Chemistry
Exploring the binding of amine and sulfonamide ligands in Rhenium(I) Tricarbonyl and Platinum(II) complexes
Abstract
dc:description.abstractPlatinum is the metal present in various classes of inorganic medicinal agents directed at important diseases such as cancer or viral infections. Several new Pt(II) complexes of polyamine ligands bearing a dansyl moiety linked by a sulfonamide group were prepared; in some cases the sulfonamide nitrogen formed a bond to Pt. The sulfonamido group donates strongly to Pt and places the dansyl group close to a vacant coordination position, allowing it to stack with bound guanine base (G) when G binds. The emission of the fluorophore decreases with decreasing distance to Pt. Metal nuclide radiopharmaceuticals contain a metal core and an inner ligating unit, usually having chelate rings. The development of the advantageous fac-[<sup>99m</sup>Tc(CO)<sub>3</sub>(H<sub>2</sub>O)<sub>3</sub>]<sup>+</sup> precursor has opened new directions for radiolabeling. The non-radioactive fac-[Re(CO)<sub>3</sub>(H<sub>2</sub>O)<sub>3</sub>]<sup>+</sup> analogue is useful in understanding the chemistry of agents derived from the [<sup>99m</sup>Tc(CO)<sub>3</sub>(H<sub>2</sub>O)<sub>3</sub>]<sup>+</sup> species. To achieve a net neutral coordination unit in radiopharmaceuticals with a fac-M(CO)<sub>3</sub><sup>+</sup> core (M = Tc, Re), facially coordinated monoanionic tridentate ligands (L<sup>-</sup>) are needed. Several fac-[Re(CO)<sub>3</sub>L] complexes containing the sulfonamido group as one terminal ligating group were synthesized and characterized by X-ray crystallography and NMR spectroscopy. For most sulfonamido complexes studied here, the two chelate rings have different pucker chirality, as is commonly found for a broad range of metal complexes. The complexes are stable at neutral and basic pH values and thus have potential for providing a neutral label in radiopharmaceuticals. The NMR signal averaging indicates that the rotations about the N-S and S-C bonds of the sulfonamido group are rapid on the NMR time scale. Understanding the chemical features of the prototypical complexes by using the fac-[Re(CO)<sub>3</sub>L]-analogue approach and the minimal ligand was the goal of this part of this investigation. fac-[Re(CO)<sub>3</sub>L]<sup>+</sup> complexes containing prototypical NNN or NSN tridentate ligands, such as diethylenetriamine (dien) and simple dien derivatives, were investigated by X-ray crystallographic and NMR methods. fac-[Re(CO)<sub>3</sub>L]<sup>+</sup> complexes with two terminal exo-NH groups exhibit unusually upfield exo-NH NMR signals, which shift downfield on addition of Cl<sup>-</sup> indicating 1:1 ion pairs forms involving one Cl<sup>-</sup> to two exo-NH's H-bonds.
Degree
thesis:*- Name thesis:degree_name
- Doctor of Philosophy (PhD)
- Level thesis:degree_level
- Dissertation
- Discipline thesis:degree_discipline
- Chemistry
- Grantor
- Chemistry
- Year dc:date.available
- 2007
Author and committee
dc:creator, dc:contributor.*- Author dc:creator
-
- Christoforou, Anna Maria
Subjects
dc:subject × 3Rights
dc:rights- Statement dc:rights
-
- restricted
- Student has submitted appropriate documentation to restrict access to LSU for 365 days after which the document will be released for worldwide access.
Identifiers
dc:identifier.*- Identifier
-
etd-07112007-142442
https://repository.lsu.edu/gradschool_dissertations/1436 - OAI identifier oai:identifier
- oai:repository.lsu.edu:gradschool_dissertations-2435