The bromoporphyrins as promising anti-tumor photosensitizers in vitro

[21] Yu W(2010)Hematoporphyrin monomethyl ether-mediated photodynamic effects on THP-1 cell-derived macrophages Journal of Photochemistry and Photobiology B: Biology 101 2669-761

[22] Zhen W(2019)Porphyrin as diagnostic and therapeutic agent Molecules 24 3842-156

[23] Zhang Q(2020)Synthesis and physicochemical properties of 2,7-disubstituted phenanthro[2,1-b:7,8-b']dithiophenes Molecules 25 3293-1552

[24] Li MY(2006)Comparison between 5,10,15,20-Tetraaryl- and 5,15-diarylporphyrins as photosensitizers: Synthesis, photodynamic activity, and quantitative structure-activity relationship modeling Journal of Medicinal Chemistry 49 758-17334

[25] Gao YH(2012)Hydrophilicity vs hydrophobicity—varying the amphiphilic structure of porphyrins related to the photosensitizer m-THPC Journal of Porphyrins and Phthalocyanines 05 146-32481

[26] Zhang JH(2018)Comparison between porphin, chlorin and bacteriochlorin derivatives for photodynamic therapy: Synthesis, photophysical properties, and biological activity European Journal of Medicinal Chemistry 160 1542-4958

[27] Knoll JD(2005)Photodynamic effects of novel XF porphyrin derivatives on prokaryotic and eukaryotic cells Antimicrobial Agents and Chemotherapy 49 1701987-14039

[28] Turro C(2017)Shorter exciton lifetimes via an external heavy-atom effect: Alleviating the effects of bimolecular processes in organic light-emitting diodes Advanced Materials 29 17327-9

[29] Plaetzer K(2018)Heavy atom effect of bromine significantly enhances exciton utilization of delayed fluorescence luminogens ACS Applied Materials & Interfaces 10 32475-44335

[30] Krammer B(2017)BODIPY derivatives for photodynamic therapy: Influence of configuration versus heavy atom effect ACS Applied Materials & Interfaces 9 4956-597

[21] Yu W(2010)Hematoporphyrin monomethyl ether-mediated photodynamic effects on THP-1 cell-derived macrophages Journal of Photochemistry and Photobiology B: Biology 101 2669-761

[22] Zhen W(2019)Porphyrin as diagnostic and therapeutic agent Molecules 24 3842-156

[23] Zhang Q(2020)Synthesis and physicochemical properties of 2,7-disubstituted phenanthro[2,1-b:7,8-b']dithiophenes Molecules 25 3293-1552

[24] Li MY(2006)Comparison between 5,10,15,20-Tetraaryl- and 5,15-diarylporphyrins as photosensitizers: Synthesis, photodynamic activity, and quantitative structure-activity relationship modeling Journal of Medicinal Chemistry 49 758-17334

[25] Gao YH(2012)Hydrophilicity vs hydrophobicity—varying the amphiphilic structure of porphyrins related to the photosensitizer m-THPC Journal of Porphyrins and Phthalocyanines 05 146-32481

[26] Zhang JH(2018)Comparison between porphin, chlorin and bacteriochlorin derivatives for photodynamic therapy: Synthesis, photophysical properties, and biological activity European Journal of Medicinal Chemistry 160 1542-4958

[27] Knoll JD(2005)Photodynamic effects of novel XF porphyrin derivatives on prokaryotic and eukaryotic cells Antimicrobial Agents and Chemotherapy 49 1701987-14039

[28] Turro C(2017)Shorter exciton lifetimes via an external heavy-atom effect: Alleviating the effects of bimolecular processes in organic light-emitting diodes Advanced Materials 29 17327-9

[29] Plaetzer K(2018)Heavy atom effect of bromine significantly enhances exciton utilization of delayed fluorescence luminogens ACS Applied Materials & Interfaces 10 32475-44335

[30] Krammer B(2017)BODIPY derivatives for photodynamic therapy: Influence of configuration versus heavy atom effect ACS Applied Materials & Interfaces 9 4956-597