TY - JOUR A1 - Tiedemann, Ralph A1 - Schneider, Anja R. R. A1 - Havenstein, Katja A1 - Blanck, Torsten A1 - Meier, Elmar A1 - Raffel, Martina A1 - Zwartepoorte, Henk A1 - Plath, Martin T1 - New microsatellite markers allow high-resolution taxon delimitation in critically endangered Asian box turtles, genus Cuora JF - Salamandra : German journal of herpetology N2 - We isolated and characterized 16 new di- and tetranudeotide microsatellite markers for the critically endangered Asian box turtle genus Cuora, focusing on the "Cuora trifasciata" species complex. The new markers were then used to analyse genetic variability and divergence amongst five described species within this complex, namely C. aurocapitata (n = 18), C. cyclornata (n = 31), C. pani (n = 6), C. trifasciata (n = 58), and C. zhoui (n = 7). Our results support the view that all five species represent valid taxa. Within two species (C. trifasciata and C. cyclornata), two distinct morphotypes were corroborated by microsatellite divergence. For three individuals, morphologically identified as being of hybrid origin, the hybrid status was confirmed by our genetic analysis. Our results confirm the controversial species (Cuora aurocapitata, C. cyclornata) and subspecies/morphotypes (C. cyclornata meieri, C. trifasciata cf. trifasciata) to be genetically distinct, which has critical implications for conservation strategies. KW - Testudines KW - Cuora KW - box turtles KW - captive breeding KW - conservation units KW - microsatellites Y1 - 2014 SN - 0036-3375 VL - 50 IS - 3 SP - 139 EP - 146 PB - Deutsche Gesellschaft für Herpetologie und Terrarienkunde CY - Darmstadt ER - TY - JOUR A1 - Hetenyi, Gyorgy A1 - Molinari, Irene A1 - Clinton, John A1 - Bokelmann, Gotz A1 - Bondar, Istvan A1 - Crawford, Wayne C. A1 - Dessa, Jean-Xavier A1 - Doubre, Cecile A1 - Friederich, Wolfgang A1 - Fuchs, Florian A1 - Giardini, Domenico A1 - Graczer, Zoltan A1 - Handy, Mark R. A1 - Herak, Marijan A1 - Jia, Yan A1 - Kissling, Edi A1 - Kopp, Heidrun A1 - Korn, Michael A1 - Margheriti, Lucia A1 - Meier, Thomas A1 - Mucciarelli, Marco A1 - Paul, Anne A1 - Pesaresi, Damiano A1 - Piromallo, Claudia A1 - Plenefisch, Thomas A1 - Plomerova, Jaroslava A1 - Ritter, Joachim A1 - Rumpker, Georg A1 - Sipka, Vesna A1 - Spallarossa, Daniele A1 - Thomas, Christine A1 - Tilmann, Frederik A1 - Wassermann, Joachim A1 - Weber, Michael A1 - Weber, Zoltan A1 - Wesztergom, Viktor A1 - Zivcic, Mladen A1 - Abreu, Rafael A1 - Allegretti, Ivo A1 - Apoloner, Maria-Theresia A1 - Aubert, Coralie A1 - Besancon, Simon A1 - de Berc, Maxime Bes A1 - Brunel, Didier A1 - Capello, Marco A1 - Carman, Martina A1 - Cavaliere, Adriano A1 - Cheze, Jerome A1 - Chiarabba, Claudio A1 - Cougoulat, Glenn A1 - Cristiano, Luigia A1 - Czifra, Tibor A1 - Danesi, Stefania A1 - Daniel, Romuald A1 - Dannowski, Anke A1 - Dasovic, Iva A1 - Deschamps, Anne A1 - Egdorf, Sven A1 - Fiket, Tomislav A1 - Fischer, Kasper A1 - Funke, Sigward A1 - Govoni, Aladino A1 - Groschl, Gidera A1 - Heimers, Stefan A1 - Heit, Ben A1 - Herak, Davorka A1 - Huber, Johann A1 - Jaric, Dejan A1 - Jedlicka, Petr A1 - Jund, Helene A1 - Klingen, Stefan A1 - Klotz, Bernhard A1 - Kolinsky, Petr A1 - Kotek, Josef A1 - Kuhne, Lothar A1 - Kuk, Kreso A1 - Lange, Dietrich A1 - Loos, Jurgen A1 - Lovati, Sara A1 - Malengros, Deny A1 - Maron, Christophe A1 - Martin, Xavier A1 - Massa, Marco A1 - Mazzarini, Francesco A1 - Metral, Laurent A1 - Moretti, Milena A1 - Munzarova, Helena A1 - Nardi, Anna A1 - Pahor, Jurij A1 - Pequegnat, Catherine A1 - Petersen, Florian A1 - Piccinini, Davide A1 - Pondrelli, Silvia A1 - Prevolnik, Snjezan A1 - Racine, Roman A1 - Regnier, Marc A1 - Reiss, Miriam A1 - Salimbeni, Simone A1 - Santulin, Marco A1 - Scherer, Werner A1 - Schippkus, Sven A1 - Schulte-Kortnack, Detlef A1 - Solarino, Stefano A1 - Spieker, Kathrin A1 - Stipcevic, Josip A1 - Strollo, Angelo A1 - Sule, Balint A1 - Szanyi, Gyongyver A1 - Szucs, Eszter A1 - Thorwart, Martin A1 - Ueding, Stefan