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Hydrogen Bonding and Protonation Effects on Excited-state Electron Transfer in meta and para-Dialkylaminopyridines

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Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Synthetic, spectral and photophysical investigations were performed for a series of dialkylaminopyridines (DAAPs) representing electron donor-acceptor systems. 4-Dimethyl aminopyridine and its analogues, substituted by an electron donor at the para position of the acceptor ring, show solvent-dependent dual luminescence from the substrate (primary excited state) and the product (TICT state) of the photoinduced electron transfer process. The investigations in mixed solvents (n-hex ane + 1-butanol) allow us to prove that dual luminescence is observed for 1:1 complexes of 4-DAAPs with the alcohol molecule hydrogen-bonded to the pyridine nitrogen atom. Contrary to 4-DAAPs, the electronic structure and geometry of the fluorescent CT state of 3-diisopropyl amino-pyridine are solvent-dependent (this 1CT state does not correspond to a full separation of charges). The spectroscopic and photophysical properties of the protonated forms of DAAPs are also presented. It is note worthy that the monocations of 4-diisopropyl-aminopyridine exhibit TICT fluorescence.
Rocznik
Strony
847--864
Opis fizyczny
Bibliogr. 48 poz., rys.
Twórcy
autor
autor
  • Institute of Physical Chemistry, Polish Academy of Sciences, Kasprzaka 44/52, 01-224 Warsaw, Poland, herbich@ichf.edu.pl
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Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BUJ6-0024-0098
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