Synthesis of Ar@C using molecular surgery

Synthesis of Ar@C 60 is described, using a route in which high-pressure argon filling of an open-fullerene and photochemical desulfinylation are the key steps for >95% encapsulation of the noble gas. Enrichment by recycling HPLC leads to quantitative incorporation of argon in the product endofull...

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Bibliographic Details
Published in:Chemical communications (Cambridge, England) England), 2020-09, Vol.56 (72), p.1521-1524
Main Authors: Bloodworth, Sally, Hoffman, Gabriela, Walkey, Mark C, Bacanu, George R, Herniman, Julie M, Levitt, Malcolm H, Whitby, Richard J
Format: Article
Language:English
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Summary:Synthesis of Ar@C 60 is described, using a route in which high-pressure argon filling of an open-fullerene and photochemical desulfinylation are the key steps for >95% encapsulation of the noble gas. Enrichment by recycling HPLC leads to quantitative incorporation of argon in the product endofullerene, with a mass recovery of tens of milligrams, allowing the first characterisation of fine structure in the solution 13 C NMR spectrum. Synthesis of Ar@C 60 is described, using a route in which high-pressure argon filling of an open-fullerene and photochemical desulfinylation are the key steps for >95% encapsulation of the noble gas.
ISSN:1359-7345
1364-548X
DOI:10.1039/d0cc04201c