Abstract

AbstractCyclic alcohols (n = 5‐7) are compounds of distinctive nonplanar structure. Effect of the alcohols on micellization of sodium dodecyl sulfate (SDS) in aqueous solution are examined by determining the critical micelle concentration (CMC) by conductometry and the micelle aggregation numbers (Nagg) by fluorometry, respectively. In general, the CMC of SDS decreases with increase in volume of a cyclic alcohol in water and increases further after attaining a minimum value. The Nagg of SDS varies little with small addition of a cyclic alcohol, but decreases when added in sufficient volume. Both the changes of the CMC and Nagg with carbon number in the ring of the alcohols occur irregularly due to their steric reasons and nonplanar nature. The irregularity makes a difference between the cyclic alcohols and their chain counterparts. Based on 1H NMR chemical shift measurements, the cyclic alcohols are found to be solubilized in the palisade layer in SDS micelles.

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