@article{AkalKoralayCandanetal.2011, author = {Akal, Cuneyt and Koralay, O. Ersin and Candan, Osman and Oberh{\"a}nsli, Roland and Chen, Fukun}, title = {Geodynamic significance of the early triassic karaburun granitoid (Western Turkey) for the opening history of Neo-Tethys}, series = {Turkish journal of earth sciences = T{\"u}rk yerbilimleri dergisi}, volume = {20}, journal = {Turkish journal of earth sciences = T{\"u}rk yerbilimleri dergisi}, number = {3}, publisher = {T{\"u}bitak}, address = {Ankara}, issn = {1300-0985}, doi = {10.3906/yer-1008-1}, pages = {255 -- 271}, year = {2011}, abstract = {The Karaburun Peninsula, which is considered part of the Anatolide-Tauride Block of Turkey, contains clastic and carbonate sequences deposited on the northern margin of Gondwana. The Palaeozoic clastic sequence, which is intruded by the Early Triassic granitoid and tectonically overlies a Mesozoic melange sequence, can be divided into three subunits: a lower clastic subunit consisting of a sandstone-shale alternation, an upper clastic subunit consisting of black chert-bearing shales, sandstone and conglomerate, and a Permo-Carboniferous carbonate subunit. The lower Triassic Karaburun I-type granitoid has a high initial Sr-87/Sr-86 ratio (0.709021-0.709168), and low Nd-143/Nd-144 ratio (0.512004-0.512023) and epsilon Nd (-5.34 to -5.70) isotopic values. Geochronological data indicate a crystallization (intrusion) age of 247.1 +/- 2.0 Ma (Scythian). Geochemically, the acidic magmatism reflects a subduction-related continental-arc basin tectonic setting, which can be linked to the opening of the northern branch of Neo-Tethys as a continental back-arc rifting basin on the northern margin of Gondwana. This can be related to the closure through southward subduction of the Palaeotethys Ocean beneath Gondwana.}, language = {en} } @article{DavidCoyEnriqueCucaSefkow2011, author = {David Coy, Ericsson and Enrique Cuca, Luis and Sefkow, Michael}, title = {Pd-NHC catalyzed biaryl coupling by direct C-H Activation-A Novel strategy for the synthesis of dibenzocyclooctane lignans}, series = {Synthetic communications : an international journal for rapid communication of synthetic organic chemistry}, volume = {41}, journal = {Synthetic communications : an international journal for rapid communication of synthetic organic chemistry}, number = {1}, publisher = {Taylor \& Francis Group}, address = {Philadelphia}, issn = {0039-7911}, doi = {10.1080/00397910903531755}, pages = {41 -- 51}, year = {2011}, abstract = {Cross-coupling reactions, such as Buchwald-Hartwig arylamination and direct intramolecular biaryl coupling by C-H activation, were carried out using various Palladium-N-heterocyclic carbenes (Pd-NHC) as catalysts. The yields were good to excellent. The latter strategy was adopted to transform two dibenzylbutane lignans, isolated from the leaves of Ocotea macrophylla (Lauraceae), into the corresponding dibenzocyclooctane lignans in good overall yields. Supplemental materials are available for this article. Go to the publisher's online edition of Synthetic Communications (R) to view the free supplemental file.}, language = {en} } @article{FeherWhelanMueller2011, author = {Feher, Kristen and Whelan, James and M{\"u}ller, Samuel}, title = {Assessing modularity using a random matrix theory approach}, series = {Statistical applications in genetics and molecular biology}, volume = {10}, journal = {Statistical applications in genetics and molecular biology}, number = {1}, publisher = {De Gruyter}, address = {Berlin}, issn = {2194-6302}, doi = {10.2202/1544-6115.1667}, pages = {36}, year = {2011}, abstract = {Random matrix theory (RMT) is well suited to describing the emergent properties of systems with complex interactions amongst their constituents through their eigenvalue spectrums. Some RMT results are applied to the problem of clustering high dimensional biological data with complex dependence structure amongst the variables. It will be shown that a gene relevance or correlation network can be constructed by choosing a correlation threshold in a principled way, such that it corresponds to a block diagonal structure in the correlation matrix, if such a structure exists. The structure is then found using community detection algorithms, but with parameter choice guided by RMT predictions. The resulting clustering is compared to a variety of hierarchical clustering outputs and is found to the most generalised result, in that it captures all the features found by the other considered methods.