75411-85-7Relevant academic research and scientific papers
Synthesis, anticancer activity and mechanism of iron chelator derived from 2,6-diacetylpyridine bis(acylhydrazones)
Yao, Qian,Qi, Jinxu,Zheng, Yunyun,Qian, Kun,Wei, Lai,Maimaitiyiming, Mukedasi,Cheng, Zhen,Wang, Yihong
, p. 1 - 8 (2019)
We synthesized five iron chelator derived from 2,6-diacetylpyridine bis(acylhydrazones) and proved their iron complexes structure by X–ray single crystal diffraction. These ligands have a significant anticancer proliferative activity and low cytotoxicity
A novel family of hepta-coordinated Cr(III) complexes with a planar pentadentate N3O2 Schiff base ligand: synthesis, structure and magnetism
Bazhenova,Zorina,Simonov,Manakin, Yu.V.,Kornev,Lyssenko,Mironov,Gilmutdinov,Yagubskii
, (2021/04/15)
A series of seven-coordinate pentagonal-bipyramidal (PBP) Cr(III) complexes with pentadentate pyridine-based ligands, 2,6-diacetylpyridine bis(4-methoxybenzoylhydrazone), H2DAPMBH (H2LOCH3) or 2,6-diacetylpyridine bis(benzoylhydrazone), H2DAPBH (H2L) and different axial ligands have been prepared. The reaction of the H2LOCH3 with CrCl2·4H2O in methanol or CrCl3·6H2O in CH3CN led to a novel seven-coordinate pentagonal-bipyramidal (PBP) complex [Cr(HLOCH3)Cl2] (1) with the mono-deprotonated chelating ligand in the equatorial plane and two apical Cl atoms. Then, taking advantage of lability of the apical Cl ligands in 1, a number of PBP CrIII complexes with charged (viz. CH3O?, N3?, CN?, NCS?) and neutral (viz. CH3OH, H2O) apical ligands was obtained and characterized: [Cr(HLOCH3)Cl2]·4CHCl3 (1), [Cr(HLOCH3)Cl2]·CH3OH (1a), [Cr(HLOCH3)(H2O)Cl]PF6·CH3OH (2), [Cr(HL)(H2O)Cl]ClO4·0.25H2O (3), [Cr(HLOCH3)(H2O)2](NO3)2·H2O·C2H5OH (4), [Cr(LOCH3)(CH3OH)(OCH3)]·CH3OH (5), [Cr(HLOCH3)(NCS)2]·1.5H2O (6), [Cr(HLOCH3)(N3)2]·xH2O (7, x = 0.2, 8, x = 0, 9, x = 0, three phases in the same synthesis), [Cr(LOCH3)(N3)2][Na(CH3OH)2]·2CH3OH (10), [Cr(LOCH3)(CN)2][Na(H2O)(C2H5OH)] (11). Single crystal X-ray analysis reveals that all the complexes 1–11 have the PBP geometry with a pentadentate ligand in a form of [HLOCH3]? or [LOCH3]2? in the equatorial plane. The PBP complexes are prone to aggregate into dimers or polymers, either due to strong hydrogen bonds or due to the transformation of terminal ligands into bridging between different metallic centers. All complexes 1–11 exhibit considerable in-plane distortion of the CrN3O2 pentagon due to the shift of the CrIII ion from the central position, which is caused by the strong first-order Jahn-Teller (JT) effect for the high-spin 3d3 configuration in the PBP ligand field. The mechanism of JT distortions is rationalized in terms of DFT calculations. DC magnetic measurements indicate a high-spin (S = 3/2) ground state of complex [Cr(HLOCH3)Cl2]·4CHCl3 (1); theoretical analysis of its magnetic properties reveals negative zero-field splitting energy with the anisotropy parameter D = –1.8 cm?1 and weak dimer-like antiferromagnetic spin coupling J = –0.23 cm?1 between neighboring PBP units [CrIII(HLOCH3)Cl2] mediated by π-stacking of planar H2LOCH3 ligands.
End-to-End Azido-Bridged Lanthanide Chain Complexes (Dy, Er, Gd, and Y) with a Pentadentate Schiff-Base [N3O2] Ligand: Synthesis, Structure, and Magnetism
Bazhenova, Tamara A.,Mironov, Vladimir S.,Yakushev, Ilya A.,Svetogorov, Roman D.,Maximova, Olga V.,Manakin, Yuriy V.,Kornev, Alexey B.,Vasiliev, Alexander N.,Yagubskii, Eduard B.
, p. 563 - 578 (2020/01/03)
The syntheses, structure and magnetic properties are reported for five novel 1D polymeric azido-bridged lanthanide complexes with the general formula {[Ln(DAPMBH)(N3)C2H5OH]C2H5OH}n where H2DAPMBH = 2,6-diacetylpyridine bis(4-methoxybenzoylhydrazone) - a new pentadentate pyridine-base [N3O2] ligand and Ln = Dy (1), Y0.930Dy0.070 (2), Er (3), Y0.923Er0.077 (4), and Gd (5). X-ray diffraction analysis of 1-5 show that the central lanthanide atoms are eight-coordinated with the N5O3 donor set originating from the ligand DAPMBH, one coordinated ethanol molecule and two end-to-end type N3- bridges connecting the metal centers into infinite chain. The [LnN5O3] coordination polyhedron can be regarded as a distorted dodecahedron (D2d). AC magnetic measurements revealed that compounds 1-4 show field-induced single-molecule magnet behavior, with estimated energy barriers Ueff ≈ 47-17 K. The experimental study of magnetic properties was complemented by theoretical analysis based on crystal-field calculations. Direct current magnetic susceptibility studies revealed marginally weak intrachain exchange interaction between Ln3+ ions mediated by the end-to-end azide bridging groups (J ≈ -0.015 cm-1 for 5). Comparative analysis of static and dynamic magnetic properties of magnetically concentrated (1, 3) and diluted (2, 4) Dy and Er compounds showed that, despite fascinating 1D azido-bridged chain structure, compounds 1 and 3 are not single-chain magnets; their magnetic behavior is largely due to single-ion magnetic anisotropy of individual Ln3+ ions.
