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N ‐Unsubstituted and N ‐Arylated Fulleropyrrolidines: New Useful Building Blocks for C 60 Functionalization †
Author(s) -
Tong ChenHua,
Wu ZongQuan,
Hou JunLi,
Li ZhanTing
Publication year - 2006
Publication title -
chinese journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.28
H-Index - 41
eISSN - 1614-7065
pISSN - 1001-604X
DOI - 10.1002/cjoc.200690220
Subject(s) - chemistry , chlorobenzene , toluene , surface modification , glycine , organic chemistry , fullerene , combinatorial chemistry , amino acid , catalysis , biochemistry
Two series of stable and soluble fulleropyrrolidines have been prepared from the reactions of C 60 , glycine or its N ‐arylated derivatives and aliphatic aldehydes or ketones in refluxing toluene or chlorobenzene. The new C 60 derivatives represent new useful building blocks for further preparation of more funcionalized C 60 derivatives.
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