Photosensitization Ability of 1,7-Phenanthroline Based Bis−BODIPYs: Perplexing Role of Intramolecular Rotation on Photophysical Properties
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DOI: 10.1021/acs.jpcc.9b09721
Abstract: 1,7Phenanthroline based bisboron dipyrromethenes (bisBODIPYs) 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… read more here.
Keywords: phenanthroline based; bis; based bis; bis bodipys ... See more keywords
Conformationally Distinct [26]Heterorubyrin(1.1.0.1.1.0) Macrocycles and Their Bis-BODIPYs: Synthesis, Structure, and Optical Properties.
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DOI: 10.1021/acs.orglett.1c04043
Abstract: Two conformationally different [26]rubyrin(1.1.0.1.1.0) macrocycles with varying heteroatoms (S/O) and their bis-BODIPYs are reported. The solid-state structure confirms O2N4 with fairly planar pyrrole-inverted conformation, whereas a thiophene-inverted structure for S2N4 is observed. Such conformational differences… read more here.
Keywords: conformationally distinct; structure; macrocycles bis; distinct heterorubyrin ... See more keywords