Transformation of rigid metal-organic frameworks into flexible gel networks and vice versa

被引:13
|
作者
Juan Marrero-Tellado, Jose [1 ]
Diaz Diaz, David [2 ,3 ]
机构
[1] Univ La Laguna, Dept Quim Organ, IUBO, E-38206 Tenerife, Spain
[2] Univ Regensburg, Inst Organ Chem, D-93040 Regensburg, Germany
[3] IQAC CSIC, Barcelona 08034, Spain
来源
CRYSTENGCOMM | 2015年 / 17卷 / 42期
关键词
CRYSTAL ENGINEERING APPROACH; SUPRAMOLECULAR GELS; CRYSTALLIZATION; TRANSITION; GROWTH; METALLOGELS; GELATION; MOFS; ORGANOGELS; GELATORS;
D O I
10.1039/c5ce01032b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Understanding and controlling phase transformations is a timely subject of investigation because they are essential for the fabrication of high-performance materials with applications in energy, sensors, biomedical, and information-related technologies. Such transformations at the nanoscale arise from both diffusion kinetics and surface thermodynamics, whose reasoning represents a major intellectual challenge in multicomponent systems. In particular, the study of interconversion routes between stable and metastable states provides a useful foundation for the rational design of hard and soft materials. Here, we highlight some recent studies that have demonstrated the possibility of transforming rigid (hard) MOFs into flexible (soft) gel materials in quantitative (or nearly quantitative) yields, and vice versa albeit involving different mechanisms and starting materials. These works represent a new paradigm in the growing areas of crystal engineering and stimuli-responsive gels by building new bridges between advanced functional materials that have been traditionally studied in very different research fields.
引用
收藏
页码:7978 / 7985
页数:8
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