Combining 3D printing and liquid handling to produce user-friendly reactionware for chemical synthesis and purification

We use two 3D-printing platforms as solid- and liquid-handling fabricators, producing sealed reactionware for chemical synthesis with the reagents, catalysts and purification apparatus integrated into monolithic devices. Using this reactionware, a multi-step reaction sequence was performed by simply rotating the device so that the reaction mixture flowed through successive environments under gravity, without the need for any pumps or liquid-handling prior to product retrieval from the reactionware in a pure form

Synthesis, Properties, and Solid-State Structures of a Series of 6,13-Dicyanoheteropentacene Analogues: Towards New Liquid Crystalline Materials

The focus of this thesis is the synthesis of novel heterocyclic pentacene analogs and the investigation of their self-organization for the development of new materials for organic electronics. The thesis consists of two interrelated projects: the first being development of an improved synthesis of a series of liquid crystalline dicyanotetraoxapentacenes (DCTOPs) while the second entails the exploratory synthesis of several novel dicyanoheteropentacene analogues and a preliminary investigation of their photophysical properties and solid-state structures. Both of these projects centre around the use of nucleophilic aromatic substitution reactions on tetrafluoroterephthalonitrile. Soluble, tetrakis(bis(alkoxy)phenyl)-substituted DCTOPs were originally synthesised via a short synthesis complicated by a tedious purification required in the last step. Despite this, derivatives bearing long alkyl chains were prepared which displayed liquid crystalline properties in addition to aggregation-induced emission. Building upon this success, but with the goal of achieving DCTOPs in an efficient synthetic manner for this thesis, changes were made which eliminated the troublesome fourfold Suzuki coupling by changing the order of reactions, which in turn required a protection-deprotection sequence. Purification in the new synthesis was greatly simplified and the target tetraaryl-DCTOPs were accessed in good overall yields and purities. The synthesis and solid state structures of these DCTOPs are discussed in Chapter 2. Building on the methods developed in Chapter 2, several novel pentacene analogues containing combinations of nitrogen, oxygen, and sulfur atoms installed within the pentacene core were also synthesised. These compounds were prepared in good yields, and preliminary photophysical studies show that all the compounds displayed luminescence in solution and the solid state. It was also shown that replacement of O with N leads to a red shift in absorption and emission spectra. The X-ray crystal structures show that several of these compounds exhibit π−stacking in the solid state, which is an important design element for applications in organic electronics. The synthesis, photophysical properties, and solid-state organization of these novel 6,13-dicyanoheteropentacene analogues are discussed in Chapter 3

First-principles design and subsequent synthesis of a material to search for the permanent electric dipole moment of the electron

We describe the first-principles design and subsequent synthesis of a new material with the specific functionalities required for a solid-state-based search for the permanent electric dipole moment of the electron. We show computationally that perovskite-structure europium barium titanate should exhibit the required large and pressure-dependent ferroelectric polarization, local magnetic moments, and absence of magnetic ordering even at liquid helium temperature. Subsequent synthesis and characterization of Eu$_{0.5}$Ba$_{0.5}$TiO$_3$ ceramics confirm the predicted desirable properties.Comment: Nature Materials, in pres

Formylation with "Supercritical” CO2: Efficient Ruthenium-Catalyzed Synthesis of N -Formylmorpholine

Formylation of morpholine with "supercritical” CO2 using the bidentate ruthenium catalyst RuCl2(dppe)2 affords high N-formylmorpholine production rate at almost 100% selectivity. The solventless reaction could be an interesting alternative to the present N-formylmorpholine synthesis routes, which are based on environmentally harmful formylation agents. Video monitoring of the reaction mixture during reaction revealed a complex phase behavior, including the formation of solid carbamate, which was most prominent at low conversion and gradually disappeared with higher conversion, i.e., with the formation of N-formylmorpholine and water as a by-product. Addition of water as an additive suppressed solid carbamate formation and enhanced the reaction rate. Infrared spectroscopy was applied to follow the changes in the liquid and dense gas phase. The ruthenium catalyst was confined to the liquid phase, containing morpholine, N-formylmorpholine, water, dissolved carbon dioxide and hydrogen. Although the solubility of the ruthenium catalyst in the liquid phase decreased with increasing conversion, good performance in the synthesis of N-formylmorpholine could be achieve

Size dependent phase diagrams of Nickel-Carbon nanoparticles

The carbon rich phase diagrams of nickel-carbon nanoparticles, relevant to catalysis and catalytic chemical vapor deposition synthesis of carbon nanotubes, are calculated for system sizes up to about 3 nanometers (807 Ni atoms). A tight binding model for interatomic interactions drives the Grand Canonical Monte Carlo simulations used to locate solid, core/shell and liquid stability domains, as a function of size, temperature and carbon chemical potential or concentration. Melting is favored by carbon incorporation from the nanoparticle surface, resulting in a strong relative lowering of the eutectic temperature and a phase diagram topology different from the bulk one. This should be taken into account in our understanding of the nanotube growth mechanisms

Taming the Base Catalyzed Sol–Gel Reaction: Basic Ionic Liquid Gels of SiO2 and TiO2

We describe the autocatalytic synthesis of SiO2 and TiO2 ionic liquid gels using a basic ionic liquid as the solvent, template, and catalyst for the sol–gel reaction. Basic gels were synthesized using a two-component mixture of the basic ionic liquid [P66614][OH] and either tetraethylorthosilicate or titanium isopropoxide (Ti(OiPr)4). The gels formed were clear glassy materials. The unstable basic ionic liquid was stabilized by the matrix and showed both increased thermal stability (by thermogravimetric analysis) and chemical stability (by solid-state NMR) after over 1 year of storage

Use of continuous solid-phase synthesis to obtain phosphors based on strontium aluminate

The effect of conditions of continuous solid-phase synthesis on particle size distribution of nanostructured powders of strontium aluminate was studied. It was shown that continuous solid-phase synthesis allows for: synthesis of strontium aluminate in the form of nanostructured powders with controlled particle size distribution directly during its synthesis; in the presence of a liquid phase strontium aluminate is synthesized with a high level of monophasity. It was shown that in order to optimize the illuminating parameters of phosphors based on strontium aluminate, it is advisable to use continuous solid-phase synthesis