Alphabet-Inspired Design of (Hetero)Aromatic Push-Pull Chromophores
Status PubMed-not-MEDLINE Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
27272649
DOI
10.1002/tcr.201600032
Knihovny.cz E-resources
- Keywords
- chromophores, conjugation, donor-acceptor systems, photochemistry, structure-activity relationships,
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Push-pull molecules represent a unique and fascinating class of organic π-conjugated materials. Herein, we provide a summary of their recent extraordinary design inspired by letters of the alphabet, especially focusing on H-, L-, T-, V-, X-, and Y-shaped molecules. Representative structures from each class were presented and their fundamental properties and prospective applications were discussed. In particular, emphasis is given to molecules recently prepared in our laboratory with T-, X-, and Y-shaped arrangements based on indan-1,3-dione, benzene, pyridine, pyrazine, imidazole, and triphenylamine. These push-pull molecules turned out to be very efficient charge-transfer chromophores with tunable properties suitable for second-order nonlinear optics, two-photon absorption, reversible pH-induced and photochromic switching, photocatalysis, and intercalation.
References provided by Crossref.org
Ferrocene donor linked to pyridine/pyridinium acceptor via a systematically enlarged π-linker