1133062-41-5Relevant academic research and scientific papers
Cubane-like tetranuclear Cu(II) complexes bearing a Cu4O4 core: Crystal structure, magnetic properties, DFT calculations and phenoxazinone synthase like activity
Sagar, Shipra,Sengupta, Swaraj,Mota, Antonio J.,Chattopadhyay, Shyamal K.,Espinosa Ferao, Arturo,Riviere, Eric,Lewis, William,Naskar, Subhendu
, p. 1249 - 1259 (2017)
In the present work, two new copper complexes 3a and 3b with a Cu4O4 cubane core are reported. Both complexes are obtained by means of the in situ conversion of the imine functionality of Schiff's base ligands 1a [(E)-4-chloro-2-((thiazol-2-ylimino)methyl)phenol] and 1b [(E)-4-bromo-2-((thiazol-2-ylimino)methyl)phenol] into amino alcohols 2a (4-chloro-2-(hydroxy(thiazol-2-ylamino)methyl)phenol) and 2b (4-bromo-2-(hydroxy(thiazol-2-ylamino)methyl)phenol), respectively. The ligand transformation may be metal assisted and the generated ligands show an interesting mode of coordination in which the alkoxo-O atom binds in a μ3-manner connecting simultaneously three copper centers and forming a Cu4O4 cubane core. The first analysis of single crystal X-ray diffraction studies reveals that both molecules possess a [4 + 2] cubane-type core, and low temperature magnetic measurements show antiferromagnetic behaviour, in agreement with DFT calculations. However, the best fit and DFT calculations point out three pairs of coupling constants, more coherent with a [2 + 2 + 2] situation, in accordance with the fine analysis of structural data. Finally, phenoxazinone synthase activity has been measured for both molecules, finding kcat = 86.3 h-1 for the chloride derivative copper(ii) complex in methanol, whereas the bromide derivative copper(ii) complex displays kcat = 3.4026 × 102 h-1 and 10.289 × 102 h-1 in methanol and DMSO, respectively.
Half-Sandwich Ruthenium Complexes with Schiff-Base Ligands: Syntheses, Characterization, and Catalytic Activities for the Reduction of Nitroarenes
Jia, Wei-Guo,Zhang, Hui,Zhang, Tai,Xie, Dong,Ling, Shuo,Sheng, En-Hong
, p. 503 - 512 (2016/03/01)
A series of ruthenium(II) p-cymene complexes containing Schiff-base ligands [Ru(p-cymene)LCl] [HL = pyridyl-salicylimine (2a-2d); HL = thiazol-salicylimine (2e-2h); HL = benzothiazol-salicylimine (2i-2l)] have been synthesized and characterized. All Schiff-base ligands and half-sandwich ruthenium complexes were fully characterized by 1H and 13C NMR spectra, mass spectrometry, and infrared spectrometry. The molecular structures of ruthenium complexes 2b and 2k were further confirmed by single-crystal X-ray diffraction methods. Furthermore, these half-sandwich ruthenium complexes are active catalysts for the mild hydrogenation of nitroarenes to aromatic anilines in the presence of sodium tetrahydroborate reducing agent in water. The most efficient catalyst, 2b, was found be compatible with nitroarenes of various functional groups.
