[1] Bunton C A, Robinson L. Catalysis of nucleophilic substitutions by micelles of dicationic detergent[J]. F J Org Chem, 1971, 36: 2 346-2 352. [2] Menger F M, Littau C A. Gemini-surfactants: synthesis and properties[J]. J Am Chem Soc, 1991, 113: 1 451-1 452. [3] Rosen M J. Gemini: A new generation of surfactants[J]. Chemtech, 1993, 3 : 30-33. [4] Zana R, Benrraou M, Rueff R. Alkanediyl-α,ω-bis(dimethylalkyiammonium bromide) Surfactants. 1. Effect of the Spacer Chain Length on the Critical Micelle Concentration and Micelle Ionization Degree[J]. Langmuir, 1991, 7: 1 072-1 075. [5] Menger F M, Littau C A. Gemini Surfactants: A New class of Self-Assembling Molecules[J]. J Am Chem Soc, 1993, 115: 10 083-10 090. [6] Menger F M, Alexey V E. Cross-linked Micelles[J]. Langmuir, 1995, 11: 1 855-1 857. [7] Menger F M, Jason S K. Gemini Surfactants[J]. Angew Chem Int Edit, 2000, 39: 1 906-1 920. [8] Zheng Ou(郑欧), Zhao Jian-xi(赵剑曦), You Yi(游毅). Effect of Spacer Chain Length on Aggregation of C12-s-C12·2Br Dimeric Surfactants in Aqueous Solutions(联接基团链长度对季铵盐二聚表面活性剂C12-s-C12·2Br在水溶液中胶团化行为的影响)[J]. Chem J Chinese Universities(高等学校化学学报), 2002, 23(7): 1 352-1 355. [9] You Yi(游毅), Zheng Ou(郑欧), Qiu Yu(邱羽), et al. Synthesis of Alkanediyl-α,ω-bis(Dimethyl Dodecylammonium Bromide) and their Micelle Formation in Aqueous Solutions (Gemini 阳离子表面活性剂的合成及胶束形成)[J]. Acta Physico-Chimica(物理化学学报), 2001, 17(1): 74-78. [10] Xiaoyong Wang, Jinben Wang, Yilin Wang, et al. Micellization of a Series of Dissymmetric Gemini Surfactants in Aqueous Solution[J]. J Phys Chem B, 2003, 107(41): 11 428-11 432. [11] Kumar A, Alami E, Holmberg K, et al. Branched Zwitterionic Gemini Surfactants Micellization and Interaction with Ionic Surfactants[J]. Collioid Surface A, 2003, 228: 197-207. [12] Zana R, Levy H, Papoutsi D, et al. Micellization of Two Triquaternary Ammonium Surfactants in Aqueous Solution[J]. Langmuir, 1995, 11: 3 694-3 698. [13] Hirata H, Norikatsu H, Makoto I, et al. Small-Angle Neutron-Scattering Study of Bis(quaternary ammonium bromide) Surfactant Micelles in Water. Effect of the Spacer Chain Length on Micellar Structure[J]. J Phys Chem, 1995, 99: 17 778-17 784. [14] Soma De, Vinod K A, Prem S G, et al. Role of Spacer Chain Length in Dimeric Micellar Organization. Small Angle Neutron Scattering and Fluorescence Studies[J]. J Phys Chem, 1996, 100: 11 664-11 671. [15] Zana R. Micellization of amphiphile: selected aspects[J]. Colloid Surface A, 1997, 123-124: 27-35. [16] Wang X Y, Wang J B, Wang Y L, et al. Effect of Nature of the Spacer on the Aggregation Properties of Gemini Surfactants in an Aqueous Solution[J]. Langmuir, 2004, 20: 53-56. [17] Menger F M, Jason S K, Mbadugha B N A, et al. Interfacial Composition of Gemini Surfactant Micelles Determined by Chemical Trapping[J]. Langmuir, 2000, 16: 9 095-9 098. [18] Kunio Esumi, Kazuhiro Taguma, Yoshifumi Koide. Aqueous Properties of Multichain Quaternary Cationic Surfactants[J]. Langmuir, 1996, 12, 4 039-4 041. [19] Soma De, Vinod K A, Prem S G, et al. SANS Studies of Different Mixed Micelles Composed of Dimeric and Monomeric Cationic Surfactants[J]. J Phys Chem B, 1997, 101: 5 639-5 645. [20] Danino D, Talmon Y, Zana R. Vesicle-to-Micelle Transformation in Systems Containing Dimeric Surfactants[J]. J Colloid Interface Sci, 1991, 185: 84-93. [21] Maja S, Ivan S, Ljerka T B, et al. Effect of Spacer Length on the Solid Phase Transitions of Dissymmetric Gemini Surfactants[J]. Langmuir, 2003, 19: 10 044-10 053. [22] Alami E, Beinert G, Marie P, et al. Alkanediyl-α,ω-bis(dimethylalkylammonium bromide) surfactants. 