@misc{YarmanKurbanogluJetzschmannetal.2018, author = {Yarman, Aysu and Kurbanoglu, Sevinc and Jetzschmann, Katharina J. and Ozkan, Sibel A. and Wollenberger, Ulla and Scheller, Frieder W.}, title = {Electrochemical MIP-Sensors for Drugs}, series = {Current Medicinal Chemistry}, volume = {25}, journal = {Current Medicinal Chemistry}, number = {33}, publisher = {Bentham Science Publishers LTD}, address = {Sharjah}, issn = {0929-8673}, doi = {10.2174/0929867324666171005103712}, pages = {4007 -- 4019}, year = {2018}, abstract = {In order to replace bio-macromolecules by stable synthetic materials in separation techniques and bioanalysis biomimetic receptors and catalysts have been developed: Functional monomers are polymerized together with the target analyte and after template removal cavities are formed in the "molecularly imprinted polymer" (MIP) which resemble the active sites of antibodies and enzymes. Starting almost 80 years ago, around 1,100 papers on MIPs were published in 2016. Electropolymerization allows to deposit MIPs directly on voltammetric electrodes or chips for quartz crystal microbalance (QCM) and surface plasmon resonance (SPR). For the readout of MIPs for drugs amperometry, differential pulse voltammetry (DPV) and impedance spectroscopy (EIS) offer higher sensitivity as compared with QCM or SPR. Application of simple electrochemical devices allows both the reproducible preparation of MIP sensors, but also the sensitive signal generation. Electrochemical MIP-sensors for the whole arsenal of drugs, e.g. the most frequently used analgesics, antibiotics and anticancer drugs have been presented in literature and tested under laboratory conditions. These biomimetic sensors typically have measuring ranges covering the lower nano-up to millimolar concentration range and they are stable under extreme pH and in organic solvents like nonaqueous extracts.}, language = {en} } @misc{WuGlebeBoeker2015, author = {Wu, Lei and Glebe, Ulrich and B{\"o}ker, Alexander}, title = {Surface-initiated controlled radical polymerizations from silica nanoparticles, gold nanocrystals, and bionanoparticles}, series = {Polymer Chemistry}, volume = {6}, journal = {Polymer Chemistry}, number = {29}, publisher = {Royal Society of Chemistry}, address = {Cambridge}, issn = {1759-9954}, doi = {10.1039/c5py00525f}, pages = {5143 -- 5184}, year = {2015}, abstract = {In recent years, core/shell nanohybrids containing a nanoparticle core and a distinct surrounding shell of polymer brushes have received extensive attention in nanoelectronics, nanophotonics, catalysis, nanopatterning, drug delivery, biosensing, and many others. From the large variety of existing polymerization methods on the one hand and strategies for grafting onto nanoparticle surfaces on the other hand, the combination of grafting-from with controlled radical polymerization (CRP) techniques has turned out to be the best suited for synthesizing these well-defined core/shell nanohybrids and is known as surface-initiated CRP. Most common among these are surface-initiated atom transfer radical polymerization (ATRP), surface-initiated reversible addition-fragmentation chain transfer (RAFT) polymerization, and surface-initiated nitroxide-mediated polymerization (NMP). This review highlights the state of the art of growing polymers from nanoparticles using surface-initiated CRP techniques. We focus on mechanistic aspects, synthetic procedures, and the formation of complex architectures as well as novel properties. From the vast number of examples of nanoparticle/polymer hybrids formed by surface-initiated CRP techniques, we present nanohybrid formation from the particularly important and most studied silica nanoparticles, gold nanocrystals, and proteins which can be regarded as bionanoparticles.}, language = {en} } @misc{WolffCaprioglioStolterfohtetal.2019, author = {Wolff, Christian Michael and Caprioglio, Pietro and Stolterfoht, Martin and Neher, Dieter}, title = {Nonradiative Recombination in Perovskite Solar Cells}, series = {Advanced materials}, volume = {31}, journal = {Advanced materials}, number = {52}, publisher = {Wiley-VCH}, address = {Weinheim}, issn = {0935-9648}, doi = {10.1002/adma.201902762}, pages = {20}, year = {2019}, abstract = {Perovskite solar cells combine high carrier mobilities with long carrier lifetimes and high radiative efficiencies. Despite this, full devices suffer from significant nonradiative recombination losses, limiting their V-OC to values well below the Shockley-Queisser limit. Here, recent