Synthesis and identification of Heterocyclic derivatives of fullerene C-60: Unexpected reaction of anionic C-60 with benzonitrile


Autoria(s): Zheng M; Li FF; Ni L; Yang WW; Gao X
Data(s)

2008

Resumo

During the reaction of reduced C-60 with benzyl bromide in benzonitrile, a novel cis-1 C-60 adduct, 1,4-dibenzyl-2,3-cyclic phenylimidate C-60 (1), Was obtained rather than the expected product of 1,4-dibenzyl C-60. The structure of compound 1 was analyzed by X-ray single-crystal diffraction, identifying the presence of a five-membered heterocycle at a [5,6] bond of C-60. One of the heteroatoms is assigned as a nitrogen atom; however, the identity of the other heteroatom cannot be determined unambiguously by crystallography due to similarity between the nitrogen and oxygen atoms.

Identificador

http://ir.ciac.jl.cn/handle/322003/11061

http://www.irgrid.ac.cn/handle/1471x/147772

Idioma(s)

英语

Fonte

Zheng M;Li FF;Ni L;Yang WW;Gao X.Synthesis and identification of Heterocyclic derivatives of fullerene C-60: Unexpected reaction of anionic C-60 with benzonitrile,JOURNAL OF ORGANIC CHEMISTRY,2008,73(8 ):3159-3168

Palavras-Chave #EFFICIENT PHOTOCURRENT GENERATION #DONOR-ACCEPTOR HETEROJUNCTIONS #SELF-ASSEMBLED MONOLAYERS #SOLUTION-PHASE GENERATION #ELECTRON-TRANSFER #REDUCTIVE ELECTROCHEMISTRY #2ND-HARMONIC GENERATION #BIOLOGICAL APPLICATIONS #CHEMICAL GENERATION #PHOTOVOLTAIC CELLS
Tipo

期刊论文