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Thieme Chemistry SYNFORM A63
People,SYNFORM Trends and Views in Synthetic Organic Chemistry 2007/06 SYNSTORIES New Catalytic Transformati- ons – On the Way to Snapshot of a Chemical Reac- Reactions Dream “ tion Intermediate Using a Syn- ” thetic Receptor Enantiocatalysis in Water Direct Synthesis of Amides (and H 2) from Alcohols and Amines This document was downloaded for personal use only. Unauthorized distribution is strictly prohibited. CONTACT Your opinion about SYNFORM is welcome, please correspond if you like: [email protected] Thieme Chemistry SYNFORM A63 Dear readers, IN THIS ISSUE The “41st World Chemistry Congress” of the International Union of Pure and SYNSTORIES Applied Chemistry (IUPAC) was held on August 5–11, 2007, in Turin New Catalytic Transformations (Italy). The congress venue was the Dream Reactions “ On the Way to former FIAT cars factory “Lingotto . .– . Conference Center” which is a modern and functional struc- ” ture that hosts concert halls, a theatre, a convention center, Enantiocatalysis in Water A64 shopping arcades and hotels. The “Gianni Agnelli” Audito- . rium, that can accommodate more than 2000 people, hosted Direct Synthesis of Amides (and H A66 the lectures of three Nobel Awardees and the play and Amines . 2. ). from. .Alcohols . “Should’ve” authored by Professor Roald Hoffmann. A rich and multidisciplinary program of lectures and posters was A68 distributed among the many lecture halls of the “Lingotto”. The conference was very well organized and scientifically very stimulating: it’s a pity that the attendance to the lec- tures has been often rather modest, at least according to my experience. Two remarkable lectures presented at the IUPAC conference are covered and analyzed in this issue of SYNFORM : one by Professor Lukas J. -
David Milstein CURRICULUM VITAE Education B.Sc. with Distinction
David Milstein CURRICULUM VITAE Education B.Sc. with distinction, Hebrew University of Jerusalem, 1968 M.Sc. with distinction, Hebrew University of Jerusalem, 1969 Ph.D. Summa Cum Laude, Hebrew University of Jerusalem, 1976. Mentor: Prof. J. Blum Employment 1977-8 Post-doctoral Fellow, Colorado State University and University of Iowa, U.S.A. (with Prof. J. K. Stille). Discovery of the Stille Reaction 1979-1982 Senior Research Chemist, Central Research and Development Department, DuPont Co., Wilmington, De. U.S.A. 1983-1986 Group Leader, Central Research and Development Department, DuPont Co., Wilmington, De. U.S.A 1987-1992 Associate Professor, Department of Organic Chemistry, The Weizmann Institute of Science 1993- Full Professor, Department of Organic Chemistry, The Weizmann Institute of Science 1996- 2005 Head, Department of Organic Chemistry, The Weizmann Institute of Science 2000- Head, The Kimmel Center for Molecular Design, The Weizmann Institute of Science Honors and Awards Elected to The Israel Academy of Sciences and Humanities, 2012 The 2012 Israel Prize (The highest honor of the State of Israel, awarded by Israel’s President) in chemistry and physics Meitner Humboldt Senior Research Award, from the Alexander von Humboldt Foundation, 2011 Sir Geoffrey Wilkinson Award, by the Royal Society of Chemistry 2010 Fellow of the Royal Society of Chemistry, 2010 ERC advanced grant (2 million Euro), 2009 The American Chemical Society National Award in Organometallic Chemistry, 2007 Research cited by Science among the top major scientific breakthroughs of the year 2007 (discovery of a new reaction (amidation)). The Israel Chemical Society Prize, 2006 Elected to the German National Academy of Sciences (Leopoldina), 2006 Member, Miller Institute for Basic Research in Science, UC Berkeley, since 2006 The I.M. -
Plenary Lecture
Plenary Lecture Time Room Name Affiliation Title Kyoto University and Emory University, Japan and Theory can Provide Insights Unavailable from Experiments PL1 4(SUN) 17:00 A Prof. Keiji MOROKUMA USA in Catalysis Bridging Heterogeneous and Homogeneous Catalysis using PL2 5(MON) 10:30 A Prof. Gabor A. SOMORJAI University of California, Berkeley, USA Supported 10-50 Atom Size Metal Nanoparticles Ruthenium Catalyzed processes from Carbenes to C-H PL3 6 (TUE) 9:00 A Prof. Pierre DIXNEUF University of Rennes, France Bond Functionalizations Discovery of Sustainable Catalytic Reactions Based on PL4 6 (TUE) 13:30 A Prof David MILSTEIN Weizmann Institute of Science, Israel