• 대한화학회지
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• 제20권4호
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• pp.270-276
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• 1976

양이온 표면활성제인 Zephiramine의 존재하에서 여러가지 술포프탈레인 지시약의 흡수스펙트럼과 해리상수를 측정하여 수용액에서의 값과 비교했다. 염기성적색형은 흡수 극대가 6${\sim}$21 nm 장파장쪽으로 이동하며 흡수도는 약간 증가하는 반면, 황색형은 흡수극대가 오히려 4${\sim}$20 nm 단파장으로 이동하고 흡수도도 약간 감소했다. pKa값은 -1.38${\sim}$0.37정도 변화했다. 이와같은 정색반응을, 색소분자가 미셀 표면에 흡착됨으로서 더 안정한 공면구조를 형성하기 때문이라는 가정으로 설명했다.

• Archives of Pharmacal Research
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• 제9권3호
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• pp.139-144
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• 1986

The solubilization sites of aniline and its derivatives in micelles were investigated with fluorescence probe technique. The fluorescence probes employed in this study are 12-(9-anthroyl) stearic acid (AS) and 2-p-toluidinylnaphthalene-6-sulfonate (TNS) which are incorporated in the interior of the micelle and attaced to its surface, respectively. As these two probes were effectively quenched by aniline and its surface, respectively. As these two probes were effectively quenched by aniline and its derivatives, the modified Stern-Volmer relationship in micellar system could be applicable to estimate the partition coefficient, $K_{p}$ of the solubilizate between aqueous and micellar phase. Because $K_{p}$ derived by this method reflects the relative proximity of the fluorophore to the quencher, the ratio of $K_{p}$ in the surface area to that in the interior of the micelle is interpreted in terms of the relative location of the solubilizate in micellar aggregate. The results show that the solubilizates are not located in a definite position but distributed in the multiple-sites of the micelle. The solubilization sites of the solubilizates in the icelle are dependent on their structures. As the solubilizate has more numbers of N-substituents of aniline and more numbers, of carbon in the substituent, it tends to incorporate in the interior of the micelle more effectively.