Fused‐pentagons results in an increase of local steric strain according to the isolated pentagon rule (IPR), and for all reported non‐IPR clusterfullerenes multiple (two or three) metals are required to stabilize the strained fused‐pentagons, making it difficult to access the single‐atom properties. Herein, we report the syntheses and isolations of novel non‐IPR mononuclear clusterfullerenes MNC@C76 (M=Tb, Y), in which one pair of strained fused‐pentagon is stabilized by a mononuclear cluster. The molecular structures of MNC@C76 (M=Tb, Y) were determined unambiguously by single‐crystal X‐ray diffraction, featuring a non‐IPR C 2v(19138)‐C76 cage entrapping a nearly linear MNC cluster, which is remarkably different from the triangular MNC cluster within the reported analogous clusterfullerenes based on IPR‐obeying C82 cages. The TbNC@C76 molecule is found to be a field‐induced single‐molecule magnet (SMM).

A natural wheat straw was used as adsorbent for removal of copper and methylene blue (MB) from aqueous solution. A batch system was applied to study the behavior of Cu2+ and MB adsorption in single and binary systems on wheat straw. In the single systems, there was no significant difference in the quantity of MB adsorbed onto wheat straw within a pH range of 4.0 to 10.0. But for Cu2+, the optimal pH is about 5. Kinetic studies indicate that Cu2+ and MB adsorption on the wheat straw follows the Elovich equation. The Cu2+ adsorption isotherm follows the Langmuir and Redlich−Peterson models, while MB adsorption follows the Redlich−Peterson isotherm. The adsorption capacities of Cu2+ and MB at 273 K and pH 5 are (7.05 and 60.66) mg·g−1, respectively. In the binary system, Cu2+ and MB exhibited competitive adsorption. The adsorption of Cu2+ or MB is considerably reduced with an increasing concentration of the other. The quantity of Cu2+ adsorbed is more strongly influenced by MB due to the higher affinity of wheat straw for the latter. As wheat straw is easily obtained and cheap, it will be promising for removal of metal ions and dyes.

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Previously reported fused-pentagon fullerenes stabilized by exohedral derivatization do not share the same cage with those stabilized by endohedral encapsulation. Herein we report the crystallographic identification of (#4348)C66Cl10, which has the same cage as that of previously reported Sc2@C66. According to the geometrical data of (#4348)C66Cl10, both strain relief (at the fused pentagons) and local aromaticity (on the remaining sp(2)-hybrided carbon framework) contribute to the exohedral stabilization of this long-sought 66 carbon atom cage.