1995
DOI: 10.1021/la00003a024
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Self-Assembled Monolayers of Long-Chain Hydroxamic Acids on the Native Oxide of Metals

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Cited by 328 publications
(271 citation statements)
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“…The minor 399.2 eV component would be consistent with an alteration product brought about by the secondary or flood-gun electrons, but the bulk complex was not significantly susceptible to such beam damage. The principal component at 401.0 eV can be assigned to protonated N in the hydroxamate ligands [9,10], and this N chemical environment is consistent with the Raman spectrum for the complex [3] and the crystal structure for the acetohydroxamate analog Fe(O 2 NHCCH 3 ) 3 ·1.5H 2 O [11]. The other photoelectron spectra from Fe hydroxamate will be reported elsewhere.…”
Section: Fe Hydroxamate Xpssupporting
confidence: 69%
“…The minor 399.2 eV component would be consistent with an alteration product brought about by the secondary or flood-gun electrons, but the bulk complex was not significantly susceptible to such beam damage. The principal component at 401.0 eV can be assigned to protonated N in the hydroxamate ligands [9,10], and this N chemical environment is consistent with the Raman spectrum for the complex [3] and the crystal structure for the acetohydroxamate analog Fe(O 2 NHCCH 3 ) 3 ·1.5H 2 O [11]. The other photoelectron spectra from Fe hydroxamate will be reported elsewhere.…”
Section: Fe Hydroxamate Xpssupporting
confidence: 69%
“…Protein adsorption and cell adhesion are reduced on the phosphorylcholine-assembled surfaces. With the intention of producing well-controlled surfaces on oxide, chlorosilanes [204], hydroxamic acid [205], carboxylic acids [206], and phosphoric and phosphonic acids [207][208][209][210] have been proposed as SAMs molecules.…”
Section: Biochemical Modification Of Titanium and Titanium Alloysmentioning
confidence: 99%
“…PA-based SAMs were chosen taking into consideration several distinct advantages over their silanebased counterparts including (i) better stability to moisture, (ii) less tendency for homocondensation between PAs, and (iii) the reaction between PA and the metal oxide substrate is not limited by the content of surface hydroxyl groups. [26] PA headgroups chemisorb readily to metal oxides [27] forming dense and robust SAMs suitable as resists for selective chemical etching [28] and patterning, [29] organic coatings for bioapplications, [30] and functional materials for organic electronics. [11,16,26b] Anthryl surface groups were chosen to combine p-p interactive forces (0-50 kJ mol À1 ) between neighboring molecules and van der Waals interactions (<5 kJ mol À1 ) [31] between aliphatic chains to promote highquality SAM formation, while providing a chemically and electrically compatible pentacene/dielectric interface.…”
Section: à2mentioning
confidence: 99%