Pincer Complexes PL5 7 (WED) 9:00 A Prof. Krzysztof MATYJASZEWSKCarnegie Mellon University, USA Catalysis in Radical Polymerization Fritz-Haber Institute of the Max-Planck Society, Model Studies on Heterogeneous Catalysis at the Atomic PL6 8 (THU) 9:00 A Prof. Hans-J. FREUND Germany Scale Controlled Functionalization of Surfaces to Access to Well- PL7 8 (THU) 13:30 A Prof. Christophe COPERET ETH Zurich, Switzerland defined Supported Nanoparticles and Single-site Catalysts. Keynote Lecture Time Room Name affiliation Title Utrecht University, Debye Institute for Nanomaterials Bridging Homogeneous and Heterogeneous Catalysis for KN1 5(MON) 13:30 A Prof. Bert WECKHUYSEN Science, The Netherlands Advancing the Field of Catalytic Biomass Valorization Design of Highly Functionalized Polyoxometalte-based KN2 5(MON) 15:10 B Prof. Noritaka MIZUNO The University of Tokyo, Japan Catalysts: From Molecular to Solid Catalysts Space-resolved XAFS Characterization of Heterogeneous KN3 6 (TUE) 10:10 A Prof. Mizuki TADA Nagoya Unversity, Japan Catalysts Turning Dihydrogen into a Highly Versatile Reagent Department of Organic Chemistry KN4 6 (TUE) 11:30 B Prof. -
Jahresbericht 2017
Jahresbericht Die GDCh vor Ort 2017 Ehrungen Studium 2 GDCh Jahresbericht 2017 Inhalt Präsidium und Vorstand 2017 3 Mitgliederentwicklung Mehr berufstätige Chemiker in der GDCh 30 Vorwort 4 Ausbildung, Fortbildung und Karriere II Stimmen Schule: Begeisterung im Klassenzimmer 31 Gemeinsam stark in die Zukunft 6 Fortbildung: Impulse für die Karriere 32 Aktivitäten und Kooperationen Netzwerke, Strukturen, Tagungen Weltweit wertgeschätzt 8 Fachgruppen: Themengestalter und Netzwerkpartner 34 Preise und Auszeichnungen Ortsverbände: Chemie vor Ort erleben 38 Preise: In den Fußstapfen großer Vorbilder 11 JungChemikerForum: Stiftungen: Ein Vermögen für die Forschung 15 Herzlichen Glückwunsch, JCF! 40 Ausbildung, Fortbildung und Karriere I Wissenschaftliche Publikationen Karriereservice und Stellenmarkt: GDCh-Fachzeitschriften: Ratschläge mit Tradition 17 The Same and Not the Same 42 A week celebrating 150 years Rechnungslegung of Chemical Societies in Germany 19 Auch im Jubiläumsjahr finanziell gut aufgestellt 46 Impressum Herausgeber und Verleger: © Gesellschaft Deutscher Chemiker e.V., Autoren, Redaktion und Herausgeber übernehmen keine Verantwor- Postfach 900440, D-60444 Frankfurt am Main, Tel.: 069 7917–0, tung für die Richtigkeit von Angaben, Hinweisen und Ratschlägen Fax: 069 7917–307, E-Mail: [email protected] sowie für Druckfehler. Alle Beiträge sind urheberrechtlich geschützt. Alle Rechte, insbeson- dere die der Übersetzung, sind vorbehalten. Kein Teil dieses Berichts Verantwortlich für den redaktionellen Inhalt: darf ohne schriftliche Zustimmung des Herausgebers in irgendeiner Prof. Dr. Wolfram Koch Form reproduziert oder in eine von Maschinen verwendbare Sprache Koordination: Christiane Dörr übertragen oder übersetzt werden. Redaktion: Dr. Brigitte Osterath Die Wiedergabe von Gebrauchsnamen, Warenbezeichnungen und Übersetzung englischsprachiger Teil: Dagmar Breitenbach ähnlichen Angaben berechtigt nicht zu der Annahme, dass solche Druckerei: Bastian Druck GmbH, Föhren Namen ohne weiteres von jedermann benutzt werden dürfen. -
Annual Report 2009
vol. 32 no. 2 annual report 2009 The Magazine of The University of Massachusetts Medical School Expanding our Reach L., the plural of life The name of this magazine encompasses the lives of those who make up the University of Massachusetts Medical School community, for which it is published. They are students, faculty, staff, alumni, volunteers, benefactors and others who aspire to help this campus achieve national distinction in education, research and public service. UMass Medical School’s mission is to advance the health and well-being of the people in the commonwealth and the world through pioneering advances in education, research, and health care delivery. As you read about this dynamic community, you’ll frequently come across references to partners and programs of UMass Medical School (UMMS), the Commonwealth of Massachusetts’ only public medical school, educating physicians, scientists and advanced practice nurses to heal, discover, teach and care, compassionately. Commonwealth Medicine UMass Medical School’s innovative public service division that assists state agencies and health care organizations to enhance the value and quality of expenditures and improve access and delivery of care for at-risk and uninsured populations. www.umassmed.edu/commed The Research Enterprise UMass Medical School’s world-class investigators, who make discoveries in basic science and clinical research and attract more than $242 million in funding annually. UMass Medical School/UMass Memorial Development Office The department that supports the academic and research enterprises of UMass Medical School and the clinical initiatives of UMass Memorial Health Care by forming vital partnerships between contributors and health care professionals, educators and researchers. -
