Dissertations / Theses on the topic 'Inorganic-organic hybrid compounds'

Metal oxides (MOs) play a key role in many areas of chemistry, physics and materials science. They are characterized by a wide variety of high technological interest compounds (e.g. TiO2, Fe3O4, Fe2O3, Y2O3, ZnO). The still increasing interest for this class of materials is mainly due to the ability to take advantage of their diversity to find new important applications in several research field. Their applicability, strengthened by the low cost, safety, ease of synthesis, ranges from (photo)catalysis to microelectronics and in vivo biological studies. Most of the MOs-based devices present outstanding performance derived from their reduced dimensions. To date, the research on nanostructured MOs is highly active in order to deeper gain knowledge about surface states and their influence on chemical and physical properties, motivating an always more multidisciplinary approach. However, some characteristics of oxides can limit their use, e.g. high band gap with almost negligible absorption in the visible, lack of optical response (luminescence) or conduction band edge not sufficiently negative to promote proton reduction (limited photocatalytic activity). The introduction of doping elements in the MO matrix to reduce these limitations can have the drawbacks of the new defects generation at the surface and/or in the bulk. Other limitations can be overcome by creating hybrid materials, such as organic and inorganic systems. In such scenario, it is necessary a detailed study aimed to characterize the properties of organic material and the means of implementation of the hybrid system. In the first part of the present thesis, we examine the stability of some exemplar metal oxides systems. The aim of this work is to extend the comprehension of nanostructured MOs phase transformation and to analyse the conditions for which the transformation takes place. The second part presents a study on carbon nitride (CN) based molecular materials performed with spectroscopy and X-ray diffraction experiments. Our characterizations reveal that CN materials present high chemical and physical stability and good control of the optical properties. Finally, we propose a structural and optical characterization of some carbon-nitride/ metal oxides hybrids. Firstly, we focus on Tb3+ doped Y2O3 system, a good candidate for nanosized phosphors, where organic passivation of the surfaces by melamine (C3H6N6) has the dual role of replacing species for hydroxides quenchers and activators of Tb by energy transfer mechanism. Then, we conclude with TiO2/CN hybrids for photocatalysis applications, realized by chemical methods and atomic layer deposition, stressing the importance of functional and terminating groups of molecular systems.

Compostos lamelares do tipo da hidrotalcita ou hidróxidos duplos lamelares (HDL), são materiais que possuem notáveis propriedades estruturais, químicas, eletrônicas, iônicas, ópticas e magnéticas. Em função dessas propriedades, os HDL apresentam uma diversidade de aplicações tais como adsorventes e catalisadores. Este trabalho tem por objetivo utilizar polímeros e macromoléculas na preparação e caracterização de HDL, visando melhorar as propriedades texturais dos HDL de MgAl-CO3 preparados em meio contendo polímeros orgânicos ou a intercalação direta de dendrímeros tipo PAMAM de gerações -0,5 e +0,5 em HDL do sistema Zn/Al. Os HDL de MgAl-CO3 foram preparados pela adaptação do método de coprecipitação a pH decrescente, com a presença de polímeros solubilizados no meio, como molde. Os materiais foram caracterizados por difração de Raios X, análise termogravimétrica, espectroscopia no infravermelho e medidas de área superficial por BET. Baseando-se nos resultados obtidos, pode-se concluir que propriedades texturais dos HDL preparados são modificadas, quando na presença de alguns polímeros. Na maioria dos casos, os valores calculados de área superficial específica foram mais elevados, em comparação com aquele obtido para o HDL preparado em meio reacional sem polímero. Isto pode ser explicado pela diminuição do tamanho de partículas e aumento no diâmetro médio de poros dos materiais preparados, provocada pela presença de polímeros no meio reacional. Os HDL intercalados com dendrímeros PAMAM G-0,5 e PAMAM G+0,5 foram preparados por duas rotas diferentes: coprecipitação a pH constante e troca iônica em fase dupla. Os materiais obtidos foram caracterizados por meio de difração de Raios X, análise de termogravimétrica associada à espectrometria de massas e espectroscopia no infravermelho. Utilizando os dois procedimentos de preparação, a intercalação de PAMAM G-0,5 deu origem a HDL com os mesmos espaçamentos basais, concordando com a intercalação dos ânions do dendrímero em um arranjo perpendicular à lamela do HDL, enquanto que para a intercalação do PAMAM G+0,5, espaçamentos basais muito menores do que o tamanho da molécula foram obtidos. A diferença entre a distância interlamelar observada e a esperada pode ser explicada por um arranjo peculiar das moléculas desse dendrímero em uma forma elipsoidal, devido às interações intramoleculares. Espectros no infravermelho confirmam a presença dos dendrímeros nos materiais Zn2Al-PAMAM G-0,5 e Zn2Al-PAMAM G+0,5. Finalmente, a presença destes dendrímeros foi confirmada por análise térmica associada com espectrometria de massas. Os estudos de Raios X com variação de temperatura in situ e as análises termogravimétricas revelaram que o material obtido pela intercalação do PAMAM G+0,5 é termicamente menos estável do que aquele intercalado com PAMAM G-0,5, concordando com a diferença de estabilidade entre os dendrímeros livres.
