Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Artificial photosynthesis enables the conversion and storage of solar energy into chemical energy, producing substances with high energy content. In this sense, the oxidation of water can provide the H+ ions and electrons needed for the energy conversion and storage processes. Since 2005, it has been known that single-site coordination compounds can act as water oxidation catalysts (WOC). Improvement of the catalytic activity, however, has occurred mainly by the choice of the redox-active metal matching with a series of compatible ligands, more specifically, paying attention to the electronic characteristics of the organic framework of the first coordination sphere. Recently, the use of dangling bases dramatically increased the catalytic activity of new species as WOC, taking advantage of what is called a second coordination sphere. With this assistance, some compounds were shown to reach turnover frequencies (TOF) of 104 s-1, while compounds with the first coordination sphere commonly exhibit TOF ca. 10-1 s-1. In this manuscript, we discuss the concept, together with a number of examples, of the use of controlled interactions between the first and second coordination spheres that have been wielded to improve the performance of ruthenium-centered complexes as WOC in water oxidation reactions.

Download full-text PDF

Source
http://dx.doi.org/10.1039/d0dt02958kDOI Listing

Publication Analysis

Top Keywords

coordination sphere
16
second coordination
12
water oxidation
12
catalytic activity
12
conversion storage
8
coordination
6
second-hand? second
4
sphere
4
sphere ruthenium
4
ruthenium complexes
4

Similar Publications

Economically viable and biologically compatible amino acids demonstrate significant potential as electrolyte microstructure modifiers in aqueous zinc-ion batteries (AZIBs). Compared to polar amino acids, nonpolar amino acids simultaneously own zincophilicity and hydrophobicity, showing great potential in the industrial application of AZIBs. However, nonpolar amino acids have been comparatively understudied in existing research investigations.

View Article and Find Full Text PDF

The crystal structure of a nitrate anion caged in spherical vanadium and oxygen structure surrounded by sodium hy-droxy and water solvent mol-ecules, systematic name poly[[hepta-deca-aqua-tetra-deca-oxidonona-sodium][penta-cosa-aqua-nitratoundeca-oxido-penta-deca-vanadium]], HNNaOV is reported. The complex crystallizes in the non-centrosymmetric space group and exhibits many inter- and intra-molecular hydrogen-bonding inter-actions. The complex contains V and V centres, which are six-coordinate or octa-hedrally coordinated.

View Article and Find Full Text PDF

The unit cell of the title compound, [Ni(CHNO)]·2CHOH, consists of a neutral complex and two methanol mol-ecules. In the complex, the two tridentate 2-[3-(benzo[][1,3]dioxol-5-yl)-1-1,2,4-triazol-5-yl]-6-(1-pyrazol-1-yl)pyridine ligands coordinate to the central Ni ion through nitro-gen atoms of the pyrazole, pyridine and triazole groups, forming a pseudo-octa-hedral coordination sphere. Neighbouring mol-ecules are linked through weak C-H(pz)⋯π(ph) inter-actions into monoperiodic chains, which are further linked through weak C-H⋯H/N/C inter-actions into diperiodic layers.

View Article and Find Full Text PDF

Ni-Catalyzed and Pentafluorobenzoate-Leaving-Group-Enabled Stereoselective -Aryl Glycosylation.

Org Lett

September 2025

College of Chemistry and Chemical Engineering and Luoyang Key Laboratory of Green Synthesis and Photofunctional Materials, Luoyang Normal University, Luoyang, Henan 471934, China.

Inspired by the excellent stereoinduction of palladium catalytic glycosylation with glycals via an inner-sphere pathway, a nickel-catalyzed, stereoselective -aryl glycosylation has been developed for glucals bearing a pentafluorobenzoate (PFB) group at the C3 position. The extremely electron-deficient nature of PFB not only endows stronger activity compared to the traditional leaving groups but also functions as an orientation group, presumably through the strong π-π interactions with the bipyridine ligand coordinated to the nickel center, thereby enabling the β-selective formation of a -aryl glycosidic bond with aryl iodides as glycosyl acceptors under mild conditions. This method features a broad substrate scope, high efficiency, and scalability, providing a general solution to the synthesis of challenging β--glycosides.

View Article and Find Full Text PDF

Although health care access among adults with Intellectual and Developmental Disabilities (IDD) improved in the past decade, persistent challenges still exist in obtaining care coordination and supportive services. As the life expectancy of individuals living with IDD increases and care succession occurs from family's community care to institutional care, the risk of maltreatment among adults with IDD is growing. Health conditions, for example, cognitive impairment pose a risk of maltreatment in adults with IDD.

View Article and Find Full Text PDF