}, language = {en} } @article{BresselPrevostAppavouetal.2011, author = {Bressel, Katharina and Prevost, Sylvain and Appavou, Marie-Sousai and Tiersch, Brigitte and Koetz, Joachim and Gradzielski, Michael}, title = {Phase behaviour and structure of zwitanionic mixtures of perfluorocarboxylates and tetradecyldimethylamine oxide-dependence on chain length of the perfluoro surfactant}, series = {Soft matter}, volume = {7}, journal = {Soft matter}, number = {23}, publisher = {Royal Society of Chemistry}, address = {Cambridge}, issn = {1744-683X}, doi = {10.1039/c1sm05618b}, pages = {11232 -- 11242}, year = {2011}, abstract = {Phase behaviour and the mesoscopic structure of zwitanionic surfactant mixtures based on the zwitterionic tetradecyldimethylamine oxide (TDMAO) and anionic lithium perfluoroalkyl carboxylates have been investigated for various chain lengths of the perfluoro surfactant with an emphasis on spontaneously forming vesicles. These mixtures were studied at a constant total concentration of 50 mM and characterised by means of dynamic light scattering (DLS), electric conductivity, small-angle neutron scattering (SANS), viscosity, and cryo-scanning electron microscopy (Cryo-SEM). No vesicles are formed for relatively short perfluoro surfactants. The extension of the vesicle phase becomes substantially larger with increasing chain length of the perfluoro surfactant, while at the same time the size of these vesicles increases. Head group interactions in these systems play a central role in the ability to form vesicles, as already protonating 10 mol\% of the TDMAO largely enhances the propensity for vesicle formation. The range of vesicle formation in the phase diagram is not only substantially enlarged but also extends to shorter perfluoro surfactants, where without protonation no vesicles would be formed. The size and polydispersity of the vesicles are related to the chain length of the perfluoro surfactant, the vesicles becoming smaller and more monodisperse with increasing perfluoro surfactant chain length. The ability of the mixed systems to form well-defined unilamellar vesicles accordingly can be controlled by the length of the alkyl chain of the perfluorinated surfactant and depends strongly on the charge conditions, which can be tuned easily by pH-variation.}, language = {en} } @article{SangoroIacobNaumovetal.2011, author = {Sangoro, J. R. and Iacob, C. and Naumov, S. and Valiullin, R. and Rexhausen, Hans and Hunger, J. and Buchner, R. and Strehmel, Veronika and Kaerger, J. and Kremer, F.}, title = {Diffusion in ionic liquids the interplay between molecular structure and dynamics}, series = {Soft matter}, volume = {7}, journal = {Soft matter}, number = {5}, publisher = {Royal Society of Chemistry}, address = {Cambridge}, issn = {1744-683X}, doi = {10.1039/c0sm01404d}, pages = {1678 -- 1681}, year = {2011}, abstract = {Diffusion in a series of ionic liquids is investigated by a combination of Broadband Dielectric Spectroscopy (BDS) and Pulsed Field Gradient Nuclear Magnetic Resonance (PFG NMR). It is demonstrated that the mean jump lengths increase with the molecular volumes determined from quantum-chemical calculations. This provides a direct means-via Einstein-Smoluchowski relation-to determine the diffusion coefficient by BDS over more than 8 decades unambiguously and in quantitative agreement with PFG NMR measurements. New possibilities in the study of charge transport and dynamic glass transition in ionic liquids are thus opened.}, language = {en} } @article{WeissBoettcherLaschewsky2011, author = {Weiss, Jan and B{\"o}ttcher, Christoph and Laschewsky, Andr{\´e}}, title = {Self-assembly of double thermoresponsive block copolymers end-capped with complementary trimethylsilyl groups}, series = {Soft matter}, volume = {7}, journal = {Soft matter}, number = {2}, publisher = {Royal Society of Chemistry}, address = {Cambridge}, issn = {1744-683X}, doi = {10.1039/c0sm00531b}, pages = {483 -- 492}, year = {2011}, abstract = {A set of double thermoresponsive diblock copolymers poly(N-n-propylacrylamide)-block-poly(N-ethylacrylamide) (PNPAM-b-PNEAM) was synthesised by sequential reversible addition-fragmentation chain transfer (RAFT) polymerisations. Using a twofold trimethylsilyl (TMS)-labeled RAFT-agent, the relative size of the two blocks was varied. While soluble as unimers below 15 degrees C, all copolymers exhibited thermally induced two-step self-assembly in water, due