Issue 1, 2020

Understanding the role of linker flexibility in soft porous coordination polymers

Abstract

Soft porous coordination polymers are a new class of materials that have the potential to combine favorable features of metal–organic polyhedra (MOP) and frameworks (MOFs) with those of soft materials: permanent porosity and chemical specificity with processability and optical, electronic, and mechanical responses. Fundamental studies are needed to guide the future technological applications of these materials. We employ topologically-based algorithms to generate crystalline structures in the fcu topology and use classical molecular modeling to calculate their mechanical properties. The generated crystals used dimetal paddlewheel based MOP with cuboctahedral topology [M2(bdc)2]12 (M = Co, Cu, Rh, and Zn; bdc = 1,3-benzenedicarboxylate) as the nodes and 1,4-diazabicyclo[2.2.2]octane (DABCO), bipyridine, 1,4-bis(imidazol-1-ylmethyl)benzene (bix), 4,4′-bis(imidazol-1-ylmethyl)biphenyl (bibPh), and 1,1′-(1,12-dodecanediyl)bis[1H-imidazole] (bidod) as the linkers. Structures containing DABCO or bipyridine are found to have bulk moduli approximately an order of magnitude higher than those containing bix, bibPh, or bidod. The differences in mechanical properties are associated with the linker flexibility, as evidenced by free energy calculations on the radius of gyration of the linkers. We also calculate free energies as a function of radius of gyration of chosen nanoparticles.

Graphical abstract: Understanding the role of linker flexibility in soft porous coordination polymers

Supplementary files

Article information

Article type
Paper
Submitted
03 ستمبر 2019
Accepted
11 اکتوٗبر 2019
First published
15 اکتوٗبر 2019

Mol. Syst. Des. Eng., 2020,5, 284-293

Understanding the role of linker flexibility in soft porous coordination polymers

Y. J. Colón and S. Furukawa, Mol. Syst. Des. Eng., 2020, 5, 284 DOI: 10.1039/C9ME00117D

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