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2008
DOI: 10.1021/ja804448p
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Azidation of Silicon(111) Surfaces

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.

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Cited by 33 publications
(41 citation statements)
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References 34 publications
(44 reference statements)
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“…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%
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“…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%
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“…[48] DeScheme 2. Representative protection/deprotection approaches to obtain functionalized organic monolayers on non-oxidized silicon.…”
Section: Preparation Of Azide-terminated Silicon Substrates and The Smentioning
confidence: 99%
“…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].…”
Section: Introductionmentioning
confidence: 99%