Hydrotalcite-like lamellar compounds or layered double hydroxides (LDH) are materials that present notable structural, chemical, electronic, ionic, optical and magnetic properties. Depending on these properties, the LDH present a great variety of applications such as adsorbents and catalysts. The aim of this work is to prepare and to characterize MgAl-CO3-LDH prepared in aqueous media containing organic polymer to improve textural properties, and to prepare HDL by intercalation of dendrimer (PAMAM) of generations -0.5 and +0.5 in ZnAl-HDL. MgAl-CO3-HDL samples were prepared by an adaptation of the coprecipitation method at decreasing pH, with the presence of polymers in the aqueous media as template. The materials were characterized by powder X-ray diffraction, termogravimetric analysis, infrared spectroscopy and BET isotherms. Based on the obtained results, it can be concluded that the textural properties of the prepared LDH were modified. The calculated values of specific surface area were higher in most of the cases compared with those obtained by the LDH prepared without polymer due to a decrease of the particle size and an increase in the average pore diameter of the prepared materials due to the presence of polymers. HDL with intercalated (PAMAM) dendrimers G-0.5 and G+0.5 were prepared by two different methods: coprecipitation at constant pH, and ionic exchange in double phase. The obtained materials were characterized by powder X-ray diffraction, thermal gravimetric analysis associated with mass spectrometry, and infrared spectroscopy. X-ray powder diffraction patterns exhibit the characteristic profiles of the lamellar materials with basal spacing depending on the nature of the dendrimer. For both preparation methods, the intercalation of PAMAM G-0.5 gives rise to LDH with basal spacing in agreement with the dendrimer molecules perpendicular to the layer of the host structure, while for PAMAM G+0.5 a basal spacing smaller than the molecule size was obtained. The difference between the obtained and the expected value is explained by an accommodation of the dendrimer molecule in an ellipsoidal shape, due to the intra-molecular interactions. Infrared spectra confirm the presence of dendrimers in the Zn2Al-PAMAM G-0.5 and Zn2Al-PAMAM G+0.5 materials. Finally, thermal analyses associated with mass spectrometry confirm the presence of these dendrimers. Powder X-ray diffraction with in situ temperature variation reveals that the material obtained by the PAMAM G+0.5 intercalation is thermally less stable than that prepared by PAMAM G-0.5 intercalation, in agreement with the difference in the thermal stability of the free dendrimers.

Die vorliegende Dissertation beschäftigt sich mit Wachstum und Aufbau von Fluorapatit-Gelatine-Nanokompositaggregaten. Diese Aggregate werden im sogenannten Doppeldiffusionsversuch biomimetisch erzeugt und ihre äußere Form bzw. Formentwicklung lässt sich anhand eines fraktalen Modells bis ins Detail nachvollziehen. Sie zeigen einen komplexen inneren Aufbau, in dem die Makromoleküle der organischen Komponente einerseits im Zentrum jeder Nanoeinheit und andererseits zu Strängen, den sogenannten Fibrillen, zusammengelagert am Aufbau der Kompositaggregate beteiligt sind. Im Fall des Kompositkeims ist die innere Architektur in hoher Detailstufe verstanden, auch wenn -- insbesondere bezüglich der späteren Wachstumsphasen -- eine Reihe ungeklärter Fragestellungen verbleibt. Ein zentrales Ergebnis der vorliegenden Arbeit bildet die Entdeckung eines weiteren Wachstumstypen, der im Vergleich zu den bekannten, fraktalen Kompositaggregaten grundsätzliche