Affiliation:
1. State Key Laboratory for Mechanical Behaviour of Materials Shaanxi International Research Center for Soft Matter Xi'an Jiaotong University 710049 Xi'an China
2. School of Chemistry and Chemical Engineering Henan University of Technology 450001 Zhengzhou China
3. Department of Materials Science and Engineering University of Sheffield S1 3JD Sheffield UK
4. Romanian Academy Coriolan Dragulescu Institute of Chemistry 300223 Timisoara Romania
Abstract
AbstractAmong 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. However, we now find that this is not the case for strongly chiral compounds. While achiral molecules follow the opposite twists of nets 1 and 2, molecules with a chiral center in their rod‐like core fail to follow the 70° twist between junctions in net 2 and instead wind against it by −110° to still match the junction orientation. The metastable chiral gyroid is a high‐entropy high‐heat‐capacity mesophase. The homochirality of its nets makes the CD signal of the thienofluorenone compounds close to that in the stable I23 phase with 3 isochiral nets.
Funder
Engineering and Physical Sciences Research Council
National Natural Science Foundation of China-Shandong Joint Fund for Marine Science Research Centers
Natural Science Foundation of Henan Province