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首页> 外文期刊>Journal of Computational Chemistry: Organic, Inorganic, Physical, Biological >Chiral Discrimination via Nuclear Magnetic Shielding Polarisabilities from NMR Spectroscopy:Theoretical Study of (R_a)-1,3-Dimethylallene,(2R)-2-Methyloxirane,and (2R)-N-Methyloxaziridine
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Chiral Discrimination via Nuclear Magnetic Shielding Polarisabilities from NMR Spectroscopy:Theoretical Study of (R_a)-1,3-Dimethylallene,(2R)-2-Methyloxirane,and (2R)-N-Methyloxaziridine

机译:核磁共振谱从核磁屏蔽极化率的手性区分:(R_a)-1,3-二甲基丙二烯,(2R)-2-甲基环氧乙烷和(2R)-N-甲基氧杂氮丙啶的理论研究

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摘要

Three medium-size optically active molecules have been studied to make a guess at candidates suitable for chiral discrimination in an isotropic medium via nuclear magnetic resonance spectroscopy.The criterion for experimental detection is given by the magnitude of the isotropic part of nuclear magnetic shielding polarisability tensors,related to a pseudoscalar of opposite sign for the two enantiomers.The pseudoscalar shielding polarisability at the ~17O nucleus in N-methyloxaziridine,calculated at the Hartree-Fock level,is approx = 7.8 x 10~(-17) mV~(-1).To obtain an experimentally observable magnetic field induced at the ~17O nucleus in N-methyloxaziridine,electric fields as large as approx = 10~7-10~8 Vm~(-1) should be applied to the probe.The molecular electric dipole moment induced by precession of the magnetic dipole of the ~(17)O nucleus in a magnetic field of 10 T is,in absolute value,approx 8.8 x 10~(42) Cm.The estimated rf-voltage at a resonance circuit is approx =10 nV.Smaller values have been estimated for N,C,and H nuclei in 1,3-dimethylallene and 2-mefhyloxirane.
机译:通过核磁共振波谱研究了三种中等大小的光学活性分子,以推测出适合各向同性介质中手性识别的候选物。实验检测的标准由核磁屏蔽极化率张量的各向同性部分的大小给出,与两个对映体的符号相反的伪标量有关。在Hartree-Fock水平计算,N-甲基恶唑烷在〜17O核的伪标量屏蔽极化率约为= 7.8 x 10〜(-17)mV〜(- 1)。为了获得在N-甲基恶唑烷中〜17O核处感应产生的实验可观察到的磁场,应对探针施加大约10〜7-10〜8 Vm〜(-1)的大电场。在10 T的磁场中,〜(17)O核的磁偶极进动引起的电偶极矩的绝对值约为8.8 x 10〜(42)Cm。在谐振电路上估算的rf电压约为= 10 nV。已估计了1,3-二甲基丙二烯和2-甲氧基环氧乙烷中N,C和H核的r值。

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