A first new porous d-p HMOF material with multiple active sites for excellent CO2 capture and catalysis.

Affiliation

Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of the Ministry of Education, Shaanxi Key Laboratory of Physico-Inorganic Chemistry, College of Chemistry & Materials Science, Northwest University, Xi'an 710127, P. R. China. [Email] [Email]

Abstract

In this work, a new monometallic metal-organic framework (MOF), namely {[Pb2(L)2(H2O)]·H2O}n (1), was prepared via a N,O-mixed 2-(imidazol-1-yl)terephthalic acid (H2L) ligand and Pb(ii) ions. Then, a first new porous d-p heterometallic MOF (HMOF), namely {[PbZn(L)2]·DMA·H2O}n (2), was yielded via Zn(ii) ions and MOF 1 as the precursor because of the different coordination affinity of oxygen and nitrogen atoms with various metal ions. MOF 1 is a condensed packing motif, whereas HMOF 2 is a porous three-dimensional (3D) framework with unsaturated Pb(ii) and Zn(ii) active sites, uncoordinated carboxylate oxygen atoms and two kinds of porous channels due to the introduction of Zn(ii) ions into the framework of MOF 1, which thus endowed HMOF 2 with excellent sorption and selectivity for CO2 over CH4. Moreover, HMOF 2 was explored to be an efficient heterogeneous catalyst for the fixation of CO2 with various epoxides because of the existence of the abundant unsaturated bimetallic sites as the Lewis acid. It is hoped that this work may supply an effective strategy to build plenty of d-p HMOF materials with excellent gas adsorption and catalytic properties.

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