2021
DOI: 10.1016/j.molstruc.2020.129707
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A novel route for the synthesis of pseudopolyrotaxane containing γ-Cyclodextrin based on environmental waste recycling

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Cited by 13 publications
(5 citation statements)
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“…The shifting that occurs in absorbance bands could strongly illustrate the formation of an inclusion complex between PEG and the macrocyclic molecules of α-CDs. The enhancement in frequencies is due to the insertion of the PEG chain through the electron-rich cavity of the cyclodextrin rings [73][74][75][76]. In contrast, the decreasing in frequencies is due to the creation of van der Waals forces, hydrogen bonds between the adjacent α-CDs and the hydrogen bonds between the hydroxyl groups of α-CDs and the oxygen ether linkages in PEG.…”
Section: Ft-ir-studiesmentioning
confidence: 99%
“…The shifting that occurs in absorbance bands could strongly illustrate the formation of an inclusion complex between PEG and the macrocyclic molecules of α-CDs. The enhancement in frequencies is due to the insertion of the PEG chain through the electron-rich cavity of the cyclodextrin rings [73][74][75][76]. In contrast, the decreasing in frequencies is due to the creation of van der Waals forces, hydrogen bonds between the adjacent α-CDs and the hydrogen bonds between the hydroxyl groups of α-CDs and the oxygen ether linkages in PEG.…”
Section: Ft-ir-studiesmentioning
confidence: 99%
“…The absorption band at 1660 cm −1 is assigned to free C=O stretching vibration 55 . The absorption bands at 1560 and 1413 cm −1 corresponding to the polymer (C=N) group bending 56 and stretching vibration of (CH 2 –OH), were shifted towards higher wave numbers and decreased in their intensities, because of the interaction between the polymer blend chains and the ZnO NPs 57 . The band at 1073 cm −1 which is attributed to C–O–C stretching became less intense and was shifted to lower wavenumber.…”
Section: Resultsmentioning
confidence: 99%
“…In addition, the bands for (PC6) appeared at 2854, 3018, 1736, and 1671, respectively, with increasing and decreasing intensity; this result is due to the overlapping between carbonyl groups with OH groups. Also, the hydrogen bond interaction between the carbonyl groups of the guest molecule and the (OH) groups of the β-CD ring causes the displacement of the C=C and carbonyl groups to higher wavenumbers and boosts their intensity [ 37 , 43 – 46 ]. Due to the inclusion of (CoP6) inside the hydrophobic cavity of β-CD, the distinctive absorption band due to (OH) groups of (PC6) became sharper than pure β-CD [ 47 ].…”
Section: Resultsmentioning
confidence: 99%
“…These results could mean that (CoP5-7) and β-CD join together to make a complexation. The maximum value is raised by incorporating (CoP5-7) chains into the cyclodextrin rings' electron-rich cavity [ 37 , 43 ]. Instead, hydrogen bonding between neighboring β-CD rings and Vander Waals forces between the OH groups of β-CDs and CO groups of copolymers are responsible for the attenuation of peaks.…”
Section: Resultsmentioning
confidence: 99%