Studies on ^<13>C Magnetic Resonance Spectroscopy. XIV. Interpretation of the ^<13>C NMR Chemical Shifts of 2-Substituted Naphthalenes and Their 6-Methoxy Derivatives
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概要
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The ^<13>C chemical shifts of 2-substituted naphthalenes and their 6-methoxy derivatives are considered in terms of empirical parameters, charge densities, and screening tensors. The ^<13>C screening tensors were calculated theoretically using LCGI-MO theory, by the MINDO/2 method. The results were consistent with the experimental data. The 2p electron charge density, the predominant factor governing the calculated ^<13>C chemical shift, also corresponded well with the experimental data.
- 社団法人日本薬学会の論文
- 1979-08-25
著者
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佐々木 喜男
Faculty of Pharmaceutical Sciences, Osaka University
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佐々木 喜男
Faculty Of Pharmaceutical Sciences Osaka University
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小谷 明
Faculty Of Pharmaceutical Sciences Osaka University
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高井 均
Faculty of Pharmaceutical Sciences, Osaka University
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高井 均
Faculty Of Pharmaceutical Sciences Osaka University
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