Nucleation Kinetics of C70

Abstract

Since the shape of C₇₀ molecule is prolate spheroidal, the same shape is assigned to the clusters of C₇₀ molecules and the nucleation parameters are evaluated using classical nucleation theory. Moreover, C₇₀ molecule is highly rotational and the rotational energy is included in the nucleation kinetics of C₇₀ molecules. the supersaturation required for condensation of C70 molecules is high compared to that of C₇₀. This theoretical prediction is compared with experimental observations.     

THE SINGLE CRYSTAL X-RAY STRUCTURE OF C70Me8; THE ORIGIN OF THE FULLERENE ADDITION PATTERNS FOR BULKY GROUPS

ABSTRACT

The first complete proof of the equatorial addition pattern in [70]fullerene is provided by a single crystal x-ray structure of C₇₀Me₈. Compared to the bonds in the parent fullerene, those having a methyl group attached are lengthened, those having two methyl groups adjacent at each end are shortened due to compression by these groups, and some hexagonal rings show greater delocalisation (more aromaticity) than the corresponding rings in the precursor fullerene. In contrast to the 1,2-addition of sterically undemanding groups, bulky groups generally undergo 1,4-addition, but only give 1,2-addition if there is a need to quench an intermediate radical. The manner in which this gives rise to the patterns seen in C₆₀ X ₆, C₆₀ X ₈ and C₇₀ X ₁₀, where X is bulky, is proposed.     

Synthesis of Radiolabeled Fullerenes C60 and C70

Abstract

The synthesis of radiolabeled C₆₀/C₇₀ for potential biochemical tracer studies was carried out. Vaporization under plasma are conditions (~3000C) of graphite rods impregnated with the ¹⁴C labeled steroid progesterone generates the expected C₆₀/C₇₀ mixture. Isolation and characterization of the ¹⁴C-C₆₀ is reported. Interestingly, the C₇₀ had more radioactivity than the C₆₀.     

Determination of C60 and/or C70 Concentrations

Abstract

Two methods of quantitative analyses of the fullerenes C₆₀ and C₇₀ are described. Quantitative Infrared Spectroscopy permits the determination of the concentrations of pure and mixed compositions of C₆₀ and C₇₀ in carbondisulfide solutions. Alternatively, the ratio of C₆₀/C₇₀ is analyzed by evaluating the lattice parameters of a solid solution of the fullerene species and cyclohexane according to Vegard's Law. Both methods show high accuracy and are suited for calibration of mass spectrometric analyses of fullerene samples.     

On the Action of Ultraviolet Light on C70 Fullerene

Abstract

C₇₀ was photopolymerized in solution of CCl₄ under nitrogen flow by an high pressure mercury lamp. The resulting photoproduct was still soluble in common solvents and has been studied by electronic and FT-IR spectroscopy. FT-IR spectroscopy reveals a very peculiar band pattern never reported to date for C₇₀ photoproduct. Since this band pattern is very similar to that of C₆₀ photopolymer, it suggests that C₇₀ photoproduct should have a chemical structure very close to that assigned to C₆₀ photopolymer and piezopolymer.

The role played by CCl₄ in C₇₀ photopolymerization seems to be comparable to that already reported for C₆₀, i.e. it acts as a polymerization promoter.     

Short Communication: Stability of C70O in Toluene

Abstract

C₇₀O dissolved in toluene transforms to as yet undetermined compounds when exposed to light at room temperature. After 140 days, only 21% of the original C₇₀O remained. C₇₀ was not formed. C₁₃₉, or C₁₄₀O were not found. One possible explanation is that the compounds formed were very insoluble in toluene and that their solids either remained in colloidal solution or attached themselves to the glass walls of the container bottles.     

Regiochemistry of Azide Additions to [70]Fullerene

Abstract

In this paper we report for the first time on the reaction of C₇₀ with alkyl azides and show that the [3+2]-cycloaddition occurs preferably at bond 7 followed by bond 5 to give two regioisomeric A/B-triazolines and one C/C-triazoline Thermal extrusion of N₂ from these triazolines leads to open [5,6]-bridged iminofullerenes as A/A- and B/C-isomers as well as to the ring closed [6,6]-bridged analogues as A/B- and C/C-isomers. These results are in line with the corresponding thermal reaction of C₇₀ with diazomethane.     

Enhancement of the quantum efficiency of radiative recombination of the fullerene C70 in a toluene solution

An investigation of the spectra and quantum efficiency of photoluminescence provided direct evidence of the presence of C₇₀ aggregates in a toluene solution. Toluene solutions of C₆₀ and C₇₀ in the proportion 1 g/l and artificial mixtures of these were studied. The hypothesis is put forward that mixed aggregates of C₆₀ and C₇₀ exist. Pis’ma Zh. Tekh. Fiz. 24, 70–75 (November 26, 1998)     

Preparation of Two Novel C60 and C70 Fullerene Pyrrolidine Derivatives

Abstract

C₆₀ reacted with paraformaldehyde and DL-valine in dry toluene under nitrogen to give a monoadduct. Under the similar conditions,C₇₀ gave a bisadduct. Both products were characterized by FT-IR,UV-Vis,EI-MS and NMR.The studies of the cyclic voltammetry showed that the abilities of donating electron of the products were increased compared to C₆₀ and C₇₀ respectively.     

A Remark on Intramolecular Transfer of an Injected Electron in C60 and C70

Abstract

A simple analysis on the intramolecular transfer of an injected electron into C₆₀ and C₇₀ has been performed based on the concept of orbital interaction. This analysis contains the partitioning of each fullerene into three parts and the examination of the frontier molecular orbital interaction for propagation of an injected electron into the whole Cgo or C70 molecule. This electron transfer process is shown to be “one-way” from energetical point of view.     

