19850-36-3Relevant articles and documents
ONS-donor ligand based Pt(II) complexes display extremely high anticancer potency through autophagic cell death pathway
Rahman, Faiz-Ur,Ali, Amjad,Duong, Hong-Quan,Khan, Inam Ullah,Bhatti, Muhammad Zeeshan,Li, Zhan-Ting,Wang, Hui,Zhang, Dan-Wei
, p. 546 - 561 (2019)
The current study unveils ONS-donor ligand based Pt(II) complexes with unusual anticancer potency showing higher anticancer effect as compared to cisplatin. This series of Pt(II)(R-salicylaldimine)Cl (C1a-C4a) (R = 5-H, 5-CH3, F, 3-CH3/su
Ruthenium complexes bearing tridentate 2-(methylthio)phenylsalicylaldimine Schiff-base ligands
Wang, Chang-Jiu,Lin, Hui,Chen, Xin,Jia, Ai-Quan,Zhang, Qian-Feng
, p. 198 - 203 (2017)
Reaction of [Ru(PPh3)3Cl2] with 2-(methylthio)phenylsalicylaldimine Schiff-base (HL) in tetrahydrofuran (THF) in the presence of triethylamine afforded a ruthenium(II) complex [Ru(ONS-L)(PPh3)2Cl]·CH3OH·2.75H2O (1). Similarly, reaction of [Ru(CO)2Cl2] with HL in N,N′-dimethylformamide (DMF) in the presence of triethylamine gave a ruthenium(II) complex [Ru(ONS-L)(CO)2Cl] (2), while the reaction between [Ru(CO)2Cl2] and HL without base resulted in a ruthenium(III) complex [Ru(ONS-L)(CO)Cl2] (3). Treatment of RuCl3·3H2O with HL in ethanol in the presence of triethylamine gave an anionic complex [Et3NH][Ru(ONS-L)Cl3] (4), which reacted with [Cp?2Ru] in the presence of sodium hydroxide to give complex [Cp?Ru(η6-1,2,3,4-Me4C6H2)][Ru(ONS-L)Cl3]·CH2Cl2 (5) with a different cation. Besides, reaction of 4 and AgNO3 afforded a dinuclear ruthenium(II) complex [Ru2(ONS-L)(μ-ONS-L)2Cl]·CH2Cl2 (6). The structures of complexes 1–6 have been established by X-ray crystallography, of which complex 4 was selected as a catalyst for the typical oxidation of 1-phenylethanol to the according acetophenone.
The enhanced catalytic performance of cobalt catalysts towards butadiene polymerization by introducing a labile donor in a salen ligand
Gong, Dirong,Wang, Baolin,Jia, Xiaoyu,Zhang, Xuequan
, p. 4169 - 4178 (2014/03/21)
A family of cobalt complexes supported by a tridentate Schiff base ligand with a labile donor (O, S, N) as a pendant arm (Co1-Co12, formulated as CoL 2) were synthesized by the treatment of the corresponding ligands with cobalt acetate tetrahyd