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Analytical data for macrocycle 8: 1H NMR (CDCl 3, 400 MHz, δ, 8.30 (d, 3J, 8 Hz, 2 H, 8.25 (d, 3J, 4 Hz, 2 H, 7.82 (d, 3J, 8 Hz, 2 H, 7.75 (s, 2 H, 7.36 (d, 3J, 4 Hz, 2 H, 7.05 (s, 4 H, 2.60-2.82 (m, 16 H, 1.79 (brs, 1.69-1.43 (m, 32 H, 0.89-0.99 ppm (m, 24 H, m/z calcd for [M+H, C80H 87N2S8, 1331.4629; found: 1331.6 [M+H, MALDI-TOF-MS, 1331.4693 [M+H, HRMS (ESI-FTICR, UV/Vis (CH2Cl2, λ max, 413 nm (ε, 8.9 × 104 L mol-1 cm-1, Analytical data for catenane 12: 1H NMR (CDCl3, 400 MHz, δ, 8.22 (d, 3J, 4 Hz, 4 H, 8.13 (d, 3J, 8 Hz, 4 H, 7.79 (d, 3J, 8 Hz, 4 H, 7.48 s, 4 H
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-1).
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According to calculations, a fully coplanar conformation of macrocycle 8 could be achieved by an anti arrangement of one inner thiophene ring, thus leading to a nonsymmetric structure.
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According to calculations, a fully coplanar conformation of macrocycle 8 could be achieved by an anti arrangement of one "inner" thiophene ring, thus leading to a nonsymmetric structure.
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