A1 - Vallocchia, Massimiliano A1 - Vecsey, Ludek A1 - Voigt, Rene A1 - Weidle, Christian A1 - Weyland, Gauthier A1 - Wiemer, Stefan A1 - Wolf, Felix A1 - Wolyniec, David A1 - Zieke, Thomas T1 - The AlpArray seismic network BT - a large-scale european experiment to image the alpine orogen JF - Surveys in Geophysics N2 - The AlpArray programme is a multinational, European consortium to advance our understanding of orogenesis and its relationship to mantle dynamics, plate reorganizations, surface processes and seismic hazard in the Alps-Apennines-Carpathians-Dinarides orogenic system. The AlpArray Seismic Network has been deployed with contributions from 36 institutions from 11 countries to map physical properties of the lithosphere and asthenosphere in 3D and thus to obtain new, high-resolution geophysical images of structures from the surface down to the base of the mantle transition zone. With over 600 broadband stations operated for 2 years, this seismic experiment is one of the largest simultaneously operated seismological networks in the academic domain, employing hexagonal coverage with station spacing at less than 52 km. This dense and regularly spaced experiment is made possible by the coordinated coeval deployment of temporary stations from numerous national pools, including ocean-bottom seismometers, which were funded by different national agencies. They combine with permanent networks, which also required the cooperation of many different operators. Together these stations ultimately fill coverage gaps. Following a short overview of previous large-scale seismological experiments in the Alpine region, we here present the goals, construction, deployment, characteristics and data management of the AlpArray Seismic Network, which will provide data that is expected to be unprecedented in quality to image the complex Alpine mountains at depth. KW - Seismology KW - Alps KW - Seismic network KW - Geodynamics KW - Seismic imaging KW - Mountain building Y1 - 2018 U6 - https://doi.org/10.1007/s10712-018-9472-4 SN - 0169-3298 SN - 1573-0956 VL - 39 IS - 5 SP - 1009 EP - 1033 PB - Springer CY - Dordrecht ER - TY - JOUR A1 - Webster, Dean C. A1 - Meier, Michael A. R. T1 - Polymer libraries : preparation and applications N2 - Polymer libraries offer straightforward opportunities for the investigation of structure property relationships and for a more thorough understanding of certain research problems. Furthermore, if combined with high-throughput methods for their preparation as well as screening, they offer the additional advantage of time savings and/or the reduction of experimental efforts. Thus, the herein discussed methods of polymer library preparation and selected literature examples of polymer libraries describe efficient and state-of-the-art methods to tackle difficult research challenges in polymer and materials science. Y1 - 2010 UR - http://www.springerlink.com/content/tk40663747722833/ U6 - https://doi.org/10.1007/12_2009_15 SN - 0065-3195 ER - TY - JOUR A1 - Türünc, Oguz A1 - Meier, Michael A. R. T1 - Fatty acid derived monomers and related polymers via Thiol-ene (click) additions N2 - Thiol-ene additions of methyl 10-undecenoate, a castor oil derived renewable platform chemical, were studied with the goal of preparing a set of renewable monomers. Good to excellent yields were obtained for these solvent and initiator free thiol-ene additions. The resulting monomers were then polymerized using TBD as a catalyst, to linear as well as hyperbranched polyesters that also contain thio-ether linkages. All thus prepared polymers were fully characterized (NMR, GPC, DSC, and TGA) and the results of these investigations will be discussed within this contribution. The thermal analysis of these polymers revealed melting points in the range from 50 to 71 degrees C. Moreover, no significant weight loss was observed below 300 degrees C. Y1 - 2010 UR - http://www3.interscience.wiley.com/cgi-bin/jhome/10003270 U6 - https://doi.org/10.1002/marc.201000291 