Unterschiede bezüglich des inneren und äußeren Aufbaus zeigt. Der Grund für die andersartige Formentwicklung liegt in der Versteifung der organischen Komponente durch eine vorangegangene Einlagerung von Calciumionen, wie sowohl experimentell als auch mit atomistischen Computersimulationen gezeigt werden konnte. Aufgrund der hohen Komplexität des Systems ist es bislang allerdings nicht möglich, lokale Ionen-Konzentrationen und pH-Werte vor bzw. während Nukleation und Wachstum der Kompositaggregate im Doppeldiffusionsversuch zu bestimmen. Deshalb wurde ein Ersatzversuch -- der sehr ähnlich strukturierte Aggregate erzeugt, sich aber mit rechnerischen Methoden analysieren lässt -- entworfen und untersucht. Anhand dieser Ergebnisse konnte erstmals die "Geschichte" von Fluorapatit-Gelatine-Nanokompositaggregaten detailliert nachvollzogen werden. Da über die Rolle der Gelatine beim Wachstum der Kompositaggregate nur wenig bekannt ist, wurde eine Reihe von Versuchen durchgeführt, in denen Gelatinen mit verschiedenen Molekülmassenverteilungen eingesetzt wurden. Es stellte sich heraus, dass für selbstorganisiertes und insbesondere fraktales Wachstum der Kompositaggregate lange, möglichst wenig gestörte Makromoleküle von zentraler Wichtigkeit sind. Um die Funktion der organischen Komponente für das Kompositwachstum näher zu untersuchen, wurden Oberflächen von Kompositkeimen mit rasterkraftmikroskopischen Methoden studiert. Durch Säuberung der Oberflächen konnten Austrittsstellen der organischen Komponente durch die Oberfläche der Kompositkeime identifiziert werden. Damit konnte gezeigt werden, dass die organische Komponente aus dem Inneren des Festkörpers teilweise durch die Oberfläche dringt und somit während des Wachstums weit in das Gel hineinreichen sollte. Für die mesoskopische Strukturbildung der Kompositaggregate spielen intrinsische elektrische Felder eine essenzielle Rolle. Deshalb wurde bislang eine Wirkung externer elektrischer Felder auf das Wachstum der Kompositaggregate vermutet. Im Rahmen der vorliegenden Arbeit wurde herausgearbeitet, dass es zwar zu keiner direkten Beeinflussung kommen kann, jedoch in den elektrodennahen Bereichen des Gels eine Ordnung der organischen Moleküle durch externe elektrische Felder zu erwarten ist. Dies könnte eine Wirkung auf wachsende Kompositaggregate zeigen. Da diese Effekte auch aufgrund der elektrischen Felder um die dipolaren Kompositaggregate zu erwarten sind, könnte eine ähnliche Strukturierung der Gelatine in der Nähe der wachsenden Kompositaggregate stattfinden. Insgesamt wurden in dieser Arbeit eine Reihe grundlegender Beiträge zur Erforschung der biomimetisch erzeugten Fluorapatit-Gelatine-Nanokompositaggregate geleistet. Es konnten neue Erkenntnisse zur inneren und äußeren Architektur der Kompositaggregate, zu Mechanismen der Morphogenese und deren wichtigsten Einflussgrößen sowie zum Verständnis der chemisch-physikalischen Vorgänge auf atomarer Größenskala gewonnen werden. Als besonders fruchtbar erwies sich die Verbindung von Experimenten mit theoretischen Untersuchungen, so dass dieser Weg auch in Zukunft grundlegende Erkenntnisse bei der Erforschung der Biomineralisation verspricht und weiterhin verfolgt werden sollte.

Thesis (Ph. D.)--Dept. of Chemistry and School of Pharmacy. University of Missouri--Kansas City, 2007.
"A dissertation in chemistry and pharmaceutical science." Advisor: Zhonghua Peng. Typescript. Vita. Description based on contents viewed Apr. 22, 2008; title from "catalog record" of the print edition. Includes bibliographical references (leaves 160-176). Online version of the print edition.

