| Literature DB >> 26574652 |
Teresa A Palazzo1, Digambara Patra2, Joung S Yang1, Elsy El Khoury2, Mackenzie G Appleton1, Makhluf J Haddadin2, Dean J Tantillo1, Mark J Kurth1.
Abstract
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(max) of excitation for DBNs with varying electronic character.Entities:
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Year: 2015 PMID： 26574652 PMCID： PMC4816217 DOI： 10.1021/acs.orglett.5b02680
Source DB: PubMed Journal: Org Lett ISSN： 1523-7052 Impact factor: 6.005