Front Cover: Synthesis of Isomerically Pure Multi‐aniline C 60  Adducts with Cyclopentadienyl Addition Pattern (Eur. J. Org. Chem. 18/2016) | Zendy

Liang Sisi | Zendy; Xu Liang | Zendy; Gan Liangbing | Zendy

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Front Cover: Synthesis of Isomerically Pure Multi‐aniline C 60 Adducts with Cyclopentadienyl Addition Pattern (Eur. J. Org. Chem. 18/2016)

Author(s) -

Liang Sisi,

Xu Liang,

Gan Liangbing

Publication year - 2016

Publication title -

european journal of organic chemistry

Language(s) - English

Resource type - Reports

SCImago Journal Rank - 0.825

H-Index - 155

eISSN - 1099-0690

pISSN - 1434-193X

DOI - 10.1002/ejoc.201670181

Subject(s) - chemistry , buckminsterfullerene , pentalene , adduct , derivative (finance) , cyclopentadienyl complex , aniline , fullerene , front cover , sulfur , nitrogen , medicinal chemistry , organic chemistry , cover (algebra) , molecule , catalysis , mechanical engineering , engineering , financial economics , economics

The cover picture shows space‐filling model of a Buckminsterfullerene (or Bucky ball C 60 ) derivative with five anilino groups around a pentagon and a benzenesulfonamido group on the center pentagon. The phenyl groups are red, nitrogen atoms are blue, sulfur and oxygen atoms are yellow. The anilino C 60 derivative was prepared by a BiCl 3 ‐mediated replacement reaction of a C 60 derivative containing secondary amino addends. Details are discussed in the article by L. Gan et al. on p. 3070 ff .

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