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- ItemA General and Highly Selective Palladium-Catalyzed Hydroamidation of 1,3-Diynes(Weinheim : Wiley-VCH, 2021) Liu, Jiawang; Schneider, Carolin; Yang, Ji; Wei, Zhihong; Jiao, Haijun; Franke, Robert; Jackstell, Ralf; Beller, MatthiasA chemo-, regio-, and stereoselective mono-hydroamidation of (un)symmetrical 1,3-diynes is described. Key for the success of this novel transformation is the utilization of an advanced palladium catalyst system with the specific ligand Neolephos. The synthetic value of this general approach to synthetically useful α-alkynyl-α, β-unsaturated amides is showcased by diversification of several structurally complex molecules and marketed drugs. Control experiments and density-functional theory (M06L-SMD) computations also suggest the crucial role of the substrate in controlling the regioselectivity of unsymmetrical 1,3-diynes. © 2020 The Authors. Published by Wiley-VCH GmbH
- ItemAmbient Hydrogenation and Deuteration of Alkenes Using a Nanostructured Ni-Core-Shell Catalyst(Weinheim : Wiley-VCH, 2021) Gao, Jie; Ma, Rui; Feng, Lu; Liu, Yuefeng; Jackstell, Ralf; Jagadeesh, Rajenahally V.; Beller, MatthiasA general protocol for the selective hydrogenation and deuteration of a variety of alkenes is presented. Key to success for these reactions is the use of a specific nickel-graphitic shell-based core–shell-structured catalyst, which is conveniently prepared by impregnation and subsequent calcination of nickel nitrate on carbon at 450 °C under argon. Applying this nanostructured catalyst, both terminal and internal alkenes, which are of industrial and commercial importance, were selectively hydrogenated and deuterated at ambient conditions (room temperature, using 1 bar hydrogen or 1 bar deuterium), giving access to the corresponding alkanes and deuterium-labeled alkanes in good to excellent yields. The synthetic utility and practicability of this Ni-based hydrogenation protocol is demonstrated by gram-scale reactions as well as efficient catalyst recycling experiments. © 2021 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH
- ItemA General Regioselective Synthesis of Alcohols by Cobalt-Catalyzed Hydrogenation of Epoxides(Weinheim : Wiley-VCH, 2020) Liu, Weiping; Leischner, Thomas; Li, Wu; Junge, Kathrin; Beller, MatthiasA straightforward methodology for the synthesis of anti-Markovnikov-type alcohols is presented. By using a specific cobalt triphos complex in the presence of Zn(OTf)2 as an additive, the hydrogenation of epoxides proceeds with high yields and selectivities. The described protocol shows a broad substrate scope, including multi-substituted internal and terminal epoxides, as well as a good functional-group tolerance. Various natural-product derivatives, including steroids, terpenoids, and sesquiterpenoids, gave access to the corresponding alcohols in moderate-to-excellent yields. © 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.
- ItemCobalt Single-Atom Catalysts with High Stability for Selective Dehydrogenation of Formic Acid(Weinheim : Wiley-VCH, 2020) Li, Xiang; Surkus, Annette-Enrica; Rabeah, Jabor; Anwar, Muhammad; Dastigir, Sarim; Junge, Henrik; Brückner, Angelika; Beller, MatthiasMetal–organic framework (MOF)-derived Co-N-C catalysts with isolated single cobalt atoms have been synthesized and compared with cobalt nanoparticles for formic acid dehydrogenation. The atomically dispersed Co-N-C catalyst achieves superior activity, better acid resistance, and improved long-term stability compared with nanoparticles synthesized by a similar route. High-angle annular dark-field–scanning transmission electron microscopy, X-ray photoelectron spectroscopy, electron paramagnetic resonance, and X-ray absorption fine structure characterizations reveal the formation of CoIINx centers as active sites. The optimal low-cost catalyst is a promising candidate for liquid H2 generation. © 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.
