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    <title>OAR@UM Collection:</title>
    <link>https://www.um.edu.mt/library/oar/handle/123456789/77289</link>
    <description />
    <pubDate>Mon, 13 Apr 2026 03:19:21 GMT</pubDate>
    <dc:date>2026-04-13T03:19:21Z</dc:date>
    <item>
      <title>Fluorescent molecular logic gates for pH and pE for cell imaging applications</title>
      <link>https://www.um.edu.mt/library/oar/handle/123456789/78449</link>
      <description>Title: Fluorescent molecular logic gates for pH and pE for cell imaging applications
Abstract: Novel molecules for sensing pH and redox potential (pE) were designed and synthesised starting from the asymmetrical 1,8-naphltalimide fluorophore. Attachment of a proton receptor and/or electron donor at either the N-imide or 4-position resulted in the molecular engineering of several positional isomers. Three novel pH-pE molecules of various modular designs were synthesised including 'fluorophore-spacer1-receptor-spacer2-electron-donor', 'electron -donor-spacer1-fluorophore-spacer2-receptor', and 'electron-donor1-spacer1-receptor1-spacer2-fluorophore-spacer2-receptor2-spacer4-electron-donor2' prototype. The receptor was either N-methylethylenediamine or piperazine, whilst the electron-donor was forrocene, both of which were connected via methylene or ethylene spacers. In addition, two model fluoroscent pH indicators were designed and studied, based on a 'fluorsphore-spacer-receptor' format, whilst a third fluorescent pH indicator was synthesised with a 'receptor1-spacer1-fluorophore-spacer2-receptor2' modular format.
Description: M.SC.CHEMISTRY</description>
      <pubDate>Sun, 01 Jan 2017 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">https://www.um.edu.mt/library/oar/handle/123456789/78449</guid>
      <dc:date>2017-01-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Crystal formation of purine salts to investigate seeding processes</title>
      <link>https://www.um.edu.mt/library/oar/handle/123456789/78113</link>
      <description>Title: Crystal formation of purine salts to investigate seeding processes
Abstract: Purines and punne salts are known to be the most widely distributed nitrogen containing compounds found in nature, and have a very important role in metabolism. &#xD;
Most purines form crystals when they precipitate out of solution, some of which deposit &#xD;
in various parts of the body, especially in the joints. The latter is responsible for the &#xD;
medical condition known as gout, which is characterised by inflammation. With this in &#xD;
mind, experiments were designed to explore whether the shape of these crystal that &#xD;
form in the body can be altered. &#xD;
In this study, aqueous solutions of purines and salts of purines were prepared. Crystals &#xD;
that precipitated out of these solutions under different conditions were isolated and &#xD;
observed under the polarised light-microscope. On the whole, theobromine formed &#xD;
small columnar prisms, while xanthine formed small and medium-sized crystals, which &#xD;
appear circular with a Maltese cross pattern at the centre. Caffeine was, by far, the &#xD;
easiest purine to crystallise, owing to its high solubility in an aqueous solution. In &#xD;
general, acicular or needle-like crystals of caffeine were formed, but at very low &#xD;
temperatures, plate-like caffeine crystals were obtained. &#xD;
Guanine and uric acid formed very few crystals owing to them being practically &#xD;
insoluble in water. Crystals of adenine were generally needle-like, comparable to those &#xD;
fonned by caffeine. Additionally, they formed bundles or clusters, with the needles &#xD;
pointing outwards from the clusters. Diversity of crystals involving theobromine &#xD;
increased when adding dicarboxylic acids in the solution. Long and slender plate-like &#xD;
crystals were observed. &#xD;
The introduction of sacchann m solution enabled the crystal morphologies to change &#xD;
drastically. Interesting dendritic crystals were formed from a saccharin-theobromine &#xD;
solution. Change in size and shape of theobromine was also observed on introducing &#xD;
alcohol in the aqueous environment. Caffeine crystals were overall unchanged on the &#xD;
introduction of dicarboxylic acids, saccharin or alcohols.
