There is general concern whether human exposure to selected Canadian bottled waters and the chemicals which may leach from them, could potentially cause deleterious effects. This research was designed to determine whether exposures to bottled water and plastic leachates caused toxicity to the freshwater Cnidarian Hydra viridissima (green hydra). Three chemicals used in the production of polycarbonate and polyethylene plastics, bisphenol A (BPA) and two phthalate esters: dibutyl phthalate (DBP) and bis (2- ethylhexyl) phthalate (DEHP) along with one type of commercial bottled water were investigated. One brand of bottled water was analyzed over four months (stored in light and dark conditions) along with lab water similarly stored in glass, polycarbonate and polyethylene bottles. Following 2, 4, 8 and 16 weeks in each of the two treatments, hydra bioassays were conducted. Chronic toxicity tests were also conducted on the two phthalates and BPA. The chronic toxicity tests showed that BPA caused effects on hydra morphology and population at low doses and DBP and DEHP both showed signs of hormesis.

Att utreda möjligheterna att etablera dataförsörjning riktade mot multimodala transporttjänster är idag av största intresse. Det är också intressant att försöka utnyttja de standarder som tagits fram när en dataförsörjningskedja ska etableras. Detta examensarbete genomfördes på Triona AB i Borlänge. Triona har utvecklat databasen Transport Network Engine (TNE), som idag används för att läsa in data från Nationella VägDataBasen (NVDB) och från skogsnäringen. Målet med arbetet var att ta fram en informationsmodell, som beskriver hur ett transportnät med nätanknutna data, som stödjer multimodala transporter och resor, kan lagras i TNE. En förlängning av målet blev att, utifrån ett givet användarfall, etablera dataförsörjning till TNE och lägga in de nödvändiga datamängderna. TNE bygger på ESRI:s produkter och funktionalitet för hantering av geografisk information och informationsmodell och datahantering i TNE baseras på internationella och svenska standarder. Idag finns all information om järnvägsnätet hos Banverket och det finns ingen koppling mellan Banverkets databas Baninformationssystemet (BIS) och Vägverkets databas NVDB. För att den kopplingen ska kunna ske, krävs att de båda verken kan samarbeta som två stora organisationer i ett väl fungerande nätverk. Ett så kallat interorganisatoriskt nätverk. Det akademiska syftet var att föreslå en arkitekturstrategi som stödjer ett sådant nätverk. Vi upptäckte att arkitekturstrategierna IRM och VBS är uppbyggda för att inrikta sig på enskilda organisationer, och det visade sig svårt att följa en specifik strategi inom ett nätverk med flera organisationer. I vårt användarfall måste nätverket mellan Banverket, Vägverket och Stora Enso samarbeta över organisationsgränserna. Därför behövs en strategi för ett interorganisatoriskt samarbete så att informationen kan struktureras på ett gemensamt sätt. Vi föreslår ett antal idealtypskriterier som vi utgått efter i struktureringen av systemarkitekturen. Den innehåller en informationsmodell för både väg- och järnvägsdata som följer standarden SS 63 70 04. Arbetet avgränsades till att endast innehålla de datamängder som användarfallet kräver. Vi har analyserat KombiTIF-rapporten som är ett avslutat projekt styrt av Banverket på uppdrag av Näringsdepartementet. Rapporten ger ett förslag på en lösning i form av en arena som ska göra data tillgänglig för användning. Vi väljer att se TNE-plattformen som en realisering av denna arena. Enligt vårt förslg så ska TNE-plattformen hämta in det mest grundläggande datat om järnvägsnät och nätanknuten data från BIS och standardiserad information om vägnät och nätanknuten data från NVDB via ett gränssnitt. I framtiden är det möjligt att på samma sätt ta in andra trafiknät såsom Sjöfartsverket, Luftfartsverket och Rikstrafiken. Vi arbetade efter en egen metod som vi tog fram med valda delar från andra metoder; kartläggning, perspektivanalys, verksamhetsanalys, utveckling och utvärdering. Arbetet genomfördes iterativt i de fem olika faserna.

Univ., Diss.-2006 u.d.T.: Heiss, Sonja: Die Interessen der Versicherten und die rechtliche Institutionalisierung der Lebensversicherung in Deutschland in der ersten Hälfte des 19. Jahrhunderts--Frankfurt/M., 2005. / Literaturverz. S. [365] - 379.

