Pillared MOFs: structure and ring opening polymerization of cyclic esters
The solvothermal reaction of Zn(NO3)2·6H2O with 5-aminoisophthalic acid and 4,4′-bipyridyl (4,4′-bipy) led to the self-assembly of the known 3-D hybrid H-bonded/covalent structure {[Zn(5-AIP)(4,4′-bipy)0.5]·DMF}n (1·DMF), but with DMF here (rather than H2O as previously): an analogous reaction using the related 4,4′-azopyridine (4,4′-azopy) in place of 4,4′-bipyridyl afforded the structurally related framework {[Zn(5-AIP)(4,4′-azopy)0.5]·0.75DMF}n (2·0.75DMF). Similar solvothermal reactions of Co(NO3)·6H2O, Mn(NO3)·4H2O and Cd(NO3)·4H2O with 5-aminoisophthalate and the potential linkers 4,4′-bipy, 2-di(4-pyridyl)ethylene (DPE), and 4,4′-azopy afforded the porous 3-D structures {[Co2(NO3)2(5-AIP)(4,4′-bipy)2]·2EtOH}n (3·2EtOH), {[Co(5-AIP)(DPE)]·2DMF}n (4·2DMF), {[Co(5-AIP)(4,4′-azopy)]·2DMA}n (5·2DMA), {[Mn(5-AIP)(4,4′-bipy)]·2DMA}n (6·2DMA), {[Mn(5-AIP)(DPE)]·6DMF}n (7·6DMF), {[Mn(5-AIP)(4,4′-azopy)]·2.5DMF}n (8·2.5DMF), the previously reported {[Cd(5-AIP)(4,4′-bipy)]·3DMF}n (9·3DMF), {[Cd(5-AIP)(DPE)]·DMF}n (10), and {Cd(5-AIP)(4,4′-azopy)(DMF)}n (11), with structures 4–10 bearing the same network topologies with metal atoms and 5-AIP ligands in sheets, bipy ligands acting as pillars, and solvent molecules of crystallisation located around the bipy ligands. The activated MOFs were employed as catalysts for the ring opening polymerization (ROP) of ε-caprolactone and δ-valerolactone. ROPs were conducted as melts, and under N2 only 1 with δ-VL (∼93% conversion) was active. In the case of ε-CL under air, all the systems were active with 1, 2, and 11 affording >90% conversion. Molecular weights (Mn) were in the range 3760–17 940 Da and the products formed were identified as both cyclic and linear PCL. For δ-VL, the catalysts performed somewhat better, with all systems (except 8) affording ∼90% conversion or more under air. Molecular weights (Mn) were in the range 2180–7940 and as for PCL, the products formed were identified as both cyclic and linear PCL.
Funding
China Scholarship Council (CSC)
History
School
- Science
Department
- Chemistry
Published in
CrystEngCommVolume
25Issue
2Pages
267 - 283Publisher
Royal Society of ChemistryVersion
- VoR (Version of Record)
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© The AuthorsPublisher statement
This is an Open Access Article. It is published by the Royal Society of Chemistry under the Creative Commons Attribution-NonCommercial 3.0 Unported Licence (CC BY-NC). Full details of this licence are available at: https://creativecommons.org/licenses/by-nc/3.0/Acceptance date
2022-11-24Publication date
2022-11-25Copyright date
2022eISSN
1466-8033Publisher version
Language
- en