SN - 1022-1336 ER - TY - JOUR A1 - Djigoué, Guy Bertrand A1 - Meier, Michael A. R. T1 - Improving the selectivity for the synthesis of two renewable platform chemicals via olefin metathesis N2 - The self-metathesis of methyl 10-undecenoate as well as its cross-metathesis with methyl acrylate was investigated in detail by a systematic variation of the reaction conditions. Unsaturated ;,;-diesters with a chain length of 20 and 12 carbon atoms were thus obtained, respectively. Four different metathesis catalysts were investigated under solvent-free conditions at catalyst loadings ranging from 0.05 mol% to 1 mol% and at temperatures ranging from 30 °C to 90 °C. In the case of the self-metathesis reactions quantitative conversions were obtained with all catalysts, but the second generation metathesis catalysts revealed high amounts of olefin isomerization side reactions at higher temperatures. Using a small quantity of the hydrogen acceptor 1,4-benzoquinone, the isomerization process was almost completely suppressed. Thus, the second generation catalysts allowed for high conversions at very low catalyst loadings. For the cross-metathesis reaction, an interesting temperature and catalyst loading dependent selectivity was observed with the second generation catalysts. Moreover, due to these optimizations, we were able to run these cross-metathesis reactions with a 1:1 ratio of the reactants and low catalysts loadings. This is an improvement over described literature procedures. Thus, we report on the detailed investigation of the described self- and cross- metathesis reactions leading to practical and optimized reaction conditions for the synthesis of unsaturated ;,;-diesters monomers from renewable raw materials in an efficient catalytic manner. Y1 - 2009 UR - http://www.sciencedirect.com/science/journal/0926860X U6 - https://doi.org/10.1016/j.apcata.2009.08.025 SN - 0926-860X ER - TY - JOUR A1 - Meier, Michael A. R. T1 - Metathesis with oleochemicals : new approaches for the utilization of plant oils as renewable resources in polymer science N2 - Due to depleting fossil resources, the ever increasing emission of greenhouse gases and toxic waste, as well as the inefficient utilization of our available resources, we have to implement the principles of green chemistry whenever and wherever possible. Plant oils are already the most important renewable resource for the chemical industry. Due to their inherent double-bond functionality, they offer the possibility of being transformed via several very efficient catalytic processes. Especially, new developments in olefin metathesis allow the chemist to directly polymerize or introduce a variety of functional groups to these renewable resources in an efficient manner. Therefore, olefin metathesis with plant-oil-derived fatty acids and their derivatives can contribute to a sustainable development of our future, since this approach has great potential for the substitution of currently used petrochemicals and a variety of value-added chemical intermediates, especially for the polymer industry, can be derived from these resources in a straightforward fashion. This contribution will address and discuss the most recent developments in this field of research. Y1 - 2009 UR - http://www3.interscience.wiley.com/journal/10003495/home U6 - https://doi.org/10.1002/macp.200900168 SN - 1022-1352 ER - TY - JOUR A1 - Fokou, Patrice A. A1 - Meier, Michael A. R. T1 - Studying and suppressing olefin isomerization side reactions during ADMET polymerizations N2 - Olefin isomerization side reactions that occur during ADMET polymerizations were studied by preparing polyesters via ADMET and subsequently degrading these polyesters via transesterification with methanol. The resulting diesters, representing the repeating units of the previously prepared polyesters, were then analyzed by GC-MS. This strategy allowed quantification of the amount of olefin isomerization that took place during ADMET