Complexes of functionalized dipyrido[3,2-a:2′,3′-c]-phenazine:: A synthetic, spectroscopic, structural, and density functional theory study

被引:93
|
作者
Lundin, NJ
Walsh, PJ
Howell, SL
McGarvey, JJ
Blackman, AG
Gordon, KC
机构
[1] Univ Otago, Dept Chem, MacDiarmid Inst Adv Mat & Nanotechnol, Dunedin, New Zealand
[2] Queens Univ Belfast, Sch Chem, Belfast BT9 5AG, Antrim, North Ireland
关键词
D O I
10.1021/ic050179k
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The ligands 11-bromodipyrido[3,2-a:2',3'-c]phenazine and ethyl dipyrido[3,2-a:2',3'-c]phenazine-11-carboxylate have been prepared and coordinated to ruthenium(II), rhenium(I), and copper(I) metal centers. The electronic effects of substitution of dipyrido[2,3-a:3',2'-c]phenazine (dppz) have been investigated by spectroscopy and electrochemistry, and some photophysical properties have been studied. The crystal structures of [Re(L)(CO)(3)Cl] (L = ethyl dipyrido[3,2-a:2',3'-c]phenazine-11-carboxylate or 11-bromodipyrido[3,2-a:2',3'-c]phenazine) are presented. Density functional theory calculations on the complexes show only small deviations in bond lengths and angles (most bonds within 0.02 angstrom, most angles within 2 degrees) from the crystallographic data. Furthermore, the vibrational spectra of the strongest Raman and IR bands are predicted to within an average 6 cm(-1) for the complexes [Re(L)(CO)(3)Cl] and [Cu(L)(triphenylphosphine)(2)]BF4 (in the 1000-1700 cm(-1) region). Spectroscopic and electrochemical evidence suggest that reduction of the complex causes structural changes across the entire dppz ligand. This is unusual as dppz-based ligands typically have electrochemical properties that suggest charge localization with reduction on the phenazine portion of the ligand. The excited-state lifetimes of the complexes have been measured, and they range from ca. 200 ns for the [Ru(L)(2,2'-bipyridine)(2)](PF6)(2) complexes to over 2,us for [Cu(11-bromodipyrido[3,2-a:2',3'c]phenazine)(PPh3)(2)](BF4) at room temperature. The emission spectra suggest that the unusually long-lived excited states of the copper complexes result from metal-to-ligand charge transfer (MLCT) transitions as they are completely quenched in methanol. Electroluminescent films may be fabricated from these compounds; they show MLCT state emission even at low doping levels [< 0.1% by weight in poly(vinylcarbazole) polymer matrix].
引用
收藏
页码:3551 / 3560
页数:10
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