2021
DOI: 10.1016/j.polymer.2021.123424
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Conformational transition of Poly-L-proline studied by IR, NMR, and SAXS

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“…In Figure 3 a, 3451 cm −1 belongs to the -OH contraction vibration peak, 2995 cm −1 is the contraction vibration peak of the N-H bond, 1653 cm −1 belongs to the stretching vibration of the C=O double bond, 1420 cm −1 belongs to the N-H deformation vibration peak, and 1088 cm −1 belongs to the C-O stretching vibration peak. After adding HAuCl 4 and hydrothermal treatment, the intensity of the transmittance peak of PPRONPs–CDs at 2995 cm −1 , 1420 cm −1 , and 1080 cm −1 decrease, compared to CDs, indicating that the N-H bond and the C-O bond decrease [ 31 ]. The reason for this is because Pro undergoes a polymerization reaction under the oxidation of HAuCl 4 , and the amino group on the heterocyclic ring reacts with the carboxyl group.…”
Section: Resultsmentioning
confidence: 99%
“…In Figure 3 a, 3451 cm −1 belongs to the -OH contraction vibration peak, 2995 cm −1 is the contraction vibration peak of the N-H bond, 1653 cm −1 belongs to the stretching vibration of the C=O double bond, 1420 cm −1 belongs to the N-H deformation vibration peak, and 1088 cm −1 belongs to the C-O stretching vibration peak. After adding HAuCl 4 and hydrothermal treatment, the intensity of the transmittance peak of PPRONPs–CDs at 2995 cm −1 , 1420 cm −1 , and 1080 cm −1 decrease, compared to CDs, indicating that the N-H bond and the C-O bond decrease [ 31 ]. The reason for this is because Pro undergoes a polymerization reaction under the oxidation of HAuCl 4 , and the amino group on the heterocyclic ring reacts with the carboxyl group.…”
Section: Resultsmentioning
confidence: 99%