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Hypothesis: Host rock weathering and incipient pedogenesis result in the exposition of minerals, e.g., clay minerals in sedimentary limestones. Once exposed, these minerals provide the surfaces for fluid-solid interactions that control the fate of dissolved or suspended compounds such as organic matter and colloids. However, the functional and compositional diversity of organic matter and colloids limits the assessment of reactivity and availability of clay mineral interfaces. Such assessment demands a mobile compound with strong affinity to clay surfaces that is alien to the subsurface., Experiment: We approached this challenge by using poly(ethylene glycol) (PEG) as interfacial tracer in limestone weathering experiments., Findings: PEG adsorption and transport was dependent on the availability of clay mineral surfaces and carbonate dissolution dynamics. In addition, PEG adsorption featured adsorption-desorption hysteresis which retained PEG mass on clay mineral surfaces. This resulted in different PEG transport for experiments conducted consecutively in the same porous medium. As such, PEG transport was reconstructed with a continuum-scale model parametrized by a Langmuir-type isotherm including hysteresis. Thus, we quantified the influence of exposed clay mineral surfaces on the transport of organic colloids in carbonate media. This renders PEG a suitable model colloid tracer for the assessment of clay surface exposition in porous media., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.)

Hypothesis: A prominent fraction of mobile organic matter in natural aqueous soil solutions is formed by molecules in sizes that seamlessly exceed the lower end of what is defined as a colloid. The hydrodynamics and the functional diversity of these molecules result in a transport behavior that is fundamentally different from smaller compounds. However, there is a lack of "reactive tracers" that allow for the study of colloidal transport phenomena appropriately. We hypothesize that tailor-made and well-defined synthetic polymers can overcome this limitation., Experiments: We prepared and characterized the hydrodynamic properties of water-soluble poly(ethylene glycol)s (PEG) and studied their adsorption to mixtures of quartz, illite, and goethite in batch and column experiments., Findings: We used this information to independently predict the transport of PEG with striking agreement to the observed mean breakthrough times in all porous media. As PEG transport can be comprehensively and quantitatively reconstructed, we conclude that functionalized PEGs are promising candidates to be used as tailorable and non-toxic tracers available in the size range of natural organic (macro-)molecules., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 The Author(s). Published by Elsevier Inc. All rights reserved.)

A new shape-memory polymer is presented, in which both the stable phase as well as the switching unit consist of two different metal complexes. Suitable metal ions, which simultaneously form labile complexes with histidine and stable ones with terpyridine ligands, are identified via isothermal titration calorimetry (ITC) measurements. Different copolymers are synthesized, which contain butyl methacrylate as the main monomer and the metal-binding ligands in the side chains. Zn(TFMS) 2 and NiCl 2 are utilized for the dual crosslinking, resulting in the formation of metallopolymer networks. The switching temperature can simply be tuned by changing the composition as well as by the choice of the metal ion. Strain fixity rates (about 99%) and very high strain recovery rates (up to 95%) are achieved and the mechanism is revealed using different techniques such as Raman spectroscopy., (© 2021 The Authors. Advanced Materials published by Wiley-VCH GmbH.)

Copolymerization of isoprene (IP) with glycidyl methacrylate (GMA) was performed under RAFT (reversible addition-fragmentation chain-transfer) polymerization conditions in a platform for high-output experimentation. Covering the range between 1 and 0.2 molar fraction of IP in the feed, four sets of reactions were carried out at 10, 15, 20, and 30 h at 115 °C. The kinetic data obtained were used to estimate the reactivity ratios using a nonlinear least-squares approach (NLLS). Reactivity ratios r GMA = 0.61 and r IP = 0.74 indicate that both monomers tend to crosspropagate in agreement with known literature values. Concerning the RAFT study, relatively good control and livingness of the copolymerization was observed except for the experiment in which IP represents 20 mol % in the feed. 1 H NMR characterization confirmed the presence of both monomers in the final copolymer, particularly the presence of the epoxy ring of GMA which is susceptible to post polymerization reactions. Finally, preliminary results on the hydrogenation of various polymers are discussed.

