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Regio- and stereo-selective intermolecular [2+2] cycloaddition of allenol esters with C 60 leading to alkylidenecyclobutane-annulated fullerenes.
Chemical Communications : Chem Comm 2016 November 2
The intermolecular [2+2] cycloaddition of allenol esters, which were in situ generated by Pt-catalyzed 1,3-acyloxy migration of propargylic esters, with C60 proceeded regio- and stereo-selectively to give a novel class of alkylidenecyclobutane-annulated fullerenes. The cyclobutane-annulated fullerene derivatives have high-lying LUMO levels, which gave a high open-circuit voltage in organic solar cell applications. The observed high electron mobility provided a good fill factor compared with the PCBM-based devices.
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