Müller, Marcus

[["dc.bibliographiccitation.firstpage","2004922"],["dc.bibliographiccitation.issue","44"],["dc.bibliographiccitation.journal","Small"],["dc.bibliographiccitation.volume","16"],["dc.contributor.author","Liu, Huan"],["dc.contributor.author","Pang, Bo"],["dc.contributor.author","Tang, Qiyun"],["dc.contributor.author","Müller, Marcus"],["dc.contributor.author","Zhang, Hua"],["dc.contributor.author","Dervişoğlu, Riza"],["dc.contributor.author","Zhang, Kai"],["dc.date.accessioned","2021-04-14T08:32:17Z"],["dc.date.available","2021-04-14T08:32:17Z"],["dc.date.issued","2020"],["dc.description.abstract","Abstract For the first time Janus‐like films of surface‐acylated cellulose nanowhiskers (CNWs) with or without graphene oxide (GO) via one‐step evaporation‐driven self‐assembly process are reported, which have reconstructible time‐dependent micro‐/nanostructures and asymmetric wettability. The heterogeneous aggregation of CNWs on rough Teflon substrates favors the formation of uniform films, leading to hydrophobic smooth bottom surface. The homogeneous nucleation of residual CNWs in bulk suspensions promotes the growth of patchy microspheres with an average diameter of 22.7 ± 2.1 µm, which precipitate on the top surface leading to enhanced hydrophobicity. These patchy microspheres are thermoresponsive and vanish after heating at 60 °C within 1 min, while they are reconstructed at room temperature with time‐dependent evolving micro‐/nanostructures in dry state within 2 d. The thermoresponsive transition of patchy microparticles leads to accompanied switchable change between transparency and opacity of Janus‐like films. Furthermore, the incorporation of GO generates more patchy microspheres with an average diameter of 13.5 ± 1.3 µm on the top surface of hybrid Janus‐like films. Different distributions of CNWs and GO in Janus‐like films and the solvent‐responsive self‐assembled patchy microparticles of CNWs facilitate their reversible actuation by showing fast curling in THF within 6 s and flattening in water for at least 25 cycles."],["dc.description.abstract","Janus‐like films of self‐assembled surface‐acylated cellulose nanowhiskers (CNWs) with or without graphene oxide (GO) have asymmetric topographies on their top and bottom surfaces showing different wettabilities, allowing fast solvent‐responsive actuation. Self‐assembled patchy microspheres on the top surface vanish upon heating and recover after cooling down to room temperature with time‐dependent morphologies, while the bottom surface remains smooth. image"],["dc.description.sponsorship","German Research Foundation http://dx.doi.org/10.13039/501100001659"],["dc.description.sponsorship","Georg‐August‐University of Goettingen"],["dc.description.sponsorship","China Scholarship Council http://dx.doi.org/10.13039/501100004543"],["dc.identifier.doi","10.1002/smll.202004922"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/83873"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-399"],["dc.relation.eissn","1613-6829"],["dc.relation.issn","1613-6810"],["dc.rights","This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes."],["dc.title","Self‐Assembly of Surface‐Acylated Cellulose Nanowhiskers and Graphene Oxide for Multiresponsive Janus‐Like Films with Time‐Dependent Dry‐State Structures"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","3161"],["dc.bibliographiccitation.issue","7"],["dc.bibliographiccitation.journal","Macromolecules"],["dc.bibliographiccitation.lastpage","3164"],["dc.bibliographiccitation.volume","43"],["dc.contributor.author","von der Heydt, Alice"],["dc.contributor.author","Mueller, Marcus"],["dc.contributor.author","Zippelius, Annette"],["dc.date.accessioned","2018-11-07T08:44:08Z"],["dc.date.available","2018-11-07T08:44:08Z"],["dc.date.issued","2010"],["dc.description.sponsorship","Deutsche Forschungsgemeinschaft [SFB-602/B6]"],["dc.identifier.doi","10.1021/ma100192n"],["dc.identifier.isi","000276232800010"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/20130"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Amer Chemical Soc"],["dc.relation.issn","0024-9297"],["dc.title","Sequence Fractionation in Symmetric Random Block Copolymers"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.artnumber","031801"],["dc.bibliographiccitation.issue","3"],["dc.bibliographiccitation.journal","PHYSICAL REVIEW E"],["dc.bibliographiccitation.volume","78"],["dc.contributor.author","Yelash, Leonid"],["dc.contributor.author","Virnau, Peter"],["dc.contributor.author","Paul, Wolfgang"],["dc.contributor.author","Binder, Kurt"],["dc.contributor.author","Mueller, Marcus"],["dc.date.accessioned","2018-11-07T11:11:52Z"],["dc.date.available","2018-11-07T11:11:52Z"],["dc.date.issued","2008"],["dc.description.abstract","In