@article{ReitenbachGeigerWangetal.2023, author = {Reitenbach, Julija and Geiger, Christina and Wang, Peixi and Vagias, Apostolos N. and Cubitt, Robert and Schanzenbach, Dirk and Laschewsky, Andr{\´e} and Papadakis, Christine M. and M{\"u}ller-Buschbaum, Peter}, title = {Effect of magnesium salts with chaotropic anions on the swelling behavior of PNIPMAM thin films}, series = {Macromolecules : a publication of the American Chemical Society}, volume = {56}, journal = {Macromolecules : a publication of the American Chemical Society}, number = {2}, publisher = {American Chemical Society}, address = {Washington}, issn = {0024-9297}, doi = {10.1021/acs.macromol.2c02282}, pages = {567 -- 577}, year = {2023}, abstract = {Poly(N-isopropylmethacrylamide) (PNIPMAM) is a stimuli responsive polymer, which in thin film geometry exhibits a volume-phase transition upon temperature increase in water vapor. The swelling behavior of PNIPMAM thin films containing magnesium salts in water vapor is investigated in view of their potential application as nanodevices. Both the extent and the kinetics of the swelling ratio as well as the water content are probed with in situ time-of-flight neutron reflectometry. Additionally, in situ Fourier-transform infrared (FTIR) spectroscopy provides information about the local solvation of the specific functional groups, while two-dimensional FTIR correlation analysis further elucidates the temporal sequence of solvation events. The addition of Mg(ClO4)2 or Mg(NO3)2 enhances the sensitivity of the polymer and therefore the responsiveness of switches and sensors based on PNIPMAM thin films. It is found that Mg(NO3)2 leads to a higher relative water uptake and therefore achieves the highest thickness gain in the swollen state.}, language = {en} } @article{GeigerReitenbachHenscheletal.2021, author = {Geiger, Christina and Reitenbach, Julija and Henschel, Cristiane and Kreuzer, Lucas and Widmann, Tobias and Wang, Peixi and Mangiapia, Gaetano and Moulin, Jean-Fran{\c{c}}ois and Papadakis, Christine M. and Laschewsky, Andr{\´e} and M{\"u}ller-Buschbaum, Peter}, title = {Ternary nanoswitches realized with multiresponsive PMMA-b-PNIPMAM films in mixed water/acetone vapor atmospheres}, series = {Advanced engineering materials}, volume = {23}, journal = {Advanced engineering materials}, number = {11}, publisher = {Wiley-VCH}, address = {Weinheim}, issn = {1438-1656}, doi = {10.1002/adem.202100191}, pages = {12}, year = {2021}, abstract = {To systematically add functionality to nanoscale polymer switches, an understanding of their responsive behavior is crucial. Herein, solvent vapor stimuli are applied to thin films of a diblock copolymer consisting of a short poly(methyl methacrylate) (PMMA) block and a long poly(N-isopropylmethacrylamide) (PNIPMAM) block for realizing ternary nanoswitches. Three significantly distinct film states are successfully implemented by the combination of amphiphilicity and co-nonsolvency effect. The exposure of the thin films to nitrogen, pure water vapor, and mixed water/acetone (90 vol\%/10 vol\%) vapor switches the films from a dried to a hydrated (solvated and swollen) and a water/acetone-exchanged (solvated and contracted) equilibrium state. These three states have distinctly different film thicknesses and solvent contents, which act as switch positions "off," "on," and "standby." For understanding the switching process, time-of-flight neutron reflectometry (ToF-NR) and spectral reflectance (SR) studies of the swelling and dehydration process are complemented by information on the local solvation of functional groups probed with Fourier-transform infrared (FTIR) spectroscopy. An accelerated responsive behavior beyond a minimum hydration/solvation level is attributed to the fast build-up and depletion of the hydration shell of PNIPMAM, caused by its hydrophobic moieties promoting a cooperative hydration character.}, language = {en} } @article{KreuzerWidmannGeigeretal.2021, author = {Kreuzer, Lucas and Widmann, Tobias and Geiger, Christina and Wang, Peixi and Vagias, Apostolos N. and Heger, Julian Eliah and Haese, Martin and Hildebrand, Viet and Laschewsky, Andr{\´e} and Papadakis, Christine M. and M{\"u}ller-Buschbaum, Peter}, title = {Salt-dependent phase transition behavior of doubly thermoresponsive poly(sulfobetaine)-based diblock copolymer thin films}, series = {Langmuir : the ACS journal of surfaces and colloids / American Chemical Society}, volume = {37}, journal = {Langmuir : the ACS journal of surfaces and colloids / American Chemical Society}, number = {30}, publisher = {American Chemical Society}, address = {Washington}, issn = {0743-7463}, doi = {10.1021/acs.langmuir.1c01342}, pages = {9179 -- 9191}, year = {2021}, abstract = {The water vapor-induced swelling, as well as subsequent phase-transition kinetics, of thin films of a diblock copolymer (DBC) loaded with different amounts of the salt NaBr, is investigated in situ. In dilute aqueous solution, the DBC features an orthogonally thermoresponsive behavior. It consists of a zwitterionic poly(sulfobetaine) block, namely, poly(4-(N-(3'-methacrylamidopropyl)-N, N-dimethylammonio) butane-1-sulfonate) (PSBP), showing an upper critical solution temperature, and a nonionic block, namely, poly(N-isopropylmethacrylamide) (PNIPMAM), exhibiting a lower critical solution temperature. The swelling kinetics in D2O vapor at 15 degrees C and the phase transition kinetics upon heating the swollen film to 60 degrees C and cooling back to 15 degrees C are followed with simultaneous time-of-flight neutron reflectometry and spectral reflectance measurements. These are complemented by Fourier transform infrared spectroscopy. The collapse temperature of PNIPMAM and the swelling temperature of PSBP are found at lower temperatures than in aqueous solution, which is attributed to the high polymer concentration in the thin-film geometry. Upon inclusion of sub-stoichiometric amounts (relative to the monomer units) of NaBr in the films, the water incorporation is significantly increased. This increase is mainly attributed to a salting-in effect on the zwitterionic PSBP block. Whereas the addition of NaBr notably shifts the swelling temperature of PSBP to lower temperatures, the collapse temperature of PNIPMAM remains unaffected by the presence of salt in the films.}, language = {en} } @article{WangGeigerKreuzeretal.2022, author = {Wang, Peixi and Geiger, Christina and Kreuzer, Lucas and Widmann, Tobias and Reitenbach, Julija and Liang, Suzhe and Cubitt, Robert and Henschel, Cristiane and Laschewsky, Andr{\´e} and Papadakis, Christine M. and M{\"u}ller-Buschbaum, Peter}, title = {Poly(sulfobetaine)-based diblock copolymer thin films in water/acetone atmosphere: modulation of water hydration and co-nonsolvency-triggered film contraction}, series = {Langmuir : the ACS journal of surfaces and colloids}, volume = {38}, journal = {Langmuir : the ACS journal of surfaces and colloids}, number = {22}, publisher = {American Chemical Society}, address = {Washington}, issn = {0743-7463}, doi = {10.1021/acs.langmuir.2c00451}, pages = {6934 -- 6948}, year = {2022}, abstract = {The water swelling and subsequent solvent exchange including co-nonsolvency behavior of thin films of a doubly thermo-responsive diblock copolymer (DBC) are studied viaspectral reflectance, time-of-flight neutron reflectometry, and Fourier transform infrared spectroscopy. The DBC consists of a thermo-responsive zwitterionic (poly(4-((3-methacrylamidopropyl) dimethylammonio) butane-1-sulfonate)) (PSBP) block, featuring an upper critical solution temperature transition in aqueous media but being insoluble in acetone, and a nonionic poly(N-isopropylmethacrylamide) (PNIPMAM) block, featuring a lower critical solution temperature transition in water, while being soluble in acetone. Homogeneous DBC films of 50-100 nm thickness are first swollen in saturated water vapor (H2OorD2O), before they are subjected to a contraction process by exposure to mixed saturated water/acetone vapor (H2OorD2O/acetone-d6 = 9:1 v/v). The affinity of the DBC film toward H2O is stronger than for D2O, as inferred from the higher film thickness in the swollen state and the higher absorbed water content, thus revealing a pronounced isotope sensitivity. During the co-solvent-induced switching by mixed water/acetone vapor, a two-step film contraction is observed, which is attributed to the delayed expulsion of water molecules and uptake of acetone molecules. The swelling kinetics are compared for both mixed vapors (H2O/acetone-d6 and D2O/acetone-d6) and with those of the related homopolymer films. Moreover, the concomitant variations of the local environment around the hydrophilic groups located in the PSBP and PNIPMAM blocks are followed. The first contraction step turns out to be dominated by the behavior of the PSBP block, where as the second one is dominated by the PNIPMAM block. The unusual swelling and contraction behavior of the latter block is attributed to its co-nonsolvency behavior. Furthermore, we observe cooperative hydration effects in the DBC films, that is, both polymer blocks influence each other's solvation behavior.}, language = {en} } @article{KreuzerLindenmeirGeigeretal.2021, author = {Kreuzer, Lucas and Lindenmeir, Christoph and Geiger, Christina and Widmann, Tobias and Hildebrand, Viet and Laschewsky, Andr{\´e} and Papadakis, Christine M. and M{\"u}ller-Buschbaum, Peter}, title = {Poly(sulfobetaine) versus poly(N-isopropylmethacrylamide)}, series = {Macromolecules : a publication of the American Chemical Society}, volume = {54}, journal = {Macromolecules : a publication of the American Chemical Society}, number = {3}, publisher = {American Chemical Society}, address = {Washington}, issn = {0024-9297}, doi = {10.1021/acs.macromol.0c02281}, pages = {1548 -- 1556}, year = {2021}, abstract = {The swelling and co-nonsolvency behaviors in pure H2O and in a mixed H2O/CH3OH vapor atmosphere of two different polar, water-soluble polymers in thin film geometry are studied in situ. Films of a zwitterionic poly(sulfobetaine), namely, poly[3-((2-(methacryloyloxy)ethyl)dimethylammonio) propane-1-sulfonate] (PSPE), and a polar nonionic polymer, namely, poly(N-isopropylmethacrylamide) (PNIPMAM), are investigated in real time by spectral reflectance (SR) measurements and Fourier transform infrared (FTIR) spectroscopy. Whereas PSPE is insoluble in methanol, PNIPMAM is soluble but exhibits cononsolvency behavior in water/methanol mixtures. First, the swelling of PSPE and PNIPMAM thin films in H2O vapor is followed. Subsequently, CH3OH is added to the vapor atmosphere, and its contracting effect on the water-swollen films is monitored, revealing a co-nonsolvency-type behavior for PNIPMAM and PSPE. SR measurements indicate that PSPE and PNIPMAM behave significantly different during the H2O swelling and subsequent exposure to CH3OH, not only with respect to the amounts of absorbed water and CH3OH, but also to the cosolvent-induced contraction mechanisms. While PSPE thin films exhibit an abrupt one-step contraction, the contraction of PNIPMAM thin films occurs in two steps. FTIR studies corroborate these findings on a molecular scale and reveal the role of the specific functional groups, both during the swelling and the cosolvent-induced switching of the solvation state.