This dissertation describes the investigation of the utility of metal–bis(oxazoline) complexes in catalytic asymmetric reactions. The development of Cu(II)-catalyzed regio- and enantioselective additions of silylketenthioacetals into diketones is discussed in the first chapter. \(Cu(OTf)_2(t-BuBox)\) complexes were found to be an effective catalyst with a broad substrate scope, providing tertiary alcohols in high yields, regioselectivities, and enantioselectivities. A model that accounts for the absolute stereochemistry of the product based on A1,3–interaction was proposed. Relative reactivities among diketones were also investigated. The second chapter reports the investigation of Diels–Alder reactions of N-allenoyloxazolidinones. The reaction between 3-buta-2,3-dienoyloxazolidin-2-one and cyclopentadiene was catalyzed by \(Cu(SbF_6)_2(H_2O)_2(t-BuBox)\) complexes, providing the cyclic product in high yield and enantioselectivity. The endo isomer was obtained as a major product with high selectivity. Relative reactivity between N-allenoyl oxazolidinones and unsaturated N-acyloxazolidinones was also studied. / Chemistry and Chemical Biology

Tetrabromobisphenol A, (TBBPA or Br4BPA), is a widely used brominated flame retardant (BFR). Although TBBPA and its breakdown products been found in river sediments, the environmental impact of their contamination is largely unknown. One breakdown product of TBBPA is bisphenol A (BPA), which has been studied intensively for its toxicology because it is used in the manufacturing of plastics and leaches from food containers, water bottles and pipes. Other breakdown products of TBBPA include tribromobisphenol A (Br3BPA), dibromobisphenol A (Br2BPA), and monobromobisphenol A (BrBPA) but little is known about their toxicology. Since TBBPA is toxic, there is a need to search for an alternative BFR, with one being tetrabromobisphenol A bis(2,3-dibromopropylether) or TBBPA-DBPE. However, almost nothing is known about the toxicology of this compound. Hence, two rainbow trout cell lines, RTL-W1 from liver and RTgill-W1 from gill, were used to evaluate the cellular toxicity of TBBPA, BPA, BrBPA, Br2BPA, Br3BPA and TBBPA-DBPE. The cells were exposed to these compounds for 24 h in the basal medium, L-15, to study their cytotoxicity and in L-15 with fetal bovine serum (FBS) to evaluate their capacity to induce 7-ethoxyresorufin o-deethylase (EROD) activity. Viability was measured with three fluorometric indicator dyes: Alamar Blue (AB) for metabolism, 5-carboxyfluorescein diacetate acetoxymethyl (CFDA AM) for cell membrane integrity, and Neutral Red (NR) for lysosomal activity. The concentrations causing a 50 % reduction in viability (EC50) as measured with these three dyes were used to compare the relative cytotoxicity of these chemicals. For both cell lines and with all viability endpoints, TBBPA was the most cytotoxic, with EC50s ranging from 2.33 to 3.11 ug/ml. BPA, BrBPA, Br2BPA, and Br3BPA also caused dose-dependent declines in cell viability but showed no consistent order of potency. None of the six compounds induced EROD activity, which suggests that they do not activate the aryl hydrocarbon receptor (AhR). Regardless of the endpoint or cell line, TBBPA-DBPE was not cytotoxic. This suggests that, from a toxicological perspective, this compound may be a suitable replacement for TBBPA as a BFR. BPA stood out from the other compounds in two regards. BPA caused a dose-dependent decline in cell viability for cultures in L-15 with FBS, whereas for the other compounds, little or no change in viability was seen in cultures with FBS. BPA elicited a decline in the ability of cells to reduce AB almost immediately upon its addition to cultures in a simple buffer, whereas as for other compounds a decline took time to develop. These results suggest that BPA exerts its cytotoxicity by a different mechanism different from the other compounds.

