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A growing field of research has evolved around the design and synthesis of a variety of porous metal-organic framework (MOF) materials. Some of the most promising areas for which these materials are potentially useful candidates include gas-separation, heterogeneous catalysis, and gas-storage, and all of these applications involve placing the MOF under pressure. There is clearly a need to understand the structural response of MOFs to applied pressure. Nevertheless, hitherto there are very few published investigations dedicated to determining the behaviour of porous hybrid materials under pressure. Through the use of high-pressure single-crystal X-ray diffraction studies, a series of MOF materials have been studied. Here we present the effect of pressure on a series of MOFs. In chapter 2, the effect of pressure on the prototypical MOF called MOF-5 was studied experimentally from ambient pressure to 3.2 GPa. Here, application of pressure was driven by the hydrostatic medium being forced into the pores of the MOF, which altered the mechanical properties of MOF-5, in particular, medium inclusion delayed the onset of amorphization. Complementary computational analysis was also performed to elucidate further the effect of medium inclusion on compressive behaviour. Detailed structural data was also collected as a function of pressure on the MOF Cu-btc. Application of pressure caused solvent to be squeezed into the pores (like MOF-5) until a phase transition occurred, driven by the sudden compression and expansion of equatorial and axial Cu–O bonds. High-pressure post-synthetic modification of a MOF is reported for the first time. On application of pressure of 0.2 GPa to the Cu-based MOF called STAM-1, a ligand exchange reaction takes place resulting in a change in pore size, shape, and hydrophilicity of the resulting pores. Here, we also demonstrate the ability to force hydrophilic molecules into hydrophobic pores using pressure, counteracting the hydrophobic effect. A high-pressure combined experimental and computational study has been carried to probe the effect of pressure on ‘breathing’ mechanisms in a zeolitic imidazolate framework (or ZIF) called ZIF-8. The penetration of guest molecules and the accommodation of pressure are shown to be inextricably linked to the rotation of methylimidazolate groups in the structure. Finally, the application of pressure to the MOF Sc₂BDC₃ and the nitro functionalized derivative Sc₂(NO₂-BDC)₃ was also studied. Here, the effect of chemical modification of the organic ligand, whilst maintaining framework topology, has been investigated as it pertains to compressibility. Directionality of compression is observed and this is rationalized with respect to the framework topology and medium inclusion/exclusion.

This thesis is built upon two areas of research concerning metal-organic frameworks (MOFs). The first focuses on the functionalisation of MOFs via post-synthetic modification (PSM). The second involves the investigation on the potential of MOFs as hosts for insect pheromones. Chapter 1 introduces the field of MOF chemistry, and covers their properties along with a brief description of their applications. The concept of PSM is introduced and a review of recent literature given. The aims of the thesis are also detailed at the end of this chapter. Chapter 2 describes the PSM of [Zr6O4(OH)4(BDC-NH2)6], UiO-66-NH2, via Aza-Michael reactions. Different functionalities were successfully introduced into its pores and the degrees of conversion were determined via 1H NMR spectroscopy. Gas sorption measurements (CO2 and N2) of the PSM products were carried out and compared. In particular, two PSM products were shown to exhibit higher CO2 over N2 selectivity than that for the starting MOF, UiO-66-NH2. Chapter 3 describes a new PSM route in obtaining azole-functionalised MOFs via Mannich reactions. The amino groups in three different MOFs were converted into a range of azole-functionalised MOFs with conversions up to 100%. In particular, one of the PSM reactions afforded a new material, formulated as [Zn3(BDC-NH2)1.32(BDC-NHCH2N2C3H3)1.68(C6H12N2)], based on single crystal X-ray crystallography, 1H NMR and TGA analyses. Gas sorption studies demonstrate increased selectivity for CO2 over N2 for the PSM products. One of the modified MOFs was shown to exhibit a high Hg(II) uptake from aqueous solutions. Chapter 4 introduces the concept of using MOFs as hosts for ant pheromones. The factors which influenced the pheromone loading in zinc and zirconium based MOFs were investigated. The MOFs containing the linker BDC-NHPr (2-(propylamino)benzene-1,4-dicarboxylate) were found to be effective at hosting two types of ant pheromones, 3-octanone and (S)-4-methyl-3-heptanone.

