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Co-ordination chemistry of sulfimidesWaring, Kevin White January 2001 (has links)
Reactions of Ph2SNH 1 with copper(II) halides in a 2:1 ratio is fast and efficiently generates species of the type trans-Cu(Ph2SNH)X2. A significant aspect of their coordination geometry comes with the observation that two distinct isomers (or allogons) of the chloro complex can be generated and we believe this is the first example of square-planar/pseudo-tetrahedral isomerism in a neutral copper(II) complex. True polymorphism is displayed by these allogons as they can be used to generate each other by crystallisation from the appropriate solvent mixtures. No such isomerism is exhibited by the bromo analogue.
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Polymères de coordination luminescents 1D et 2D avec des ligands rigides contenant du Pt(II) montrants des propriétés d’adsorption du CO2 / Luminescent 1D-and 2D-coordination polymers constructed with rigid Pt(II)-containing ligands exhibiting CO2 adsorption propertiesJuvenal, Frank January 2017 (has links)
La conception de nouveaux matériaux fonctionnels a une longue histoire. Durant les deux dernières décennies, le domaine des polymères organiques et inorganiques a attiré l'attention des chercheurs. Plus important encore, les matériaux poreux tels que les Metal Organic Frameworks (MOFs), en anglais, Covalent Organic Frameworks (COFs), en anglais, ainsi que des polymères de coordination poreux sont maintenant étudiés de manière intensive en raison de leurs applications potentielles, comprenant le stockage de gaz, la séparation de gaz, la catalyse et la détection. D'un autre côté, les polymères contenant du Pt ont montré l'application potentielle dans les cellules solaires et les diodes électroluminescentes. Le mémoire est divisé en trois sections principales présentant des résultats nouveaux. Dans la première section, le chapitre 2 traite essentiellement de la formation de polymères de coordination (CP) avec des sels CuX (X = Cl, Br, I) et trans-[p-MeSC6H4C≡C-Pt(PMe3)2-C≡CC6H4SMe] (L1), soit dans le PrCN ou PhCN. Les polymères résultants sont soit 2D (bidimensionel) ou 1D (unidimensionel). Cependant, en presence de PrCN ou de PhCN, le CP 2D obtenu avec le CuBr n'a pas incorporé de solvant dans ses espaces vides. D'autre part, le CP 2D et le reste des CP 1D obtenus avaient soit des molécules de solvant de cristallisation dans leurs cavités ou coordonnés au cuivre sur la chaîne. Les unités cuivre-halogénures étaient soit des rhomboïdes Cu2X2 ou le cubane Cu4I4. Leurs mesures photophysiques en présence et en l'absence de molécules de solvant de cristallisation ont été effectuées. En outre, la porosité du CP a été évaluée par BET (N2 à 77 K). Le vapochromisme du CP 2D sans solvant et des CP 1D ont été étudiés, ainsi que les mesures de sorption du CO2 ont été effectuées. De plus, nous avons utilisé CuCN et L1 dans MeCN pour former de nouveaux CP’s. Ceci est rapporté dans la deuxième section, le chapitre 3. Le CP obtenu était inattendu : L1 s’est rompu et du cyanure CN‾ s’est coordonné sur le Pt. Ceci a conduit à la formation d’un CP 1D zigzag. Généralement, les CP sont formés avec L1 via des liens Cu-S ou/et Cu([éta]2-C≡C), mais pas dans le cas du CuCN qui lui forme une chaîne 1D (CuCN)n où le L1 rompu se lie avec cette chaîne via un lien Cu-N. Les propriétés photophysiques et de stabilité thermique ont été étudiées. La troisième section (Chapitre 4) traite d'une exploration des CP formés par la reaction des sels CuX (X = Cl, Br, I) et le trans-[p-MeSC6H4C≡C-Pt(PMe3)2-C≡CC6H4SMe] (L1) ou le trans-[p-MeSC6H4C≡C-Pt(PEt3)2-C≡CC6H4SMe] (L2) dans du MeCN afin de trouver des tendances. L'utilisation de L1 a donné lieu à un CP 2D ou 1D CPs avec le MeCN piégé à l'intérieur des cavités, il y a de l’espace vide. L2 a conduit uniquement à des CP 1D sans molecules de solvant de cristallisation. Des analyses thermogravimétriques, photophysique et des mesures d’adsorption de gaz (uniquement pour ceux avec du solvant) ont été étudiées. / Abstract: The design of new functional materials has a long history. For the past two decades, the field of organic and inorganic polymers has attracted attention of researchers. More importantly, porous materials such as Metal Organic Frameworks (MOFs), Covalent Organic Frameworks (COFs) as well as porous coordination polymers are now being intensively studied due to their potential applications including gas storage, gas separations, catalyst and sensing. On another hand, Pt-containing polymers have shown potential applications in solar cells and light emitting diodes. The masters’ thesis is mainly divided into three main sections presenting new results. In the first section; Chapter 2 mainly discusses the formation of coordination polymers with CuX salts (X= Cl, Br, I) and trans-[p-MeSC6H4C≡C-Pt(PMe3)2-C≡CC6H4SMe] (L1), in either PrCN or