Infrared spectroscopy of endohedral HD and D2 in C60

We report on the dynamics of two hydrogen isotopomers, D(2) and HD, trapped in the molecular cages of a fullerene C(60) molecule. We measured the infrared spectra and analyzed them using a spherical potential for a vibrating rotor. The potential, vibration-rotation Hamiltonian, and dipole moment parameters are compared with previously studied H(2)@C(60) parameters [M. Ge, U. Nagel, D. Hüvonen, T. R??m, S. Mamone, M. H. Levitt, M. Carravetta, Y. Murata, K. Komatsu, J. Y.-C. Chen, and N. J. Turro, J. Chem. Phys. 134, 054507 (2011)]. The isotropic part of the potential is similar for all three isotopomers. In HD@C(60), we observe mixing of the rotational states and an interference effect of the dipole moment terms due to the displacement of the HD rotation center from the fullerene cage center.     

Interaction potential and infrared absorption of endohedral H2 in C60

We have measured the temperature dependence of the infrared spectra of a hydrogen molecule trapped inside a C(60) cage, H(2)@C(60), in the temperature range from 6 to 300 K and analyzed the excitation spectrum by using a five-dimensional model of a vibrating rotor in a spherical potential. The electric dipole moment is induced by the translational motion of endohedral H(2) and gives rise to an infrared absorption process where one translational quantum is created or annihilated, ΔN = ±1. Some fundamental transitions, ΔN = 0, are observed as well. The rotation of endohedral H(2) is unhindered but coupled to the translational motion. The isotropic and translation-rotation coupling part of the potential are anharmonic and different in the ground and excited vibrational states of H(2). The vibrational frequency and the rotational constant of endohedral H(2) are smaller than those of H(2) in the gas phase. The assignment of lines to ortho- and para-H(2) is confirmed by measuring spectra of a para enriched sample of H(2)@C(60) and is consistent with the earlier interpretation of the low temperature infrared spectra [Mamone et al., J. Chem. Phys. 130, 081103 (2009)].     

Synthesis and properties of water-soluble derivatives of fullerene C60

Procedures for synthesized of water-soluble forms of fullerene C₆₀ and its derivatives were developed.     

Geometric and electronic properties of endohedral Si @ C74

The generalized gradient approximation based on density functional theory is used to analyze the geometric and electronic properties of Si @ C(74). It is found that among the five possible optimized geometries of Si @ C(74), the most favorable endohedral site of Si atom is under the center of a pentagon ring on the sigma(h) plane, i.e., Si @ C(74)-5, which is different from the center stable site for Si in C(74) calculated by the semiempirical molecular orbital calculations and molecular mechanics calculations, and it is also different from the stable site, i.e., under a [6, 6] bond along the C(2) axis on the sigma(h) plane in C(74) for metal atoms Ba, Ca, and Eu. The deformation charge density on the sigma(h) plane reveals that the Si-C bonds in Si @ C(74)-5 have covalent character, while the Mulliken charge analysis together with a longer Si-C bond length reveals that the Si-C bonds in Si @ C(74)-5 have ionic character. Therefore, we infer that Si-C bonds in Si @ C(74)-5 contain both covalent and ionic characters.     

Synthesis and properties of metal-ligand complexes with endohedral amine functionality

A series of tetracationic M(2)L(4) palladium-pyridyl complexes with endohedral amine functionality have been synthesized. The complexes were analyzed by NMR techniques (including Diffusion NMR and 2D NOESY), electrospray ionization (ESI) mass spectrometry, and X-ray crystallography. The solid state analysis shows a large change in crystal morphology upon introduction of the endohedral amine groups, caused by deleterious interactions between the amines and the triflate counterions from the coordination process. Combination of different ligands allows analysis of ligand exchange rates via NMR analysis, with half-lives on the order of 3 h, independent of the donor properties of the ligand. Self-sorting behavior is observed, with more electron-rich ligands being favored. The amine-containing and extended complexes are strongly fluorescent, giving quantum yields of up to 83%.     