Metal-Organic Frameworks (MOFs) are hybrid materials and are acknowledged as an important class of functional solid-state materials with high scientific interest in academia and industry alike. Their modular nature in terms of structural and compositional diversity, tunability, high surface area, and controlled pore size renders MOFs as the ideal candidate to address various persistent challenges pertaining to gas storage/separation, catalysis, drug delivery, and smart sensing. Through the field of reticular chemistry, targeted structures can be constructed through multiple design approaches, based on preselected building blocks prior to the assembly process. This thesis illustrates the merit of the supermolecular building layer (SBL) approach for the rational construction and discovery of highly connected and porous MOFs based on rare earth cations. Specifically, the emphasis of this study is on (i) the rational design and synthesis of 3-periodic MOFs based on SBLs pillared by ditopic ligands through post-synthetic modification (PSM) and in situ reactions. (ii) The investigation of the mixed-ligand system with different lengths and geometry of ditopic ligands on the isolation of metal clusters with distinct pore sizes. (iii) Gaining an overall insight into the exploration of different synthetic pathways that control the assembly of rare earth MOFs.

Yes / Pesticide contamination is a global issue, affecting nearly 44% of the global farming population, and disproportionately affecting farmers and agricultural workers in developing countries. Despite this, global pesticide usage is on the rise, with the growing demand of global food production with increasing population. Different types of porous materials, such as carbon and zeolites, have been explored for the remediation of pesticides from the environment. However, there are some limitations with these materials, especially due to lack of functional groups and relatively modest surface areas. In this regard, metal-organic frameworks (MOFs) provide us with a better alternative to conventionally used porous materials due to their versatile and highly porous structure. Recently, a number of MOFs have been studied for the extraction of pesticides from the environment as well as for targeted and controlled release of agrochemicals. Different types of pesticides and conditions have been investigated, and MOFs have proved their potential in agricultural applications. In this review, the latest studies on delivery and extraction of pesticides using MOFs are systematically reviewed, along with some recent studies on greener ways of pest control through the slow release of chemical compounds from MOF composites. Finally, we present our insights into the key issues concerning the development and translational applications of using MOFs for targeted delivery and pesticide control.

Porous materials are essential to our everyday lives, for example as an effective catalyst in the cracking of crude oil, or as water softeners in washing powder. When developing novel functional porous materials, it is necessary to fully understand their structure-property relationships to maximise their ability to be used in industrially relevant settings. This thesis aims to understand the mechanical and adsorption properties of a class of porous solids metal-organic frameworks (or MOFs), which have many potential applications owing to their tuneable structures. Due to the inherent 3-D crystalline structure of MOFs, a wide range crystallographic techniques were used to determine structure-property relationships. To achieve maximum in-depth structural knowledge, both classical and quantum theoretical approaches were also applied to complement the understanding of both the energetics and structural details. Chapters One and Two begin with an overview of the state of the art studies carried out on MOFs, focusing on the use of high-pressure crystallography to understand their properties. In addition, there is emphasise on the importance of complementary computational methods that are used in the characterisation of MOFs. In Chapter Three, an isostructural series of MOFs (zeolitic imidazolate frameworks, or ZIFs) were studied for methanol adsorption by employing both experimental and molecular simulation techniques. These frameworks are gating materials, where the imidazole linker rotates upon adsorption of guest, and it was found that through ligand substitution the gate opening angle and onset pressure to gating could be tuned. By using high-pressure Xray crystallography the structure of the ZIFs were studied upon the uptake of guest and the degree of ring rotation quantified. In combination with periodic DFT and grand canonical Monte Carlo simulations the energy barrier to rotation and energies of adsorption could be calculated, respectively. Chapter Four focuses on one ZIF in particular, ZIF-8 ((Zn6(MeIm)12, MeIm = 2- methylimidazole) and details the adsorption of a selection of gases into the pores. The experimental method of cryogenic gas loading into a diamond anvil cell in this chapter is novel to MOFs. This method, in combination with molecular crystallography, is used to determine the structural response of the framework to guest-uptake as well as the crystallographic positions of the adsorption sites. In combination with in silico methods, the adsorption energies of guest-sites could be calculated, detailing which interactions drive the gating behaviour. The method of cryogenic loading highlighted how extreme conditions can be used to extract useful information about structural behaviour of MOFs on uptake of gas molecules into the pores, and when used in combination with computational methods, we have a powerful tool to analyse both positions and energies of adsorption sites. With this information, progress can be made in developing MOFs to maximize favourable interactions and lead to the development of MOFs with better selective gas storage properties. Chapter Five focuses on the synthesis and characterisation of the physical properties of a series of Zr-containing MOFs, called UiO-MOFs. The high valency of Zr(IV) and 12-fold coordination of the metal cluster in these materials, are associated with high shear and bulk moduli, which surpass those of other MOFs. A combination of single-crystal nano-indentation, high-pressure X-ray diffraction studies, density functional theory (DFT) calculations, and first-principles molecular dynamics (MD) simulations were used to determine the compressibility, elasticity and hardness of these materials, whose mechanical robustness was correlated to their different structural features, in-particular, how using non-linear linkers between the metal clusters stabilises the framework to compression. Chapter Six expands upon the series of Zr-MOFs in Chapter Five, and looks at how the mechanical properties of these MOFs are affected upon increasing the linker length. The experimentally determined elastics modulus of one of the frameworks, UiO-sdc (Zr6O4(OH)4(sdc)6 where sdc =4,4’-stillbene dicarboxylate), was found to lie above those of other highly porous MOFs. In addition, the elastic modulus was found to decrease linearly as a function of increasing the linker length, extending the structure-property relationships determined in Chapter Five.