Shape memory polymers represent an interesting class of stimuli-responsive polymers. With their ability to memorize and recover their original shape, they could be useful in almost every area of our daily life. We herein present the synthesis of shape-memory metallopolymers in which the switching unit is designed by using bis(pyridine-triazole) metal complexes. The polymer networks were synthesized via free radical polymerization of methyl-, ethyl- or butyl-methacrylate, tri(ethylene glycol) dimethacrylate and a methacrylate moiety of the triazole-pyridine ligand. By the addition of zinc(II) or cobalt(II) acetate it was possible to achieve metallopolymer networks featuring shape-memory abilities. The successful formation of the metal-ligand complex was proven by Fourier transform infrared (FT-IR) spectroscopy and by 1 H NMR spectroscopy. Furthermore, the shape-recovery behavior was studied in detailed fashion and even triple-shape memory behavior could be revealed.

The determination of diol impurities in methoxy poly(ethylene glycol)s (mPEG)s is of high importance, e.g., in the area of pharmaceutical applications, since mPEGs are considered the gold standard-based on properties of biocompatibility, stealth effect against the immune system, and well-established procedures used in PEGylation reactions. Herein, we communicate a straightforward and fast approach for the resolution of the PEGdiol impurities in mPEG products by liquid chromatography on reversed-phase monolithic silica-rods. Thus, we utilize fine, in-house prepared and narrow dispersity mPEGs ( Ð ≤ 1.1) and commercial PEGdiol standards as a reference. Most efficient analysis of diol impurities becomes possible with reversed-phase liquid chromatography that results in selective elution of the PEGdiol from mPEG macromolecule populations in partition/adsorption mode. We do this by a minimum selectivity of the population of macromolecules characterizing the narrow molar mass distributions of mPEG. Control experiments with intentionally added water at the start of the well-controlled mPEG synthesis via the living anionic ring opening polymerization of ethylene oxide clearly reconciled the existence of PEGdiol impurity in chromatographed samples. The here-demonstrated methodology allows for the resolution of diol impurities of less than one percent in elution times of only a few minutes, confirmed by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS) of the collected elution fractions. The unique combination of the open flow-through pore structure of the monolithic silica rods and resultant varying accessibility of C18-derivatized pore surfaces indicates beneficial properties for robust and end-group-specific adsorption/partition liquid chromatography of synthetic macromolecules.

Metallopolymers combine properties of metal complexes and polymers and are thus interesting materials for a wide field of different applications. One current major field is the utilization as self-healing polymers, and for this purpose, palladium-SCS pincer complexes are synthesized. Well-defined copolymers featuring those metal complexes in the side chain are obtained using the reversible addition-fragmentation chain-transfer polymerization technique. By the addition of a tetravalent pyridine cross-linkers, reversible cross-linked supramolecular networks are prepared, enabling self-healing properties. By utilizing density functional theory calculations, IR, and Raman spectroscopy, as well as isothermal titration calorimetry, the complex formation, reversibility, and stability are studied. The information of these experiments also enables further optimizations for the design of similar reversible systems in the future., (© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Aspartate incorporated into the protein structure of mussel byssal threads is believed to play an important role, besides the reversible histidine-zinc interactions, in the self-healing behavior of mussel byssal threads. Therefore, copolymers containing both aspartate and histidine moieties are synthesized in order to investigate the influence of aspartate on the complexation of zinc(II) as well as on the self-healing behavior and the mechanical properties of the resulting supramolecular networks. For this purpose, isothermal titration calorimetry measurements of a model aspartate compound as well as of these copolymers are performed and the thermodynamic parameters are utilized for the design of self-healing copolymers. For this purpose, n-lauryl methacrylate-based copolymers containing histidine and aspartate are synthesized and crosslinked with zinc(II) acetate. The self-healing behavior of the supramolecular networks is investigated using scratch healing tests and the mechanical properties by nanoindentation., (© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