simulations of phase separation kinetics, large length and time scales are involved due to the mesoscopic size of the polymer coils, and the structure formation on still larger scales of length and time. We apply a coarse-grained model of hexadecane dissolved in supercritical carbon dioxide, for which in previous work the equilibrium phase behavior has been established by Monte Carlo methods. Using parallelized simulations on a multiprocessor supercomputer, large scale molecular dynamics simulations of phase separation following pressure jumps are presented for systems containing N=435 136 coarse- grained particles, which correspond to several millions of atoms in a box with linear dimension 447 angstrom. Even for large systems the phase separation can be observed up to the final, macroscopically segregated, equilibrium state. It is shown that in the segregation process the two order parameters of the system (density and concentration) are strongly coupled. The system does not follow the predicted growth law for the characteristic domain size l(t)proportional to t in binary fluid mixtures for the range of times accessible in the simulation. Instead, it exhibits a distinctly slower growth, presumably due to the dynamic asymmetry of the constituents."],["dc.description.sponsorship","John von Neumann Institute for Computing (NIC)"],["dc.identifier.doi","10.1103/PhysRevE.78.031801"],["dc.identifier.isi","000259682700077"],["dc.identifier.pmid","18851056"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/53533"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Amer Physical Soc"],["dc.relation.issn","1550-2376"],["dc.relation.issn","1539-3755"],["dc.title","Spinodal decomposition of polymer solutions: A parallelized molecular dynamics simulation"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.artnumber","024903"],["dc.bibliographiccitation.issue","2"],["dc.bibliographiccitation.journal","The Journal of Chemical Physics"],["dc.bibliographiccitation.volume","128"],["dc.contributor.author","Mueller, Marcus"],["dc.contributor.author","Daoulas, Kostas Ch."],["dc.date.accessioned","2018-11-07T11:19:08Z"],["dc.date.available","2018-11-07T11:19:08Z"],["dc.date.issued","2008"],["dc.description.abstract","We discuss a method for calculating free energy differences between disordered and ordered phases of self-assembling systems utilizing computer simulations. Applying an external, ordering field, we impose a predefined structure onto the fluid in the disordered phase. The structure in the presence of the external, ordering field closely mimics the structure of the ordered phase (in the absence of an ordering field). Self-consistent field theory or density functional theory provides an accurate estimate for choosing the strength of the ordering field. Subsequently, we gradually switch off the external, ordering field and, in turn, increase the control parameter that drives the self-assembly. The free energy difference along this reversible path connecting the disordered and the ordered state is obtained via thermodynamic integration or expanded ensemble simulation techniques. Utilizing Single-Chain-in-Mean-Field simulations of a symmetric diblock copolymer melt we illustrate the method and calculate the free energy difference between the disordered phase and the lamellar structure at an intermediate incompatibility chi N=20. Evidence for the first-order character of the order-disorder transition at fixed volume is presented. The transition is located at chi(ODT)N=13.65 +/- 0.10 for an invariant degree of polymerization of ($) over barN=14 884. The magnitude of the shift of the transition from the mean field prediction qualitatively agrees with other simulations. (c) 2008 American Institute of Physics."],["dc.identifier.doi","10.1063/1.2818565"],["dc.identifier.isi","000252450100038"],["dc.identifier.pmid","18205471"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/55199"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Amer Inst Physics"],["dc.relation.issn","0021-9606"],["dc.title","Calculating the free energy of self-assembled structures by thermodynamic integration"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","5256"],["dc.bibliographiccitation.issue","14"],["dc.bibliographiccitation.journal","Macromolecules"],["dc.bibliographiccitation.lastpage","5265"],["dc.bibliographiccitation.volume","49"],["dc.contributor.author","Leonforte, Fabien"],["dc.contributor.author","Mueller, Marcus"],["dc.date.accessioned","2018-11-07T10:11:29Z"],["dc.date.available","2018-11-07T10:11:29Z"],["dc.date.issued","2016"],["dc.description.abstract","Molecular dynamics simulations of a coarse-grained model with soft, nonbonded