Expanded bite angles in tridentate ligands. Improving the photophysical properties in bistridentate RuII polypyridine complexes

2010 ◽  
Vol 254 (21-22) ◽  
pp. 2546-2559 ◽  
Author(s):  
Leif Hammarström ◽  
Olof Johansson
Molecules ◽  
2020 ◽  
Vol 25 (24) ◽  
pp. 5991
Author(s):  
Mohamed Darari ◽  
Antonio Francés-Monerris ◽  
Bogdan Marekha ◽  
Abdelatif Doudouh ◽  
Emmanuel Wenger ◽  
...  

The control of ligand-field splitting in iron (II) complexes is critical to slow down the metal-to-ligand charge transfer (MLCT)-excited states deactivation pathways. The gap between the metal-centered states is maximal when the coordination sphere of the complex approaches an ideal octahedral geometry. Two new iron(II) complexes (C1 and C2), prepared from pyridylNHC and pyridylquinoline type ligands, respectively, have a near-perfect octahedral coordination of the metal. The photophysics of the complexes have been further investigated by means of ultrafast spectroscopy and TD-DFT modeling. For C1, it is shown that—despite the geometrical improvement—the excited state deactivation is faster than for the parent pseudo-octahedral C0 complex. This unexpected result is due to the increased ligand flexibility in C1 that lowers the energetic barrier for the relaxation of 3MLCT into the 3MC state. For C2, the effect of the increased ligand field is not strong enough to close the prominent deactivation channel into the metal-centered quintet state, as for other Fe-polypyridine complexes.


Inorganics ◽  
2019 ◽  
Vol 7 (1) ◽  
pp. 4 ◽  
Author(s):  
Johannes Karges ◽  
Philippe Goldner ◽  
Gilles Gasser

Cancer is known to be one of the major causes of death nowadays. Among others, chemotherapy with cisplatin is a commonly used treatment. Although widely employed, cisplatin is known to cause severe side effects, such as nerve and kidney damage, nausea, vomiting, and bone marrow suppression. Most importantly, a number of cancer tumors are acquiring resistance to cisplatin, limiting its clinical use. There is therefore a need for the discovery of novel anticancer agents. Complementary to chemotherapy, Photodynamic Therapy (PDT) has expanded the range of treatment opportunities of numerous kinds of cancer. Nonetheless, the currently approved PDT photosensitizers (PSs) suffer from major drawbacks, which include poor water solubility or photobleaching, in addition to a slow clearance from the body that causes photosensitivity. Due to these limitations, there is a need for the development of new PDT PSs. To overcome these problems, a lot of research groups around the world are currently focusing their attention towards the development of new metal complexes as PDT PSs. However, most synthesized compounds reported so far show limited use due to their poor absorption in the phototherapeutic window. Herein, we report on the preparation and characterization of three Fe(II) polypyridine complexes (4–6) and evaluate their potential as both anticancer agents and PDT PSs. Very importantly, these compounds are stable in human plasma, photostable upon continuous LED irradiation, and absorb in the red region of the spectrum. We could demonstrate that through additional sulfonic acid groups on the polypyridine ligand being used (bphen: 4,7-diphenyl-1,10-phenanthroline), the water solubility of the complexes could be highly improved, whereas the photophysical properties did not significantly change. One of these complexes (4) shows interesting toxicity, with IC50 values in the low micromolar range in the dark as well as some phototoxicity upon irradiation at 480 and 540 nm against RPE-1 and HeLa cells.


2009 ◽  
pp. 1700 ◽  
Author(s):  
Misa Ashizawa ◽  
Lifen Yang ◽  
Katsuaki Kobayashi ◽  
Hisako Sato ◽  
Akihiko Yamagishi ◽  
...  

2006 ◽  
Vol 110 (13) ◽  
pp. 4348-4358 ◽  
Author(s):  
Maurilio Galletta ◽  
Fausto Puntoriero ◽  
Sebastiano Campagna ◽  
Claudio Chiorboli ◽  
Manuel Quesada ◽  
...  

2019 ◽  
Vol 48 (26) ◽  
pp. 9692-9702 ◽  
Author(s):  
Steve Po-Yam Li ◽  
Justin Shum ◽  
Kenneth Kam-Wing Lo

The synthesis, characterization, and photophysical properties of novel iridium(iii) polypyridine complexes as thiol-sensing probes and cytotoxic agents are reported.


1997 ◽  
Vol 488 ◽  
Author(s):  
Po King Ng ◽  
Wai Yue Ng ◽  
Xiong Gong ◽  
Wai Kin Chan

AbstractA series of conjugated polymers functionalized with different ruthenium polypyridine metal complexes were synthesized by the palladium catalyzed reaction. Two conjugated polymer systems have been studied: 1. poly(phenylenevinylene) with bis(2,2':6',2”-terpyridine) ruthenium (II) on the mainchain and 2. quinoxaline based polymers with tris(2,2'-bipyridine) ruthenium (II). The ruthenium polypyridine complexes exhibit a long-lived metal to ligand charge transfer excited state which can enhance the photosensitivity of the resulting polymers. Different physical properties such as the photoconductivity and charge mobility in these polymers are also studied.


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