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Photosensitization Ability of 1,7-Phenanthroline Based Bis−BODIPYs: Perplexing Role of Intramolecular Rotation on Photophysical Properties

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1,7Phenanthroline based bisboron dipyrromethenes (bisBODIPYs) B1 and B2 obtained via small substitutional changes (Cl/SCH3) have been described. The effect of RIR in emission enhancement in a viscous solvent (glycerol) has… Click to show full abstract

1,7Phenanthroline based bisboron dipyrromethenes (bisBODIPYs) B1 and B2 obtained via small substitutional changes (Cl/SCH3) have been described. The effect of RIR in emission enhancement in a viscous solvent (glycerol) has been studied besides vital role of intermolecular interactions scrutinized by Xray single crystal studies. The efficiency of intersystem crossing (ISC) in generation of singlet oxygen (ΦΔ∼ 19.2% and 56.7%) by photoirradiation using visible light along with distinct photostability has been investigated by 1,3-diphenylisobenzofuran (DPBF) titration studies. The 1O2 generation quantum yield and photosensitizing durability of the bisBODIPYs have been investigated by photooxidation of 1,5-dihydroxynaphthalene (DHN) in presence of B1 and B2 as photosensitizers. The pseudo-first-order rate constants for photooxidation reactions and consumption rates of DHN reflected appreciable 1O2 generation quantum yields (ΦΔ: B1, 29.0; B2, 57.8%). Density functional theory (DFT) studies showed distri...

Keywords: phenanthroline based; bis; based bis; bis bodipys

Journal Title: Journal of Physical Chemistry C
Year Published: 2019

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