Exploring the enantiomeric 13C position-specific isotope fractionation: challenges and anisotropic NMR-based analytical strategy
نویسندگان
چکیده
Trying to answer the intriguing and fundamental question related chiral induction/amplification at origin of homochirality in Nature: “Is there a relationship between enantiomeric isotopic fractionation carbon 13 molecules?” is difficult but stimulating challenge. Although isotropic 13C-PSIA NMR promising tool for determination (13C/12C) ratios capable providing key 13C data understanding reaction mechanisms biological processes or artificial transformations, this method does not provide access any unless mirror-image isomers are first physically separated. Interestingly, spectral enantiodiscriminations can be potentially performed situ presence enantiopure entities as chiral-europium complexes liquid crystals (CLCs). In work, we explored time capabilities anisotropic 13C-{1H} using PBLG-based lyotropic CLCs enantiodiscriminating media context position-specific isotope (EPSIF), within requested precision order permil. As signals discriminated on basis difference residual chemical shift anisotropy (13C-RCSA) prior being deconvoluted, analysis mixtures becomes possible. The analytical potential approach when poly-?-benzyl-L-glutamate (PBLG) presented, preliminary quantitative results small model molecules obtained 17.5 T with cryogenic probe reported discussed. Graphical abstract
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ژورنال
عنوان ژورنال: Analytical and Bioanalytical Chemistry
سال: 2021
ISSN: ['1618-2642', '1618-2650']
DOI: https://doi.org/10.1007/s00216-021-03599-8