Corannulene polysulfides: Molecular bowls with multiple arms and flaps

被引:41
|
作者
Bancu, M
Rai, AK
Cheng, PC
Gilardi, RD
Scott, LT [1 ]
机构
[1] Boston Coll, Merkert Chem Ctr, Dept Chem, Chestnut Hill, MA 02467 USA
[2] USN, Lab Struct Matter, Washington, DC 20375 USA
关键词
nucleophilic aromatic substitutions; sulfur; arenes; polycycles; supramolecular chemistry;
D O I
10.1055/s-2003-44965
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Nucleophilic aromatic substitution of all the chlorine atoms in 1,3,5,7,9-pentachlorocorannulene and in decachloro-corannulene by sodium alkanethiolates gives 1,3,5,7,9- pentakis(1-alkylthio)corannulenes, C20H5(SR)(5), and decakis(1-alkylthio)corannulenes, C-20(SR)(10), respectively, with arms of varying lengths attached around the perimeter (R = n-propyl, n-hexyl, and n-dodecyl). The corresponding reaction of decachlorocorannulene with ortho-C6H4(SNa)(2) gives pentakis(1,4-benzodithiino)corannulene, a molecular bowl with 6 Angstrom flaps on all five sides. Such compounds represent attractive candidates for the formation of discotic liquid crystals and/or supramolecular complexes with fullerenes and other convex guests.
引用
收藏
页码:173 / 176
页数:4
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