Spin-Selective Correlation Experiment for Measurement of Long-Range J Couplings and for Assignment of (R/S) Enantiomers from the Residual Dipolar Couplings and DFT

被引:14
作者
Nath, Nilamoni [1 ,2 ,3 ]
Suryaprakash, N. [1 ]
机构
[1] Indian Inst Sci, NMR Res Ctr, Bangalore 560012, Karnataka, India
[2] Indian Inst Sci, Solid State & Struct Chem Unit, Bangalore 560012, Karnataka, India
[3] Sanjay Gandhi Postgrad Inst Med Sci, Ctr Biomed Magnet Resonance, Lucknow 226014, Uttar Pradesh, India
关键词
LIQUID-CRYSTALLINE PHASE; RELATIVE CONFIGURATION; NMR EXPERIMENTS; CONSTANTS; ALIGNMENT; PREDICTION; H-1-NMR; SPECTRA; RDCS;
D O I
10.1021/jp112416q
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We report the C-HETSERF experiment for determination of long- and short-range homo- and heteronuclear scalar couplings ((n)J(HH) and (n)J(XH), n >= 1) of organic molecules with a low sensitivity dilute heteronucleus in natural abundance. The method finds significant advantage in measurement of relative signs of long-range heteronuclear total couplings in chiral organic liquid crystal. The advantage of the method is demonstrated for the measurement of residual dipolar couplings (RDCs) in enantiomers oriented in the chiral liquid crystal with a focus to unambiguously assign R/S designation in a 2D spectrum. The alignment tensor calculated from the experimental RDCs and with the computed structures of enantiomers obtained by DFT calculations provides the size of the back-calculated RDCs. Smaller root-mean-square deviations (rmsd) between experimental and calculated RDCs indicate better agreement with the input structure and its correct designation of the stereogenic center.
引用
收藏
页码:6868 / 6875
页数:8
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