Palazzo, Teresa A. Patra, Digambara Yang, Joung S. Khoury, Elsy El Appleton, Mackenzie G. Haddadin, Makhluf J. Tantillo, Dean J. Kurth, Mark J. Dibenzonaphthyridinones: Heterocycle-to-Heterocycle Synthetic Strategies and Photophysical Studies A heterocycle-to-heterocycle strategy is presented for the preparation of highly fluorescent and solvatochromic dibenzo­naph­thyridinones (DBNs) via methodology that leads to the formation of a tertiary, spiro-fused carbon center. A linear correlation between the results of photophysical experiments and time dependent density functional theory calculations was observed for the λ<sub>max</sub> of excitation for DBNs with varying electronic character. dibenzo;Strategy;theory calculations;StudiesA;density;strategy;methodology;solvatochromic;excitation;photophysical experiments;λ max;formation;center;DBN;preparation;Photophysical;correlation;Dibenzonaphthyridinone 2015-12-04
    https://acs.figshare.com/articles/journal_contribution/Dibenzonaphthyridinones_Heterocycle_to_Heterocycle_Synthetic_Strategies_and_Photophysical_Studies/2102947
10.1021/acs.orglett.5b02680.s001