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971.
Yan Ping Wang Wen Fa Xie Bin Li Wen Lian Li 《中国化学快报》2007,18(12):1501-1504
A new 1,3,4-oxadiazole-contanining rhenium(I) complex,with the formula [Re(CO)_3(Bphen)(PTOP)],(Bphen=bathophe- nardine,PTOP=4-(5-p-tolyl-1,3,4-oxadiazd-2-yl)pyridine),is synthesized and characterized by elemental analysis,IR,~1H NMR, UV-vis and luminescence spectroscopy.The double-layer electroluminescence devices based on the Re(I) complex have been fabricated by spin-coating technique.The turn-on voltage,maximum efficiency,and brightness for green emission obtained from the devices are 9V,2.1cd/A and 165cd/m~2,respectively. 相似文献
972.
双金属氰化物配合物的制备、表征及催化性能 总被引:7,自引:0,他引:7
制备了基于钴氰化锌的双金属氰化物配合物(DMC)催化剂,并\r\n用元素分析、X射线衍射和红外光谱等手段进行了表征,考察了催化剂\r\n的结构与组成对其催化活性的影响以及该催化体系催化环氧烷烃开环聚\r\n合的特点.结果表明,含ZnCl2和叔丁醇的非晶态DMC催化剂具有最高的\r\n催化活性.该催化体系使聚合物的分子量可控,不饱和度很低(<14μ\r\neq/g),逐步聚合所得到的聚合物的分子量分布较窄(Mn/Mw<1.4\r\n8).13CNMR分析结果表明,甲基氧丙环均聚物的链结构具有无规立构\r\n的特点,且链节分布几乎都为头-尾方式.IR分析结果表明,甲基氧丙\r\n环-环氧乙烷共聚物的链结构是无规分布的. 相似文献
973.
Jóna E. Kubranová M. Sirota A. Šimon P. 《Journal of Thermal Analysis and Calorimetry》1998,52(2):373-382
The stoichiometry of thermal decomposition and enthalpy and structural changes were studied for the compounds formed by penetration
of [Ni(4-Etpy)4(NCS)2] (I) into Ca-montmorillonite (II) or Cr-, Zr- and Al-pillared analogues (III, IV and V, respectively).
The mass fractions of complex I in II, III, IV or V are different. It was found for all studied compounds that the release
of L (L=4-Etpy) is a three-step process (-2L, -1L, -1L), and differences occurred in enthalpy changes (δH in kJ per mole of
I) corresponding to the individual processes. These differences and the changes in diffraction and spectral properties of
the species formed after intercalation are assumed to have their roots in different intramolecular guest-host interactions
in the studied compounds.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
974.
The equilibrium constants and molar absorptivities for the fast formation of a 1:3 complex between cadmium(II) (Cd(II)) and dithizonate anion, in the presence of cationic and non-ionic surfactants, allowed a simple and fast spectrophotometric determination of total cadmium. Indeed, the molar absorptivities of the Cd(II)-dithizone (Dz) complex formed in the presence of the neutral Triton X-100 and cationic cetyltrimethylammonium bromide (CTAB) surfactants are almost twice the value observed in the standard method and the maxima of absorption are shifted by about 40 nm when compared with the standard method. Clearly, the use of neutral and cationic surfactants promotes a higher value of the molar absorptivities of the complex, resulting in an increase in the sensitivity of the method. Application of the method to the desorption of Cd(II) ions from clays is illustrated. 相似文献
975.
976.
Ksenia Shilyaeva Nils Elander Evgeny Yarevsky 《International journal of quantum chemistry》2007,107(6):1301-1315
Peaks in collision cross sections are often interpreted as resonances. The complex dilation method, as well as other methods relying on analytic continuation of the scattering formalism, can be used to clarify whether these structures are true resonances in the sense that they are poles of the S‐matrix and the associated Green function. The performance of the Mittag–Leffler expansion and T‐matrix Green function expansion methods are formally and computationally compared. The two methods are applied to two model potentials. Eigenenergies, s‐wave residues, and cross sections are computed with both methods. The resonance contributions to the cross sections are further analyzed by removing the residue contributions from the Mittag–Leffler and Green function expansion sums, respectively. It is suggested that the contribution of a resonance to a cross section should be defined through its S‐matrix residue. © 2006 Wiley Periodicals, Inc. Int J Quantum Chem, 2007 相似文献
977.
