correlations of the specific rates of solvolysis of aromatic carbamoyl chlorides, chloroformates, chlorothionoformates, and chlorodithioformates revisited芳香的特定的溶剂分解率的相关性[氨基甲酰氯,氯甲酸酯,chlorothionoformates,chlorodithioformates再现.pdfVIP
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correlations of the specific rates of solvolysis of aromatic carbamoyl chlorides, chloroformates, chlorothionoformates, and chlorodithioformates revisited芳香的特定的溶剂分解率的相关性[氨基甲酰氯,氯甲酸酯,chlorothionoformates,chlorodithioformates再现
Int. J. Mol. Sci. 2007, 8, 346-362 International Journal of Molecular Sciences ISSN 1422-0067 © 2007 by MDPI /ijms Full Research Paper Correlations of the Specific Rates of Solvolysis of Aromatic Carbamoyl Chlorides, Chloroformates, Chlorothionoformates, and Chlorodithioformates Revisited Dennis N. Kevill 1,*, Fumie Koyoshi 2 and Malcolm J. D’Souza 2,* 1 Department of Chemistry and Biochemistry, Northern Illinois University, DeKalb, Illinois 60115- 2862, USA; E-mail: dkevill@ 2 Department of Chemistry, Wesley College, 120 N. State Street, Dover, Delaware 19901-3875, USA; E-mail: DSouzaMa@W * Authors to whom correspondence should be addressed. Received: 22 March 2007 / Accepted: 24 April 2007 / Published: 30 April 2007 Abstract: Additional specific rates of solvolysis are determined for phenyl chloroformate. These values are combined with literature values to give a total of 49 data points, which are used within simple and extended Grunwald-Winstein treatments. Literature values are also brought together to allow treatments in more solvents than previously for three N-aryl-N- methylcarbamoyl chlorides, phenyl chlorothionoformate, phenyl chlorodithioformate, and N,N-diphenylcarbamoyl chloride. For the last two listed, moderately strong evidence for a meaningful inclusion of a term governed by the aromatic ring parameter (I) was indicated. No evidence was found requiring inclusion of this parameter for ionization reactions with only one aromatic ring on t
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