Diol-substituted boron complexes of dipyrrolyl diketones as anion receptors and covalently linked ‘pivotal’ dimers
Literature Information
Yasunobu Fujii, Yuta Mihashi
Diol-substitution at a boron unit results in the formation of anion receptors consisting of dipyrrolyl diketones and covalently linked dimers, which exhibit selective binding for dianions with appropriate lengths.
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![6-Benzyl-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridin-3(2H)-one structure 6-Benzyl-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridin-3(2H)-one structure](https://static.chemtradehub.com/structs/909/909187-64-0-f54f.webp)
![tert-Butyl N-[(2-chloropyridin-4-yl)methyl]carbamate structure tert-Butyl N-[(2-chloropyridin-4-yl)methyl]carbamate structure](https://static.chemtradehub.com/structs/916/916210-27-0-9f95.webp)
![Pyrazolo[1,5-a]pyridine-3-carbothioamide structure Pyrazolo[1,5-a]pyridine-3-carbothioamide structure](https://static.chemtradehub.com/structs/885/885275-44-5-aae0.webp)

