Photophysical Characterization of a Benzo-Fused Analogue of Brooker’s Merocyanine: Solvent Polarity and pH Effects
2012
The photophysical properties of 4-[2-(6-hydroxy-2-naphthalenyl)-ethenyl]-1-methyl-pyridinium (HNEP+) and its deprotonated form (NEP), a benzofused derivative of Brooker’s merocyanine (BM), were investigated through a combined spectroscopic and computational approach. Despite their structural similarities and similar pKa values, HNEP+/NEP and BMH+/BM differ in the extent of charge delocalization in the ground and excited states. NEP exhibits the spectral characteristics of a charge transfer species in solvents in which BM exists in a charge-delocalized quinoid; however, quantum chemical calculations show that the CT absorption of NEP is not necessarily a consequence of the zwitterionic character. HNEP+ displays larger Stokes shifts than BMH+, and NEP demonstrates enhanced solvatochromism relative to BM as a consequence of benzofusion.
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