“…2924, 2853, 2131, 1689, 1595, 1463, 1392, 1379, 1316. (1E,1'E)-1,1'-(5-azido-1,3-phenylene)bis(N-(1,10-phenanthrolin-5-yl)methanimine) (11): The compound 11 was synthesised using asimilar procedure reported in literature with some modifications. [37] Compound 10 (100 mg, 0.57 mmol) and 8 (330 mg, 1.71 mmol) were stirred in 10 mL dry MeOH under reflux and overnight with catalytic amount of glacial acetic acid. Afterwards, ah ot filtration was performed.…”