Issue 16, 2021

Nanochannel-based heterometallic {ZnIIHoIII}–organic framework with high catalytic activity for the chemical fixation of CO2

Abstract

The exquisite combination of ZnII and HoIII generated the highly robust [ZnHo(CO2)6(OH2)]-based heterometallic framework of {[ZnHo(TDP)(H2O)]·5H2O·3DMF}n (NUC-30, H6TDP = 2,4,6-tri(2′,4′-dicarboxyphenyl)pyridine), which featured outstanding physicochemical properties, including honeycomb nanochannels, high porosity, large specific surface area, the coexistence of highly open Lewis acid–base sites, good thermal and chemical stability, and resistance to most organic solvents. Due to its extremely unsaturated metal tetra-coordinated Zn(II) ions, hepta-coordinated Ho(III) and high faveolate void volume (61.3%), the conversion rate of styrene oxide and CO2 into cyclic carbonates in the presence of 2 mol% activated NUC-30 and 5 mol% n-Bu4NBr reached 99% under the mild conditions of 1.0 MPa and 60 °C. Furthermore, the luminescence sensing experiments proved that NUC-30 could be used as a fast, sensitive and highly efficiency sensor for the detection of Fe3+ in aqueous solution. Therefore, these results prove that nanoporous MOFs assembled from pyridine-containing polycarboxylate ligands have wide applications, such as catalysis and as luminescent materials.

Graphical abstract: Nanochannel-based heterometallic {ZnIIHoIII}–organic framework with high catalytic activity for the chemical fixation of CO2

Supplementary files

Article information

Article type
Paper
Submitted
22 Jan 2021
Accepted
15 Feb 2021
First published
04 Mar 2021
This article is Open Access
Creative Commons BY license

RSC Adv., 2021,11, 9731-9739

Nanochannel-based heterometallic {ZnIIHoIII}–organic framework with high catalytic activity for the chemical fixation of CO2

T. Zhang, H. Chen, H. Lv, Q. Li and X. Zhang, RSC Adv., 2021, 11, 9731 DOI: 10.1039/D1RA00590A

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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