2012
DOI: 10.1007/s00216-012-5862-5
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Ambient-ageing processes in amine self-assembled monolayers on microarray slides as studied by ToF-SIMS with principal component analysis, XPS, and NEXAFS spectroscopy

Abstract: We investigated the ageing of amine-terminated self-assembled monolayers (amine-SAMs) on different silica substrates due to exposure to different ambient gases, pressures, and/or temperatures using time-of-flight secondary ion mass spectrometry (ToF-SIMS) with principal component analysis and complementary methods of surface analysis as X-ray photoelectron spectroscopy (XPS) and near edge X-ray absorption fine structure (NEXAFS). The goal of this study is to examine the durability of primary amine groups of am… Show more

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Cited by 77 publications
(68 citation statements)
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“…Three components corresponding to primary amino function at 399 eV, nitrogen from amide bonds at 400.2 eV and primary ammonium function (NH 3 + ) and nitrogen from residual activated ester at 401.9 eV were observed . An increase in the contribution from NH 3 + and nitrogen from residual activated ester, was found, compared to those made in normal activation condition (about 1.5–2 for polysaccharides immobilized by an excess of activation reagents).…”
Section: Resultsmentioning
confidence: 88%
“…Three components corresponding to primary amino function at 399 eV, nitrogen from amide bonds at 400.2 eV and primary ammonium function (NH 3 + ) and nitrogen from residual activated ester at 401.9 eV were observed . An increase in the contribution from NH 3 + and nitrogen from residual activated ester, was found, compared to those made in normal activation condition (about 1.5–2 for polysaccharides immobilized by an excess of activation reagents).…”
Section: Resultsmentioning
confidence: 88%
“…Amides are often observed as aging products of nitrogen containing organic molecules. They are typically formed by oxidation when the samples were exposed to ambient air for a while . In the given case, while the origin of amide species is probably not an amide contamination of educt amines which should be visible in IR spectra shown as supplementary material (Figure S2), oxidation of amines re‐formed by partial hydrolysis of the product imines could possibly play a role.…”
Section: Resultsmentioning
confidence: 89%
“…From Figure 2b, the main peaks of the C 1s spectrum of CKB at binding energies of 284.8, 285.3, 286.98, and 288.58 eV can be assigned to C-C, C-N, C-O-C, and C=O groups [28], respectively, which belong to both chitosan and kenaf biochar. N 1s spectrum in Figure 2c shows three peaks at 399.9, 400.4, and 402.5 eV, referring to -NH2, -NHCO-, and C-N, respectively [29,30]. Figure 2d shows XPS peak deconvolution for O1s spectrum of CKB.…”
Section: Xpsmentioning
confidence: 97%