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
dc.contributor.author | Ashe, Arthur J. | en_US |
dc.contributor.author | Kampf, Jeffrey W. | en_US |
dc.contributor.author | Savla, Paresh M. | en_US |
dc.date.accessioned | 2006-04-28T17:04:39Z | |
dc.date.available | 2006-04-28T17:04:39Z | |
dc.date.issued | 1994-04 | en_US |
dc.identifier.citation | Ashe, Arthur J.; Kampf, Jeff W.; Savla, Paresh M. (1994)."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." Heteroatom Chemistry 5(2): 113-119. <http://hdl.handle.net/2027.42/38566> | en_US |
dc.identifier.issn | 1042-7163 | en_US |
dc.identifier.issn | 1098-1071 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/38566 | |
dc.description.abstract | 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. | en_US |
dc.format.extent | 576864 bytes | |
dc.format.extent | 3118 bytes | |
dc.format.mimetype | application/pdf | |
dc.format.mimetype | text/plain | |
dc.language.iso | en_US | |
dc.publisher | VCH Publishers, Inc. | en_US |
dc.publisher | Wiley Periodiocals, Inc. | en_US |
dc.subject.other | Chemistry | en_US |
dc.title | 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 | en_US |
dc.type | Article | en_US |
dc.rights.robots | IndexNoFollow | en_US |
dc.subject.hlbsecondlevel | Biological Chemistry | en_US |
dc.subject.hlbsecondlevel | Chemical Engineering | en_US |
dc.subject.hlbsecondlevel | Chemistry | en_US |
dc.subject.hlbsecondlevel | Materials Science and Engineering | en_US |
dc.subject.hlbtoplevel | Health Sciences | en_US |
dc.subject.hlbtoplevel | Science | en_US |
dc.subject.hlbtoplevel | Engineering | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | Department of Chemistry, The University of Michigan, Ann Arbor, MI 48109–1055 ; Department of Chemistry, The University of Michigan, Ann Arbor, MI 48109–1055 | en_US |
dc.contributor.affiliationum | Department of Chemistry, The University of Michigan, Ann Arbor, MI 48109–1055 | en_US |
dc.contributor.affiliationum | Department of Chemistry, The University of Michigan, Ann Arbor, MI 48109–1055 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/38566/1/520050206_ftp.pdf | en_US |
dc.identifier.doi | http://dx.doi.org/10.1002/hc.520050206 | en_US |
dc.identifier.source | Heteroatom Chemistry | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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