THE REACTION OF SULFUR WITH DILITHIO COMPOUNDS - THE SYNTHESES AND STRUCTURES OF PHENANTHRO[1,10-CD]-1,2-DITHIOLE AND PHENANTHRO[4,5-CDE][1,2]DITHIIN

被引:34
作者
ASHE, AJ
KAMPF, JW
SAVLA, PM
机构
[1] Department of Chemistry, The University of Michigan, Ann Arbor, Michigan
关键词
D O I
10.1002/hc.520050206
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The sequential reaction of selected polycyclic aromatic hydrocarbons with butyllithium/TMEDA/hexane and sulfur allows preparation of ring-fused dithiins, dithioles, and thiophenes. In this manner, phenanthrene has been converted to phenanthro[4,5-cde][1,2]dithiin and phenanthro[1,10cd]-1,2-dithiole. Yellow crystals of the dithiin form in C2/c (#15) space group with Z = 4, a = 13.537(3) angstrom, b = 8.933(2) angstrom, c = 9.601(4) angstrom, and beta = 116.19 (2)-degrees; while orange crystals of the dithiole form in P2(1)2(1)2(1) (#19) space group with Z = 4, a = 4.1507(5) angstrom, b = 14.436(3) angstrom, and c = 16.972(3) angstrom. Full structures have been determined for both compounds.
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页码:113 / 119
页数:7
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