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Beilstein J. Org. Chem. 2010, 6, 932–937, doi:10.3762/bjoc.6.104
Graphical Abstract
Scheme 1: Preparation of the four [2.2]paracyclophane dialdehydes 4 by cycloaddition (ps - pseudo).
Scheme 2: Spin systems of the CH2CH2 protons in the isomeric dialdehydes 4. Protons at C-9 and C-10 in ps-gem...
Figure 1: CH2CH2 regions of the 600 MHz 1H NMR spectra of the isomeric dialdehydes 4, a: ps-gem, b: ps-meta, ...
Scheme 3: NOEs observed for ps-ortho-4 when the 5-H resonance is irradiated.
Beilstein J. Org. Chem. 2009, 5, No. 20, doi:10.3762/bjoc.5.20
Figure 1: Schematic representation of a photochromic system. The reverse reaction can be a photochemical or t...
Figure 2: Photochromic reaction of pseudo-gem disubstituted tetraene [2.2]cyclophane 1 in acetonitrile, conc....
Figure 3: Molecular structure of 4,13-bis[(1E,3E)-4-(9-anthracenyl)-buta-1,3-dienyl][2.2]paracyclophane (2).
Scheme 1: Preparation of 2 (last step), using the Wittig reaction. The preparation of 3 has been described in...
Figure 4: Molecular structure of 2 in the crystal. Radii are arbitrary; only selected H atoms are shown.
Figure 5: Projection of the molecular structure of 2 exhibiting the closest internuclear distances (distances...
Figure 6: Electronic absorption spectra of 2 (conc. ca 10−4 M) in MCH (full line) and CH3CN (dotted line) at ...
Figure 7: Irradiation of 2 (2.6 × 10−5 M) in CH3CN at 400 nm at 20 °C. The spectra were recorded at various t...
Figure 8: Irradiation at 306 nm of the photoproduct 4 obtained at 400 nm in the same setup; the spectra were ...
Figure 9: Reversibility of the formation of the photoproduct 4 at 400 nm (40 min) and photodissociation of 4 ...
Figure 10: 1H NMR spectra (400 MHz, CDCl3). A: Compound 2, B: Compound 4.
Figure 11: Proposed structure of 4 (1,4 : 2′,3′-cycloadduct).