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Reversibly switchable methanofullerene by photoexcitation and reduction†
Sofia V. Gracheva,Tatiana S. Yankova,Maria P. Kosaya,Victor A. Brotsman,Ilya N. Ioffe,Natalia S. Lukonina,Alexey A. Goryunkov
Physical Chemistry Chemical Physics Pub Date : 10/25/2022 00:00:00 , DOI:10.1039/D2CP03945A
Abstract

A cyclopropanated derivative of the trifluoromethylated fullerene Cs-C70(CF3)8 demonstrates reversible switching behavior triggered by excited state electron transfer or by negative charging. The switching between the state with connected 62-electron π-system and the state with disjoint 28- and 32-electron conjugated caps is effected by opening/closure of the cyclopropanated bond. A pronounced alteration of the electronic properties upon seemingly minor changes in a large fullerene molecule is an attractive feature for the organic electronic devices where similar fullerene compounds are commonly utilized as electron acceptor materials.

Graphical abstract: Reversibly switchable methanofullerene by photoexcitation and reduction
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