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      The Complex Reactivity of [(salen)Fe] 2(μ-O) with HBpin and Its Implications in Catalysis

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          Abstract

          We report a detailed study into the method of precatalyst activation during alkyne cyclotrimerization. During these studies we have prepared a homologous series of Fe(III)-μ-oxo(salen) complexes and use a range of techniques including UV–vis, reaction monitoring studies, single crystal X-ray diffraction, NMR spectroscopy, and LIFDI mass spectrometry to provide experimental evidence for the nature of the on-cycle iron catalyst. These data infer the likelihood of ligand reduction, generating an iron(salan)-boryl complex as a key on-cycle intermediate. We use DFT studies to interrogate spin states, connecting this to experimentally identified diamagnetic and paramagnetic species. The extreme conformational flexibility of the salan system appears connected to challenges associated with crystallization of likely on-cycle species.

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          Most cited references61

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          A review of the problem of distinguishing true homogeneous catalysis from soluble or other metal-particle heterogeneous catalysis under reducing conditions

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            Earth-abundant transition metal catalysts for alkene hydrosilylation and hydroboration

            The addition of a silicon-hydrogen or a boron-hydrogen bond across a carbon-carbon multiple bonds is a well-established method for the introduction of versatile silane and borane functional groups to base hydrocarbon feedstocks. Transition metal catalysis, historically with precious second- and third- row transition metals, has been used to broaden the scope of the hydrofunctionalization reaction, improve reaction rate and enhance selectivity. The anti-Markovnikov selectivity of platinum-catalyzed hydrosilylation of alkenes, for example, is an enabling synthetic technology in the multibillion-dollar silicones industry. Increased emphasis on sustainable catalytic methods and more economic processes has shifted focus to catalysis with more earth-abundant transition metals such as iron, cobalt and nickel. This review describes contemporary approaches and offers a contextual analysis of catalytic alkene hydrosilylation and hydroboration reactions using first-row transition metals. Emphasis is placed on defining advances in the field, what constitutes catalyst cost, safety, and important design features to enable precious metal-like reactivity, as well as new chemistry that is unique to first-row transition metals.
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              Metal-Salen Schiff base complexes in catalysis: practical aspects.

              Schiff base ligands are considered "privileged ligands" because they are easily prepared by the condensation between aldehydes and imines. Stereogenic centres or other elements of chirality (planes, axes) can be introduced in the synthetic design. Schiff base ligands are able to coordinate many different metals, and to stabilize them in various oxidation states, enabling the use of Schiff base metal complexes for a large variety of useful catalytic transformations. Practical guidelines for the preparation and use of different Schiff base metal complexes in the field of catalytic transformations are discussed in this tutorial review.
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                Author and article information

                Journal
                ACS Catal
                ACS Catal
                cs
                accacs
                ACS Catalysis
                American Chemical Society
                2155-5435
                23 August 2023
                01 September 2023
                : 13
                : 17
                : 11841-11850
                Affiliations
                []Department of Chemistry, University of Bath , Claverton Down, Bath, United Kingdom BA2 7AY
                []Department of Chemistry, TU Darmstadt , Peter-Grünberg-Str. 4, 64287 Darmstadt, Germany
                Author notes
                [* ]Email for M.M.: m.f.mahon@ 123456bath.ac.uk .
                [* ]Email for R.L.W.: r.l.webster@ 123456bath.ac.uk .
                Author information
                https://orcid.org/0000-0003-2506-2753
                https://orcid.org/0000-0001-9936-117X
                https://orcid.org/0000-0002-4749-4357
                https://orcid.org/0000-0001-9199-7579
                Article
                10.1021/acscatal.3c02898
                10476159
                37671182
                7bdb68b1-cec4-4c80-8b50-9dcbd01e53cc
                © 2023 The Authors. Published by American Chemical Society

                Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 26 June 2023
                : 01 August 2023
                Funding
                Funded by: Engineering and Physical Sciences Research Council, doi 10.13039/501100000266;
                Award ID: NA
                Funded by: Leverhulme Trust, doi 10.13039/501100000275;
                Award ID: RPG-2020-313
                Categories
                Research Article
                Custom metadata
                cs3c02898
                cs3c02898

                iron,cyclotrimerization,mechanism,salen,ligand reduction
                iron, cyclotrimerization, mechanism, salen, ligand reduction

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