Nanotechnology

Synthesis of novel inflexible constructions derived from 1,1′-biadamantane: Fullerenes, Nanotubes and Carbon Nanostructures: Vol 0, No 0

Synthesis of novel inflexible constructions derived from 1,1′-biadamantane: Fullerenes, Nanotubes and Carbon Nanostructures: Vol 0, No 0
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Summary

In the present day adamantane, the only diamondoid, has attracted a lot consideration, attributable to its distinctive construction and properties for the development of nanostructured entities. 1,1′-biadamantane is an almost inflexible hydrocarbon fashioned from the covalent attachment of the 2 adamantane models. On this research, adamantane was first transformed to 1,1′-biadamantane, and the obtained 1,1′-biadamantane was brominated to present its hexabromo spinoff. The six bromine atoms within the hexabromo spinoff had been then substituted by six phenols through a Friedel-Crafts alkylation response to yield the novel hexakis (4-hydroxyphenyl) spinoff. Additionally, hydrolysis of the heaxabromo spinoff afforded the novel hexahydroxy spinoff.

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