polymerization with second generation ruthenium metathesis catalysts. In a second step, it was shown that the addition of benzoquinone to the polymerization mixture prevented the olefin isomerization. Therefore, second generation ruthenium metathesis catalysts may now be used for the preparation of well-defined polymers via ADMET with very little isomerization, which was not possible before. Y1 - 2010 UR - http://www3.interscience.wiley.com/cgi-bin/jhome/10003270 U6 - https://doi.org/10.1002/marc.200900678 SN - 1022-1336 ER - TY - JOUR A1 - de Espinosa, Lucas Montero A1 - Meier, Michael A. R. A1 - Ronda, Juan C. A1 - Galiß, Marina A1 - Cßdiz, Virginia T1 - Phosphorus-containing renewable polyester-polyols via ADMET polymerization : synthesis, functionalization, and radical crosslinking N2 - An alpha,omega-diene containing hydroxyl groups was prepared from plant oil-derived platform chemicals. The acyclic diene metathesis copolymerization (ADMET) of this monomer with a phosphorus-containing alpha,omega-cliene (DOPO II), also plant oil derived, afforded a series of phosphorus containing linear polyesters, which have been fully characterized. The backbone hydroxyls of these polyesters have been acrylated and radically polymerized to produce crosslinked polymers. The thermomechanical and mechanical properties, the thermal stability, and the flame retardancy of these phosphorus-based thermosets have been studied. Moreover, methyl 10-undecenoate has been used as chain stopper in selected ADMET polymerizations to study the effect of the prepolymers' molecular weights on the different properties of the final materials. Y1 - 2010 UR - http://www3.interscience.wiley.com/journal/117932467/tocgroup U6 - https://doi.org/10.1002/Pola.23887 SN - 0887-624X ER - TY - JOUR A1 - Biermann, Ursula A1 - Metzger, Juergen O. A1 - Meier, Michael A. R. T1 - Acyclic triene metathesis oligo- and polymerization of high oleic sun flower oil N2 - High oleic sunflower oil, a renewable raw material consisting of triglycerides with internal C=C-double bonds, was polymerized via acyclic triene metathesis (ATMET) to highly branched and functionalized polyesters. If the Hoveyda- Grubbs second generation catalyst was used and methyl acrylate was introduced as a chain stopper, the molecular weight of the obtained polymers could be tuned by varying the ratio of the triglyceride and methyl acrylate. Using the first generation Grubbs catalyst for the polymerization of high oleic sunflower oil, no cross-linking was observed, even without the use of a chain stopper. The resulting branched materials were characterized by GPC, H-1 and C-13 NMR, and ESI-MS. Y1 - 2010 UR - http://www3.interscience.wiley.com/journal/10003495/home U6 - https://doi.org/10.1002/macp.200900615 SN - 1022-1352 ER - TY - JOUR A1 - Kreye, Oliver A1 - Türünc, Oguz A1 - Sehlinger, Ansgar A1 - Rackwitz, Jenny A1 - Meier, Michael A. R. T1 - Structurally diverse polyamides obtained from monomers derived via the Ugi multicomponent reaction JF - Chemistry - a European journal N2 - The combination of the Ugi four-component reaction (Ugi-4CR) with acyclic diene metathesis (ADMET) or thiolene polymerization led to the formation of poly-1-(alkylcarbamoyl) carboxamides, a new class of substituted polyamides with amide moieties in the polymer backbone, as well as its side chains. 10-Undecenoic acid, obtained by pyrolysis of ricinoleic acid, the main fatty acid of castor oil, was used as the key renewable building block. The use of different primary amines, as well as isonitriles (isocyanides) for the described Ugi reactions provided monomers with high structural diversity. Furthermore, the possibility of versatile post-modification of functional groups in the side chains of the corresponding polymers should be of considerable interest in materials science. The obtained monomers were polymerized by ADMET, as well as thiolene, chemistry and all polymers were fully characterized. Finally, ortho-nitrobenzylamide-containing