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Coordination-Driven Poly[2]Pseudorotaxanes in Highly Polar Organic Solvent
Self-assembly of polypseudorotaxanes in high-polar organic solvents is difficult due to remarkably weak interactions between macrocycles and axles. Reported here is a novel metal-coordinated poly[2]pseudorotaxane constructed by pillar[5]arene, 1,4-bis(4-pyridyl pyridinium)butane, and [PdCl(2)(PhCN)(...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7406859/ https://www.ncbi.nlm.nih.gov/pubmed/32850622 http://dx.doi.org/10.3389/fchem.2020.00579 |
Sumario: | Self-assembly of polypseudorotaxanes in high-polar organic solvents is difficult due to remarkably weak interactions between macrocycles and axles. Reported here is a novel metal-coordinated poly[2]pseudorotaxane constructed by pillar[5]arene, 1,4-bis(4-pyridyl pyridinium)butane, and [PdCl(2)(PhCN)(2)] in highly polar organic solvent of dimethyl sulfoxide (DMSO). Utilizing a combination of (1)H NMR, NOESY, DOSY, DLS, SEM, and viscosity measurements, the formation of polypseudorotaxane was shown to be dependent on the concentration of [2]pseudorotaxanes/[PdCl(2)(PhCN)(2)] and temperature. Furthermore, a temperature-responsive supramolecular gel with reversibly gel–sol transformation was obtained via spontaneous assembly of the polypseudorotaxanes at high concentrations. |
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