Abstract:
A series of expanded corroles containing electron donating and electron withdrawing groups on the opposite meso-phenyl groups have been synthesized through a simple [3 + 2] oxidative coupling reaction of a tripyr-rane containing electron donating group (-OMe, -Me) and dipyrromethane containing an electron withdrawing group (-NO2, -CN) in moderate yields. The photophysical studies reveal decrease in singlet lifetimes and quantum yields relative to normal corrole. The quantum yield, lifetime and Stokes shift depend on the nature of solvent and the largest Stokes shifts are observed in the polar solvents, suggesting a polar nature of the excited state. The molecular first hyperpolarizability (beta) measured for expanded corroles shows moderate values (24-30 x 10(-30) esu). These values are approximately 5-6 times larger than those observed for structurally similar 18 a substituted tetraphenyl porphyrins, revealing that the nonlinear optical (NLO) response can be increased by increasing the number of pi electrons in conjugation. An attempt has been made to correlate the observed beta values with structure of the molecule and orientation of donor acceptor groups. The single crystal X-ray structure of 13 and 14 reveals nonplanarity of macrocycle and the dihedral angles between the macrocyclic pi system and the meso-aryl rings vary in the range of (33-75 degrees) preventing an effective charge transfer interaction between the donor and acceptor groups required for observation of large beta value. Formation of supramolecular ladder type structure for Compound 13 through noncovalent C-(HO)-O-... hydrogen bonding interactions is also described.
