Vana, Philipp

[["dc.bibliographiccitation.firstpage","170"],["dc.bibliographiccitation.issue","2"],["dc.bibliographiccitation.journal","Journal of Polymer Science"],["dc.bibliographiccitation.lastpage","181"],["dc.bibliographiccitation.volume","59"],["dc.contributor.author","Wang, Shuang"],["dc.contributor.author","Vana, Philipp"],["dc.contributor.author","Zhang, Kai"],["dc.date.accessioned","2021-04-14T08:30:54Z"],["dc.date.available","2021-04-14T08:30:54Z"],["dc.date.issued","2020"],["dc.description.abstract","Abstract In living organisms, carbohydrate‐protein interactions play key roles in physiological and pathological processes, which are amplified by the “glycol‐cluster effect.” In this work, we synthesized novel fluorescent cellulose derivatives bearing mannose moieties via thiol‐ene click reactions by sequentially conjugating hydrophilic mannose‐oxyethoxylpropane‐thiol (Mann‐SH) and fluorescent coumarin‐oxyhexyl‐thiol (Coum‐SH) and rhodamine B‐ethyl‐thiol (RhB‐SH) to cellulose undecenoate with terminal double bonds. The amphiphilic fluorescent cellulose derivatives were converted into nanoparticles (NPs) by dropping into low ionic strength solutions (\\u0026lt;0.085 M). Obtained NPs have average sizes between 240 and 554 nm depending on the solution concentrations, exhibiting uniform size distributions (PDI values \\u0026lt;0.12). These uniform NPs exhibited excellent dispersion stability even at elevated temperatures. The mannose moieties were accessible to 1,4‐benzenediboronic acid (BDBA) in NaOH aqueous solutions. Under irradiation with UV light of 320–400 nm, the fluorescence of NPs increased by the formation of open‐ring rhodamine spiroamide, which could be a promising candidate for biomedical application."],["dc.description.abstract","A novel fluorescent cellulose derivative bearing mannose, coumarin, and rhodamine moieties is synthesized via two‐step photo‐/thermo‐initiated thiol‐ene click reactions, and stable uniform nanoparticles (NPs) are formed. The mannose moieties of NPs are accessible to 1,4‐benzenediboronic acid (BDBA) in NaOH solutions, and NPs are stabilized in strong alkaline solutions at elevated temperatures. The fluorescence intensity of NPs is increased under irradiation with UV light of 320–400 nm, which allows them to be promising candidates for biomedical applications. image"],["dc.description.sponsorship","China Scholarship Council http://dx.doi.org/10.13039/501100004543"],["dc.description.sponsorship","Georg‐August‐Universität Göttingen http://dx.doi.org/10.13039/501100003385"],["dc.description.sponsorship","Verband der Chemischen Industrie http://dx.doi.org/10.13039/100007215"],["dc.description.sponsorship","Fonds der Chemischen Industrie (FCI)"],["dc.identifier.doi","10.1002/pol.20200714"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/83407"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-399"],["dc.publisher","John Wiley \\u0026 Sons, Inc."],["dc.relation.eissn","2642-4169"],["dc.relation.issn","2642-4150"],["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","Mannosylated fluorescent cellulose‐based glycopolymers for stable uniform nanoparticles"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","2787"],["dc.bibliographiccitation.issue","13"],["dc.bibliographiccitation.journal","Nanoscale Advances"],["dc.bibliographiccitation.lastpage","2793"],["dc.bibliographiccitation.volume","4"],["dc.contributor.author","Cai, Yingying"],["dc.contributor.author","Peng, Wentao"],["dc.contributor.author","Vana, Philipp"],["dc.date.accessioned","2022-10-04T10:22:01Z"],["dc.date.available","2022-10-04T10:22:01Z"],["dc.date.issued","2022"],["dc.description.abstract","Polymer-grafted gold nanoparticles are attached to silica nanoparticles forming core–satellite structures, which rearrange into ring arrays when cast to surface. By etching away the silica core, ring-shaped patterns of gold nanoparticles are formed."],["dc.description.abstract","Polyethylene glycol-grafted gold nanoparticles are attached to silica nanoparticle cores\r\n via\r\n hydrogen bonding in a controlled fashion, forming well-defined core–satellite structures in colloidal solution. For separating these complex structures effectively from the parental nanoparticles, a straightforward and easy protocol using glass beads has been developed. The attached gold nanoparticles show unique surface mobility on the silica core surface, which allows for nanoparticle rearrangement into a 2D ring pattern surrounding the silica nanoparticle template when the core–satellite structures are cast to a planar