}, language = {en} } @article{SchoenemannKocKarthaeuseretal.2021, author = {Sch{\"o}nemann, Eric and Koc, Julian and Karth{\"a}user, Jana and {\"O}zcan, Onur and Schanzenbach, Dirk and Schardt, Lisa and Rosenhahn, Axel and Laschewsky, Andr{\´e}}, title = {Sulfobetaine methacrylate polymers of unconventional polyzwitterion architecture and their antifouling properties}, series = {Biomacromolecules : an interdisciplinary journal focused at the interface of polymer science and the biological sciences}, volume = {22}, journal = {Biomacromolecules : an interdisciplinary journal focused at the interface of polymer science and the biological sciences}, number = {4}, publisher = {American Chemical Society}, address = {Washington}, issn = {1525-7797}, doi = {10.1021/acs.biomac.0c01705}, pages = {1494 -- 1508}, year = {2021}, abstract = {Combining high hydrophilicity with charge neutrality, polyzwitterions are intensely explored for their high biocompatibility and low-fouling properties. Recent reports indicated that in addition to charge neutrality, the zwitterion's segmental dipole orientation is an important factor for interacting with the environment. Accordingly, a series of polysulfobetaines with a novel architecture was designed, in which the cationic and anionic groups of the zwitterionic moiety are placed at equal distances from the backbone. They were investigated by in vitro biofouling assays, covering proteins of different charges and model marine organisms. All polyzwitterion coatings reduced the fouling effectively compared to model polymer surfaces of poly(butyl methacrylate), with a nearly equally good performance as the reference polybetaine poly(3-(N-(2-(methacryloyloxy)ethyl)-N,N-dimethylammonio)propanesulfonate). The specific fouling resistance depended on the detailed chemical structure of the polyzwitterions. Still, while clearly affecting the performance, the precise dipole orientation of the sulfobetaine group in the polyzwitterions seems overall to be only of secondary importance for their antifouling behavior.}, language = {en} } @article{KocSchardtNolteetal.2020, author = {Koc, Julian and Schardt, Lisa and Nolte, Kim and Beyer, Cindy and Eckhard, Till and Schwiderowski, Philipp and Clarke, Jessica L. and Finlay, John A. and Clare, Anthony S. and Muhler, Martin and Laschewsky, Andr{\´e} and Rosenhahn, Axel}, title = {Effect of dipole orientation in mixed, charge-equilibrated self-assembled monolayers on protein adsorption and marine biofouling}, series = {ACS applied materials \& interfaces}, volume = {12}, journal = {ACS applied materials \& interfaces}, number = {45}, publisher = {American Chemical Society}, address = {Washington}, issn = {1944-8244}, doi = {10.1021/acsami.0c11580}, pages = {50953 -- 50961}, year = {2020}, abstract = {While zwitterionic interfaces are known for their excellent low-fouling properties, the underlying molecular principles are still under debate. In particular, the role of the zwitterion orientation at the interface has been discussed recently. For elucidation of the effect of this parameter, self-assembled monolayers (SAMs) on gold were prepared from stoichiometric mixtures of oppositely charged alkyl thiols bearing either a quaternary ammonium or a carboxylate moiety. The alkyl chain length of the cationic component (11-mercaptoundecyl)-N,N,N-trimethylammonium, which controls the distance of the positively charged end group from the substrate's surface, was kept constant. In contrast, the anionic component and, correspondingly, the distance of the negatively charged carboxylate groups from the surface was varied by changing the alkyl chain length in the thiol molecules from 7 (8-mercaptooctanoic acid) to 11 (12-mercaptododecanoic acid) to 15 (16-mercaptohexadecanoic acid). In this way, the charge neutrality of the coating was maintained, but the charged groups exposed at the interface to water were varied, and thus, the orientation of the dipoles in the SAMs was altered. In model biofouling studies, protein adsorption, diatom accumulation, and the settlement of zoospores were all affected by the altered charge distribution. This demonstrates the importance of the dipole orientation in mixed-charged SAMs for their inertness to nonspecific protein adsorption and the accumulation of marine organisms. Overall, biofouling was lowest when both the anionic and the cationic groups were placed at the same distance from the substrate's surface.}, language = {en} } @article{HuLinMetwallietal.2023, author = {Hu, Neng and Lin, Li and Metwalli, Ezzeldin and Bießmann, Lorenz and Philipp, Martine and Hildebrand, Viet and Laschewsky, Andr{\´e} and Papadakis, Christine M. and Cubitt, Robert and Zhong, Qi and M{\"u}ller-Buschbaum, Peter}, title = {Kinetics of water transfer between the LCST and UCST thermoresponsive blocks in diblock copolymer thin films monitored by in situ neutron reflectivity}, series = {Advanced materials interfaces}, volume = {10}, journal = {Advanced materials interfaces}, number = {3}, publisher = {Wiley-VCH}, address = {Weinheim}, issn = {2196-7350}, doi = {10.1002/admi.202201913}, pages = {11}, year = {2023}, abstract = {The kinetics of water transfer between the lower critical solution temperature (LCST) and upper critical solution temperature (UCST) thermoresponsive blocks in about 10 nm thin films of a diblock copolymer is monitored by in situ neutron reflectivity. The UCST-exhibiting block in the copolymer consists of the zwitterionic poly(4((3-methacrylamidopropyl)dimethylammonio)butane-1-sulfonate), abbreviated as PSBP. The LCST-exhibiting block consists of the nonionic poly(N-isopropylacrylamide), abbreviated as PNIPAM. The as-prepared PSBP80-b-PNIPAM(400) films feature a three-layer structure, i.e., PNIPAM, mixed PNIPAM and PSBP, and PSBP. Both blocks have similar transition temperatures (TTs), namely around 32 degrees C for PNIPAM, and around 35 degrees C for PSBP, and with a two-step heating protocol (20 degrees C to 40 degrees C and 40 degrees C to 80 degrees C), both TTs are passed. The response to such a thermal stimulus turns out to be complex. Besides a three-step process (shrinkage, rearrangement, and reswelling), a continuous transfer of D2O from the PNIPAM to the PSBP block is observed. Due to the existence of both, LCST and UCST blocks in the PSBP80-b-PNIPAM(400 )film, the water transfer from the contracting PNIPAM, and mixed layers to the expanding PSBP layer occurs. Thus, the hydration kinetics and thermal response differ markedly from a thermoresponsive polymer film with a single LCST transition.}, language = {en} } @misc{SchoenemannKocAldredetal.2019, author = {Sch{\"o}nemann, Eric and Koc, Julian and Aldred, Nick and Clare, Anthony S. and Laschewsky, Andr{\´e} and Rosenhahn, Axel and Wischerhoff, Erik}, title = {Synthesis of novel sulfobetaine polymers with differing dipole orientations in their side chains, and their effects on the antifouling properties}, series = {Postprints der Universit{\"a}t Potsdam : Mathematisch-Naturwissenschaftliche Reihe}, journal = {Postprints der Universit{\"a}t Potsdam : Mathematisch-Naturwissenschaftliche Reihe}, number = {1}, issn = {1866-8372}, doi = {10.25932/publishup-52482}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-524820}, pages = {9}, year = {2019}, abstract = {The impact of the orientation of zwitterionic groups, with respect to the polymer backbone, on the antifouling performance of thin hydrogel films made of polyzwitterions is explored. In an extension of the recent discussion about differences in the behavior of polymeric phosphatidylcholines and choline phosphates, a quasi-isomeric set of three poly(sulfobetaine methacrylate)s is designed for this purpose. The design is based on the established monomer 3-[N-2-(methacryloyloxy)ethyl-N,N-dimethyl]ammonio-propane-1-sulfonate and two novel sulfobetaine methacrylates, in which the positions of the cationic and the ionic groups relative to the polymerizable group, and thus also to the polymer backbone, are altered. The effect of the varied segmental dipole orientation on their water solubility, wetting behavior by water, and fouling resistance is compared. As model systems, the adsorption of the model proteins bovine serum albumin (BSA), fibrinogen, and lysozyme onto films of the various polyzwitterion surfaces is studied, as well as the settlement of a diatom (Navicula perminuta) and barnacle cyprids (Balanus improvisus) as representatives of typical marine fouling communities. The results demonstrate the important role of the zwitterionic group's orientation on the polymer behavior and fouling resistance}, language = {en} } @article{SchoenemannKocAldredetal.2019, author = {Sch{\"o}nemann, Eric and Koc, Julian and Aldred, Nick and Clare, Anthony S. and Laschewsky, Andr{\´e} and Rosenhahn, Axel and Wischerhoff, Erik}, title = {Synthesis of Novel Sulfobetaine Polymers with Differing Dipole Orientations in Their Side Chains, and Their Effects on the Antifouling Properties}, series = {Macromolecular rapid communications}, volume = {41}, journal = {Macromolecular rapid communications}, number = {1}, publisher = {Wiley-VCH}, address = {Weinheim}, issn = {1022-1336}, doi = {10.1002/marc.201900447}, pages = {7}, year = {2019}, abstract = {The impact of the orientation of zwitterionic groups, with respect to the polymer backbone, on the antifouling performance of thin hydrogel films made of polyzwitterions is explored. In an extension of the recent discussion about differences in the behavior of polymeric phosphatidylcholines and choline phosphates, a quasi-isomeric set of three poly(sulfobetaine methacrylate)s is designed for this purpose. The design is based on the established monomer 3-[N-2-(methacryloyloxy)ethyl-N,N-dimethyl]ammonio-propane-1-sulfonate and two novel sulfobetaine methacrylates, in which the positions of the cationic and the ionic groups relative to the polymerizable group, and thus also to the polymer backbone, are altered. The effect of the varied segmental dipole orientation on their water solubility, wetting behavior by water, and fouling resistance is compared. As model systems, the adsorption of the model proteins bovine serum albumin (BSA), fibrinogen, and lysozyme onto films of the various polyzwitterion surfaces is studied, as well as the settlement of a diatom (Navicula perminuta) and barnacle cyprids (Balanus improvisus) as representatives of typical marine fouling communities. The results demonstrate the important role of the zwitterionic group's orientation on the polymer behavior and fouling resistance.