Two types of two-component gels formed from pseudoenantiomeric ethynylhelicene oligomers

Two-component gels formed from pseudoenantiomeric ethynylhelicene oligomers in toluene exhibited two different properties depending on difference in numbers of helicenes in the two components. The combinations (M)-5/(P)-4, (M)-6/(P)-4, and (M)-7/(P)-4, which contained oligomers with comparable numbe...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1992. - 28(2012), 32 vom: 14. Aug., Seite 11939-47
1. Verfasser: Yamamoto, Koji (VerfasserIn)
Weitere Verfasser: Oyamada, Naohiro, Mizutani, Marie, An, Zengjian, Saito, Nozomi, Yamaguchi, Masahiko, Kasuya, Motohiro, Kurihara, Kazue
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2012
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Gels Polycyclic Compounds Polymers ethynylhelicene Toluene 3FPU23BG52
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520 |a Two-component gels formed from pseudoenantiomeric ethynylhelicene oligomers in toluene exhibited two different properties depending on difference in numbers of helicenes in the two components. The combinations (M)-5/(P)-4, (M)-6/(P)-4, and (M)-7/(P)-4, which contained oligomers with comparable numbers of helicenes, formed transparent gels (Type I gels). The combinations (M)-6/(P)-3, (M)-7/(P)-3, and (M)-8/(P)-3, which contained oligomers with considerably different numbers of helicenes, formed turbid gels (Type II gels). Negative Cotton effects were observed for the Type I gels in the region between 350 and 450 nm, and were positive for the Type II gels, despite the use of (M)-oligomers for the longer components. UV/vis exhibited absorption maxima at 350 nm for the Type I gels and at 338 nm for the Type II gels. Different behaviors in gel formation processes were observed by fluorescence studies. Atomic force microscopy analysis showed fiber structures of 25-50 nm diameter for Type I gels and bundles of 100-150 nm diameter for Type II gels. The stoichiometry in gel formation also differed: The Type I gels showed 1:1 stoichiometry of the two components; the Type II gels showed no 1:1 stoichiometry, likely 1:2 stoichiometry. Using the Type I and II gels, two-layer gel systems were constructed 
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650 4 |a Research Support, Non-U.S. Gov't 
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650 7 |a Polycyclic Compounds  |2 NLM 
650 7 |a Polymers  |2 NLM 
650 7 |a ethynylhelicene  |2 NLM 
650 7 |a Toluene  |2 NLM 
650 7 |a 3FPU23BG52  |2 NLM 
700 1 |a Oyamada, Naohiro  |e verfasserin  |4 aut 
700 1 |a Mizutani, Marie  |e verfasserin  |4 aut 
700 1 |a An, Zengjian  |e verfasserin  |4 aut 
700 1 |a Saito, Nozomi  |e verfasserin  |4 aut 
700 1 |a Yamaguchi, Masahiko  |e verfasserin  |4 aut 
700 1 |a Kasuya, Motohiro  |e verfasserin  |4 aut 
700 1 |a Kurihara, Kazue  |e verfasserin  |4 aut 
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773 1 8 |g volume:28  |g year:2012  |g number:32  |g day:14  |g month:08  |g pages:11939-47 
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