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Alkylthiol SAMs

An alternative photo-SIP approach was described by Kang and coworkers, where they used an argon plasma to oxidize alkylthiolate SAMs on planar gold [55]. The plasma treatment oxidized carboxy-terminated SAMs to peroxide moieties. UV irradiation in the presence of acryhc acid and allylpentafluorobenzene yielded ultra-thin graft layers of 6-7nm. The poly(acrylic acid) layers were found to adsorb Fe " ions from solution. This particular photoinitiation method yields low-density polymer brush films. [Pg.61]

Protein-resistant surfaces based on alkylthiol SAMs... [Pg.12]

Self-assembly of one- or two-component alkylthiol SAMs provides a convenient tool for tailoring, at a molecular level, the chemical reactivity of a gold surface by choosing and modulating the nature and amount of surface-bound chemically reactive groups (e.g., -OH, -COOH, or -NH2) in the monolayer. Particularly, mixed alkylthiol SAMs prepared by coadsorption of alkylthiols... [Pg.14]

Scheme 4. Idealized sketches of gold surfaces for DNA hybridization sensors prepared by (a) chemisorption of thiolated ssDNA capture probes followed by chemisorption of a dilutor alkylthiol [168] and by (b) chemisorption of a mixed alkylthiol SAM followed by covalent attachment of an amino-terminated ssDNA capture probe (surface-bound carboxylic groups are activated by reaction with 0-(N-auccimrmdyl)-N,N,N, N -tetramethyluronium tetrafluoroborate in acetonitrile in the presence of N, A-diisopropylethylamine, [172]). Scheme 4. Idealized sketches of gold surfaces for DNA hybridization sensors prepared by (a) chemisorption of thiolated ssDNA capture probes followed by chemisorption of a dilutor alkylthiol [168] and by (b) chemisorption of a mixed alkylthiol SAM followed by covalent attachment of an amino-terminated ssDNA capture probe (surface-bound carboxylic groups are activated by reaction with 0-(N-auccimrmdyl)-N,N,N, N -tetramethyluronium tetrafluoroborate in acetonitrile in the presence of N, A-diisopropylethylamine, [172]).
Multipoint attachment of proteins to gold electrode surfaces modified with an alkylthiol SAM... [Pg.33]

Multipoint covalent attachment of proteins to electrode surfaces modified with a functionalized alkylthiol SAM gives rise to protein films in which... [Pg.40]

LDH-modified electrodes, prepared by affinity binding to CB-anchored alkylthiol SAMs, electrocatalyse the oxidation of L-lactate only in the presence of exogenous NAD and a soluble redox mediator in the reaction mixture. [Pg.44]

Scheme 11. Idealized sketch showing the electroen matic oxidation of L-lactate at gold modified electrode surfaces, (a) Lactate dehydrogenase bound to CB-terminated alkylthiol SAMs prepared by covalent attachment of CB to 3-mercaptopropionic acid SAM derivatized with 1,4-diaminobutane. The electroenzymatic oxidation of lactate is observed only in the presence of soluble coenzyme (NAD" ") and a redox mediator (phenazine methosulfate) [215]. (b) Lactate deh3tdrogenase bound to NAD-terminated alkylthiol SAMs prepared by covalent attachment of Af -(2-aminoethyl)-NAD to a cystamine SAM derivatized with pjrrroloquinoline quinone. The reconstituted enzyme is electrically wired to the electrode surface via two NAD" -binding pockets involved in the affinity-binding surface reaction [242]. Scheme 11. Idealized sketch showing the electroen matic oxidation of L-lactate at gold modified electrode surfaces, (a) Lactate dehydrogenase bound to CB-terminated alkylthiol SAMs prepared by covalent attachment of CB to 3-mercaptopropionic acid SAM derivatized with 1,4-diaminobutane. The electroenzymatic oxidation of lactate is observed only in the presence of soluble coenzyme (NAD" ") and a redox mediator (phenazine methosulfate) [215]. (b) Lactate deh3tdrogenase bound to NAD-terminated alkylthiol SAMs prepared by covalent attachment of Af -(2-aminoethyl)-NAD to a cystamine SAM derivatized with pjrrroloquinoline quinone. The reconstituted enzyme is electrically wired to the electrode surface via two NAD" -binding pockets involved in the affinity-binding surface reaction [242].

See other pages where Alkylthiol SAMs is mentioned: [Pg.49]    [Pg.211]    [Pg.12]    [Pg.13]    [Pg.14]    [Pg.15]    [Pg.16]    [Pg.17]    [Pg.18]    [Pg.18]    [Pg.22]    [Pg.23]    [Pg.23]    [Pg.24]    [Pg.25]    [Pg.26]    [Pg.27]    [Pg.27]    [Pg.30]    [Pg.30]    [Pg.33]    [Pg.33]    [Pg.39]    [Pg.39]    [Pg.40]    [Pg.42]    [Pg.42]    [Pg.44]    [Pg.44]    [Pg.47]    [Pg.48]    [Pg.48]    [Pg.50]    [Pg.50]    [Pg.50]    [Pg.52]    [Pg.53]    [Pg.53]    [Pg.54]    [Pg.55]    [Pg.55]   
See also in sourсe #XX -- [ Pg.11 , Pg.449 ]




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Carboxylic-terminated alkylthiols SAMs

Mixed alkylthiol SAM

SAMs

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