Exohedral Addition Chemistry of the Fullerenide Anions C60 2- and C60 ⋠.

A systematic screening study of the exohedral reactivity of the reduced fullerenes (fullerenides) C60 2- and C60 ⋅- is reported. These doubly and singly negatively charged carbon cages were prepared by two-fold reduction of C60 with potassium, leading to K2 C60 , or by in situ monoreduction with the radical anion of benzonitrile PhCN⋅- , respectively. Several series of electrophiles, including geminal and distant dihalides, benzyl bromides, and diazonium compounds, were employed as addition partners. In general, the investigated bromides proved to be the most suitable reaction partners. A series of fullerene adducts and cycloadducts involving either 1,2- or 1,4-addition patterns, depending on the precise architecture and the steric demand of the addends, were synthesized and fully characterized. Some of the reaction products are unprecedented and inaccessible forms of neutral C60 . The fullerenide chemistry presented here closely resembles related reactions of graphenides and carbon nanotubides, which are the most powerful methods for the functionalization of these macromolecular forms of synthetic carbon allotropes (SCAs). Activation of C60 by negative charging represents a little explored concept of fullerene chemistry, providing both new insights of fullerene reactivity itself and new types of exohedral derivatives.

Fullerene Building Blocks with Tailor-Made Solubility and New Insights into Their Hierarchical Self-Assembly.

Herein, the synthesis of fullerene derivatives with adjustable polarities and lyotropic aggregation properties is reported. The polarity range spans from superhydrophobic to hydrophilic, while simultaneously providing a further reactive position with a view to graft them onto other materials. The synthetic strategy relies on a selective protection with an isoxazoline moiety. The remaining octahedral positions were further functionalized with the desired groups to tune their solubility, yielding mixed [5:1] hexakisadducts. The subsequent deprotection by clean photolytic reaction led to fullerene pentakisadducts with an incomplete octahedral addition pattern, which are useful forerunners for the synthesis of building blocks. Their hydrophobic/hydrophilic behavior has been characterized both in solution and surface through octanol/water partition coefficients (log P) and contact angle measurements. Furthermore, these derivatives can form supramolecular constructions which have been studied by dynamic light scattering (DLS) and cryo-TEM.