}, language = {en} } @article{LaschewskyRosenhahn2019, author = {Laschewsky, Andr{\´e} and Rosenhahn, Axel}, title = {Molecular design of zwitterionic polymer interfaces}, series = {Langmuir}, volume = {35}, journal = {Langmuir}, number = {5}, publisher = {American Chemical Society}, address = {Washington}, issn = {0743-7463}, doi = {10.1021/acs.langmuir.8b01789}, pages = {1056 -- 1071}, year = {2019}, abstract = {The widespread occurrence of zwitterionic compounds in nature has incited their frequent use in designing biomimetic materials. Therefore, zwitterionic polymers are a thriving field. A particular interest for this particular polymer class has currently focused on their use in establishing neutral, low-fouling surfaces. After highlighting strategies to prepare model zwitterionic surfaces as well as those that are more suitable for practical purposes relying strongly on radical polymerization methods, we present recent efforts to diversify the structure of the hitherto quite limited variety of zwitterionic monomers and of the derived polymers. We identify key structural variables, consider their influence on essential properties such as overall hydrophilicity and long-term stability, and discuss promising targets for the synthesis of new variants.}, language = {en} } @article{KreuzerWidmannHohnetal.2019, author = {Kreuzer, Lucas and Widmann, Tobias and Hohn, Nuri and Wang, Kun and Biessmann, Lorenz and Peis, Leander and Moulin, Jean-Francois and Hildebrand, Viet and Laschewsky, Andr{\´e} and Papadakis, Christine M. and M{\"u}ller-Buschbaum, Peter}, title = {Swelling and exchange behavior of poly(sulfobetaine)-based block copolymer thin films}, series = {Macromolecules : web edition}, volume = {52}, journal = {Macromolecules : web edition}, number = {9}, publisher = {American Chemical Society}, address = {Washington}, issn = {0024-9297}, doi = {10.1021/acs.macromol.9b00443}, pages = {3486 -- 3498}, year = {2019}, abstract = {The humidity-induced swelling and exchange behavior of a block copolymer thin film, which consists of a zwitterionic poly(sulfobetaine) [poly(N,N-dimethyl-N-(3-(methacrylamido)propyl)ammoniopropanesulfonate) (PSPP)] block and a nonionic poly(N-isopropylacrylamide) (PNIPAM) block, are investigated by time-of-flight neutron reflectometry (TOF-NR). We monitor in situ the swelling in the H2O atmosphere, followed by an exchange with D2O. In the reverse experiment, swelling in the D2O atmosphere and the subsequent exchange with H2O are studied. Both, static and kinetic TOF-NR measurements indicate significant differences in the interactions between the PSPP80-b-PNIPAM(130) thin film and H2O or D2O, which we attribute to the different H- and D-bonds between water and the polymer. Changes in the chain conformation and hydrogen bonding are probed with Fourier transform infrared spectroscopy during the kinetics of the swelling and exchange processes, which reveals the key roles of the ionic SO3- group in the PSPP block and of the polar amide groups of both blocks during water uptake and exchange.}, language = {en} } @article{KocSimovichSchoenemannetal.2019, author = {Koc, Julian and Simovich, Tomer and Sch{\"o}nemann, Eric and Chilkoti, Ashutosh and Gardner, Harrison and Swain, Geoffrey W. and Hunsucker, Kelli and Laschewsky, Andr{\´e} and Rosenhahn, Axel}, title = {Sediment challenge to promising ultra-low fouling hydrophilic surfaces in the marine environment}, series = {Biofouling : the journal of bioadhesion and biofilm research}, volume = {35}, journal = {Biofouling : the journal of bioadhesion and biofilm research}, number = {4}, publisher = {Taylor \& Francis}, address = {London}, issn = {0892-7014}, doi = {10.1080/08927014.2019.1611790}, pages = {454 -- 462}, year = {2019}, abstract = {Hydrophilic coatings exhibit ultra-low fouling properties in numerous laboratory experiments. In stark contrast, the antifouling effect of such coatings in vitro failed when performing field tests in the marine environment. The fouling release performance of nonionic and zwitterionic hydrophilic polymers was substantially reduced compared to the controlled laboratory environment. Microscopy and spectroscopy revealed that a large proportion of the accumulated material in field tests contains inorganic compounds and diatomaceous soil. Diatoms adhered to the accumulated material on the coating, but not to the pristine polymer. Simulating field tests in the laboratory using sediment samples collected from the test sites showed that incorporated sand and diatomaceous earth impairs the fouling release characteristics of the coatings. When exposed to marine sediment from multiple locations, particulate matter accumulated on these coatings and served as attachment points for diatom adhesion and enhanced fouling. Future developments of hydrophilic coatings should consider accumulated sediment and its potential impact on the antifouling performance.}, language = {en} } @article{VishnevetskayaHildebrandNizardoetal.2019, author = {Vishnevetskaya, Natalya S. and Hildebrand, Viet and Nizardo, Noverra Mardhatillah and Ko, Chia-Hsin and Di, Zhenyu and Radulescu, Aurel and Barnsley, Lester C. and M{\"u}ller-Buschbaum, Peter and Laschewsky, Andr{\´e} and Papadakis, Christine M.}, title = {All-in-One "Schizophrenic" self-assembly of orthogonally tuned thermoresponsive diblock copolymers}, series = {Langmuir}, volume = {35}, journal = {Langmuir}, number = {19}, publisher = {American Chemical Society}, address = {Washington}, issn = {0743-7463}, doi = {10.1021/acs.langmuir.9b00241}, pages = {6441 -- 6452}, year = {2019}, abstract = {Smart, fully orthogonal switching was realized in a highly biocompatible diblock copolymer system with variable trigger-induced aqueous self-assembly. The polymers are composed of nonionic and zwitterionic blocks featuring lower and upper critical solution temperatures (LCSTs and UCSTs). In the system investigated, diblock copolymers from poly(N-isopropyl methacrylamide) (PNIPMAM) and a poly(sulfobetaine methacrylamide), systematic variation of the molar mass of the latter block allowed for shifting the UCST of the latter above the LCST of the PNIPMAM block in a salt-free condition. Thus, successive thermal switching results in "schizophrenic" micellization, in which the roles of the hydrophobic core block and the hydrophilic shell block are interchanged depending on the temperature. Furthermore, by virtue of the strong electrolyte-sensitivity of the zwitterionic polysulfobetaine block, we succeeded to shift its UCST below the LCST of the PNIPMAM block by adding small amounts of an electrolyte, thus inverting the pathway of switching. This superimposed orthogonal switching by electrolyte addition enabled us to control the switching scenarios between the two types of micelles (i) via an insoluble state, if the LCST-type cloud point is below the UCST-type cloud point, which is the case at low salt concentrations or (ii) via a molecularly dissolved state, if the LCST-type cloud point is above the UCST-type cloud point, which is the case at high salt concentrations. Systematic variation of the block lengths allowed for verifying the anticipated behavior and identifying the molecular architecture needed. The versatile and tunable self-assembly offers manifold opportunities, for example, for smart emulsifiers or for sophisticated carrier systems.}, language = {en} } @misc{SchoenemannLaschewskyRosenhahn2018, author = {Sch{\"o}nemann, Eric and Laschewsky, Andr{\´e} and Rosenhahn, Axel}, title = {Exploring the long-term hydrolytic behavior of zwitterionic polymethacrylates and polymethacrylamides}, series = {Postprints der Universit{\"a}t Potsdam : Mathematisch-Naturwissenschaftliche Reihe}, journal = {Postprints der Universit{\"a}t Potsdam : Mathematisch-Naturwissenschaftliche Reihe}, number = {1091}, issn = {1866-8372}, doi = {10.25932/publishup-47305}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-473052}, pages = {25}, year = {2018}, abstract = {The hydrolytic stability of polymers to be used for coatings in aqueous environments, for example, to confer anti-fouling properties, is crucial. However, long-term exposure studies on such polymers are virtually missing. In this context, we synthesized a set of nine polymers that are typically used for low-fouling coatings, comprising the well-established poly(oligoethylene glycol methylether methacrylate), poly(3-(N-2-methacryloylethyl-N,N-dimethyl) ammoniopropanesulfonate) ("sulfobetaine methacrylate"), and poly(3-(N-3-methacryamidopropyl-N,N-dimethyl)ammoniopropanesulfonate) ("sulfobetaine methacrylamide") as well as a series of hitherto rarely studied polysulfabetaines, which had been suggested to be particularly hydrolysis-stable. Hydrolysis resistance upon extended storage in aqueous solution is followed by ¹H NMR at ambient temperature in various pH regimes. Whereas the monomers suffered slow (in PBS) to very fast hydrolysis (in 1 M NaOH), the polymers, including the polymethacrylates, proved to be highly stable. No degradation of the carboxyl ester or amide was observed after one year in PBS, 1 M HCl, or in sodium carbonate buffer of pH 10. This demonstrates their basic suitability for anti-fouling applications. Poly(sulfobetaine methacrylamide) proved even to be stable for one year in 1 M NaOH without any signs of degradation. The stability is ascribed to a steric shielding effect. The hemisulfate group in the polysulfabetaines, however, was found to be partially labile.}, language = {en} } @misc{Laschewsky2014, author = {Laschewsky, Andr{\´e}}, title = {Structures and synthesis of zwitterionic polymers}, series = {Postprints der Universit{\"a}t Potsdam : Mathematisch-Naturwissenschaftliche Reihe}, journal = {Postprints der Universit{\"a}t Potsdam : Mathematisch-Naturwissenschaftliche Reihe}, number = {1043}, issn = {1866-8372}, doi = {10.25932/publishup-47616}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-476167}, pages = {60}, year = {2014}, abstract = {The structures and synthesis of polyzwitterions ("polybetaines") are reviewed, emphasizing the literature of the past decade. Particular attention is given to the general challenges faced, and to successful strategies to obtain polymers with a true balance of permanent cationic and anionic groups, thus resulting in an overall zero charge. Also, the progress due to applying new methodologies from general polymer synthesis, such as controlled polymerization methods or the use of "click" chemical reactions is presented. Furthermore, the emerging topic of responsive ("smart") polyzwitterions is addressed. The considerations and critical discussions are illustrated by typical examples.}, language = {en} } @misc{EnzenbergLaschewskyBoeffeletal.2017, author = {Enzenberg, Anne and Laschewsky, Andr{\´e} and Boeffel, Christine and Wischerhoff, Erik}, title = {Influence of the near molecular vicinity on the temperature regulated fluorescence response of poly(N-vinylcaprolactam)}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-400634}, pages = {21}, year = {2017}, abstract = {A series of new fluorescent dye bearing monomers, including glycomonomers, based on maleamide and maleic esteramide was synthesized. The dye monomers were incorporated by radical copolymerization into thermo-responsive poly(N-vinyl-caprolactam) that displays a lower critical solution temperature (LCST) in aqueous solution. The effects of the local molecular environment on the polymers' luminescence, in particular on the fluorescence intensity and the extent of solvatochromism, were investigated below as well as above the phase transition. By attaching substituents of varying size and polarity in the close vicinity of the fluorophore, and by varying the spacer groups connecting the dyes to the polymer backbone, we explored the underlying structure-property relationships, in order to establish rules for successful sensor designs, e.g., for molecular thermometers. Most importantly, spacer groups of sufficient length separating the fluorophore from the polymer backbone proved to be crucial for obtaining pronounced temperature regulated fluorescence responses.