Description: M.SC.CHEMISTRY</description>
      <pubDate>Sun, 01 Jan 2017 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">https://www.um.edu.mt/library/oar/handle/123456789/78113</guid>
      <dc:date>2017-01-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Fluorescent molecular logic gates for the early detection of corrosion</title>
      <link>https://www.um.edu.mt/library/oar/handle/123456789/77941</link>
      <description>Title: Fluorescent molecular logic gates for the early detection of corrosion
Abstract: Four novel molecules for sensing pH and redox potential (pE) were designed and &#xD;
synthesised based on the asymmetrical 1,8-naphthalimide fluorophore. Attachment of the &#xD;
proton receptor and electron donor at either the N-imide or 4-position produced two pairs &#xD;
of positional isomers. Two of the molecules are designed based on an 'electron donor-spacen- fluorophore-spacer-recepton' modular format with dimethylamine or &#xD;
morpholine as the proton receptors and ferrocene as the electron donor. The two other &#xD;
molecules consist of the same chemical units, but adopt a 'recepton-spaceri-fluorophore &#xD;
-spacer-electron-donor' arrangement. The ferrocene and proton receptors are connected &#xD;
to the fluorophore via a methylene and ethylene spacers, respectively. Furthennore, a &#xD;
three-input logic gate for Na+, pH and pE was synthesised based on 'electron donor-spacen-fluorophore-spacer-recepton- space-recepton' design. A piperazine &#xD;
unit was employed as recepton for protons and a benzo-15-crown-5 as receptor2 for Na+ &#xD;
separated by a methylene group.
Description: M.SC.CHEMISTRY</description>
      <pubDate>Sun, 01 Jan 2017 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">https://www.um.edu.mt/library/oar/handle/123456789/77941</guid>
      <dc:date>2017-01-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>The interaction of lanthanides and lanthanide-carbene complexes with crown ethers</title>
      <link>https://www.um.edu.mt/library/oar/handle/123456789/77875</link>
      <description>Title: The interaction of lanthanides and lanthanide-carbene complexes with crown ethers
Abstract: The syntheses of novel organometallic compounds, using cyclic and semi-cyclic &#xD;
compounds, were investigated. These included the synthesis of an air-sensitive &#xD;
lanthanide complex, by using a carbene as the ligands. This was achieved by using &#xD;
lanthanum as the metal centre, and a bis(iminophosphorano )methanide as the ligand. &#xD;
The intermediates of this reaction were successfully observed, but the final product was &#xD;
not obtained successfully. &#xD;
The syntheses of several air-stable lanthanide complexes, with the use of different &#xD;
oxygen-based crown ethers, were also carried out. The lanthanides used included &#xD;
lanthanum, europium, gadolinium, and ytterbium. The crown ethers which were used &#xD;
included 18-crown-6, 21-crown-7, and 24-crown-8. &#xD;
The synthesis of lanthanide-crown ether complexes, as high-quality single &#xD;
crystals, was carried out by using standard crystallisation techniques, such as grinding &#xD;
and vapour diffusion, using water-ethanol and water-propanone as solvent pairs. &#xD;
Crystals of a sufficient quality were analysed by means of microscopy, infra-red &#xD;
spectroscopy, hot-stage microscopy, and single crystal X-ray diffraction. A total of 32 &#xD;
unique samples were prepared, and eight of these samples produced adequate crystals &#xD;
for analysis. &#xD;
Single crystal X-ray diffraction was used to collect diffraction data for eight &#xD;
samples, all of which have now been analysed. These samples are not new complexes, &#xD;
but are instead identical to certain lanthanide-crown ether complexes which were &#xD;
previously produced. However, one sample (GG2112) showed intrinsic modulation of &#xD;
the crystal structure at low temperatures, which is not visible at room temperature.
Description: M.SC.CHEMISTRY</description>
      <pubDate>Sun, 01 Jan 2017 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">https://www.um.edu.mt/library/oar/handle/123456789/77875</guid>
      <dc:date>2017-01-01T00:00:00Z</dc:date>
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