The dipole moment and polarizability changes have been determined from electroabsorption (EA) spectroscopy of solid films of fac tris(2-(phenyl)pyridinato,N,C2′)iridium (III) [Ir(ppy)3]. The maximum changes in the dipole moment |Δμ|S=(5.0±0.5) D/f (f is the local field correction factor: 1.3–1.7) accompany ground state to the lowest singlet, and |Δμ|T=(1.7±0.5) D/f ground state to the lowest triplet metal-to-ligand charge transfer (MLCT) excited states formation, while the average polarizability change
Å3/f2 follows from the fitting procedure throughout the visible absorption spectrum range. The experimental values of |Δμ| as well as energy positions of the MLCT states correlate with the literature results of time-dependent density functional theory. 相似文献
978.
Chun-Long?Chen Andrea?M.?Goforth Mark?D.?Smith William?R.?Gemmill Cheng-Yong?Su Hans-Conrad?zur?LoyeEmail author 《Journal of Cluster Science》2005,16(4):477-487
A new flexible ligand, 1,5-bis(8-oxaquinoline)-3-methylpentane (C5MeOQ), was synthesized and used in the preparation of the
new dinuclear copper(II) complex 1: [Cu2(μ-OMe)2(μ-C5MeOQ)(NO3)2]. Single crystal X-ray analysis revealed that complex 1 contains dinuclear Cu(II) units with bridging methoxo groups. The ligand, C5MeOQ, takes on a bent conformation in order to
connect to and complete the square planar coordination environment of both copper centers; and one of the two Cu(II) centers
adopts a distorted square planar configuration as a result of the ligand conformation. The magnetic properties of complex
1 were investigated by variable-temperature magnetic susceptibility measurements in the 100–300 K range. Interestingly, the
susceptibility data for complex 1 reveals that the compound is diamagnetic, suggesting the presence of very strong antiferromagnetic coupling interactions
between the adjacent Cu(II) centers. 相似文献
979.
The complex Eu(btfa)3 (phen) (btfa=4,4,4‐trifluoro‐1‐phenyl‐1, 3‐butanedione, phen = 1,10‐phenanthroline) has been prepared and characterized by elemental analysis, IR and UV spectroscopies. The crystal and molecular structures of the complex have been determined by X‐ray diffraction analysis. It belongs to the monoclinic crystal system, space group P21/c with a = 0.9700(2) nm, b = 3.7450(5) nm, c = 1.0917(3) nm, β = 92.51(2)°, V = 3.962(1) nm5, Z = 4, Dc = 1.639 g/cm3, μ = 1.676 mm?1, F(000) = 1936, R1, = 0.0388, wR2 = 0.0775. Structure analysis shows that the europium(III) ion is coordinated to six oxygen atoms of β‐diketonate anions and two nitrogen atoms of phenanthroline molecule. The coordination polyhedron is an approximate square antiprism. 相似文献
980.
Reactions of SmI2 in THF with ArSSAr produced two binuclear samarium thiolate complexes [(THF)3I2- Sm(μ-SAr)]2 [Ar=Ph (1), 4-Me2NC6H4 (2)] in high yields. The structure of 2 was characterized by single crystal X-ray crystallography. The crystal of 2 belongs to the triclinic system with space group P 1 and a=0.95705(13) nm, b= 1.22287(14) nm, c= 1.26450(14) nm, a=64.194(11)°, B=78.491(13)°, y=76.176(12)°, V= 1.2860(3) nm^3, Z= 1,μ=4.783 mm^-1, Dc= 1.964 Mg/m^3, M= 1521.19, S= 1.046, R1=0.0358, wR2=0.0910. X-ray analysis revealed that 2 is a thiolate-bridged dimer in which each Sm atom adopts a distorted pentagonal bipyramidal coordi- nation geometry. 相似文献