al (1990) and Rosado et al (1998). The D-alanine spectra were compared with spectra of L-alanine in KBr pellets determined by Fischer (1999, 2000) and Rozenberg et al (2003).…”
Section: Resultsmentioning
confidence: 99%
“…Uvdal et al (1990) reported that in a thin layer of Gly on a Cu substrate, the NH3+-stretching vibration of zwitterionic Gly shifted to higher frequency, from 3169 to 3180 cm-L Jang and Condrate (1972) also observed that the NH3+-stretching band occurred at 3220 cm i in the Hmontmorillonite-Gly intercalate and concluded that the intercalated Gly molecules involved less intermolecu- A similar mechanism is assumed for the KH-amino acid intercalates. Amino acid in the crystalline (zwitterionic) state forms a strong NH3 + -.. CO0-intermolecular hydrogen bond between adjacent molecules.…”
Section: Discussionmentioning
confidence: 97%
“…In Figure 5A, trace a, the broad and strong absorption band between 3300-2300 cm -1 occurs in most amino acids in the crystalline (zwitterionic) state and is characteristic of the intermolecular hydrogen-bonding, COO-... NH3 § (Uvdal et al, 1990). In the Gly intercalate, several of these strong bands were shifted to 3300-2800 cm -~ ( Figure 5A, trace e).…”
Section: Intercalation Of Amino Acidsmentioning
confidence: 95%
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