Matches in SemOpenAlex for { <https://semopenalex.org/work/W2044711915> ?p ?o ?g. }
- W2044711915 endingPage "5065" @default.
- W2044711915 startingPage "5065" @default.
- W2044711915 abstract "Triazolophanes have recently surfaced as a new class of shape-persistent macrocycles that bind anions. Bearing only triazole- and phenyl-derived CH hydrogen bond donors, these receptors have shown extraordinary Cl− binding strengths (>106 M−1, CH2Cl2). The attributes of the triazolophane that are responsible are presented herein alongside recent literature accounts that have utilized similar strategies in new and exciting supramolecular systems. This review describes how triazolophanes leverage the structural pre-organization characteristic of spherands to take advantage of non-traditional hydrogen bonds originating from extrinsic CH donors." @default.
- W2044711915 created "2016-06-24" @default.
- W2044711915 creator A5008334206 @default.
- W2044711915 creator A5017840845 @default.
- W2044711915 creator A5062354047 @default.
- W2044711915 creator A5072699347 @default.
- W2044711915 date "2012-01-01" @default.
- W2044711915 modified "2023-09-26" @default.
- W2044711915 title "Shape persistence delivers lock-and-key chloride binding in triazolophanes" @default.
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