polyamides obtained by this route were shown to be photoresponsive and exhibited a dramatic change of their properties upon irradiation with light. KW - metathesis KW - polyamides KW - polymerization KW - renewable resources KW - Ugi reaction KW - thiol-ene reactions Y1 - 2012 U6 - https://doi.org/10.1002/chem.201103341 SN - 0947-6539 VL - 18 IS - 18 SP - 5767 EP - 5776 PB - Wiley-VCH CY - Weinheim ER - TY - JOUR A1 - Kreye, Oliver A1 - Toth, Tommy A1 - Meier, Michael A. R. T1 - Copolymers derived from rapeseed derivatives via ADMET and thiol-ene addition JF - European polymer journal N2 - Novel (co)polymers were synthesized from substances obtained from rapeseed via ADMET and thiol-ene additions. alpha,omega-Dienes derived from oleic and erucic acid were copolymerized with a ferulic acid derivative, a representative phenolic acid (p-hydroxycinnamic acid) present, for instance, in rapeseed cake. Copolymers with different ratios of these monomers were prepared via two different routes (ADMET and thiol-ene) and studied in detail. Both monomer and polymer synthesis were optimized in order to achieve high yielding synthetic procedures that meet the requirements of green chemistry. Some thermal properties of the resulting copolymer series were then studied and correlated to the co-monomer composition. KW - Rapeseed oil KW - Rapeseed cake KW - p-Hydroxycinnamic acids KW - alpha,omega-Dienes KW - ADMET polymerization KW - Thiol-ene addition Y1 - 2011 U6 - https://doi.org/10.1016/j.eurpolymj.2011.06.012 SN - 0014-3057 VL - 47 IS - 9 SP - 1804 EP - 1816 PB - Elsevier CY - Oxford ER - TY - JOUR A1 - Kreye, Oliver A1 - Toth, Tommy A1 - Meier, Michael A. R. T1 - Introducing multicomponent reactions to polymer science passerini reactions of renewable monomers JF - Journal of the American Chemical Society N2 - Combination of the Passerini three component-reaction (3CR) and olefin metathesis led to the formation of poly[1-(alkyl carbamoyl)alkyl alkanoates], a new class of polyesters with amide moieties in their side chain, from renewable resources. Two different approaches were studied and compared to each other. First, monomers were synthesized by the Passerini-3CR and then polymerized via acyclic diene metathesis. Alternatively, bifunctional monomers were synthesized by self-metathesis and then polymerized by Passerini-3CR. Both approaches led to the formation of high-molecular-weight polymers. Moreover, Passerini-3CRs were shown to be a versatile grafting-onto method. The results clearly demonstrate that the Passerini-3CR offers an interesting new access to monomers and polymers and thus broadens the synthetic portfolio of polymer science. Y1 - 2011 U6 - https://doi.org/10.1021/ja1113003 SN - 0002-7863 VL - 133 IS - 6 SP - 1790 EP - 1792 PB - American Chemical Society CY - Washington ER - TY - GEN A1 - Dahm, Torsten A1 - Becker, Dirk A1 - Bischoff, Monika A1 - Cesca, Simone A1 - Dost, B. A1 - Fritschen, R. A1 - Hainzl, Sebastian A1 - Klose, C. D. A1 - Kuhn, D. A1 - Lasocki, S. A1 - Meier, Thomas A1 - Ohrnberger, Matthias A1 - Rivalta, Eleonora A1 - Wegler, Ulrich A1 - Husen, Stephan T1 - Recommendation for the discrimination of human-related and natural seismicity T2 - Journal of seismology N2 - Various techniques are utilized by the seismological community, extractive industries, energy and geoengineering companies to identify earthquake nucleation processes in close proximity to engineering operation points. These operations may comprise fluid extraction or injections, artificial water reservoir impoundments, open pit and deep mining, deep geothermal power generations or carbon sequestration. In this letter to the editor, we outline several lines of investigation that we suggest to follow to address the discrimination problem between natural seismicity and seismic events induced or triggered by geoengineering activities. These suggestions have been developed by a group of experts during several meetings and workshops, and we feel