3-Methylindole-Based Tripodal Tetraphosphine Ruthenium Complexes in N2 Coordination and Reduction and Formic Acid Dehydrogenation
Author:
Funder
Nederlandse Organisatie voor Wetenschappelijk Onderzoek
Publisher
MDPI AG
Subject
Inorganic Chemistry
Link
http://www.mdpi.com/2304-6740/5/4/73/pdf
Reference45 articles.
1. Synthesis and Properties of Iron(II) Hydride Complexes Containing the Tripodal Tetraphosphine Ligand P(CH2CH2PMe2)3
2. Ruthenium in Catalysis;Bruneau,2014
3. Stoichiometric and catalytic functionalization reactions of alkynes at transition metal complexes stabilized by tripodal polyphosphine ligands
4. Synthesis and Reactions of Molybdenum Triamidoamine Complexes Containing Hexaisopropylterphenyl Substituents
5. Terminal FeIN2 and FeII⋅⋅⋅HC Interactions Supported by Tris(phosphino)silyl Ligands
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1. Well‐defined Nickel P 3 C Complexes as Hydrogenation Catalysts of N ‐Heteroarenes Under Mild Conditions;ChemCatChem;2022-04-14
2. Triphosphines-containing ruthenium-acetato complexes: Synthesis, characterization, DFT, mer/fac isomerization and formic acid dehydrogenation;Journal of Molecular Structure;2020-01
3. Coordination of 3‐Methylindole‐Based Tripodal Tetraphosphine Ligands to Iron(+II), Cobalt(+II), and Nickel(+II) and Investigations of their Subsequent Two‐Electron Reduction;European Journal of Inorganic Chemistry;2018-02-12
4. From Mechanisms in Homogeneous Metal Catalysis to Applications in Chemical Synthesis;Inorganics;2018-01-24
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