Die photochemische Acylierung von Chinonen und deren mögliche solarchemische Anwendung

Ziel dieser Arbeit war es, Untersuchungen zur photochemischen Acylierung von Chinonen durchzuführen, um, in Hinblick auf eine mögliche Nutzung in der Solarchemie, deren synthetisches Potential zu erschließen. Hierzu wurden unterschiedliche Aldehyde mit verschiedenen Chinonen umgesetzt. Die Oxidationen zu den entsprechenden Chinonderivaten gelang in einem präparativ sehr einfachen Verfahren mit Ag₂O. Mit dieser Methode konnten mehrere Chinone dargestellt werden

Photochemie von Phthalimiden: photodecarboxylative Addition von Carboxylaten und PET-induzierte Makrocyclisierungen

[Extract] This PhD thesis describes the development of photodecarboxylative additions to phthalimides as a green alternative to Grignard reactions and photoinduced electron transfer cyclizations to macrocyclic products

Continuous flow photochemical and thermal multi-step synthesis of bioactive 3-arylmethylene-2,3-dihydro-1H-isoindolin-1-ones

An effective multi-step continuous flow approach towards N-diaminoalkylated 3-arylmethylene-2,3-dihydro-1H-isoindolin-1-ones, including the local anesthetic compound AL-12, has been realized. Compared to the traditional decoupled batch processes, the combined photochemical–thermal–thermal flow setup rapidly provides the desired target compounds in superior yields and significantly shorter reaction times

The effects of ultraviolet radiation and climate on oil toxicity to coral reef organisms – a review

Oil pollution remains a significant local threat to shallow tropical coral reef environments, but the environmental conditions typical of coral reefs are rarely considered in oil toxicity testing and risk assessments. Here we review the effects of three environmental co-factors on petroleum oil toxicity towards coral reef organisms, and show that the impacts of oil pollution on coral reef taxa can be exacerbated by environmental conditions commonly encountered in tropical reef environments. Shallow reefs are routinely exposed to high levels of ultraviolet radiation (UVR), which can substantially increase the toxicity of some oil components through phototoxicity. Exposure to UVR represents the most likely and harmful environmental co-factor reviewed here, leading to an average toxicity increase of 7.2-fold across all tests reviewed. The clear relevance of UVR co-exposure and its strong influence on tropical reef oil toxicity highlights the need to account for UVR as a standard practice in future oil toxicity studies. Indeed, quantifying the influence of UVR on toxic thresholds of oil to coral reef species is essential to develop credible oil spill risk models required for oil extraction developments, shipping management and spill responses in the tropics. The few studies available indicate that co-exposure to elevated temperature and low pH, both within the range of current daily and seasonal fluctuations and/or projected under continued climate change, can increase oil toxicity on average by 3.0- and 1.3-fold, respectively. While all three of the reviewed environmental co-factors have the potential to substantially increase the impacts of oil pollution in shallow reef environments, their simultaneous effects have not been investigated. Assessments of the combined effects of oil pollution, UVR, temperature and low pH will become increasingly important to identify realistic hazard thresholds suitable for future risk assessments over the coming century

TiO2 photocatalysis of naproxen: Effect of the water matrix, anions and diclofenac on degradation rates

The TiO2 photocatalytic degradation of the active pharmaceutical ingredient (API) naproxen (NPX) has been studied using a laboratory-scale photoreactor equipped with a medium pressure mercury lamp. UV/TiO2 photocatalysis proved highly efficient in the elimination of NPX from a variety of water matrices, including distilled water, unfiltered river water and drinking water, although the rate of reaction was not always proportional to TiO2 concentration. However, the NPX degradation rate, which follows first-order kinetics, was appreciably reduced in river water spiked with phosphate and chloride ions, a dual anion system. Addition of chloride into drinking water enhanced the TiO2-photocatalysed degradation rate. Competitive degradation studies also revealed that the NPX degradation was greatly reduced in the presence of increased concentrations of another API, diclofenac (DCF). This was established by (i) the extent of mineralization, as determined by dissolved organic carbon (DOC) content, and (ii) the formation of intermediate NPX by-products, identified using liquid chromatography and electrospray ionization (positive and negative mode) mass spectrometry techniques. This study demonstrates that competition for active sites (anions or DCF) and formation of multiple photoproducts resulting from synergistic interactions (between both APIs) are key to the TiO2-photocatalysed NPX degradation

