New mesomorphic benzothiazol derivatives:Synthesis and characterization
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关键词:
- Benzothiazole
- / Nematic
- / Smectic C
- / Mesomorphic
English
New mesomorphic benzothiazol derivatives:Synthesis and characterization
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Key words:
- Benzothiazole
- / Nematic
- / Smectic C
- / Mesomorphic
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[17] Analytical and spectroscopic data for the representative compound C2H5O-9BSPEP: EI-MS m/z (rel. int. %): 544 (22) [M+], 247 (100), IR vmax (KBr, cm-1): v 3056 (C-H aromatic); 2922, 2851 (C-H aliphatic); 1740 (C5O ester); 1609 (C5N thiazole), 1273 (C-O, aromatic ether) 1H NMR (400 MHz, CDCl3): d 0.9 (t, 3H, J = 6.6 Hz, CH3-), 1.3 (m, 10H, CH3-(CH2)5-(CH2)3-O-), 1.4 (t, 3H, J = 6.8 Hz, CH3-CH2-O-), 1.5 (p, 2H, J = 6.1 Hz,-CH2-CH2-CH2-O-), 1.8 (p, 2H, J = 7.1 Hz,-CH2-CH2-O-), 4.0 (t, 2H, J = 6.6 Hz,-CH2-O-), 4.1 (t, 2H, J = 7.1 Hz, CH3-CH2-O-), 7.0 (d, 2H, J = 8.8 Hz, Ar-H), 7.1 (d, 1H, J = 9.0 Hz, Ar-H), 7.3 (s, 1H, Ar-H), 7.4 (d, 2H, J = 8.6 Hz, Ar-H), 7.9 (d, 1H, J = 8.8 Hz, Ar-H), 8.1 (d, 2H, J = 8.6 Hz, Ar-H), 8.2 (d, 2H, J = 8.8 Hz, Ar-H), 9.0 (s, 1H,-N5CH-); 13C NMR (100 MHz, CDCl3): δ 14.23 (CH3-), 14.94 (CH3-CH2O-), 15.01, 22.77, 26.07, 29.17, 29.35, 29.46, 29.61, 31.97 for methylene carbons (CH3-(CH2)8-), 64.18 (-CH2O-), 68.47 (CH3-CH2O-), 105.14, 114.50, 116.22, 121.06, 122.70, 123.85, 131.44, 132.50, 133.98, 135.93, 146.06, 154.91, 156.04, 157.18 for aromatic carbons, 163.88 (N=CH, Schiff base), 164.47 (N=C, thiazole), 169.20 (-COO-). Anal. calcd. for C32H36N2O4S: C, 70.56, H, 6.66, N, 5.14; Found: C, 70.48, H, 6.74, N, 5.03.[17] Analytical and spectroscopic data for the representative compound C2H5O-9BSPEP: EI-MS m/z (rel. int. %): 544 (22) [M+], 247 (100), IR vmax (KBr, cm-1): v 3056 (C-H aromatic); 2922, 2851 (C-H aliphatic); 1740 (C5O ester); 1609 (C5N thiazole), 1273 (C-O, aromatic ether) 1H NMR (400 MHz, CDCl3): d 0.9 (t, 3H, J = 6.6 Hz, CH3-), 1.3 (m, 10H, CH3-(CH2)5-(CH2)3-O-), 1.4 (t, 3H, J = 6.8 Hz, CH3-CH2-O-), 1.5 (p, 2H, J = 6.1 Hz,-CH2-CH2-CH2-O-), 1.8 (p, 2H, J = 7.1 Hz,-CH2-CH2-O-), 4.0 (t, 2H, J = 6.6 Hz,-CH2-O-), 4.1 (t, 2H, J = 7.1 Hz, CH3-CH2-O-), 7.0 (d, 2H, J = 8.8 Hz, Ar-H), 7.1 (d, 1H, J = 9.0 Hz, Ar-H), 7.3 (s, 1H, Ar-H), 7.4 (d, 2H, J = 8.6 Hz, Ar-H), 7.9 (d, 1H, J = 8.8 Hz, Ar-H), 8.1 (d, 2H, J = 8.6 Hz, Ar-H), 8.2 (d, 2H, J = 8.8 Hz, Ar-H), 9.0 (s, 1H,-N5CH-); 13C NMR (100 MHz, CDCl3): δ 14.23 (CH3-), 14.94 (CH3-CH2O-), 15.01, 22.77, 26.07, 29.17, 29.35, 29.46, 29.61, 31.97 for methylene carbons (CH3-(CH2)8-), 64.18 (-CH2O-), 68.47 (CH3-CH2O-), 105.14, 114.50, 116.22, 121.06, 122.70, 123.85, 131.44, 132.50, 133.98, 135.93, 146.06, 154.91, 156.04, 157.18 for aromatic carbons, 163.88 (N=CH, Schiff base), 164.47 (N=C, thiazole), 169.20 (-COO-). Anal. calcd. for C32H36N2O4S: C, 70.56, H, 6.66, N, 5.14; Found: C, 70.48, H, 6.74, N, 5.03.
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