interactions and implicit solvent are used to study the temperature- and pH sensitive response of mixed brushes composed of poly(N-isopropylacrylamide) [PNIPAm] and poly(acrylic acid) [PAA] polymers. The model is developed in order to address experimentally relevant, large invariant degrees of polymerization, and nonbonded interactions are expressed via a third-order virial expansion of the equation of state. The choice of interaction parameters for PNIPAm mimics the swelling behavior in water as the temperature increases toward the lower critical solution temperature, T-LCST, and the model captures the pH-dependent response of PAA at fixed ionic strength (IS). For this case, the solvent-mediated Flory-Huggins parameter is adapted to reproduce the experimental pH swelling of the homopolymer brush. Mixed brushes incorporating various amounts of PAA are considered, and the effect of mixing polymers on the response of the mixed brushes to both temperature and pH changes is discussed. Additionally, nanoparticles (NPs) that preferably interact with the PAA portion of the polymers are considered. As a function of their radius and the size of the functional NP-attractive groups on PAA chains, the capability to capture NP and allow them to penetrate inside brushes is studied at various temperatures and fixed pH. Moreover, the kinetics of adsorption and release of NPs is investigated."],["dc.identifier.doi","10.1021/acs.macromol.6b00535"],["dc.identifier.isi","000380576900027"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/40054"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Amer Chemical Soc"],["dc.relation.issn","1520-5835"],["dc.relation.issn","0024-9297"],["dc.title","Functional Poly(N-isopropylacrylamide)/Poly(acrylic acid) Mixed Brushes for Controlled Manipulation of Nanoparticles"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","371"],["dc.bibliographiccitation.issue","4"],["dc.bibliographiccitation.journal","The Journal of Heart and Lung Transplantation"],["dc.bibliographiccitation.lastpage","378"],["dc.bibliographiccitation.volume","24"],["dc.contributor.author","Wittwer, Thorsten"],["dc.contributor.author","Franke, Ulrich F. W."],["dc.contributor.author","Fehrenbach, A."],["dc.contributor.author","Ochs, Matthias"],["dc.contributor.author","Sandhaus, T."],["dc.contributor.author","Schuette, A."],["dc.contributor.author","Richter, S."],["dc.contributor.author","Dreyer, N."],["dc.contributor.author","Knudsen, L."],["dc.contributor.author","Mueller, T."],["dc.contributor.author","Schubert, H."],["dc.contributor.author","Richter, J."],["dc.contributor.author","Wahlers, T."],["dc.date.accessioned","2018-11-07T11:12:02Z"],["dc.date.available","2018-11-07T11:12:02Z"],["dc.date.issued","2005"],["dc.description.abstract","Background: Ischemia-reperfusion injury accounts for one-third of early deaths after lung transplantation. To expand the limited donor pool, lung retrieval from non-heart-beating donors (NHBD) has been introduced recently. However, because of potentially deleterious effects of warm ischemia on microvascular integrity, use of NHBD lungs is limited by short tolerable time periods before preservation. After intravenous prostanoids are routinely used to ameliorate reperfusion injury, the latest evidence suggests. similar efficacy of inhaled prostacyclin. Therefore, the impact of donor pretreatment with the prostacyclin analogue iloprost on postischemic NHBD lung function and preservation quality was evaluated. Methods: Asystolic pigs (5 per group) were ventilated for 180 minutes of warm ischemia (Group 2). In Group 3, 100 mu g iloprost was aerosolized during the final 30 minutes of ventilation with a novel mobile ultrasonic nebulizer. Lungs were then retrogradely preserved with Perfadex and stored for 3 hours. After left lung transplantation and contralateral lung exclusion, hemodynamics, rO(2)/FiO(2), and dynamic compliance were monitored for 6 hours and compared with sham-operated controls (Group 1). Pulmonary edema was determined both stereologically and by wet-to-dry weight ratio (W/D). Statistics comprised analysis of variance with repeated measures and Mann-Whitney test. Results: Flush preservation pressures, dynamic compliance, inspiratory pressures, and W/D were significantly superior in iloprost-treated lungs, and oxygenation and pulmonary hemodynamics were comparable between groups. Stereology revealed a trend toward lower intraalveolar edema formation in iloprost-treated lungs compared with untreated grafts. Conclusions: Alveolar deposition of Iloprost in NHBD lungs before preservation ameliorates postischemic edema and significantly improves lung compliance. This easily applicable innovative approach, which uses