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  - Haas, Maria
A1  - Holzendorf, Ulf
A1  - Künzel, Matthias
A1  - Lenk, Michael
A1  - Meier, Bernd
A1  - Ordnung, M.
ED  - Meier, Bernd
ED  - Schmid, Margarete
T1  - Wirtschaft-Technik-Haushalt
Y1  - 2003
SN  - 3-486-88747-5
PB  - Oldenbourg
CY  - München
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  - BOOK
A1  - Mette, Dieter
A1  - Meier, Bernd
A1  - Schmid, Margarete
A1  - Lenk, Michael
A1  - Nissen, Heike
A1  - Peschk, Sylvia
A1  - Priebe, Ulrike
A1  - Schubert, Arndt
A1  - Lenk, Jenny
T1  - Wirtschaft, Technik, Haushalt : Neubearbeitung zum Lehrplan Wirtschaft, Technik, Haushalt/Soziales in Sachsen ; Arbeitsheft 9
Y1  - 2005
SN  - 978-3-637-00948-6
PB  - Oldenbourg Schulbuchverl. GmbH
CY  - München
ER  - 
TY  - BOOK
A1  - Mette, Dieter
A1  - Meier, Bernd
A1  - Schmid, Margarete
A1  - Lenk, Michael
A1  - Nissen, Heike
A1  - Peschk, Sylvia
A1  - Priebe, Ulrike
A1  - Schubert, Arndt
T1  - Wirtschaft, Technik, Haushalt/Soziales : zum Lehrplan Wirtschaft, Technik, Haushalt/Soziales in Sachsen ; Schülerbuch 10 - Vertiefungskurse
Y1  - 2008
SN  - 978-3-637-00605-8
PB  - Oldenbourg Schulbuchverl. GmbH
CY  - München
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  -