The effect of pressure on the nanostructure of a thermotropic cubic (Cub) mesogen 1,2-bis(4'-n-alkoxybenzoyl)hydrazine (BABH-n; n is the number of carbon atoms in the alkyl chain) was investigated under elevated pressures up to 140 MPa by an X-ray diffraction (XRD) technique. Four compounds, BABH-12, -14, -16 and -18, were examined and the type of Cub mesophase formed at ambient pressure is Ia3d for BABH-12 and -18, Im3m for BABH-14, and both for BABH-16. The high-pressure XRD enabled the discrimination of the Cub phase type in the low-pressure Cub phase regions of BABH-14 and BABH-16 and the revision of the phase diagrams reported previously. New insight in this work is changes in the lattice constant a of the Cub phases upon pressurization. The lattice constant a of the Im3m-Cub phase in BABH-14 decreases as only an exception, while those of the Ia3d-Cub phases in BABH-16 and -18 increased gradually, with increasing pressure, up to about 24 and 25% in the unit cell volume, respectively, in their optimal situations of pressure and temperature. The a values of the Ia3d-Cub phases in BABH-12, -14, -16 and -18 at elevated pressures were roughly on an extrapolated line of the a vs. n linear relationship determined for the corresponding data of the short-chain BABH-n (6 ≤ n ≤ 13) at ambient pressure. The pressure-induced expansion of the Ia3d-Cub lattice is well explained by reduced lateral expansion of a terminal alkyl chain and apparent reduction of the effective core size (from "double-layered core" to the "single-layered core" states).
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http://dx.doi.org/10.1039/c3cp54471k | DOI Listing |
Chemistry
December 2024
Department of Chemistry, University of Calgary, 2500 University Drive NW, Calgary, AB, T2N 1N4, Canada.
Amphiphilic supramolecular materials based on biodegradable cyclodextrins (CDs) have been known to self-assemble into different types of thermotropic liquid crystals, including smectic and hexagonal columnar mesophases. Previous studies on amphiphilic CDs bearing 14 aliphatic chains at the secondary face and 7 oligoethylene glycol (OEG) chains at the primary face showed that the stability of the mesophase can be rationally tuned through implementation of terminal functional groups to the OEG chains. Here, we report the syntheses of first examples of crown ether-functionalized amphiphilic cyclodextrins that unexpectedly form thermotropic bicontinuous cubic phases.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
November 2024
Key Laboratory of Medicinal Chemistry from Natural Resources, Ministry of Education, Yunnan University, 650091, Kunming, P. R. China.
Gyroid, double diamond and the body-centred "Plumber's nightmare" are the three most common bicontinuous cubic phases in lyotropic liquid crystals and block copolymers. While the first two are also present in solvent-free thermotropics, the latter had never been found. Containing six-fold junctions, it was unlikely to form in the more common phases with rod-like cores normal to the network columns, where a maximum of four branches can join at a junction.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
June 2024
State Key Laboratory for Mechanical Behaviour of Materials, Shaanxi International Research Center for Soft Matter, Xi'an Jiaotong University, 710049, Xi'an, China.
Among the intriguing bicontinuous self-assembled structures, the gyroid cubic is the most ubiquitous. It is found in block and star polymers, surfactants with or without solvent, in thermotropic liquid crystals with end- or side-chains, and in biosystems providing structural color and modelling cell mitosis. It contains two interpenetrating networks of opposite chirality and is thus achiral if, as usual, the content of the two nets is the same.
View Article and Find Full Text PDFSoft Matter
November 2023
Laboratory of Molecular Science and Engineering, Johan Gadolin Process Chemistry Centre, Åbo Akademi University, FI-20500, Finland.
Conformational rigidity controls the bulk self-assembly and liquid crystallinity from amphiphilic block molecules to copolymers. The effects of block stereochemistry on the self-assembly have, however, been less explored. Here, we have investigated amphiphilic block molecules involving eight open-chain monosaccharide-based polyol units possessing different stereochemistries, derived from D-glucose, D-galactose, L-arabinose, D-mannose and L-rhamnose (allylated monosaccharides -Glc*, -Glc*, -Gal*, -Gal*, -Ara*, -Ara*, -Man*, and -Rha*), end-functionalized with repulsive tetradecyl alkyl chain blocks to form well-defined amphiphiles with block molecule structures.
View Article and Find Full Text PDFJ Phys Chem Lett
February 2023
Key Laboratory of Colloid and Interface Chemistry of Ministry of Education and School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, People's Republic of China.
Incorporating carbon dots (CDs) into chiral self-assemblies will endow the system with intriguing optoelectronic, catalytic, and chiroptical activities. Utilization of chiral substituents to rationally manipulate chiral self-assembly of the CDs, however, remains a major challenge. In this work, cholesteryl monoprotected ethylene diamine was used as a precursor to synthesize CDs with a cholesteryl periphery.
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