Raman Spectra of Chlorinated C60 and C70 Fullerenes

Abstract

Raman spectra of chlorinated C₆₀ and C₇₀ fullerenes prepared by photochlorination have been reported and discussed. The Raman lines suggest structural analogies with already fully characterized brominated fullerenes. Intense laser light irradiation cause a decomposition of fullerene chloro-derivatives leading to the formation of C₆₀ polymer.     

Quantitative Determination of C60 and C70 in Soot Extracts by High Performance Liquid Chromatography and Mass Spectrometric Characterization

Abstract

A quantitative HPLC method was applied to determine the amounts of C₆₀ and C₇₀ present in extracts of soot produced in the electric arc reactor and in flames. The combustion method was found to yield a higher C₇₀/C₆₀ ratio (0.67) compared with the evaporation experiment where the C₇₀/C₆₀ ratio amounts to 0.27.     

Effect of pressure on electrical resistivity of Mg70Zn30 metallic glass

Abstract

The variation of the electrical resistivity of amorphous simple metal alloy Mg₇₀Zn₃₀ as a function of non-hydrostatic pressure has been studied. Measurements have been made in the range 0–10 kbar. The resistivity is found to increase with increasing pressure.

MST/982     

New Developments on the Photochlorination of C60 and C70 Fullerene and Preparation of Fullerene Derivatives: Polyfluorofullerenes and Polyfullerols.

Abstract

Improved methods for photochlorination of C₆₀ and C₇₀ are described. The photoproducts fit respectively the average formulae C₆₀ Cl₄₀ and C₇₀ Cl₄₇. It is also shown that these photoproducts can be easily fluorinated by means of KF to give fluorofullerenes.

Polyhydroxyfullerene (fullerol) can be easily produced by the action of a methanolic solution of alkali over C₆₀ Cl₄₀.     

Trifluoromethylation of [60]- and [70]Fullerene in the Ionization Chamber of a Mass Spectrometer

Abstract

Both [60]- and [70]fullerene react with either the Scherer radical (perfluorodiisopropylethylmethyl, C₉F₁₉), a mixture of branched perfluorononenes (C₉F₁₈, the product of hexafluoropropene trimerization), or β-fluorosulphatotetrafluoroethyldiheptafluoroisopropylmethyl radical (C₉F₁₈OSO₂F) in the ionization chamber of a mass spectrometer to give the positive parent ions of trifluoromethylation products, the reaction being accompanied by hydrogen addition. The reaction occurs at least partly on the walls of the ionization chamber, by a radical mechanism employing CF₃ radicals formed from the radical reactants both thermally and under electron impact; only the latter route occurs with the perfluorononenes.     

Effect of Molecular Rotation on Vapor Phase Nucleation: Fullerenes C60 and C70

Abstract

The effect of rotational free energy of fullerenes C₆₀ and C₇₀ on homogeneous nucleation of crystals from vapor phase have been studied. Classical nucleation parameters have been estimated for the case of nucleation and crystal growth of C₆₀ and C₇₀ by Physical Vapor Transport (PVT) method under different supercooling in the range of 20–150 K, keeping the source temperatures constant. The result shows that the growth of large size single crystals is more feasible in the lower supercooling range. The effect of change in interfacial tension on the critical free energy of formation of the nuclei is also studied.     

Solubility of Fullerenes C60 and C70 in Seven Normal Alcohols and Their Deduced Solubility in Water

Abstract

The solubilities of C₆₀ and C₇₀ at 25°C in seven normal alcohols obey the relationship InY = a + bX + cX², where Y is solubility and X is the Hildebrand solubility parameter of the solvent. Extrapolation to the solubility parameter of water yields solubilities in water of 1.3′10^?11 (C₆₀) and 1.3′10^?10(C₇₀) ng/ml with an uncertainty of one order of magnitude.     

Penultimate Intermediates to C60 and C70

Abstract

Penultimate intermediates leading to C₆₀ and C₇₀ fullerenes contain one or two pairs of pentalene units and 32 to 55 kcal/mol less stable than the final products. Energy barriers of pyracylene rearrangements from these intermediates to the final products are computed to be 118 to 125 kcal/mol in height by MOPAC/AM1, which are comparable to those of preceding steps in the Stone-Wales rearrangement cascade.     

Nonlinear Stern-Volmer Fluorescence Quenching of Pyrene by C60/70

Abstract

The Stern-Volmer plot of fluorescence quenching of pyrene by C₆₀ (or C₇₀) is upward, and non linearly proportional to the fullerene concentration. Electronic absorption measurements show that pyrene and C₆₀ do not form static complexes under the experimental condition. a novel “inner filter effect” model is proposed to rationalize the observed non linear upward Stern Volmer behavior. At a given C₆₀ concentration, increasing either solvent polarity or temperature (T > 280 K) causes diminishment in the I₀/I ratio. the data strongly suggest that even at concentrations far below saturation, fullerenes form aggregates in organic solvents.     

Anisotropic Carbon Phases Prepared from Fullerite C70 under High Pressure

Abstract

We present the structural and ultrasonic study of carbon phases prepared by quenching after heating of fullerite C₇₀ in the temperature range 300–1100°C at pressures 4 and 7.5 GPa. The main aspect of the work concerns the structural and elastic anisotropy of samples resulted as consequence of quasi hydrostatic pressure with an additional pressure component along the axis of pressure load. Structural anisotropy correlates with anisotropy of the tensor of effective elastic constants taken for the medium with single axis of anisotropy. Comparison of the data obtained with anisotropy effects, earlier observed in the phases synthesized from C₆₀ in the similar quasi hydrostatic conditions, clarifies the role of non‐spherical symmetry of C₇₀ molecule.