244 Papers
3.1K Citations
Sally Brooker is an academic researcher from MacDiarmid Institute for Advanced Materials and Nanotechnology. The author has contributed to research in topics: Chemistry & Spin crossover. The author has an hindex of 45, co-authored 235 publications. Previous affiliations of Sally Brooker include University of Canterbury & University of Otago.
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Papers
Review of Purely 4f and Mixed‐Metal Nd‐4f Single‐Molecule Magnets Containing Only One Lanthanide Ion
TL;DR: In this paper, a very basic tutorial-style introduction to single-molecule magnetism is provided, followed by a review of the synthesis, structures and magnetic properties of SMMs that contain just one lanthanide ion and are either (a) monometallic or (b) di- or polymetallic.
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Dicopper(II) and dinickel(II) complexes of Schiff-base macrocycles derived from 5,5-dimethyl-1,9-diformyldipyrromethane
TL;DR: In this paper, the synthesis and characterisation of two dicopper(II) and two dinickel(II)-macrocyclic complexes, [Cu II 2 L Pr ] (10), [Ni II 2 2 L Bu ] (11 ), [Ni 2 2 l P ] (12 ), and [NiII 2 l B L P ](13 ), are reported.
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Selective gas adsorption in a pair of robust isostructural MOFs differing in framework charge and anion loading.
Matthew G. Cowan,Reece G. Miller,Peter D. Southon,Jason R. Price,Ozgur Yazaydin,Joseph R. Lane,Cameron J. Kepert,Sally Brooker +7 more
TL;DR: The increased anion loading in the channels of Co(III)-based MOF 1 relative to Ni(II)- based MOF 2 results in increased selectivity for CO2 over N2 but a decrease in the sorption kinetics and storage capacity of the framework.
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Monomeric, dimeric and 1D chain polymeric copper(II) complexes of a pyrrole-containing tridentate Schiff-base ligand and its 4-brominated analogue
TL;DR: Variable temperature magnetic susceptibility measurements carried out on the structurally characterised dimeric and polymeric copper(ii) complexes, and revealed weak antiferromagnetic exchange.
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Redox-adaptable copper hosts. pyridazine-linked cryptands accommodate copper in a range of redox states
TL;DR: Electrochemical studies indicate that L(A) stabilizes the copper(II) oxidation state more effectively than L(I); no copper redox state lower than II,II has been isolated in the solid state using this ligand.
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