advances in understanding nonradiative recombination in perovskite solar cells from picoseconds to steady state are presented, with an emphasis on the interfaces between the perovskite absorber and the charge transport layers. Quantification of the quasi-Fermi level splitting in perovskite films with and without attached transport layers allows to identify the origin of nonradiative recombination, and to explain the V-OC of operational devices. These measurements prove that in state-of-the-art solar cells, nonradiative recombination at the interfaces between the perovskite and the transport layers is more important than processes in the bulk or at grain boundaries. Optical pump-probe techniques give complementary access to the interfacial recombination pathways and provide quantitative information on transfer rates and recombination velocities. Promising optimization strategies are also highlighted, in particular in view of the role of energy level alignment and the importance of surface passivation. Recent record perovskite solar cells with low nonradiative losses are presented where interfacial recombination is effectively overcome-paving the way to the thermodynamic efficiency limit.}, 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} } @misc{VankarLinker2015, author = {Vankar, Yashwant D. and Linker, Torsten}, title = {Recent Developments in the Synthesis of 2-C-Branched and 1,2-Annulated Carbohydrates}, series = {European journal of organic chemistry}, journal = {European journal of organic chemistry}, number = {35}, publisher = {Wiley-VCH}, address = {Weinheim}, issn = {1434-193X}, doi = {10.1002/ejoc.201501176}, pages = {7633 -- 7642}, year = {2015}, abstract = {The importance of carbohydrate chemistry in biological and medicinal chemistry has led to enormous developments in the synthesis of carbohydrate mimics. In this context, the synthesis of branched sugars in general and of 2-C-branched carbohydrates in particular, as well as the synthesis of 1,2-annulated sugars, have received immense attention. They serve not only as carbohydrate mimics in the form of stand-alone molecules, but also as useful intermediates in the synthesis of many natural products, their analogues, and glycosidase inhibitors. This microreview covers the recent synthetic efforts in this area and puts the subject matter into proper perspective for future developments.}, language = {en} } @misc{UnuabonahTaubert2014, author = {Unuabonah, Emmanuel Iyayi and Taubert, Andreas}, title = {Clay-polymer nanocomposites (CPNs): Adsorbents of the future for water treatment}, series = {Applied clay science : an international journal on the application and technology of clays and clay minerals}, volume = {99}, journal = {Applied clay science : an international journal on the application and technology of clays and clay minerals}, publisher = {Elsevier}, address = {Amsterdam}, issn = {0169-1317}, doi = {10.1016/j.clay.2014.06.016}, pages = {83 -- 92}, year = {2014}, abstract = {A class of adsorbents currently receiving growing attention is the clay-polymer nanocomposite (CPN) adsorbents. CPNs effectively treat water by adsorption and flocculation of both inorganic and organic micropollutants from aqueous solutions. Some of these CPNs - when modified with biocides - also have the ability to efficiently remove microorganisms such as Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus and Candida albicans from water. CPNs are far more easily recovered from aqueous media than neat clay. They also exhibit far better treatment times than either polymer or clay adsorbents. They have higher adsorption capacity and better life cycles compared with clay alone. CPNs therefore show an excellent potential as highly efficient water and waste treatment agents. This article reviews the various CPNs that have been prepared recently and used as adsorbents in the removal of micropollutants (inorganic, organic and biological) from aqueous solutions. A special focus is placed on CPNs that are not only interesting from an academic point of view but also effectively reduce the concentration of micropollutants in water to safe limits and also on new developments bordering on CPN use as water treatment agent that have not yet realized their full potential. (C) 2014 Elsevier B.V. All rights reserved.