“…The structure and dynamic properties of their self-aggregated micelles have been thoroughly studied by various methods, including 1 H NMR measurements (11)(12)(13)(14)(15)(16). By the use of the 1D and 2D NMR techniques we have recently shown (17) that the α-methylene group of CTAB is located in the near vicinity of the phenoxy ring of the nonionic surfactant, Triton X-100 (TX-100), in their mixed micelles, and the end methyl group of CTAB is close to those of TX-100. Furthermore, the closely packed (coiled) hydrophilic polyethylene chains in the exterior part of the mixed micelles gradually extend with an increase in the CTAB component in the mixed solution, whereas the mixing of TX-100 with the anionic surfactant, SDS, does not show this effect (18).…”