The absorption and emission of 4-(N,N-dimethylarnino)benzonitrile (DMABN) in a-cyclodextrine (a-CD) cavities is reported. The twisted intramolecular charge transfer emission is enhanced on complexation with a-CD. This is attributed to the reduced polarity of the CD environment.
Normal and twisted intramolecular charge-transfer fluorescence of 4-dimethylaminobenzonitrile in α-cyclodextrine cavities
✍ Scribed by Khader A. Al-Hassan; Uwe K.A. Klein; A. Suwaiyan
- Publisher
- Elsevier Science
- Year
- 1993
- Tongue
- English
- Weight
- 501 KB
- Volume
- 212
- Category
- Article
- ISSN
- 0009-2614
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✦ Synopsis
Dual fluorescence of 4dimethylaminobenzonitrile (DMABN) has been used to study the behavior of DMABN in a-cyclodextrine (a-CD). Results obtained indicate that DMABN in an aqueous a-CD solution probably exists in three different environmental conditions; polar, slightly polar and hydrophobic. DMABN surrounded by water molecules represents the most polar and least rigid environment. DMABN molecules have two different possible positions inside the CC-CD cavity. The first position could arise when the dimethylamino group of the DMABN molecule is headed towards the larger rim of the a-CD cavity representing the slightly polar and slightly rigid environment. The second position could arise when the dimethylamino group of the DMABN molecule is headed towards the smaller rim ofthe a-CD cavity representing the least polar and most rigid environment. Therefore, it is suggested that the relative positions and contributions of the two fluorescence bands of DMABN in a-CD are determined by restricted molecular motion (controlled by the polarity and free volume of the a-CD cavity) rather than by the polarity alone.
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