Cranfield, Jason (2009) Ladder-structured conjugated oligomers. (MSc(R) thesis), Kingston University.Full text not available from this archive.
This project's aim was to synthesis and investigate the properties of series of even-numbered polyazacenes in comparison with an analogous odd numbered series. Three compounds were initially planned to be synthesized, pyrazino [2,3-b] phenazine (L4), 4, 13-dihydro-2,4,6,9, 11, 13-pentaazahexacene (L6H2) and 3,14- dihydro1 ,3,5,7,12,14,16, 18heptaazaoctacene (L8H2) but only L4 was successfully prepared. Standard spectroscopic techniques such as FTIR, NMR and UV-Visible spectroscopy and thermogravimetric analysis have been used to characterize this compound, and to use in its comparison against the previously documented analogous series. The oligomers L4 and quinoxalino [2,3-b] phenazine (L5H2) were vacuum coated onto ITO coated glass slides and analyzed by cyclic voltammetry. Solubility problems led to the need for solution cyclic voltammetry to be used. L4 was compared against phenazine (L5H2) 7,16-Dihydro-5,7,9,14,16,18- hexaazaheptacene (L7H2) and.7,20-Dihydro5,7,9, 11,16,9,18,20,22- octaazanonacene (L9H2). Evidence has been found that L4 does not follow a trend in behavious. defined by "odd-numbered" oligomers of the same general structure.
|Item Type:||Thesis (MSc(R))|
|Physical Location:||This item is held in stock at Kingston University Library.|
|Faculty, School or Research Centre:||Faculty of Science (until 2011) > School of Pharmacy and Chemistry|
|Depositing User:||Katrina Clifford|
|Date Deposited:||23 Feb 2012 14:33|
|Last Modified:||21 Aug 2013 08:21|
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