Syntheses and coordination chemistry of methylpyridylphosphine oxide ligands with copper(II)

被引:13
|
作者
Hung-Low, Fernando [1 ]
Klausmeyer, Kevin K. [1 ]
机构
[1] Baylor Univ, Dept Chem & Biochem, Waco, TX 76798 USA
关键词
Copper; Jahn-Teller effect; Coordination modes; SILVER(I) 3-AMINOMETHYLPYRIDINE COMPLEXES; PI-STACKING; PHOSPHINE OXIDES; RATIO; CRYSTAL; BIPYRIDINE; MOLECULES; ANION; SALTS; PALLADIUM(II);
D O I
10.1016/j.poly.2010.02.019
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The coordination properties of three heterofunctional phosphine oxide ligands, 2-methylpyridyldiphenylphosphine oxide (L1), phenylphosphino-bis-2-methylpyridine oxide (L2) and phenylphosphino-bis-2-methylpyridine N,N',P-trioxide (L3) with Cu(II) is described. The X-ray crystal structures of the compounds display a distorted octahedral geometry, which exhibit Jahn-Teller distortions. In compounds 1 and 2, the L1 and 12 ligands react with Cu(BF4)(2) in a 2:1 ligand to metal ratio, respectively, with the BF4 anions interacting with the metal center. L3 reacts with Cu(BF4)(2) in 1:1 and 2:1 ligand/metal ratios to form compounds 3 and 4, respectively. Addition of either 2,2'-bipyridine or 4,4'-bipyridine to reaction solutions containing Cu(BF4)(2) and U produces a discrete molecule (5) and a polymeric structure (7), respectively. The reaction of both bipyridines in the presence of Cu(BF4)(2) and L3 gives rise to a discrete molecule (6) characterized by two octahedral coppers interconnected by the 4,4'-bipyridine. The electrochemical and photophysical properties of all compounds were investigated by cyclic voltammetry (CV) and UV-Vis, as they exhibited no emission or excitation in fluorimetric experiments. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1676 / 1686
页数:11
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