Visible and near-IR spectroscopy of endohedral Gd@C82(C 2v ) and Ho@C82(C 2v ) metallofullerenes and their monoanions

Solutions of endohedral Gd@C₈₂(C _2v ) and Ho@C₈₂(C _2v ) metallofullerenes are studied by means of visible and near-IR spectroscopy upon their conversion from neutral to the anionic form via a redox reaction with the electron donor potassium perchlorotriphenylmethide K(18-crown-6)[C(C₆Cl₅)₃]. The concentrations of the studied solutions of endohedral Gd@C₈₂(C _2v ) and Ho@C₈₂(C _2v ) metallofullerenes in o-dichlorobenzene were determined from the spectroscopic data, and their molar extinction coefficients are calculated.

     

Asymmetric orbital-lattice interactions in ultrathin correlated oxide films

Using resonant x-ray spectroscopies combined with density functional calculations, we find an asymmetric biaxial strain-induced d-orbital response in ultrathin films of the correlated metal LaNiO3 which are not accessible in the bulk. The sign of the misfit strain governs the stability of an octahedral "breathing" distortion, which, in turn, produces an emergent charge-ordered ground state with an altered ligand-hole density and bond covalency. Control of this new mechanism opens a pathway to rational orbital engineering, providing a platform for artificially designed Mott materials.     

Endohedral gadolinium-containing metallofullerenes in the trifluoromethylation reaction

An efficient method for the synthesis of trifluoromethyl derivatives of endohedral gadolinium-containing metallofullerenes was proposed. High-purity (98–99%) trifluoromethyl derivatives Gd@C₈₂(CF₃)₅ (two isomers) and Gd₂@C₈₀(CF₃) have been synthesized for the first time. They were isolated and characterized by HPLC, MALDI-TOF mass spectrometry, and UV-Vis spectroscopy. Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 7, pp. 1457–1462, July, 2008.     

Energy spectrum of isomer no. 3 of C82 fullerene of C 2 symmetry

Physics of the Solid State - The energy spectrum of C82 fullerene (isomer no. 3 of C 2 symmetry) is calculated within the Hubbard model in the approximation of static fluctuations. Based on the...     

Reaction of C60 with KMnF4 : Isolation and characterization of a new isomer of C60F8 and re-evaluation of the structures of C60F7(CF3) and the known isomer of C60F8

The volatile fluorofullerene products of high-temperature reactions of C₆₀ with the ternary manganese(III, IV) fluorides KMnF₄, KMnF₅, A₂MnF₆ (A⁺ = Li⁺, K⁺, Cs⁺), and K₃MnF₆ were monitored as a function of reaction temperature, reaction time, and stoichiometric ratio by in situ Knudsen-cell mass spectrometry. When combined with fluorofullerene product ratios from larger-scale (bulk) screening reactions with the same reagents, an optimized set of conditions was found that yielded the greatest amount of C₆₀F₈ (KMnF₄/C₆₀ mol ratio 28-30, 470 °C, 4-5 h). Two isomers of C₆₀F₈ were purified by HPLC, one of which has not been previously reported. Quantum chemical calculations at the DFT level combined with 1D and 2D ¹⁹F NMR, FTIR, and FT-Raman spectroscopy indicate that the C₆₀F₈ isomer previously reported to be 1,2,3,8,9,12,15,16-C₆₀F₈ is actually 1,2,3,6,9,12,15,18-C₆₀F₈, making it the first high-temperature fluorofullerene with non-contiguous fluorine atoms. The new isomer, which was found to be 1,2,7,8,9,12,13,14-C₆₀F₈, is predicted to be 5.5 kJ mol⁻¹ more stable than 1,2,3,6,9,12,15,18-C₆₀F₈ at the DFT level. In addition, new DFT calculations and spectroscopic data indicate that the compound previously isolated from the high-temperature reaction of C₆₀ and K₂PtF₆ and reported to be 16-CF₃-1,2,3,8,9,12,15-C₆₀F₇ is actually 18-CF₃-1,2,3,6,8,12,15-C₆₀F₇.     

Trifluoromethyl derivatives of cerium endohedral metallofullerenes

A method was developed for the synthesis of trifluoromethyl derivatives of endohedral metallofullerenes (EMF) encapsulating cerium based on the high-temperature solid-state reaction of silver trifluoroacetate with a DMF extract of EMF enriched with Ce@C₈₂. The trifluoromethyl derivatives Ce@C₈₂(CF₃)₅ (isomers I–III) with high purity (98–99%) were synthesized and isolated for the first time. These compounds were characterized by HPLC, S8-MALDI-TOF mass spectrometry, and optical spectroscopy.     

Mott physics near the insulator-to-metal transition in NdNiO3

An optical study of NdNiO(3) ultrathin films with insulating and metallic ground states reveals new aspects of the insulator-to-metal transition that point to Mott physics as the driving force. In contrast with the behavior of charge-ordered systems, we find that the emergence of the Drude resonance across the transition is linked to a spectral weight transfer over an energy range of the order of the Coulomb repulsion U, as the energy gap is filled with states instead of closing continuously.     

Energy and optical absorption spectra of endohedral metallofullerenes with Gd or Ho as strongly correlated π-electron systems

Isomerically pure endohedral metallofullerenes Gd@C82(C2v), Ho@C₈₂(C_2v), and their monoanions have been synthesized and separated. The optical absorption spectra of solutions of obtained compounds in o-dichlorobenzene have been studied. Within the Hubbard model, the energy spectrum of isomer of C_2v symmetry (no. 9) of fullerene С₈₂ has been calculated. Based on the obtained spectrum, optical absorption spectra of endohedral metallofullerenes Gd@C₈₂ and Ho@C₈₂ and their monoanions have been simulated. The calculated optical absorption spectra have been compared with experimental ones; it has been found that qualitative agreement between them is observed.     

X-ray structure and DFT study of C1-C60(CF3)12. A high-energy, kinetically-stable isomer prepared at 500 degrees C

The title compound, prepared from C(60) and CF(3)I at 500 degrees C, exhibits an unusual fullerene(X)12 addition pattern that is 40 kJ mol(-1) less stable than the previously reported C(60)(CF(3))12 isomer.