Density functional theory calculations for endohedral complexes of non-pi C60H60 cage with small guest molecules

Hybrid density-functional theory (B3LYP) calculations were carried out to determine the structures and energies of endohedral complexes of non-pi C(60)H(60) with H(2), CO, and LiH. It was demonstrated that the endohedral complexes of C(60)H(60) with the above three guest molecules are more stable than the corresponding complexes with C(60). Furthermore, the interaction between C(60)H(60) and the inside H(2) or CO is negligible, but the formation of the LiH-C(60)H(60) complex is exothermic with a stabilization energy of -6.0 kcal/mol. While the bond lengths of H(2) and CO changed a little when placed inside the cages, that of the LiH molecule increased and decreased inside C(60)H(60) and C(60), respectively.     

Redox-induced hydrogen transfer from hydrofullerene C60H36 to fullerene C60

The possibility of hydrogen transfer from hydrofullerene C₆₀H₃₆ to electrogenerated radical anion C₆₀ ^.− or dianion C₆₀ ²⁻ in propylene carbonate-toluence (3∶2, v/v) was demonstrated by cyclic voltammetry. The process affords C₆₀H₂ as the product. The reaction found is the typical redox-induced process. Translated fromIzvestiya Akodemii Nauk. Seriya Khimicheskaya, No. 6, pp. 1136–1139, June, 1998.     

Quantum states of the endohedral fullerene Li@C60

We present a theoretical study of the eigenstates of the endohedral fullerene Li@C60 for the case that the C 60 cage is assumed to be stationary. These eigenstates represent the three-dimensional nuclear dynamics of a Li atom confined to the interior of the carbon cage. The potential function employed, based on density functional theory calculations that we performed, has a variety of minima corresponding to complex hindered rotations of the Li atom in a shell about 1.5 A from the cage center. The energies and wave functions of the lowest 1200 states have been calculated, and the characteristic features of selected states and the far-IR spectrum are discussed. An interesting result of the calculations is the finding that the ground-state eigenfunction can become strongly localized when the cage atoms are just slightly perturbed from icosahedral symmetry.     

Synthesis and reaction of fullerene C70 encapsulating two molecules of H2

New endohedral fullerene C(70) encapsulating one and two H(2) molecule(s) has been synthesized by organic reactions, the so-called "molecular surgery" method, and the first organic derivatization of H(2)@C(70) and (H(2))(2)@C(70) has been conducted. Although the interaction between inner H(2) and outer C(70) is rather weak, (H(2))(2)@C(70) exhibits smaller equilibrium constants in the Diels-Alder reaction with 9,10-dimethylanthracene than those of H(2)@C(70).     

Structural and electronic properties of endohedral metallofullerenes

This account presents an overview of our achievements in structural and chemical understanding of endohedral metallofullerenes (EMFs), a new class of metal‐carbon hybrid materials formed by encapsulation of metals inside fullerene cavities. Structural determination of EMFs is of fundamental importance for understanding their intrinsic properties and the formation mechanism, and for broadening their applications. We have developed an effective method for determining the structures of paramagnetic EMFs, and also succeeded in observing the motion of cluster in a di‐metal EMF for the first time. Recently, we unambiguously established the structures of some carbide EMFs which had been wrongly assumed as conventional EMFs previously. More importantly, we have obtained some insoluble EMF species which had never been explored or even expected before. Meanwhile, the chemical properties of various EMFs with different cage structures or different metallic cores have been systematically investigated by means of both covalent and supramolecular considerations, yielding many fascinating results relating to the dictating effect of internal metals. It is noteworthy that all these achievements are based on unambiguous X‐ray results of pristine or functionalized EMFs. DOI 10.1002/tcr.201100038     

SynthesisofFullereneC＿（60）DerivativesbyOne－potProcedure

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Synthesis of C60H2 by rhodium-catalyzed hydrogenation of C60.

Reduction of C60 with rhodium(0) on alumina and hydrogen in deuterated benzene (C6D6) at ambient temperature and pressure yields a mixture of hydrogenated compounds; C60H2 has been characterized as the major product in 14% yield based on 1H NMR.     