3.Behavior at the air-water interface[J]. Langmuir, 1993, 9: 1 465-1 467. [23] Manne S, Schaffer T E, Huo O, et al. Gemini at Solid-Liquid Interface: Control of Interfacial Aggregate Geometry[J]. Langmuir, 1997, 13: 6 382-6 387. [24] Letian Liu, Rosen M J. The Interaction of some Novel Diquaternary Gemini Surfactants with Anionic Surfactants[J]. J Colloid Interface Sci, 1996, 179: 454-459. [25] Shui Ling-ling(水玲玲), Zheng Li-qiang(郑利强), Zhao Jian-xi(赵剑曦), et al. The Surface Tension Study of Gemini Surfactant Systems(双子表面活性剂体系的界面活性研究)[J]. Fine Chemicals(精细化工), 2001, 18: 67-69. [26] Sharma K S, Christopher Rodgers, Rama M P, et al. Studies of Mixed Surfactants with Cationic Dimeric (Gemini) Surfactant with Nonionic Surfactant C12E6 in aqueous Medium[J]. J Colloid Interface Sci, 2003, 268: 482-488. [27] Zana R, Levy H, Kwetkat K. Mixed Micellization of Dimeric (Gemini) Surfactants and conventional Surfactants. Ⅰ. Mixtures of an anionic Dimeric Surfactant and of the Nonionic Surfactants C12E5 and C12E8[J]. J Colloid Interface Sci, 1998, 197: 370-376. [28] Giulio Caracciolo, Giovanna Mancini, Cecilia Bombelli, et al. The Structure of Gemini Surfactant Self-Assemblies Investigated by Energy Dispersive X-ray Diffraction[J]. J Phys Chem B, 2003, 107: 12 268-12 274. [29] Luciana Luchetti, Giovanna Mancini. NMR Investigation on the Various Aggregates Formed by a Gemini Chiral Surfactant[J]. Langmuir, 2000, 16: 161-165. [30] Alami S A, Alami E, Eastoe J, et al. Interaction between a Novel Gemini Surfactant and Cyclodextrin: NMR and Surface Tension Studies[J]. J Colloid Interface Sci, 2002, 246: 191-202. [31] Cesare Oliviero, Luigi Coppola, Camillo La Mesa, et al. Gemini Surfactant-water Mixtures: Some Physical-chemical Properties[J]. Colloid Surface A, 2002, 201: 247-260. [32] Alami E, Alami S A, Eastoe J. Investigation of Microstucture and Dynamics of Novel Gemini Surfactant Micelles by Small-Angle Neutron Scattering (SANS) and NMR Self-Diffusion[J]. Langmuir, 2003, 19: 18-23. [33] Alami E, Holmberg K. Heterogemini Surfactants Based on Fatty Acid Synthesis and Interfacial Properties[J]. J Colloid Interface Sci, 2001, 239: 230-240. [34] Damien Berthier, Thierry Buffeteau, Jean-Michel Leger, et al. From Chiral Counterions to Twisted Membranes[J]. J Am Chem Soc, 2002, 124: 13 486-13 494. [35] Norikatsu Hattori, Akihiro Yoshino, Hirofumi Okabayashi, et al. Conformational Analysis of (Phenylenedimethylene) bis(n-otcylammonium) dibromides in Aqueous Solution. Conformational Change upon Micellization[J]. J Phys Chem B, 1998, 102: 8 965-8 973. [36] Keisuke Matsuoka, Yoshikiyo Moroi. Micellization of Fluorinated Amphiphiles[J]. Curr Opin Colloid Interface Sci, 2003, 8: 227-235. [37] Du Ding-zhun(杜定准). 19F NMR on Perfluoroheptanoic Acid and Perfluorooctanoic Acid(表面活性剂全氟庚酸和全氟辛酸的19F NMR研究)[J]. Chinese J Magn Reson(波谱学杂志), 2003, 20(1): 29-36. [38] David A J, Yapin Wang, Richard L P. Pyrophosphate-Based Gemini Surfactants[J]. Langmuir, 2002, 18: 9 259-9 266. [39] Apiradee W, David J M, Pavinee C, et al. Two-Dimensional rotatibg-frame Overhauser spectroscopy (ROESY) and 13C NMR study of the interactions between maltodextrin and an anionic surfactant[J]. Carbohyd Res, 2004, 339: 1 105-1 111. [40] Feng Y(冯杨), Fang X W(方晓雯), Mao S Z(毛诗珍), et al. Interactions of Water-soluble Polymers with Sodium Dodecyl Sulfate in Aqueous Solution Studied by 1H NMR(水溶性聚合物与十二烷基硫酸钠相互作用的1H NMR)[J]. Chinese J Magn Reson(波谱学杂志), 2004, 21(1): 49-55. |