Effect of Addition Pattern on the Electrochemical and Spectroscopic Properties of Neutral and Reduced 1,2- and 1,4-(C6H5CH2)2C60 Isomers
- 30 March 2000
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Physical Chemistry A
- Vol. 104 (17) , 3878-3883
- https://doi.org/10.1021/jp993708c
Abstract
No abstract availableThis publication has 46 references indexed in Scilit:
- Formation of C60Adducts with Two Different Alkyl Groups via Combination of Electron Transfer and SN2 ReactionsJournal of the American Chemical Society, 1998
- Synthesis and Spectroscopic and Electrochemical Characterization of Di- and Tetrasubstituted C60 DerivativesThe Journal of Physical Chemistry A, 1998
- Theoretical studies of derivatized buckyballs and buckytubesTetrahedron, 1996
- Covalent Fullerene ChemistryScience, 1996
- Chemical Generation of C602- and Electron Transfer Mechanism for the Reactions with Alkyl BromidesThe Journal of Physical Chemistry, 1996
- An Unusual Addition−Rearrangement of a Dialkoxycarbene to C60: Exclusion of Methanofullerene ProductsThe Journal of Organic Chemistry, 1996
- Reaction of [60]fullerene with morpholine and piperidine: preferred 1,4-additions and fullerene dimer formationJournal of the Chemical Society, Chemical Communications, 1995
- Silylmethylations of C60 with Grignard Reagents: Selective Synthesis of HC60CH2SiMe2Y and C60(CH2SiMe2Y)2 with Selection of SolventsThe Journal of Organic Chemistry, 1994
- Selective electrosynthesis of dimethylfullerene [(CH3)2C60]: a novel method for the controlled functionalization of fullerenesJournal of the American Chemical Society, 1993
- Semiempirical calculations of dihydrogenated buckminsterfullerenes, C60H2The Journal of Physical Chemistry, 1992