Cationic allyl nickel complexes containing N,O-donor labile ligands: Synthesis and molecular characterisation

被引:4
|
作者
Belkhiria, Marwa [1 ]
Mechria, Ali [1 ]
Cruz, Tiago F. C. [2 ]
Gomes, Clara S. B. [2 ]
Msaddek, Moncef [1 ]
Gomes, Pedro T. [2 ]
机构
[1] Fac Sci Monastir, LCHPNR, Bd Environm, Monastir 5000, Tunisia
[2] Univ Lisbon, Ctr Quim Estrutural, Inst Super Tecn, Dept Engn Quim, Av Rovisco Pais, P-1049001 Lisbon, Portugal
关键词
eta(3)-allyl complexes; Cationic nickel(II) complexes; N; O-chelates; Hemilabile ligands; DFT calculations; EFFECTIVE CORE POTENTIALS; GAUSSIAN-BASIS SETS; METAL-COMPLEXES; SCHIFF-BASE; PALLADIUM(II) COMPLEXES; OCTAHEDRAL NICKEL(II); BIOLOGICAL-ACTIVITY; THIOSEMICARBAZONES; 2-FURALDEHYDE; ETHYLENE;
D O I
10.1016/j.molstruc.2019.01.045
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Three 2-iminofuran ligands 2-(N-2,6-diisopropylphenylformimino)furan (L1), 2-(N-2,6-dimethylphenylformimino)furan (L2) and 2-(N-4-methoxyphenylformimino)furan (L3) were obtained by condensation reactions of the respective anilines with furfural. The eta(3)-allyl Ni(II) cationic complexes 1-3 have been synthesised by reacting [Ni(eta(3)-C3H5)(mu-Br)](2) with the corresponding ligands L1-L3, in the presence of TIPF6. All complexes have been characterised by FT-IR, NMR spectroscopy and elemental analysis. The molecular structure of complex 2 has been determined by single crystal X-Ray diffraction. Complexes 1 and 2 have displayed a mono bidentate chelation mode of the respective ligand, while complex 3 showed a bis monodentate coordination framework. The respective complexes were studied by DFT calculations, showing a tendency to form the bis monodentate species, the formation of complex 3 being clearly the most favoured one. (C) 2019 Elsevier B.V. All rights reserved.
引用
收藏
页码:260 / 265
页数:6
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