This search combines search strings from the content search (i.e. "Full Text", "Author", "Title", "Abstract", or "Keywords") with "Article Type" and "Publication Date Range" using the AND operator.
Beilstein J. Org. Chem. 2014, 10, 1006–1016, doi:10.3762/bjoc.10.100
Graphical Abstract
Figure 1: Phenothiazine–anthraquinone dyad 1, donor-only (2) and acceptor-only (3) models assembled by Ugi 4C...
Scheme 1: Ugi 4CR synthesis of donor–anthraquinone dyads 8.
Scheme 2: Ugi 4CR synthesis of donor-only reference systems 10.
Figure 2: Molecular structure of S(O)-1 (left) (30% ellipsoids, except for the CH3CH2 end of the hexyl group,...
Figure 3: Cyclic voltammogram of dyad 8c (recorded in CH2Cl2, T = 298 K, c (8c) = 0.1 mol·L−1, Pt working ele...
Figure 4: DFT-computed (B3LYP, 6-311G*) frontier molecular orbitals HOMO (bottom) and LUMO (top) of the pheno...
Figure 5: Normalized absorption spectra of the phenothiazine–anthraquinone dyad 8c (recorded in CH2Cl2, c (8c...
Figure 6: Absorption spectra of Do–anthraquinone dyads 8c (top) and 8e (bottom) with the corresponding refere...
Figure 7: Normalized absorption and emission spectra of Ugi-donor compounds 2 and 10 (recorded in CH2Cl2, T =...
Figure 8: Emission spectra of donor-only system 2 phenothiazine–anthraquinone dyads 8a,b (top), and the donor...