The majority of research in this thesis uses X-ray crystallography to investigate the structural features of peri-substituted naphthalene compounds. X-ray crystallography is introduced in chapter one, followed by a discussion on modes of distortion peri-substituted naphthalene derivatives can undergo, in chapter two. In chapter three, compounds having non-bonded -SPh and -EPh (E = S, Se, or Te) peri-substituents are compared. These similar compounds react differently when oxidized with bromine. The oxidation products are used to discuss a recently proposed mechanism and a more specific mechanism is suggested. In chapter four, a one-pot synthesis for naphtho[1,8-c,d]-1,2-diselenole (Se₂naph) is reported. Substituents were added to Se₂naph to form two new naphthalene compounds. The substituents are found to distort the Se-Se bond and influence packing. In chapter five, several diselenium-containing compounds are used as ligands in platinum(II)-bisdiphosphine complexes. The preference for platinum(II) to stay square planar dictates the geometry around the metal center, not the rigidity of the naphthalene backbone. Chapter six introduces (8-phenylsulfanylnaphth-1-yl)diphenylphosphine, a peri-substituted naphthalene containing -SPh and -PPh₂ substituents, and several derivatives. This ligand is used in a variety of complexes containing platinum(II), ruthenium(II), and copper(I) metal halides, whose coordination geometries are discussed in chapter 7. The naphthalene-based ligands in Cu(I) and Ru(II) seem to determine the geometry around the metal, whereas the metal center d-orbitals dominate in the Pt(II) examples. Chapters eight and nine deviate from the naphthalene theme. In chapter eight, X-ray analysis of sulfoxide compounds is used to discuss the structural environment around the sulfur. Various intra- and inter-molecular interactions were discovered in crystal packing. Finally, chapter 9 uses STANDARD (St ANDrews Automated Robotic Diffractometer) to statistically analyze numerous E₂Ph₂ (E = S, Se, or Te) crystals to determine chirality. It is intriguing that Te₂Ph₂ shows a preference for one enantiomer over the other.
| Identifer | oai:union.ndltd.org:bl.uk/oai:ethos.bl.uk:552309 |
| Date | January 2010 |
| Creators | Fuller, Amy L. |
| Contributors | Slawin, Alexandra M. Z. : Woollins, J. Derek |
| Publisher | University of St Andrews |
| Source Sets | Ethos UK |
| Detected Language | English |
| Type | Electronic Thesis or Dissertation |
| Source | http://hdl.handle.net/10023/826 |
Page generated in 0.1125 seconds