Die vorliegende Dissertation beschäftigt sich mit Wachstum und Aufbau von Fluorapatit-Gelatine-Nanokompositaggregaten. Diese Aggregate werden im sogenannten Doppeldiffusionsversuch biomimetisch erzeugt und ihre äußere Form bzw. Formentwicklung lässt sich anhand eines fraktalen Modells bis ins Detail nachvollziehen. Sie zeigen einen komplexen inneren Aufbau, in dem die Makromoleküle der organischen Komponente einerseits im Zentrum jeder Nanoeinheit und andererseits zu Strängen, den sogenannten Fibrillen, zusammengelagert am Aufbau der Kompositaggregate beteiligt sind. Im Fall des Kompositkeims ist die innere Architektur in hoher Detailstufe verstanden, auch wenn -- insbesondere bezüglich der späteren Wachstumsphasen -- eine Reihe ungeklärter Fragestellungen verbleibt. Ein zentrales Ergebnis der vorliegenden Arbeit bildet die Entdeckung eines weiteren Wachstumstypen, der im Vergleich zu den bekannten, fraktalen Kompositaggregaten grundsätzliche Unterschiede bezüglich des inneren und äußeren Aufbaus zeigt. Der Grund für die andersartige Formentwicklung liegt in der Versteifung der organischen Komponente durch eine vorangegangene Einlagerung von Calciumionen, wie sowohl experimentell als auch mit atomistischen Computersimulationen gezeigt werden konnte. Aufgrund der hohen Komplexität des Systems ist es bislang allerdings nicht möglich, lokale Ionen-Konzentrationen und pH-Werte vor bzw. während Nukleation und Wachstum der Kompositaggregate im Doppeldiffusionsversuch zu bestimmen. Deshalb wurde ein Ersatzversuch -- der sehr ähnlich strukturierte Aggregate erzeugt, sich aber mit rechnerischen Methoden analysieren lässt -- entworfen und untersucht. Anhand dieser Ergebnisse konnte erstmals die "Geschichte" von Fluorapatit-Gelatine-Nanokompositaggregaten detailliert nachvollzogen werden. Da über die Rolle der Gelatine beim Wachstum der Kompositaggregate nur wenig bekannt ist, wurde eine Reihe von Versuchen durchgeführt, in denen Gelatinen mit verschiedenen Molekülmassenverteilungen eingesetzt wurden. Es stellte sich heraus, dass für selbstorganisiertes und insbesondere fraktales Wachstum der Kompositaggregate lange, möglichst wenig gestörte Makromoleküle von zentraler Wichtigkeit sind. Um die Funktion der organischen Komponente für das Kompositwachstum näher zu untersuchen, wurden Oberflächen von Kompositkeimen mit rasterkraftmikroskopischen Methoden studiert. Durch Säuberung der Oberflächen konnten Austrittsstellen der organischen Komponente durch die Oberfläche der Kompositkeime identifiziert werden. Damit konnte gezeigt werden, dass die organische Komponente aus dem Inneren des Festkörpers teilweise durch die Oberfläche dringt und somit während des Wachstums weit in das Gel hineinreichen sollte. Für die mesoskopische Strukturbildung der Kompositaggregate spielen intrinsische elektrische Felder eine essenzielle Rolle. Deshalb wurde bislang eine Wirkung externer elektrischer Felder auf das Wachstum der Kompositaggregate vermutet. Im Rahmen der vorliegenden Arbeit wurde herausgearbeitet, dass es zwar zu keiner direkten Beeinflussung kommen kann, jedoch in den elektrodennahen Bereichen des Gels eine Ordnung der organischen Moleküle durch externe elektrische Felder zu erwarten ist. Dies könnte eine Wirkung auf wachsende Kompositaggregate zeigen. Da diese Effekte auch aufgrund der elektrischen Felder um die dipolaren Kompositaggregate zu erwarten sind, könnte eine ähnliche Strukturierung der Gelatine in der Nähe der wachsenden Kompositaggregate stattfinden. Insgesamt wurden in dieser Arbeit eine Reihe grundlegender Beiträge zur Erforschung der biomimetisch erzeugten Fluorapatit-Gelatine-Nanokompositaggregate geleistet. Es konnten neue Erkenntnisse zur inneren und äußeren Architektur der Kompositaggregate, zu Mechanismen der Morphogenese und deren wichtigsten Einflussgrößen sowie zum Verständnis der chemisch-physikalischen Vorgänge auf atomarer Größenskala gewonnen werden. Als besonders fruchtbar erwies sich die Verbindung von Experimenten mit theoretischen Untersuchungen, so dass dieser Weg auch in Zukunft grundlegende Erkenntnisse bei der Erforschung der Biomineralisation verspricht und weiterhin verfolgt werden sollte.

博士
國立中央大學
化學研究所
97
In this thesis, our work mainly focuses on the synthesis of metal compounds with novel structures by a hydrothermal method. Compared with a large number of publications of transition-metal compounds, the research on the synthesis of novel uranium or lanthanide compounds is considerable less. At the same time, the past studies also show that uranium- and(or) lanthanide-bearing materials display many interesting structural chemistry and potential applications, therefore, we aim at synthesizing new metal compounds with various architectures by adjusting the ratio of reactant in a hydrothermal method and then characterize their properties, such as luminescence and catalytic properties. 34 compounds in this research are divided into two series based on metal centers. The first series is to synthesize and characterize novel uranium-containing compounds by choosing appropriately organic templates or(and) ligands into fluoride or phosphate systems. U-1 is an organically templated mixed-valent uranium(IV)/uranium(VI) oxyfluoride with a hybrid network structure (1D + 2D). U-2 is the first example of a mixed-metal uranium oxyfluoride incorporating an organic ligand. Bimetallic compounds are highly interesting because the second metal provides the possibility of incorporating organic ligands into the extended structures. U-3 is a new uranium(IV) fluorooxalate, in which oxalate ligands show bisbidentate coordination to the U atoms acting as pillars between adjacent uranium fluoride layers to produce an extended 3D network. U-4 and U-5 are the first examples of organically templated uranium fluorooxalates. Both of them consist of anionic [U2F6(C2O4)3]4- layers separated by organic ammonium cations and lattice water molecules. The building units within the layers are connected in different ways, which are very likely directed by the organic templates. U-6 and U-7 are two mixed-metal uranium compounds with a pillared layer structure. The organic ligands coordinate to the Cu atoms within adjacent uranium/copper phosphate( or arsenate) layers to generate a pillared layer structure. The other uranium compounds are categorized in appendix A. The second series focuses on synthesis, characterization, and properties of novel lanthanide phosphates or phosphates. The 12 compounds (Ln-1-Ln-12) are isostructural and feature a 3D architecture in which 2D layers of [Ln(H2O)(HPO3)]+ are pillared by oxalate ligands. The structures of four isostructural organically templated lanthanide oxalatophosphates (Ln-13-Ln-16) contain 2D layers of lanthanide oxalates which are linked by dihydrogen phosphate units and bismonodentate oxalate ligands to form 3D frameworks. The three isostructural lanthanide phosphates (Ln-17-Ln-19) are observed for the first time by using a multidentate organic ligand, which was never used in metal phosphate and(or) phosphite systems before. Some of those lanthanide-bearing materials display red, blue, green, and near-IR luminescence. At the same time, it is also proved that the Yb and Gd compounds are effective catalysts for the Biginelli reaction.