TropEco Research Award 2014: the Eradicate Insect-borne Diseases with Sunlight Initiative at JCU

The Eradicate Insect-borne Diseases with Sunlight Initiative (EIDSI) at JCU is utilizing Queensland's two major natural resources, sunlight and biomass. Its research activities, for which it received the TropEco Research Award 2014, help to safeguard public health in the region and covers prophylaxis, treatment as well as cure

A laboratory-scale annular continuous flow reactor for UV photochemistry using excimer lamps for discrete wavelength excitation and its use in a wavelength study of a photodecarboxlyative cyclisation

This paper describes a new annular reactor for continuous UV photochemistry, which uses easily interchangeable excimer lamps of different wavelengths. The reactor has narrow clearance to form thin films of material for efficient irradiation of molecules. Its use is demonstrated by investigating the effect of discrete wavelength lamps (222, 282 and 308 nm) on the reaction of potassium N-phthalimidobutanoate 1. The ability of the reactor to be integrated into multistep processes is illustrated by combining it with an Amberlyst scavenger and a solid acid catalyst, NbOPO4, to access a second product 3 that is obtained in a single telescoped process. The tricyclic scaffold in 3 is a motif found in several biologically active compounds and has possibilities as a synthon for new pharmaceutical products

The photodecarboxylative addition of carboxylates to phthalimides as a key-step in the synthesis of biologically active 3-arylmethylene-2,3-dihydro-1H-isoindolin-1-ones

The synthesis of various 3-arylmethylene-2,3-dihydro-1H-isoindolin-1-ones was realized following a simple three-step process. The protocol utilized the photodecarboxylative addition of readily available carboxylates to N-(bromoalkyl)phthalimides as a versatile and efficient key step. The initially obtained hydroxyphthalimidines were readily converted to the desired N-diaminoalkylated 3-arylmethylene-2,3-dihydro-1H-isoindolin-1-ones via acid-catalyzed dehydration and subsequent nucleophilic substitution with the corresponding secondary amines. The procedure was successfully applied to the synthesis of known local anesthetics (AL-12, AL-12B and AL-5) in their neutral forms

TiO2 photocatalysis of naproxen : effect of the water matrix, anions and diclofenac on degradation rates

The TiO2 photocatalytic degradation of the active pharmaceutical ingredient (API) naproxen (NPX) has been studied using a laboratory-scale photoreactor equipped with a medium pressure mercury lamp. UV/TiO2 photocatalysis proved highly efficient in the elimination of NPX from a variety of water matrices, including distilled water, unfiltered river water and drinking water, although the rate of reaction was not always proportional to TiO2 concentration. However, the NPX degradation rate, which follows first-order kinetics, was appreciably reduced in river water spiked with phosphate and chloride ions, a dual anion system. Addition of chloride into drinking water enhanced the TiO2-photocatalysed degradation rate. Competitive degradation studies also revealed that the NPX degradation was greatly reduced in the presence of increased concentrations of another API, diclofenac (DCF). This was established by (i) the extent of mineralization, as determined by dissolved organic carbon (DOC) content, and (ii) the formation of intermediate NPX by-products, identified using liquid chromatography and electrospray ionization (positive and negative mode) mass spectrometry techniques. This study demonstrates that competition for active sites (anions or DCF) and formation of multiple photoproducts resulting from synergistic interactions (between both APIs) are key to the TiO2-photocatalysed NPX degradation

Photooxygenation in an advanced led-driven flow reactor module: experimental investigations and modelling

The photooxygenation of  α-terpinene was investigated as a benchmark reaction in an advanced LED-driven flow reactor module, both from an experimental and modelling point of view. Ethanol was used as a green solvent and rose Bengal was chosen as a cheap sensitizer of industrial importance. Firstly, the kinetic law based on all mechanistic steps was established for the chosen photooxygenation. From this, the set of operating parameters potentially influencing the photoreaction rate were identified. Subsequently, experiments were carried out under continuous-flow conditions to screen these operating parameters, namely concentration of α-terpinene, concentration of photosensitizer, residence time, structure of the segmented gas-liquid flow and nature of the reagent gas phase (air versus pure oxygen). Finally, the conditions enabling minimization of sensitizer bleaching were established. It was also shown that the hydrodynamic characteristics of the gas-liquid flow can have an effect on the conversion levels. From this, a simplified model was proposed to predict the conversion at the reactor’s outlet when pure oxygen was used