@misc{Kleinpeter2014, author = {Kleinpeter, Erich}, title = {Quantification and visualization of the anisotropy effect in NMR spectroscopy by through-space NMR shieldings}, series = {Annual reports on NMR spectroscopy}, volume = {82}, journal = {Annual reports on NMR spectroscopy}, editor = {Webb, GA}, publisher = {Elsevier}, address = {San Diego}, isbn = {978-0-12-800184-4}, issn = {0066-4103}, doi = {10.1016/B978-0-12-800184-4.00003-5}, pages = {115 -- 166}, year = {2014}, abstract = {The anisotropy effect of functional groups (respectively the ring-current effect of aryl moieties) in H-1 NMR spectra has been computed as spatial NICS (through-space NMR chemical shieldings) and visualized by iso-chemical-shielding surfaces of various size and low(high) field direction. Hereby, the anisotropy/ring-current effect, which proves to be the molecular response property of spatial NICS, can be quantified and can be readily employed for assignment purposes in proton NMR spectroscopy-characteristic examples of stereochemistry and position assignments (the latter in supramolecular structures) will be given. In addition, anisotropy/ring-current effects in H-1 NMR spectra can be quantitatively separated from the second dominant structural effect in proton NMR spectra, the steric compression effect, pointing into the reverse direction, and the ring-current effect, by far the strongest anisotropy effect, can be impressively employed to visualize and quantify (anti) aromaticity and to clear up standing physical-organic phenomena as are pseudo-, spherical, captodative, homo-and chelatoaromaticity, to characterize the pi-electronic structure of, for example, fulvenes, fulvalenes, annulenes or fullerenes and to differentiate aromatic and quinonoid structures.}, 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{Laschewsky2012, author = {Laschewsky, Andr{\´e}}, title = {Recent trends in the synthesis of polyelectrolytes}, series = {Current opinion in colloid \& interface science : current chemistry}, volume = {17}, journal = {Current opinion in colloid \& interface science : current chemistry}, number = {2}, publisher = {Elsevier}, address = {London}, issn = {1359-0294}, doi = {10.1016/j.cocis.2011.08.001}, pages = {56 -- 63}, year = {2012}, abstract = {Recent developments in the synthesis of polyelectrolytes are highlighted, with respect to the nature of the ionic groups, the polymer backbones, synthetic methods, and additional functionality given to the polyelectrolytes. In fact, the synthesis of new polyelectrolytes is mostly driven by material aspects, currently. The article pays particular attention to strong polyelectrolytes, and the new methods of controlled polymerization. These methods and the so-called click reactions have enabled novel designs of polyelectrolytes. Nevertheless, the polymerization of unprotected ionic monomers is still challenging and limits the synthetic possibilities. The structural aspects are complemented by considerations with respect to the aspired uses of the new polyelectrolytes.}, language = {en} } @misc{FudickarLinker2018, author = {Fudickar, Werner and Linker, Torsten}, title = {Release of Singlet Oxygen from Organic Peroxides under Mild Conditions}, series = {ChemPhotoChem}, volume = {2}, journal = {ChemPhotoChem}, number = {7}, publisher = {Wiley-VCH}, address = {Weinheim}, issn = {2367-0932}, doi = {10.1002/cptc.201700235}, pages = {548 -- 558}, year = {2018}, abstract = {Singlet oxygen can be released in the dark in nearly quantitative yield from endoperoxides of naphthalenes, anthracenes and pyridones as an alternative to its generation by photosensitization. Recently, new donor systems have been designed which operate at very low temperatures but which are prepared from their parent forms at acceptable rates. Enhancement of the reactivity of donors is conveniently achieved by the design of the substitution pattern or through the use of plasmonic heating of nanoparticle-bound donors. The most important aim of these donor molecules is to transfer singlet oxygen in a controlled and directed manner to a target. Low temperatures and the linking between donors and acceptors reduce the random walk of oxygen and may force an attack at the desired position. By using chiral donor systems, new stereocenters might be introduced into prochiral acceptors.}, language = {en} } @misc{LendleinKelchSchulteetal.2004, author = {Lendlein, Andreas and Kelch, S. and Schulte, J. and Kratz, K.}, title = {Shape-memory polymers}, year = {2004}, 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{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} } @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{BornhorstKippHaaseetal.2018, author = {Bornhorst, Julia and Kipp, Anna Patricia and Haase, Hajo and Meyer, Soeren and Schwerdtle, Tanja}, title = {The crux of inept biomarkers for risks and benefits of trace elements}, series = {Trends in Analytical Chemistry}, volume = {104}, journal = {Trends in Analytical Chemistry}, publisher = {Elsevier}, address = {Oxford}, issn = {0165-9936}, doi = {10.1016/j.trac.2017.11.007}, pages = {183 -- 190}, year = {2018}, abstract = {Nowadays, the role of trace elements (TE) is of growing interest because dyshomeostasis of selenium (Se), manganese (Mn), zinc (Zn), and copper (Cu) is supposed to be a risk factor for several diseases. Thereby, research focuses on identifying new biomarkers for the TE status to allow for a more reliable description of the individual TE and health status. This review mirrors a lack of well-defined, sensitive, and selective biomarkers and summarizes technical limitations to measure them. Thus, the capacity to assess the relationship between dietary TE intake, homeostasis, and health is restricted, which would otherwise provide the basis to define adequate intake levels of single TE in both healthy and diseased humans. Besides that, our knowledge is even more limited with respect to the real life situation of combined TE intake and putative interactions between single TE.}, language = {en} } @misc{HoogenboomSchlaad2017, author = {Hoogenboom, Richard and Schlaad, Helmut}, title = {Thermoresponsive poly(2-oxazoline)s, polypeptoids, and polypeptides}, series = {Polymer Chemistry}, volume = {8}, journal = {Polymer Chemistry}, number = {1}, publisher = {Royal Society of Chemistry}, address = {Cambridge}, issn = {1759-9954}, doi = {10.1039/c6py01320a}, pages = {24 -- 40}, year = {2017}, abstract = {This review covers the recent advances in the emerging field of thermoresponsive polyamides or polymeric amides, i.e., poly(2-oxazoline)s, polypeptoids, and polypeptides, with a specific focus on structure-thermoresponsive property relationships, self-assembly, and applications.}, language = {en} }