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Synthesis and spectral properties of arylmercury derivatives of α-thiopicolinanilide

Synthesis and spectral properties of arylmercury derivatives of α-thiopicolinanilide
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摘要 A series of thirteen arylmercury derivatives of α-thiopicolinanilide have been synthesized and characterized by elemental analysis,IR,~1H NMR and MS.The intramolecular coordination and the substituent effects on the MS and ^(199)Hg NMR behaviours have been studie6.It has been shown that a linear correlation exists between the ^(199)Hg chemical shifts and the Hammett-Brown constants σ^+,and the electron-donating groups cause the chemical shift to move upfield. A series of thirteen arylmercury derivatives of α-thiopicolinanilide have been synthesized and characterized by elemental analysis,IR,~1H NMR and MS.The intramolecular coordination and the substituent effects on the MS and ^(199)Hg NMR behaviours have been studie6.It has been shown that a linear correlation exists between the ^(199)Hg chemical shifts and the Hammett-Brown constants σ^+,and the electron-donating groups cause the chemical shift to move upfield.
出处 《Chinese Journal of Chemistry》 SCIE CAS CSCD 1993年第1期45-52,共8页 中国化学(英文版)
基金 Project supported by the National Natural Science Foundation of China and the Natural Science Foundation of Henan Province
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