Supramolecular self-assembly between symmetric tetramethyl cucurbit[6]uril and 1,2-Di(4-pyridyl)ethylene derivative-Reference-Cited by-同舟云学术

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Supramolecular self-assembly between symmetric tetramethyl cucurbit[6]uril and 1,2-Di(4-pyridyl)ethylene derivative

Published:2023-09-22 Issue:12 Volume:77 Page:7625-7631
ISSN:0366-6352
Container-title:Chemical Papers
language:en
Short-container-title:Chem. Pap.

Author:

Yue Cai-Lai,Wang Hai-Yan,Yang Mao-Xia,Luo Yang,Zhang Qian-Jun,Tao Zhu,Xiao Xin^ORCID

Funder

Science and Technology Fund of Guizhou Province and the Innovation Program for High-level Talents of Guizhou Province

Publisher

Springer Science and Business Media LLC

Subject

Materials Chemistry,Industrial and Manufacturing Engineering,General Chemical Engineering,Biochemistry,General Chemistry

Link

https://link.springer.com/content/pdf/10.1007/s11696-023-03074-x.pdf

Reference36 articles.

1. Bai H, He W, Chau JH, Zheng CZ, Kwok RTK, Lam JWY, Tang BZ (2021) AIEgens for microbial detection and antimicrobial therapy. Biomaterials 268:120598. https://doi.org/10.1016/j.biomaterials.2020.120598

2. Bardelang D, Udachin AK, Leeka MD, Ripmeester AJ (2007) Highly symmetric columnar channels in metal-free cucurbit[n]uril hydrate crystals (n = 6, 8). CrystEngComn 9:973–975. https://doi.org/10.1039/B711285H

3. Cen R, Liu M, Lu JH, Zeng X, Zhang WF, Dai JJ, Tao Z, Xiao X (2022) Synthesis and characterization of asensitive and selective Fe3+ fluorescent sensor based on novel sulfonated calix[4]arene-basedhost-guestcomplex. Chinese Chem Lett 33:2469–2472. https://doi.org/10.1016/j.cclet.2021.12.005

4. Chen K, Zhu ZQ, Zhang MH, Yang X, Li J, Chen C, Redshaw C (2023) 4,4′-Biphenyldisulfonic acid induced coordination polymers of symmetrical tetramethyl cucurbit[6]uril with alkaline-earth metals for detection of antibiotics. CrystEngComm 25:961–970. https://doi.org/10.1039/D2CE01470J

5. Cong H, Ni XL, Xiao X, Huang Y, Zhu QJ, Xue SF, Tao Z, Lindoy LF, Wei G (2016) Synthesis and separation of cucurbit[n]urils and their derivatives. Org Biomol Chem 14:4335–4364. https://doi.org/10.1039/C6OB00268D

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