IrCytoToxDB: a dataset of iridium(III) complexes cytotoxicities against various cell lines.

Iridium(III) complexes nowadays became rising stars in various health-related applications. Thus, there is a necessity to assess cytotoxicity of the synthesized molecules against cancer/normal cell lines. In this report, we present a dataset of 2694 experimental cytotoxicity values of 803 iridium complexes against 127 different cell lines.

Tailoring the π-system of benzimidazole ligands towards stable light-harvesting cyclometalated iridium(III) complexes.

The synthesis, structure, optical and redox properties as well as photovoltaic studies of iridium(III) complexes with cyclometalated 2-arylbenzimidazoles decorated with various polyaromatic fragments and an ancillary aromatic β-diketone are reported. Despite the strong preference of the iridium(III) ion to form bis- or tris-cyclometalated complexes in which the metal participates in five-membered metallacycles, the cyclometalation of the benzimidazole ligands containing rigid π-extended systems yields dimeric complexes containing strained five- or six-membered metallacycles and allows for generating an extremely rare monocyclometalated complex. X-ray crystallography shows that the steric strain observed in the dimers is retained in heteroleptic diketonate complexes which is also corroborated by gas-phase DFT calculations.

A Panchromatic Cyclometalated Iridium Dye Based on 2-Thienyl-Perimidine.

Though 2-arylperimidines have never been used in iridium(III) chemistry, the present study on structural, electronic and optical properties of -unsubstituted and -methylated 2-(2-thienyl)perimidines, supported by DFT/TDDFT calculations, has shown that these ligands are promising candidates for construction of light-harvesting iridium(III) complexes. In contrast to -H perimidine, the -methylated ligand gave the expected cyclometalated μ-chloro-bridged iridium(III) dimer which was readily converted to a cationic heteroleptic complex with 4,4'-dicarboxy-2,2'-bipyridine. The resulting iridium(III) dye exhibited panchromatic absorption up to 1000 nm and was tested in a dye-sensitized solar cell.

Syntheses and crystal structures of 2-(-tol-yl)-1-perimidine hemihydrate and 1-methyl-2-(-tol-yl)-1-perimidine.

The title compounds, 2-(4-methylphenyl)-1-perimidine hemihydrate (, CHN·0.5HO) and 1-methyl-2-(4-methylphenyl)-1-perimidine (, CHN), were prepared and characterized by H NMR and single-crystal X-ray diffraction. The organic mol-ecule of the hemihydrate lies on a twofold rotation axis while the water mol-ecule lies on the inter-section of three twofold rotation axes (point group symmetry 222).

Synthesis and crystal structures of -H, -phenyl and -benzyl-2-(4-hexyl-oxyphen-yl)benzimidazoles.

The title compounds, 2-(4-hexyl-oxyphen-yl)-1-benzimidazole (CHNO; ), 2-(4-hexyl-oxyphen-yl)-1-phenyl-1-benzimidazole (CHNO; ) and 1-benzyl-2-(4-hexyl-oxyphen-yl)-1-benzimidazole (CHNO; ) were synthesized and their structures were determined by single-crystal X-ray analysis. The N-substituent at the imidazole moiety slightly affects the inter-planar angle between the 4-hexyl-oxyphenyl ring and the benzimidazole system. The unsubstituted benzimidazole () forms inter-molecular N-H⋯N bonds while in the crystal structures of and , the mol-ecules are assembled only through π-π and C-H⋯π inter-actions.

Cyclometalated Ru(II) complexes with tunable redox and optical properties for dye-sensitized solar cells.

Cyclometalated Ru(ii) complexes with 2-arylbenzimidazole antenna ligands bearing electron-donor/withdrawing substituents and anchoring 4,4'-dimethoxycarbonyl-2,2'-bipyridine have been prepared and their structure, optical and electrochemical properties have been studied. The complexes possess enhanced light-harvesting characteristics compared to those of the standard N719 dye and absorb light up to 750 nm. In addition, they demonstrate reversible redox behavior with Ru3+/Ru2+ potentials being finely tuned by the change of the electron-donating ability of cyclometalated ligands.