Study of parameters affecting microcontact printing of thiols on gold-coated substrate

2019 ◽  
Vol 34 (01n03) ◽  
pp. 2040040
Author(s):  
Swapna A. Jaywant ◽  
Khalid Mahmood Arif
Keyword(s):  
Molecular Weight ◽  
Soft Lithography ◽  
Ph Value ◽  
Microcontact Printing ◽  
Gold Surface ◽  
Self Assembled Monolayers ◽  
Wide Range ◽  
Assembled Monolayers ◽  
Time Required ◽  
Compound Concentration

Microcontact printing ([Formula: see text]CP) is a type of soft-lithography technique, which is widely used for patterning self-assembled monolayers (SAMs). It is a convenient method to form SAMs of bio/chemical ink onto different surfaces such as polymers, palladium, silver and gold. A wide range of applications of this technology includes micromachining, patterning proteins, cells or DNA in biosensors. However, the application primarily depends on the type of the ink used. Here, we present an experimental study that provides information about the parameters that affect the [Formula: see text]CP process. Two different thiol inks (dithiothreitol (DTT) and glutathione (GSH)) have been used for obtaining SAMs on gold-coated substrates. Our findings suggest that transferring the alkanethiols over the gold surface is extremely dependent upon the molecular weight of thiol compound, concentration of the thiol solution and pH value of the buffer used. Furthermore, higher the molecular weight, concentration and pH value of the ink, lower is the time required for the process of [Formula: see text]CP.

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.

scholarly journals Molecular recognition of surface-immobilized carbohydrates by a synthetic lectin

2014 ◽  
Vol 10 ◽  
pp. 1354-1364 ◽  
Author(s):  
Melanie Rauschenberg ◽  
Eva-Corrina Fritz ◽  
Christian Schulz ◽  
Tobias Kaufmann ◽  
Bart Jan Ravoo
Keyword(s):  
Molecular Recognition ◽  
Self Assembled Monolayers ◽  
Carbohydrate Binding ◽  
Air Oxidation ◽  
Acetylneuraminic Acid ◽  
Physiological Processes ◽  
Wide Range ◽  
Assembled Monolayers ◽  
Synthetic Carbohydrate ◽  
Derivatives Of

The molecular recognition of carbohydrates and proteins mediates a wide range of physiological processes and the development of synthetic carbohydrate receptors (“synthetic lectins”) constitutes a key advance in biomedical technology. In this article we report a synthetic lectin that selectively binds to carbohydrates immobilized in a molecular monolayer. Inspired by our previous work, we prepared a fluorescently labeled synthetic lectin consisting of a cyclic dimer of the tripeptide Cys-His-Cys, which forms spontaneously by air oxidation of the monomer. Amine-tethered derivatives of N-acetylneuraminic acid (NANA), β-D-galactose, β-D-glucose and α-D-mannose were microcontact printed on epoxide-terminated self-assembled monolayers. Successive prints resulted in simple microarrays of two carbohydrates. The selectivity of the synthetic lectin was investigated by incubation on the immobilized carbohydrates. Selective binding of the synthetic lectin to immobilized NANA and β-D-galactose was observed by fluorescence microscopy. The selectivity and affinity of the synthetic lectin was screened in competition experiments. In addition, the carbohydrate binding of the synthetic lectin was compared with the carbohydrate binding of the lectins concanavalin A and peanut agglutinin. It was found that the printed carbohydrates retain their characteristic selectivity towards the synthetic and natural lectins and that the recognition of synthetic and natural lectins is strictly orthogonal.

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

Microcontact Printing of Lipophilic Self-Assembled Monolayers for the Attachment of Biomimetic Lipid Bilayers to Surfaces

1999 ◽  
Vol 121 (22) ◽  
pp. 5274-5280 ◽  
Author(s):  
A. Toby A. Jenkins ◽  
Neville Boden ◽  
Richard. J. Bushby ◽  
Stephen. D. Evans ◽  
Peter. F. Knowles ◽  
...  
Keyword(s):  
Lipid Bilayers ◽  
Microcontact Printing ◽  
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.

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.

Realizing high aspect ratio silver micro and nanostructures by microcontact printing of alkyl thiol self-assembled monolayers

MRS Advances ◽  
2019 ◽  
Vol 4 (44-45) ◽  
pp. 2441-2451
Author(s):  
Amare Benor ◽  
Asman Tamang ◽  
Veit Wagner ◽  
Alberto Salleo ◽  
Dietmar Knipp
Keyword(s):  
Aspect Ratio ◽  
Noble Metal ◽  
Microcontact Printing ◽  
Self Assembled Monolayers ◽  
Head Group ◽  
Material System ◽  
Printing Process ◽  
Aspect Ratios ◽  
Assembled Monolayers ◽  
Self Assembled

ABSTRACTThe patterning of gold and silver micro and nanostructures on rigid and flexible substrates is investigated by microcontact printed thiol based self-assembled monolayers. The aspect ratio of the noble metal micro and nanostructures is determined by interaction of the -SH head group of the CH3(CH2)19SH molecules and the surface of the noble metal. Silver micro and nanostructures with >10 times higher aspect ratios can be realized in comparison to commonly realized gold micro and nanostructures. The printing process is described, and the etching process is characterized in terms of etching window and etching selectivity. Potential electronic and photonic applications of the micro and nanostructures are discussed taking the boundary conditions of the printing process and the selected material system into consideration.

Patterning of Surface Chemistry and Topography for Biological Applications

1998 ◽  
Vol 4 (S2) ◽  
pp. 888-889
Author(s):  
H. G. Craighead ◽  
R. C. Davis ◽  
M. Foquet ◽  
M. Isaacson ◽  
C. James ◽  
...  
Keyword(s):  
Microcontact Printing ◽  
Biological Systems ◽  
Inorganic Materials ◽  
Self Assembled Monolayers ◽  
Chemical Patterning ◽  
Critical Function ◽  
Assembled Monolayers ◽  
Cell Surface Interactions ◽  
Mechanical Devices ◽  
Glass Surfaces

The technologies of nanofabrication as applied to inorganic materials and substrates are advanced and continue to develop. These sophisticated processes enable the formation of complex electronic, optical and mechanical devices with feature sizes down to tens of nanometers. Adaptation of these types of processes to surface chemical patterning and topographical patterning provides a new set of experimental tools for investigating biological systems and realizing sensors and devices that require the interaction of biological systems and fluids with inorganic materials and surfaces.In this talk we discuss methods of pattering self assembled monolayers, proteins and antibodies on silicon and glass surfaces by lithography and microcontact printing. This is of utility in a variety of experiments in cell-surface interactions and in sensor devices. In certain types of devices the manipulation of fluids and sieving of molecules is a critical function such as in DNA sequencing6 by electrophoretic separation.

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