}, language = {en} } @misc{Taubert2015, author = {Taubert, Andreas}, title = {Electrospinning of Ionogels: Current Status and Future Perspectives}, series = {European journal of inorganic chemistry : a journal of ChemPubSoc Europe}, journal = {European journal of inorganic chemistry : a journal of ChemPubSoc Europe}, number = {7}, publisher = {Wiley-VCH}, address = {Weinheim}, issn = {1434-1948}, doi = {10.1002/ejic.201402490}, pages = {1148 -- 1159}, year = {2015}, abstract = {Ionogels (IGs), also termed ion gels, are functional hybrid materials based on an ionic liquid (IL) and a polymeric, hybrid, or inorganic matrix. IGs combine the properties of the matrix such as mechanical strength with IL properties like high ionic conductivity, high thermal stability, or catalytic activity. IGs are thus attractive for many applications, but the vast majority of IGs made and published so far are bulk materials or dense films. Applications like sensing or catalysis, however, would benefit from IGs with high surface areas or defined surface morphologies or architectures. In spite of this, only relatively few examples of high-surface-area IGs have been made so far; this has mostly been achieved by electrospinning, which has proven to be a promising strategy towards advanced IGs. The current review discusses first developments and outlines the future potential of electrospun ionogels, predominantly from a materials and inorganic chemistry perspective.}, language = {en} } @misc{SuriyanarayananCywinskiMoroetal.2012, author = {Suriyanarayanan, Subramanian and Cywinski, Piotr J. and Moro, Artur J. and Mohr, Gerhard J. and Kutner, Wlodzimierz}, title = {Chemosensors based on molecularly imprinted polymers}, series = {Topics in current chemistry}, volume = {325}, journal = {Topics in current chemistry}, number = {4}, editor = {Haupt, K}, publisher = {Springer}, address = {Berlin}, isbn = {978-3-642-28421-2}, issn = {0340-1022}, doi = {10.1007/128_2010_92}, pages = {165 -- 265}, year = {2012}, language = {en} } @misc{SchoeneRochSchulzetal.2017, author = {Sch{\"o}ne, Anne-Christin and Roch, Toralf and Schulz, Burkhard and Lendlein, Andreas}, title = {Evaluating polymeric biomaterial-environment interfaces by Langmuir monolayer techniques}, series = {Interface : journal of the Royal Society}, volume = {14}, journal = {Interface : journal of the Royal Society}, publisher = {Royal Society}, address = {London}, issn = {1742-5689}, doi = {10.1098/rsif.2016.1028}, pages = {18}, year = {2017}, abstract = {Polymeric biomaterials are of specific relevance in medical and pharmaceutical applications due to their wide range of tailorable properties and functionalities. The knowledge about interactions of biomaterials with their biological environment is of crucial importance for developing highly sophisticated medical devices. To achieve optimal in vivo performance, a description at the molecular level is required to gain better understanding about the surface of synthetic materials for tailoring their properties. This is still challenging and requires the comprehensive characterization of morphological structures, polymer chain arrangements and degradation behaviour. The review discusses selected aspects for evaluating polymeric biomaterial-environment interfaces by Langmuir monolayer methods as powerful techniques for studying interfacial properties, such as morphological and degradation processes. The combination of spectroscopic, microscopic and scattering methods with the Langmuir techniques adapted to polymers can substantially improve the understanding of their in vivo behaviour.}, language = {en} } @misc{MutludeEspinosaMeier2011, author = {Mutlu, Hatice and de Espinosa, Lucas Montero and Meier, Michael A. R.}, title = {Acyclic diene metathesis a versatile tool for the construction of defined polymer architectures}, series = {Chemical Society reviews}, volume = {40}, journal = {Chemical Society reviews}, number = {3}, publisher = {Royal Society of Chemistry}, address = {Cambridge}, issn = {0306-0012}, doi = {10.1039/b924852h}, pages = {1404 -- 1445}, year = {2011}, abstract = {Two decades have passed since the metathesis polymerisation of alpha,omega-dienes was successfully demonstrated by the group of Wagener and the term acyclic diene metathesis (ADMET) polymerisation was coined. Since then, the advances of metathesis chemistry have allowed to expand the scope of this versatile polymerisation reaction that nowadays finds applications in different fields, such as polymer, material, or medicinal chemistry. This critical review provides an insight into the historical aspects of ADMET and a detailed overview of the work done to date applying this versatile polymerisation reaction (221 references).}, language = {en} }