<?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>2026-09-23T19:27:56Z</responseDate><request verb="GetRecord" identifier="oai:mro.massey.ac.nz:10179/1854" metadataPrefix="dim">https://mro.massey.ac.nz/server/oai/request</request><GetRecord><record><header><identifier>oai:mro.massey.ac.nz:10179/1854</identifier><datestamp>2025-11-11T14:02:05Z</datestamp><setSpec>com_10179_294</setSpec><setSpec>col_10179_296</setSpec></header><metadata><dim:dim xmlns:dim="http://www.dspace.org/xmlns/dspace/dim" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.dspace.org/xmlns/dspace/dim http://www.dspace.org/schema/dim.xsd">
   <dim:field mdschema="dc" element="contributor" qualifier="author">Stephenson, Adam Wayne Ian</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2010-11-15T20:30:39Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available" lang="en_US">NO_RESTRICTION</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2010-11-15T20:30:39Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued">2010</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">http://hdl.handle.net/10179/1854</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="wikidata">Q112884598</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="wikidata-uri">https://www.wikidata.org/wiki/Q112884598</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">Porphyrins are useful chromophores and have been used in numerous biological&#xd;
applications including light harvesting, oxygen transport and energy transfer. DNA is a&#xd;
perfect template for the controlled assembly of organic chromophores. By combining&#xd;
DNA and porphyrins in a controlled manner we have developed a novel range of&#xd;
porphyrin-DNA supramolecular constructs for future applications in&#xd;
nanobiotechnology.&#xd;
A number of β-pyrrolic functionalised porphyrin precursors were synthesised to be used&#xd;
as building blocks in the construction of both covalently and non-covalently modified&#xd;
DNAs. Using these porphyrins we have created several lipophilic porphyrin-DNA&#xd;
complexes through non-covalent attachment methods. Using a CuI catalysed azide&#xd;
alkyne cycloaddition (CuAAC) reaction of azido functionalised porphyrins we have&#xd;
developed a versatile approach for the covalent, site specific internal porphyrin insertion&#xd;
into oligonucleotides in a post-synthetic manner. We have investigated a number of&#xd;
duplex structures where porphyrins were located in the major or minor grooves of the&#xd;
duplex. Additionally, porphyrins were studied as intercalating moieties when they were&#xd;
inserted as a bulge in the middle of the duplexes or parallel triplexes. Additionally,&#xd;
when porphyrins were placed in both strands of the duplex they formed a zipper type&#xd;
structure in the minor groove. This resulted in a significant increase in the duplex&#xd;
thermal stability due to the formation of porphyrin H-aggregates. UV-Vis and CD&#xd;
spectroscopy as well as molecular modelling were used to help understand the&#xd;
interactions between porphyrins in the duplex.&#xd;
These findings lay the foundation for the future design of artificial DNA-chromophore&#xd;
supramolecular architectures and for their applications in material science and&#xd;
nanotechnology.</dim:field>
   <dim:field mdschema="dc" element="language" qualifier="iso" lang="en_US">en</dim:field>
   <dim:field mdschema="dc" element="publisher" lang="en_US">Massey University</dim:field>
   <dim:field mdschema="dc" element="rights" lang="en_US">The Author</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">Chromophores</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">Nanobiotechnology</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">DNA modification</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">Porphyrin interactions</dim:field>
   <dim:field mdschema="dc" element="subject" qualifier="other" lang="en_US">Fields of Research::250000 Chemical Sciences::259900 Other Chemical Sciences::259904 Supramolecular chemistry</dim:field>
   <dim:field mdschema="dc" element="title" lang="en_US">Supramolecular helical arrangement of porphyrins along DNA : a thesis submitted in the partial fulfilment of the requirements for the degree of Doctor of Philosophy in Chemistry, Massey University, Palmerston North, New Zealand</dim:field>
   <dim:field mdschema="dc" element="type" lang="en_US">Thesis</dim:field>
   <dim:field mdschema="thesis" element="degree" qualifier="discipline" lang="en_US">Chemistry</dim:field>
   <dim:field mdschema="thesis" element="degree" qualifier="grantor" lang="en_US">Massey University</dim:field>
   <dim:field mdschema="thesis" element="degree" qualifier="level" lang="en_US">Doctoral</dim:field>
   <dim:field mdschema="thesis" element="degree" qualifier="level" lang="en">Doctoral</dim:field>
   <dim:field mdschema="thesis" element="degree" qualifier="name" lang="en_US">Doctor of Philosophy (Ph.D.)</dim:field>
   <dim:field mdschema="massey" element="contributor" qualifier="author">Stephenson, Adam Wayne Ian</dim:field>
   <dim:field mdschema="others" element="access-status">open.access</dim:field>
</dim:dim>
</metadata></record></GetRecord></OAI-PMH>