to distinct lower critical solution temperature (LCST) phase transitions of PNPAM (around 20 degrees C) and PNEAM (around 70 degrees C). Their temperature-dependent self-organisation in dilute aqueous solution was studied by turbidimetry, dynamic light scattering, transmission electron microscopy, and (1)H NMR spectroscopy. The copolymers show distinct, two-step self-organisation behaviour with respect to transition temperatures, aggregate type and size, which can be correlated to the relative lengths of the low and high LCST blocks. For polymers having short blocks with low LCST, the first thermal transition induces the formation of individual micelles. Further heating above the second thermal transition results reversibly either in a shrink of the micelle size or in aggregation of the micelles, with hydrodynamic diameters below 250 nm. In contrast in the case of polymers having a long block with low LCST, the first thermal transition already leads to clusters of micelles, while the second thermal transition makes the clusters shrink. Noteworthy, the twofold TMS-labeled end groups report not only on the molar masses of the polymers, but can simultaneously serve as NMR-probes for the self-assembly process. The signal of the TMS-aryl end group displays a reversible temperature dependent, two-step splitting that is indicative of the self-organisation of the block copolymers.}, language = {en} } @article{StoyanovKolloscheRisseetal.2011, author = {Stoyanov, Hristiyan and Kollosche, Matthias and Risse, Sebastian and McCarthy, Denis N. and Kofod, Guggi}, title = {Elastic block copolymer nanocomposites with controlled interfacial interactions for artificial muscles with direct voltage control}, series = {Soft matter}, volume = {7}, journal = {Soft matter}, number = {1}, publisher = {Royal Society of Chemistry}, address = {Cambridge}, issn = {1744-683X}, doi = {10.1039/c0sm00715c}, pages = {194 -- 202}, year = {2011}, abstract = {Soft, physically crosslinking, block copolymer elastomers were filled with surface-treated nanoparticles, in order to evaluate the possibility for improvement of their properties when used as soft dielectric actuators. The nanoparticles led to improvements in dielectric properties, however they also reinforced the elastomer matrix. Comparing dielectric spectra of composites with untreated and surface-treated particles showed a measurable influence of the surface on the dielectric loss behaviour for high filler amounts, strongly indicating an improved host-guest interaction for the surface-treated particles. Breakdown strength was measured using a test bench and was found to be in good agreement with the results from the actuation measurements. Actuation responses predicted by a model for prestrained actuators agreed well with measurements up to a filler amount of 20\%(vol). Strong improvements in actuation behaviour were observed, with an optimum near 15\%(vol) nanoparticles, corresponding to a reduction in electrical field of 27\% for identical actuation strains. The use of physically crosslinking elastomer ensured the mechanical properties of the matrix elastomer were unchanged by nanoparticles effecting the crosslinking reaction, contrary to similar experiments performed with chemically crosslinking elastomers. This allows for a firm conclusion about the positive effects of surface-treated nanoparticles on actuation behavior.}, language = {en} } @misc{Sorge2011, author = {Sorge, Arndt}, title = {Too big to fail the inside story of how wall street and washington fought to save the financial system from crisis-and themselves}, series = {Socio-economic review}, volume = {9}, journal = {Socio-economic review}, number = {1}, publisher = {Oxford Univ. Press}, address = {Oxford}, issn = {1475-1461}, pages = {169 -- 186}, year = {2011}, language = {en} } @misc{Sorge2011, author = {Sorge, Arndt}, title = {This time is different eight centuries of financial folly}, series = {Socio-economic review}, volume = {9}, journal = {Socio-economic review}, number = {1}, publisher = {Oxford Univ. Press}, address = {Oxford}, issn = {1475-1461}, pages = {169 -- 186}, year = {2011}, language = {en} } @misc{Sorge2011, author = {Sorge, Arndt}, title = {How markets fail the logic of economic calamities}, series = {Socio-economic review}, volume = {9}, journal = {Socio-economic review}, number = {1}, publisher = {Oxford Univ. Press}, address = {Oxford}, issn = {1475-1461}, pages = {169 -- 186}, year = {2011}, language = {en} }