Acid/base responsive assembly/dis-assembly of a family of zirconium(iv) clusters with a cyclic imide-dioxime ligand-Reference-Cited by-同舟云学术

Acid/base responsive assembly/dis-assembly of a family of zirconium(iv) clusters with a cyclic imide-dioxime ligand

Published:2022 Issue:5 Volume:51 Page:1806-1818
ISSN:1477-9226
Container-title:Dalton Transactions
language:en
Short-container-title:Dalton Trans.

Author:

Passadis Stamatis S.¹,Hadjithoma Sofia²,Papanikolaou Michael G.¹,Keramidas Anastasios D.²^ORCID,Miras Haralampos N.³^ORCID,Kabanos Themistoklis A.¹^ORCID

Affiliation:

1. Section of Inorganic and Analytical Chemistry, Department of Chemistry, University of Ioannina, Ioannina 45110, Greece

2. Department of Chemistry, University of Cyprus, Nicosia 2109, Cyprus

3. West CHEM, School of Chemistry, University of Glasgow, Glasgow G12 8QQ, U.K

Abstract

The hydrolytically stable dioxime ligand not only acts as an excellent metal sequestering agent but it can give rise to the formation of a family of Zr-clusters which can convert to each other via a reversible pH driven dis-assembly/re-assembly process.

Funder

Hellenic Foundation for Research and Innovation

European Regional Development Fund

Research and Innovation Foundation

Engineering and Physical Sciences Research Council

Publisher

Royal Society of Chemistry (RSC)

Subject

Inorganic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/DT/D1DT03641F

Reference48 articles.

1. A gigantic polyoxozirconate with visible photoactivity

2. Synthesis, Structural, and Physicochemical Characterization of a Ti6 and a Unique Type of Zr6 Oxo Clusters Bearing an Electron-Rich Unsymmetrical {OON} Catecholate/Oxime Ligand and Exhibiting Metalloaromaticity

3. Synthesis and photocatalytic H2 evolution properties of four titanium-oxo-clusters based on a cyclohex-3-ene-1-carboxylate ligand

4. Synthesis, Crystal Structures, and Photochemical Properties of a Family of Heterometallic Titanium Oxo Clusters

5. A Titanium Oxo Cluster Model Study of Synergistic Effect of Co-coordinated Dye Ligands on Photocurrent Responses

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