In the European Convention and the EU charter the principle ne bis in idem is provided, which implies that a person can not be tried or punished twice for the same offense. Since the European Convention was incorporated into Swedish law in 1995 the principles application has been discussed in tax law. Several cases have been examined by the European Court and the Supreme Court (HD) in order to determine whether dual punishment has occurred in the national rules concerning tax surcharge, tax crime and accounting fraud. The judicial trials have brought different assessments concerning the matter, which have resulted in a lack of clarity on the application of the principle in Swedish law. The thesis purpose is to clarify whether the principle ne bis in idem is applicable on the relationship between tax surcharge and tax crime, and the relationship between tax surcharge and accounting fraud. The authors' conclusion is that the principle ne bis in idem is applicable on the relationship between tax surcharge and tax crime because both sanctions are considered criminal in nature and concern the same crime, since they are based on substantially the same circumstances. Furthermore, the principle ne bis in idem is considered applicable on the relationship tax surcharge and accounting fraud, because both sanctions are criminal in nature and their circumstances have a connection, therefore they are considered as the same crime. / I Europakonventionen och EU:s stadga föreskrivs principen ne bis in idem som innebär att en person inte kan bli dömd eller straffad två gånger för samma gärning. Sedan Europakonventionen inkorporerades i svensk rätt år 1995 har principens tillämpningsområde på det skatterättsliga området blivit omdiskuterad. Flera fall har prövats av både Europadomstolen och Högsta Domstolen (HD), i strävan att avgöra huruvida dubbelbestraffning har förekommit vid tillämpning av de svenska skatterättsliga bestämmelserna om skattetillägg, skattebrott och bokföringsbrott. Rättsinstansernas prövningar har resulterat i olika bedömningar, varpå rättsläget för principens tillämpningsområde i svensk rätt anses oklart. Uppsatsens syfte är att klargöra om ne bis in idem är tillämplig på förhållandet mellan skattetillägg och skattebrott samt förhållandet mellan skattetillägg och bokföringsbrott. Författarnas slutsats är att principen ne bis in idem är tillämplig på förhållandet mellan skattetillägg och skattebrott för att båda sanktionerna skattetillägg och skattebrott har straffrättslig karaktär samt att sanktionerna vid en jämförelse av omständigheterna är väsentligen samma och därför avser samma brott. Avseende förhållandet mellan skattetillägg och bokföringsbrott, som prövas av HD för tillfället, är författarnas bedömning att båda sanktionerna har straffrättslig karaktär och baseras på samma omständigheter för att en anknytning mellan omständigheterna för sanktionerna föreligger och därför utgör de samma gärning. Principen ne bis in idem ska därför vara tillämplig även på förhållandet mellan skattetillägg och bokföringsbrott.

Twelve porphyrin dyads linked by an ethene bridge were synthesised as model systems for conjugated polymers. The extent of interporphyrin interaction was investigated for meso-meso and meso-β linked homo- and heterobimetallo-porphyrin dyads. To complement these dyads, model monomers with alkenyl substituents were also studied. Once the synthesis of these compounds was achieved, the extent of interaction was studied using UV-visible and fluorescence spectroscopy and molecular modelling. In order to gain a true indication of the extent of interaction in a dyad, the effect of the bridge as a substituent must be accounted for. This was achieved by studying the series of monomers by UV-visible and fluorescence spectroscopy. The increased conjugation resulting from mono- and bis-alkenyl substituents results in a red shift of the origin of transition energies in the absorption spectrum which is accompanied by a broadened and less intense Soret band and an increase in the intensity of the Q bands. The emission of these compounds also displays an increase in Stokes shift and a loss of vibronic coupling due to the increased conjugation. The serendipitous synthesis of three asymmetric meso-β ethene-linked porphyrin dyads was achieved by the use of palladium-catalysed Heck coupling of mesoethenyl- with meso-bromoporphyrins. A possible mechanism for this meso to β rearrangement was proposed. A series of nine meso-meso ethene-linked dyads was synthesised by palladium-catalysed Suzuki coupling of meso-(2-iodoethenyl)- with meso-borolanylporphyrins. All of these dyads were characterised by 1D and 2D NMR as well as MS analysis. The absorption spectra of ethene-linked dyads exhibit a split Soret band and a red-shifted and intensified HOMO-LUMO band. In the meso-β dyads, the degree of splitting in the Soret band is sufficient only to generate a shoulder on the red edge, whereas in the meso-meso dyads two separate bands appear. The extent of splitting is believed to be an indication of the amount of porphyrin-porphyrin interaction. The fluorescence profiles of the dyads change dramatically depending upon the central substituents in the porphyrins and the wavelength used for irradiation, which suggests that different conformations of these compounds give rise to different parts of their absorption and emission profiles. The fluorescence profiles of the dyads also do not reflect their absorption profiles, and therefore the excitation of the dyad is believed to be accompanied also by a change in geometry. All ethene-linked dyads exhibited an anti-Stokes shift, and the excitation spectra of the different parts of the fluorescence envelope also support the possibility of different conformers contributing to the fluorescence spectra. Molecular mechanics and time-dependent quantum mechanical calculations were performed on seven ethene-linked porphyrin dyads. These calculations further support the proposal of different conformations contributing to the physical properties of ethene-linked dyads. Electronic structure calculations also show considerable electron density on the alkene for the meso-meso ethene-linked dyads, which highlights the important influence of this bridge upon the electronic nature of these conjugated diporphyrins.

Business School, Diss.--København, 2007.

Univ., Diss.--Linz.

Mainz, Univ., Diss., 2002. / Computerdatei im Fernzugriff.