PhCN. The resulting polymers obtained were 2D (bidimensional) CPs or 1D (unidimensional) CPs in all cases. However, 2D CPs obtained when CuBr salt is used by either using PrCN or PhCN did not incorporate the solvents in their cavities. On the other hand, the 2D CP and the rest of 1D CPs obtained had either the crystallization molecules in the cavities or coordinated to the copper cluster. The copper-halide clusters were either the rhomboids Cu2X2 fragments or the step cubane Cu4I4. The photophysical measurements in the presence and absence of solvent crystallization molecules were performed. In addition, the porosity of the CPs was evaluated by adsorption isotherms. The vapochromism of the solvent-free 2D and 1D CPs were investigated as well as CO2 sorption measurements were perfomed. Furthermore, we then attempted to use CuCN and L1 in MeCN which is reported in the second section as Chapter 3. The obtained CP was unexpected as L1 broke and a cyanide (CN‾) ion coordinated to the Pt atom leading to the formation of zigzag 1D CP. The coordination bonds Cu-S or/and Cu([eta]2-C≡C) were generally observed with L1, but not in the CuCN case. Instead a 1D chain of (CuCN)n was made and the broken L1 now binds the chain via a Cu-N bond. The photophysical and thermal stability properties were studied. Lastly, the third section, Chapter 4 deals with a potential predictability of CP formation by using CuX salts (X= Cl, Br, I) and either trans-[p-MeSC6H4C≡C-Pt(PMe3)2-C≡CC6H4SMe] (L1) or trans-[p-MeSC6H4C≡C-Pt(PEt3)2-C≡CC6H4SMe] (L2) in MeCN as the solvent. The use of L1 resulted in either 2D or 1D CPs with the MeCN trapped inside of the cavities while L2 resulted in 1D CPs without MeCN being present in their cavities. The thermogravimetric, photophysical as well as gas sorption measurements (only for those with crystalisation molecules) were perfomed.
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Synthesis and Characterization of Copper Halide Complex Materials / Syntes och karakterisering av material baserade på kopparhalogenid-komplexTomita, Hiroki January 2021 (has links)
Energiförbrukning är ett hett ämne i världen idag, eftersom världens befolkning fortsätter att växa. Som ett resultat ökar också den globala energiförbrukningen snabbt och utsläppen av koldioxid därmed, vilket påverkar global uppvärmning och klimatförändringar. Således kommer utvecklingen av förnybara energikällor att bli en av nödvändighet. Solenergi utgör en förnybar energikälla och uppvisar en enorm potential för att tillgodose det globala energibehovet. En solcell är kan användas för att omvandla solljus till elektricitet. Många typer av solceller har utvecklats under det senaste decenniet, och forskning för att förbättra effektiviteten kommer att fortsätta i framtiden. Material baserade på kopparhalogenidkomplex har uppvisat intressanta optiska och elektrokemiska egenskaper på grund av flera laddningsöverföringsexciterade tillstånd. Genom att kombinera kopparhalogenidsystem med organiska ligander med två bindningsgrupper, kommer komplexet att kunna bilda nätverksstrukturer i flera dimensioner och därmed effektivt kunna leda ström. Eftersom kopparhalogenidkomplex uppvisar unika optiska och elektriska egenskaper, är det värt att undersöka dem för användning i solceller. Syftet med examensarbete har varit att undersöka kopparhalogenidkomplex med optiska och elektrokemiska egenskaper. Kopparhalogenidkomplex med bidentatligander har syntetiserats och applicera som tunna filmer undersöktes. I kapitel 1 och 2 av uppsatsen presenteras bakgrunden och en introduktion av denna studie, samt de experimentella metoderna. I kapitel 3 beskrivs syntesen av kopparjodid-4,4'-bipyridinkomplex och karakteriseringen av detsamma. Applicering av det resulterande materialet på glassubstrat diskuteras också. I kapitel 4 beskrivs syntesen av kopparhalogenid-N-oxid-4,4'-bipyridinkomplex med efterföljande karakterisering. I kapitel 5 undersöks metoder för att applicera kopparjodidpyridin på koppar-folie och FTO-belagda glassubstrat. / Energy consumption is presently a hot topic in the world since the world’s population continues to grow. As a result, global energy consumption is increasing rapidly and the emission of carbon dioxide is also increasing, which causes global warming and climate change. Thus, the development of renewable energy sources will be one of the solutions. Solar energy is one of the renewable energy sources and has a huge potential to satisfy the global energy demand. A solar cell harvests light and converts it to electricity. Many kinds of solar cells have been developed in the past decades, and investigation for the improvement of the efficiency will be continued in the future. Copper halide organic complex materials have some potential for optical and electrochemical properties due to several charge transfer states inside the structure. By combining copper halide with bidentate organic ligands, the complex will form high dimensional network structure and will have electrical property due to the formation of electron conducting paths. Since copper halide complex has potential for unique optical and electrical properties, it is worth investigating for the further photovoltaic application. The aim of the thesis is to investigate copper halide complex material showing optical and electrochemical property. Copper halide complex with bidentate ligands were synthesized and the way to apply copper halide complex to films were also investigated in this thesis. In chapter 1 and 2, the background and the introduction of this study and the experimental methods are presented. In chapter 3, the synthesis of copper iodide 4,4’-bipyridine complex and the characterization of the complex sample are presented. The application of the complex to glass substrate is also discussed. In chapter 4, the synthesis of copper halide N-oxide-4,4’-bipyridine complex and the characterization are discussed. In chapter 5, the way to apply copper iodide pyridine to copper foil and FTO-coated glass substrate is discussed.
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Photochemistry of Copper Coordination Complexes / Fotokemi av kopparkoordinationskomplexBlad, Amanda, Glisén, Helena, Ludvig, Filippa January 2021 (has links)
The United Nations have set a number of sustainability goals, Agenda 2030, in order to combat the worlds largest challenges and injustices. The energy market is one of these urgent issues which must be solved. Solar energy is expected to be the fastest growing energy source in the future energy mix. It can be a great way to provide zero emission energy and also become a key part in equality as it can provide energy to people who live off the grid today and raise quality of life all over the world. The aim of this study is to compare different ligands in a copper halide complex to conclude what structural properties of the ligand might be better suited for photoluminescent applications, and especially in solar cells. Eight ligands were chosen for the complexes depending on their level of conjugation: 4,4’-bipyridine, tri(o-tolyl)phosphine, 3,6-di-2-pyridyl-1,2,4,5-tetrazine, pyridine, pyrimidine, pyrazine, phenanthroline, and 2,2’-bipyridine. A series of analytical methods were used to compare the complexes properties; X-Ray diffraction, emission and excitation spectroscopy, time-resolved photoluminescence spectroscopy, microscopy and thermochromism. From these measurements, pyridine and pyrimidine proved to have the greatest potential for working in a solar cell. This was deduced because of the detected crystallinity, having luminescence under UV-light, forming distinct wavelength peaks during excitation and emission in the flourometer, having the longest excited state lifetime and and finally, emitting distinctive colours during thermochromism. When creating the solar cell, pyridine was chosen as ligand due to higher availability than pyrimidine. The method used in this project for making the solar cell is directly applied form a previously tested method, but which was designed for another type of electron donor. This project compared the different ways of applying the copper halide complex on to the cell. The methods used were spin-coating and SILAR for creating the copper iodide thin film and vapour diffusion and immersion to introduce the ligand. These four methods were combined systematically for all combinations. The solar cells were then put in a solar simulator where voltage, current, efficiency and fill factor was measured. The best results came form the solar cell where spin coating and immersion was used, though the overall efficiency of the created cells were low. Copper halide complexes in previous studies have been proven to be reactive with oxygen and the experiments in this project were not carried out in an inert environment. This could have had significant impact on the measurements, as reactions between the complexes and oxygen may have resulted in oxidation and thus inactivation of the complexes. Therefore, it would be interesting to conduct the syntheses again but instead in an inert environment to determine whether oxygen made a major impact on the measurements. In further studies, it would also be worthwhile to investigate how the different layers of the solar cell would have to be adapted for this particular complex to obtain higher efficiency and voltage. Also, making thin film of pyrimidine to be used in a solar cell as it showed the attributes required for a solar cell. Furthermore, it would be interesting to use derivatives of pyrimidine, such as uracil and cytosine which are abundant in nature, as they might be more sustainable choices. This is due to their inherent biodegradability and not posing a threat to either health or environment when handled.
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