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Spectroscopic results of macrocycles 4-6 were shown as follows. 4: 80% yield; mp 124.5 °C; FTIR (KBr, cm1, 1480 (vs, tri-substituted benzene, 1213 (vs. C-N stretching, 1053 (s, C-O-C, 1 H NMR (400 MHz, CDCl3, δH 1.94 (3H, s, N-CH3, 2.11 (2H, t, CH2-CH2-CH2, 2.25 (12H, s, Ar-CH3, 3.62 (4H, s, Ar-CH2-N, 4.11 (4H, t, Ar-O-CH2, 6.79 (2H, s. Ar-H, 6.91 (2H, s, Ar-H, MALDI-TOF MS: m/z 340.23 [M+H, Anal. Calcd for C22H 29NO2: C, 77.84; H, 8.61; N, 4.13, Found: C, 77.63; H, 8.40; N, 4.12, 5: 76% yield; mp 172.8°C; FTIR (KBr, cm -1, 1481 (vs, tri-substituted benzene, 1213 (vs, C-N stretching, 1076 (s, C-O-C, 1HNMR (400MHz, CDCl3, δH 1.96 (3H, s, N-CH3, 2.00 (4H, t, O-CH 2-CH2, 2.25 15H, s, Ar-CH3
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3: C, 75.53; H, 8.87; N, 3.52%. Found: C, 75.24; H, 8.76; N, 3.49%.
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11
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67650420323
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Crystallographic data reported in this manuscript have been deposited with Cambridge Crystallographic Data Centre as supplementary publication number CCDC 671193 (4), 671194 (5), 692237 (6), and 692236 (7). Copies of the data can be obtained free of charge via www.ccdc.cam.ac.uk/conts/retrieving.html.
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Crystallographic data reported in this manuscript have been deposited with Cambridge Crystallographic Data Centre as supplementary publication number CCDC 671193 (4), 671194 (5), 692237 (6), and 692236 (7). Copies of the data can be obtained free of charge via www.ccdc.cam.ac.uk/conts/retrieving.html.
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