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Journal articles on the topic 'Herrmann’s Catalyst'

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1

Bourouina, Amine, Alexis Oswald, Valentin Lido, et al. "Kinetic Study of the Herrmann–Beller Palladacycle-Catalyzed Suzuki–Miyaura Coupling of 4-Iodoacetophenone and Phenylboronic Acid." Catalysts 10, no. 9 (2020): 989. http://dx.doi.org/10.3390/catal10090989.

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This article presents an experimental kinetic study of the Suzuki–Miyaura reaction of 4-iodoacetophenone with phenylboronic acid catalyzed by the Herrmann–Beller palladacycle. This catalyst, together with the solvent (ethanol) and the base (sodium methylate), were chosen to ensure catalyst stability and reactants solubility all along the reaction. Based on the study of initial reaction rates, a quasi-first-order was found for 4-iodoacetophenone with a first-order dependence on the initial concentration of palladium. A zero-order was found for the base and the phenylboronic acid. The oxidative
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2

Krause, Jens O, Said Lubbad, Oskar Nuyken, and Michael R Buchmeiser. "Monolith- and Silica-Supported Carboxylate-Based Grubbs–Herrmann-Type Metathesis Catalysts." Advanced Synthesis & Catalysis 345, no. 8 (2003): 996–1004. http://dx.doi.org/10.1002/adsc.200303037.

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3

Tkatchenko, Igor. "Book Review: Applied Homogeneous Catalysis with Organometallic Compounds. Vols. 1–3. 2nd. Edition. Edited by Boy Cornils and Wolfgang A. Herrmann." Angewandte Chemie International Edition 41, no. 23 (2002): 4586–87. http://dx.doi.org/10.1002/1521-3773(20021202)41:23<4586::aid-anie4586>3.0.co;2-8.

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4

Walter, Olaf. "Multiphase Homogeneous Catalysis. Edited by B. Cornils, W. A. Herrmann, I. T. Horváth, W. Leitner, S. Mecking, H. Olivier-Bourbigou and D. Vogt." Angewandte Chemie International Edition 45, no. 13 (2006): 2005. http://dx.doi.org/10.1002/anie.200585366.

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5

Heinrich, Lothar. "Book Review: Catalysis from A to Z. A Concise Encyclopedia. Edited by Boy Cornils, W. A. Herrmann, R. Schlögl and Ch.-H. Wong." Angewandte Chemie International Edition 40, no. 9 (2001): 1785. http://dx.doi.org/10.1002/1521-3773(20010504)40:9<1785::aid-anie17851>3.0.co;2-5.

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6

Baker, R. Tom. "B. Cornils, W. A. Herrmann, I. T. Horváth, W. Leitner, S. Mecking, H. Olivier-Bourbigou, D. Vogt: Multiphase Homogeneous Catalysis." Advanced Synthesis & Catalysis 349, no. 3 (2007): 469–70. http://dx.doi.org/10.1002/adsc.200600490.

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7

Centi, Gabriele. "Catalysis from A to Z. A Concise Encyclopedia. Vols. 1–3, 3rd ed. Edited by Boy Cornils, Wolfgang A. Herrmann, Martin Muhler and Chi-Huey Wong." Angewandte Chemie International Edition 47, no. 9 (2008): 1547–48. http://dx.doi.org/10.1002/anie.200785548.

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8

Tkatchenko, Igor. "Book Review: The Success Story of Organometallic Chemistry!: Applied Homogeneous Catalysis with Organometallic Compounds. A Comprehensive Handbook.(Volumes 1 and 2). Edited by B. Cornils and W. A. Herrmann." Angewandte Chemie International Edition in English 36, no. 1314 (1997): 1547–49. http://dx.doi.org/10.1002/anie.199715471.

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9

Drießen-Hölscher, Birgit. "Umfassende Übersicht zur Organometall-Katalyse in Wasser: Aqueous-Phase Organometallic Catalyis - Concepts and Applications. Hrsg. von B. Cornils und W. A. Herrmann. Wiley-VCH, Weinheim, 1998. 306 S., geb., 398- DM. ISBN 3-527-29478-3." Nachrichten aus Chemie, Technik und Laboratorium 47, no. 5 (1999): 572. http://dx.doi.org/10.1002/nadc.19990470524.