碩士
國立中央大學
化學研究所
91
Abstract In the thesis, we report five novel metal phosphates have been syn- thesized under hydrothermal conditions and structurally characterized by single X-ray diffaction. Type Ⅰ:The first mixed-metal phosphate and metal phosphate incorporate isonicotinate ligand, CuVO2(HINT)(PO4), 1; Zn2(HINT)2(HPO4)2, 2. Type Ⅱ:Two mixed metal organic-inorganic hybrid compounds, CuVO2(4,4’-bipyridine)(PO4), 3; CuVO2(4,4’-bipyridine)(AsO4), 4, have a pillared layer structure. Type Ⅲ:The clustered vanadium phosphate, (4,4’H2bipyridine)[(VO2)4(PO4)2], 5, was a layer structure. The formulations were confirmed by single-crystal X-ray diffraction, Energy-dispersive X-ray fluorescence spectroscopy (EDS), powder X-ray diffraction, thermogravimetric analysis (TGA), elemental analysis (EA), magnetic susceptibility measurements, and solid state NMR spectroscopy. The compound 1 was the first mixed-metal phosphate. The structure consists of 2D neutral sheets of bimetallic oxide layers with the isonicotinate ligand being coordinated to copper in a bidentate fashion as a pendent group. The compound 2 was a noval zinc phosphate combined with isonicotinate ligand. Each Zn is tetrahedrally coordinated by three phosphate groups and one carboxylate group of the ligand in a mono- dentate fashion. So two compounds 1 and 2 being successfully synthesiz- ed would be the start for the study of the Metals/isonicotinate ligand/ phosphate system. The compounds 3 and 4 were isostructure linked through 4,4’-bipyridine pillars into a 3D framework. The compound 5 was a novel vanadium phosphate with V4O84+ clusters. The structure consists of phosphate-bridged vanadium (Ⅴ) clusters to form a layer structure in the presence of the protonated 4,4’-H2bipyridine as the structure-directing agent.

A dissertation submitted to the Faculty of Science, University of the Witwatersrand, Johannesburg, in fulfilment of the requirements for degree of Master of Science in Chemistry
The mandate for renewable energy sources to replace the current reliance on fossil fuels as a primary energy source has recently attracted a lot of research interest. The research has also focussed on bringing the technologies that take into consideration the goal of reducing environmental pollution. Consequently, approaches using photovoltaic (PV) technologies have been a promising arena to tackle the problem facing energy sources. Recently, more focus has been placed on improving the power conversion efficiency (PCE) of PV devices, such as organic and/or organic-inorganic hybrid perovskite solar cells. Therefore, in this work two different materials were applied in two independent PV devices, namely organic and/or organic-inorganic hybrid perovskite solar cells. One study employed nitrogen doped broken hollow carbon spheres (N-bHCSs), with an aim of enhancing the electronic properties of the P3HT:PCBM active layer of an organic photovoltaic (OPV) solar cell. N-bHCSs were successfully synthesized using a horizontal chemical vapour deposition method (H-CVD) employing a template-based method and the carbon was doped using in-situ and ex-situ doping techniques. Pyridine, acetonitrile and toluene were used as both carbon and nitrogen precursors. The dispersity of the SiO2 spheres (i.e. templates) was found to play a role on the breakage of the N-bHCSs. Incorporation of the N-bHCSs into the P3HT:PCBM active layer was found to enhance the charge transfer and this led to less recombination of photogenerated charges in the interface between the donor and acceptor. The current-voltage (I-V) characteristics of the ITO/PEPOT:PSS/P3HT:PCBM:N-bHCSs/Al solar cell devices revealed an increased chargetransport distance due to increased electron density by n-type doping from the N-bHCSs. The second study employed the organic-inorganic hybrid perovskite (CH3NH3PbI3) material as a light harvesting layer in an ITO/PEDOT:PSS/CH3NH3PbI3/PC6BM/Al solar cell device. Initially, the device parameters were optimised to obtain the best performing device. These include parameters such as the degradation of the hybrid film as a function of time and air exposure. A rapid degradation was seen on the device after 24 h of air exposure which was accompanied by the decrease in the PV performance of the device. The degradation was visually seen by the formation of crystal grains (i.e. “islands”) on the perovskite film.