}, language = {en} } @article{CramerGambinossiWischerhoffetal.2015, author = {Cramer, Ashley D. and Gambinossi, Filippo and Wischerhoff, Erik and Laschewsky, Andr{\´e} and Miller, Reinhard and Ferri, James K.}, title = {Flexible thermoresponsive nanomembranes at the aqueous-air interface}, series = {Chemical communications}, volume = {51}, journal = {Chemical communications}, number = {5}, publisher = {Royal Society of Chemistry}, address = {Cambridge}, issn = {1359-7345}, doi = {10.1039/c4cc07359b}, pages = {877 -- 880}, year = {2015}, abstract = {A synthetic pathway is described to construct thermoresponsive freestanding nanomembranes at the aqueous-air interface of a pendant drop. Dynamic control of the reaction kinetics allows formation of viscoelastic interfaces supporting anisotropic stresses and mechanical stability, which can be tuned by external stimuli.}, language = {en} } @article{GambinossiSefcikWischerhoffetal.2015, author = {Gambinossi, Filippo and Sefcik, Lauren S. and Wischerhoff, Erik and Laschewsky, Andr{\´e} and Ferri, James K.}, title = {Engineering Adhesion to Thermoresponsive Substrates: Effect of Polymer Composition on Liquid-Liquid-Solid Wetting}, series = {ACS applied materials \& interfaces}, volume = {7}, journal = {ACS applied materials \& interfaces}, number = {4}, publisher = {American Chemical Society}, address = {Washington}, issn = {1944-8244}, doi = {10.1021/am507418m}, pages = {2518 -- 2528}, year = {2015}, abstract = {Adhesion control in liquidliquidsolid systems represents a challenge for applications ranging from self-cleaning to biocompatibility of engineered materials. By using responsive polymer chemistry and molecular self-assembly, adhesion at solid/liquid interfaces can be achieved and modulated by external stimuli. Here, we utilize thermosensitive polymeric materials based on random copolymers of di(ethylene glycol) methyl ether methacrylate (x = MEO(2)MA) and oligo(ethylene glycol) methyl ether methacrylate (y = OEGMA), that is, P(MEO(2)MA(x)-co-OEGMA(y)), to investigate the role of hydrophobicity on the phenomenon of adhesion. The copolymer ratio (x/y) dictates macromolecular changes enabling control of the hydrophilic-to-lipophilic balance (HBL) of the polymer brushes through external triggers such as ionic strength and temperature. We discuss the HBL of the thermobrushes in terms of the surface energy of the substrate by measuring the contact angle at waterdecaneP(MEO(2)MA(x)-co-OEGMA(y)) brush contact line as a function of polymer composition and temperature. Solid supported polyelectrolyte layers grafted with P(MEO(2)MA(x)-co-OEGMA(y)) display a transition in the wettability that is related to the lower critical solution temperature of the polymer brushes. Using experimental observation of the hydrophilic to hydrophobic transition by the contact angle, we extract the underlying energetics associated with liquidliquidsolid adhesion as a function of the copolymer ratio. The change in cellular attachment on P(MEO(2)MA(x)-co-OEGMA(y)) substrates of variable (x/y) composition demonstrates the subtle role of compositional tuning on the ability to control liquidliquidsolid adhesion in biological applications.}, language = {en} } @article{AdelsbergerBivigouKoumbaMiasnikovaetal.2015, author = {Adelsberger, Joseph and Bivigou Koumba, Achille Mayelle and Miasnikova, Anna and Busch, Peter and Laschewsky, Andr{\´e} and M{\"u}ller-Buschbaum, Peter and Papadakis, Christine M.}, title = {Polystyrene-block-poly (methoxy diethylene glycol acrylate)-block-polystyrene triblock copolymers in aqueous solution-a SANS study of the temperature-induced switching behavior}, series = {Colloid and polymer science : official journal of the Kolloid-Gesellschaft}, volume = {293}, journal = {Colloid and polymer science : official journal of the Kolloid-Gesellschaft}, number = {5}, publisher = {Springer}, address = {New York}, issn = {0303-402X}, doi = {10.1007/s00396-015-3535-6}, pages = {1515 -- 1523}, year = {2015}, abstract = {A concentrated solution of a symmetric triblock copolymer with a thermoresponsive poly(methoxy diethylene glycol acrylate) (PMDEGA) middle block and short hydrophobic, fully deuterated polystyrene end blocks is investigated in D2O where it undergoes a lower critical solution temperature-type phase transition at ca. 36 A degrees C. Small-angle neutron scattering (SANS) in a wide temperature range (15-50 A degrees C) is used to characterize the size and inner structure of the micelles as well as the correlation between the micelles and the formation of aggregates by the micelles above the cloud point (CP). A model featuring spherical core-shell micelles, which are correlated by a hard-sphere potential or a sticky hard-sphere potential together with a Guinier form factor describing aggregates formed by the micelles above the CP, fits the SANS curves well in the entire temperature range. The thickness of the thermoresponsive micellar PMDEGA shell as well as the hard-sphere radius increase slightly already below the cloud point. Whereas the thickness of the thermoresponsive micellar shell hardly shrinks when heating through the CP and up to 50 A degrees C, the hard-sphere radius decreases within 3.5 K at the CP. The volume fraction decreases already significantly below the CP, which may be at the origin of the previously observed gel-sol transition far below the CP (Miasnikova et al., Langmuir 28: 4479-4490, 2012). Above the CP, small, and at higher temperatures, large aggregates are formed by the micelles.}, language = {en} } @article{deMolinaIhlefeldtPrevostetal.2015, author = {de Molina, Paula Malo and Ihlefeldt, Franziska Stefanie and Prevost, Sylvain and Herfurth, Christoph and Appavou, Marie-Sousai and Laschewsky, Andr{\´e} and Gradzielski, Michael}, title = {Phase Behavior of Nonionic Microemulsions with Multi-end-capped Polymers and Its Relation to the Mesoscopic Structure}, series = {Langmuir}, volume = {31}, journal = {Langmuir}, number = {18}, publisher = {American Chemical Society}, address = {Washington}, issn = {0743-7463}, doi = {10.1021/acs.langmuir.5b00817}, pages = {5198 -- 5209}, year = {2015}, abstract = {The polymer architecture of telechelic or associative polymers has a large impact on the bridging of self-assembled structures. This Work presents: the phase behavior, small angle neutron scattering (SANS), dynamic light scattering (DLS), and fluorescence correlation spectroscopy (FCS) of a nonionic oil-in-water (O/W) microemulsion with hydrophobically end-capped multiarm polymers With functionalities f = 2, 3, and 4. For high polymer concentrations and large average interdroplet distance relative to the end-to-end distance of the polymer, d/R-ee; the system phase separates into a dense, highly connected droplet network phase, in equilibrium with a dilute phase. The extent of the two-phase region is larger for polymers With similar length but higher f. The Interaction potential between the droplets in the presence of polymer has both a repulsive and an attractive contribution as a result of the counterbalancing effects of the exclusion by polymer chains and bridging between droplets. This study experimentally demonstrates that higher polymer functionalities induce a stronger attractive force between droplets, which is responsible for a more extended phase separation region., and correlate with lower Collective droplet diffusivities and higher amplitude of the second relaxation time in DLS. The viscosity and the droplet self-diffusion obtained from FCS, however, are dominated by the end-capped chain concentration.}, language = {en} } @article{CouturierSuetterlinLaschewskyetal.2015, author = {Couturier, Jean-Philippe and S{\"u}tterlin, Martin and Laschewsky, Andr{\´e} and Hettrich, Cornelia and Wischerhoff, Erik}, title = {Responsive Inverse Opal Hydrogels for the Sensing of Macromolecules}, series = {Angewandte Chemie : a journal of the Gesellschaft Deutscher Chemiker ; International edition}, volume = {54}, journal = {Angewandte Chemie : a journal of the Gesellschaft Deutscher Chemiker ; International edition}, number = {22}, publisher = {Wiley-VCH}, address = {Weinheim}, issn = {1433-7851}, doi = {10.1002/anie.201500674}, pages = {6641 -- 6644}, year = {2015}, abstract = {Dual responsive inverse opal hydrogels were designed as autonomous sensor systems for (bio)macromolecules, exploiting the analyte-induced modulation of the opal's structural color. The systems that are based on oligo(ethylene glycol) macromonomers additionally incorporate comonomers with various recognition units. They combine a coil-to-globule collapse transition of the LCST type with sensitivity of the transition temperature toward molecular recognition processes. This enables the specific detection of macromolecular analytes, such as glycopolymers and proteins, by simple optical methods. While the inverse opal structure assists the effective diffusion even of large analytes into the photonic crystal, the stimulus responsiveness gives rise to strong shifts of the optical Bragg peak of more than 100nm upon analyte binding at a given temperature. The systems' design provides a versatile platform for the development of easy-to-use, fast, and low-cost sensors for pathogens.}, language = {en} } @article{FandrichBullerSchaeferetal.2015, author = {Fandrich, Artur and Buller, Jens and Sch{\"a}fer, Daniel and Wischerhoff, Erik and Laschewsky, Andr{\´e} and Lisdat, Fred}, title = {Electrochemical characterization of a responsive macromolecular interface on gold}, series = {Physica status solidi : A, Applications and materials science}, volume = {212}, journal = {Physica status solidi : A, Applications and materials science}, number = {6}, publisher = {Wiley-VCH}, address = {Weinheim}, issn = {1862-6300}, doi = {10.1002/pssa.201431698}, pages = {1359 -- 1367}, year = {2015}, abstract = {This study reports on the investigation of a thermoresponsive polymer as a thin film on electrodes and the influence of coupling a peptide and an antibody to the film. The utilized polymer from the class of poly(oligoethylene glycol)-methacrylate polymers (poly(OEGMA)) with carboxy functions containing side chains was synthesized and properly characterized in aqueous solutions. The dependence of the cloud point on the pH of the surrounding media is discussed. The responsive polymer was immobilized on gold electrodes as shown by electrochemical, quartz crystal microbalance (QCM), and atomic force microscopy (AFM) techniques. The temperature dependent behavior of the polymer covalently grafted to gold substrates is investigated using cyclic voltammetry (CV) in ferro-/ferricyanide solution. Significant changes in the slope of the temperature-dependence of the voltammetric peak current and the peak separation values clearly indicate the thermally induced conformational change on the surface. Finally, a biorecognition reaction between a short FLAG peptide (N-Asp-Tyr-Lys-Asp-Asp-Asp-Asp-Lys-C) covalently immobilized on the polymer interface and the corresponding IgG antibody was performed. The study shows that the responsiveness of the electrode is retained after peptide coupling and antibody binding, although the response is diminished.