Geometrical and electronic cooperativity in cation-mediated electrochemical reductions of anthraquinone-substituted podands
β Scribed by Deborah A Gustowski; Milagros Delgado; Vincent J Gatto; Luis Echegoyen; George W Gokel
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- French
- Weight
- 212 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Unlike their nitroaromatic counterparts, podands based upon the anthraquinone skeleton bind cations more strongly when reduced because of a combination of geometrical and electronic factors.
We wish to report the first example of an electrochemically switched anthraquinone podand, the success of which can be attributed to a combination of electronic and geometrical factors.
L.: Goli.
π SIMILAR VOLUMES
The oxidation and reduction potentials of a series of related even non-alternant derivatives of 7,14-disubstituted acenaphth[1,2-k] fluoranthenes, and also fluoranthene, 7,10-diphenylfluoranthene and 8,9-dihydrodiindeno[1,2-j;2Π,1Π-] fluoranthene, were determined in organic solvents by cyclic voltam