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10

Jones, Richard A. "Applied Homogeneous Catalysis with Organometallic Compounds: A Comprehensive Handbook in Three Volumes. Second, Completely Revised and Enlarged Edition Edited by Boy Cornils (Hofheim, Germany) and Wolfgang A. Herrmann (Universität München). Wiley-VCH: Weinheim. 2002. 1450 pp. $520.00. ISBN 3-527-30434-7." Journal of the American Chemical Society 125, no. 21 (2003): 6598. http://dx.doi.org/10.1021/ja0252936.

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11

Atwood, Jim D. "Multiphase Homogeneous Catalysis: Volumes 1−2 Edited by Boy Cornils (Hofheim, Germany), Wolfgang A. Herrmann (Universität München, Germany), Istvan T. Horvath (Eötvös University, Hungary), Walter Leitner (RWTH, Aachen, Germany), Stefan Mecking (Universität Konstanz, Germany), Hélène Olivier-Bourbigou (Institut Français du Pétrole, Vernaison, France), and Dieter Vogt (Eindhoven University of Technology, the Netherlands). Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim. 2005. xxxiv + xxxiv + 872 pp. $385.00. ISBN 3-527-30721-4." Journal of the American Chemical Society 128, no. 28 (2006): 9258. http://dx.doi.org/10.1021/ja0598762.

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12

"Carl Duisberg Plaque: R. Zellner / Karl Wamsler Award: W. A. Herrmann / Primo Levi Award: V. Balzani." Angewandte Chemie International Edition 58, no. 52 (2019): 18743. http://dx.doi.org/10.1002/anie.201915178.

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13

"Catalysis from A to Z: A Concise Encyclopedia. Second, Completely Revised, and Enlarged Edition Edited by Boy Cornils (Hofheim, Germany), Wolfgang A. Herrmann (Technical University of Munich), R. Schlögl (Fritz-Haber-Institute of the Max-Planck Society, Berlin), and Chi-Huey Wong (The Scripps Research Institute, La Jolla, CA). Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim. 2003. xxii + 840 pp. $145.00. ISBN: 3-527-30373-1." Journal of the American Chemical Society 126, no. 22 (2004): 7153. http://dx.doi.org/10.1021/ja0336628.

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14

"Catalysis from A to Z: A Concise Encyclopedia, Volumes 1−3, Completely Revised and Enlarged 3rd ed Edited by Boy Cornils (Hofheim, Germany), Wolfgang A. Herrmann (Technische Universität München, Germany), Martin Muhler (Ruhr-Universität, Bochum, Germany), and Chi-Huey Wong (Scripps Research Institute, La Jolla, CA). Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim. 2007. 1560 pp. $560.00. ISBN 978-3-527-31438-6." Journal of the American Chemical Society 129, no. 32 (2007): 10043. http://dx.doi.org/10.1021/ja076972p.

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15

Ha, Nguyen Van, Doan Thanh Dat, and Trieu Thi Nguyet. "Stereoelectronic Properties of 1,2,4-Triazole-Derived N-heterocyclic Carbenes - A Theoretical Study." VNU Journal of Science: Natural Sciences and Technology 35, no. 4 (2019). http://dx.doi.org/10.25073/2588-1140/vnunst.4935.

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A theoretical study on stereo and electronic properties of a series of six 1,2,4-triazole-derived carbenes bearing different N4-substituents, namely isopropyl (1), benzyl (2), phenyl (3), mesityl (4), 2,6-diisopropylphenyl (5) and 1-naphthyl (6), has been carried out. Structures of the six carbenes were first optimized using Gaussian® 16 at B3LYP level. Their molecular geometries and electronic structures of the frontier orbitals were examined. The results suggest the similarity in nature of their HOMOs, which all posses s symmetry with respect to the heterocycle and essentially be the lone el
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