surface. When etching away the silica core under conditions in which the polymer shell fixes the satellites to the substrate, highly ordered ring-shaped patterns of gold nanoparticles are formed. By variation of the size of the parental particles – 13 to 28 nm for gold nanoparticles and 39 to 62 nm for silica nanoparticles – a great library of different ring-structures regarding size and particle number is accessible with relative ease. The proposed protocol is low-cost and can easily be scaled up. It moreover demonstrates the power of hydrogen bonds in polymers as a dynamic anchoring tool for creating nanoclusters with rearrangement ability. We believe that this concept constitutes a powerful strategy for the development of new and innovative nanostructures."],["dc.description.sponsorship","Open-Access-Publikationsfonds 2022"],["dc.identifier.doi","10.1039/D2NA00204C"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/114565"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-606000"],["dc.relation.eissn","2516-0230"],["dc.rights","CC BY 3.0"],["dc.rights.uri","http://creativecommons.org/licenses/by/3.0/"],["dc.title","Gold nanoparticle ring arrays from core–satellite nanostructures made to order by hydrogen bond interactions"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.subtype","original_ja"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","1"],["dc.bibliographiccitation.issue","4"],["dc.bibliographiccitation.journal","Polymers"],["dc.bibliographiccitation.lastpage","3"],["dc.bibliographiccitation.volume","10"],["dc.contributor.author","Wagner, Jannik"],["dc.contributor.author","Peng, Wentao"],["dc.contributor.author","Vana, Philipp"],["dc.date.accessioned","2018-08-14T14:52:30Z"],["dc.date.available","2018-08-14T14:52:30Z"],["dc.date.issued","2018"],["dc.description.abstract","We report an efficient synthesis route for the formation of gold/silver-core-PE-shell nanohybrids in a simple self-assembly approach using PE with strong aurophilicity and argentophilicity, via thiol- and trithiocarbonate terminated moieties. This united the unique properties of polyethylene (PE) with gold and silver nanoparticles, using the well-defined end-group design of PE. These nanocomposites showed a similar solubility as PE, as confirmed by dynamic light scattering, and could be fully incorporated into a polyethylene matrix with different particle contents, as visualized by transmission electron microscopy. Using UV/vis-spectroscopy, we observed reversible, thermoresponsive aggregation/deaggregation properties in the nanohybrids, validating the strong and effective anchoring of PE on gold/silver surfaces."],["dc.description.sponsorship","Open-Access-Publikationsfonds 2018"],["dc.identifier.doi","10.3390/polym10040407"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/15112"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/15294"],["dc.language.iso","en"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","final"],["dc.publisher","MDPI"],["dc.relation.eissn","2073-4360"],["dc.rights","CC BY 4.0"],["dc.rights.uri","https://creativecommons.org/licenses/by/4.0"],["dc.title","Polyethylene-Grafted Gold and Silver Nanoparticles Using Catalyzed Chain Growth (CCG)"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","2000595"],["dc.bibliographiccitation.issue","2"],["dc.bibliographiccitation.journal","Macromolecular Materials and Engineering"],["dc.bibliographiccitation.volume","306"],["dc.contributor.author","Rauschendorfer, Judith Elisabeth"],["dc.contributor.author","Thien, Katharina Maria"],["dc.contributor.author","Denz, Manuela"],["dc.contributor.author","Köster, Sarah"],["dc.contributor.author","Ehlers, Florian"],["dc.contributor.author","Vana, Philipp"],["dc.date.accessioned","2021-04-14T08:30:55Z"],["dc.date.available","2021-04-14T08:30:55Z"],["dc.date.issued","2020"],["dc.description.abstract","Abstract Polymer layered silicate nanocomposites (PLSNs) made of montmorillonite (MMT) nanosheets and poly(methyl acrylate) (PMA) are synthesized and systematically characterized. MMT is first modified with a surface‐bound monomer and then functionalized with PMA via radical addition–fragmentation chain transfer (RAFT) polymerization using a grafting through approach. PMA‐modified MMT nanosheets with grafted polymer chains of variable length are obtained. The successful surface modification is demonstrated by near‐field scanning optical microscopy, thermogravimetric analysis, attenuated total reflection Fourier transform infrared spectroscopy, small‐angle X‐ray scattering, and size‐exclusion chromatography. The