- ItemLigand-Controlled Palladium-Catalyzed Carbonylation of Alkynols : Highly Selective Synthesis of α-Methylene-β-Lactones(Weinheim : Wiley-VCH, 2020) Ge, Yao; Ye, Fei; Liu, Jiawang; Yang, Ji; Spannenberg, Anke; Jiao, Haijun; Jackstell, Ralf; Beller, MatthiasThe first general and regioselective Pd-catalyzed cyclocarbonylation to give α-methylene-β-lactones is reported. Key to the success for this process is the use of a specific sterically demanding phosphine ligand based on N-arylated imidazole (L11) in the presence of Pd(MeCN)2Cl2 as pre-catalyst. A variety of easily available alkynols provide under additive-free conditions the corresponding α-methylene-β-lactones in moderate to good yields with excellent regio- and diastereoselectivity. The applicability of this novel methodology is showcased by the direct carbonylation of biologically active molecules including natural products. © 2020 The Authors. Published by Wiley-VCH GmbH
- ItemRecent Advances in Catalytic Hydrosilylations: Developments beyond Traditional Platinum Catalysts(Weinheim : Wiley-VCH, 2021) de Almeida, Leandro Duarte; Wang, Hongli; Junge, Kathrin; Cui, Xinjiang; Beller, MatthiasHydrosilylation reactions, which allow the addition of Si−H to C=C/C≡C bonds, are typically catalyzed by homogeneous noble metal catalysts (Pt, Rh, Ir, and Ru). Although excellent activity and selectivity can be obtained, the price, purification, and metal residues of these precious catalysts are problems in the silicone industry. Thus, a strong interest in more sustainable catalysts and for more economic processes exists. In this respect, recently disclosed hydrosilylations using catalysts based on earth-abundant transition metals, for example, Fe, Co, Ni, and Mn, and heterogeneous catalysts (supported nanoparticles and single-atom sites) are noteworthy. This minireview describes the recent advances in this field. © 2020 The Authors. Published by Wiley-VCH GmbH
- ItemA Unified Research Data Infrastructure for Catalysis Research – Challenges and Concepts(Weinheim : Wiley-VCH, 2021) Wulf, Christoph; Beller, Matthias; Boenisch, Thomas; Deutschmann, Olaf; Hanf, Schirin; Kockmann, Norbert; Kraehnert, Ralph; Oezaslan, Mehtap; Palkovits, Stefan; Schimmler, Sonja; Schunk, Stephan A.; Wagemann, Kurt; Linke, DavidModern research methods produce large amounts of scientifically valuable data. Tools to process and analyze such data have advanced rapidly. Yet, access to large amounts of high-quality data remains limited in many fields, including catalysis research. Implementing the concept of FAIR data (Findable, Accessible, Interoperable, Reusable) in the catalysis community would improve this situation dramatically. The German NFDI initiative (National Research Data Infrastructure) aims to create a unique research data infrastructure covering all scientific disciplines. One of the consortia, NFDI4Cat, proposes a concept that serves all aspects and fields of catalysis research. We present a perspective on the challenging path ahead. Starting out from the current state, research needs are identified. A vision for a integrating all research data along the catalysis value chain, from molecule to chemical process, is developed. Respective core development topics are discussed, including ontologies, metadata, required infrastructure, IP, and the embedding into research community. This Concept paper aims to inspire not only researchers in the catalysis field, but to spark similar efforts also in other disciplines and on an international level. © 2021 The Authors. ChemCatChem published by Wiley-VCH GmbH
- ItemEfficient methylation of anilines with methanol catalysed by cyclometalated ruthenium complexes(London : RSC Publ., 2021) Piehl, Patrick; Amuso, Roberta; Spannenberg, Anke; Gabriele, Bartolo; Neumann, Helfried; Beller, MatthiasCyclometalated ruthenium complexes4-10allow the effective methylation of anilines with methanol to selectively giveN-methylanilines. This hydrogen autotransfer procedure proceeds under mild conditions (60 °C) in a practical manner (NaOH as base). Mechanistic investigations suggest an active homogenous ruthenium complex and β-hydride elimination of methanol as the rate determining step. © The Royal Society of Chemistry 2021.
- ItemAerobic iron-catalyzed site-selective C(sp3)–C(sp3) bond cleavage in N-heterocycles(Amsterdam : Elsevier, 2021) Leonard, David K.; Li, Wu; Rockstroh, Nils; Junge, Kathrin; Beller, MatthiasThe kinetic and thermodynamic stability of C(sp3)–C(sp3) bonds makes the site-selective activation of these motifs a real synthetic challenge. In view of this, herein a site-selective method of C(sp3)–C(sp3) bond scission of amines, specifically morpholine and piperazine derivatives, using a cheap iron catalyst and air as a sustainable oxidant is reported. Furthermore, a statistical design of experiments (DoE) is used to evaluate multiple reaction parameters thereby allowing for the rapid development of a catalytic process. © 2021
- ItemFacile synthesis of iron-titanate nanocomposite as a sustainable material for selective amination of substitued nitro-arenes(Basel : MDPI, 2020) Sohail, Manzar; Tahir, Nimra; Rubab, Anosha; Beller, Matthias; Sharif, MuhammadThe fabrication of durable and low-cost nanostructured materials remains important in chemical, biologic and medicinal applications. Particularly, iron-based nanomaterials are of central importance due to the ‘noble’ features of iron such as its high abundance, low cost and non-toxicity. Herein we report a simple sol–gel method for the synthesis of novel iron–titanium nanocomposite-based material (Fe9TiO15@TiO2). In order to prepare this material, we made a polymeric gel using ferrocene, titanium isopropoxide and THF precursors. The calcination of this gel in air at 500◦C produced Fe-Ti bimetallic nanoparticles-based composite and nano-TiO2 as support. Noteworthy, our methodology provides an excellent control over composition, size and shape of the resulting nanoparticles. The resulted Fe-based material provides a sustainable catalyst for selective synthesis of anilines, which are key intermediates for the synthesis of several chemicals, dyes and materials, via reduction of structurally diverse and functionalized nitroarenes. © 2020 by the authors. Licensee MDPI, Basel, Switzerland.