2019
DOI: 10.1016/j.jiec.2019.07.038
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Synthesis of poly[2-(3-butenyl)-2-oxazoline] with abundant carboxylic acid functional groups as a fiber-based sol–gel reaction supporter for catalytic applications

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Cited by 4 publications
(4 citation statements)
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“…46 PBuOxz n was modified by cysteamine hydrochloride and 3-mercaptopropionic acid to generate PBuOxz n -g-NH 2 and PBuOxz n -g-COOH, respectively. 63,64 The chemical structures and molecular characteristics were confirmed by FTIR, 1 H NMR, and 13 C NMR spectra and GPC (Figures S3b, S4d−e, S5d−e, and S6b).…”
Section: ■ Results and Discussionmentioning
confidence: 87%
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“…46 PBuOxz n was modified by cysteamine hydrochloride and 3-mercaptopropionic acid to generate PBuOxz n -g-NH 2 and PBuOxz n -g-COOH, respectively. 63,64 The chemical structures and molecular characteristics were confirmed by FTIR, 1 H NMR, and 13 C NMR spectra and GPC (Figures S3b, S4d−e, S5d−e, and S6b).…”
Section: ■ Results and Discussionmentioning
confidence: 87%
“…Similarly, poly­[2-(3-butenyl)-2-oxazoline] n (PBuOxz) n with various DPs ( n = 32, 41 and 80) and dispersity ( D̵ ) ≤ 1.30 were synthesized according to the reported procedure . PBuOxz n was modified by cysteamine hydrochloride and 3-mercaptopropionic acid to generate PBuOxz n - g -NH 2 and PBuOxz n - g -COOH, respectively. , The chemical structures and molecular characteristics were confirmed by FTIR, 1 H NMR, and 13 C NMR spectra and GPC (Figures S3b, S4d−e, S5d−e, and S6b).…”
Section: Resultsmentioning
confidence: 99%
“…27 The PBuOxz 80 precursor was subsequently quantitatively modified with cysteamine hydrochloride and 3-mercaptopropionic acid to obtain PBuOxz 80 -g-NH 2 and PBuOxz 80 -g-COOH, respectively. 34,35 The molecular structures and characteristics of these polymers were confirmed by 1 H NMR spectroscopy and GPC. The assemblies were prepared by mixing aqueous solutions of oppositely charged PBuOxz 80 -g-NH 2 and PBuOxz 80 -g-COOH at charge-matched stoichiometry and a total polymer concentration of 1 mg/mL at neutral pH in water.…”
Section: ■ Results and Discussionmentioning
confidence: 91%
“…Poly(2-oxazoline)s are peptidomimetic polymers that possess similar chemical structure to polypeptides yet are devoid of hydrogen-bond donating sites and chirality. This results in tunable molecular interactions, processability, and excellent water affinity, offering an excellent nanoreactor platform. ,, By employing ring-opening polymerization (ROP) of BuOxz, we synthesized oppositely charged PBuOxz 80 with a degree of polymerization (DP) of 80 and a dispersity ( D̵ ) of 1.31 according to the reported procedure (Figures S2–S4). The PBuOxz 80 precursor was subsequently quantitatively modified with cysteamine hydrochloride and 3-mercaptopropionic acid to obtain PBuOxz 80 - g -NH 2 and PBuOxz 80 - g -COOH, respectively. , The molecular structures and characteristics of these polymers were confirmed by 1 H NMR spectroscopy and GPC.…”
Section: Resultsmentioning
confidence: 99%