Metal-organic frameworks (MOFs) are a relatively new class of porous materials, assembled from inorganic metal nodes and organic ligands. MOFs have garnered significant attention in the porous materials and adsorption fields in recent years due to their various attractive features such as high surface areas and pore volumes, tunable and uniform pore sizes, chemically functionalized adsorption sites, and potential for post-synthetic modification. These features give MOFs enormous potential for use in applications such as air purification, methane and hydrogen storage, separations, catalysis, sensing, and drug delivery. Therefore, synthesis and adsorption studies of MOFs have increased tremendously in recent years. Among the aforesaid applications, air purification and air quality control are important topics because existing porous media are ineffective at the adsorptive removal of toxic industrial chemicals (TICs) and chemical warfare agents. Thus, there is a critical need for radical improvements in these purification systems. MOFs have shown great potential to become next-generation filter media as they outperform the traditional porous materials such as activated carbons and zeolites in the air purification of TICs such as ammonia and sulfur dioxide. In spite of the numerous desirable attributes of MOFs, the practical use of these new materials in most applications hinges on their stability in humid or aqueous environments. The sensitivity of certain MOFs under humid conditions is well known, but systematic studies of the water stability properties of MOFs are lacking. This information is critical for identifying structural factors that are important for development of next-generation, water stable MOFs. In addition to the water stability issue, difficulty in the scale up of MOF synthesis has also plagued MOFs. Hence, the goal of this Ph.D. dissertation research is to design ammonia-selective, water stable MOFs that can be synthesized on a large scale. This work will have a direct impact on moving the MOF field forward to the commercial level. To achieve the aforementioned goal, this Ph.D. dissertation research has been divided into following three objectives: (1) Advance our understanding of the water stability of MOFs and develop design criteria for the construction of water stable MOFs. (2) Design water stable, ammonia-selective MOFs for next-generation chemical, biological, radiological, and nuclear (CBRN) filter media. (3) Investigate the scale-up of the UiO-66 MOF scaffold. Through the research efforts over the past four years, it is discovered that it is possible to adjust the water stability of pillared MOFs in both positive and negative directions by proper shielding of the ligand via functional groups. This study is the first of its kind and is of high value for the MOF community. This shielding concept is further extended by synthesizing 4 novel isostructural MOFs with methyl functional groups at different positions on the ligand. For the first time, light is shed on the important distinction between kinetic and thermodynamic water stability and experimental evidence for a kinetically governed water stability mechanism in these MOFs is provided. It is also demonstrated that, using catenation in combination with a pillaring strategy, it is possible to obtain water stable MOFs even when the pillar ligand has lower basicity (pKa value). Ammonia breakthrough measurements have shown that a hydroxyl functionalized Zr-based UiO-66 material is promising as it could offer a method for targeting the removal of specific chemical threats in a chemically stable framework that does not degrade in the presence of water. Large scale synthesis of a water stable MOF, UiO-66, is studied using glass vials and Teflon lined autoclaves. UiO-66 synthesis methods have been refined such that it is now possible to produce more than 70 times the yield obtained from the original synthesis report using the same reaction volume. This would result in a significant reduction of the MOF production cost at the industrial scale. Methane and hydrogen are ‘clean fuels’ (less CO2 emissions than petroleum) and MOFs are being tested for their on-board storage in cars due to the extremely high storage capacities of MOFs being promising enough to meet the requirements. Hence, more broadly, this Ph.D. dissertation work will lead to commercial applications of MOFs, which can revolutionize a variety of gas separation and storage problems such as CO2 capture, natural gas upgrading, and methane and hydrogen storage for clean fuel technologies. This would greatly reduce the environmental concerns faced by our society today.