This paper presents the synthesis and characterization of d-fructose modified poly(ethylene glycol) (Fru-PEG) and fructose modified poly(ethylene glycol)-block-poly(ethyl hexyl glycidyl ether) (Fru-PEG-b-PEHG) that are both prepared by initiation with isopropyliden protected fructose, followed by deprotection of the sugar. The block copolymers are self-assembled into micelles, and are subsequently characterized by cryo-TEM and dynamic light scattering. The fluorescent dye Nile red is encapsulated as a model hydrophobic compound and fluorescent marker to perform initial uptake tests with breast cancer cells. The uptake of sugar and nonsugar decorated micelles is compared., (© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

The self-healing ability of self-healing materials is often analyzed using morphologic microscopy images. Here it was possible to show that morphologic information alone is not sufficient to judge the status of a self-healing process and molecular information is required as well. When comparing molecular coherent anti-Stokes Raman scattering (CARS) and morphological laser reflection images during a standard scratch healing test of an intrinsic self-healing polymer network, it was found that the morphologic closing of the scratch and the molecular crosslinking of the material do not take place simultaneously. This important observation can be explained by the fact that the self-healing process of the thiol-ene based polymer network is limited by the mobility of alkene-containing compounds, which can only be monitored by molecular CARS microscopy and not by standard morphological imaging. Additionally, the recorded CARS images indicate a mechanochemical activation of the self-healing material by the scratching/damaging process, which leads to an enhanced self-healing behavior in the vicinity of the scratch., (© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

The synthesis and comprehensive characterization of a systematic series of cleft-type anion receptors imbedded into a polymeric architecture is presented. For the first time, isothermal calorimetric titrations on polymeric halogen-bond-based donors were exploited to evaluate the dependence of the anion affinity on different key parameters (i.e. monomeric versus polymeric receptor, halogen versus hydrogen bonding, charge assistance). The combination of these donor systems with a copolymer bearing accepting carboxylate groups led to supramolecular cross-linked polymer networks showing excellent intrinsic self-healing behavior. FT-Raman spectroscopy and nano-indentation measurements were utilized to clarify the thermally induced self-healing mechanism based on the formation of halogen bonds. These first self-healing materials based on halogen bonds pave the way for new applications of halogen-bond donors in polymer and material science., (© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

The solution behavior originating from molecular characteristics of synthetic macromolecules plays a pivotal role in many areas, in particular the life sciences. This situation necessitates the use of complementary hydrodynamic analytical methods as the only means for a complete structural understanding of any macromolecule in solution. To this end, we present a combined hydrodynamic approach for studying in-house prepared, low dispersity poly(ethylene glycols)s (PEGs), also known as poly(ethylene oxide)s (PEOs) depending on the classification used, synthesized from varying initiation sites by the living anionic ring opening polymerization. The series of linear PEGs in the molar mass range of only a few thousand to 50 000 g mol -1 have been studied in detail via viscometry and sedimentation-diffusion analysis by analytical ultracentrifugation. The obtained estimations for intrinsic viscosity, diffusion coefficients, and sedimentation coefficients of the macromolecules in the solution-based analysis clearly showed self-consistency of the followed hydrodynamic approach. This self-consistency is underpinned by appropriate and physically sound values of hydrodynamic invariants, indicating adequate values of derived absolute molar masses. The classical scaling relations of Kuhn-Mark-Houwink-Sakurada of all molar-mass dependent hydrodynamic estimates show linear trends, allowing for interrelation of all parametric macromolecular characteristics. Differences among these are ascribed to the observation of α-end and chain-length dependent solvation of the macromolecules, identified from viscometric studies. This important information allows for analytical tracing of variations of scaling relationships and a physically sound estimation of hydrodynamic characteristics. The demonstrated self-sufficient methodology paves an important way for a complete structural understanding and potential replacement of pharmaceutically relevant PEGs by alternative macromolecules offering a suite of similar or tractably distinct physicochemical properties.

