Porphyrin/Ionic-Liquid Co-assembly Polymorphism Controlled by Liquid-Liquid Phase Separation

被引:56
作者
Yuan, Chengqian [1 ]
Yang, Mengyao [1 ,2 ]
Ren, Xiaokang [1 ,2 ]
Zou, Qianli [1 ]
Yan, Xuehai [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Inst Proc Engn, State Key Lab Biochem Engn, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Sch Chem Engn, Beijing 100049, Peoples R China
[3] Chinese Acad Sci, Ctr Mesosci, Inst Proc Engn, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
co-assembly; ionic liquids; liquid-liquid phase separation; nucleation; porphyrin; IONIC LIQUIDS; PEPTIDE; NUCLEATION;
D O I
10.1002/anie.202007459
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Understanding and controlling multicomponent co-assembly is of primary importance in different fields, such as materials fabrication, pharmaceutical polymorphism, and supramolecular polymerization, but these aspects have been a long-standing challenge. Herein, we discover that liquid-liquid phase separation (LLPS) into ion-cluster-rich and ion-cluster-poor liquid phases is the first step prior to co-assembly nucleation based on a model system of water-soluble porphyrin and ionic liquids. The LLPS-formed droplets serve as the nucleation precursors, which determine the resulting structures and properties of co-assemblies. Co-assembly polymorphism and tunable supramolecular phase transition behaviors can be achieved by regulating the intermolecular interactions at the LLPS stage. These findings elucidate the key role of LLPS in multicomponent co-assembly evolution and enable it to be an effective strategy to control co-assembly polymorphism as well as supramolecular phase transitions.
引用
收藏
页码:17456 / 17460
页数:5
相关论文
共 40 条
[1]  
[Anonymous], 2018, ANGEW CHEM INT EDIT
[2]  
[Anonymous], 2019, ANGEW CHEM, V131, P19279
[3]   Kinetically Controlled Coassembly of Multichromophoric Peptide Hydrogelators and the Impacts on Energy Transport [J].
Ardona, Herdeline Ann M. ;
Draper, Emily R. ;
Citossi, Francesca ;
Wallace, Matthew ;
Serpell, Louise C. ;
Adams, Dave J. ;
Tovar, John D. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2017, 139 (25) :8685-8692
[4]  
Aumiller WM, 2016, NAT CHEM, V8, P129, DOI [10.1038/NCHEM.2414, 10.1038/nchem.2414]
[5]  
Birks J. B., 1970, PHOTOPHYSICS AROMATI, DOI DOI 10.1002/BBPC.19700741223
[6]   Ultralong Phosphorescence from Organic Ionic Crystals under Ambient Conditions [J].
Cheng, Zhichao ;
Shi, Huifang ;
Ma, Huili ;
Bian, Lifang ;
Wu, Qi ;
Gu, Long ;
Cai, Suzhi ;
Wang, Xuan ;
Xiong, Wei-wei ;
An, Zhongfu ;
Huang, Wei .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2018, 57 (03) :678-682
[7]   Dehydration-driven solvent exposure of hydrophobic surfaces as a driving force in peptide folding [J].
Daidone, Isabella ;
Ulmschneider, Martin B. ;
Di Nola, Alfredo ;
Amadei, Andrea ;
Smith, Jeremy C. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (39) :15230-15235
[8]   Multiscale Studies on Ionic Liquids [J].
Dong, Kun ;
Liu, Xiaomin ;
Dong, Haifeng ;
Zhang, Xiangping ;
Zhang, Suojiang .
CHEMICAL REVIEWS, 2017, 117 (10) :6636-6695
[9]   Pharmaceutical cocrystals: along the path to improved medicines [J].
Duggirala, Naga K. ;
Perry, Miranda L. ;
Almarsson, Oern ;
Zaworotko, Michael J. .
CHEMICAL COMMUNICATIONS, 2016, 52 (04) :640-655
[10]   Role of the Hydrophobic Effect in the Transfer of Chirality from Molecules to Complex Systems: From Chiral Surfactants to Porphyrin/Surfactant Aggregates [J].
El-Hachemi, Zoubir ;
Mancini, Giovanna ;
Ribo, Josep M. ;
Sorrenti, Alessandro .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (45) :15176-15184