Synthesis of polycrystalline, vs. single-crystalline porous materials, such as metal-organic frameworks (MOFs), is usually beneficial due to shorter synthetic time and higher yields. However, the structural characterization of these materials by X-ray powder diffraction can be complicated. Even more difficult, is to track structural changes of MOFs by in situ experiments. Hence, we designed several successful techniques for the structural investigation of porous MOFs. These methods utilize the Structure Envelope (SE) density maps. SEs are surfaces which describing the pore system with the framework. It was shown that these maps can be easily generated from the structure factors of a few (1 to 10) of the most intense low index reflections. Application of SE in Charge Flipping calculations shortens and simplifies structure determination of MOF materials. This method provides excellent MOF models which can be used as a good starting point for their refinement. However, the most interesting results have been found by using Difference Envelope Density (DED) analysis. DED plots are made by taking the difference between observed and calculated SE densities. This allows us to study guest related issues of MOFs such as, location of guest molecules in the pores, tracking activation of MOFs and gas loading, etc. We also have shown that, DED created from routine powder diffraction patterns might provide very important information about MOF structure itself. In fact DED can be used for study of interpenetration, substituents locations and effects conformational changes in the MOF ligands. Generation and analysis of SEs and DEDs are easy and straightforward. It provides the information needed to explain major deviations in structure-property relationship in MOFs. In our opinion, this method might become one of the important and routine techniques for MOFs structural analysis.

Submitted by JADER BARBOSA DA SILVA FLOR null (jader@iq.unesp.br) on 2017-05-22T17:08:38Z No. of bitstreams: 1 TESE VERSÃO FINAL para a impressão.pdf: 8986552 bytes, checksum: 9b079a86ffb72f7d5def9d9e6c6ba45e (MD5) / Approved for entry into archive by Luiz Galeffi (luizgaleffi@gmail.com) on 2017-05-23T17:35:16Z (GMT) No. of bitstreams: 1 flor_jbs_dr_araiq.pdf: 8986552 bytes, checksum: 9b079a86ffb72f7d5def9d9e6c6ba45e (MD5) / Made available in DSpace on 2017-05-23T17:35:16Z (GMT). No. of bitstreams: 1 flor_jbs_dr_araiq.pdf: 8986552 bytes, checksum: 9b079a86ffb72f7d5def9d9e6c6ba45e (MD5) Previous issue date: 2017-05-03 / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) / Neste projeto foram sintetizados e caracterizados materiais porosos conhecidos como Metal-Organic Frameworks (MOFs) que abrangem uma área da química que tem experimentado um crescimento muito grande nas duas últimas décadas. MOFs são compostos cristalinos contendo espaços potencialmente vazios (poros) construídos a partir de íons ou clusters metálicos interconectados por espaçadores orgânicos. Além da diversidade estrutural e topológica, estes materiais têm enorme potencial para muitas aplicações. Dentro desse contexto, o objetivo central do trabalho foi a preparação de MOFs de cobre(II) e zinco(II) e investigação da potencialidade de aplicação em catálise heterogênea. Dentre outros materiais, a MOF MOF-INZ foi preparada pela primeira vez a partir da funcionalização da HKUST-1 via processo PSM (Pos-Synthetic Modification) pela coordenação da isoniazida nos centros coordenativamente insaturados (CUSs) do íon cobre(II) do material precursor ativado. A utilização desse material como catalisador em reações de cicloadição de CO2 frente ao epóxido de propileno resultou em 95% de conversão do reagente em carbonato de propileno (após 72 horas, em presença de TBAI). A última etapa do trabalho consistiu na preparação das MOFs ZIF-8 e HKUST-1 em escala nanométrica, usando moduladores de concentração, e no desenvolvimento de uma técnica muito elegante para a formação de filmes finos sobre nanotubos de dióxido de titânio (com diâmetros da ordem de 50-100 nm). Os materiais híbridos preparados foram então submetidos a reações foto- e fotoeletrocatalíticas de redução de CO2. As MOFs adsorvidas nos eletrodos nanoestruturados mostraram atividades significativamente mais altas em comparação com o eletrodo não modificado. Sob irradiação de luz e na presença de ácido ascórbico, o compósito Ti/TiO2-ZIF-8 gerou cerca de 30 mmol/L de etanol e 2 mmol/L de metanol em fase gasosa, enquanto que reações fotoeletrocatalíticas de redução de CO2 produziram 104 mmol/L e 17 mmol/L desses mesmos produtos, respectivamente. Do que seja do nosso conhecimento, essa é a primeira vez que a redução fotoeletrocatalítica desse importante gás causador do efeito estufa é realizada sobre materiais baseado em MOFs e abre uma frente de pesquisa bastante promissora no que tange a introdução dessa importante classe de materiais porosos no design de fotoeletrocatalisadores para reações gasosas. / In