The Polytope Formalism: isomerism and associated unimolecular isomerisation

This thesis concerns the ontology of isomerism, this encompassing the conceptual frameworks and relationships that comprise the subject matter; the necessary formal definitions, nomenclature, and representations that have impacts reaching into unexpected areas such as drug registration and patent specifications; the requisite controlled and precise vocabulary that facilitates nuanced communication; and the digital/computational formalisms that underpin the chemistry software and database tools that empower chemists to perform much of their work. Using conceptual tools taken from Combinatorics, and Graph Theory, means are presented to provide a unified description of isomerism and associated unimolecular isomerisation spanning both constitutional isomerism and stereoisomerism called the Polytope Formalism. This includes unification of the varying approaches historically taken to describe and understand stereoisomerism in organic and inorganic compounds. Work for this Thesis began with the synthesis, isolation, and characterisation of compounds not adequately describable using existing IUPAC recommendations. Generalisation of the polytopal-rearrangements model of stereoisomerisation used for inorganic chemistry led to the prescriptions that could deal with the synthesised compounds, revealing an unrecognised fundamental form of isomerism called akamptisomerism. Following on, this Thesis describes how in attempting to place akamptisomerism within the context of existing stereoisomerism reveals significant systematic deficiencies in the IUPAC recommendations. These shortcomings have limited the conceptualisation of broad classes of compounds and hindered development of molecules for medicinal and technological applications. It is shown how the Polytope Formalism can be applied to the description of constitutional isomerism in a practical manner. Finally, a radically different medicinal chemistry design strategy with broad application, based upon the principles, is describe

Entangled graphs on surfaces in space

In the chemical world, as well as the physical, strands get tangled. When those strands form loops, the mathematical discipline of ‘knot theory’ can be used to analyse and describe the resultant tangles. However less has been studied about the situation when the strands branch and form entangled loops in either finite structures or infinite periodic structures. The branches and loops within the structure form a ‘graph’, and can be described by mathematical ‘graph theory’, but when graph theory concerns itself with the way that a graph can fit in space, it typically focuses on the simplest ways of doing so. Graph theory thus provides few tools for understanding graphs that are entangled beyond their simplest spatial configurations. This thesis explores this gap between knot theory and graph theory. It is focussed on the introduction of small amounts of entanglement into finite graphs embedded in space. These graphs are located on surfaces in space, and the surface is chosen to allow a limited amount of complexity. As well as limiting the types of entanglement possible, the surface simplifies the analysis of the problem – reducing a three-dimensional problem to a two-dimensional one. Through much of this thesis, the embedding surface is a torus (the surface of a doughnut) and the graph embedded on the surface is the graph of a polyhedron. Polyhedral graphs can be embedded on a sphere, but the addition of the central hole of the torus allows a certain amount of freedom for the entanglement of the edges of the graph. Entanglements of the five Platonic polyhedra (tetrahedron, octahedron, cube, dodecahedron, icosahedron) are studied in depth through their embeddings on the torus. The structures that are produced in this way are analysed in terms of their component knots and links, as well as their symmetry and energy. It is then shown that all toroidally embedded tangled polyhedral graphs are necessarily chiral, which is an important property in biochemical and other systems. These finite tangled structures can also be used to make tangled infinite periodic nets; planar repeating subgraphs within the net can be systematically replaced with a tangled version, introducing a controlled level of entanglement into the net. Finally, the analysis of entangled structures simply in terms of knots and links is shown to be deficient, as a novel form of tangling can exist which involves neither knots nor links. This new form of entanglement is known as a ravel. Different types of ravels can be localised to the immediate vicinity of a vertex, or can be spread over an arbitrarily large scope within a finite graph or periodic net. These different forms of entanglement are relevant to chemical and biochemical self-assembly, including DNA nanotechnology and metal-ligand complex crystallisation

Quantum mechanics in complex systems

This document should be considered in its separation; there are three distinct topics contained within and three distinct chapters within the body of works. In a similar fashion, this abstract should be considered in three parts. Firstly, we explored the existence of multiply-charged atomic ions by having developed a new set of dimensional scaling equations as well as a series of relativistic augmentations to the standard dimensional scaling procedure and to the self-consistent field calculations. Secondly, we propose a novel method of predicting drug efficacy in hopes to facilitate the discovery of new small molecule therapeutics by modeling the agonist-protein system as being similar to the process of Inelastic Electron Tunneling Spectroscopy. Finally, we facilitate the instruction in basic quantum mechanical topics through the use of quantum games; this method of approach allows for the generation of exercises with the intent of conveying the fundamental concepts within a first year quantum mechanics classroom. Furthermore, no to be mentioned within the body of the text, yet presented in appendix form, certain works modeling the proliferation of cells types within the confines of man-made lattices for the purpose of facilitating artificial vascular transplants. ^ In Chapter 2, we present a theoretical framework which describes multiply-charged atomic ions, their stability within super-intense laser fields, also lay corrections to the systems due to relativistic effects. Dimensional scaling calculations with relativistic corrections for systems: H, H-, H 2-, He, He-, He2-, He3- within super-intense laser fields were completed. Also completed were three-dimensional self consistent field calculations to verify the dimensionally scaled quantities. With the aforementioned methods the system\u27s ability to stably bind \u27additional\u27 electrons through the development of multiple isolated regions of high potential energy leading to nodes of high electron density is shown. These nodes are spaced far enough from each other to minimized the electronic repulsion of the electrons, while still providing adequate enough attraction so as to bind the excess elections into orbitals. We have found that even with relativistic considerations these species are stably bound within the field. It was also found that performing the dimensional scaling calculations for systems within the confines of laser fields to be a much simpler and more cost-effective method than the supporting D=3 SCF method. The dimensional scaling method is general and can be extended to include relativistic corrections to describe the stability of simple molecular systems in super-intense laser fields.^ Chapter 3, we delineate the model, and aspects therein, of inelastic electron tunneling and map this model to the protein environment. G protein-coupled receptors (GPCRs) constitute a large family of receptors that sense molecules outside of a cell and activate signal transduction pathways inside the cell. Modeling how an agonist activates such a receptor is important for understanding a wide variety of physiological processes and it is of tremendous value for pharmacology and drug design. Inelastic electron tunneling spectroscopy (IETS) has been proposed as the mechanism by which olfactory GPCRs are activated by an encapsulated agonist. In this note we apply this notion to GPCRs within the mammalian nervous system using ab initio quantum chemical modeling. We found that non-endogenous agonists of the serotonin receptor share a singular IET spectral aspect both amongst each other and with the serotonin molecule: a peak that scales in intensity with the known agonist activities. We propose an experiential validation of this model by utilizing lysergic acid dimethylamide (DAM-57), an ergot derivative, and its isotopologues in which hydrogen atoms are replaced by deuterium. If validated our theory may provide new avenues for guided drug design and better in silico prediction of efficacies. ^ Our final chapter, explores methods which may be explored to assist in the early instruction in quantum mechanics. The learning of quantum mechanics is contingent upon an understanding of the physical significance of the mathematics that one must perform. Concepts such as normalization, superposition, interference, probability amplitude and entanglement can prove challenging for the beginning student. This paper outlines several class exercises that use a non-classical version of tic-tac-toe to instruct several topics in an undergraduate quantum mechanics course. Quantum tic-tac-toe (QTTT) is a quantum analogue of classical tic-tac-toe (CTTT) benefiting from the use of superposition in movement, qualitative (and later quantitative) displays of entanglement and state collapse due to observation. QTTT can be used for the benefit of the students understanding in several other topics with the aid of proper discussion