Abstract:A two-step chlorination/azidation process was reported to prepare azide-modified silicon(111) surfaces. XPS and IR analyses show the covalent bonding of azide with silicon. In combination with scanning tunneling microscopy and spectroscopy analyses, different kinetic rates, azide coverages, and surface-area distributions were derived depending on the azidation solvent.
“…It is approximately consistent with azide-terminated monolayers on planar Au [22,23] and Si [3,27] surfaces, and also on nanoparticles [50][51][52][53], as well as with azide-carried polymers [54,55]. These azide groups behave normally as organic groups, different from the direct bonding of AN 3 to silicon metal (SiAN 3 ), which was reported at 2168 cm À1 (v a (AN@N + @N À )), due to the proximity effect of silicon metals [8]. In our case, azides were attached on polymer brushes; therefore the density of azides is enhanced greatly, compared to monolayer azides [3,4,[7][8][9][22][23][24]26,48].…”
Section: Conversion Of Terminal Hydroxyls Of Si-g-p(pegmaaoh) To Chlosupporting
confidence: 77%
“…As a reactive intermediate, surface terminal chlorines can be easily substituted with azide groups [3,8,26,27,47,48].…”
Section: Conversion Of Terminal Hydroxyls Of Si-g-p(pegmaaoh) To Chlomentioning
confidence: 99%
“…Especially click chemistry is widely recognized in biomedical applications recently for its reaction in aqueous media and under room temperature. Either acetylene or azide moieties can be conveniently introduced onto solid surfaces [2][3][4][5][6][7][8][9][10][11][12][13][14] or combined with functional or biological molecules [4,6,[15][16][17][18][19][20][21]. Furthermore through click chemistry, a variety of probe molecules can be anchored onto solid surfaces for sensors and biochips.…”
“…It is approximately consistent with azide-terminated monolayers on planar Au [22,23] and Si [3,27] surfaces, and also on nanoparticles [50][51][52][53], as well as with azide-carried polymers [54,55]. These azide groups behave normally as organic groups, different from the direct bonding of AN 3 to silicon metal (SiAN 3 ), which was reported at 2168 cm À1 (v a (AN@N + @N À )), due to the proximity effect of silicon metals [8]. In our case, azides were attached on polymer brushes; therefore the density of azides is enhanced greatly, compared to monolayer azides [3,4,[7][8][9][22][23][24]26,48].…”
Section: Conversion Of Terminal Hydroxyls Of Si-g-p(pegmaaoh) To Chlosupporting
confidence: 77%
“…As a reactive intermediate, surface terminal chlorines can be easily substituted with azide groups [3,8,26,27,47,48].…”
Section: Conversion Of Terminal Hydroxyls Of Si-g-p(pegmaaoh) To Chlomentioning
confidence: 99%
“…Especially click chemistry is widely recognized in biomedical applications recently for its reaction in aqueous media and under room temperature. Either acetylene or azide moieties can be conveniently introduced onto solid surfaces [2][3][4][5][6][7][8][9][10][11][12][13][14] or combined with functional or biological molecules [4,6,[15][16][17][18][19][20][21]. Furthermore through click chemistry, a variety of probe molecules can be anchored onto solid surfaces for sensors and biochips.…”
Copper-catalyzed azide-alkyne cycloaddition (CuAAC), combined with the chemical stability of the SiÀC-bound organic layer, serves as an efficient tool for the modification of silicon substrates, particularly for the immobilization of complex biomolecules. This review covers recent advances in the preparation of alkynyl-or azido-terminated "clickable" platforms on non-oxidized silicon and their further derivatization by means of the CuAAC reaction. The exploitation of these "click"-functionalized organic thin films as model surfaces to study many biological events was also addressed, as they are directly relevant to the on-going effort of creating siliconbased molecular electronics and chemical/biomolecular sensors.
“…The monolayer formation with unsaturated groups of acetylene, alcohols and thiols has been reperted. And the modifications of Si-H with halogenations and click reaction have been also reported [5,6]. In this way, Si-H surfaces can be modified by various methods, but the modification was not investigated in the unified treatment [7][8][9][10].…”
We report on the monolayer formation of hydrocarbons with terminal groups of thiol, hydroxyl and alkynyl groups on H-terminated silicon using UV light in order to clarify the ability to form the well-defined monolayer. The each molecule was dissolved in the solution (100 mM) and irradiated with UV light on the Si-H substrate. The monolayer formation was investigated by water contact angle, XPS, AFM and ellipsometry. The molecules formed hydrophobic monolayer, but the densities of the monolayers were loose. The hydrocarbons with thiol and vinyl formed the most densely packed monolayer based on the photochemical reactivity with Si-H.
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