}, language = {en} } @article{ZhongMetwalliRawolleetal.2015, author = {Zhong, Qi and Metwalli, Ezzeldin and Rawolle, Monika and Kaune, Gunar and Bivigou Koumba, Achille Mayelle and Laschewsky, Andr{\´e} and Papadakis, Christine M. and Cubitt, Robert and M{\"u}ller-Buschbaum, Peter}, title = {Rehydration of Thermoresponsive Poly(monomethoxydiethylene glycol acrylate) Films Probed in Situ by Real-Time Neutron Reflectivity}, series = {Macromolecules : a publication of the American Chemical Society}, volume = {48}, journal = {Macromolecules : a publication of the American Chemical Society}, number = {11}, publisher = {American Chemical Society}, address = {Washington}, issn = {0024-9297}, doi = {10.1021/acs.macromol.5b00645}, pages = {3604 -- 3612}, year = {2015}, abstract = {The rehydration of thermoresponsive poly(monomethoxydiethylene glycol acrylate) (PMDEGA) films exhibiting a lower critical solution temperature (LCST) type demixing phase transition in aqueous environments, induced by a decrease in temperature, is investigated in situ with real-time neutron reflectivity. Two different starting conditions (collapsed versus partially swollen chain conformation) are compared. In one experiment, the temperature is reduced from above the demixing temperature to well below the demixing temperature. In a second experiment, the starting temperature is below the demixing temperature, but within the transition regime, and reduced to the same final temperature. In both cases, the observed rehydration process can be divided into three stages: first condensation of water from the surrounding atmosphere, then absorption of water by the PMDEGA film and evaporation of excess water, and finally, rearrangement of the PMDEGA chains. The final rehydrated film is thicker and contains more absorbed water as compared with the initially swollen film at the same temperature well below the demixing temperature.}, language = {en} } @article{ZerballLaschewskyvonKlitzing2015, author = {Zerball, Maximilian and Laschewsky, Andr{\´e} and von Klitzing, Regine}, title = {Swelling of Polyelectrolyte Multilayers: The Relation Between, Surface and Bulk Characteristics}, series = {The journal of physical chemistry : B, Condensed matter, materials, surfaces, interfaces \& biophysical chemistry}, volume = {119}, journal = {The journal of physical chemistry : B, Condensed matter, materials, surfaces, interfaces \& biophysical chemistry}, number = {35}, publisher = {American Chemical Society}, address = {Washington}, issn = {1520-6106}, doi = {10.1021/acs.jpcb.5b04350}, pages = {11879 -- 11886}, year = {2015}, abstract = {The odd even effect, i.e., the influence of the outermost layer of polyelectrolyte multilayers (PEMs) on their swelling behavior, is investigated. For that purpose poly(styrene sodium sulfonate) (PSS)/poly(diallyl-dimethylammonium chloride) (PDADMAC) polyelectrolyte multilayers are studied in air with 1\% relative humidity (RH), 30\% RH, 95\% RH, and in liquid water by ellipsometry, atomic force microscopy (AFM), and X-ray reflectometry (XRR). Since the total amount of water uptake in swollen PEMs is divided into two fractions, the void water and the swelling water, a correct evaluation of the odd even effect is only possible if both fractions are examined separately. In order to allow measuring samples over a larger thickness regime the investigation of a larger amount of samples is required. Therefore, the concept of separating void water from swelling water using neutron reflectometry is for the first time transferred to ellipsometry. The subsequent analysis of swelling water, void water, and roughness revealed the existence of two types of odd even effects: an odd even effect which addresses only the surface of the PEM (surface-odd even effect) and an odd even effect which addresses also the bulk of the PEM (bulk-odd even effect). The appearance of both effects is dependent on the environment; the surface-odd even effect is only detectable in humid air while the bulk-odd even effect is only detectable in liquid water. The bulk-odd even effect is related to the osmotic pressure between the PEM and the surrounding water. A correlation between the amount of void water and both odd even effects is not found. The amount of void water is independent of the terminated layer and the thickness of PEMs.}, language = {en} } @article{KopecLapokLaschewskyetal.2014, author = {Kopec, Maciej and Lapok, Lukasz and Laschewsky, Andr{\´e} and Zapotoczny, Szczepan and Nowakowska, Maria}, title = {Polyelectrolyte multilayers with perfluorinated phthalocyanine selectively entrapped inside the perfluorinated nanocompartments}, series = {Soft matter}, volume = {10}, journal = {Soft matter}, number = {10}, publisher = {Royal Society of Chemistry}, address = {Cambridge}, issn = {1744-683X}, doi = {10.1039/c2sm26938d}, pages = {1481 -- 1488}, year = {2014}, abstract = {A novel perfluorinated magnesium phthalocyanine (MgPcF64) was synthesized and employed to probe nanodomains in hydrophobically modified, amphiphilic cationic polyelectrolytes bearing alkyl and/or fluoroalkyl side chains. MgPcF64 was found to be solubilized exclusively in the aqueous solutions of the fluorocarbon modified polycations, occupying the perfluorinated nanocompartments provided, while analogous polyelectrolytes with alkyl side chains forming hydrocarbon nanocompartments could not host the MgPcF64 dye. Multilayer films were fabricated by means of the layer-by-layer (LbL) deposition method using sodium poly(styrene sulfonate) as a polyanion. Linear multilayer growth was confirmed by UV-Vis spectroscopy and spectroscopic ellipsometry. Atomic force microscopy studies indicated that the micellar conformation of the polycations is preserved in the multilayer films. Fluorescence spectroscopy measurements confirmed that MgPcF64 stays embedded inside the fluorocarbon domains after the deposition process. This facile way of selectively incorporating water-insoluble, photoactive molecules into the structure of polyelectrolyte multilayers may be utilized for nanoengineering of ultrathin film-based optoelectronic devices.}, language = {en} } @article{HildebrandLaschewskyZehm2014, author = {Hildebrand, Viet and Laschewsky, Andr{\´e} and Zehm, Daniel}, title = {On the hydrophilicity of polyzwitterion poly (N, N-dimethyl-N(3-(methacrylamido)propyl)ammoniopropane sulfonate) in water, deuterated water, and aqueous salt solutions}, series = {Journal of biomaterials science : Polymer edition}, volume = {25}, journal = {Journal of biomaterials science : Polymer edition}, number = {14-15}, publisher = {Routledge, Taylor \& Francis Group}, address = {Abingdon}, issn = {0920-5063}, doi = {10.1080/09205063.2014.939918}, pages = {1602 -- 1618}, year = {2014}, language = {en} } @article{CommingesFrascaSuetterlinetal.2014, author = {Comminges, Clement and Frasca, Stefano and Suetterlin, Martin and Wischerhoff, Erik and Laschewsky, Andr{\´e} and Wollenberger, Ursula}, title = {Surface modification with thermoresponsive polymer brushes for a switchable electrochemical sensor}, series = {RSC Advances}, volume = {4}, journal = {RSC Advances}, number = {81}, publisher = {Royal Society of Chemistry}, address = {Cambridge}, issn = {2046-2069}, doi = {10.1039/c4ra07190e}, pages = {43092 -- 43097}, year = {2014}, abstract = {Elaboration of switchable surfaces represents an interesting way for the development of a new generation of electrochemical sensors. In this paper, a method for growing thermoresponsive polymer brushes from a gold surface pre-modified with polyethyleneimine (PEI), subsequent layer-by-layer polyelectrolyte assembly and adsorption of a charged macroinitiator is described. We propose an easy method for monitoring the coil-to-globule phase transition of the polymer brush using an electrochemical quartz crystal microbalance with dissipation (E-QCM-D). The surface of these polymer modified electrodes shows reversible switching from the swollen to the collapsed state with temperature. As demonstrated from E-QCM-D measurements using an original signal processing method, the switch is operating in three reversible steps related to different interfacial viscosities. Moreover, it is shown that the one electron oxidation of ferrocene carboxylic acid is dramatically affected by the change from the swollen to the collapsed state of the polymer brush, showing a spectacular 86\% decrease of the charge transfer resistance between the two states.}, language = {en} } @article{KopecNiemiecLaschewskyetal.2014, author = {Kopec, Maciej and Niemiec, Wiktor and Laschewsky, Andr{\´e} and Nowakowska, Maria and Zapotoczny, Szczepan}, title = {Photoinduced energy and electron transfer in micellar multilayer films}, series = {The journal of physical chemistry : C, Nanomaterials and interfaces}, volume = {118}, journal = {The journal of physical chemistry : C, Nanomaterials and interfaces}, number = {4}, publisher = {American Chemical Society}, address = {Washington}, issn = {1932-7447}, doi = {10.1021/jp410808z}, pages = {2215 -- 2221}, year = {2014}, abstract = {Micellar multilayer films were prepared from an amphiphilic comb-like polycation ("polysoap") and the polyanion poly(styrene sulfonate) (PSS) using alternate polyelectrolyte layer-by-layer (LbL) self-assembly. Linear growth of the film thickness was evidenced by UV-vis spectroscopy and spectroscopic ellipsometry. Imaging by atomic force microscopy (AFM) indicated that the micellar conformation adopted by the polycation in solutions was preserved in the films. Thus, hydrophobic photoactive molecules, which were solubilized by the hydrophobic nanodomains of the micellar polymer prior to deposition, could be transferred into the films. Photoinduced energy transfer was observed in the nanostructured multilayers between naphthalene (donor) and perylene (acceptor) molecules embedded inside the polymer micelles. The efficiency of the energy transfer process can be controlled to some extent by introducing spacer layers between the layers containing the donor or acceptor, revealing partial stratification of the micellar LbL films. Also, photoinduced electron transfer was evidenced between perylene (donor) and butyl viologen (acceptor) molecules embedded inside the multilayers by steady-state fluorescence spectroscopy. The obtained photoactive nanostructures are promising candidates for solar-to-chemical energy conversion systems.