
Chemistry Letters p. 1333 - 1336 (1994)
Update date:2022-08-05
Topics:
Kawase, Takeshi
Ohsawa, Takeshi
Enomoto, Tetsuya
Oda, Masaji
2,3,4,5-Tetra(2-thienyl)cyclopentadienone and the related compounds, here first synthesized, show large bathochromic shift of visible absorptions and appreciably higher amphoteric redox properties than tetraphenylcyclopentadienone; 2-thienyl groups at 2,5-positions exert stronger substituent effects than those at 3,4-positions.
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