GR2019

In organic-inorganic hybrid compounds an organic and an inorganic component are combined to form either a coordination or an ionic material. Relevant to the current study are hybrid materials composed of an organic part that contains one or more functional groups, for example amine, amide or carboxylic acid functional groups, and a metal halide inorganic portion. These functional materials display a range of interesting and desired properties, as evidenced from numerous literature reports on their properties. In order to utilise these properties in applications, a detailed understanding of the way that the crystal structure influences the properties of a material is required. However, before this step can be achieved, it is necessary to obtain information on the structural trends of the materials, and to use the approach of crystal engineering to identify robust supramolecular synthons that may afford structural control and prediction. The aim of the current study was to investigate the synthesis and crystal structures of hybrid materials, both ionic and coordination, composed of divalent transition metal halides and the organic components 4-aminobenzoic acid, 4-aminobenzamide and isonicotinic acid, and to identify the structural trends and crystal engineering synthons displayed by these materials. A secondary objective was the preliminary identification of properties exhibited by selected materials, in order to decide on the suitability of the materials for detailed future property investigations. Part of the work describes the investigation of the structural characteristics of coordination materials prepared by the combination of the organic and inorganic components. Five novel crystal structures of coordination materials were determined, and these are compared with six related coordination structures reported in the literature. Two of the novel structures display interesting one-dimensional coordination polymers, one of which has never been reported previously in the literature. The molecular and structural characteristics of both the novel and the literature coordination structures are presented in detail, and this discussion includes a description of the coordination geometry, the molecular geometry, packing trends, hydrogen bonding interactions and aromatic interactions. A comparison study across the three families of organic components in which the structural trends, hydrogen bonding interactions, aromatic interactions, ligand geometry and coordination modes are compared, is included. The results of the synthesis of the coordination materials by means of a mechanochemical method are presented, and the products afforded by this method are compared with those prepared via solution crystallisation. Finally, the results of preliminary studies of the thermal and electronic propertries of the materials are presented and interpreted. The combination of the hybrid components as cations and anions to form ionic materials yielded nine novel structures, and these were compared with five related ionic structures reported in the literature. The novel structures include three polar structures that contain the 4-ammoniumbenzamide cation, and to our knowledge no structures containing this cation have ever been reported in the literature, hence a significant contribution to the structural knowledge of perhalometallate salts of 4-ammoniumbenzamide is made by this study. In addition two novel structures display interesting one-dimensional and two-dimensional polymeric anions, respectively, are reported. The discussion of the novel and literature ionic structures includes a description of the molecular geometry of each of the components, the identification of packing trends, and an analysis of the hydrogen bonding and aromatic interactions occurring in the structures. The structures of all three families of organic components are compared, and trends in structural type, anion geometry, water inclusion, hydrogen bonding and functional group recognition are presented. In addition, a detailed analysis of robust crystal engineering synthons occurring in these structures is presented. Lastly the results of preliminary property investigations of the thermal and electronic properties of the materials are presented and discussed
Dissertation (MSc)--University of Pretoria, 2011.
Chemistry
unrestricted

Open–framework inorganic materials are an important class of compounds because of their many applications in the areas of ion–exchange, separation and catalysis. Ever since the discovery of microporous aluminophosphates by Flanigen and co–workers in the early 80’s, the field of open–framework compounds has witnessed explosive growth. It is now established that the open–framework compounds comprise of almost all the elements of the periodic table. In addition, it has been shown that the inorganic anions in the open–framework compounds can be partially substituted by rigid organic linkers such as the oxalate. The resulting inorganic–organic hybrid structures are interesting due to the variable nature of the binding properties of the organic and inorganic moieties. The present thesis consists of systematic studies on the formation of amine–templated inorganic open–framework structures and inorganic–organic hybrid compounds based on the main group, transition metal and actinide elements. In Chapter 1 of the thesis an overview of inorganic open-framework materials is presented, with an emphasis on the elements that have been employed in the present study. Chapter 2 has two parts (Parts A and B) describing the synthesis and structure of open-framework tin(II) containing compounds. In Part A, the syntheses and structures of amine–templated tin(II) phosphates are presented, and in Part B, the syntheses and structures of a family of tin(II) oxalate compounds are discussed. Weak intermolecular forces such as hydrogen-bond interactions, π•••π interactions, and lone-pair–π interactions have been observed in these compounds, and appear to lend structural stability. As part of this study, efforts have been made to evaluate the energies associated with the π•••π interactions and the lone-pair–π interactions using suitable theoretical models. In Chapter 3, a new family of organically templated hybrid materials based on indium, synthesized by partially substituting the inorganic anion (phosphite/phosphate/suphate) by the oxalate group, is presented. These compounds exhibit a wide range of structures in which the oxalates play a variety of roles. The observation of the first zero-dimensional molecular hybrid structure and the isolation of concomitant polymorphic compounds is noteworthy. The molecular hybrid structure is reactive and undergoes transformation reactions under both acidic and basic conditions. In Chapter 4, the synthesis and structural studies of five new open–framework phosphate and phosphite compounds of gallium are presented. All the compounds have three-dimensional structures, and the formation of a gallium phosphate based on only one type of building unit (spiro–5) is noteworthy. While a large number of organically templated transition metal phosphates have been synthesized, studies on transition metal phosphites are not many. In Chapter 5, the synthesis, structure and magnetic properties of a family of transition metal (cobalt, vanadium, manganese) phosphite structures templated by the organic amines are presented. A previously known vanadyl phosphite has also been isolated and investigated by temperature dependent ESR and magnetic susceptibility studies. All the transition metal compounds exhibit antiferromagnetic behavior. In Chapter 6, the synthesis, structure, and transformation reactions in amine-templated actinide phosphonoacetates are presented. The compounds, which are based on uranium and thorium, are built up from the connectivity between the metal polyhedra and the phosphonoacetate/oxalate units, forming two– and three–dimensional structures. It has been shown that the two–dimensional uranyl phosphonoacetate–oxalate compound can be prepared by two different synthetic approaches: (i) solvent–free solid state reaction at 150˚C and (ii) room temperature mechanochemical (grinding) route. The formation of oxalate hybrids using the phosphonocarboxylate ligand is a new approach in the synthesis of multi-component hybrid compounds.

碩士
國立中央大學
化學研究所
95
Four organic-inorganic hybrid compounds, (H4A)[U2F6(C2O4)3]‧4H2O [A = tris(2-aminoethyl)amine (A1) and 1,4-bis-(3-aminopropyl)piperazine (A2)] and M(H2O)(C2O4)0.5(HPO3)‧H2O [M = Er (B1) and Yb (B2)], have been synthesized by hydrothermal methods and structurally characterized by single-crystal X-ray diffraction, thermogravimetric analysis, and magnetic analysis. Both A1 and A2 consist of anionic layers, [U2F6(C2O4)3]4-, separated by organic ammonium cations and lattice water molecules. The UF3O6 polyhedra are connected by oxalate ligands with different types within the layers. A1 and A2 are the first example of organically-templated uranium fluorooxalates. Both B1 and B2 comprise LnO8 decahedra and HPO3 tetrahedra forming 2-D layers which connected via bisbidentate oxalate anions to form a 3-D framework, and delimit 8-membered ring channels alone a axis. B1 and B2 are the first example of lanthanide oxalatophosphite.

