1609575-00-9Relevant academic research and scientific papers
Pre-/post-functionalization in dipyrrin metal complexes-antitumor and antibacterial activity of their glycosylated derivatives
Gutsche, Claudia S.,Gr?fe, Susanna,Gitter, Burkhard,Flanagan, Keith J.,Senge, Mathias O.,Kulak, Nora,Wiehe, Arno
, p. 12373 - 12384 (2018)
A post-functionalization route to tris(dipyrrinato) metal complexes is presented giving access to a range of new complexes relevant in the context of medicinal inorganic chemistry. A pentafluorophenyl group in the meso-position of the dipyrrin ligand serves as an anchor for the connection with alcohols and thiocarbohydrates. The photochemotherapeutic activity of the complexes has been assessed in cellular assays with tumor cell lines and against the Gram-positive bacterium S. aureus. Finally, it is shown that this post-functionalization is also applicable to other dipyrrinato metal complexes.
Synthesis, characterization, DNA binding and cytotoxicity of fluoro-dipyrrin based arene ruthenium(II) complexes
Paitandi, Rajendra Prasad,Singh, Roop Shikha,Mukhopadhyay, Sujay,Sharma, Gunjan,Koch, Biplob,Vishnoi, Pratap,Pandey, Daya Shankar
, p. 117 - 127 (2017)
Synthesis of four new arene ruthenium(II) complexes [(η6-C10H14)RuCl(MFPdpm)] (1); [(η6-C12H18)Ru-Cl(MFPdpm)] (2); [(η6-C10H14)RuCl(PFPdpm)] (3) and [(ηsup
Near-IR photoresponse of ruthenium dipyrrinate terpyridine sensitizers in the dye-sensitized solar cells
Li, Guocan,Yella, Aswani,Brown, Douglas G.,Gorelsky, Serge I.,Nazeeruddin, Mohammad K.,Graetzel, Michael,Berlinguette, Curtis P.,Shatruk, Michael
supporting information, p. 5417 - 5419 (2014/06/23)
Coordination of bidentate 5-pentafluorophenyldipyrrinate (pfpdp) or 5-(2-thienyl)dipyrrinate (2-tdp) to a RuII center bearing 2,2:6,2″-terpyridine-4,4,4″-tricarboxylate (tctpy) and a NCS - ligand results in strongly light-absorbing complexes [Ru(tctpy)(L)(NCS)] (L = pfpdp or 2-tdp). Anchored to a mesoporous TiO 2 electrode, these complexes afford a photoaction spectral response at wavelengths of up to 950 nm, one of the most red-shifted values reported to date for molecular dyes in the dye-sensitized solar cell (DSSC).
