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- ItemMechanistic Understanding of the Heterogeneous, Rhodium-Cyclic (Alkyl)(Amino)Carbene-Catalyzed (Fluoro-)Arene Hydrogenation(Washington, DC : American Chemical Society, 2020) Moock D.; Wiesenfeldt M.P.; Freitag M.; Muratsugu S.; Ikemoto S.; Knitsch R.; Schneidewind J.; Baumann W.; Schäfer A.H.; Timmer A.; Tada M.; Hansen M.R.; Glorius F.Recently, chemoselective methods for the hydrogenation of fluorinated, silylated, and borylated arenes have been developed providing direct access to previously unattainable, valuable products. Herein, a comprehensive study on the employed rhodium-cyclic (alkyl)(amino)carbene (CAAC) catalyst precursor is disclosed. Mechanistic experiments, kinetic studies, and surface-spectroscopic methods revealed supported rhodium(0) nanoparticles (NP) as the active catalytic species. Further studies suggest that CAAC-derived modifiers play a key role in determining the chemoselectivity of the hydrogenation of fluorinated arenes, thus offering an avenue for further tuning of the catalytic properties. Copyright © 2020 American Chemical Society.
- ItemFabrication of a new photo-sensitized solar cell using TiO2\ZnO Nanocomposite synthesized via a modified sol-gel Technique(London [u.a.] : Institute of Physics, 2020) Mahdi Rheima, Ahmed; Hadi Hussain, Dhia; Jawad Abed, HayderThe current research synthesized was carried out using a modified solgel Technique for titanium dioxide ( TiO2) and zinc oxide (ZnO) nanocomposite. The morphology and optical properties of the synthesized nanocomposite were examined using a transmission electron microscope ( TEM) and UV-Visible spectroscopy. The structure of the synthesized nanocomposite was proved using X-ray Diffraction(XRD). The particle size of the ZnO/TiO2 nanocomposites was found to be range between 11 to 27.37 nm. The product of TEM has proof of the inclusion in the ZnO matrix of spherical TiO2particles. Also found were TiO2 sections attached to the ZnO-like rodlike particles., the ZnO/TiO2 Nanocomposites had better optical absorbing properties. The nanocomposite has been used to create a new photosensitizer solar cell with the efficiency of energy conversion of approximately 4.6%, using (E)-ethyl 4- ((4-nitrobenzylidene)) aminobenzoate as organic photo-sensitized (OPS) by (ITO/TiO2\ZnO nanocomposite/POS/iodine/silver (Ag) nanofilm/ITO).
- 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
- ItemElectrocatalytic Reduction of CO2 to Acetic Acid by a Molecular Manganese Corrole Complex(Weinheim : Wiley-VCH, 2020) De, Ratnadip; Gonglach, Sabrina; Paul, Shounik; Haas, Michael; Sreejith, S.S.; Gerschel, Philipp; Apfel, Ulf-Peter; Vuong, Thanh Huyen; Rabeah, Jabor; Roy, Soumyajit; Schöfberger, WolfgangThe controlled electrochemical reduction of carbon dioxide to value added chemicals is an important strategy in terms of renewable energy technologies. Therefore, the development of efficient and stable catalysts in an aqueous environment is of great importance. In this context, we focused on synthesizing and studying a molecular MnIII-corrole complex, which is modified on the three meso-positions with polyethylene glycol moieties for direct and selective production of acetic acid from CO2. Electrochemical reduction of MnIII leads to an electroactive MnII species, which binds CO2 and stabilizes the reduced intermediates. This catalyst allows to electrochemically reduce CO2 to acetic acid in a moderate acidic aqueous medium (pH 6) with a selectivity of 63 % and a turn over frequency (TOF) of 8.25 h−1, when immobilized on a carbon paper (CP) electrode. In terms of high selectivity towards acetate, we propose the formation and reduction of an oxalate type intermediate, stabilized at the MnIII-corrole center. © 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
- ItemHighly Efficient and Atom Economic Route for the Production of Methyl Acrylate and Acetic Acid from a Biorefinery Side Stream(Washington, DC : American Chemical Society, 2020) El Ouahabi F.; Polyakov M.; Van Klink G.P.M.; Wohlrab S.; Tin S.; De Vries J.G.We report a highly efficient and 100% atom economic synthesis of methyl acrylate and acetic acid via gas phase pyrolysis of methyl 3-acetoxypropionate at 600 °C. The latter can be produced in a single step from methyl levulinate, a side product of Avantium's FDCA process. Copyright © 2020 American Chemical Society.
