2016
DOI: 10.1002/mrc.4491
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Rate of a Click Chemistry reaction under catalysis by trace‐amounts of copper as evaluated by NMR spectroscopy

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Cited by 3 publications
(3 citation statements)
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“…As shown in Figure S4, the conversion of both monomers in the click reaction leads to a decrease in the intensity of monomer signals and the appearance of new peaks. Specifically, peaks at 4.64 and 4.00 were attributed to the adjoining protons of the newly formed triazole ring . Based on this mechanism, the LbL assembly started with PAA-PEG 2 -Azi on substrates treated with piranha solution followed by the addition of PAA-Alk with the existence of Cu­(I).…”
Section: Results and Discussionmentioning
confidence: 97%
See 1 more Smart Citation
“…As shown in Figure S4, the conversion of both monomers in the click reaction leads to a decrease in the intensity of monomer signals and the appearance of new peaks. Specifically, peaks at 4.64 and 4.00 were attributed to the adjoining protons of the newly formed triazole ring . Based on this mechanism, the LbL assembly started with PAA-PEG 2 -Azi on substrates treated with piranha solution followed by the addition of PAA-Alk with the existence of Cu­(I).…”
Section: Results and Discussionmentioning
confidence: 97%
“…Specifically, peaks at 4.64 and 4.00 were attributed to the adjoining protons of the newly formed triazole ring. 35 Based on this mechanism, the LbL assembly started with PAA-PEG 2 -Azi on substrates treated with piranha solution followed by the addition of PAA-Alk with the existence of Cu(I). During this process, the formation of triazole occurs together with a simultaneous attachment of the PAA-Alk layer to the underlying PAA-PEG 2 -Azi layer.…”
Section: Fabrication Of Fully Negatively Charged (Fnc) Lbl Nanofilmsmentioning
confidence: 99%
“…The first evidence of the reaction's occurrence was the immediate quenching of the methylene proton signal next to alkyne groups at 4.25 ppm due to the rapid complexation with Cu(I) 27 (Figure S6). Furthermore, the conversion of the azide groups led to a decrease in the intensity of -CH 2 -N 3 (peak q) and the appearance of new proton signals that were assigned to the adjoining protons next to the triazole rings 28 (peaks o and p) (Figure 1b). The reagents' peaks showed a decreasing trend with reaction time, while the triazole's peaks displayed the opposite behavior (Figure 1c).…”
Section: ■ Experimental Sectionmentioning
confidence: 99%