第23讲-抗磁各向异性和自旋分裂Lecture 23 - Diamagnetic Anisotropy and Spin-Spin Splitting |
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课程网址: | http://videolectures.net/yalespan125bs2011_mcbride_lec23/ |
主讲教师: | J. Michael McBride |
开课单位: | 耶鲁大学 |
开课时间: | 2014-08-19 |
课程语种: | 英语 |
中文简介: | 通过固定强度和方向的磁铁之间的空间相互作用,在随机分子翻滚过程中,平均值为零,这表明质子周围的局部场应该只对围绕自身运行的电子敏感。如果轨道的数量随分子取向的变化而变化,那么化学位移可能对在别处轨道运行的电子很敏感。这种“抗磁各向异性”通常用于解释乙炔、芳香族和反芳香族化合物中质子的异常化学位移。质子局部场的另一个来源是附近的磁核,可以用分裂多重数来计算。与化学位移不同,化学位移是以分数单位测量的,因为它取决于外加磁场的强度,而这种自旋分裂(J)是以赫兹为单位测量的,它只取决于分子结构。J不取决于空间接近度,而是取决于轨道重叠,这对于反日食构象来说明显大于日食构象。 |
课程简介: | Through-space interaction between magnets of fixed strength and orientation averages to zero during random molecular tumbling, suggesting that the local field about a proton should be sensitive only to electrons that orbit about itself. The chemical shift can be sensitive to electrons orbiting elsewhere if the amount of orbiting varies with molecular orientation. This "diamagnetic anisotropy" is commonly used to rationalize the unusual chemical shifts of protons in acetylene and in aromatic and antiaromatic compounds. The other source of a proton's local field is nearby magnetic nuclei, which can be counted by the splitting multiplicity. Unlike chemical shift, which is measured in fractional units because it depends on the strength of the applied field, this spin-spin splitting (J), measured in Hz, is dependent only on molecular structure. J depends not on spatial proximity, but on orbital overlap, which, remarkably, is larger for anti- than for eclipsed conformations. |
关 键 词: | 抗磁各向异性; 分子结构; 异常化学位移 |
课程来源: | 视频讲座网 |
数据采集: | 2021-11-19:zkj |
最后编审: | 2021-11-19:zkj |
阅读次数: | 72 |