| Abstract
| - Spectroscopic properties for a series of 2,5-diarylidenecyclopentanones in weak and strong acid environmentsare reported. Electronic absorption and fluorescence spectra have been measured for the all-E configurationsof 2,5-dibenzylidenecyclopentanone (1), 2,5-bis(3-phenylallylidene)cyclopentanone (2), and 2,5-bis(5-phenylpenta-2,4-dienylidene)cyclopentanone (3) in acetic acid and sulfuric acid solutions. The spectroscopicevidence indicates that in 96% sulfuric acid 1, 2, and 3 are protonated both in the ground state and on the S1potential energy surface. This assignment is supported by Zerner's intermediate neglect of differential overlap(ZINDO) and time-dependent density functional theory (TD-DFT) calculations. In glacial acetic acid, 1, 2,and 3 are unprotonated in the ground state. The absence of observable fluorescence from 1 in glacial aceticacid indicates that S1 is nπ*, whereas the observation of fluorescence from 2 and 3 in acetic acid is consistentwith S1 being ππ*. A combination of spectroscopic data, molecular orbital calculations, and fluorescencelifetime measurements indicate that 2 and 3 undergo intermolecular excited-state proton transfer in glacialacetic acid and diluted sulfuric acid solutions. Photochemical studies reveal that, unlike its behavior in organicsolvents, 1 does not undergo efficient E,E → E,Z photoisomerization in 96% sulfuric acid.
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