On the reactivity of naphthalene and biphenyl dianions: tying up loose ends concerning an S(N)2-ET dichotomy in alkylation reactions

摘要

Naphthalene and biphenyl dianions are interesting compounds that can be obtained by double reduction of the corresponding arenes in solution with certain alkali metals. These dianions are highly reactive and rather elusive species with very high laying and highly delocalized electrons. They share many aspects of the reactivity of the alkali metal they originated from and consequently behave primarily as strong electron transfer (ET) reagents. We report here kinetic evidence for a different type of reactivity in their alkylation reactions with alkyl fluorides. By using cyclopropylmethyl fluoride (c-C3H5CH2F) as a very fast radical probe, we were able to settle that this alkylation does not involve the classical electron transfer reaction followed by radical coupling between diffusing radicals, but supports the alternative S(N)2 concerted mechanism, discerning thus this mechanistic S(N)2-ET dichotomy. Copyright (c) 2015 John Wiley & Sons, Ltd.