Coordination nature of europium(III) with tBuPNP (2,6-bis(di-tert-butylphosphinomethyl) pyridine) ligand

被引:2
作者
Goni, Md. A. [1 ]
Daniels, Lee M. [2 ]
Siddiquee, Tasneem A. [1 ]
机构
[1] Tennessee State Univ, Dept Chem, Nashville, TN 37209 USA
[2] Rigaku Americas Corp, The Woodlands, TX 77381 USA
关键词
Europium-PNP complex; Bis-(di-tert-butylphosphinomethyl)pyridine; Hydrated europium(III)chloride; Oxygen insertion; X-ray structure; CRYSTAL-STRUCTURES; COMPLEXES; AUTOXIDATION; FRAMEWORKS; O-2; H-2; LN;
D O I
10.1016/j.ica.2012.09.023
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The reaction of 2,6-bis(di-tert-butylphosphinomethyl)pyridine (PNP) with hydrated europium(III) chloride yields a novel complex, dichlorotriaqua-(2,6-bis(di-tert-butylphosphinoxidomethyl) pyridine)europium(III) chloride. The complex crystallizes as a dihydrate. IR, H-1 and P-31 NMR spectroscopic studies were undertaken along with X-ray diffraction studies for structural elucidation. The solid state structure of the compound reveals the insertion of oxygen atoms in the inner coordination sphere bridging phosphorus and europium atoms. The metal center is a seven coordinate system ligated by two chloride ligands, three water ligands and two oxygen atoms from the oxidized phosphine moiety of the PNP ligand. The nitrogen atom of the pyridine unit of the ligand is not coordinated to the metal center. (C) 2012 Elsevier B. V. All rights reserved.
引用
收藏
页码:645 / 648
页数:4
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