<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-23T12:22:50Z</responseDate><request verb="GetRecord" identifier="oai:www.repository.cam.ac.uk:1810/242016" metadataPrefix="uketd_dc">https://api.repository.cam.ac.uk/server/oai/request</request><GetRecord><record><header><identifier>oai:www.repository.cam.ac.uk:1810/242016</identifier><datestamp>2024-06-27T12:54:06Z</datestamp><setSpec>com_1810_721</setSpec><setSpec>com_1810_256064</setSpec><setSpec>col_1810_218856</setSpec></header><metadata><uketd_dc:uketddc xmlns:uketd_dc="http://naca.central.cranfield.ac.uk/ethos-oai/2.0/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:uketdterms="http://naca.central.cranfield.ac.uk/ethos-oai/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://naca.central.cranfield.ac.uk/ethos-oai/2.0/ http://naca.central.cranfield.ac.uk/ethos-oai/2.0/uketd_dc.xsd">
   <dc:title>Self-assembly of synthetic and biological components in water using cucurbit[8]uril</dc:title>
   <dc:identifier xsi:type="dcterms:DOI">10.17863/CAM.16287</dc:identifier>
   <dc:creator>Zayed, Jameel Majed</dc:creator>
   <dcterms:abstract>This thesis discusses progress made towards assembling molecular building blocks in the presence of our molecular host of choice, cucurbit[8]uril (CB[8]). Our studies on the self-assembly of synthetic and biological components in water bridge overlapping concepts&#xd;
and techniques drawn from the fields of synthetic organic chemistry, supramolecular self-assembly, and applied NMR techniques.&#xd;
Chapter 1 introduces the reader to chemical complexity, and how supramolecular chemists&#xd;
have advanced in their capability of assembling more complex molecular architectures.&#xd;
The discussion focusses particularly on self-assembly carried out in the aqueous&#xd;
phase, and how, like in biology, molecular design of the building blocks become critical&#xd;
in enabling non-covalent assembly to occur in this dynamic, and relatively competitive&#xd;
environment. The cucurbit[n]uril family of molecular hosts are then introduced with an&#xd;
overview of their modes of binding, and affinities towards typical guests. Finally, a practical&#xd;
introduction to NMR methods gaining prominence in supramolecular chemistry is&#xd;
presented. In particular, the use of diffusion NMR, a key tool for probing the solution&#xd;
dynamics of molecular assemblies, is highlighted.&#xd;
Chapter 2 details work carried out on the CB[8]-mediated self-assembly of supramolecular&#xd;
block copolymers from polymeric, and small molecule building blocks. Here, end&#xd;
group-functionalised polymer guests were shown to assemble with small molecule ditopic&#xd;
guests in the presence of CB[8] to form block copolymers. Copolymers of various molecular&#xd;
weights were assembled, and the supramolecular complexes were studied using&#xd;
solution viscometry and diffusion NMR. This study represented the first use of diffusion&#xd;
NMR for probing the assembly of polymeric guests with CB[8].&#xd;
Chapter 3 describes the self-assembly of CB[8] with complementary ditopic guests. High&#xd;
molecular weight supramolecular polymers are known to form through the step-growth&#xd;
assembly of complementary ditopic building blocks. Here we sought to probe CB[8]’s&#xd;
ability to drive supramolecular polymerisation. Solution viscometry, ESI-MS, and diffusion&#xd;
NMR were used to investigate the self-assembly process, which indicated that cyclic&#xd;
oligomers had formed. The relatively low solubility of CB[8] in water was thought to be&#xd;
a major limitation to polymer formation in this instance.&#xd;
Important observations relating to the effect of salts on the solution viscosities and stabilities&#xd;
of the complexes, are also discussed.&#xd;
Chapter 4 places emphasis on the synthetic methods employed towards preparing multivalent&#xd;
guests for CB[8] binding studies. Our synthetic guests were based on watersoluble&#xd;
oligomers of ethylene glycol. A bidirectional elongation route is presented for&#xd;
accessing higher molecular weight, and monodisperse ethylene glycol oligomers (n = 12)&#xd;
in suitable purity.&#xd;
Chapter 5 describes the assembly of protein-polymer conjugates, and the versatility of&#xd;
diffusion NMR as a means to probe the assembly process. Here, end group-functionalised&#xd;
poly(ethylene glycol) guests were appended to bovine serum albumin (BSA) through a&#xd;
mixed chemical ligation-self assembly protocol. The NMR studies conducted are emphasised&#xd;
here, which served to complement other characterisation methods used that&#xd;
are reported elsewhere.&#xd;
Chapter 6 discusses ongoing work on lipid-based guests, and the resulting liposome assemblies&#xd;
formed. Head group-functionalised phospholipid guests, and cholesterol-based&#xd;
guests were synthesised. Phospholipid guests were obtained through an enzymatic route,&#xd;
a novelty in our group. Dye-encapsulated liposomes were then assembled, purified, and&#xd;
characterised by fluorescence microscopy. Finally, we sought to optimise lipid formulations&#xd;
to enhance liposome stability, towards conducting molecular recognition studies in&#xd;
the presence of CB[8].&#xd;
Chapter 7 then closes the thesis with concluding remarks that summarise the described&#xd;
research, while highlighting points of note.</dcterms:abstract>
   <uketdterms:institution>University of Cambridge</uketdterms:institution>
   <dcterms:issued>2012-02-07</dcterms:issued>
   <dc:type>Thesis</dc:type>
   <uketdterms:qualificationlevel>Doctoral</uketdterms:qualificationlevel>
   <uketdterms:qualificationname>Doctor of Philosophy (PhD)</uketdterms:qualificationname>
   <dc:language>en</dc:language>
   <dcterms:isReferencedBy xsi:type="dcterms:URI">http://www.dspace.cam.ac.uk/handle/1810/242016</dcterms:isReferencedBy>
   <dcterms:isReferencedBy xsi:type="dcterms:URI">https://www.repository.cam.ac.uk/handle/1810/242016</dcterms:isReferencedBy>
   <dc:identifier xsi:type="dcterms:URI">https://apollo8-f-pro.lib.cam.ac.uk/bitstreams/6b138a12-76ff-47f1-92b5-2b6a61cb042b/download</dc:identifier>
   <uketdterms:checksum xsi:type="uketdterms:MD5">f1ba17da60535740a5ee4d22cc9b042d</uketdterms:checksum>
   <dcterms:license>https://apollo8-f-pro.lib.cam.ac.uk/bitstreams/2f099a7f-88d9-419c-a67e-54a78531c05e/download</dcterms:license>
   <uketdterms:checksum xsi:type="uketdterms:MD5">48dcdf38f646da27e5e4bc6c1893d4fc</uketdterms:checksum>
   <dc:rights>http://creativecommons.org/licenses/by-nc-nd/2.0/uk/</dc:rights>
   <dc:subject>Supramolecular</dc:subject>
   <dc:subject>Diffusion/DOSY NMR</dc:subject>
   <dc:subject>Host-guest</dc:subject>
   <dc:subject>Chemistry</dc:subject>
   <dc:subject>Water</dc:subject>
   <dc:subject>Organic</dc:subject>
   <dc:subject>Self-assembly</dc:subject>
   <dc:subject>Complexity</dc:subject>
</uketd_dc:uketddc>
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