Issue 5, 2021

Effect of pyridyl donors from organic ligands versus metalloligands on material design

Abstract

A pyridyl group, one of the most ubiquitous functionalities, has been widely used by researchers working at the forefront of framework materials such as coordination polymers (CPs) including metal–organic frameworks (MOFs) due to its versatile coordination abilities. As the coordination mode of a ligand or a linker plays a critical role in dictating the architecture of the resultant framework material, numerous pyridyl-based ligands and linkers have been developed. In recent times, various metalloligands offering appended pyridyl groups have also been developed. A metalloligand is typically rigid when compared to a flexible organic ligand and therefore a ligand versus a metalloligand is expected to afford different framework materials. Although a large number of pyridyl-based CPs including MOFs have been studied in terms of their synthesis, characterization and application, no systematic investigation on the impact of pyridyl donors emerging from an organic ligand versus a metalloligand on the material design has been attempted and the present review article is an attempt to fill this gap. This review article presents design strategies, crystal structures and topologies for various framework materials synthesized using assorted flexible as well as rigid organic ligands and rigid metalloligands offering appended pyridyl groups. The focus has been placed to delineate the effect of flexibility versus rigidity on the architectures of the resultant material.

Graphical abstract: Effect of pyridyl donors from organic ligands versus metalloligands on material design

Article information

Article type
Review Article
Submitted
28 jún 2020
Accepted
08 aug 2020
First published
10 aug 2020

Inorg. Chem. Front., 2021,8, 1334-1373

Effect of pyridyl donors from organic ligands versus metalloligands on material design

G. Kumar, G. Kumar and R. Gupta, Inorg. Chem. Front., 2021, 8, 1334 DOI: 10.1039/D0QI00768D

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements