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

Synthesis and surface characterization of alkylthioacetyl-capped self-assembled monolayers on gold surface

2006 ◽  
Vol 252 (14) ◽  
pp. 5158-5167 ◽  
Author(s):  
Abdiaziz A. Farah ◽  
Raluca Voicu ◽  
Raluca Barjovanu ◽  
Farid Bensebaa ◽  
Kidus Tufa ◽  
...  
Keyword(s):  
Surface Characterization ◽  
Gold Surface ◽  
Self Assembled Monolayers ◽  
Assembled Monolayers ◽  
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.

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.

scholarly journals Adsorption and desorption of self-assembled L-cysteine monolayers on nanoporous gold monitored by in situ resistometry

2019 ◽  
Vol 10 ◽  
pp. 2275-2279
Author(s):  
Elisabeth Hengge ◽  
Eva-Maria Steyskal ◽  
Rupert Bachler ◽  
Alexander Dennig ◽  
Bernd Nidetzky ◽  
...  
Keyword(s):  
Gold Surface ◽  
Research Field ◽  
Nanoporous Gold ◽  
Self Assembled Monolayers ◽  
Initial Surface ◽  
Resistance Change ◽  
Adsorption And Desorption ◽  
Assembled Monolayers ◽  
Self Assembled

Surface modifications of nanoporous metals have become a highly attractive research field as they exhibit great potential for various applications, especially in biotechnology. Using self-assembled monolayers is one of the most promising approaches to modify a gold surface. However, only few techniques are capable of characterizing the formation of these monolayers on porous substrates. Here, we present a method to in situ monitor the adsorption and desorption of self-assembled monolayers on nanoporous gold by resistometry, using cysteine as example. During the adsorption an overall relative change in resistance of 18% is detected, which occurs in three distinct stages. First, the cysteine molecules are adsorbed on the outer surface. In the second stage, they are adsorbed on the internal surfaces and in the last stage the reordering accompanied by additional adsorption takes place. The successful binding of cysteine on the Au surface was confirmed by cyclic voltammetry, which showed a significant decrease of the double-layer capacitance. Also, the electrochemically controlled desorption of cysteine was monitored by concomitant in situ resistometry. From the desorption peak related to the (111) surface of the structure, which is associated with a resistance change of 4.8%, an initial surface coverage of 0.48 monolayers of cysteine could be estimated.

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