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Electrochemical Study Of 1,3-Indandione Derivatives Of Terthiophenes, Mieczyslaw Lapkowski, Sylwia Plewa, Pawel Wagner, David L. Officer
Electrochemical Study Of 1,3-Indandione Derivatives Of Terthiophenes, Mieczyslaw Lapkowski, Sylwia Plewa, Pawel Wagner, David L. Officer
Australian Institute for Innovative Materials - Papers
Properties and behavior of a group of four newly synthesized derivatives of terthiophene and terthienylenvinylene was studied. All four investigated monomers bear a 1,3-indandione substituent at the central thiophene ring and two of them (ThIV, ThIVM) have additional vinyl bonds introduced between the thiophene rings. In addition, ThIM and ThIVM have 5 positions of the two terminal rings blocked with methyl groups. The measurements were done using cyclic voltamperometry (CV) in solutions of 0.1M Bu4NBF4 in CH2Cl2. It was found that ThI and ThIV polymerise easily. CV of ThI reveals a reduction peak …
The Effect Of Oxidation On The Structure Of Styryl-Substituted Sexithiophenes: A Resonance Raman Spectroscopy And Density Functional Theory Study, Tracy Clarke, Keith Gordon, David L. Officer, Daina K. Grant
The Effect Of Oxidation On The Structure Of Styryl-Substituted Sexithiophenes: A Resonance Raman Spectroscopy And Density Functional Theory Study, Tracy Clarke, Keith Gordon, David L. Officer, Daina K. Grant
Australian Institute for Innovative Materials - Papers
The structures and vibrational properties of a series of styryl-substituted sexithiophenes and their charged species have been examined using resonance Raman spectroscopy in conjunction with density functional theory calculations. The calculated geometries of the radical cations and dications indicate that the quinoidal charged defects are more strongly localized in the center of the thiophene backbone than is observed in other sexithiophenes. This defect confinement, induced by the positions of the styryl substituents, is particularly evident in the dication species. However, the defect confinement weakens when alkoxy groups are added onto the phenyl rings by causing the extension of the charged …