Marina Carravetta

Find an error

Name:
Organization: University of Southampton , England
Department:
Title: Research Fellow(PhD)
Co-reporter:James A. Jarvis, Ibraheem M. Haies, Philip T. F. Williamson and Marina Carravetta  
Physical Chemistry Chemical Physics 2013 vol. 15(Issue 20) pp:7613-7620
Publication Date(Web):05 Apr 2013
DOI:10.1039/C3CP50787D
Nitrogen is one of the most abundant elements and plays a key role in the chemistry of biological systems. Despite its widespread distribution, the study of the naturally occurring isotope of nitrogen, 14N (99.6%), has been relatively limited as it is a spin-1 nucleus that typically exhibits a large quadrupolar interaction. Accordingly, most studies of nitrogen sites in biomolecules have been performed on samples enriched with 15N, limiting the application of NMR to samples which can be isotopically enriched. This precludes the analysis of naturally occurring samples and results in the loss of the wealth of structural and dynamic information that the quadrupolar interaction can provide. Recently, several experimental approaches have been developed to characterize 14N sites through their interaction with neighboring ‘spy’ nuclei. Here we describe a novel version of these experiments whereby coherence between the 14N site and the spy nucleus is mediated by the application of a moderate rf field to the 14N. The resulting 13C/14N spectra show good sensitivity on natural abundance and labeled materials; whilst the 14N lineshapes permit the quantitative analysis of the quadrupolar interaction.
Co-reporter:James A. Jarvis, Ibraheem M. Haies, Philip T. F. Williamson and Marina Carravetta
Physical Chemistry Chemical Physics 2013 - vol. 15(Issue 20) pp:NaN7620-7620
Publication Date(Web):2013/04/05
DOI:10.1039/C3CP50787D
Nitrogen is one of the most abundant elements and plays a key role in the chemistry of biological systems. Despite its widespread distribution, the study of the naturally occurring isotope of nitrogen, 14N (99.6%), has been relatively limited as it is a spin-1 nucleus that typically exhibits a large quadrupolar interaction. Accordingly, most studies of nitrogen sites in biomolecules have been performed on samples enriched with 15N, limiting the application of NMR to samples which can be isotopically enriched. This precludes the analysis of naturally occurring samples and results in the loss of the wealth of structural and dynamic information that the quadrupolar interaction can provide. Recently, several experimental approaches have been developed to characterize 14N sites through their interaction with neighboring ‘spy’ nuclei. Here we describe a novel version of these experiments whereby coherence between the 14N site and the spy nucleus is mediated by the application of a moderate rf field to the 14N. The resulting 13C/14N spectra show good sensitivity on natural abundance and labeled materials; whilst the 14N lineshapes permit the quantitative analysis of the quadrupolar interaction.
2-Propenamide, N-methoxy-N-(phenylmethyl)-
Methanesulfonic acid, trifluoro-, 2,6,6-trimethyl-1-cyclohexen-1-yl ester
BENZENEMETHANAMINE, N-METHOXY-
ACETAMIDE, 2-CHLORO-N-METHOXY-N-(PHENYLMETHYL)-
2,4-Pentadienoic acid, 3-methyl-5-(2,6,6-trimethyl-1-cyclohexen-1-yl)-,ethyl ester, (2E,4E)-
Silanetriamine, 1-chloro-N,N,N',N',N'',N''-hexaethyl-
Nitrogen oxide (15N2O)(8CI,9CI)
(2Z,4Z,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethyl-1-cyclohexenyl)nona-2,4,6,8-tetraen-1-ol
O-tert-Butyldimethylsilyl 11,12-Didehydro Retinol