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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
1

A design strategy for group 15 supramolecular assemblies /

Vickaryous, William Jake. January 2008 (has links)
Thesis (Ph. D.)--University of Oregon, 2008. / Typescript. Includes vita and abstract. Includes bibliographical references (leaves 69-81). Also available online in ProQuest, free to University of Oregon users.
2

Využití interaktivní tabule ve výuce anorganické chemie na SŠ - V.A (15.) skupina / The Use of Interactive Whiteboard in Inorganic Chemistry Teaching (Secondary Education) - Group 15 of the Periodic Table of Elements

Matušková, Eva January 2014 (has links)
The subject of this thesis was creating of teaching material for an interactive whiteboard using ActivInspire program. The material was created in a form of interactive presentations designed to be used in chemistry lessons at secondary schools. The theme of these presentations was the 15th group of the periodic table of elements. The thesis also includes a description of the way the presentations were made and instructions for teachers how to work with them.
3

Phosphorus (III) tricationic and dicationic complexes

Sinclair, Hannah 01 August 2017 (has links)
Coordination chemistry usually applies to transition metals, but has recently been extended to the p-block elements. For the pnictogen atoms (group 15), this type of coordination chemistry has already been applied to antimony and bismuth, where they behave as Lewis acceptor centres. However, complexes with nitrogen and phosphorus as Lewis acidic centres are rare, due to their relatively small atomic radii and inherent basic nature. Instead, these elements (Pn(III)) are typically observed as donor centres because they are better at donating their electron pair, than they are at accepting them. To enhance the Lewis acidity at the phosphorus and nitrogen centres, a cationic charge can be introduced by heterolytically abstracting a halide and replacing it with a weakly coordinating anion, providing more opportunities for new reactivity. The presence of a stereochemically active lone pair at the acceptor site also introduces new reactivity patterns to be explored. The formation of these main group coordination complexes opens doors to potential applications in catalysis, small molecule activation, or as material precursors. 2,2’-bipyridine (bipy) has been a prototypical ligand used in transition metal coordination chemistry due to its high basicity and oxidative resistance. This property has been exploited to enable a comprehensive study of a series of Pn(III) tricationic and dicationic complexes using 2,2’-bipyridine (bipy); 4,4’-di-tert-butyl-2,2’-bipyridine (tBu2bipy); 4-dimethylaminopyridine (DMAP); and other main group containing ligands. / Graduate

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