New Cyclophanes as Supramolecular Scaffolds: The Synthesis of Tribenzo-1,4,7-Triazacyclononatriene.

<p>Supramolecular chemistry involves the formation of complex molecular entities that have the capacity to participate in specific molecular recognition of guest molecules. A commonly employed scaffold in supramolecular chemistry is the trimeric crown-shaped molecule cyclotriveratrylene (CTV). CTV has been studied extensively for its capability of binding a number of smaller organic and organometallic guests within its bowl-shaped cleft and has been used as a building block enabling the construction of more complex cryptophanes. The goal of this research is the synthesis and characterization of a novel cyclophane, tribenzo-1,4,7-triazacyclononene and derivatives thereof. These new cyclophanes should have greater versatility than the parent hydrocarbon macrocycle including greatly enhanced water solubility, ability to coordinate to metal ligands, the potential for use in drug delivery, and unique optical and liquid crystal properties. Progress towards these molecules have employed both Buchwald-Hartwig palladium catalyzed N-arylation as well as benzyne chemistry. The synthesis of tribenzo-1,4,7-triazacyclononatriene and its derivatives will be discussed.</p>

Name thesis:degree_name

Doctor of Philosophy (PhD)

Level thesis:degree_level

Dissertation

Discipline thesis:degree_discipline

Chemistry

Year dc:date.available

2010

Author dc:creator

• Panagopoulos, Andria M.

• Biochemistry

Repository record dc:identifier

https://ecommons.luc.edu/luc_diss/88

OAI identifier oai:identifier

oai:ecommons.luc.edu:luc_diss-1087