Synthesis of a new class of fullerene derivative Li⁺@C₆₀O⁻(OH)₇ as a "cation-encapsulated anion nanoparticle".

Nanoscale

Division of Applied Chemistry, Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871, Japan.

Published: March 2013

Metal encapsulation into a cage and chemical modification on the outer surface of fullerenes endow them with some unique characteristic properties. Although the derivatization of endohedral fullerenes holds promise for producing novel new nano-carbon materials, there are few reports about such compounds. Herein, we report the synthesis of lithium encapsulated fullerenol Li(+)@C60O(-)(OH)7 using a fuming sulfuric acid method from [Li(+)@C60](PF6(-)) and characterization of its structure by IR, NMR, FAB mass spectroscopy, and elemental analysis. The hydroxylation of [Li(+)@C60](PF6(-)) is site-selective to preferentially give a single isomer (ca. 70%) with two minor isomers in marked contrast to the reaction of empty C60. We conclude from the analysis of radical species produced in the reaction of a C60 cage with fuming sulfuric acid that this unusual site-selective hydroxylation is caused by the lower HOMO level of Li(+)@C60 than that of empty C60. Furthermore, our results clearly indicate that the internal lithium cation is interacted with the introduced hydroxyl groups, and thus the properties of endohedral fullerenes can be controlled by the external modification of a fullerene cage.

Download full-text PDF

Source
http://dx.doi.org/10.1039/c3nr33608eDOI Listing

Publication Analysis

Top Keywords

endohedral fullerenes
8
fuming sulfuric
8
sulfuric acid
8
empty c60
8
synthesis class
4
class fullerene
4
fullerene derivative
4
derivative li⁺@c₆₀o⁻oh₇
4
li⁺@c₆₀o⁻oh₇ "cation-encapsulated
4
"cation-encapsulated anion
4

Similar Publications

Dinuclear iridium complexes ligated by lithium-ion endohedral fullerene Li@C.

Chem Commun (Camb)

January 2025

Department of Chemistry, Graduate School of Science, Tohoku University, Sendai 980-8578, Japan.

The diiridium complexes of lithium-ion endohedral fullerene Li@C were synthesised in high yields. X-ray crystallography revealed the η:η-coordination of Li@C and the disorder of the Li ion over two sites close to the coordinated carbons. C NMR study suggested the presence of dynamic behaviour haptotropic rearrangements.

View Article and Find Full Text PDF

Endohedral vs exohedral boron in C60: Bonding nature and impact on hot-electron relaxation dynamics.

J Chem Phys

January 2025

MOE Key Laboratory for Non-Equilibrium Synthesis and Modulation of Condensed Matter, School of Physics, Xi'an Jiaotong University, Xi'an 710049, People's Republic of China.

Endohedral and exohedral fullerenes have both been employed as electron acceptors in polymer solar cells (PSCs). However, their differences in hot-electron relaxation dynamics remain unclear. Previous studies have shown that the location of a single atom, whether inside or outside the fullerene cage, results in significant differences in charge distribution.

View Article and Find Full Text PDF

Fluoride Clusterfullerenes: Tuning Metal-Metal Bonding and Magnetic Properties via Single Fluorine Atom Doping.

J Am Chem Soc

December 2024

College of Chemistry, Chemical Engineering and Materials Science, and State Key Laboratory of Radiation Medicine and Protection, Soochow University, Suzhou, Jiangsu 215123, P. R. China.

Article Synopsis
  • Endohedral fullerenes are molecules that can encapsulate metal clusters, and this study introduces a new type called fluoride clusterfullerenes (FCFs).
  • The researchers successfully synthesized FCFs using various actinides, rare earth metals, and alkaline earth metals without needing extra modifications, revealing that adding a fluorine atom alters the metal-metal bonding significantly.
  • Their findings indicate that compounds like ThF@(7)-C and CaScF@(6)-C exhibit unique bonding interactions and promising magnetic properties, showcasing the potential of FCFs in future applications.
View Article and Find Full Text PDF

n- to p-Type Conductivity Transition of LuN@C Due to Anisotropic Deformation of Fullerene and Pyramidalization of Endohedral Clusters.

Nano Lett

December 2024

Center for High Pressure Science (CHiPS), State Key Laboratory of Metastable Materials Science and Technology, Yanshan University, Qinhuangdao, Hebei 066004, China.

The endohedral fullerene LuN@C was examined using in situ high-pressure measurements, which included electrical transport, Fourier-transform infrared spectroscopy, and Raman spectroscopy, in combination with theoretical calculations. LuN@C was found to undergo a reversible n- to p-type conversion at ∼8.9 GPa.

View Article and Find Full Text PDF

Spin probe for dynamics of the internal cluster in endohedral metallofullerenes.

Chem Commun (Camb)

December 2024

MOE Key Laboratory of Cluster Science, School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing 102488, China.

Endohedral metallofullerenes (EMFs) are constructed by fullerene cages encapsulating various metal atoms or metal clusters, which usually exhibit some motion. However, due to the fact that the elusive endohedral dynamics are related to many factors, it remains a challenge to image the motion of internal species. Recently, the electron spin was found to be a sensitive probe to detect the motion of internal species in EMFs.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!