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Lee, Ji Ha, Fujii, Shota, Takahashi, Rintaro, Sakurai, Kazuo (2019) Tuning of the aggregation number of Platonic micelles with a binary mixture of calix[4]arene surfactants. Chemical Communications, 55 (9). 1303-1305 doi:10.1039/c8cc09621j

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Reference TypeJournal (article/letter/editorial)
TitleTuning of the aggregation number of Platonic micelles with a binary mixture of calix[4]arene surfactants
JournalChemical Communications
AuthorsLee, Ji HaAuthor
Fujii, ShotaAuthor
Takahashi, RintaroAuthor
Sakurai, KazuoAuthor
Year2019Volume55
Issue9
PublisherRoyal Society of Chemistry (RSC)
DOIdoi:10.1039/c8cc09621jSearch in ResearchGate
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Mindat Ref. ID8165788Long-form Identifiermindat:1:5:8165788:3
GUID0
Full ReferenceLee, Ji Ha, Fujii, Shota, Takahashi, Rintaro, Sakurai, Kazuo (2019) Tuning of the aggregation number of Platonic micelles with a binary mixture of calix[4]arene surfactants. Chemical Communications, 55 (9). 1303-1305 doi:10.1039/c8cc09621j
Plain TextLee, Ji Ha, Fujii, Shota, Takahashi, Rintaro, Sakurai, Kazuo (2019) Tuning of the aggregation number of Platonic micelles with a binary mixture of calix[4]arene surfactants. Chemical Communications, 55 (9). 1303-1305 doi:10.1039/c8cc09621j
In(2019) Chemical Communications Vol. 55 (9) Royal Society of Chemistry (RSC)

See Also

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Lee, Ji Ha, Fujii, Shota, Takahashi, Rintaro, Sakurai, Kazuo (2018) Morphological Transition of Oppositely Charged Calix[4]arene Surfactant Mixture. Langmuir, 34. 12109-12115 doi:10.1021/acs.langmuir.8b02542
Fujii, Shota, Yamada, Shimpei, Araki, Masataka, Lee, Ji Ha, Takahashi, Rintaro, Sakurai, Kazuo (2019) Discrete and Discontinuous Increase in the Micellar Aggregation Number: Effects of the Alkyl Chain Length on Platonic Micelles. Langmuir, 35. 3156-3161 doi:10.1021/acs.langmuir.8b04204
Fujii, Shota, Lee, Ji Ha, Takahashi, Rintaro, Sakurai, Kazuo (2018) Rediscovering the Monodispersity of Sulfonatocalix[4]arene-Based Micelles. Langmuir, 34. 5072-5078 doi:10.1021/acs.langmuir.8b00802
Fujii, Shota, Takahashi, Rintaro, Sakurai, Kazuo (2017) Glutamic Acids Bearing Calix[4]arene Micelles: pH-Controllable Aggregation Number Corresponding to Regular Polyhedra. Langmuir, 33. 4019-4027 doi:10.1021/acs.langmuir.7b00603
Yoshida, Kenta, Fujii, Shota, Takahashi, Rintaro, Matsumoto, Sakiko, Sakurai, Kazuo (2017) Self-Assembly of Calix[4]arene-Based Amphiphiles Bearing Polyethylene Glycols: Another Example of “Platonic Micelles”. Langmuir, 33. 9122-9128 doi:10.1021/acs.langmuir.7b02196
Fujii, Shota, Miyake, Rika, Campo, Liliana de, Lee, Ji Ha, Takahashi, Rintaro, Sakurai, Kazuo (2020) Structural Polymorphism of Resorcinarene Assemblies. Langmuir, 36 (22) 6222-6227 doi:10.1021/acs.langmuir.0c00861
Miwa, Shotaro, Takahashi, Rintaro, Rössel, Carsten, Matsumoto, Sakiko, Fujii, Shota, Lee, Ji Ha, Schacher, Felix H., Sakurai, Kazuo (2018) Core–Shell–Corona Micelles from a Polyether-Based Triblock Terpolymer: Investigation of the pH-Dependent Micellar Structure. Langmuir, 34. 7813-7820 doi:10.1021/acs.langmuir.8b01168
Mylonas, Efstratios, Yagi, Naoto, Fujii, Shota, Ikesue, Kodai, Ueda, Tomoya, Moriyama, Hideaki, Sanada, Yusuke, Uezu, Kazuya, Sakurai, Kazuo, Okobira, Tadashi (2019) Structural analysis of a calix[4]arene-based Platonic Micelle. Scientific Reports, 9. doi:10.1038/s41598-018-38280-1
Matsumoto, Sakiko, Takahashi, Rintaro, Yamada, Shimpei, Fujii, Shota, Sakurai, Kazuo (2017) Salt-induced Morphology Transition of a Micelle Formed of a Calix[4]arene-Derivative Cationic Surfactant in Aqueous Solution. Chemistry Letters, 46 (5). 750-752 doi:10.1246/cl.170032
Takahashi, Rintaro, Matsumoto, Sakiko, Fujii, Shota, Narayanan, Theyencheri, Sakurai, Kazuo (2017) Frontispiz: Monitoring the Discontinuous Dodecamer-Icosamer Transition of a Calix[4]arene-Derived Surfactant by Time-Resolved Small-Angle X-ray Scattering. Angewandte Chemie, 129 (24). doi:10.1002/ange.201782461
Takahashi, Rintaro, Matsumoto, Sakiko, Fujii, Shota, Narayanan, Theyencheri, Sakurai, Kazuo (2017) Frontispiece: Monitoring the Discontinuous Dodecamer-Icosamer Transition of a Calix[4]arene-Derived Surfactant by Time-Resolved Small-Angle X-ray Scattering. Angewandte Chemie International Edition, 56 (24). doi:10.1002/anie.201782461
 
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