10.1021/acs.orglett.5b02680.s001
Teresa
A. Palazzo
Teresa
A.
Palazzo
Digambara Patra
Digambara
Patra
Joung S. Yang
Joung S.
Yang
Elsy El Khoury
Elsy El
Khoury
Mackenzie G. Appleton
Mackenzie G.
Appleton
Makhluf J. Haddadin
Makhluf J.
Haddadin
Dean J. Tantillo
Dean J.
Tantillo
Mark J. Kurth
Mark J.
Kurth
Dibenzonaphthyridinones: Heterocycle-to-Heterocycle
Synthetic Strategies and Photophysical Studies
American Chemical Society
2015
dibenzo
Strategy
theory calculations
StudiesA
density
strategy
methodology
solvatochromic
excitation
photophysical experiments
λ max
formation
center
DBN
preparation
Photophysical
correlation
Dibenzonaphthyridinone
2015-12-04 00:00:00
Journal contribution
https://acs.figshare.com/articles/journal_contribution/Dibenzonaphthyridinones_Heterocycle_to_Heterocycle_Synthetic_Strategies_and_Photophysical_Studies/2102947
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.