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Isoreticular expansion of polyMOFs achieves high surface area materials
Author(s) -
Giulia E. M. Schukraft,
Sergio Ayala,
Benjamin L. Dick,
Seth M. Cohen
Publication year - 2017
Publication title -
chemical communications
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.837
H-Index - 333
eISSN - 1364-548X
pISSN - 1359-7345
DOI - 10.1039/c7cc04222a
Subject(s) - surface (topology) , stability (learning theory) , materials science , polymer , chemical engineering , nanotechnology , composite material , computer science , mathematics , engineering , geometry , machine learning
The concept of isoreticular chemistry has become a core principle in metal-organic framework (MOF) materials. Isoreticular chemistry has shown that organic ligands of different sizes, but with a common geometry/symmetry can be used to generate MOFs of related topologies, but with expanded pore sizes and volumes. In this report, polymer-MOF hybrid materials (polyMOFs) with a UiO (UiO = University of Oslo) architecture are shown to adhere to the principle of isoreticular expansion, generating polyMOFs with large surface areas and enhanced stability.

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