2019
DOI: 10.1002/ppap.201800160
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XPS investigation on the reactivity of surface imine groups with TFAA

Abstract: The chemical reaction of imine groups with vapors of trifluoroacetic anhydride (TFAA) was investigated in detail with X‐ray photoelectron spectroscopy (XPS) for the potential application in chemical derivatization (CD) studies of plasma treated surfaces. Imine groups were at first prepared by converting surface amine groups of a polymer precursor using a common vapor phase derivatization reaction with fluorine tagged aldehydes and ketones. The originally low yield for the imine forming reaction of approx. 50%,… Show more

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Cited by 150 publications
(82 citation statements)
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“…As far as nitrogen is concerned, the N1s band ( Figure S6 ) can be well-fitted only by assuming the overlap of two different components, having approximately the same intensity, centered at 399.8 and at 401.1 eV of binding energy. The first component is in agreement with the presence of nitrogen involved in amine functional groups, the second one in amide compounds [ 39 ].…”
Section: Resultsmentioning
confidence: 55%
“…As far as nitrogen is concerned, the N1s band ( Figure S6 ) can be well-fitted only by assuming the overlap of two different components, having approximately the same intensity, centered at 399.8 and at 401.1 eV of binding energy. The first component is in agreement with the presence of nitrogen involved in amine functional groups, the second one in amide compounds [ 39 ].…”
Section: Resultsmentioning
confidence: 55%
“…This is supported by Ahmad and colleagues' results, who observed a B-F component in a comparable region 52 . Furthermore, the peak centered 195 eV could be assigned to BF 4 + species following a similar argument that charged ammonium species are located at higher energies than their corresponding neutral nitrogen functionalities in the N1s area 53 55 . Lastly, the position of the feature in the F1s area is also in line with the literature regarding the expected position for an F-B functionality 52 .…”
Section: Resultsmentioning
confidence: 69%
“…The high-resolution B1s scan in Figure 2 b shows that 75% of the boron is B-C bonded and the remaining 25% is B-B bonded [ 38 , 39 ]. The high-resolution C1s scan in Figure 2 c shows that 9% of the carbon is C-O bonded and the high-resolution O1s scan also shows C-O bonding in Figure 2 d [ 40 , 41 ]. Figure 2 c also shows that 22% of the carbon is C-C bonded and the remaining 69% is B-C bonded [ 38 , 39 ].…”
Section: Resultsmentioning
confidence: 99%