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Two bis urea based acyclic receptors (1 and 2) containing two pyridyl moieties with different spacers are synthesized. These receptors are further transformed to metallo-macrocyclic receptors (3 and 4) by coordinating with metal center through pyridine ring ‘N’. The binding-behavior as well as selectivity of the receptors towards anions upon metal coordinated cyclization is studied and the results are compared with parent acyclic receptors. Receptors 2 and 4 containing a naphthalene moiety as a spacer as well as a fluorophore behave as ‘on-off’ sensors towards anions.