“…1 H NMR (300 MHz, DMSO- d 6 ), δ (TMS, ppm): 1.02 (m, 183H, OCH 2 CH(C H 3 )), 3.28–3.33 (m, 28H, H 2 and H 4 of β-CD), 3.45 (m, 122H, OC H 2 CH(CH 3 )), 3.55 (m, 1022H, OC H 2 C H 2 O of EPE and H 5 of β-CD), 3.60–3.64 (m, 28H, H 3 and H 6 of β-CD), 4.44 (t, 12H, primary hydroxyl of β-CD), 4.82 (d, 14H, H l of β-CD), 5.65–5.70 (m, 28H, secondary hydroxyl of β-CD), 6.90–7.20 (br, 6H, Ar– H ), 7.93 (s, 4H, ArN H COO). 1 H NMR spectra of EPE-CD agreed with literature data . FT-IR (KBr): υ (cm –1 ) 2880 (C–H stretching), 1964, 1727(C–H scissoring of phenyl ring), 1466, 1348, 1281, and 1241 (C–H scissoring), 1095 (C–O stretching).…”