Photoswitchable Hydrogel Surface Topographies by Polymerisation‐Induced Diffusion

Herein, we describe the preparation of patterned photoresponsive hydrogels by using a facile method. This polymer‐network hydrogel coating consists of N‐isopropylacrylamide (NIPAAM), cross‐linking agent tripropylene glycol diacrylate (TPGDA), and a new photochromic spiropyran monoacrylate. In a pre‐study, a linear NIPAAM copolymer (without TPGDA) that contained the spiropyran dye was synthesised, which showed relatively fast photoswitching behaviour. Subsequently, the photopolymerisation of a similar monomer mixture that included TPGDA afforded freestanding hydrogel polymer networks. The light‐induced isomerisation of protonated merocyanine into neutral spiropyran under slightly acidic conditions resulted in macroscopic changes in the hydrophilicity of the entire polymer film, that is, shrinkage of the hydrogel. The degree of shrinkage could be controlled by changing the chemical composition of the acrylate mixture. After these pre‐studies, a hydrogel film with spatially modulated cross‐link density was fabricated through polymerisation‐induced diffusion, by using a patterned photomask. The resulting smooth patterned hydrogel coating swelled in slightly acidic media and the swelling was higher in the regions with lower cross‐linking densities, thus yielding a corrugated surface. Upon exposure to visible light, the surface topography flattened again, thus showing that a hydrogel coating could be created, the topography of which could be controlled by light irradiation.     

Aqueous Solution-Gel Synthesis of Strontium Bismuth Niobate (SrBi2Nb2O9)

The synthesis of multimetal oxides containing pentavalent elements like Nb and Ta out of an aqueous solution is very complicated due to the extremely high sensitivity of these metals towards hydrolysis. Moreover the only water-soluble starting compound is the oxalate which is not very suited for gel formation. Nevertheless, from Nb-oxalate it is possible to prepare a water-soluble Nb(V)-precursor by chemical modification. The synthesized precursor remains stable in the pH-range needed for gel formation. This Nb(V)-precursor is used for the synthesis of the ferroelectric material SrBi₂Nb₂O₉ (SBN). An aqueous acetate-citrate solution-gel precursor for SBN was prepared. The chemical homogeneity of this precursor was investigated by means of TEM-experiments. All metal ions were found to be homogeneously dispersed in the precursor gel at least down to 10 nm. The SBN phase formation is followed by means of X-ray Diffraction. It has been shown that the perovskite phase already forms at 550°C.     

Glow Discharge as a Tool for Surface and Interface Analysis

Abstract

This review article focuses on the analytical capabilities of glow discharge optical emission spectrometry (GD‐OES) and mass spectrometry (GD‐MS) to perform compositional depth profiling (GD‐CDP). The properties of the Grimm‐type glow discharge as well as basic processes of sputtering are described and their influence on the GD as a surface and interface analytical tool are discussed. A series of examples from recent literature ranging from computer hard disks to molecular monolayers on copper substrates are presented to illustrate the excellent depth resolution that can be achieved with GD surface analytical techniques. The conditions for obtaining nanometer or even atomic‐layer depth resolution are discussed. Following this introduction is the possibilities of the technique a selection of applications principally chosen from our laboratories, demonstrating that GD‐OES and GD‐MS can be successfully employed as an analytical tool assisting the development of new materials and coatings. The applications cover common industrial tasks such as heat treatments, studies of diffusion processes at interfaces, and electrochemical depositions for biocompatible material. However, limitations and known artifacts are also discussed.     

Vibrational Fingerprinting of Defects Sites in Thin Films of Zeolitic Imidazolate Frameworks

Surface-mounted metal–organic frameworks (SURMOFs) are crystalline films of MOFs and have garnered a great deal of attention in the past years. So far, thin-film MOF research has been mainly focused on the synthesis and the exploration of potential applications of these materials, while a detailed understanding of their growth is still lacking. In this report evidence is provided for the inter-grown nature of surface-mounted thin films of Zn-ZIF-8 (SURZIF-8; ZIF=zeolitic imidazolate framework). Two distinct SURZIF-8 thin films have been made through layer-by-layer (LBL) growth after applying 20 and 50 LBL cycles. They have been characterized with atomic force microscopy (AFM) and Raman micro-spectroscopy. A detailed analysis of the Raman mapping data, inter alia using principal component analysis (PCA), revealed the existence of phase boundaries within the 20-cycle thin film, while the 50-cycle thin film is chemically more homogeneous. To further analyze these chemical heterogeneities, density functional theory (DFT) calculations were performed of three theoretical models providing spectroscopic fingerprints of the molecular vibrations associated with the Zn-ZIF-8 thin films. Based on these calculations and the experimental data distinct vibrational markers indicative for the presence of defects sites were identified.     

Guidelines for tuning the macropore structure of monolithic columns for high‐performance liquid chromatography

The ability to control the external porosity and to tune the dimensions of the macropore size on multiple length scales provides the possibility of tailoring the monolithic support structure towards separation performance. This paper discusses the properties of conventional polymer–monolithic stationary phases and its limitations regarding the effects of morphology on kinetic performance. Furthermore, guidelines to improve the macropore structure are discussed. The optimal monolithic macropore structure is characterized by high external porosity (while maintaining ultra‐high‐pressure stability), high structure homogeneity, polymer globule clusters in the submicron range, and macropores with a diameter tuned toward speed (small diameter in the 100–500 nm range using short beds) or efficiency (larger macropores in the range of 500 nm–1 μm allowing the use of longer column formats). Finally, promising approaches to control the morphology are discussed.     

Reversed-phase liquid chromatography coupled on-line to estrogen receptor bioaffinity detection based on fluorescence polarization

We describe the development and validation of a high-resolution screening (HRS) platform which couples gradient reversed-phase high-performance liquid chromatography (RP-HPLC) on-line to estrogen receptor α (ERα) affinity detection using fluorescence polarization (FP). FP, which allows detection at high wavelengths, limits the occurrence of interference from the autofluorescence of test compounds in the bioassay. A fluorescein-labeled estradiol derivative (E2-F) was synthesized and a binding assay was optimized in platereader format. After subsequent optimization in flow-injection analysis (FIA) mode, the optimized parameters were translated to the on-line HRS bioassay. Proof of principle was demonstrated by separating a mixture of five compounds known to be estrogenic (17β-estradiol, 17α-ethinylestradiol and the phytoestrogens coumestrol, coumarol and zearalenone), followed by post-column bioaffinity screening of the individual affinities for ERα. Using the HRS-based FP setup, we were able to screen affinities of off-line-generated metabolites of zearalenone for ERα. It is concluded that the on-line FP-based bioassay can be used to screen for the affinity of compounds without the disturbing occurrence of autofluorescence.