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Fullerene Pipes

Science, 1998
Single-wall fullerene nanotubes were converted from nearly endless, highly tangled ropes into short, open-ended pipes that behave as individual macromolecules. Raw nanotube material was purified in large batches, and the ropes were cut into 100- to 300-nanometer lengths.
, Liu   +14 more
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Fullerene Quantum Gyroscope

Physical Review Letters, 2004
We report the observation of quantized rotational states of a diatomic C2 unit in solid endohedral fullerene C(2)Sc(2)@C(84). The rotational transitions induce a periodic line pattern in the low energy Raman spectrum. The rotational constant B and the C-C distance were found to be 1.73 cm(-1) and 0.127 nm, respectively.
Krause, M.   +8 more
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Fullerene-fullerene collisions: Fragmentation and electron capture

Physical Review A, 1995
In this paper, we describe collisions between high-energy (100-keV) fullerene ions (${\mathrm{C}}_{60}^{+}$, ${\mathrm{C}}_{60}^{2+}$, ${\mathrm{C}}_{70}^{2+}$, and ${\mathrm{C}}_{70}^{3+}$) and ${\mathrm{C}}_{60}$. The fast, forward-directed charged collision products are identified, leading to information on electron capture and loss as well as ...
, Shen   +6 more
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Conformational Barrier for Fullerene−Porphyrin−Fullerene Triad

The Journal of Physical Chemistry B, 2008
A recent study (J. Phys. Chem. B 2006, 110, 5337) proposed that fullerene-porphyrin-fullerene triad (C60PC60) could be utilized as a photoinduced switch due to the difference in electron transfer directionality for the cis and trans conformer. It is found that the rotational barrier between the SS and AA conformers of C60PC60 is about 3-5 kcal/mol ...
Shihai, Yan   +4 more
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Fluorinated Fullerenes

Chemistry - A European Journal, 2001
Recent developments in fluorination of fullerenes coupled with HPLC separation have permitted the isolation and subsequent structural characterisation of many derivatives, a number of which have novel and unexpected structures. The good solubility of fluorofullerenes, high reactivity towards nucleophiles and enhanced dienophilicity of the unsubstituted
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Medicinal chemistry with fullerenes and fullerene derivatives

Chemical Communications, 1999
The study of the biological applications of fullerenes has attracted increasing attention despite the low solubility of the carbon spheres in physiological media. The organic functionalisation of fullerenes has helped solubilisation by covalent attachment of hydrophilic appendages.
DA ROS, TATIANA, PRATO, MAURIZIO
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Fullerenes

ChemInform, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
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FULLERENES AND FULLERENE NANOSTRUCTURES

Fullerenes and Fullerene Nanostructures, 1996
H Kuzmany, J Fink, M Mehring, S Roth
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Unexpected Dimerization of Oxidized Fullerene-Oligothiophene-Fullerene Triads

Advanced Materials, 2000
Can bulky fullerene substituents reduce the dimerization tendency of oligothiophene radical cations? These authors prepared the dumbbell-shaped bis-C60-substituted oligothiophene shown in the Figure in order to address this question. Contrary to expectation, the molecules display extensive dimerization, even at room temperature, in remarkable contrast ...
Apperloo, Joke J.   +4 more
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Fullerenes

1992
Synthesis of C[6[0 from Small Carbon Clusters: A Model Based on Experiment and Theory Crystalline Fullerenes: Round Pegs in Square Holes Low-Resolution Single-Crystal X-ray Structure of Solvated Fullerenes and Spectroscopy and Electronic Structure of Their Monoanions Solid C[6[0: Structure.
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