A novel ruthenium polypyridyl complex of [Ru(bpy) 2(FcIP)](PF 6) 2(bpy=2,2′-bipyridine, FcIP=2-ferrocenyl-imidazo[4,5-f]-1, 10-phenanthroline) was synthesized and characterized by elementary analysis and 1H NMR. The binding of the complex to calf thymus(ct) DNA was investigated with absorption and luminescence spectroscopy titrations, steady-state emission quenching, and viscosity measurements. The results suggest that the complex acted as a ct-DNA intercalator with an intrinsic binding constant of (2.0±0.4)×10 5 L/mol in buffered 50 mmol/L NaCl.
合成和表征了1个新的钌(Ⅱ)配合物[R u(bpy)2(dpapz)](C lO4)2,其中bpy=2,2′-联吡啶,dpapz=联吡啶并[3,2-a:2,′3-′c]-6-氮杂-吩嗪.通过紫外可见光谱、荧光光谱、与溴化乙锭的竞争键合实验和粘度测量研究了该配合物与小牛胸腺DNA的键合性质,并研究了该配合物的紫外可见光谱和荧光光谱的溶剂变色性质.结果表明,该配合物是具有键合常数Kb=6.9×105L/m o l(50 mm o l/L N aC l)的DNA嵌入键合试剂和优良的荧光溶剂传感分子.
A new ruthenium（Ⅱ） complex,[Ru（bpy）2bdpq](ClO4)2,where bpy=2,2′-bipyridine,（bdpq=2-（benzoxazol-2-yl）-dipyrido） [2,3-f: 2′,3′-h]quinoxaline,was synthesized and characterized by IR,（）1H NMR,MALDI-TOF MS,and elemental analysis.The electronic absorption and emission spectral titrations with calf thymus DNA,steady-state emission quenching by [Fe（CN）6]4-,and viscosity measurements were carried out to study the binding of [Ru（bpy）2bdpq](ClO4)2 with the DNA.The results indicate that the（Ru（Ⅱ）） complex acts as a DNA intercalator with a binding constant of（1.9±0.1）×106 L/mol at 50 mmol/L NaCl,and can serve as a good "DNA molecular light switches" with a luminescence enhancement factor of 180.
Three ternary Eu(III) complexes with general formula of Eu(DBM)3LN (DBM = dibenzoylmethanate, and LN (N = 13 ) stand for three different 1,10-phenanthroline derivatives) have been synthesized for vacuum deposition films-based electroluminescent devices. The complex Eu(DBM)3L3 (L3 = 2-phenyl-3-[3-(carbazol-9-yl)propyl]imidazo[4,5-f]1,10-phenan- throline) was designed with an effort to combine the electron-transporting phenanthroline plat-form and the hole-transporting carbazole group into one molecule expecting to improve both electron and hole transporting properties simultaneously. The results show that the variation of the neutral ligands in Eu(III) mixed ligand complexes is a simple and effective approach to the improvement in the thermal stability, PL and EL properties of materials. A double-layer device with the configuration of ITO/TPD (50 nm)/Eu(DBM)3L3 (50 nm)/Mg0.9Ag0.1 (200 nm)/Ag (100 nm) exhibited Eu(III)-based pure red emission with a maximum brightness of 561 cd/m2 at 16 V, and an onset driving voltage of 8 V. A device with the configuration of ITO/TPD (50 nm)/[Eu(DBM)3L3 (5 nm):BCP (5 nm)]4/BCP (20 nm)/AlQ (10 nm) Mg0.9Ag0.1 (110 nm)/Ag (100 nm) gave high effi-cient and pure red light emission with a luminance of 1419 cd/m2.
BIAN Zuqiang1,2, GAO Deqing1, GUAN Min1, XIN Hao1, LI Fuyou1, HUANG Chunhui1, WANG Kezhi2 & JIN Linpei2 1. State Key Laboratory of Rare Earth Materials Chemistry and Applications, Peking University, Beijing 100871, China
Three kinds of new electrostatic self-assembled multilayer films were prepared with alternating adsorption of H3PMo12O40 and hemicyanine derivatives,and characterized with UV-visible absorption spectroscopy and cyclic voltammetry.The results show that these films are vertically uniform and electrochemically active with surface-controlled behavior,and the charge transfer may occur between H3PMo12O40 and hemicyanine derivatives in the films.The electron transfer rates of the three films are derived to be 0.0027,0.0019 and 0.00066 s-1,respectively,which decrease with increasing the thickness of the hemicyanine layers in the films.
The dimerization of a well-known DNA light-switch [Ru(phen)2dppz]2+(phen=1,10-phenanthroline, dppz=dipyrido[3,2-a:2′,3′-c]phenazine), and its effect on calf thymus binding properties were studied by UV-Vis and emission spectroscopy in Tris-HCl buffered 50 mmol/L NaCl(pH=7.1). The results show that the complex has a strong tendency to dimerize with a dimerization constant of (1.8±0.3)×106 L/mol at the same order of magnitude as the DNA binding constant of (6.0±1.2)×106 L/mol for the Ru(Ⅱ) complex dimer, but one order of magnitude less than (4.9±1.5)×107 L/mol for the Ru(Ⅱ) complex monomer. This study has provided insight into a fundamental but important issue that should be taken into account for the DNA binding studies.
