Abstract
Despite the fact that numerous studies have been conducted to explore the crystalline structures of various metal-organic polyhedrons (MOPs), the direct probing of solvated and deformed structures of MOPs is still rare but critical to the development of processing protocols and the understanding of their structure-property relationship for gas separation and ion transportation. Here, MOPs from the coordination of isophthalic acids and Cu2+ are covalently functionalized with alkyl chains for studies in solutions and at the air/water interface, respectively. As suggested from small-angle scattering studies, the MOP structures in the solvated state remain intact while the grafted linear alkyl arms exhibit an extended conformation, allowing solvent molecules to penetrate into the cavity of MOPs. Meanwhile, under surface pressure at the water/air interface, the hairy MOP structures, as suggested by in situ neutron reflectivity studies, can be deformed and MOP cores are close together while the grafted chains are squeezed upward and downward toward liquid and air phases, respectively. This discovery provides the first direct evidence for the existence of an ion transportation active conformation of hairy MOPs.
Original language | English |
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Pages (from-to) | 15656-15662 |
Number of pages | 7 |
Journal | Journal of Physical Chemistry C |
Volume | 124 |
Issue number | 28 |
DOIs | |
State | Published - Jul 16 2020 |
Funding
The work is supported by the National Natural Science Foundation of China (nos. 51873067, U1832220, and 21961142018), the National Key Research and Development Program of China (no. 2018YFB0704200), the Natural Science Foundation of Guangdong Province (no. 2018A030313503), the Fundamental Research Funds for the Central Universities (no. 2018JQ04), the Guangdong Provincial Key Laboratory of Functional and Intelligent Hybrid Materials and Devices (no. 2019B121203003), and the Guangdong Innovative and Entrepreneurial Research Team Program (no. 2016ZT06C322). We are grateful to 12-ID-B of the Advanced Photon Source and BL19U2 station of the Shanghai Synchrotron Radiation Facility for the access to the synchrotron-based SAXS. We would like to thank C.M.R.R. for the collection of SANS measurements. The portion of this research at the ORNL’s Spallation Neutron Source was sponsored by the Scientific User Facilities Division, Office of Basic Energy Sciences, U.S. Department of Energy. We acknowledge funding from the National Natural Science Foundation of China (nos. U1832220, 21961142018, and 51873067), the National Key Research and Development Program of China (no. 2018YFB0704200), the Natural Science Foundation of Guangdong Province (no. 2018A030313503), the Fundamental Research Funds for the Central Universities (no. 2018JQ04), the Guangdong Provincial Key Laboratory of Functional and Intelligent Hybrid Materials and Devices (no. 2019B121203003), and the Guangdong Innovative and Entrepreneurial Research Team Program (no. 2016ZT06C322).
Funders | Funder number |
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Guangdong Provincial Key Laboratory of Functional and Intelligent Hybrid Materials and Devices | 2019B121203003 |
Scientific User Facilities Division | |
U.S. Department of Energy | |
Basic Energy Sciences | |
Oak Ridge National Laboratory | |
Guangdong Innovative and Entrepreneurial Research Team Program | 2016ZT06C322 |
National Natural Science Foundation of China | 51873067, 21961142018, U1832220 |
Natural Science Foundation of Guangdong Province | 2018A030313503 |
National Key Research and Development Program of China | 2018YFB0704200 |
Fundamental Research Funds for the Central Universities | 2018JQ04 |