Seminar Program
2012 Seminar Program Sponsored by Av. Països Catalans, 16, Campus Sescelades (St. Pere i St. Pau), Tarragona. Tel. 977920200 Discovery of Catalytic Reactions For Sustainable Chemistry Prof. David Milstein The Weizmann Institute of Science (Israel) Thursday 18th October, 2012. ICIQ Auditorium, 12 p.m. Professional career David Milstein received his Ph.D. degree at the Hebrew University of Jerusalem in 1976 with Prof Blum. He carried out postdoctoral at Colorado State University, where together with his advisor, John Stille, he discovered the Stille Reaction. In 1979 he joined the DuPont Company in Wilmington, Delaware, where he became a Group Leader in the homogeneous catalysis area. In 1987 he accepted a professorial appointment at the Weizmann Institute of Science, where he was Head of the Department of Organic Chemistry in 1996-2005. In 2000 he became Head of the Kimmel Center for Molecular Design. He is the Israel Matz Professor of Organic Chemistry since 1996. His research interests focus on the development of fundamental organometallic chemistry, particularly the activation of strong bonds, and its application to the design and implementation of new environmentally benign processes catalyzed by transition metal complexes. Awards Awards received by DM include: the Kolthoff Prize by the Technion (2002), the Israel Chemical Society Prize (2006), the Miller Professorship, UC Berkeley (2006); the ACS Award in Organometallic Chemistry (2007); the RSC Sir Geoffrey Wilkinson Award (2010); the Humboldt Senior Award (2011); and the Israel Prize (2012, Israel’s highest honor). DM was elected to the German National Academy of Sciences-Leopoldina (in 2006) and to the Israel National Academy of Sciences and Humanities (in 2012). -
By Prof. David Milstein
IAS Distinguished Lecture Design and Applications of Catalytic Reactions for Sustainable Synthesis and Energy ProfessorProfessor DavidDavid MilsteinMilstein The Israel Matz Professorial Chair of Organic Chemistry Department of Organic Chemistry The Weizmann Institute of Science, Israel Date : 23 January 2019 (Wednesday) Time : 4:30pm – 6:00pm ( ) Venue : Connie Fan Multi-media Conference Room, 4/F, Cheng Yick-chi Building City University of Hong Kong AbstractAbstract The design of ”green” synthetic methodology and new approaches to sustainable energy are major goals of modern catalysis. Traditionally, catalysis by metal complexes has been based on the reactivity of the metal center, while the ligands bound to it influence its reactivity, but do not interact directly with the substrate. In a major advance in homogeneous catalysis, complexes based on “cooperating” ligands were developed, in which both the metal and ligand undergo bond making and breaking in key steps of the catalytic cycle, thus providing exciting opportunities for catalytic design. We have developed a new mode of metal-ligand cooperation, involving ligand aromatization – dearomatization, which provides a new approach to the activation of chemical bonds. Pincer-type complexes of several transition metals exhibit such cooperation, including complexes of Ru, Fe, Co, Rh, Ir, Ni, Pd, Pt, Mn and Re. This has led to fundamentally new, environmentally benign catalytic reactions, including several reactions which either produce dihydrogen or consume it. Synthetic and energy-relaed applications based on these reactions will be described. BiographyBiography David Milstein is the Israel Matz Professor of Chemistry at the Weizmann Institute of Science in Israel. He received a Ph.D. degree at the Hebrew University in Israel in 1976 with Prof. -
Synthesis of Oxalamides by Acceptorless Dehydrogenative Coupling of Ethylene Glycol and Cite This: Chem
