CrossRef 27. Tsafack VC, Marquette CA, Leca B, Blum LJ: An electrochemiluminescence – based fibre optic biosensor for choline flow injection analysis . Analyst 2000, 125:151–155.CrossRef 28. Jiao T, Leca-Bouvier BD, Boullanger P, Blum LJ, Girard-Egrot AP: Phase behavior and optical investigation of two synthetic luminol Ku-0059436 ic50 derivatives and glycolipid mixed monolayers at the air-water interface. Colloid Surf A-Physicochem Eng Asp 2008, 321:137–142.CrossRef 29. Jiao T, Leca-Bouvier BD, Boullanger P, Blum LJ, Girard-Egrot AP:
Electrochemiluminescent detection of hydrogen peroxide using amphiphilic luminol derivatives in solution. Colloid Surf A-Physicochem Eng Asp 2008, 321:143–146.CrossRef 30. Jiao T, Leca-Bouvier BD, Boullanger P, Blum LJ, Girard-Egrot AP: A chemiluminescent Langmuir–Blodgett membrane as the sensing layer for the reagentless monitoring of an immobilized enzyme activity. Colloid Surf A-Physicochem selleck Eng Asp 2010, MAPK Inhibitor Library price 354:284–290.CrossRef 31. Jiao TF, Wang
YJ, Gao FQ, Zhou JX, Gao FM: Photoresponsive organogel and organized nanostructures of cholesterol imide derivatives with azobenzene substituent groups. Prog Nat Sci 2012, 22:64–70.CrossRef 32. Jiao TF, Gao FQ, Wang YJ, Zhou JX, Gao FM, Luo XZ: Supramolecular gel and nanostructures of bolaform and trigonal cholesteryl derivatives with different aromatic spacers. Curr Nanosci 2012, 8:111–116.CrossRef 33. Yang H, Yi T, Zhou Z, Zhou Y, Wu J, Xu M, Li F, Huang C: Switchable fluorescent organogels and mesomorphic superstructure based on naphthalene derivatives. Langmuir 2007, 23:8224–8230.CrossRef 34. Omote Y, Miyake T, Ohmori S, Sugiyama N: The chemiluminescence C1GALT1 of acyl luminols. Bull Chem Soc Jpn 1966, 39:932–935.CrossRef 35. Omote Y, Miyake T, Ohmori S, Sugiyama N: The chemiluminescence of luminol and acetyl-luminol. Bull Chem Soc Jpn 1967, 40:899–903.CrossRef 36. Zhu X, Duan P, Zhang L, Liu M: Regulation of the chiral twist and supramolecular chirality in co-assemblies of amphiphilic L -glutamic acid with bipyridines. Chem Eur J 2011, 17:3429–3437.CrossRef 37. Duan P, Qin L, Zhu X, Liu M: Hierarchical
self-assembly of amphiphilic peptide dendrons: evolution of diverse chiral nanostructures through hydrogel formation over a wide pH range. Chem Eur J 2011, 17:6389–6395.CrossRef 38. Zhu GY, Dordick JS: Solvent effect on organogel formation by low molecular weight molecules. Chem Mater 2006, 18:5988–5995.CrossRef 39. Xin H, Zhou X, Zhao C, Wang H, Lib M: Low molecular weight organogel from the cubic mesogens containing dihydrazide group. J Mol Liq 2011, 160:17–21.CrossRef 40. Nayak MK: Functional organogel based on a hydroxyl naphthanilide derivative and aggregation induced enhanced fluorescence emission. J Photochem Photobiol A: Chem 2011, 217:40–48.CrossRef 41. Atsbeha T, Bussotti L, Cicchi S, Foggi P, Ghini G, Lascialfari L, Marcelli A: Photophysical characterization of low-molecular weight organogels for energy transfer and light harvesting. J Mol Struct 2011, 993:459–463.