- ItemSelective Construction of C−C and C=C Bonds by Manganese Catalyzed Coupling of Alcohols with Phosphorus Ylides(Weinheim : Wiley-VCH Verlag, 2020) Liu X.; Werner T.Herein, we report the manganese catalyzed coupling of alcohols with phosphorus ylides. The selectivity in the coupling of primary alcohols with phosphorus ylides to form carbon-carbon single (C−C) and carbon-carbon double (C=C) bonds can be controlled by the ligands. In the conversion of more challenging secondary alcohols with phosphorus ylides the selectivity towards the formation of C−C vs. C=C bonds can be controlled by the reaction conditions, namely the amount of base. The scope and limitations of the coupling reactions were thoroughly evaluated by the conversion of 21 alcohols and 15 ylides. Notably, compared to existing methods, which are based on precious metal complexes as catalysts, the present catalytic system is based on earth abundant manganese catalysts. The reaction can also be performed in a sequential one-pot reaction generating the phosphorus ylide in situ followed manganese catalyzed C−C and C=C bond formation. Mechanistic studies suggest that the C−C bond was generated via a borrowing hydrogen pathway and the C=C bond formation followed an acceptorless dehydrogenative coupling pathway. (Figure presented.). © 2020 The Authors. Advanced Synthesis & Catalysis published by Wiley-VCH GmbH
- ItemIncreasing the efficiency of optimized v-sba-15 catalysts in the selective oxidation of methane to formaldehyde by artificial neural network modelling(Basel : MDPI, 2020) Kunkel, Benny; Kabelitz, Anke; Buzanich, Ana Guilherme; Wohlrab, SebastianThe present study investigates the possibility of improving the selective oxidation of methane to formaldehyde over V-SBA-15 catalysts in two different ways. In a classical approach of catalyst optimization, the in situ synthesis of V-SBA-15 catalysts was optimized with regard to the applied pH value. Among the set of catalysts synthesized, a higher amount of incorporated vanadium, a higher content of polymeric VOx species as well as a less ordered structure of the support material were observed by increasing the pH values from 2.0 to 3.0. An optimum in performance during the selective oxidation of methane to formaldehyde with respect to activity and selectivity was found over V-SBA-15 prepared at a pH value of 2.5. With this knowledge, we have now evaluated the possibilities of reaction control using this catalyst. Specifically, artificial neural network modelling was applied after the collection of 232 training samples for obtaining insight into the influence of different reaction parameters (temperature; gas hourly space velocity (GHSV); and concentration of O2, N2 and H2O) onto methane conversion and selectivity towards formaldehyde. This optimization of reaction conditions resulted in an outstanding high space-time yield of 13.6 kgCH2O·kgcat·h−1. © 2020 by the authors. Licensee MDPI, Basel, Switzerland.
- ItemPlasma-Assisted Immobilization of a Phosphonium Salt and Its Use as a Catalyst in the Valorization of CO2(Weinheim : Wiley-VCH, 2020) Hu, Yuya; Peglow, Sandra; Longwitz, Lars; Frank, Marcus; Epping, Jan Dirk; Breser, Volker; Werner, ThomasThe first plasma-assisted immobilization of an organocatalyst, namely a bifunctional phosphonium salt in an amorphous hydrogenated carbon coating, is reported. This method makes the requirement for prefunctionalized supports redundant. The immobilized catalyst was characterized by solid-state 13C and 31P NMR spectroscopy, SEM, and energy-dispersive X-ray spectroscopy. The immobilized catalyst (1 mol %) was employed in the synthesis of cyclic carbonates from epoxides and CO2. Notably, the efficiency of the plasma-treated catalyst on SiO2 was higher than those of the SiO2 support impregnated with the catalyst and even the homogeneous counterpart. After optimization of the reaction conditions, 13 terminal and four internal epoxides were converted with CO2 to the respective cyclic carbonates in yields of up to 99 %. Furthermore, the possibility to recycle the immobilized catalyst was evaluated. Even though the catalyst could be reused, the yields gradually decreased from the third run. However, this is the first example of the recycling of a plasma-immobilized catalyst, which opens new possibilities in the recovery and reuse of catalysts. © 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.