Answers are grounded in this paper and cite their sources.
We herein report a β-cyclodextrin-based secondary assembly (β-CD SA) obtained from an aqueous solution. It was found that the addition of a very small amount of organic molecule 2-phenyl-5-(4-diphenylyl) 1,3,4-oxadiazole (PBD) into an aqueous solution of 10 mM β-CD led to the formation of a micrometer-sized rodlike SA, which made the mixture turbid immediately. After careful characterization, the structure and the formation mechanism of the β-CD SA were suggested. PBD first induces β-CDs to form rigid nanotubes through head-to-head or tail-to-tail routes. Using the "solid" nanotubes as recrystallization centers, other β-CDs assembled to channel in the c axis direction and hexagonally aligned in the b axis direction, leading to the formation of a β-CD SA. In the β-CD SA, most of the β-CDs were not occupied by PBD. In the course of formation , intermolecular hydrogen-bonding plays a prominent role. The results reported herein would be helpful in constructing cyclodextrin-based architectures in water.
No takes yet. Share an insight, caveat, or question.
He et al. (2010) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: