|
|
|
|
LEADER |
01000naa a22002652 4500 |
001 |
NLM266854818 |
003 |
DE-627 |
005 |
20231224215429.0 |
007 |
cr uuu---uuuuu |
008 |
231224s2017 xx |||||o 00| ||eng c |
024 |
7 |
|
|a 10.1002/mrc.4548
|2 doi
|
028 |
5 |
2 |
|a pubmed24n0889.xml
|
035 |
|
|
|a (DE-627)NLM266854818
|
035 |
|
|
|a (NLM)27921330
|
040 |
|
|
|a DE-627
|b ger
|c DE-627
|e rakwb
|
041 |
|
|
|a eng
|
100 |
1 |
|
|a Jézéquel, Tangi
|e verfasserin
|4 aut
|
245 |
1 |
4 |
|a The new face of isotopic NMR at natural abundance
|
264 |
|
1 |
|c 2017
|
336 |
|
|
|a Text
|b txt
|2 rdacontent
|
337 |
|
|
|a ƒaComputermedien
|b c
|2 rdamedia
|
338 |
|
|
|a ƒa Online-Ressource
|b cr
|2 rdacarrier
|
500 |
|
|
|a Date Completed 05.03.2018
|
500 |
|
|
|a Date Revised 05.03.2018
|
500 |
|
|
|a published: Print-Electronic
|
500 |
|
|
|a Citation Status PubMed-not-MEDLINE
|
520 |
|
|
|a Copyright © 2016 John Wiley & Sons, Ltd.
|
520 |
|
|
|a The most widely used method for isotope analysis at natural abundance is isotope ratio monitoring by Mass Spectrometry (irm-MS) which provides bulk isotopic composition in 2 H, 13 C, 15 N, 18 O or 34 S. However, in the 1980s, the direct access to Site-specific Natural Isotope Fractionation by Nuclear Magnetic Resonance (SNIF-NMRTM ) was immediately recognized as a powerful technique to authenticate the origin of natural or synthetic products. The initial - and still most popular - application consisted in detecting the chaptalization of wines by irm-2 H NMR. The approach has been extended to a wide range of methodologies over the last decade, paving the way to a wide range of applications, not only in the field of authentication but also to study metabolism. In particular, the emerging irm-13 C NMR approach delivers direct access to position-specific 13 C isotope content at natural abundance. After highlighting the application scope of irm-NMR (2 H and 13 C), this article describes the major improvements which made possible to reach the required accuracy of 1‰ (0.1%) in irm-13 C NMR. The last part of the manuscript summarizes the different steps to perform isotope analysis as a function of the sample properties (concentration, peak overlap) and the kind of targeted isotopic information (authentication, affiliation). Copyright © 2016 John Wiley & Sons, Ltd
|
650 |
|
4 |
|a Journal Article
|
650 |
|
4 |
|a Position-Specific Isotope Analysis
|
650 |
|
4 |
|a SNIF-NMR
|
650 |
|
4 |
|a internal standard
|
650 |
|
4 |
|a irm-NMR
|
650 |
|
4 |
|a isotope analysis
|
700 |
1 |
|
|a Joubert, Valentin
|e verfasserin
|4 aut
|
700 |
1 |
|
|a Giraudeau, Patrick
|e verfasserin
|4 aut
|
700 |
1 |
|
|a Remaud, Gérald S
|e verfasserin
|4 aut
|
700 |
1 |
|
|a Akoka, Serge
|e verfasserin
|4 aut
|
773 |
0 |
8 |
|i Enthalten in
|t Magnetic resonance in chemistry : MRC
|d 1985
|g 55(2017), 2 vom: 15. Feb., Seite 77-90
|w (DE-627)NLM098179667
|x 1097-458X
|7 nnns
|
773 |
1 |
8 |
|g volume:55
|g year:2017
|g number:2
|g day:15
|g month:02
|g pages:77-90
|
856 |
4 |
0 |
|u http://dx.doi.org/10.1002/mrc.4548
|3 Volltext
|
912 |
|
|
|a GBV_USEFLAG_A
|
912 |
|
|
|a SYSFLAG_A
|
912 |
|
|
|a GBV_NLM
|
912 |
|
|
|a GBV_ILN_350
|
951 |
|
|
|a AR
|
952 |
|
|
|d 55
|j 2017
|e 2
|b 15
|c 02
|h 77-90
|