}, language = {en} } @article{WeissWienkBoelensetal.2014, author = {Weiss, Jan and Wienk, Hans and Boelens, Rolf and Laschewsky, Andr{\´e}}, title = {Block copolymer micelles with an intermediate star-/flower-like structure studied by H-1 NMR relaxometry}, series = {Macromolecular chemistry and physics}, volume = {215}, journal = {Macromolecular chemistry and physics}, number = {9}, publisher = {Wiley-VCH}, address = {Weinheim}, issn = {1022-1352}, doi = {10.1002/macp.201300753}, pages = {915 -- 919}, year = {2014}, abstract = {H-1 NMR relaxation is used to study the self-assembly of a double thermoresponsive diblock copolymer in dilute aqueous solution. Above the first transition temperature, at which aggregation into micellar structures is observed, the trimethylsilyl (TMS)-labeled end group attached to the shell-forming block shows a biphasic T-2 relaxation. The slow contribution reflects the TMS groups located at the periphery of the hydrophilic shell, in agreement with a star-like micelle. The fast T-2 contribution corresponds to the TMS groups, which fold back toward the hydrophobic core, reflecting a flower-like micelle. These results confirm the formation of block copolymer micelles of an intermediate nature (i.e., of partial flower-like and star-like character), in which a part of the TMS end groups folds back to the core due to hydrophobic interactions.}, language = {en} } @misc{Laschewsky2014, author = {Laschewsky, Andr{\´e}}, title = {Structures and synthesis of zwitterionic polymers}, series = {Polymers}, volume = {6}, journal = {Polymers}, number = {5}, publisher = {MDPI}, address = {Basel}, issn = {2073-4360}, doi = {10.3390/polym6051544}, pages = {1544 -- 1601}, year = {2014}, abstract = {The structures and synthesis of polyzwitterions ("polybetaines") are reviewed, emphasizing the literature of the past decade. Particular attention is given to the general challenges faced, and to successful strategies to obtain polymers with a true balance of permanent cationic and anionic groups, thus resulting in an overall zero charge. Also, the progress due to applying new methodologies from general polymer synthesis, such as controlled polymerization methods or the use of "click" chemical reactions is presented. Furthermore, the emerging topic of responsive ("smart") polyzwitterions is addressed. The considerations and critical discussions are illustrated by typical examples.}, language = {en} } @article{OrtmannAhrensMilewskietal.2014, author = {Ortmann, Thomas and Ahrens, Heiko and Milewski, Sven and Lawrenz, Frank and Groening, Andreas and Laschewsky, Andr{\´e} and Garnier, Sebastien and Helm, Christiane A.}, title = {Lipid monolayers with adsorbed oppositely charged polyelectrolytes: Influence of reduced charge densities}, series = {Polymers}, volume = {6}, journal = {Polymers}, number = {7}, publisher = {MDPI}, address = {Basel}, issn = {2073-4360}, doi = {10.3390/polym6071999}, pages = {1999 -- 2017}, year = {2014}, abstract = {Polyelectrolytes in dilute solutions (0.01 mmol/L) adsorb in a two-dimensional lamellar phase to oppositely charged lipid monolayers at the air/water interface. The interchain separation is monitored by Grazing Incidence X-ray Diffraction. On monolayer compression, the interchain separation decreases to a factor of two. To investigate the influence of the electrostatic interaction, either the line charge density of the polymer is reduced (a statistic copolymer with 90\% and 50\% charged monomers) or mixtures between charged and uncharged lipids are used (dipalmitoylphosphatidylcholine (DPPC)/dioctadecyldimethylammonium bromide (DODAB)) On decrease of the surface charge density, the interchain separation increases, while on decrease of the linear charge density, the interchain separation decreases. The ratio between charged monomers and charged lipid molecules is fairly constant; it decreases up to 30\% when the lipids are in the fluid phase. With decreasing surface charge or linear charge density, the correlation length of the lamellar order decreases.}, language = {en} } @article{KyriakosAravopoulouAugsbachetal.2014, author = {Kyriakos, Konstantinos and Aravopoulou, Dionysia and Augsbach, Lukas and Sapper, Josef and Ottinger, Sarah and Psylla, Christina and Rafat, Ali Aghebat and Benitez-Montoya, Carlos Adrian and Miasnikova, Anna and Di, Zhenyu and Laschewsky, Andr{\´e} and M{\"u}ller-Buschbaum, Peter and Kyritsis, Apostolos and Papadakis, Christine M.}, title = {Novel thermoresponsive block copolymers having different architectures-structural, rheological, thermal, and dielectric investigations}, series = {Colloid and polymer science : official journal of the Kolloid-Gesellschaft}, volume = {292}, journal = {Colloid and polymer science : official journal of the Kolloid-Gesellschaft}, number = {8}, publisher = {Springer}, address = {New York}, issn = {0303-402X}, doi = {10.1007/s00396-014-3282-0}, pages = {1757 -- 1774}, year = {2014}, abstract = {Thermoresponsive block copolymers comprising long, hydrophilic, nonionic poly(methoxy diethylene glycol acrylate) (PMDEGA) blocks and short hydrophobic polystyrene (PS) blocks are investigated in aqueous solution. Various architectures, namely diblock, triblock, and starblock copolymers are studied as well as a PMDEGA homopolymer as reference, over a wide concentration range. For specific characterization methods, polymers were labeled, either by partial deuteration (for neutron scattering studies) or by fluorophores. Using fluorescence correlation spectroscopy, critical micellization concentrations are identified and the hydrodynamic radii of the micelles, r (h) (mic) , are determined. Using dynamic light scattering, the behavior of r (h) (mic) in dependence on temperature and the cloud points are measured. Small-angle neutron scattering enabled the detailed structural investigation of the micelles and their aggregates below and above the cloud point. Viscosity measurements are carried out to determine the activation energies in dependence on the molecular architecture. Differential scanning calorimetry at high polymer concentration reveals the glass transition of the polymers, the fraction of uncrystallized water and effects of the phase transition at the cloud point. Dielectric relaxation spectroscopy shows that the polarization changes reversibly at the cloud point, which reflects the formation of large aggregates upon heating through the cloud point and their redissolution upon cooling.}, language = {en} } @article{KyriakosPhilippAdelsbergeretal.2014, author = {Kyriakos, Konstantinos and Philipp, Martine and Adelsberger, Joseph and Jaksch, Sebastian and Berezkin, Anatoly V. and Lugo, Dersy M. and Richtering, Walter and Grillo, Isabelle and Miasnikova, Anna and Laschewsky, Andr{\´e} and M{\"u}ller-Buschbaum, Peter and Papadakis, Christine M.}, title = {Cononsolvency of water/methanol mixtures for PNIPAM and PS-b-PNIPAM: pathway of aggregate formation investigated using time-resolved SANS}, series = {Macromolecules : a publication of the American Chemical Society}, volume = {47}, journal = {Macromolecules : a publication of the American Chemical Society}, number = {19}, publisher = {American Chemical Society}, address = {Washington}, issn = {0024-9297}, doi = {10.1021/ma501434e}, pages = {6867 -- 6879}, year = {2014}, abstract = {We investigate the cononsolvency effect of poly(N-isopropylacrylamide) (PNIPAM) in mixtures of water and methanol. Two systems are studied: micellar solutions of polystyrene-b-poly(N-isopropylacrylamide) (PS-b-PNIPAM) diblock copolymers and, as a reference, solutions of PNIPAM homopolymers, both at a concentration of 20 mg/mL in DO. Using a stopped-flow instrument, fully deuterated methanol was rapidly added to these solutions at volume fractions between 10 and 20\%. Time-resolved turbidimetry revealed aggregate formation within 10-100 s. The structural changes on mesoscopic length scales were followed by time-resolved small-angle neutron scattering (TR-SANS) with a time resolution of 0.1 s. In both systems, the pathway of the aggregation depends on the content of deuterated methanol; however, it is fundamentally different for homopolymer and diblock copolymer solutions: In the former, very large aggregates (>150 nm) are formed within the dead time of the setup, gradient appears at their surface in the late stages. In contrast, the growth of the aggregates in the latter system features different regimes, and the final aggregate size is 50 nm, thus much smaller than for the homopolymer. For the diblock copolymer, the time dependence of the aggregate radius can be described by two models: In the initial stage, the diffusion-limited coalescence model describes the data well; however, the resulting coalescence time is unreasonably high. In the late stage, a logarithmic coalescence model based on an energy barrier which is proportional to the aggregate radius is successfully applied. and a concentration}, 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{BullerLaschewskyLutzetal.2011, author = {Buller, Jens and Laschewsky, Andr{\´e} and Lutz, Jean-Francois and Wischerhoff, Erik}, title = {Tuning the lower critical solution temperature of thermoresponsive polymers by biospecific recognition}, series = {Polymer Chemistry}, volume = {2}, journal = {Polymer Chemistry}, number = {7}, publisher = {Royal Society of Chemistry}, address = {Cambridge}, issn = {1759-9954}, doi = {10.1039/c1py00001b}, pages = {1486 -- 1489}, year = {2011}, abstract = {A thermosensitive statistical copolymer based on oligo(ethylene glycol) methacrylates incorporating biotin was synthesized by free radical copolymerisation. The influence of added avidin on its thermoresponsive behaviour was investigated. The specific binding of avidin to the biotinylated copolymers provoked a marked increase of the lower critical solution temperature.}, language = {en} } @article{ZehmLaschewskyHeunemannetal.2011, author = {Zehm, Daniel and Laschewsky, Andr{\´e} and Heunemann, Peggy and Gradzielski, Michael and Prevost, Sylvain and Liang, Hua and Rabe, J{\"u}rgen P. and Lutz, Jean-Francois}, title = {Synthesis and self-assembly of amphiphilic semi-brush and dual brush block copolymers in solution and on surfaces}, series = {Polymer Chemistry}, volume = {2}, journal = {Polymer Chemistry}, number = {1}, publisher = {Royal Society of Chemistry}, address = {Cambridge}, issn = {1759-9954}, doi = {10.1039/c0py00200c}, pages = {137 -- 147}, year = {2011}, abstract = {The combination of two techniques of controlled free radical polymerization, namely the reversible addition fragmentation chain transfer (RAFT) and the atom transfer radical polymerization (ATRP) techniques, together with the use of a macromonomer allowed the synthesis of symmetrical triblock copolymers, designed as amphiphilic dual brushes. One type of brush was made of poly(n-butyl acrylate) as soft hydrophobic block, i.e. characterized by a low glass transition temperature, while the other one was made of hydrophilic poly(ethylene glycol) (PEG). The new triblock polymers represent "giant surfactants" according to their molecular architecture. The hydrophobic and hydrophilic blocks microphase separate in the bulk. In aqueous solution, they aggregate into globular micellar aggregates, their size being determined by the length of the stretched polymer molecules. As determined by the combination of various scattering techniques for the dual brush copolymer, a rather compact structure is formed, which is dominated by the large hydrophobic poly(n-butyl acrylate) block. The aggregation number for the dual brush is about 10 times larger than for the "semi-brush" precursor copolymer, due to the packing requirements for the much bulkier hydrophobic core. On mica surfaces the triblock copolymers adsorb with worm-like backbones and stretched out side chains.