π-Extended Open-[70]Fullerenes with a Fused Azaacene.
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DOI: 10.1021/acs.orglett.3c00726
Abstract: By the reaction with aromatic diamines, π-extended open-[60]fullerenes were synthesized, in which the nucleophilicity of the diamine switched annulation and orifice-cutting modes, thus generating a fused pyrazine or imidazole. Employing this method for [70]fullerene analogues,… read more here.
Keywords: fused azaacene; fullerenes fused; open fullerenes; extended open ... See more keywords