mechanical properties of various nanocomposites are evaluated via tensile testing. It can be shown that the mechanical properties (Young's modulus, tensile strength, toughness, and ductility) of these PLSNs can be fully controlled by using two major strategies, i.e., by the variation of the overall content of polymer‐modified MMT and by the variation of the chain length of the surface‐grafted polymer."],["dc.description.abstract","The mechanical properties of nanocomposites of poly(methyl acrylate) and surface‐functionalized montmorillonite nanosheets are explored. Polymer functionalization is achieved using radical addition–fragmentation chain transfer polymerization. Young's modulus, tensile strength, ductility, and toughness are investigated using tensile testing and can be specifically tailored by variation of filler content and surface‐grafted polymer chain length. image"],["dc.identifier.doi","10.1002/mame.202000595"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/83411"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-399"],["dc.relation.eissn","1439-2054"],["dc.relation.issn","1438-7492"],["dc.relation.orgunit","Institut für Röntgenphysik"],["dc.relation.workinggroup","RG Köster (Cellular Biophysics)"],["dc.rights","This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited."],["dc.subject.gro","x-ray scattering"],["dc.subject.gro","molecular biophysics"],["dc.title","Tuning the Mechanical Properties of Poly(Methyl Acrylate) via Surface‐Functionalized Montmorillonite Nanosheets"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.subtype","original_ja"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","706"],["dc.bibliographiccitation.issue","2"],["dc.bibliographiccitation.journal","Polymers"],["dc.bibliographiccitation.lastpage","729"],["dc.bibliographiccitation.volume","5"],["dc.contributor.author","Foerster, Nadja"],["dc.contributor.author","Poeppler, Ann-Christin"],["dc.contributor.author","Stalke, Dietmar"],["dc.contributor.author","Vana, Philipp"],["dc.date.accessioned","2018-11-07T09:23:49Z"],["dc.date.available","2018-11-07T09:23:49Z"],["dc.date.issued","2013"],["dc.description.abstract","This paper describes the Z-RAFT-star copolymerization of n-butyl acrylate (BA) and N-isopropyl acrylamide (NIPAm), respectively, with N-ethylacrylate-3,4-dimethylmaleimide (1.1), a monomer carrying a UV-reactive unit that undergoes photocrosslinking. Addition of 1.1 slows down the polymerization rate both for BA and for NIPAm polymerization. Double star formation due to radical attack to the 3,4-dimethylmaleimide moiety was found in the case of BA. Dead polymer formation, presumably due to aminolysis as side-reaction, was pronounced in the NIPAm system. These two effects broadened the molar mass distributions, but did not impede the formation of functional star polymers. The composition of the copolymers as well as the reactivity ratios for the applied comonomers were determined via NMR spectroscopy (BA-co-1.1 r(1.1) = 2.24 r(BA) = 0.95; NIPAm-co-1.1 r(1.1) = 0.96 r(NIPAm) = 0.05). In both cases, the comonomer is consumed preferably in the beginning of the polymerization, thus forming gradient copolymer stars with the UV-reactive units being located in the outer sphere."],["dc.identifier.doi","10.3390/polym5020706"],["dc.identifier.isi","000321948400013"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/10027"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/29674"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Mdpi Ag"],["dc.relation.issn","2073-4360"],["dc.rights","Goescholar"],["dc.rights.uri","https://goescholar.uni-goettingen.de/licenses"],["dc.title","Photocrosslinkable Star Polymers via RAFT-Copolymerizations with N-Ethylacrylate-3,4-dimethylmaleimide"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","2100054"],["dc.bibliographiccitation.journal","Macromolecular Materials and Engineering"],["dc.contributor.author","Rauschendorfer, Judith E."],["dc.contributor.author","Möckelmann, Jytte"],["dc.contributor.author","Vana, Philipp"],["dc.date.accessioned","2021-04-14T08:29:23Z"],["dc.date.available","2021-04-14T08:29:23Z"],["dc.date.issued","2021"],["dc.description.abstract","Abstract Matrix‐free nanocomposite films of poly(methyl acrylate) (PMA) and montmorillonite (MMT) nanosheets that imitate the microscopic structure of nacre are developed and their mechanical properties are studied in detail via tensile testing. The exfoliated MMT nanosheets are grafted with PMA via a grafting‐through radical addition–fragmentation chain transfer polymerization in presence of a