Investigation into the molecular structure and energetic stability of endohedral and exohedral metallofullerene derivatives of C24

Density-functional theory was applied to the investigation of the structural and electronic properties of C₂₄ fullerene derivatives. Transition metals (TMs) from groups 11 and 12, in various oxidation and spin-states, are inserted at either endohedral (TM@C₂₄) or exohedral (TM-C₂₄) sites and their subsequent energetic stabilities are assessed. With the exception of Ag@C₂₄, all derivatives are predicted to occupy a minimum on the potential energy surface. The optimized exohedral TM-C₂₄ geometries yield TM-C bond lengths that are consistent with comparable carbon-metal bond lengths, and the overwhelming majority of the derivatives result in a slight deformation of the C₂₄ cage as the bonding carbon takes on more sp³ character. All of the TM@C₂₄ equilibrium structures maintain the integrity of the cage structure with a moderate increase in the diameter. All neutral exohedral and endohedral complexes favor the low spin-state; conversely, all of the charged exohedral complexes prefer the high spin-state, with the exception of Cu-C₂₄¹⁺ molecular ion. The Group 12 charged endohedral derivatives prefer the low spin-state, whereas the Group 11 molecular ions do not necessarily exhibit a definitive trend. Analysis of the energetic data predicts that of the lowest energy endohedral molecular species only four are predicted to be energetically favorable in terms of insertion energy and an advantageous HOMO-LUMO gap: Cu@C₂₄²⁺, Ag@C₂₄¹⁺, Au@C₂₄³⁺, and Zn@C₂₄²⁺.     

DFT studies on endohedral fullerene C@C60: C centers the C60 cage

Structural and electronic properties of C@C₆₀ were studied via Hartree–Fock self-consistent field (SCF) and density functional B3LYP levels of theory with the STO-3G, 6-31G(d) and 6-31G(d, p) basis sets. Both singlet and triplet were considered. The triplet structure with C on the center of the C₆₀ cage was proved to be global minimum on the C@C₆₀ molecular potential energy surface. The calculated HOMO-LUMO gaps as well as the electron affinity (EA) and the ionization potential (IP) were also presented as an indicator of the kinetic stability.     

Synthesis and characterization of tetrakis-silylated C60 isomers

A photochemical reaction of C(60) with disilane in a 2:3 ratio affords the isomer mixture of the tetrakis-adduct of C(60)((t)BuPh(2)Si)(4) as the major product. The use of a three-stage HPLC separation system isolated three of their isomers. Their structural assignments were based on FAB mass, UV-vis, NMR, and cyclic voltammetry (CV) measurements. The CV analysis showed that the terakis-adduct has lower oxidation and higher reduction potentials than the bis-adduct C(60)((t)BuPh(2)Si)(2) and the parent C(60).     

豆荚型纳米材料C60@SWNTs的制备和表征

通过气相扩散的方法将C60填入单壁碳纳米管（SWNTs）,制备了豆荚型纳米材料C60@SWNTs,并利用高分辨电子显微镜（HRTEM）和拉曼光谱（Raman spectra）对其进行了表征.结果均证明C60以较高的比例填充入单壁碳纳米管中.HRTEM结果表明,填入单壁碳纳米管的C60之间的距离与面心立方C60晶体中C60之间的距离有细微的差别,说明C60分子与SWNTs间存在弱的范德华相互作用.此外,还观察到在电子束的照射下,C60在SWNT中两两聚合的现象.     

Synthesis and identification of endohedral metallofullerenes La@C82

The effect of the procedure of preparation of lanthanum-graphite electrodes and the regime of their evaporation in the electric arc on the yield of endometallofullerene La@C₈₂ has been studied. La@C₈₂ was identified by ESR spectroscopy, optical spectroscopy, and mass spectrometry. The fractional extraction of the fullerene-containing soot witho-xylene makes it possible to separate La@C₈₂ from higher fullerenes containing no metal atorns and to obtain fullerene extracts enriched in La@C₈₂. Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 2, pp. 254–258, February, 1997.     

Synthesis of an Octacyclic C60 Fragment

Fragments of buckminsterfullerene (C₆₀) include the monumental three compounds corannulene, sumanene, and truxene. These three have served as leading molecules in ongoing research for curved, fused, and π-extended polyaromatic materials. Achieving more structural variations that join the ranks of these three archetypes remains challenging. Herein we report synthesis of an octacyclic hydrocarbon that is an unexplored C₆₀-fragment, namely, a 4,11-dihydrodiindeno[7,1,2-ghi:7′,1′,2′-pqr]chrysene (C₂₈H₁₆, which we named Metelykene). The key to success was solution-compatible synthesis in which double pentagonal rings flank hexagonal ones. This solution-phase approach, coupled with the resulting non-planar π-conjugation, is so straightforward that it offers an entry to a derivative such as a cardo aromatic monomer.