Preparation and Optical and Electrochemical Properties of Phthalocyanines with the Ttf Unit

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• 4 dark green powder; mp. 280 °C (decomp); 1H NMR (500 MHz, CDCl3) δ 0.17 (br, 2H), 0.76 (t, J = 6.5 Hz, 24H, CH3), 1.09–1.22 (m, 48H), 1.22–1.33 (m, 16H), 1.42–1.53 (m, 16H, CH2), 1.87–1.96 (m, 16H, CH2), 2.51 (s, 24H, SCH3), 4.19–4.37 (m, 16H, CH2Ar); MALDI-TOF-MS (m/z) 2842.451 [M+]; Anal. Calcd for C120H162N8S24: C, 57.97; H, 6.57; N, 4.51%. Found: C, 57.95; H, 6.47; N, 4.51%; 5: mp 285 °C (decomp); 1H NMR (500 MHz, CDCl3) δ –3.71 (s, 2H, NH), 0.84 (t, J = 6.9 Hz, 6H, CH3), 0.93–1.07 (m, 18H, CH3), 1.16–1.60 (m, 56H, CH2), 1.60–1.70 (m, 12H, CH2), 1.70–1.78 (m, 4H, CH2), 1.78–1.94 (m, 12H, CH2), 2.15–2.32 (m, 12H, CH2), 2.60 (s, 6H, SCH3), 3.43–3.99 (m, 4H, CH2), 4.29 (br, 4H, OCH2), 4.52–4.71 (m, 8H, OCH2), 7.94 (br, 2H, ArH), 8.43 (br, 2H, ArH), 8.46 (br, 2H, ArH); MALDI-TOF-MS (m/z) 1775.575 [M+]; Anal. Calcd for C102H150N8O6S8: C, 68.95; H, 8.51; N, 6.31%. Found: C, 68.90; H, 8.54; N, 6.16%; 6: 1H NMR (500 MHz, CDCl3) δ 0.19 (s, 2H, NH), 0.67 (t, J = 6.9 Hz, 6H, CH3), 0.79–0.86 (m, 18H, CH3), 0.86–1.70 (m, 80H, CH2), 2.01 (quint, J = 7.3 Hz, 4H, CH2), 2.19 (quint, J = 7.3 Hz, 8H, CH2), 2.26 (quint, J = 7.3 Hz, 4H, CH2), 2.51 (s, 6H, SCH3), 4.63 (t, J = 7.3 Hz, 4H, CH2), 4.67 (t, J = 7.3 Hz, 4H, CH2), 4.84 (t, J = 7.3 Hz, 8H, CH2), 7.52 (d, J = 7.9 Hz, 2H, ArH), 7.585 (d, J = 7.9 Hz, 2H, ArH), 7.593 (s, 2H, ArH); MALDI-TOF-MS (m/z) 1774.173 [M+]
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