Abstract

AbstractTwo nucleophilicity scales (N′ and N″) including 96 nucleophiles, spanning 1017 in rate constant, have been constructed directly from experimental rate constants for reactions of nucleophiles with dianisyl (log k = N′) or dimethylaminobenzhydrylium (log k = N″) cations in dichloromethane at 20 °C. The two scales are linked/unified by the formula: N′ − N″ = 6.6. In contrast, published procedures (H. Mayr et al. J. Am. Chem. Soc. 2001, 123, 9500, and later work) involve 23 benzhydrylium cations and over 200 adjustable parameters obtained from the equation log k = s(E + N), where k is the rate constant, E is an electrophilicity parameter and s is a nucleophile‐specific sensitivity parameter. The definitions of N′ and N″ avoid a floating N scale, i.e. having less than the usual attachment to fixed reference points. New equations, log k = (E + sN′) or log k = (E + sN″), where s is now an electrophile‐specific parameter, are then used to correlate over 350 second‐order rate constants for reactions of other benzhydrylium cations with nucleophiles. For weaker, less polar, nucleophiles, s ∼ 1 and the new E and N′ parameters are in satisfactory agreement with published data for E and N. For more polar nucleophiles, s ≠ 1 and values of N − N″ vary by five log units. Copyright © 2010 John Wiley & Sons, Ltd.

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