m, 8 H, anthracene), 8.18 (m, 9 H, tolyl and anthracene), 8.05 (m, 6 H, tolyl and anthracene), 7.55 (m, 16 H, tolyl and anthracene), 6.32 (s, 2 H, -OCH 2 , peripheral), 5.65 (s, 4 H, -OCH 2 , axial), 2.75 (s, 9 H, CH 3 ); 13 C NMR (50 MHz, CDCl 3 , 258C, TMS): 63.4 (-OCH 2 , peripheral), 57.2 (-OCH
✦ LIBER ✦
Orientation Dependence of Energy Transfer in an Anthracene–Porphyrin Donor–Acceptor System
✍ Scribed by L. Giribabu; A. Ashok Kumar; V. Neeraja; Bhaskar G. Maiya
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 92 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0044-8249
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## Abstract We describe the preparation as well as a detailed photophysical study of Fmoc‐amino acid building blocks carrying different carbostyril (=quinolin‐2(1__H__)‐one) heterocycles as donors in a FRET (fluorescence‐resonance‐energy transfer) system in combination with a [Ru^II^(bathophenanthr