Abstract Photophysical study of highly photoactive bis-2-benzylidenemalononitrile (BBM) has been investigated in solution using UV–vis, fluorescence and NMR spectroscopic techniques. The seletive photodissociation can be attributed to the presence of… Click to show full abstract
Abstract Photophysical study of highly photoactive bis-2-benzylidenemalononitrile (BBM) has been investigated in solution using UV–vis, fluorescence and NMR spectroscopic techniques. The seletive photodissociation can be attributed to the presence of highly polarized C C bond, attached to dicyno groups (CN). Nevertheless, the observed photodissociation of BBM is highly solvent specific and temperature sensitive. The product A (2-(4-formylbenzylidene)malononitrile), formed by the selective photodissociation of BBM under UV irradiation has been isolated and identified by NMR studies. The photodissociation followed the pseudo 1st order kinetics with a rate constant (k) 10−3-10-4.s-1. Moreover the mechanistic study of selective photodissociation of bis-2-benzylidenemalononitrile (BBM) has been investigated and found to follow the dipolar mechanism path during photochemical reaction.
               
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