Internal Referencing for 13C Position-Specific Isotope Analysis Measured by NMR Spectrometry

被引:17
作者
Bayle, Kevin [1 ]
Grand, Mathilde [1 ]
Chaintreau, Alain [2 ]
Robins, Richard J. [1 ]
Fieber, Wolfgang [2 ]
Sommer, Horst [2 ]
Akoka, Serge [1 ]
Remaudt, Gerald S. [1 ]
机构
[1] Univ Nantes, CNRS, Interdisciplinary Chem Synth Anal Modeling CEISAM, EBSI Team,UMR 6230, F-44322 Nantes 3, France
[2] Firmenich Co, Corp R&D Div, CH-1211 Geneva 8, Switzerland
关键词
NUCLEAR-MAGNETIC-RESONANCE; ACETIC-ACID; FRACTIONATION; H-1-NMR; PRECISE; PATHWAY; PATTERN; ETHANOL; ORIGIN;
D O I
10.1021/acs.analchem.5b02094
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The intramolecular C-13 composition of a molecule retains evidence relevant to its (bio)synthetic history and can provide valuable information in numerous fields ranging from biochemistry to environmental sciences. Isotope ratio monitoring by C-13 NMR spectrometry (irm-C-13 NMR) is a generic method that offers the potential to conduct C-13 position-specific isotope analysis with a precision better than 1 parts per thousand. Until now, determining absolute values also required measurement of the global (or bulk) C-13 composition (delta C-13(g)) by mass spectrometry. In a radical new approach, it is shown that an internal isotopic chemical reference for irm-C-13 NMR can be used instead. The strategy uses H-1 NMR to quantify both the number of moles of the reference and of the studied compound present in the NMR tube. Thus, the sample preparation protocol is greatly simplified, bypassing the previous requirement for precise purity and mass determination. The key to accurate results is suppressing the effect of radiation damping in H-1 NMR which produces signal distortion and alters quantification. The methodology, applied to vanillin with dimethylsulfone as an internal standard, has an equivalent accuracy (<1 parts per thousand) to that of the conventional approach. Hence, it was possible to clearly identify vanillin from different origins based on the C-13 isotopic profiles.
引用
收藏
页码:7550 / 7554
页数:5
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