Chemical Science View Article Online EDGE ARTICLE View Journal | View Issue Synthesis of oxalamides by acceptorless dehydrogenative coupling of ethylene glycol and Cite this: Chem. Sci., 2020, 11,7188 All publication charges for this article amines and the reverse hydrogenation catalyzed by have been paid for by the Royal Society † of Chemistry ruthenium You-Quan Zou, ‡§a Quan-Quan Zhou,‡a Yael Diskin-Posner, b Yehoshoa Ben- Davida and David Milstein *a A sustainable, new synthesis of oxalamides, by acceptorless dehydrogenative coupling of ethylene glycol Received 9th April 2020 with amines, generating H , homogeneously catalyzed by a ruthenium pincer complex, is presented. The Accepted 20th June 2020 2 reverse hydrogenation reaction is also accomplished using the same catalyst. A plausible reaction DOI: 10.1039/d0sc02065f mechanism is proposed based on stoichiometric reactions, NMR studies, X-ray crystallography as well as rsc.li/chemical-science observation of plausible intermediates. Creative Commons Attribution-NonCommercial 3.0 Unported Licence. Introduction desirable and remains an important goal both in chemical and pharmaceutical industries. Oxalamide skeletons are prevalent in many biologically active In 2007, we reported the ruthenium catalyzed dehydro- molecules and pharmaceuticals, such as Lixiana (1, Fig. 1), genative coupling of alcohols with amines leading to the 1 widely used as an anticoagulant. Oxalamide 2 shows promising environmentally benign synthesis of amides with H2 libera- 8 9a antiviral activity of entry inhibitors targeting the CD4-binding tion as the sole byproduct (Fig. 2b). Guan's group and our b site of HIV-1.2 Additionally, oxalamides are employed as robust group9 also demonstrated the ruthenium pincer complex ligands in copper catalyzed cross coupling reactions (e.g., oxa- catalyzed dehydrogenative coupling of diols and diamines, to This article is licensed under a lamides 3–5).3 Besides these, oxalamides are also popular in form polyamides. -
Kar 2020 ACSC Hydrogenatio
This is an open access article published under a Creative Commons Attribution (CC-BY) License, which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. pubs.acs.org/acscatalysis Letter Selective Room-Temperature Hydrogenation of Amides to Amines and Alcohols Catalyzed by a Ruthenium Pincer Complex and Mechanistic Insight Sayan Kar, Michael Rauch, Amit Kumar, Gregory Leitus, Yehoshoa Ben-David, and David Milstein* Cite This: ACS Catal. 2020, 10, 5511−5515 Read Online ACCESS Metrics & More Article Recommendations *sı Supporting Information ABSTRACT: We report a room-temperature protocol for the hydro- genation of various amides to produce amines and alcohols. Compared with most previous reports for this transformation, which use high − ° − temperatures (typically, 100 200 C) and H2 pressures (10 100 bar), this system proceeds under extremely mild conditions (RT, 5−10 bar of fi H2). The hydrogenation is catalyzed by well-de ned ruthenium-PNNH pincer complexes (0.5 mol %) with potential dual modes of metal−ligand cooperation. An unusual Ru-amidate complex was formed and crystallo- graphically characterized. Mechanistic investigations indicate that the room-temperature hydrogenation proceeds predominantly via the Ru−N amido/amine metal−ligand cooperation. KEYWORDS: amide, hydrogenation, metal−ligand cooperation, ruthenium-pincer, room-temperature, ruthenium amidate complex eduction of the amide group has useful applications in of amide hydrogenation with C−N bond cleavage appeared in R diverse areas of chemical transformations including 20106a followed by reports of several other research groups.6 synthesis of amines, alcohols, peptide chemistry, total syn- Hydrogenation and dehydrogenative formation of the amide 1,2 thesis, CO2 recycling, and others. -
Cooperation and Discrimination in Academic Publishing
COOPERATION AND DISCRIMINATION IN ACADEMIC PUBLISHING A thesis submitted for the degree of Doctor of Philosophy by Boontarika Paphawasit Department of Economics and Finance College of Business, Arts and Social Sciences Brunel University London, UK June 2017 ABSTRACT This thesis consists of four essays in collaboration and discrimination. The first essay examines the role of collaboration as a determinant of publication productivity in the field of economics, measured by means of citations, journal rank, and journal impact factor. The analysis employs cross-sectional data of 1,512 journal publications published in 2012 in 16 economics journals. The findings show a