2020
DOI: 10.1016/j.bioorg.2020.103994
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New nitroindazole-porphyrin conjugates: Synthesis, characterization and antibacterial properties

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Cited by 4 publications
(2 citation statements)
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“…Our interest is centered on the functionalization of β-pyrrolic positions of meso -tetraarylporphyrins aiming to prepare new porphyrinic derivatives with adequate properties to be used in different fields [ 57 ], namely as photosensitizers in Photodynamic Therapy (PDT) or antimicrobial PDT [ 13 , 58 , 59 , 60 , 61 , 62 , 63 , 64 ]. We then report here an efficient synthetic approach to obtain a novel series of mononuclear heteroleptic porphyrin-iridium(III) complexes 4 and 5 via porphyrin derivatives 2 bearing a bipyridine unit (see Scheme 1 and Scheme 2 ).…”
Section: Introductionmentioning
confidence: 99%
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“…Our interest is centered on the functionalization of β-pyrrolic positions of meso -tetraarylporphyrins aiming to prepare new porphyrinic derivatives with adequate properties to be used in different fields [ 57 ], namely as photosensitizers in Photodynamic Therapy (PDT) or antimicrobial PDT [ 13 , 58 , 59 , 60 , 61 , 62 , 63 , 64 ]. We then report here an efficient synthetic approach to obtain a novel series of mononuclear heteroleptic porphyrin-iridium(III) complexes 4 and 5 via porphyrin derivatives 2 bearing a bipyridine unit (see Scheme 1 and Scheme 2 ).…”
Section: Introductionmentioning
confidence: 99%
“…, and H-4 C ), 6.76-6.64 (4H, m, H-5 C , H-5 F , H-4 E , and H-2 G , 6 G ), 6 59. 6.53 (2H, m, H-5 E , and H-4 D ), 6.29 (1H, td, J = 7.6 and 1.2 Hz, H-5 D ), 6.00 (1H, d, J = 7.5 Hz, H-6 C ), 5.85 (1H, d, J = 7.1 Hz, 6 E ), 5.48 (1H, d, J = 7.4 Hz, H-6 D ) ppm.…”
mentioning
confidence: 99%