Soil organic matter (SOM) and its water-soluble components play an important role in terrestrial carbon cycling and associated ecosystem functions. Chemically, they are complex mixtures of organic compounds derived from decomposing plant material, microbial residues, as well as root exudates, and soil biota. To test the effect of the ecosystem type (forest and grassland) and fires events on the chemistry of dissolved organic matter (DOM), we applied a combination of laser-desorption/ionization time-of-flight mass spectrometry (LDI-TOF-MS) and 2D ( 1 H and 13 C) nuclear magnetic resonance (NMR) spectroscopy to water-extractable organic matter (WEOM) from a range of top soil samples. The aim was to assess the suitability of LDI-TOF-MS for the rapid characterization of WEOM. Therefore, we evaluated the effects of sample (pH and dilution) conditions and use of positive or negative reflector mode to identify the conditions under which LDI-TOF-MS best distinguished between WEOM from different sources. Thirty-six samples were measured with both analytical techniques and their chemical patterns were statistically evaluated to distinguish firstly the effect of the type of ecosystem (forest versus grassland) on WEOM characteristics, and secondly the impact of fire on the chemical composition of WEOM. The nonmetric multidimensional scaling (NMDS) analysis of the most suitable experimental LDI-TOF-MS conditions showed a clear separation between the type of vegetation and fire-induced changes, mostly reflecting the presence of poly(ethylene glycol) in grassland soils. Discrimination among WEOM from different vegetation types was preserved in the fire treated samples. The calculation of the relative abundance of certain functional structures in the WEOM samples revealed a common composition of forest and grassland WEOM, with polysaccharides and proteins making up to 60%. The compositional impact of forest fire on WEOM was more pronounced compared to the one of grassland, leading to a decline in the main components, and an increase in amino-sugars, fatty acids, and sterols. The recorded 1 H NMR and heteronuclear single quantum coherence (HSQC) spectra showed a decrease of the carbohydrate signal in WEOM from fire-treated samples, which was more pronounced in forest than in grassland soils., (Copyright © 2016 Elsevier B.V. All rights reserved.)

The analysis of synthetic polymers represents today an important part of polymer science to determine their physical properties and to optimize the performance of polymeric materials for block copolymers as well as blend systems. The characterization can easily and rapidly be performed by mass spectrometry. In particular, the film formation of a synthetic polymer is of interest in material research and quality control, which can be determined by employing mass spectrometric imaging (MSI) using secondary ion mass spectrometry (SIMS) or matrix-assisted laser desorption/ionization (MALDI) mass spectrometry. MALDI-MSI has been rapidly improved for the analysis of tissue cross-sections due to its soft ionization and accessible m/z range, which both also play an important role in polymer science. On the other hand, SIMS-MSI enables a sub-micrometer molecular spatial resolution, which is limited in MALDI-MSI due to the spatial resolution capabilities of the laser desorption process. The aim of the present contribution is to summarize recent advances in both imaging techniques for the analysis of synthetic polymers and to highlight their capabilities to correlate several imaging modalities in future applications., (Copyright © 2013 Elsevier B.V. All rights reserved.)

The use of solvents produces the largest amount of auxiliary waste in polymer science. Due to the fact that sustainable chemistry is becoming more and more important in polymer research, alternative reaction media have been investigated in order to reduce or replace the use of organic solvents. The most commonly used green solvents in polymer chemistry are water, supercritical carbon dioxide and ionic liquids. The progress of utilizing these green solvents in polymerization processes is reviewed and discussed in this critical review on the basis of results mainly published during the last five years (216 references).

Dextran was functionalized with 6-(2,2':6',2″-terpyridin-4'-yloxy)-hexanoic acid using two different ratios of terpyridine to dextran, leading to terpyridine-functionalized dextran esters possessing different degrees of substitution (DS = 0.23-0.41). The intra- and intermolecular complexation behavior of both functionalized biopolymers was studied using Fe(II) metal ions as well as activated Ru(III) complexes. The complexation behavior in the first case was studied by UV-visible and viscosity titration experiments. In the latter case, a water soluble comb-polymer could be obtained when using a PEG- functionalized terpyridine Ru(II) moiety for complexation. Moreover, nanoprecipitation was applied to self-assemble the functionalized dextrans into nanoparticles., (Copyright © 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)