}, language = {en} } @article{DodooSteitzLaschewskyetal.2011, author = {Dodoo, S. and Steitz, R. and Laschewsky, Andr{\´e} and von Klitzing, Regine}, title = {Effect of ionic strength and type of ions on the structure of water swollen polyelectrolyte multilayers}, series = {Physical chemistry, chemical physics : a journal of European Chemical Societies}, volume = {13}, journal = {Physical chemistry, chemical physics : a journal of European Chemical Societies}, number = {21}, publisher = {Royal Society of Chemistry}, address = {Cambridge}, issn = {1463-9076}, doi = {10.1039/c0cp01357a}, pages = {10318 -- 10325}, year = {2011}, abstract = {This study addresses the effect of ionic strength and type of ions on the structure and water content of polyelectrolyte multilayers. Polyelectrolyte multilayers of poly(sodium-4-styrene sulfonate) (PSS) and poly(diallyl dimethyl ammonium chloride) (PDADMAC) prepared at different NaF, NaCl and NaBr concentrations have been investigated by neutron reflectometry against vacuum, H2O and D2O. Both thickness and water content of the multilayers increase with increasing ionic strength and increasing ion size. Two types of water were identified, "void water" which fills the voids of the multilayers and does not contribute to swelling but to a change in scattering length density and "swelling water" which directly contributes to swelling of the multilayers. The amount of void water decreases with increasing salt concentration and anion radius while the amount of swelling water increases with salt concentration and anion radius. This is interpreted as a denser structure in the dry state and larger ability to swell in water (sponge) for multilayers prepared from high ionic strengths and/or salt solution of large anions. No exchange of hydration water or replacement of H by D was detected even after eight hours incubation time in water of opposing isotopic composition.}, language = {en} } @misc{TrollKulkarniWangetal.2011, author = {Troll, K. and Kulkarni, Amit and Wang, W. and Darko, C. and Koumba, A. M. Bivigou and Laschewsky, Andr{\´e} and M{\"u}ller-Buschbaum, Peter and Papadakis, Christine M.}, title = {The collapse transition of poly(styrene-b-(N-isopropyl acrylamide)) diblock copolymers in aqueous solution and in thin films}, series = {Colloid and polymer science : official journal of the Kolloid-Gesellschaft}, volume = {289}, journal = {Colloid and polymer science : official journal of the Kolloid-Gesellschaft}, number = {2}, publisher = {Springer}, address = {New York}, issn = {0303-402X}, doi = {10.1007/s00396-010-2344-1}, pages = {227 -- 227}, year = {2011}, language = {en} } @misc{WischerhoffBadiLaschewskyetal.2011, author = {Wischerhoff, Erik and Badi, Nezha and Laschewsky, Andr{\´e} and Lutz, Jean-Francois}, title = {Smart polymer surfaces concepts and applications in biosciences}, series = {Advances in polymer science = Fortschritte der Hochpolymeren-Forschung}, volume = {240}, journal = {Advances in polymer science = Fortschritte der Hochpolymeren-Forschung}, number = {1}, editor = {B{\"o}rner, Hans Gerhard and Lutz, JF}, publisher = {Springer}, address = {Berlin}, isbn = {978-3-642-20154-7}, issn = {0065-3195}, doi = {10.1007/12_2010_88}, pages = {1 -- 33}, year = {2011}, abstract = {Stimuli-responsive macromolecules (i.e., pH-, thermo-, photo-, chemo-, and bioresponsive polymers) have gained exponential importance in materials science, nanotechnology, and biotechnology during the last two decades. This chapter describes the usefulness of this class of polymer for preparing smart surfaces (e.g., modified planar surfaces, particles surfaces, and surfaces of three-dimensional scaffolds). Some efficient pathways for connecting these macromolecules to inorganic, polymer, or biological substrates are described. In addition, some emerging bioapplications of smart polymer surfaces (e.g., antifouling surfaces, cell engineering, protein chromatography, tissue engineering, biochips, and bioassays) are critically discussed.}, language = {en} } @article{SkrabaniaMiasnikovaBivigouKoumbaetal.2011, author = {Skrabania, Katja and Miasnikova, Anna and Bivigou Koumba, Achille Mayelle and Zehm, Daniel and Laschewsky, Andr{\´e}}, title = {Examining the UV-vis absorption of RAFT chain transfer agents and their use for polymer analysis}, series = {Polymer Chemistry}, volume = {2}, journal = {Polymer Chemistry}, number = {9}, publisher = {Royal Society of Chemistry}, address = {Cambridge}, issn = {1759-9954}, doi = {10.1039/c1py00173f}, pages = {2074 -- 2083}, year = {2011}, abstract = {The absorption characteristics of a large set of thiocarbonyl based chain transfer agents (CTAs) were studied by UV-vis spectroscopy in order to identify appropriate conditions for exploiting their absorbance bands in end-group analysis of polymers prepared by reversible addition-fragmentation chain transfer (RAFT) polymerisation. Substitution pattern and solvent polarity were found to affect notably the wavelengths and intensities of the pi-pi*- and n-pi*-transition of the thiocarbonyl bond of dithioester and trithiocarbonate RAFT agents. Therefore, it is advisable to refer in end group analysis to the spectral parameters of low molar mass analogues of the active polymer chain ends, rather than to rely on the specific RAFT agent engaged in the polymerisation. When using appropriate conditions, the quantification of the thiocarbonyl end-groups via the pi-pi* band of the thiocarbonyl moiety around 300-310 nm allows a facile, sensitive and surprisingly precise estimation of the number average molar mass of the polymers produced, without the need of particular end group labels. Moreover, when additional methods for absolute molar mass determination can be applied, the quantification of the thiocarbonyl end-groups by UV-spectroscopy provides a good estimate of the degree of active end group for a given polymer sample.}, language = {en} } @article{PrevostWattebledLaschewskyetal.2011, author = {Prevost, Sylvain and Wattebled, Laurent and Laschewsky, Andr{\´e} and Gradzielski, Michael}, title = {Formation of monodisperse charged vesicles in mixtures of cationic gemini surfactants and anionic SDS}, series = {Langmuir}, volume = {27}, journal = {Langmuir}, number = {2}, publisher = {American Chemical Society}, address = {Washington}, issn = {0743-7463}, doi = {10.1021/la103976p}, pages = {582 -- 591}, year = {2011}, abstract = {The aggregation behavior of catanionics formed by the mixture of cationic geminis derived from dodecyltrimethylammonium chloride (DTAC) and anionic sodium dodecylsulfate (SDS) was studied by means of phase studies and comprehensive small-angle neutron scattering (SANS) experiments at 25 degrees C and 50 mM overall concentration. The results are compared to those for the previously studied SDS + DTAC system. Various gemini spacers of different natures and geometries were used, but all of them had similar lengths: an ethoxy bridge, a double bond, and an aromatic ring binding the two DTACs in three different substitutions (ortho, meta, and para). SANS and SAXS data analysis indicates that the spacer has no large effect on the spheroidal micelles of pure surfactants formed at low concentration in water; however, specific effects appear with the addition of electrolytes. Microstructures formed in the catanionic mixtures are rather strongly dependent on the nature of the spacer. The most important finding is that for the hydrophilic, flexible ethoxy bridge, monodisperse vesicles with a fixed anionic/cationic charge ratio (depending only on the surfactant in excess) are formed. Furthermore, the composition of these vesicles shows that strongly charged aggregates are formed. This study therefore provides new opportunities for developing tailor-made gemini surfactants that allow for the fine tuning of catanionic structures.}, language = {en} } @article{GlatzelLaschewskyLutz2011, author = {Glatzel, Stefan and Laschewsky, Andr{\´e} and Lutz, Jean-Francois}, title = {Well-Defined uncharged polymers with a sharp UCST in water and in physiological milieu}, series = {Macromolecules : a publication of the American Chemical Society}, volume = {44}, journal = {Macromolecules : a publication of the American Chemical Society}, number = {2}, publisher = {American Chemical Society}, address = {Washington}, issn = {0024-9297}, doi = {10.1021/ma102677k}, pages = {413 -- 415}, year = {2011}, language = {en} } @article{AdelsbergerMeierKollBivigouKoumbaetal.2011, author = {Adelsberger, Joseph and Meier-Koll, Andreas and Bivigou Koumba, Achille Mayelle and Busch, Peter and Holderer, Olaf and Hellweg, Thomas and Laschewsky, Andr{\´e} and M{\"u}ller-Buschbaum, Peter and Papadakis, Christine M.}, title = {The collapse transition and the segmental dynamics in concentrated micellar solutions of P(S-b-NIPAM) diblock copolymers}, series = {Colloid and polymer science : official journal of the Kolloid-Gesellschaft}, volume = {289}, journal = {Colloid and polymer science : official journal of the Kolloid-Gesellschaft}, number = {5-6}, publisher = {Springer}, address = {New York}, issn = {0303-402X}, doi = {10.1007/s00396-011-2382-3}, pages = {711 -- 720}, year = {2011}, abstract = {We investigate concentrated solutions of poly(styrene-b-N-isopropyl acrylamide) (P(S-b-NIPAM)) diblock copolymers in deuterated water (D2O). Both structural changes and the changes of the segmental dynamics occurring upon heating through the lower critical solution temperature (LCST) of PNIPAM are studied using small-angle neutron scattering and neutron spin-echo spectroscopy. The collapse of the micellar shell and the cluster formation of collapsed micelles at the LCST as well as an increase of the segmental diffusion coefficient after crossing the LCST are detected. Comparing to our recent results on a triblock copolymer P(S-b-NIPAM-b-S) [25], we observe that the collapse transition of P(S-b-NIPAM) is more complex and that the PNIPAM segmental dynamics are faster than in P(S-b-NIPAM-b-S).}, language = {en} } @article{MarsatHeydenreichKleinpeteretal.2011, author = {Marsat, Jean-Noel and Heydenreich, Matthias and Kleinpeter, Erich and Berlepsch, Hans V. and Boettcher, Christoph and Laschewsky, Andr{\´e}}, title = {Self-Assembly into multicompartment micelles and selective solubilization by Hydrophilic-Lipophilic-Fluorophilic block copolymers}, series = {Macromolecules : a publication of the American Chemical Society}, volume = {44}, journal = {Macromolecules : a publication of the American Chemical Society}, number = {7}, publisher = {American Chemical Society}, address = {Washington}, issn = {0024-9297}, doi = {10.1021/ma200032j}, pages = {2092 -- 2105}, year = {2011}, abstract = {Amphiphilic linear ternary block copolymers (ABC) were synthesized in three consecutive steps by the reversible addition fragmentation chain transfer (RAFT) method. Using oligo(ethylene oxide) monomethyl ether acrylate, benzyl acrylate, and 1H,1H-perfluorobutyl acrylate monomers, the triblock copolymers consist of a hydrophilic (A), a lipophilic (B), and a fluorophilic (C) block. The block sequence of the triphilic copolymers was varied systematically to provide all possible variations: ABC, ACB, and BAC. All blocks have glass transition temperatures below 0 degrees C. Self-assembly into spherical micellar aggregates was observed in aqueous solution, where hydrophobic cores undergo local phase separation into various ultrastructures as shown by cryogenic transmission electron microscopy (cryo-TEM). Selective solubilization of substantial quantities of hydrocarbon and fluorocarbon low molar mass compounds by the lipophilic and fluorophilic block, respectively, is demonstrated.