this project, porous materials known as Metal-Organic Frameworks (MOFs) were synthesized and characterized, which cover a chemistry area that has experienced a very large growth in the last two decades. MOFs are crystalline compounds containing potentially empty spaces (pores) constructed from ions or metal clusters interconnected by organic spacers. In addition to structural and topological diversity, these materials have enormous potential for many applications. In this context, the main objective of the work was the preparation of copper (II) and zinc (II) MOFs and the investigation of the potentiality of application in heterogeneous catalysis. Among other materials, MOF MOF-INZ was prepared for the first time from the functionalization of HKUST-1 via PSM (Post-Synthetic Modification) process by the coordination of isoniazid to the coordinated unsaturated (CUSs) centers of the copper (II) activated precursor. The use of this material as a catalyst in CO2-cycloaddition reactions to propylene epoxide resulted in 95% conversion of the reactant into propylene carbonate (after 72 hours in the presence of TBAI). The last stage of the work consisted in the preparation of the ZIF-8 and HKUST-1 MOFs at nanoscale using concentration modulators and the development of a very elegant technique for the formation of thin films on titanium dioxide nanotubes (with diameters in the order of 50-100 nm). The prepared hybrid materials were then submitted to photo- and photoelectrocatalytic CO2 reduction reactions. The MOFs adsorbed on the nanostructured electrodes showed significantly higher activities compared to the unmodified electrode. Under light irradiation and in the presence of ascorbic acid, the Ti / TiO2-ZIF-8 composite generated about 30 mmol / L of ethanol and 2 mmol / L of methanol in the gas phase, while photoelectrocatalytic CO2 reduction reactions produced 104 Mmol / L and 17 mmol / L of these same products, respectively. To our knowledge, this is the first time that the photoelectrocatalytic reduction of this important greenhouse gas is carried out on materials based on MOFs and opens a very promising research front regarding the introduction of this important class of porous materials in the design of photoelectrocatalysts for gaseous reactions.

Gaining control over the assembly of crystalline solid-state materials has been significantly advanced through the field of reticular chemistry and metal organic frameworks (MOFs). MOFs have emerged as a unique modular class of porous materials amenable to a rational design with targeted properties for given applications. Several design approaches have been deployed to construct targeted functional MOFs, where desired structural and geometrical attributes are incorporated in preselected building units prior to the assembly process. This dissertation illustrates the merit of the molecular building block approach (MBB) for the rational construction and discovery of stable and highly porous MOFs, and their exploration as potential gas storage medium for sustainable and clean energy applications. Specifically, emphasis was placed on gaining insights into the structure-property relationships that impact the methane (CH4) storage in MOFs and its subsequent delivery. The foreseen gained understanding is essential for the design of new adsorbent materials or adjusting existing MOF platforms to encompass the desired features that subsequently afford meeting the challenging targets for methane storage in mobile and stationary applications.In this context, we report the successful use of the MBB approach for the design and deliberate construction of a series of novel isoreticular, highly porous and stable, aluminum based MOFs with the square-octahedral (soc) underlying net topology. From this platform, Al-soc-MOF-1, with more than 6000 m2/g apparent Langmuir specific surface area, exhibits outstanding gravimetric CH4 uptake (total and working capacities). It is shown experimentally, for the first time, that the Al-soc-MOF platform can address the U.S. Department of Energy (DOE) challenging gravimetric and volumetric targets for the CH4 working capacity for on-board CH4 storage. Furthermore, Al-soc-MOF-1 exhibits the highest total gravimetric and volumetric uptake for carbon dioxide and the utmost total and deliverable uptake for oxygen at relatively high pressures among all microporous MOFs. Additionally, the research studies presented in this dissertation highlight the latest discoveries on our continuous quest for highly-connected nets. Specifically, we report the discovery of two fascinating and highly-connected minimal edge-transitive nets in MOF chemistry, namely pek and aea topologies, via a systematic exploration of rare earth metal salts in combination with relatively less symmetrical 3-connected tricarboxylate ligands. Adsorption studies revealed that pek-MOF-1 offers excellent volumetric CO2 and CH4 uptakes at high pressures.