positive effect of team size on publication productivity, whereas research teams consisting of only one gender perform better in terms of research quality than gender-mixed teams. The analysis also indicates a negative relationship between female-dominated teams and research productivity. The second essay examines the impact of physical attractiveness on productivity. As literature found a strong impact on wages and career progression, it can be either due to discrimination in favour of good-looking people or can reflect an association between attractiveness and productivity. We utilise a context of academic publishing where there is no or limited face-to-face interaction. Using data on 2,800 authors, the results suggest that physical attractiveness has significantly important benefits. The third essay also considers the effect of physical attractiveness, as assessed based on pictures of top scientists, on their probability of winning the Nobel Prize. In contrast, the results show that attractiveness is negatively correlated with the probability of being awarded the Nobel, with the magnitude of this effect being not negligible. -
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SynformPeople, Trends and Views in Chemical Synthesis 2019/01 Approaching Sub-ppm-Level Asymmetric Organocatalysis of a Highly Challenging and Scalable Carbon–Carbon Bond-Forming Reaction Highlighted article by H. Y. Bae, D. Höfler, P. S. J. Kaib, P. Kasaplar, C. K. De, A. Döhring, S. Lee, K. Kaupmees, I. Leito, B. List This document was downloaded for personal use only. Unauthorized distribution is strictly prohibited. Contact Your opinion about Synform is welcome, please correspond if you like: [email protected] Thieme A2 Synform Dear Readers, First of all, Happy New Year! In this issue At the beginning of every year there is a “trend” going Editorial Board Focus on in magazines, newspapers and the online marketing Trends in Organic Synthesis .................................. A3 community: asking a number of experts about the Literature Coverage upcoming trends in the New Year and beyond. As these Exploring the Performance of Nanostructured Reagents articles are very popular, we thought we could apply with Organic-Group-Defined Morphology in Cross- the same concept to our beloved field of chemistry and Coupling Reaction. A5 ask our Editors for their opinion on the hottest trends Literature Coverage or topics in organic synthesis. Answers from a few of us Approaching Sub-ppm-Level Asymmetric Organo- can be found in the first article of this year. catalysis of a Highly Challenging and Scalable Carbon– Carbon Bond-Forming Reaction ............................. A8 I hope you like the idea, which – I have to confess – Literature Coverage is not mine but comes from our creative Marketing Acceptorless Dehydrogenative Coupling Using Ammonia: Associate Evelyn Hosner. -
Hydrogenative Depolymerization of Nylons
This is an open access article published under a Creative Commons Attribution (CC-BY) License, which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. pubs.acs.org/JACS Article Hydrogenative Depolymerization of Nylons Amit Kumar, Niklas von Wolff, Michael Rauch, You-Quan Zou, Guy Shmul, Yehoshoa Ben-David, Gregory Leitus, Liat Avram, and David Milstein* Cite This: https://dx.doi.org/10.1021/jacs.0c05675 Read Online ACCESS Metrics & More Article Recommendations *sı Supporting Information ABSTRACT: The widespread crisis of plastic pollution demands discovery of new and sustainable approaches to degrade robust plastics such as nylons. Using a green and sustainable approach based on hydrogenation, in the presence of a ruthenium ° fi pincer catalyst at 150 C and 70 bar H2, we report here the rst example of hydrogenative depolymerization of conventional, widely used nylons and polyamides, in general. Under the same catalytic conditions, we also demonstrate the hydrogenation of a polyurethane to produce diol, diamine, and methanol. Additionally, we demonstrate an example where monomers (and oligomers) obtained from the hydrogenation process can be dehydrogenated back to a poly(oligo)amide of approximately similar molecular weight, thus completing a closed loop cycle for recycling of polyamides. Based on the experimental and density functional theory studies, we propose a catalytic cycle for the process that is facilitated by metal−ligand cooperativity. Overall, this unprecedented trans-