}, language = {en} } @article{WeissLaschewsky2011, author = {Weiss, Jan and Laschewsky, Andr{\´e}}, title = {Temperature-induced self-assembly of triple-responsive triblock copolymers in aqueous solutions}, series = {Langmuir}, volume = {27}, journal = {Langmuir}, number = {8}, publisher = {American Chemical Society}, address = {Washington}, issn = {0743-7463}, doi = {10.1021/la200115p}, pages = {4465 -- 4473}, year = {2011}, abstract = {A series of triple-thermoresponsive triblock copolymers from poly(N-n-propylacrylamide) (PNPAM, A), poly(methoxydiethylene glycol acrylate) (PMDEGA, B), and poly(N-ethylacrylamide) (PNEAM, C) was synthesized by sequential reversible addition-fragmentation chain transfer polymerizations. Polymers of differing block sequences, ABC, BAC, and ACB, with increasing phase transition temperatures in the order A < B < C were prepared. Their aggregation behavior in dilute aqueous solution was investigated using dynamic light scattering, turbidimetry, and NMR spectroscopy. The self-organization of such polymers was found to dependent strongly on the block sequence. While polymers with a terminal low-LCST (lower critical solution temperature) block undergo aggregation above the first phase transition temperature at 20-25 degrees C, triblock copolymers with the low-LCST block in the middle show aggregation only above the second phase transition. The collapse of the middle block is not sufficient to induce aggregation but produces instead stable, unimolecular micelles with a collapsed middle block, as supported by NMR and fluorescence probe data. Continued heating of all copolymers led to two additional thermal transitions at 40-55 and 70-80 degrees C, which could be correlated to the phase transitions of the B and C blocks, respectively. All polymers show a high tendency for cluster formation, once aggregation is induced. The carrier abilities of the triple responsive triblock copolymers for hydrophobic agents were probed with the solvatochromic fluorescence dye Nile Red. With passing through the first thermal transition, the block copolymers are capable of solubilizing Nile Red. In the case of block copolymers with sequences ABC or ACB, which bear the low-LCST block at one terminus, notable amounts of dye are solubilized already at this stage. In contrast, the hydrophobic probe is much less efficiently incorporated by the BAC triblock copolymer, which forms unimolecular micelles. Only after the collapse of the B block, when reaching the second phase transition at about 45 degrees C, does aggregation occur and solubilization becomes efficient. In the case of ABC and ACB polymers, the hydrophobic probe seems to partition between the originally collapsed A chains and the additional hydrophobic chains formed after the collapse of the less hydrophobic B block.}, language = {en} } @article{KristenHochreinLaschewskyMilleretal.2011, author = {Kristen-Hochrein, Nora and Laschewsky, Andr{\´e} and Miller, Reinhard and von Klitzing, Regine}, title = {Stability of foam Films of oppositely charged polyelectrolyte/surfactant mixtures - effect of isoelectric point}, series = {The journal of physical chemistry : B, Condensed matter, materials, surfaces, interfaces \& biophysical chemistry}, volume = {115}, journal = {The journal of physical chemistry : B, Condensed matter, materials, surfaces, interfaces \& biophysical chemistry}, number = {49}, publisher = {American Chemical Society}, address = {Washington}, issn = {1520-6106}, doi = {10.1021/jp206964k}, pages = {14475 -- 14483}, year = {2011}, abstract = {In the present paper, the influence of the surfactant concentration and the degree of charge of a polymer on foam film properties of oppositely charged polyelectrolyte/surfactant mixtures has been investigated. To verify the assumption that the position of the isoelectric point (IEP) does not change the character of the foam film stabilities, the position of the IEP of the polyelectrolyte/surfactant mixtures has been shifted in two different ways. Within the first series of experiments, the foam. film properties were studied using a fixed surfactant concentration of 3 x 10(-5) M in the mixture. Due to the low surfactant concentration, this is a rather dilute system. In the second approach, a copolymer of nonionic and ionic monomer units was Used to lower the charge density of the polymer. This gave rise to additional interactions between the polyelectrolyte and the surfactant, which makes the description of the foam film behavior more complex. In both systems, the same characteristics of the foam film stabilities were found: The foam film stability is reduced toward the IEP of the system, followed by a destabilization around the IEP., At polyelectrolyte concentrations above the IEP, foam films are very stable. However, the concentration range where unstable films were formed was rather broad, and the mechanisms leading to the destabilization had different origins. The results were compared with former findings on PAMPS/C(14)TAB mixtures with an IEP of 10(-4)M.(1)}, language = {en} } @article{ZehmLaschewskyLiangetal.2011, author = {Zehm, Daniel and Laschewsky, Andr{\´e} and Liang, Hua and Rabe, J{\"u}rgen P.}, title = {Straightforward access to amphiphilic dual bottle brushes by combining RAFT, ATRP, and NMP polymerization in one sequence}, series = {Macromolecules : a publication of the American Chemical Society}, volume = {44}, journal = {Macromolecules : a publication of the American Chemical Society}, number = {24}, publisher = {American Chemical Society}, address = {Washington}, issn = {0024-9297}, doi = {10.1021/ma2015613}, pages = {9635 -- 9641}, year = {2011}, abstract = {Molecular brush diblock copolymers were synthesized by the orthogonal overlay of the RAFT (reversible addition-fragmentation chain transfer), the ATRP (atom transfer radical polymerization), and the NMP (nitroxide-mediated polymerization) techniques. This unique combination enabled the synthesis of the complex amphiphilic polymers without the need of postpolymerization modifications, using a diblock copolymer intermediate made from two selectively addressable inimers and applying a sequence of four controlled free radical polymerization steps in total. The resulting polymers are composed of a thermosensitive poly(N-isopropylacrylamide) brush as hydrophilic block and a polystyrene brush as hydrophobic block, thus translating the structure of the established amphiphilic diblock copolymers known as macro surfactants to the higher size level of "giant surfactants". The dual molecular brushes and the aggregates formed on ultra flat solid substrates were visualized by scanning force microscopy (SFM).}, language = {en} } @article{HerfurthVollBulleretal.2012, author = {Herfurth, Christoph and Voll, Dominik and Buller, Jens and Weiss, Jan and Barner-Kowollik, Christopher and Laschewsky, Andr{\´e}}, title = {Radical addition fragmentation chain transfer (RAFT) polymerization of ferrocenyl (meth)acrylates}, series = {Journal of polymer science : A, Polymer chemistry}, volume = {50}, journal = {Journal of polymer science : A, Polymer chemistry}, number = {1}, publisher = {Wiley-Blackwell}, address = {Malden}, issn = {0887-624X}, doi = {10.1002/pola.24994}, pages = {108 -- 118}, year = {2012}, abstract = {We report on the controlled free radical homopolymerization of 1-ferrocenylethyl acrylate as well as of three new ferrocene bearing monomers, namely 4-ferrocenylbutyl acrylate, 2-ferrocenylamido-2-methylpropyl acrylate, and 4-ferrocenylbutyl methacrylate, by the RAFT technique. For comparison, the latter monomer was polymerized using ATRP, too. The ferrocene containing monomers were found to be less reactive than their analogues free of ferrocene. The reasons for the low polymerizability are not entirely clear. As the addition of free ferrocene to the reaction mixture did not notably affect the polymerizations, sterical hindrance by the bulky ferrocene moiety fixed on the monomers seems to be the most probable explanation. Molar masses found for 1-ferrocenylethyl acrylate did not exceed 10,000 g mol(-1), while for 4-ferrocenylbutyl (meth) acrylate molar masses of 15,000 g mol(-1) could be obtained. With PDIs as low as 1.3 in RAFT polymerization of the monomers, good control over the polymerization was achieved.}, language = {en} } @article{WeissLiWischerhoffetal.2012, author = {Weiss, Jan and Li, Ang and Wischerhoff, Erik and Laschewsky, Andr{\´e}}, title = {Water-soluble random and alternating copolymers of styrene monomers with adjustable lower critical solution temperature}, series = {Polymer Chemistry}, volume = {3}, journal = {Polymer Chemistry}, number = {2}, publisher = {Royal Society of Chemistry}, address = {Cambridge}, issn = {1759-9954}, doi = {10.1039/c1py00422k}, pages = {352 -- 361}, year = {2012}, abstract = {Random copolymers of 4-vinylbenzyl tri(oxyethylene) and tetra(oxyethylene) ethers, as well as alternating copolymers of 4-vinylbenzyl methoxytetra(oxyethylene) ether and a series of N-substituted maleimides, were synthesised by conventional free radical polymerisation, reversible addition fragmentation chain transfer (RAFT) and atom transfer radical polymerisation (ATRP). Their thermosensitive behaviour in aqueous solution was studied by turbidimetry and dynamic light scattering. Depending on the copolymer composition, a LCST type phase transition was observed in water. The transition temperature of the obtained random as well as alternating copolymers could be varied within a broad temperature window. In the case of the random copolymers, transition temperatures could be easily fine-tuned, as they showed a linear dependence on the copolymer composition, and were additionally modified by the nature of the polymer end-groups. Alternating copolymers were extremely versatile for implementing a broad range of variations of the phase transition temperatures. Further, while alternating copolymers derived from 4-vinylbenzyl methoxytetra(oxyethylene) ether and maleimides with small hydrophobic side chains underwent macroscopic phase separation when dissolved in water and heated above their cloud point, the incorporation of maleimides bearing larger hydrophobic substituents resulted in the formation of mesoglobules above the phase transition temperature, with hydrodynamic diameters of less than 100 nm.}, language = {en} }