C60H18 has been shown by 1H NMR spectroscopy to be 1,2,3,4,8,9,10,16,17,18,22,23,24,36,37,38,39,40-octadecahydro[60]fullerene, a crown-shaped molecule with C3v symmetry, and a sub-structure of T C60H36; both hydride structures are derived from multiple addition of 6 H in a constant pattern governed by the semi-aromaticity of [60]fullerene
Fullerenes, the highly symmetric molecular carbon clusters, have been in the limelight of scientific...
Benkeser reduction was used to synthesize highly hydrogenated fullerenes, C60H36, C60H38, C 60H40, C...
Fluorination of C-60 at 550 degrees C leads to milligram quantities of two stable fullerene derivati...
Isomers of the higher fullerenes were analyzed using 3He NMR spectroscopy. Structures have been assi...
Density functional calculations accurately reproduce the known bond lengths for C60F18, shown recent...
Tetrahedral C60F36 is shown by its single-crystal X-ray structure to be the most aromatic (and disto...
Unconventional fullerenes are those smaller than C-60 or those intermediate between C-60 and C-70, w...
Under Birch reduction conditions, $C_{60}$ predominantly forms $C_{60}H_{36}$. Spectroscopic results...
The 1H NMR spectrum of the fulleroid C61H26- consists two high field doublets, providing experimenta...
The endohedral fullerene CH4@C60, in which each C60 fullerene cage encapsulates a single methane mol...
A single-crystal X-ray structure determination of the main isomer of C60F18O shows it to be an intra...
Reaction of freshly prepared C60Cl6 (from chlorination of [60]fullerene by ICI in benzene) with meth...
From the reaction of [60]fullerene with K2PtF6 at 470 degreesC, we have isolated C60F4, C60F6 (mixed...
[[abstract]]We present the results of a semiempirical study of C60 (Ih, D6h, C3v, C3, D5), C76 (Td, ...
We describe the existence and structure of large fullerenes in terms of symmetry breaking of the C60...
Fullerenes, the highly symmetric molecular carbon clusters, have been in the limelight of scientific...
Benkeser reduction was used to synthesize highly hydrogenated fullerenes, C60H36, C60H38, C 60H40, C...
Fluorination of C-60 at 550 degrees C leads to milligram quantities of two stable fullerene derivati...
Isomers of the higher fullerenes were analyzed using 3He NMR spectroscopy. Structures have been assi...
Density functional calculations accurately reproduce the known bond lengths for C60F18, shown recent...
Tetrahedral C60F36 is shown by its single-crystal X-ray structure to be the most aromatic (and disto...
Unconventional fullerenes are those smaller than C-60 or those intermediate between C-60 and C-70, w...
Under Birch reduction conditions, $C_{60}$ predominantly forms $C_{60}H_{36}$. Spectroscopic results...
The 1H NMR spectrum of the fulleroid C61H26- consists two high field doublets, providing experimenta...
The endohedral fullerene CH4@C60, in which each C60 fullerene cage encapsulates a single methane mol...
A single-crystal X-ray structure determination of the main isomer of C60F18O shows it to be an intra...
Reaction of freshly prepared C60Cl6 (from chlorination of [60]fullerene by ICI in benzene) with meth...
From the reaction of [60]fullerene with K2PtF6 at 470 degreesC, we have isolated C60F4, C60F6 (mixed...
[[abstract]]We present the results of a semiempirical study of C60 (Ih, D6h, C3v, C3, D5), C76 (Td, ...
We describe the existence and structure of large fullerenes in terms of symmetry breaking of the C60...
Fullerenes, the highly symmetric molecular carbon clusters, have been in the limelight of scientific...
Benkeser reduction was used to synthesize highly hydrogenated fullerenes, C60H36, C60H38, C 60H40, C...
Fluorination of C-60 at 550 degrees C leads to milligram quantities of two stable fullerene derivati...