z-logo
open-access-imgOpen Access
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
Author(s) -
Ashe Arthur J.,
Kampf Jeff W.,
Savla Paresh M.
Publication year - 1994
Publication title -
heteroatom chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.283
H-Index - 42
eISSN - 1098-1071
pISSN - 1042-7163
DOI - 10.1002/hc.520050206
Subject(s) - chemistry , phenanthrene , sulfur , hexane , butyllithium , orange (colour) , ring (chemistry) , medicinal chemistry , organic chemistry , food science
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) Å, b = 8.933(2) Å, c = 9.601(4) Å, and β = 116.19 (2)°; while orange crystals of the dithiole form in P2 1 2 1 2 1 (#19) space group with Z = 4, a = 4.1507(5) Å, b = 14.436(3) Å, and c = 16.972(3) Å. Full structures have been determined for both compounds.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom