Abstract
dc:description.abstractChapter 1 of this Dissertation presents a brief overview of the history of tetrapyrrole derivatives and of their fundamental properties. Overviews of porphyrins, benzoporphyrins, chlorins and porphycenes are presented. Work presented in Chapter 2 through Chapter 4 mainly focuses on the syntheses and functionalization of chromophore-extended porphyrin derivatives. Several new synthetic routes for the syntheses and functionalizations of extended porphyrins either at the β-position or at the meso-position of porphyrin are developed. From these improved synthetic routes, the regio-selective syntheses of porphyrin derivatives are described. Chapter 2 mainly focuses on the syntheses of β,β'-fused methylenepropanoporphyrins and related porphyrin dimers. Chapter 3 mainly describes a new synthetic route for selective synthesis of benzoporphyrin regioisomers and Chapter 4 mainly discusses new work on the efficient synthesis of the so-called "Hangman Porphyrin" analogs. Chapter 5 consists two parts. The first part is devoted results of work on the total synthesis of an important porphycene derivative, 9-capronyl-oxytetrakis(methyoxyethyl)-porphycene, which has already been shown to have attractive potential applications in photodynamic therapy of tumors. The second part of Chapter 5 concerns the improved syntheses of 2,2'-bipyrrole, which is an important part of our effort to improve the synthesis of porphycene and related tetrapyrrole derivatives. The potential utility of these 2,2'-bipyrroles as bio-probes and ion-binding reagents are also tested. Chapter 6 reports mechanistic studies on the unique regio-selective formation of mono-(L)-aspartylchlorin-e<sub>6</sub>. This important photodynamic therapy (PDT) photosensitizer has recently undergone a structural revision, and the work reported in this Chapter provides a rationale for the formation of the unexpected regioisomeric structure now known to belong to mono-(L)-aspartylchlorin-e<sub>6</sub>.
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
-
- Jiao, Lijuan
Subjects
dc:subject × 5Rights
dc:rights- Statement dc:rights
-
- unrestricted
- Release the entire work immediately for access worldwide.
Identifiers
dc:identifier.*- Identifier
-
etd-10232007-121548
https://repository.lsu.edu/gradschool_dissertations/1309 - OAI identifier oai:identifier
- oai:repository.lsu.edu:gradschool_dissertations-2308