a mobile ultrasonic nebulizer, offers an important strategy for improvement of pulmonary preservation quality and might expand the pool of donor lungs. Copyright (c) 2005 by the International Society for Heart and Lung Transplantation."],["dc.identifier.doi","10.1016/j.healun.2004.02.014"],["dc.identifier.isi","000227922400002"],["dc.identifier.pmid","15812907"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/53571"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Elsevier Science Inc"],["dc.publisher.place","New york"],["dc.relation.conference","23rd Annual Meeting of the International-Society-for-Heart-and-Lung-Transplantation"],["dc.relation.eventlocation","Vienna, AUSTRIA"],["dc.relation.issn","1053-2498"],["dc.title","Donor pretreatment using the aerosolized prostacyclin analogue iloprost optimizes post-ischemic function of non-heart beating donor lungs"],["dc.type","conference_paper"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","140"],["dc.bibliographiccitation.issue","1-2"],["dc.bibliographiccitation.journal","Computer Physics Communications"],["dc.bibliographiccitation.lastpage","145"],["dc.bibliographiccitation.volume","177"],["dc.contributor.author","Binder, Kurt"],["dc.contributor.author","Horbach, Juergen"],["dc.contributor.author","Milchev, Andrey"],["dc.contributor.author","Mueller, Marcus"],["dc.contributor.author","Vink, Richard L. C."],["dc.date.accessioned","2018-11-07T11:00:56Z"],["dc.date.available","2018-11-07T11:00:56Z"],["dc.date.issued","2007"],["dc.description.abstract","When simple or complex fluids are confined to ultrathin films or channels or other cavities of nanoscopic linear dimensions, the interplay of finite size and surface controls the phase behavior, and may lead to phase transitions rather different from the corresponding phenomena in the bulk. Monte Carlo simulation is a very suitable tool to clarify the complex behavior of such systems, since the boundary conditions providing the confinement can be controlled and arbitrarily varied, and detailed structural information on the inhomogeneous states of the considered systems is available. Examples used to illustrate these concepts include simple Ising models in pores and double-pyramid-shaped cavities with competing surface fields, where novel types of interface local ization-delocalization phenomena occur accompanied by \"macroscopic\" fluctuations, and colloid-polymer mixtures confined in slit pores. Finite size scaling concepts are shown to be a useful tool also for such systems \"in between\" the dimensionalities. (C) 2007 Elsevier B.V. All rights reserved."],["dc.identifier.doi","10.1016/j.cpc.2007.02.039"],["dc.identifier.isi","000248161700060"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/51036"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Elsevier Science Bv"],["dc.publisher.place","Amsterdam"],["dc.relation.conference","Conference on Computational Physics (CCP 2006)"],["dc.relation.eventlocation","Gyeongju, SOUTH KOREA"],["dc.relation.issn","0010-4655"],["dc.title","Monte Carlo simulations of phase transitions of systems in nanoscopic confinement"],["dc.type","conference_paper"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","724"],["dc.bibliographiccitation.issue","4"],["dc.bibliographiccitation.journal","European Journal of Organic Chemistry"],["dc.bibliographiccitation.lastpage","748"],["dc.contributor.author","Wu, Y."],["dc.contributor.author","Flynn, B."],["dc.contributor.author","Schirmer, H."],["dc.contributor.author","Funke, Frank"],["dc.contributor.author","Mueller, S."],["dc.contributor.author","Labahn, T."],["dc.contributor.author","Notzel, M."],["dc.contributor.author","de Meijere, Armin"],["dc.date.accessioned","2018-11-07T10:51:08Z"],["dc.date.available","2018-11-07T10:51:08Z"],["dc.date.issued","2004"],["dc.description.abstract","The beta-amino-substituted mu,beta-unsaturated Fischer carbene complexes 3 are readily available by a four step one-pot procedure from terminal alkynes, chromium hexacarbonyl and secondary amines (24 examples with yields of 68-99% and 7 examples with yields of 26-63%). The formal [3+2] cycloadditions of complexes 3 with different alkynes including diynes and enynes performed in donor solvents such as pyridine or acetonitrile afforded highly substituted 5-(dialkylamino)-3-ethoxycyclopentadienes 7, generally in medium to excellent yields (25 examples with yields of 60-95% and 7 examples with yields of 18-53%). The steric and electronic effects of the substituents on the carbene complexes and the incorporated alkynes on the regio- and stereo selectivity of the ring-forming reaction have been elaborated. An interesting 1,5- or, more likely, 1,2-migration of the dimethylamino group was