Abstract

The pillared layer motif is a commonly used route to porous coordination polymers or metal organic frameworks (MOFs). Materials based on the pillared cyano-bridged architecture, [Ni’(L)Ni(CN)4]n (L = pillar organic ligands), also known as PICNICs, have been shown to be especially diverse where pore size and pore functionality can be varied by the choice of pillar organic ligand. In addition, a number of PICNICs form soft porous structures that show reversible structure transitions during the adsorption and desorption of guests. The structural flexibility in these materials can be affected by relatively minor differences in ligand design, and the physical driving force for variations in host-guest behavior in these materials is still not known. One key to understanding this diversity is a detailed investigation of the crystal structures of both rigid and flexible PICNIC derivatives. This article gives a brief review of flexible MOFs. It also reports the crystal structures of five PICNICS from our laboratories including three 3-D porous frameworks (Ni-Bpene, NI-BpyMe, Ni-BpyNH2), one 2-D layer (Ni-Bpy), and one 1-D chain (Ni-Naph) compound. The sorption data of BpyMe for CO2, CH4 and N2 is described. The important role of NH3 (from the solvent of crystallization) as blocking ligands which prevent the polymerization of the 1-D chains and 2-D layers to become 3D porous frameworks in the Ni-Bpy and Ni-Naph compounds is also addressed.

Highlights

  • The continual rise in anthropogenic CO2 concentration since the dawn of the Industrial Revolution and its effect on climate change underlie the urgent need for the implementation of carbon mitigation approaches to stabilize the CO2 concentration in the atmosphere, which would result in a more sustainable global development [1,2,3]

  • According to Zhou and Kitagawa [12], the surge of metal organic frameworks (MOFs) research in recent years has been due to five factors: (1) advances in cluster chemistry; (2) maturation of organic synthesis; (3) improvements for evaluation of sorption and structural properties; (4) interdisciplinary growth of MOFs, and (5) their expanding potential in applications

  • The goals of this article are to give a brief description of flexible MOFs, with emphasis on the flexible PICNICs, and to discuss the crystallography of flexible and rigid PICNICs based on our recent crystallographic investigations on five Ni(CN)4 -based compounds

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Summary

Introduction

The continual rise in anthropogenic CO2 concentration since the dawn of the Industrial Revolution and its effect on climate change underlie the urgent need for the implementation of carbon mitigation approaches to stabilize the CO2 concentration in the atmosphere, which would result in a more sustainable global development [1,2,3]. Porous materials which offer a wide range of compositions and structures suitable for adsorption and capture of CO2 [4] near atmospheric pressure and over various temperature ranges include zeolites [5,6], activated carbon [7], smectites [8], oxide materials such as calcium oxide [9], lithium zirconates [10], and hydrotalcites [11]. MOFs consist of metal centers and/or metal clusters connected by organic linkers, forming 3-D porous structures with 1-D, 2-D, or 3-D channel systems. According to Zhou and Kitagawa [12], the surge of MOF research in recent years has been due to five factors: (1) advances in cluster chemistry; (2) maturation of organic synthesis (ligand design and post-synthetic modification on linkers); (3) improvements for evaluation of sorption and structural properties; (4) interdisciplinary growth of MOFs, and (5) their expanding potential in applications

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