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Since the pioneering independent reports of Akiyama and Terada, the use of chiral phosphoric acids (CPAs) and derivatives as a versatile tool for asymmetric synthesis with good reactivity, regioselectivity, diastereoselectivity and enantioselectivity has emerged, forming an important part of the implementation of asymmetric counteranion-directed catalysis reported to date. In these achievements, the combination of metals with CPAs has enabled various catalytic modes beyond the scope of typical acid catalysis, such as relay catalysis, ion-pairing catalysis, and binary acid catalysis. The first-row transition metals (Sc-Zn) are considered to be sustainable transition metals and have received a great deal of attention. These naturally abundant metals display excellent Lewis acidity and function as powerful redox catalysts in synthesis involving both one and two-electron transfers. Hence, in this chapter, we summarize recent advances in the development of asymmetric reactions using a combination of first-row transition metals and CPAs. Furthermore, we provide a detailed discussion of the mechanisms involved in order to understand the interaction of the metal/phosphate and the origins of the asymmetric control of the transformations.
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http://dx.doi.org/10.1007/s41061-019-0249-0 | DOI Listing |
Inorg Chem
September 2025
Department of Chemistry and Biochemistry, University of Delaware, Newark, Delaware 19716 United States.
Electrochemical valorization of biomass-derived substrates has become a prominent area of research due to its potential to produce value-added products from renewable feedstocks in a more sustainable way. First-row transition-metal electrodes are compelling candidates for these conversions due to their stability, abundance, and cost-effectiveness. Herein, we report on the colloidal synthesis of MnZnO ( = 0.
View Article and Find Full Text PDFMolecules
July 2025
Department of Chemistry, Missouri University of Science and Technology, Rolla, MO 65409, USA.
A 12-membered pyridinophane scaffold containing two pyridine and two tertiary amine residues is examined as a prototype ligand (N4) for supporting nitrene transfer to olefins. The known [(N4)M(MeCN)] (M = Mn, Fe, Co, and Ni) and [(N4)Cu(MeCN)] cations are synthesized with the hexafluorophosphate counteranion. The aziridination of para-substituted styrenes with PhI=NTs (Ts = tosyl) in various solvents proved to be high yielding for the Cu(I) and Cu(II) reagents, in contrast to the modest efficacy of all other metals.
View Article and Find Full Text PDFJ Comput Chem
August 2025
Department of Chemistry, Birla Institute of Technology Mesra, Ranchi, India.
Metal ligand cooperation (MLC) is a catalyst design technique where both the metal center and the ligand framework aid in the binding of the reactant. Recently, a first-row transition metal Mn-PNP pincer complex that works via an aromatisation-dearomatisation mechanism of MLC was reported for base-free dinitrile coupling. We perform microkinetic modeling of the pertinent reaction considering competitive binding of the reactants and branching pathways in the overall scheme.
View Article and Find Full Text PDFChem Sci
August 2025
Department of Chemistry, Michigan State University East Lansing USA
Exploration of the photophysical and photochemical properties of transition metal complexes has driven ground-breaking advancements in solar energy conversion technologies, including photoredox catalysis. While significant research has been devoted to understanding excited state properties of second- and third-row transition metal complexes, earth-abundant first-row metal complexes have received comparatively little attention in this context until very recently. In particular, the role of ion-pairing - which has been identified as a potentially significant factor for Ir(iii)-based photosensitizers - has not been examined with regard to its influence on the ligand-field excited states that dominate much of first-row photophysics.
View Article and Find Full Text PDFJ Am Chem Soc
August 2025
Department of Chemistry, University of Basel, St. Johanns-Ring 19, Basel 4056, Switzerland.
Co complexes have recently become an important focus in photophysics and photoredox catalysis due to metal-centered excited states with strong oxidizing properties. Optimizing chelate ligand bite angles is a widely used strategy to strengthen metal-ligand interactions in coordination complexes, with the resulting enhanced ligand fields often contributing to extended excited-state lifetimes that are advantageous for photochemical applications. We demonstrate that bite-angle optimization exerts the opposite effect on Co polypyridines compared to previously studied transition metal complexes, as polypyridine ligands function as π-donors to Co rather than π-acceptors.
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