Leveraging Macromolecular Isomerism for Phase Complexity in Janus Nanograins

被引:13
作者
Shao, Yu [1 ]
Han, Di [2 ]
Tao, Yangdan [2 ]
Feng, Fengfeng [3 ]
Han, Ge [2 ]
Hou, Bo [1 ]
Liu, Hao [3 ]
Yang, Shuguang [3 ]
Fu, Qiang [2 ]
Zhang, Wen-Bin [1 ]
机构
[1] Peking Univ, Ctr Soft Matter Sci & Engn, Beijing Natl Lab Mol Sci, Key Lab Polymer Chem & Phys,Minist Educ,Coll Chem, Beijing 100871, Peoples R China
[2] Sichuan Univ, Coll Polymer Sci & Engn, State Key Lab Polymer Mat Engn, Chengdu 610065, Peoples R China
[3] Donghua Univ, Ctr Adv Low Dimens Mat, State Key Lab Modificat Chem Fibers & Polymer Mat, Shanghai 201620, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
SYMMETRY-BREAKING; GIANT MOLECULES; BLOCK-COPOLYMER; CUBIC PHASE; SHAPE; SURFACTANTS; CHEMISTRY; PATTERNS; CRYSTAL; POSS;
D O I
10.1021/acscentsci.2c01405
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
It remains intriguing whether macromolecular isomerism, along with competing molecular interactions, could be leveraged to create unconventional phase structures and generate considerable phase complexity in soft matter. Herein, we report the synthesis, assembly, and phase behaviors of a series of precisely defined regioisomeric Janus nanograins with distinct core symmetry. They are named B2DB2 where B stands for iso-butyl-functionalized polyhedral oligomeric silsesquioxanes (POSS) and D stands for dihydroxylfunctionalized POSS. While BPOSS prefers crystallization with a flat interface, DPOSS prefers to phase-separate from BPOSS. In solution, they form 2D crystals owing to strong BPOSS crystallization. In bulk, the subtle competition between crystallization and phase separation is strongly influenced by the core symmetry, leading to distinct phase structures and transition behaviors. The phase complexity was understood based on their symmetry, molecular packing, and free energy profiles. The results demonstrate that regioisomerism could indeed generate profound phase complexity.
引用
收藏
页码:289 / 299
页数:11
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