Mechanisms and applications of cyclometalated Pt(ii) complexes in photoredox catalytic trifluoromethylation† †Electronic supplementary information (ESI) available: Experimental details and the syntheses of the Pt(ii) catalysts; Fig. S1–S55, showing the phosphorescence spectra, femto- and nanosecond laser flash photolysis results, cyclic and differential pulse voltammograms, phosphorescence quenching experiment results, photoinduced ESR spectrum, spectroelectrochemical UV-vis-NIR absorption spectrum, dark-state reaction results, and 1H, 13C, and 19F NMR spectra; Scheme S1, presenting the synthetic routes to the Pt(ii) complexes; Tables S1–S6, listing optimization results for the trifluoromethylation of 1-dodecene, 3-methylindole and N-methylpyrrole, and the Cartesian coordinates for the optimized geometries of one-electron oxidized species of the Pt complexes. See DOI: 10.1039/c4sc02537g Click here for additional data file.
نویسندگان
چکیده
Department of Advanced Materials Engin Kyung Hee University, Yongin, Gyeonggi-do 4 Department of Applied Chemistry & Depa University, Ansan, Gyeonggi-do 426-791, Ko Department of Material and Life Science, University, ALCA, Japan Science and Tech 0871, Japan. E-mail: [email protected] † Electronic supplementary information ( the syntheses of the Pt(II) catalysts; Fig. spectra, femtoand nanosecond laser differential pulse voltammograms, pho results, photoinduced ESR spectrum absorption spectrum, dark-state reaction spectra; Scheme S1, presenting the syn Tables S1–S6, listing optimization res 1-dodecene, 3-methylindole and N-methy for the optimized geometries of onecomplexes. See DOI: 10.1039/c4sc02537g Cite this: Chem. Sci., 2015, 6, 1454
منابع مشابه
Development of a cyclometalated iridium complex with specific intramolecular hydrogen-bonding that acts as a fluorescent marker for the endoplasmic reticulum and causes photoinduced cell death† †Electronic supplementary information (ESI) available: Detailed synthesis; photophysical data (Table S1); pH dependent phosphorescence lifetime of complex C2 (Table S2); crystallographic parameters of C2; selected bond distances and angles of C2 (Table S3); cyclic voltammetric data of complexes C1–C11 (Table S4); 1H NMR spectra of ligands and complexes (Fig. S1 and S3); ESI-MS spectra of ligands and complexes (Fig. S2 and S4); fluorescence spectra of the complexes in acetonitrile and at pH 4, 7 and 9, exponential decay curve of C2 (Fig. S5); pH dependent fluorescence spectrum of complexes C1–C11 (Fig. S6); DIC and confocal fluorescence images of live MCF7 cells not treated with C2 but exposed to photoirradiation at 405 nm for 30 min; the cells were treated with DCFDA and fluorescence images were obtained at 529 nm after excitation at 495 nm (Fig. S7). ESI videos 1 and 2. CCDC 967841. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c4dt00845f Click here for additional data file. Click here for additional data file. Click here for additional data file. Click here for additional data file. Click here for additional data file.
Cyclometalated iridium complexes have important applications as phosphorescent probes for cellular imaging due to their photophysical properties. Moreover, these properties also make them potential candidates as photosensitizers for photodynamic therapy (PDT) of tumors and skin diseases. Treatment of MCF7 breast carcinoma cells with a heteroleptic phosphorescent cyclometalated iridium(III) comp...
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Institut für Anorganische Chemie, Julius Hubland, 97074 Würzburg, Germany. E-ma School of Medicine, Pharmacy and Health, Stockton-on-Tees, TS17 6BH, UK Department of Chemistry, University of Tor M5S 3H6, Canada Institut für Organische Chemie, JuliusHubland, 97074 Würzburg, Germany † Electronic supplementary information Additional views of the molecular stru voltammograms of 2 and 3. Plots of ca...
متن کاملAcid/base-regulated reversible electron transfer disproportionation of N–N linked bicarbazole and biacridine derivatives† †Electronic supplementary information (ESI) available: Experimental information, synthesis and characterization data, NMR spectra, solid state NMR data, X-ray data, ESR spectra, UV-Vis-NIR spectra, fluorescence spectra, kinetic experiments, theoretical calculations, Tables S1–S8, Scheme S1, Fig. S1–12, References. CCDC 1025063, 1038914, 1049677 and 1040722. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c5sc00946d
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