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801.
Two cobalt(II) coordination polymers formed from bte (bte = 1,2-bis(1,2,4-triazol-1-yl)ethane), namely [Co(bte)2(dca)2]n (1) and {[Co(bte)(dca)2] · H2O}n (2), have been synthesized and characterized by elementary analyses, IR, thermogravimetric analyses, X-ray diffraction analyses and magnetic measurements. Compound 1 is a double-chain with Co(II) centers bridged by bte, containing metallocycles of [Co2(bte)2] and trans dca as termination ligands. In 2, each Co(II) center is bonded by two bridging bte ligands and four dca as μ-1,5-dca in different orientations in the 3D network. 相似文献
802.
Van Lokeren L Maheut G Ribot F Escax V Verbruggen I Sanchez C Martins JC Biesemans M Willem R 《Chemistry (Weinheim an der Bergstrasse, Germany)》2007,13(24):6957-6966
Diffusion-ordered NMR spectroscopy (DOSY NMR) is presented as a tool for the determination of the diffusion coefficients of organic ligands in suspensions of titanium dioxide nanoparticles. The nanoparticles were prepared by a sol-gel process by hydrolysis and condensation reactions of titanium tetra-n-butoxide in the presence of pentane-2,4-dione (acacH: acetylacetone), as well as para-toluenesulfonic acid (pTsA) and n-butanol (nBuOH). NMR spectroscopic studies were performed in various deuterated solvents, on both dispersed xerosols and diluted sols. The bipolar-pulsed field gradient longitudinal eddy-current delay (LED) pulse sequence was used for data acquisition. The data were processed by inverse Laplace transformation (ILT), by using a maximum entropy algorithm, to afford 2D DOSY spectra. Different diffusion regimes for organic ligands in the bound and unbound states were successfully discriminated, more particularly in [D3]acetonitrile, thus allowing assessment of their interactions with the nanoparticles. 相似文献
803.
804.
Seggio A Lannou MI Chevallier F Nobuto D Uchiyama M Golhen S Roisnel T Mongin F 《Chemistry (Weinheim an der Bergstrasse, Germany)》2007,13(35):9982-9989
Metalation of N-phenylpyrrole by using an in situ mixture of ZnCl(2)TMEDA (0.5 equiv; TMEDA=N,N,N',N'-tetramethylethylenediamine) and LiTMP (1.5 equiv; TMP=2,2,6,6-tetramethylpiperidino) was optimized. The reaction carried out at room temperature in THF resulted in incomplete metalation (56 % conversion) and selectivity (mixture of 2-iodo and 2,2'-diiodo derivatives in an 86:14 ratio after trapping with iodine). By using diethyl ether (DEE), toluene, or hexane instead of THF, low conversions of 17, 38, or 23 % were observed, respectively, but the formation of the diiodide was avoided. When hexane was used as solvent, strong lithium-complexing ligands such as [12]crown-4 and N,N'-dimethylpropylideneurea (DMPU) inhibited the reaction whereas more (hemi)labile ligands (TMEDA>THF approximately DME) favored it. This result shows that a temporary accessibility of lithium to interact with the rest of the base and/or the substrate is a prerequisite for an efficient metalation. A 75 % yield of 2-iodo-N-phenylpyrrole was obtained after reaction with the base in the presence of five equivalents of TMEDA for two hours at room temperature, and subsequent trapping with iodine. We were able to successfully replace the spare TMP with a less expensive butyl group. 相似文献
805.
利用小分子配合物[Cu(2-mpac)2(H2O)]•3H2O (1)作为配合物配体, 以其两侧未配位的羰基氧原子与金属配位合成了一个Cu-Cd异核配位聚合物[Cu(2-mpac)2(H2O)2Cd(H2O)4(NO3)2]n (2) (2-mpac=5-methyl-2-pyrazinecarboxylic acid), 并利用元素分析、红外光谱以及X射线单晶衍射法对标题化合物进行了表征. 晶体学数据: 三斜晶系, P-1空间群, a=0.7654(7) nm, b=0.8903(8) nm, c=0.9745(9) nm, α=116.116(1)°, β=98.408(1)°, γ=90.335(1)°, V=0.5880(9) nm3, Z=1, S=1.053, 最终残差因子[I>2σ(I)] R1=0.0280, wR2=0.0718, 对于全部数据R1=0.0305, wR2=0.0741. 相似文献
806.
