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NIR Absorbing Aromatic E-Ethylene Bridged Hexaphyrins (2.1.1.2.1.1): Synthesis, Characterization, and Protonation
Sumit Sahoo1, Maheshwari Horalavadi Mahadavaiah2, Dandamudi Usharani2
1School of Chemical Sciences, Indian Association for the Cultivation of Science, 2A/2B Raja S.C Mullick Road, Jadavpur, Kolkata, West Bengal 700 032, India.
Abstract:
Judicious syntheses, spectroscopic analyses, and solid state structural evidence of two structural variants (with planar geometry) of strongly aromatic hybrid [30] E-ethylene bridged hexaphyrins (2.1.1.2.1.1) exhibiting strong NIR absorption are reported. The induced correspondence of fused phenanthrene on the pyrrole moieties has led to a further red-shift of up to ∼45 nm in the neutral and protonated form of the macrocycles. The electronic nature and aromaticity of both hexaphyrins are fully supported by DFT calculations.
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