Show simple item record

Synthesis and Application of Double Cavity Cucurbit[n]urils

dc.contributor.advisorIsaacs, Lyleen_US
dc.contributor.authorWittenberg, Jamesen_US
dc.date.accessioned2013-07-06T05:30:38Z
dc.date.available2013-07-06T05:30:38Z
dc.date.issued2012en_US
dc.identifier.urihttp://hdl.handle.net/1903/14339
dc.description.abstractMolecular containers are a unique set of compounds that are able to recognize and associate with other molecules. It is these molecular recognition properties that has resulted in a large number of research groups studying such phenomena. The cucurbit[n]uril (CB[n]) family of macrocyclic hosts are well known for their high binding affinities and selectivity towards guests, particularly ammonium compounds, in water. Synthesizing new types of CB[n] hosts will lead to new and exciting applications for these exceptional molecular receptors. Chapter 1 introduces the concept and importance of noncovalent interactions. A review of cucurbit[n]uril chemistry, including the nor-seco-cucurbit[n]urils and glycoluril hexamer, is covered. The potential applications of the double cavity host, bis-nor-seco-cucurbit[10]uril (bis-ns-CB[10]), and of the mono-functionalized CB[6] derivatives recently synthesized are discussed. The wide range of applications incorporating CB[8] as a host for ternary complexes is also reviewed. Chapter 2 describes the synthesis of a new double cavity host (II-1) derived from bis-ns-CB[10]. Host II-1 is synthesized by the double bridging reaction of bis-ns-CB[10] with II-2 under acidic conditions. Host II-1 binds a variety of aliphatic and aromatic ammonium ions (II-3-II-17) in water as the corresponding ternary complexes. Conducting the bridging reaction in the presence of guest II-4 delivers [3]rotaxane II-1*II-42 by a clipping process, the first published rotaxane of a cucurbituril prepared via a clipping mechanism. Chapter 3 describes the synthesis and potential application of two new double cavity hosts (III-1 and III-2) synthesized through condensation of two equivalents of glycoluril hexamer (III-3) with one equivalent of tetra-aldehydes III-4 and III-5, respectively. Host III-1 has been shown to bind four different PEG derivatives (III-16300, III-161000, III-163350, III-1610000) in D2O, and the degree of polymerization was measured by diffusion ordered spectroscopy (DOSY). The highly symmetrical and rigid host III-2 binds to synthesized guests III-20 - III-23 to form discrete complexes and supramolecular ladders.en_US
dc.titleSynthesis and Application of Double Cavity Cucurbit[n]urilsen_US
dc.typeDissertationen_US
dc.contributor.publisherDigital Repository at the University of Marylanden_US
dc.contributor.publisherUniversity of Maryland (College Park, Md.)en_US
dc.contributor.departmentChemistryen_US
dc.subject.pqcontrolledChemistryen_US
dc.subject.pquncontrolledcucurbiturilen_US
dc.subject.pquncontrolledsupramolecularen_US


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record