ORCID Profile
0000-0002-9043-8369
Current Organisations
The Hong Kong Polytechnic University
,
University of Adelaide
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Publisher: Royal Society of Chemistry (RSC)
Date: 2023
DOI: 10.1039/D3TA04707E
Publisher: Wiley
Date: 27-07-2022
Publisher: Elsevier BV
Date: 09-2017
Publisher: CSIRO Publishing
Date: 2019
DOI: 10.1071/CH19220
Abstract: A diruthenium(ii) complex involving the di(terpyridine) ligand 1,2-bis{5-(5″-methyl-2,2′:6′,2″-terpyridinyl)}ethane was synthesised by heating an equimolar ratio of RuCl3 and the ligand under reflux conditions in ethylene glycol for 3 days, realising double-stranded helicate and mesocate forms which were chromatographically separated. The two species were obtained in relatively low yield (each ~7–9%) from the reaction mixture. X-Ray structural studies revealed differences in the cavity sizes of the two structures, with the helicate structure having a significantly smaller cavity. Furthermore, the helicate and mesocate forms pack with notably different arrangements of the structures with the helicate having large solvent and anion filled pores. 1D/2D NMR studies revealed rigidity in the mesocate structure relative to that of the helicate, such that the –CH2CH2– signal was split in the former and appeared as a singlet in the latter. In a manner analogous to the behaviour of the parent [Ru(tpy)2]2+ coordination moiety (tpy=2,2′:6′,2″-terpyridine), photophysical studies indicated that both the helicate and mesocate forms were non-emissive at ~610nm at room temperature, but at 77K in n-butyronitrile, both isomers showed emission at ~610nm (λex 472nm). However, the temporal emission characteristics were very different: time-resolved studies showed the emission of the helicate species decayed with a dominant emission lifetime of ~10 μs (similar to the emissive properties of free [Ru(tpy)2]2+ under the same conditions), whereas for the mesocate the emission lifetime was at least three orders of magnitude lower (~4 ns).
Publisher: American Chemical Society (ACS)
Date: 27-10-2023
Publisher: Royal Society of Chemistry (RSC)
Date: 2023
DOI: 10.1039/D3TA02784H
Abstract: Boron-modified cobalt-free single-crystal cathode enables to ultra-low c -axis lattice contraction and anchors lattice oxygen for high safety Li-ion batteries.
Publisher: Elsevier BV
Date: 05-2019
DOI: 10.1016/J.BBAGEN.2019.02.016
Abstract: Actinobacteria, including the Mycobacteria, have a large component of cytochrome P450 family monooxygenases. This includes Mycobacterium tuberculosis, M. ulcerans and M. marinum, and M. vanbaalenii. These enzymes can abstract CH bonds and have important roles in natural product biosynthesis. Two members of the bacterial CYP150 family, CYP150A5 and CYP150A6 from M. marinum, were produced, purified and characterised. The potential substrate ranges of both enzymes were analysed and the monooxygenase activity of CYP150A5 was reconstituted using a physiological electron transfer partner system. CYP150A6 was structurally characterised by X-ray crystallography. CYP150A5 was shown to bind various norisoprenoids and terpenoids. It could regioselectively hydroxylate β-ionol. The X-ray crystal structure of substrate-free CYP150A6 was solved to 1.5 Å. This displayed an open conformation with short F and G helices, an unresolved F-G loop region and exposed active site pocket. The active site residues could be identified and important variations were found among the CYP150A enzymes. Haem-binding azole inhibitors were identified for both enzymes. The structure of CYP150A6 will facilitate the identification of physiological substrates and the design of better inhibitors for members of this P450 family. Based on the observed differences in substrate binding preference and sequence variations among the active site residues, their roles are predicted to be different. Multiple CYP150 family members were found in many bacteria and are prevalent in the Mycobacteria including several human pathogens. Inhibition and structural data are reported here for these enzymes for the first time.
Publisher: American Chemical Society (ACS)
Date: 06-09-2023
DOI: 10.1021/JACS.3C05488
Publisher: Wiley
Date: 14-06-2022
Abstract: A series of ligands containing a 1,4‐disubstituted 1,2,3‐triazole unit have been used for the formation of triple‐stranded dinuclear Ru(II) complexes. In contrast to the previously reported complexes of labile metals, the use of inert Ru(II) enabled stereoisomeric mixtures of triple‐stranded diruthenium(II) complexes to be accessed. The chromatographic resolution of the enantiomers of a reported helicate containing a more rigid 1,4‐xylyl spacer was carried out on cellulose. The ligand spacer was modified and as the flexibility increased the production of isomeric mixtures was detected the mesocate and helicate forms were separated when an n ‐propyl spacer was used. This pair of diastereomers was found to exhibit photoconversion, a unique observation for Ru(II) compounds of this type. Partial separation via chromatographic resolution was achieved for compounds containing an n ‐butyl spacer, and the presence of a mesocate/helicate pair confirmed.
Publisher: Elsevier BV
Date: 07-2023
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