surface‐anchored ionic monomer. The mechanical properties are precisely tailored a) via the variation of the degree of polymerization of the surface‐grafted polymer, illustrating the impact of chain entanglement and the MMT content on the performance of the material, and b) via cross‐linking of the surface‐grafted polymer, either by partial change of the polymer topology from linear to star‐shape or by the introduction of hydrogen‐bonding units within the polymer. These experiments demonstrate the strong influence of the chain mobility of the surface‐grafted polymer on the mechanical properties of the nanocomposite material."],["dc.description.abstract","Matrix‐free nanocomposite films of poly(methyl acrylate) and montmorillonite are generated viaradical addition–fragmentation chain transfer polymerization. The mechanical properties are optimized viavariation of the degree of polymerization of the surface‐grafted polymer and via cross‐linking of the surface‐grafted polymer, by partial change of the polymer topology or by introduction of hydrogen‐bonding units within the polymer. image"],["dc.identifier.doi","10.1002/mame.202100054"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/82886"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-399"],["dc.relation.eissn","1439-2054"],["dc.relation.issn","1438-7492"],["dc.rights","This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited."],["dc.title","Enhancing the Mechanical Properties of Matrix‐Free Poly(Methyl Acrylate)‐Grafted Montmorillonite Nanosheets by Introducing Star Polymers and Hydrogen Bonding Moieties"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","695"],["dc.bibliographiccitation.issue","4"],["dc.bibliographiccitation.journal","Polymers"],["dc.bibliographiccitation.lastpage","716"],["dc.bibliographiccitation.volume","7"],["dc.contributor.author","Förster, Nadja"],["dc.contributor.author","Schmidt, Sonja"],["dc.contributor.author","Vana, Philipp"],["dc.date.accessioned","2018-08-16T13:10:52Z"],["dc.date.available","2018-08-16T13:10:52Z"],["dc.date.issued","2015"],["dc.description.abstract","A new pathway to nano-sized hollow-sphere particles from six-arm star polymers with an amphiphilic core-corona structure, synthesized in a four-step-procedure by means of reversible addition-fragmentation chain transfer (RAFT) polymerization is presented, in order to achieve more stable and versatile nano-container systems, which could be applied in the fields of drug delivery or catalyst storage. Star-shaped amphiphilic, diblock copolymers serve as globular platforms for synthesizing uniform hollow structures. By the introduction of monomer units carrying UV-cross-linkable dimethyl maleimido functionalities into the outer sphere of these star polymers, the carrier's shell could be stabilized under UV-irradiation. After removal of the RAFT-core-constituting the central hub of the star polymer-by aminolysis, the carrier is ready for loading."],["dc.identifier.doi","10.3390/polym7040695"],["dc.identifier.fs","612089"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/13660"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/15359"],["dc.language.iso","en"],["dc.notes.status","final"],["dc.rights.access","openAccess"],["dc.title","Tailoring Confinement"],["dc.title.subtitle","Nano-Carrier Synthesis via Z-RAFT Star Polymerization"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","2474"],["dc.bibliographiccitation.issue","8"],["dc.bibliographiccitation.journal","Macromolecules"],["dc.bibliographiccitation.lastpage","2480"],["dc.bibliographiccitation.volume","44"],["dc.contributor.author","Meiser, Wibke"],["dc.contributor.author","Barth, Johannes"],["dc.contributor.author","Buback, Michael"],["dc.contributor.author","Kattner, Hendrik"],["dc.contributor.author","Vana, Philipp"],["dc.date.accessioned","2018-11-07T08:56:56Z"],["dc.date.available","2018-11-07T08:56:56Z"],["dc.date.issued","2011"],["dc.description.abstract","The kinetics of reversible addition fragmentation chain transfer (RAFT) polymerization of butyl acrylate with ethyl S-thiobenzoyl-2-thiopropionate (ETTP) as the RAFT agent has been studied. The concentrations of propagating (P-center dot) and intermediate radicals (INT\") were measured via highly time-resolved EPR spectroscopy after initiation by a laser single pulse. Predici simulation of experimental data results in rate coefficients for -40 degrees C of k(ad) = (1.4 +/- 0 4) x 10(6)L mol(-1) s(-1), k(beta) = (4.7 +/- 1.5) s(-1), and k(t)(cross) = 0.25 x k(upsilon), where k(t) is the rate coefficient for termination of two