Dual Substituent Effects on Anilinolysis of Bis(aryl) Chlorothiophosphates 


Vol. 34,  No. 12, pp. 3597-3601, Dec.  2013
10.5012/bkcs.2013.34.12.3597


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  Abstract

The reactions of bis(Y-aryl) chlorothiophosphates (1) with substituted anilines and deuterated anilines are investigated kinetically in acetonitrile at 55.0 oC. The Hammett plots for substituent Y variations in the substrates show biphasic concave upwards with a break point at Y = H. The cross-interaction constants (ρXY) are positive for both electron-donating and electron-withdrawing Y substituents. The kinetic results of 1 are compared with those of Y-aryl phenyl chlorothiophosphates (2). The cross-interaction between Y and Y, due to additional substituent Y, is significant enough to result in the change of the sign of ρXY from negative with 2 to positive with 1. The effect of the cross-interaction between Y and Y on the rate changes from negative role with electron-donating Y substituents to positive role with electron-withdrawing Y substituents, resulting in biphasic concave upward free energy correlation with Y. A stepwise mechanism with a rate-limiting leaving group departure from the intermediate involving a predominant frontside attack hydrogen bonded, four-centertype transition state is proposed based on the positive sign of ρXY and primary normal deuterium kinetic isotope effects.

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  Cite this article

[IEEE Style]

H. R. Barai and H. W. Lee, "Dual Substituent Effects on Anilinolysis of Bis(aryl) Chlorothiophosphates," Bulletin of the Korean Chemical Society, vol. 34, no. 12, pp. 3597-3601, 2013. DOI: 10.5012/bkcs.2013.34.12.3597.

[ACM Style]

Hasi Rani Barai and Hai Whang Lee. 2013. Dual Substituent Effects on Anilinolysis of Bis(aryl) Chlorothiophosphates. Bulletin of the Korean Chemical Society, 34, 12, (2013), 3597-3601. DOI: 10.5012/bkcs.2013.34.12.3597.

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ISSN(Print) 0253-2964
ISSN(Online) 1229-5949