The preparation and acetolysis of some [π-phenylchromium tricarbonyl] benzyl p-toluenesulfonates and their noncomplexed analogs. a search for σ π delocalization
RS Bly, KK Tse, RK Bly
Index: Bly,R.S. et al. Journal of Organometallic Chemistry, 1976 , vol. 117, p. 35 - 54
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Citation Number: 7
Abstract
Abstract The substituted benzyl tosylates p-phenyl, p-(π-phenylchromium tricarbonyl), p-(p′- nitrophenyl), m-phenyl, m-(π-phenylchromium tricarbonyl) and m-(p′-nitrophenyl) have been prepared and their solvolysis rates in buffered and/or unbuffered acetic acid determined. At 69.0 C their reactivities relative to benzyl tosylate (1.00) are: 10.8, 7.14, 0.742, 0.571, 0.134 and 0.173, respectively. Conjugative substituent parameters are ...
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