2010
DOI: 10.1016/j.orggeochem.2010.05.018
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Limitations in interpreting TMAH thermochemolysis of natural organic matter via consideration of glycine and alanine derivatives

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Cited by 6 publications
(5 citation statements)
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“…The most abundant features in the chromatogram of the clear coating were N,N-Dimethylglycine methyl ester, followed by an unknown compound eluting at 5.5 min (Figure 10B). This unknown compound has a base peak at m/z 72 and an apparent mass of 131 amu, which is similar to the reported fragmentation pattern for N-N-dimethylalanine methyl ester [32]. As neither pyrrole nor indole are identified here, it is likely that these compounds are instead related to TMAH itself.…”
Section: Surface Coatingsupporting
confidence: 82%
“…The most abundant features in the chromatogram of the clear coating were N,N-Dimethylglycine methyl ester, followed by an unknown compound eluting at 5.5 min (Figure 10B). This unknown compound has a base peak at m/z 72 and an apparent mass of 131 amu, which is similar to the reported fragmentation pattern for N-N-dimethylalanine methyl ester [32]. As neither pyrrole nor indole are identified here, it is likely that these compounds are instead related to TMAH itself.…”
Section: Surface Coatingsupporting
confidence: 82%
“…MTBSTFA is a silyl reagent (Figure 1), which replaces any labile (reactive) hydrogen in chemical bonds (e.g., -OH, -NH 2 , -SH, and -COOH) with the nonpolar moiety -Si (CH 3 ) 2 C(CH 3 ) 3 (Kataoka, 1996). Thermochemolysis thermally degrades molecules before the substitution of acidic hydrogen by apolar groups from TMAH (i.e., methyl groups -CH 3 ; Challinor, 2001;Gallois et al, 2010;Shadkami & Helleur, 2010). After sample preparation, the stream of helium is divided: a 1:800 fraction is sent directly to the quadrupole mass spectrometer, while the sample is heated at a rate of 35°C/min (evolved gas analysis modes).…”
Section: The Quest For Organics On Marsmentioning
confidence: 99%
“…MTBSTFA is a silyl reagent (Figure ), which replaces any labile (reactive) hydrogen in chemical bonds (e.g., ‐OH, ‐NH 2 , ‐SH, and ‐COOH) with the nonpolar moiety ‐Si (CH 3 ) 2 C(CH 3 ) 3 (Kataoka, ). Thermochemolysis thermally degrades molecules before the substitution of acidic hydrogen by apolar groups from TMAH (i.e., methyl groups –CH 3 ; Challinor, ; Gallois et al, ; Shadkami & Helleur, ).…”
Section: Introductionmentioning
confidence: 99%
“…Nitrogen-containing pyrolysate compounds are derived from proteins, nucleic acids and amino acids via decarboxylation, homolysis, cyclization and fragmentation. 20,22,26 Peaks of Nos. 40, 41, 43 and 45, which are common in plants, animals and fungi, 27 were detected in all HAs in this study.…”
Section: Detail Structural Character Of Hasmentioning
confidence: 99%
“…4), which is regarded as a pyrolysate product of polyphenol or proteins. 26,29,30 The conspicuous peaks of 3,4-dimethoxy-benzoic acid (No. 32) and 3,4,5-trimethoxybenzoic acid methyl esters (No.…”
Section: Detail Structural Character Of Hasmentioning
confidence: 99%