1998
DOI: 10.1016/s0022-0728(98)00041-2
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Constructing different `bridges' for interfacial electron transfer in azobenzene LB/SAM composite bilayers

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Cited by 15 publications
(9 citation statements)
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“…It has been previously reported that, in the case of both aromatic and heteroaromatic thiols, the electron-transfer reaction is facilitated by the presence of highly delocalized π-electrons in the aromatic ring and also by the extended conjugation of the molecules. This property of the aromatic SAM is extensively used for sensor and catalysis applications. The aromatic SAM can also be used as a molecular bridge to study the effects of different interaction forces and ionic and hydrogen bonding in the long-range electron-transfer reaction. The observed results were attributed to the tunneling process because of the presence of delocalized π-electrons in the aromatic ring, which acts as a bridge between the electrode surface and the redox probe. In our case, the facile nature of the electron-transfer reaction of the ruthenium complex at the SAM−solution interface suggests a tunneling process, where the naphthalene ring with the delocalized π-electrons acts as a bridge between the monolayer-modified electrode and the ruthenium complex.…”
Section: Resultsmentioning
confidence: 62%
See 1 more Smart Citation
“…It has been previously reported that, in the case of both aromatic and heteroaromatic thiols, the electron-transfer reaction is facilitated by the presence of highly delocalized π-electrons in the aromatic ring and also by the extended conjugation of the molecules. This property of the aromatic SAM is extensively used for sensor and catalysis applications. The aromatic SAM can also be used as a molecular bridge to study the effects of different interaction forces and ionic and hydrogen bonding in the long-range electron-transfer reaction. The observed results were attributed to the tunneling process because of the presence of delocalized π-electrons in the aromatic ring, which acts as a bridge between the electrode surface and the redox probe. In our case, the facile nature of the electron-transfer reaction of the ruthenium complex at the SAM−solution interface suggests a tunneling process, where the naphthalene ring with the delocalized π-electrons acts as a bridge between the monolayer-modified electrode and the ruthenium complex.…”
Section: Resultsmentioning
confidence: 62%
“…The observed results were attributed to the tunneling process because of the presence of delocalized π-electrons in the aromatic ring, which acts as a bridge between the electrode surface and the redox probe. [31][32][33] In our case, the facile nature of the electron-transfer reaction of the ruthenium complex at the SAM-solution interface suggests a tunneling process, where the naphthalene ring with the delocalized π-electrons acts as a bridge between the monolayer-modified electrode and the ruthenium complex.…”
Section: Effect Of Potential Cycling and Annealingmentioning
confidence: 65%
“…Homogeneous and well-dispersed CNTs in aqueous and nonaqueous media formed with the aid of polymers and surfactants were reported earlier [44][45][46][47][48]. Here we have used analogous method to disperse the SWNTs in pH 6.5 phosphate buffer solution.…”
Section: Preparation Of Swnt Functionalized Cyt C Electrodes: (Cyt C/mentioning
confidence: 89%
“…Recently Ashwell et al have studied the rectification behavior in hybrid Au/SAM/LB device [8]. Yu et al have studied the different bridges for interfacial electron transfer in azobenzene LB/SAM composite bilayers [9]. While cholesterol and its derivatives are known to form Langmuir monolayers at airwater interface [10][11][12][13] and LB films on substrates coated with hexamethyldisilazane [14], there are very few studies of these film using electrochemical and surface probe techniques [15].…”
Section: Introductionmentioning
confidence: 99%