Abstract
Charge-transfer (CT) complexes formed between piperidine (Pip) as donor with monoiodobromide (IBr), 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ), 2,6-dichloroquinone-4-chloroimide (DCQ), and 2,6-dibromoquinone-4-chloroimide (DBQ), as acceptors have been studied spectrophotometrically. The synthesis and characterization of piperidine CT-complexes of monoiodobromide, [(Pip)(IBr)], 2,3-dichloro-5,6-dicyano-1,4-benzoquinone, [(Pip)(DDQ)], 2,6-dichloroquinone-4-chloroimide, [(Pip)(DCQ)] and 2,6-dibromoquinone-4-chloroimide, [(Pip)(DBQ)] were described. These complexes are readily prepared from the reaction of Pip with IBr, DDQ, DCQ and DBQ within CHCl3 solvent. IR, UV–Vis techniques and elemental analyses (CHN), characterize the four piperidine charge-transfer complexes. Benesi–Hildebrand and its modification methods were applied to the determination of association constant (K), molar extinction coefficient (ɛ).