A Foldable Metal–Organic Framework with cds Topology Assembled via Four-Connected Square-Planar Single Ni2+-Ion Nodes and Linear Bidentate Linkers

Author:

Shi Zhi-Chun1ORCID,Wang Xiaoliang2ORCID,Drozd Vadym3,Raptis Raphael G.1ORCID

Affiliation:

1. Department of Chemistry and Biochemistry, Florida International University, Miami, FL 33199, USA

2. Department of Chemistry, Northwestern University, Evanston, IL 60208, USA

3. Center for Study of Matter at Extreme Conditions, Florida International University, Miami, FL 33199, USA

Abstract

A binary, three-dimensional (3D), foldable, Metal–Organic Framework (MOF) of formula {[trans-Ni(H2O)2(μ-4,4′-bpy)2](ClO4)2}n (1), with CdSO4 (65 8), cds, topology, based on four-connected (4-c) square-planar single Ni2+ ion nodes and two-connected (2-c) linear rigid 4,4′-bipyridine (4,4′-bpy) ligands, was synthesized and structurally characterized via single crystal X-ray crystallography. The 41° dihedral angle between two distinct coordination environments within the 3D network of 1 produced the self-dual topology of Ni2+ nodes. Two rectangular 1D channels ran parallel to the crystallographic a-axis and b-axis, respectively, creating a 44.2% volume porosity, probed by gas (N2, CO2, and H2) sorption studies. The PXRD, FT-IR, Raman, EDS, and SEM methods were employed for the study of 1. A thermogravimetric analysis (TGA) showed that coordinated water molecules were readily removed upon heating, whereas the 3D lattice remained intact up to 370 °C.

Funder

National Science Foundation

Publisher

MDPI AG

Subject

Inorganic Chemistry,Condensed Matter Physics,General Materials Science,General Chemical Engineering

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