Open-framework inorganic and inorganic-organic hybrid materials constitute an important area of study in materials chemistry, because of their potential applications in areas such as sorption and catalysis. Besides aluminosilicate zeolites, the metal phosphates and carboxylates constitute large families of open-framework structures. The possibility of building open architectures with the sulfate and selenate anions as the basic building units has been explored in this thesis. Investigations of a variety of open-framework metal sulfates and selenates, as well as a family of jarosites of different transition metals are presented. More importantly, studies directed towards the synthesis and understanding of the magnetic properties of various Kagome compounds formed by the transition metal ions is discussed at length. After providing an introduction to inorganic open-framework compounds (Part 1), the thesis presents the results of the investigations of various transition and rare earth metal sulfates with diverse structures and dimensionalities in Part 2. Some of these compounds show interesting properties. For example, a two-dimensional Ni(II) sulfate exhibits ferrimagnetism whereas a three-dimensional Ni(II) sulfate with 10-membered channels is paramagnetic. A family of three-dimensional co-ordination polymers of Co(II) sulfate wherein the Co(II) sulfate layers are linked by diaminoalkanes of varying chain length has been synthesized and characterized. Organically-templated neodymium and thorium sulfates with layered and three-dimensional structure have also been prepared. The jarosite family of compounds with the Kagome structure is considered as an ideal model for studying frustrated magnetism. This type of materials, however, is difficult to prepare in a pure and highly crystalline form. We have synthesized analogues of the jarosite containing magnetic ions other than Fe3+ by solvothermal techniques and discussed them in Part 3. In particular, we have prepared and explored the magnetic properties of Mn2+(S = 5/2), Fe2+ (S = 2), Co2+(S = 3/2) and Ni2+ (S = 1) jarosites. Based on the results presented, it becomes clear that the magnetic properties vary with the spin of the transition metal ion. It appears that those Kagome compounds with transition metalions with non-integer spins show antiferromagnetic interactions and magnetic frustration while those with integer spins exhibit ferro/ferrimagnetic properties. A theoretical study has also supports this observation. We have been able to isolate for the first time 1,4-diazacubane as the part of the structure of the nickel Kagome compound. The possibility of building open architectures with the selenate anion as the basic building unit has been explored in Part 4. The results have been rewarding and an organically-templated three-dimensional lanthanum selenate with 12-membered channels has thus been obtained for the first time.

Crystal growth and characterization of few multifunctional materials with perovskite (ABX3) structure are discussed in this thesis. Efforts were made to modify the magnetic and electric behaviour of these materials by selective tuning of A, B and X components. Structural, magnetic and dielectric characterization are detailed in various chapters for doped (A and B site) rare-earth manganites and organometallic compounds with different (Chloride or formate) anions. The relevant aspects of crystal structure and its relationship with ordered ground states are discussed in the introductory chapter. A detailed review of prominent theories pertaining to magnetic and ferroelectric ordering in the literature is provided. Growth of various inorganic compounds by solid-state reaction and floating zone method as well as use of solvothermal techniques for growing organometallic compounds are discussed. Material preparation, optimization of crystal growth processes and results of characterization are addressed in various chapters. The effect of Yttrium doping on structural, magnetic and dielectric properties of rare-earth manganites (RMnO3 where R = Nd, Pr) has been investigated. Neutron diffraction studies (Pr compounds) confirm A-type antiferromagnetic structure and fall in transition temperature as the Yttrium doping level increases. Diffraction experiments in conjunction with dc magnetization and ac susceptibility studies reveal magnetic frustration in excess Yttrium dopedcompounds. When mutliglass properties of 50% B-site doped Nd2NiMnO6 were investigated, evidence of re-entrant cluster glass phase was seen probably due to presence of anti-site disorder. The relaxor-like dielectric behaviour arises from crossover of relaxation time in grain and grain boundary regions. Multiferroic behaviour of the organometallic compound (C2H5NH3)2CuCl4 as well as the ferroelectric transition were investigated in detail. The role of Hydrogen bond ordering in driving structural transitions is elucidated by low temperature dielectric and Raman studies in (C2H5NH3)2CdCl4. It was found possible to tune the magnetic and ferroelectric properties in metal formate compounds (general formula AB(HCOO)3) by selectively choosing organic cations [(CH3)2NH2+; C(NH3)3+] and transition metal ion [B = Mn, Co and Cu]. The nature of magnetic ordering and transition temperature could be altered by the transition metal ion. The effect of reorientation of organic cations which leads to ferroelectric nature is discussed using dielectric and pyroelectric data. Significant results are summarized in the chapter outlining general conclusions. Future prospects of work based on these observations are also provided. The conclusions are corroborated by detailed analysis of experimental data.

碩士
中國文化大學
應用化學研究所
86
The hydrothermai synthesis and characterization of a novel organic/inorganichybrid compound:viz.[WO3(2,2-bipyridinee)],is presented. This compound was characteriztion by various techniques incuding Raman and IR spectroscopy, XRDand thermogravimetric analysis. Structural analyses of this compound by Ramanand IR data shows that it consists a novel tungstate structure with 2,2-bipyridineis coordinated to the tungsten atom.The X-ray powder diffraction data of thecompound is indexed to a monoclinic cell with a=14.313(4),b=9.603(2),c=7.288(2) AB=102.07(2).The structure of [WO3(2,2-bipyridine)] adopts a chain-like framework consisting of cornerishareed distorted octahedron (WO4N2) with the 2,2-bipyridineserving as a bidentate ligand whose ring fanning out from the chain.Upon thermal threatment,[WO3(2,2-bipyridine)] retains its structural integrity below 300c,followed by a gradual lossof 2,2-bipyridine which leads to formation of WO3 around 475c. The thermaldecomposition is observed to proceed through a transtional intermediate:viz.[WO4O12(2,2-bipyridine)]whose stucture is proposeed and discussed.