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Beilstein J. Org. Chem. 2020, 16, 2032–2045, doi:10.3762/bjoc.16.170
Graphical Abstract
Figure 1: Structures of investigated compounds stressing steric differences in linker length attached to the ...
Scheme 1: Synthesis of water-soluble naphthalene diimides 3a,b, and 5.
Figure 2: UV–vis absorption (solid line) and fluorescence spectra (dashed line) of NDI 3a,b, and 5 (c = 4.5 ×...
Figure 3: Calculations for Cl-NDI-NMe model compound (at the B3LYP/6-31+G** level of theory) in water (PCM). ...
Figure 4: (a) Melting curve of poly(dA-dT)2 alone and after the addition of NDI 3a,b, and 5 (r = 0.3 ([NDI]/[...
Figure 5: Changes in fluorescence intensity (spectra are normalized) of (a) 3a (c = 1.0 × 10−6 M), (b) 3b (c ...
Figure 6: Calorimetric titration of a poly(dG-dC)2 solution in sodium cacodylate buffer (pH 5.0) at 298 K wit...
Figure 7: CD titration of poly(dG-dC)2 (c = 2.0 × 10−5 M) with (a) 3a, (b) 3b, and (c) 5 with increasing mola...
Figure 8: Schematic representation of the alignment of the intercalating 3a (left) and 3b (right) between the...
Beilstein J. Org. Chem. 2010, 6, 1070–1078, doi:10.3762/bjoc.6.122
Scheme 1: Structure of the quarterthiophene derivative T1.
Scheme 2: Synthetic route to T1. Reagent and conditions: a) Boc anhydride, CH2Cl2, 6 h, 0 °C–rt, 97%; b) NBS,...
Figure 1: AFM height images of a film spin-coated from diluted gel solution of T1 in MCH (2 × 10−3 M) onto HO...
Figure 2: a) UV-vis spectra of T1 in chloroform (dashed line) and n-heptane (solid line); b) UV-vis spectra o...
Scheme 3: Proposed mode of self-assembly of T1.
Figure 3: UV-vis spectra of T1 (concentration 5 x 10−5 M) in cyclohexane (solid line) and 2.4% MeOH in cycloh...
Figure 4: AFM height images (A and B) of a film spin-coated from MCH solution (concentration 5 x 10−4 M) of a...
Figure 5: Variation of dose-normalized conductivity transients (Δσ/D) with time for T1.