Supramolecular structures of V(III) complexes supported by PNP pincer ligands

被引:2
|
作者
Ruivo, Rita [1 ]
Alves, Luis G. [1 ]
Kirchner, Karl [2 ]
Martins, Ana M. [1 ]
机构
[1] Univ Lisbon, Inst Super Tecn, Ctr Quim Estrutural, Av Rovisco Pais 1, P-1049001 Lisbon, Portugal
[2] Vienna Univ Technol, Inst Appl Synthet Chem, Getreidemarkt 9, A-1060 Vienna, Austria
关键词
PNP ligands; V(III) complexes; Hydrogen bonds; Solvates; Supramolecular structures; CRYSTAL-STRUCTURE; EFFICIENT; HYDROGENATION; COORDINATION; ALDEHYDES; CATALYSTS;
D O I
10.1016/j.molstruc.2017.07.066
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
The syntheses of vanadium complexes with tridentate PNP pincer ligands based on 2,6-diaminopyridine of the type [(PNP)VCl3] are reported. All compounds reveal distorted octahedral metal coordination geometry with three meridionally placed donor atoms of the PNP ligand and one chlorine atom occupying the equatorial plane of the octahedron. The axial positions are occupied by the other two chloride ligands. Complexes [(PNP)VCl3] were obtained as different solvates displaying hydrogen bonds between the PNP ligands and solvent molecules. The NH spacer groups in the PNP ligands are responsible for the establishment of hydrogen bonds that determines the solid state supramolecular architectures. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:229 / 234
页数:6
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