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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)(...

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Detalles Bibliográficos
Autores principales: Su, Hang, Chen, Wei, Li, Liang, Li, Bin, Zhang, Zhi-Yuan, Li, Chunju
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
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
Descripción
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.