A mixture of a pseudoenantiomeric ethynylhelicene (M)-tetramer and a (P)-pentamer forms a hetero-double-helix in a solution, which self-assembles and gelates solvents. When gelation was conducted in the presence of chiral silica (P)-nanoparticles grafted with (P)-helicene, the resulting hetero-double-helix intermediate was adsorbed on the (P)-nanoparticles, and was removed from the solution by aggregation and precipitation. The resulting precipitates contained only the hetero-double-helix, not random coil or clusters of the hetero-double-helix. (P)-Nanoparticles did not extract the hetero-double-helix from the self-assembly gels. The hetero-double-helix was then isolated by liberating it from the precipitates in 2-bromopropionic acid, and was crystallized from the solution. The crystalline hetero-double-helices were isolated for several other combinations of pseudoenantiomeric ethynylhelicene oligomers.
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http://dx.doi.org/10.1002/chem.201406482 | DOI Listing |
Langmuir
April 2019
Institute of Multidisciplinary Research for Advanced Materials , Tohoku University, Aoba, Sendai 980-8577 , Japan.
Long-range anisotropic structural materials exhibit notable optical and mechanical properties, and an efficient method for synthesizing such materials involving self-assembly of well-defined monodispersed organic molecules is described here. Hetero-double-helices are formed in toluene using a pseudoenantiomeric mixture of an ethynylhelicene ( M)-tetramer with C terminal groups and a ( P)-pentamer. When the concentration of the mixture was increased, the hetero-double-helices self-assembled to form lyotropic liquid crystal gels.
View Article and Find Full Text PDFChemistry
June 2015
Department of Organic Chemistry, Graduate School of Pharmaceutical Sciences, Tohoku University, 6-3 Aoba, Sendai 980-8578 (Japan), Fax: (+81) 22-795-6811.
A mixture of a pseudoenantiomeric ethynylhelicene (M)-tetramer and a (P)-pentamer forms a hetero-double-helix in a solution, which self-assembles and gelates solvents. When gelation was conducted in the presence of chiral silica (P)-nanoparticles grafted with (P)-helicene, the resulting hetero-double-helix intermediate was adsorbed on the (P)-nanoparticles, and was removed from the solution by aggregation and precipitation. The resulting precipitates contained only the hetero-double-helix, not random coil or clusters of the hetero-double-helix.
View Article and Find Full Text PDFJ Am Chem Soc
May 2015
‡Department of Organic Chemistry, Graduate School of Pharmaceutical Sciences, Tohoku University, Aoba, Sendai 980-8578, Japan.
A self-assembled lyotropic liquid crystal (LLC) system exhibiting dynamic and reversible polymorphism was developed using the synthetic cyclic ethynylhelicene oligomers cyclobis[(M)-D-n] (n = 4 and 6), in which two oligomer moieties are connected by two flexible linkers. The cyclic molecular structure was designed to control aggregation properties ranging from the molecular level to the macroscopic level. The cyclic oligomer changed its structure between random coils and an intramolecular homo-double helix induced by temperature and solvents.
View Article and Find Full Text PDFChemistry
August 2013
Department of Organic Chemistry, Graduate School of Pharmaceutical Sciences, Tohoku University, 6-3 Aoba, Sendai, 980-8578, Japan.
Pseudoenantiomeric ethynylhelicene oligomers containing a disulfide group formed two-component gels, which showed different solvent properties from gels without the disulfide group. The disulfide gels reacted with gold nanoparticles, and the resulting organic-inorganic composite materials exhibited fluorescence emission between 600-800 nm, along with emission from the oligomers at 450 nm. The disulfide gels and isolated gold nanoparticles loaded with the oligomers did not show the former emission.
View Article and Find Full Text PDFLangmuir
August 2012
Department of Organic Chemistry, Graduate School of Pharmaceutical Sciences, Tohoku University, Aoba 6-3, Sendai 980-8578, Japan.
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).
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