Electron Transfer Behavior through Densely Packed Self-Assembled Monolayers of a Novel Heteroaromatic Thiol Derivative onto the Gold Surface

2008 ◽  
Vol 20 (5) ◽  
pp. 513-519 ◽  
Author(s):  
Mojtaba Shamsipur ◽  
Sayed Habib Kazemi ◽  
Ali Mehdinia ◽  
Mir Fazlollah Mousavi ◽  
Hashem Sharghi
Keyword(s):  
Electron Transfer ◽  
Gold Surface ◽  
Self Assembled Monolayers ◽  
Assembled Monolayers ◽  
Transfer Behavior ◽  
Self Assembled

scholarly journals Electron-Transfer Properties of Phenyleneethynylene Linkers Bound to Gold via a Self-Assembled Monolayer of Molecular Tripod

Molecules ◽  
2018 ◽  
Vol 23 (11) ◽  
pp. 2893 ◽  
Author(s):  
Toshikazu Kitagawa ◽  
Takashi Kawano ◽  
Takahiro Hase ◽  
Ikuma Hayakawa ◽  
Katsuyuki Hirai ◽  
...  
Keyword(s):  
Electron Transfer ◽  
High Surface ◽  
Gold Surface ◽  
Solid Surfaces ◽  
Self Assembled Monolayers ◽  
Self Assembled Monolayer ◽  
Assembled Monolayers ◽  
Self Assembled ◽  
Electron Transfer Properties ◽  
Transfer Properties

The three-point adsorption of tripod-shaped molecules enables the formation of robust self-assembled monolayers (SAMs) on solid surfaces, where the component molecules are fixed in a strictly upright orientation. In the present study, SAMs of a rigid molecular tripod consisting of an adamantane core and three CH2SH groups were employed to arrange ferrocene on a gold surface through oligo(p-phenyleneethynylene) linkers. Cyclic voltammetry of the monolayers demonstrated high surface coverage of ferrocene, yet the molecular interaction among adjacent ferrocene units was negligible. This was because of the extended intermolecular distance caused by the bulky tripod framework. The rates of electron transfer from the ferrocene to the gold surface through different linker lengths were determined by electrochemical measurements, from which the decay factor for oligo(p-phenyleneethynylene) wire was evaluated.

Electron transfer behavior at polyoxometalate-adsorbed alkanethiol self-assembled monolayers

2011 ◽  
Vol 257 (22) ◽  
pp. 9490-9497 ◽  
Author(s):  
Yeonyi Chu ◽  
Jandee Kim ◽  
Suhee Choi ◽  
Choong Kyun Rhee ◽  
Jongwon Kim
Keyword(s):  
Electron Transfer ◽  
Self Assembled Monolayers ◽  
Assembled Monolayers ◽  
Transfer Behavior ◽  
Self Assembled

Self-Assembled Monolayers of Heme Derivatives on a Gold Surface

2000 ◽  
Vol 73 (9) ◽  
pp. 1993-2000 ◽  
Author(s):  
Kazutoshi Kobayashi ◽  
Shin'ichiro Imabayashi ◽  
Katsuhiko Fujita ◽  
Kazuhide Nonaka ◽  
Takashi Kakiuchi ◽  
...  
Keyword(s):  
Gold Surface ◽  
Self Assembled Monolayers ◽  
Assembled Monolayers ◽  
Self Assembled

Spectral and cyclic voltammetric characterization of self-assembled monolayers on gold of pyrene end-labeled oligonucleotide duplexes

1999 ◽  
Vol 77 (5-6) ◽  
pp. 1077-1084 ◽  
Author(s):  
R Scott Reese ◽  
Marye Anne Fox
Keyword(s):  
Gold Surface ◽  
Self Assembled Monolayers ◽  
Self Assembled Monolayer ◽  
Surface Emission ◽  
Assembled Monolayers ◽  
Oligonucleotide Duplex ◽  
Self Assembled ◽  
Duplex Formation

Self-assembled monolayers of sulfur-terminated oligonucleotide duplexes were formed on flat gold surfaces, either by exposure of a self-assembled monolayer bearing one oligonucleotide strand to the complementary strand or by preformation of a oligonucleotide duplex that was then deposited on a fresh gold surface. Virtually identical spectral behavior was observed whether the duplex was produced before deposition or by in situ complementary association. With a duplex bearing an appropriate pyrene end-label, the resulting thin film was photoresponsive. Surface emission measurements show no evidence for pyrene aggregation on the modified surfaces. The polarity of the photocurrent, reflecting photoinduced electron transfer initiated by photoexcitation of pyrene, is opposite that expected from the oligonucleotide-mediated reduction of the appended pyrene excited state.Key words: oligonucleotide, self-assembled monolayer, duplex formation, photoelectrochemistry, surface emission.

scholarly journals Density Functional Theory with Modified Dispersion Correction for Metals Applied to Self-Assembled Monolayers of Thiols on Au(111)

2013 ◽  
Vol 2013 ◽  
pp. 1-9 ◽  
Author(s):  
M. P. Andersson
Keyword(s):  
Density Functional Theory ◽  
Density Functional ◽  
Dimethyl Disulfide ◽  
Gold Surface ◽  
Self Assembled Monolayers ◽  
Dispersion Correction ◽  
Dissociative Chemisorption ◽  
Functional Theory ◽  
Assembled Monolayers ◽  
Self Assembled

Using sound physical principles we modify the DFT-D2 atom pairwise semiempirical dispersion correction to density functional theory to work for metallic systems and in particular self-assembled monolayers of thiols on gold surfaces. We test our approximation for two functionals PBE-D and revPBE-D for lattice parameters and cohesive energies for Ni, Pd, Pt, Cu, Ag, and Au, adsorption energies of CO on (111) surfaces of Pd, Pt, Cu, Ag, and Au, and adsorption energy of benzene on Ag(111) and Au(111). Agreement with experimental data is substantially improved. We apply the method to self-assembled monolayers of alkanethiols on Au(111) and find reasonable agreement for PBE-D and revPBE-D for both physisorption of n-alkanethiols as well as dissociative chemisorption of dimethyl disulfide as an Au-adatom-dithiolate complex. By modifying the C6 coefficient for Au, we obtain quantitative agreement for physisorption and chemisorption for both PBE-D and revPBE-D using the same set of parameters. Our results confirm that inclusion of dispersion forces is crucial for any quantitative analysis of the thiol and thiolate bonds to the gold surface using quantum chemical calculations.

Self-Assembled Monolayers of Hexapeptides on Gold:  Surface Characterization and Orientation Distribution Analysis†

2004 ◽  
Vol 108 (45) ◽  
pp. 9673-9681 ◽  
Author(s):  
Xingu Wen ◽  
Richard W. Linton ◽  
Fernando Formaggio ◽  
Claudio Toniolo ◽  
Edward T. Samulski
Keyword(s):  
Surface Characterization ◽  
Gold Surface ◽  
Orientation Distribution ◽  
Self Assembled Monolayers ◽  
Distribution Analysis ◽  
Assembled Monolayers ◽  
Self Assembled

Evaluation of the Tunneling Constant for Long Range Electron Transfer in Azobenzene Self-Assembled Monolayers on Gold

Langmuir ◽  
1997 ◽  
Vol 13 (21) ◽  
pp. 5774-5778 ◽  
Author(s):  
H. Z. Yu ◽  
H. B. Shao ◽  
Y. Luo ◽  
H. L. Zhang ◽  
Z. F. Liu
Keyword(s):  
Electron Transfer ◽  
Long Range ◽  
Self Assembled Monolayers ◽  
Assembled Monolayers ◽  
Self Assembled

Specific Immobilization of Streptavidin on Mixed Self-Assembled Monolayers as Mixing Ratio

2007 ◽  
Vol 121-123 ◽  
pp. 495-498 ◽  
Author(s):  
Jun Hyung Park ◽  
Buyng Su Park ◽  
Gu Huh ◽  
Seung Hyun Lee ◽  
Hyun Sook Lee ◽  
...  
Keyword(s):  
Colorimetric Detection ◽  
Gold Surface ◽  
Self Assembled Monolayers ◽  
Scanning Tunneling ◽  
Local Domain ◽  
Mixing Ratio ◽  
Tunneling Microscopy ◽  
Self Assembled Monolayer ◽  
Assembled Monolayers ◽  
Self Assembled

We report on the distribution of mixed self-assembled monolayers (SAMs) composed of biotinylated and diluent alkylthiolates for streptavidin immobilization. Two thiol derivatives, 11-mercapto-1-undecanol (MUOH) and 11-mercaptoundecanoic-(8-biotinylamido-3,6-dioxaoctyl) amide (MBDA), were employed for mixed SAM. These thiols formed self-assembled monolayer without local domain, and streptavidins were immobilized onto biotinylated gold surface without nonspecific binding. In order to find the optimized condition of immobilization of streptavidin, we controlled the mixing ratio of two kind thiols by colorimetric detection assay, and the immobilization was characterized by atomic force microscopy (AFM), scanning tunneling microscopy (STM), and ellipsometer.

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