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. UV/Vis and CV characteristics were also investigated experimentally and theoretically.
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http://dx.doi.org/10.1039/d4cc05485g | DOI Listing |
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 PDFSci Rep
October 2024
Department of Pure and Applied Chemistry, University of Calabar, PMB 1115, Calabar, Nigeria.
Nanostructured materials have gained significant attention as anode material in rechargeable lithium-ion batteries due to their large surface-to-volume ratio and efficient lithium-ion intercalation. Herein, we systematically investigated the electronic and electrochemical performance of pristine and endohedral doped (O and Se) GeC and SiC nanocages as a prospective negative electrode for lithium-ion batteries using high-level density functional theory at the DFT/B3LYP-GD3(BJ)/6-311 + G(d, p)/GEN/LanL2DZ level of theory. Key findings from frontier molecular orbital (FMO) and density of states (DOS) revealed that endohedral doping of the studied nanocages with O and Se tremendously enhances their electrical conductivity.
View Article and Find Full Text PDFBeilstein J Org Chem
March 2024
Division of Applied Chemistry, Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871, Japan.
Lithium ion-endohedral fullerene (Li@C), a member of the burgeoning family of ion-endohedral fullerenes, holds substantial promise for diverse applications owing to its distinctive ionic properties. Despite the high demand for precise property tuning through chemical modification, there have been only a few reports detailing synthetic protocols for the derivatization of this novel material. In this study, we report the synthesis of Li@C derivatives via the thermal [2 + 2] cycloaddition reaction of styrene derivatives, achieving significantly higher yields of monofunctionalized Li@C compared to previously reported reactions.
View Article and Find Full Text PDFChemistry
February 2024
Department of Chemistry, Graduate School of Science, Tohoku University, Sendai, 980-8578, Japan.
Ion-endohedral-fullerene has attracted growing interest due to the unique electronic and structural characteristics arising from its distinctive ionic nature. Although there has been only one reported ion-encapsulated fullerene, Li @C , a significant number of fundamental and applied studies have been conducted, making a substantial impact not only in chemistry and physics but also across various interdisciplinary research fields. Nevertheless, studies on ion-endohedral fullerenes are still in their infancy due to the limitations in variety, and hence, it remains an open question how the size and symmetry of fullerene, as well as the motion and position of the encapsulated ion, affect their physical/chemical properties.
View Article and Find Full Text PDFChem Commun (Camb)
January 2023
Graduate School of Pharmaceutical Sciences, Tohoku University, 6-3, Aoba, Aramaki, Aoba-ku, Sendai, Miyagi 980-8578, Japan.
A versatile method for the chemical modification of a lithium-ion endohedral fullerene (Li@C) to connect various small molecules is described. The designed dieneazide linker enables the facile connection of Li@C with small molecules bearing a terminal alkyne Huisgen annulation and a subsequent Diels-Alder reaction. This strategy significantly expands the diversity of small molecules to be attached by Li@C.
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