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Fast and simultaneous determination of 1H-1H and 1H-19F scalar couplings in complex spin systems: Application of PSYCHE homonuclear broadband decoupling
被引:9
|作者:
Kakita, Veera Mohana Rao
[1
]
Rachineni, Kavitha
[1
]
Hosur, Ramakrishna V.
[1
,2
]
机构:
[1] Univ Mumbai, UM DAE Ctr Excellence Basic Sci, Kalina Campus, Bombay 400098, Maharashtra, India
[2] TIFR, Dept Chem Sci, 1 Homi Bhabha Rd, Bombay 400005, Maharashtra, India
关键词:
H-1-H-1 and H-1-F-19 scalar couplings;
broadband decoupling;
PSYCHE;
spectral aliasing;
steroids;
PURE-SHIFT NMR;
HETERONUCLEAR COUPLINGS;
ORGANIC-MOLECULES;
H-1;
SPECTRA;
SPECTROSCOPY;
RESOLUTION;
H-1-NMR;
CONSTANTS;
MIXTURES;
BIRD;
D O I:
10.1002/mrc.4635
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
The present manuscript focuses on fast and simultaneous determination of H-1-H-1 and H-1-F-19 scalar couplings in fluorinated complex steroid molecules. Incorporation of broadband PSYCHE homonuclear decoupling in the indirect dimension of zero-quantum filtered diagonal experiments (F1-PSYCHE-DIAG) suppresses H-1-H-1 scalar couplings; however, it retains H-1-F-19 scalar couplings (along F1 dimension) for the F-19 coupled protons while preserving the pure-shift nature for H-1 resonances uncoupled to F-19. In such cases, along the direct dimensions, H-1-H-1 scalar coupling multiplets deconvolute and they appear as duplicated multiplets for the F-19 coupled protons, which facilitates unambiguous discrimination of F-19 coupled H-1 chemical sites from the others. Further, as an added advantage, data acquisition has been accelerated by invoking the known ideas of spectral aliasing in the F1-PSYCHE-DIAG scheme and experiments demand only similar to 10min of spectrometer times.
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页码:1043 / 1046
页数:4
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