离子液体
材料科学
聚合物
离子键合
多孔性
物质状态
离子电导率
纳米技术
同步加速器
液晶
金属
化学物理
化学
物理化学
冶金
有机化学
离子
复合材料
凝聚态物理
光电子学
光学
物理
催化作用
电解质
电极
作者
Satoshi Horike,Sanjog S. Nagarkar,Tomohiro Ogawa,Susumu Kitagawa
标识
DOI:10.1002/anie.201911384
摘要
Abstract There are two categories of coordination polymers (CPs): inorganic CPs (i‐CPs) and organic ligand bridged CPs (o‐CPs). Based on the successful crystal engineering of CPs, we here propose noncrystalline states and functionalities as a new research direction for CPs. Control over the liquid or glassy states in materials is essential to obtain specific properties and functions. Several studies suggest the feasibility of obtaining liquid/glassy states in o‐CPs by design principles. The combination of metal ions and organic bridging ligands, together with the liquid/glass phase transformation, offer the possibility to transform o‐CPs into ionic liquids and other ionic soft materials. Synchrotron measurements and computational approaches contribute to elucidating the structures and dynamics of the liquid/glassy states of o‐CPs. This offers the opportunity to tune the porosity, conductivity, transparency, and other material properties. The unique energy landscape of liquid/glass o‐CPs offers opportunities for properties and functions that are complementary to those of the crystalline state.
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