Please use this identifier to cite or link to this item:
Scopus Web of Science® Altmetric
Type: Journal article
Title: Isolating reactive metal-based species in Metal-Organic Frameworks - viable strategies and opportunities
Author: Young, R.J.
Huxley, M.T.
Pardo, E.
Champness, N.R.
Sumby, C.J.
Doonan, C.J.
Citation: Chemical Science, 2020; 11(16):4031-4050
Publisher: Royal Society of Chemistry
Issue Date: 2020
ISSN: 2041-6520
Statement of
Rosemary J. Young, Michael T. Huxley, Emilio Pardo, Neil R. Champness, Christopher J. Sumby and Christian J. Doonan
Abstract: Structural insight into reactive species can be achieved via strategies such as matrix isolation in frozen glasses, whereby species are kinetically trapped, or by confinement within the cavities of host molecules. More recently, Metal–Organic Frameworks (MOFs) have been used as molecular scaffolds to isolate reactive metal-based species within their ordered pore networks. These studies have uncovered new reactivity, allowed observation of novel metal-based complexes and clusters, and elucidated the nature of metal-centred reactions responsible for catalysis. This perspective considers strategies by which metal species can be introduced into MOFs and highlights some of the advantages and limitations of each approach. Furthermore, the growing body of work whereby reactive species can be isolated and structurally characterised within a MOF matrix will be reviewed, including discussion of salient examples and the provision of useful guidelines for the design of new systems. Novel approaches that facilitate detailed structural analysis of reactive chemical moieties are of considerable interest as the knowledge garnered underpins our understanding of reactivity and thus guides the synthesis of materials with unprecedented functionality.
Rights: This journal is © The Royal Society of Chemistry 2020
DOI: 10.1039/d0sc00485e
Grant ID:
Appears in Collections:Aurora harvest 8
Chemistry publications

Files in This Item:
There are no files associated with this item.

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.