P-center dot species. Fast fragmentation of the intermediate radical is thus observed at this low temperature. Measuring the ratio of INT center dot to P-center dot concentrations during stationary polymerization at -40 and -70 degrees C yields K-eq = k(ad)/k(beta) values of (2.3 +/- 0.6) x 10(5) and 75 +/- 15 L mol(-1), respectively, which correspond to an apparent activation energy difference, E-A(k(ad)/k(beta)), of -49.5 kJ mol(-1)."],["dc.description.sponsorship","Fonds der Chemischen Industrie"],["dc.identifier.doi","10.1021/ma102491x"],["dc.identifier.isi","000289593200013"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/9445"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/23267"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Amer Chemical Soc"],["dc.relation.issn","0024-9297"],["dc.rights","Goescholar"],["dc.rights.uri","https://goescholar.uni-goettingen.de/licenses"],["dc.title","EPR Measurement of Fragmentation Kinetics in Dithiobenzoate-Mediated RAFT Polymerization"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","4100"],["dc.bibliographiccitation.issue","24"],["dc.bibliographiccitation.journal","Polymer Chemistry"],["dc.bibliographiccitation.lastpage","4105"],["dc.bibliographiccitation.volume","7"],["dc.contributor.author","Wöll, Dominik"],["dc.contributor.author","Nölle, Jan Martin"],["dc.contributor.author","Primpke, Sebastian"],["dc.contributor.author","Vana, Philipp"],["dc.contributor.author","Müllen, Klaus"],["dc.date.accessioned","2018-08-16T12:17:40Z"],["dc.date.available","2018-08-16T12:17:40Z"],["dc.date.issued","2016"],["dc.description.abstract","Free radical bulk polymerizations exhibit complex kinetics due to the viscosity increase during the polymerization process. Especially the termination rate constant can be strongly influenced by the mobility of polymer chains in the polymerization mixture. As a consequence an autoacceleration period, the so-called Trommsdorff effect, can be observed often. In order to investigate this behaviour on a nanoscopic scale, we directly visualized the mobility of molecules and macromolecules in polymerizing MMA solutions using a combination of highly sensitive fluorescence correlation spectroscopy and widefield fluorescence microscopy. For this purpose, rather monodisperse PMMA chains were synthesized by RAFT polymerization and fluorescence-labelled with perylenediimide derivatives. The behaviour of the different fluorescent probes could be related to their size and flexibility. Our studies show that diffusional heterogeneities must be accounted for when modeling bulk polymerization."],["dc.identifier.doi","10.1039/C6PY00590J"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/14185"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/15342"],["dc.language.iso","en"],["dc.notes.status","final"],["dc.rights.access","openAccess"],["dc.title","Diffusion of single molecular and macromolecular probes during the free radical bulk polymerization of MMA"],["dc.title.subtitle","Towards a better understanding of the Trommsdorff effect on a molecular level"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","1714"],["dc.bibliographiccitation.issue","10"],["dc.bibliographiccitation.journal","Polymer Chemistry"],["dc.bibliographiccitation.lastpage","1726"],["dc.bibliographiccitation.volume","6"],["dc.contributor.author","Schuetz, Jan-Hendrik"],["dc.contributor.author","Peng, Wentao"],["dc.contributor.author","Vana, Philipp"],["dc.date.accessioned","2018-08-23T13:03:51Z"],["dc.date.available","2018-08-23T13:03:51Z"],["dc.date.issued","2015"],["dc.description.abstract","Polycyclic polymers based on cyclic (ABC)n-multiblock-copolymers are formed via stepwise polymerization of three individual blocks and exploiting the ring merging reaction of these ring polymers. The so-obtained precursor ring-polymers were interconnected via click reaction. Small blocks within the rings with the ability to form self-complementary hydrogen bonds lead to intra- and intermolecular links between polycyclic polymers. The obtained materials, which mimic nature's paragon Titin, have some extraordinary material properties concerning elasticity and energy dissipation."],["dc.identifier.doi","10.1039/C4PY01458H"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/11668"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/15503"],["dc.language.iso","en"],["dc.notes.status","final"],["dc.rights.access","openAccess"],["dc.title","Titin-mimicking polycyclic polymers with shape regeneration and healing properties"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]