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   <subfield code="a">Living cationic polymerization of styrene by the 1-phenylethyl chloride/tin tetrachloride initiating system in the presence of tetra-n-butylammonium chloride</subfield>
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   <subfield code="c">[Yoshiyuki Ishihama, Mitsuo Sawamoto, Toshinobu Higashimura]</subfield>
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   <subfield code="a">Summary: An initiating system, consisting of 1-phenylethyl chloride, tin tetrachloride, and tetra-n-butylammonium chloride [CH3CH(Ph)C1/SnCl4/nBu4NCl], led to living cationic polymerization of styrene in CH2Cl2 solvent at-15°C; typically, CH3CH(Ph)Cl/SnCl4/nBu4NCl=20/100/40 mM for 1.0 M of styrene. The living nature of the process was confirmed by an increase in the number-average molecular weight ( $$\bar M_n $$ ) of the polymers in direct proportion to monomer conversion and its continuation on supplying a fresh feed of styrene after the polymerization; the observed $$\bar M_n $$ was close to the calculated value assuming that one molecule of CH3CH(Ph)Cl yields one living polymer. Throughout these reactions, the polymer's molecular weight distribution (MWD) stayed very narrow ( $$\bar M_w /\bar M_n \leqslant 1.1$$ ), though slightly broadening after the second monomer addition. In the absence of nBu4NCl, the CH3CH(Ph)Cl/SnCl4 system yielded polystyrene with a bimodal MWD where the lower polymer fraction alone was apparently of a long lifetime. Styrene polymerization with the H2O/SnCl4 system was also examined, both with and without added nBu4NCl, and a long-lived propagating species was obtained in the presence of nBu4NCl.</subfield>
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   <subfield code="u">Department of Polymer Chemistry, Faculty of Engineering, Kyoto University, 606, Kyoto, Japan</subfield>
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