A new method for the synthesis of azo Schiff an base ligand in which the azo and azomethine groups are coordination sites was developed through a Schiff base precursor. The precursor, N-4-methoxybenzylidene-3-hydroxyphenylamine (SB) derived from 3-aminophenol was regioselectively coupled with a diazonium ion para to the hydroxyl group of the amine component of the Schiff base. The para selectivity was controlled by the directing effect of the hydroxyl group. The ligand and its nickel(Ⅱ) complex were characterized by elemental analyses, IR and UV-Vis spectroscopy. The analytical and spectral data supported the mononuclear formulation of the complex with metal to ligand ratio (M : L = 1 : 2) and suggested a square planar geometry for the complex. 相似文献
807.
The mononuclear vanadium(Ⅴ) complex with 2-hydroxyl-1-naphthaldehyde isoncotinoyl hydrazone was synthesized and characterized by single-crystal X-ray diffraction.The crystal is of monoclinic,space group P2 1/n with a = 10.3153(15),b = 7.4024(11 ),c = 24.413(4) (A),β= 101.911(2)°,V= 1824.0(5) (A)3,Z = 4,Mr = 427.28,Dc = 1.556 g/cm3,F(000) = 880,μ(MoKα) =0.591,the final R = 0.0372 and wR = 0.0926.The vanadium(Ⅴ) atom adopts a distorted square-pyramidal geometry coordinated by the tridentate ligand and two oxygen atoms.The hydrogen bonds and strong π…π stacking interactions link the complex molecules into a 3-D network structure. 相似文献
808.
The title compound (13,27-dimethyl-3,6,9,17,20,23-hexaazatricyclo-[23.3.1.111,15]-triaconta- 1 (29),2,9,11,13,15(30), 16,23,25,27-decaene-29,30-diol-N3,N6,N9,O29,O30)-bis(nitrato-O,O')-holmium(Ⅲ) nitrate hydrate has been prepared and characterized by elemental analysis, infrared spectra, and electrospray mass spectra. Its crystal and molecular structures were determined by X-ray diffraction methods. The crystal crystallizes in the monoclinic system, space group C2/c with a = 23.737(12), b = 14.237(7), c = 19.801(10) (A), β = 91.36(1)°, Mr = 831.57, V = 6690(6) (A)3, Z = 8,Dc = 1.651 g/cma, F(000) = 3344, R = 0.0482 and wR = 0.0923. The holmium ion is located in one of the compartments of the macrocyclic ligand and presents a distorted tricapped trigonal prismatic coordination geometry. The macrocycle is coordinated with two oxygen and three nitrogen atoms.Two nitrates are chelated in the opposite positions of the macrocycle, and the third one is ionic. 相似文献
809.
合成了一种新的含有3个配体的稀土配合物Eu(TTA)2(N-HPA)Phen(TTA-噻吩甲酰基三氟丙酮,N—HPA=N-苯基邻氨基苯甲酸,phen=邻菲咯啉)。将稀土配合物作为掺杂物与基质PVK按照不同质量比混合共溶,旋涂成膜。通过荧光光谱,分析了薄膜的发光特性,并将其应用于有机电致发光。研究了PVK和Eu(TTA)2(N—HPA)Phen之间的能量传递,并且制备了发光层为PVK:Eu(TTA)2(N—HPA)Phen,结构为ITO/PVK:Eu(TrA)2(N—HPA)Phen/BCP/Alq3/Al的多层器件,发现改变PVK和稀土配合物的掺杂比,可以不同程度地抑制PVK的发光,最终得到纯的Eu^3+的红色发光。实验结果证明,在PVK:Eu(TTA)2(N—HPA)Phen=5:1的质量比下,从PVK到稀土配合物之间存在充分的能量传递。 相似文献
810.