Two mono meso-functionalized [20]di-[Formula: see text]-benzihomoporphyrins containing [Formula: see text]-formylphenyl and [Formula: see text]-iodophenyl groups at meso-position respectively were synthesized by condensing one equivalent of appropriate tetrapyrrane with one equivalent of [Formula: see text]-formyl benzaldehyde/[Formula: see text]-iodo benzaldehyde in CH2Cl2 under mild acid catalyzed conditions. The meso-formylphenyl and meso-iodophenyl functionalized di-[Formula: see text]-benzihomoporphyrins were used to synthesize two covalently linked di-[Formula: see text]-benzihomoporphyrins-BODIPY conjugates. The meso-formylphenyl-functionalized di-[Formula: see text]-benzihomoporphyrin was converted to corresponding meso-dipyrrolyl substituted di-[Formula: see text]-benzihomoporphyrin by treating with excess pyrrole under acid catalyzed conditions. In the next step, the meso-dipyrrolyl di-[Formula: see text]-benzihomoporphyrin was subjected to oxidation followed by BF2 complexation to afford the directly linked di-[Formula: see text]-benzihomoporphyrin-BODIPY conjugate. The meso-iodophenyl functionalized di-[Formula: see text]-benzihomoporphyrin was coupled with ethynyl-functionalized BODIPY under mild Pd(0) coupling condition to synthesize diphenylethyne-bridged di-[Formula: see text]-benzihomoporphyrin-BODIPY conjugate. The two conjugates were characterized by HR-MS, NMR, absorption, electrochemical, fluorescence and DFT studies. The spectral and electrochemical studies indicated that the two constituents, di-[Formula: see text]-benzihomoporphyrin and BODIPY units in the conjugates interact weakly and retain their individual characteristic features. DFT studies indicated a possibility of charge transfer between di-[Formula: see text]-benzihomoporphyrin and BODIPY units in conjugates.
