Modulating Photochemical Properties to Enhance the Stability of Electronically Dimmable Eye Protection Devices†

The study evaluates compatibility of stabilizers with dye doped liquid crystal (LC) scaffolds that are used in electronically dimmable materials. The photodegradation of the materials was investigated and suitable stabilizers were evaluated to slow the degradation process. Various types of benzotriazole-based stabilizers were evaluated for stabilizing the liquid crystals. Based on spin trapping experiments, radicals generated upon UV exposure is likely responsible for the degradation of the system. The radical generation is competitively inhibited by the addition of stabilizers.     

Model systems for poly(acrylic acid) main-chain radicals based on the Kemp's triacid framework

Kemp's triacid (KTA) and cyclohexane tricarboxylic acid (CTA) are small-molecule model systems for acrylic acid polymers, having the same functionalities and stereoregularities as isotactic poly(methacrylic acid) (PMAA) and poly(acrylic acid) (PAA), respectively. As part of an ongoing investigation of radicals produced by photolysis of acrylic polymers, the photochemistry and free radicals from the model systems have been studied using time-resolved EPR spectroscopy as a function of temperature and pH. Radicals are created by direct photolysis of the acids at 248 nm or by sensitized photo-oxidation using quinone triplet states at 308 nm. The two methods of radical production lead to different chemically induced electron spin polarization (CIDEP) patterns in the ensuing radicals, which are simulated and discussed. Well-resolved spectra are obtained at all temperatures for the model system radicals, which are determined to be in the slow motion condition. DFT calculations of the model system radicals are presented and discussed in support of the experimental data.     

The energetics of lanthanum tantalate materials

Lanthanum tantalates are important refractory materials with application in photocatalysis, solid oxide fuel cells, and phosphors. Soft-chemical synthesis utilizing the Lindqvist ion, [Ta₆O₁₉]⁸⁻, has yielded a new phase, La₂Ta₂O₇(OH)₂. Using the hydrated phase as a starting material, a new lanthanum orthotantalate polymorph was formed by heating to 850 °C, which converts to a previously reported LaTaO₄ polymorph at 1200 °C. The stabilities of La₂Ta₂O₇(OH)₂ (LaTa−OH), the intermediate LaTaO₄ polymorph (LaTa-850), and the high temperature phase (LaTa-1200) were investigated using high-temperature oxide melt solution calorimetry. The enthalpy of formation from the oxides were calculated from the enthalpies of drop solution to be −87.1±9.6, −94.9±8.8, and −93.1±8.7 kJ/mol for LaTa−OH, LaTa-850, and LaTa-1200, respectively. These results indicate that the intermediate phase, LaTa-850, is the most stable. This pattern of energetics may be related to cation-cation repulsion of the tantalate cations. We also investigated possible LnTaO₄ and Ln₂Ta₂O₇(OH)₂ analogues of Ln=Pr, Nd to examine the relationship between cation size and the resulting phases.     

Sulfenylation chemistry using polymer-supported sulfides

Clean sulfenylations are observed upon reaction of activated methylenes with phenyl succinimidyl sulfide. When working with diethyl benzylmalonate, the sulfenylated product can be selectively oxidized and thermally fragmented affording phenylsulfenic acid, initially, and diethyl benzylidenemalonate. The developed method was applied using a polymer-supported thioanisole derivative (JandaJel). Formation of the enedicarboxylate documents proof of principle of polymer-supported sulfides as sulfenylating agents onto activated methylenes.     

Structural evolution and epitaxial stabilisation of pulsed laser deposited Sm0.55Nd0.45NiO3 solid solution nanostructured films on undoped Si (1 0 0) and NdGaO3 substrates

We report on the effects of substrate, ambient oxygen pressure and deposition time on the crystal structure, and morphology of Sm_0.55Nd_0.45NiO₃ solid solution nanostructured films synthesized by pulsed-laser deposition. In each film the structure was found to be consistent with a perovskite structure with preferential planes growth and reveals a strong orientation along the orthorhombic (2 1 0) plane of the perovskite subcell for the film deposited on NdGaO₃ where highly crystalline films were obtained within 15 min deposition time with a low surface roughness of 8.79 nm. Similar structure is observed on Si (1 0 0) substrate only at O₂ pressure of 0.4 mbar. The surface morphology of the different samples shows a net dense film structure with several droplets population. The nano-scaled droplets are in general spherical in shape; a detailed analysis indicates that the laser ablation of this nickelate family is governed to a certain extent by a heat transfer phenomenon.     

Einen compendi?sen Apparat zur Kohlens?urebestimmung

Ohne Zusammenfassung     

Ueber die Bestimmung der Titans?ure

Ohne Zusammenfassung     

Jargonium, ein neues Element

Ohne Zusammenfassung     

Oxidation of Benzyl Alcohol Using Cobalt Oxide Supported Inside and Outside Hollow Carbon Spheres

Cobalt oxide nanoparticles (6 nm) supported both inside and outside of hollow carbon spheres (HCSs) were synthesized by using two different polymer templates. The oxidation of benzyl alcohol was used as a model reaction to evaluate the catalysts. PXRD studies indicated that the Co oxidation state varied for the different catalysts due to reduction of the Co by the carbon, and a metal oxidation step prior to the benzyl alcohol oxidation enhanced the catalytic activity. The metal loading influenced the catalytic efficiency, and the activity decreased with increasing metal loading, possibly due to pore filling effects. The catalysts showed similar activity and selectivity (to benzaldehyde) whether placed inside or outside the HCS (63 % selectivity at 50 % conversion). No poisoning was observed due to product build up in the HCS.