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Steady State and Time Resolved Fluorescence Studies of Anthrylacrylic Ester

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Figure

Figure 1. (a) Ground state conformers at room temperature (at very low energy) [Orientation of the carbonyl group with respect to double bond is different, it can be S-Cis or it can be S-Trans]; (b) Excited state geometric isomers (Cis- Trans isomers are d
Figure 2. Absorption spectra of Anthrylacrylic ester at 1 nol; (4) Tetrahydrofuran; (5) Methanol; (6) Toluene; (7) Dio- xane; (8) Benzene; (9) Cyclohexane
Figure 6. Emission spectra of Anthrylacrylic ester in Ace-tonitrile as a function of excitation wavelength at 1 nm ( 10–5 mol·dm–3 (1) 320 nm (    ); (2) 340 nm (  ); (3) 360 ); (4) 380 nm (    ) and (5) 400 nm (  )
Table 2. Solvent shift data for Anthrylacrylic ester in various solvents at 1  10–5 mol·dm–3
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