that their publication as a summary report is helpful for the geoscientific community. Specific investigation procedures and discrimination approaches, on which our recommendations are based, are also published in this Special Issue (SI) of Journal of Seismology. KW - Triggered seismicity KW - Induced seismicity Y1 - 2013 U6 - https://doi.org/10.1007/s10950-012-9295-6 SN - 1383-4649 VL - 17 IS - 1 SP - 197 EP - 202 PB - Springer CY - Dordrecht ER - TY - JOUR A1 - Kreye, Oliver A1 - Toth, Tommy A1 - Meier, Michael A. R. T1 - Poly-alpha,beta-unsaturated aldehydes derived from castor oil via ADMET polymerization JF - European journal of lipid science and technology N2 - 10-Undecenal, derived by pyrolysis and reduction from castor oil, was almost quantitatively transformed into the corresponding aldol condensation product under basic conditions. This alpha,omega-diene monomer was polymerized using acyclic diene metathesis (ADMET) polymerization. In a catalyst screening, four of nine different ruthenium-based metathesis catalysts showed good reactivity under neat conditions at 80 degrees C in the presence of 1,4-benzoquinone and polymers with molecular weights up to 11 kDa were formed. Furthermore, the (1)H NMR spectra showed that the metathesis catalysts tolerate the alpha,beta-unsaturated aldehyde function and due to the addition of benzoquinone, the degree of double bond isomerization was low. Further experiments investigating reduced catalyst amounts (down to 0.2 mol%) and the temperature dependence of these ADMET polymerizations gave also satisfying results for the formation of poly-alpha,beta-unsaturated aldehydes. Moreover, ADMET polymerizations with different amounts of methyl 10-undecenoate as chain-stopper were performed and the integrals of the corresponding (1)H NMR spectra allowed the determination of an absolute degree of polymerization. Finally, a reduction of a poly-alpha,beta-unsaturated aldehyde with sodium borohydride was accomplished. The resulting poly-(allyl alcohol) could be a useful compound in the generation of polymer networks like polyesters, polyurethanes, and polycarbonates and thus be of high interest in materials research. KW - ADMET KW - Aldol condensation KW - Castor oil KW - Poly(allyl alcohol)s KW - Poly-alpha,beta-unsaturated aldehydes Y1 - 2011 U6 - https://doi.org/10.1002/ejlt.201000108 SN - 1438-7697 VL - 113 IS - 1 SP - 31 EP - 38 PB - Wiley-VCH CY - Weinheim ER - TY - JOUR A1 - Biermann, Ursula A1 - Meier, Michael A. R. A1 - Butte, Werner A1 - Metzger, Jürgen O. T1 - Cross-metathesis of unsaturated triglycerides with methyl acrylate synthesis of a dimeric metathesis product JF - European journal of lipid science and technology N2 - Highly functionalized dimeric triglycerides, such as compound 2, are obtained as minor products besides branched macromolecules from the acyclic triene metathesis (ATMET) polymerization of unsaturated triglycerides such as glyceryl triundec-10-enoate 1 and methyl acrylate (MA) in the presence of the second generation Hoveyda-Grubbs catalyst. The formed amount of interesting products of lower molecular weight during the ATMET reaction depends on the ratio of MA and triglyceride, reaction time, and temperature. We isolated the dimeric metathesis product 2 and synthesized the respective partially hydrogenated dimer 3 regioselectivly in a seven step reaction sequence starting from 10-undecenoic acid 7 and glycerol. Product 3 was unambiguously characterized by (13)C and (1)H NMR and MS as well as the further intermediate products of the seven step reaction including 10,11 bromo-undecanoic acid 8, the respective brominated 1,3-diglyceride 9, the brominated 1,3-triglyceride 6, and the self-metathesis products 4 and 5 which were isolated and purified. KW - Highly functionalized dimeric triglycerides KW - Olefin self- and cross-metathesis KW - Renewable resources Y1 - 2011 U6 - https://doi.org/10.1002/ejlt.201000109 SN - 1438-7697 VL - 113 IS - 1 SP - 39 EP - 45 PB - Wiley-VCH CY - Weinheim ER - TY - JOUR A1 - de Espinosa, Lucas Montero A1 - Meier, Michael A. R. T1 - Synthesis of star- and block-copolymers using ADMET head-to-tail selectivity during step-growth polymerization JF - Chemical communications N2 - Control over molecular architectures obtained via ADMET polymerization is limited by the step-growth nature of this technique. A new approach to this polycondensation method is described allowing for the synthesis of diblock and star-shaped polymers with molecular weight control by using the selectivity of olefin cross-metathesis between acrylates and terminal olefins. Y1 - 2011 U6 - https://doi.org/10.1039/c0cc04161k SN - 1359-7345 VL - 47 IS - 6 SP - 1908 EP - 1910 PB - Royal Society of Chemistry CY - Cambridge ER - TY - JOUR A1 - Mutlu, Hatice A1 - de Espinosa, Lucas Montero A1 - Meier, Michael A. R. T1 - Acyclic diene metathesis a versatile tool for the construction of defined polymer architectures JF - Chemical Society reviews N2 - Two decades have passed since the metathesis polymerisation of alpha,omega-dienes was successfully demonstrated by the group of Wagener and the term acyclic diene metathesis (ADMET) polymerisation was coined. Since then, the advances of metathesis chemistry have allowed to expand the scope of this versatile polymerisation reaction that nowadays finds applications in different fields, such as polymer, material, or medicinal chemistry. This critical review provides an insight into the historical aspects of ADMET and a detailed overview of the work done to date applying this versatile polymerisation reaction (221 references). Y1 - 2011 U6 - https://doi.org/10.1039/b924852h SN - 0306-0012 VL - 40 IS - 3 SP - 1404 EP - 1445 PB - Royal Society of Chemistry CY - Cambridge ER - TY - JOUR A1 - von Czapiewski, Marc A1 - Kreye, Oliver A1 - Mutlu, Hatice A1 - Meier, Michael A. R. T1 - Cross-metathesis versus palladium-catalyzed C-H activation acetoxy ester functionalization of unsaturated fatty acid methyl esters JF - European journal of lipid science and technology N2 - Two synthetic approaches to functionalize plant oil derived platform chemicals were investigated. For this purpose, methyl 10-undecenoate, which can be obtained by pyrolysis of castor oil, was used in olefin cross-metathesis under neat conditions forming an unsaturated a,?-acetoxy ester. A catalyst screening with 11 different ruthenium-based metathesis catalysts was performed, revealing that well-suited catalysts allow for full conversion and very good cross-metathesis selectivity at a loading of only 0.5?mol%. An alternative possibility to the aforementioned synthetic method is a palladium-catalyzed reaction of methyl 10-undecenoate with acetic acid in the presence of dimethyl sulfoxide. Here, the formation of linear and branched unsaturated acetoxy esters as well as a ketone was observed. The conversion as well as the selectivity of this procedure was studied under different reaction conditions and compared to the cross-metathesis results. Based on the successful functionalization of methyl 10-undecenoate, methyl oleate was investigated in this palladium-catalyzed C?H activation reaction. Due to the lower reactivity of the internal double bond the desired acetoxy ester was only obtained in moderate conversion in this case. In summary, this study clearly shows that palladium-catalyzed functionalization of unsaturated fatty compounds via C?H activation is an attractive alternative to the well-established olefin cross-metathesis procedure. KW - a KW - -Acetoxy esters KW - C?H oxidation KW - Cross-metathesis KW - Fatty acids KW - Pd catalysis Y1 - 2013 U6 - https://doi.org/10.1002/ejlt.201200196 SN - 1438-7697 VL - 115 IS - 1 SP - 76 EP - 85 PB - Wiley-Blackwell CY - Hoboken ER - TY - JOUR A1 - Kallies, Bernd A1 - Meier, R. T1 - The electronic structure od 3 [M(H20)6)3+ions from Sc(III)till Fe (III) : a quantum mechanical study based on DFT computations and natural bond orbital analyses Y1 - 2001 ER -