observed for 5-(dimethylamino)-3-ethoxycyclopentadienes with trimethylsilyl and jPr substituents at C-5. Attempted asymmetric syntheses of cyclopentadienes 7 from complexes 3 with chiral amino groups or substituents were only moderately successful. At a center of chirality in the secondary amino group, complexes of type 3 gave compounds 7 with diastereomeric excesses of, at best, 59% in yields of 54%, and with a stereogenic center in the substituent R-1 attached to the vinyl group of 3, diastereomeric excesses as high as 94% could be achieved, but with poor chemical yields (21%). In general, cyclopentenones 21 could be easily obtained from the cyclopentadienes 7 under acidic conditions in very good yields (4 examples with yields of 81-98%, 1 example with an overall yield of 50% from complex 3). Intramolecular aldol reactions of dicarbonyl compounds generated by hydrolysis of cyclopentadienes 7 with acetal-protected aldehyde or ketone carbonyl groups in either the 5-substituent R-1 or the N-substituent R-2 led to the bicyclic compounds 22 and 23. The dimethylamino group in cyclopentenones 21 could be either eliminated or transformed into other functional groups via the quaternary ammonium salts 24. The elimination product, cyclopentadienone 27 can undergo dimerization either by a formal [4+2] or [2+2] cycloaddition. Cyclopentenone 21naaa with a bromovinyl-terminated side chain undergoes an intramolecular Heck reaction to form 5-methyl-4,6-dimethylenebicyclo[3.3.0]oct-1-en-3one (32) (37% yield). (C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004."],["dc.identifier.doi","10.1002/ejoc.200300534"],["dc.identifier.isi","000189310700007"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/48821"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Wiley-v C H Verlag Gmbh"],["dc.relation.issn","1434-193X"],["dc.title","From alpha,beta-unsaturated Fischer carbene complexes to highly substituted 3-ethoxycyclopentadienes, masked cyclopentenones"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","105"],["dc.bibliographiccitation.journal","Solid State Phenomena"],["dc.bibliographiccitation.lastpage","114"],["dc.bibliographiccitation.volume","94"],["dc.contributor.author","Kaganovskii, Y."],["dc.contributor.author","Antonov, I."],["dc.contributor.author","Ianetz, D."],["dc.contributor.author","Rosenbluh, M."],["dc.contributor.author","Ihlemann, Juergen"],["dc.contributor.author","Mueller, S."],["dc.contributor.author","Marowsky, Gerd"],["dc.contributor.author","Lipovskii, A. A."],["dc.date.accessioned","2018-11-07T10:42:29Z"],["dc.date.available","2018-11-07T10:42:29Z"],["dc.date.issued","2003"],["dc.description.abstract","In a glass matrix containing nanocrystalline Ag clusters (quantum dots) and illuminated by nanosecond and sub-picosecond pulsed lasers, the metal nanocrystals are observed to move rapidly toward the surface. The motion leads to agglomeration and coalescence of the clusters at the surface. Processes responsible for the motion and coalescence are suggested, and the motional kinetics based on the model are estimated and are found to be in agreement with the experimental observations."],["dc.identifier.isi","000186633600017"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/46810"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Trans Tech Publications"],["dc.publisher.place","Zürich"],["dc.relation.conference","Symposium on Interfacial Effects in Nanostructured Materials"],["dc.relation.eventend","2002-09-18"],["dc.relation.eventlocation","Warsaw, Poland"],["dc.relation.eventstart","2002-09-14"],["dc.relation.isbn","3-908450-80-2"],["dc.relation.ispartof","Interfacial effects and novel properties of nanomaterials"],["dc.title","Mass transfer in optical nanocomposites induced by pulsed laser irradiation"],["dc.type","conference_paper"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.journal","ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY"],["dc.bibliographiccitation.volume","236"],["dc.contributor.author","Mueller, Marcus"],["dc.contributor.author","Wang, J."],["dc.date.accessioned","2018-11-07T11:12:05Z"],["dc.date.available","2018-11-07T11:12:05Z"],["dc.date.issued","2008"],["dc.identifier.isi","000270280001192"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/53581"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Amer Chemical Soc"],["dc.publisher.place","Washington"],["dc.relation.conference","236th National Meeting of the American-Chemical-Society"],["dc.relation.eventlocation","Philadelphia, PA"],["dc.relation.issn","0065-7727"],["dc.title","PMSE 66-Microphase separation of dibock copolymer brushes in different solvents"],["dc.type","conference_abstract"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]