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41.
Solid state reactions of lanthanide oxide, MoO3 and SeO2 (or TeO2) at high temperature in an evacuated quartz tube lead to four new Ln-Mo-Se(Te)-O quaternary phases with four different types of structures, namely, Nd2MoSe2O10, Gd2MoSe3O12, La2MoTe3O12, and Nd2MoTe3O12. The structure of Nd2MoSe2O10 features a 3D architecture built by the intergrowth of the Nd-Se-O layers with the Nd-Mo-O layers. The structure of Gd2MoSe3O12 contains a 3D network of gadolinium selenite with the MoO6 octahedra occupying the cavities of the structure. The structure of La2MoTe3O12 features a 3D network of La2(Te3O8)2+ with the tunnels along the a axis occupied by the MoO4 tetrahedra. Nd2MoTe3O12 features a 2D layer built by the lanthanide ions interconnected by tellurite groups and ditellurite groups, with the MoO4 tetrahedra as the interlayer pendant groups. Room temperature and low temperature luminescent studies indicate that Nd2MoSe2O10 and Nd2MoTe3O12 exhibit strong luminescence in the near-IR region. 相似文献
42.
He H Zhu X Hou A Guo J Wong WK Wong WY Li KF Cheah KW 《Dalton transactions (Cambridge, England : 2003)》2004,(23):4064-4073
Dimerization of monoporphyrinate lanthanide complexes [Yb(Por)(H(2)O)(3)]Cl, (Por = TTP(2-), TMPP(2-) and TPP(2-)) in the presence of sterically hindered tripodal ligand, zinc Schiff-base, dilute HCl, K(2)CO(3) solution, 4,4'-bipyridine (bipy), and basic 8-hydroxyquinaldine (HQ) solution was observed in CH(2)Cl(2) at room temperature. Six neutral dimeric lanthanide porphyrinate complexes, [Yb(TTP)(mu-OH)](2)(mu-THF) (1), [Yb(TMPP)(mu-OH)(H(2)O)](2) (2), [Yb(TPP)(mu-OH)(mu-H(2)O)](2) (4), [Yb(TMPP)(mu-Cl)(H(2)O)](2) (5), [Yb(TMPP)(mu-OH)](2)(THF) (6) and [Yb(TPP)](2)(mu-OH)(mu-Q) (7), were obtained. X-Ray diffraction studies showed that for the dimers, the two lanthanide ions were bridged by OH(-), Cl(-) or H(2)O. Photoluminescent studies showed that the porphyrinate dianion acted as an antenna, transferred its absorbed visible energy to the lanthanide ion and enabled the latter emitting in the near-infrared (NIR) region. In general, the NIR emission is more intense for the dimers than for the monomers, and the NIR emission intensity decreases as the number of O-H oscillators present in the molecule increases. 相似文献
43.
Intermediates formed during reduction of Fe(2)(mu-PPh(2))(2)(CO)(6) (1) in the presence of protons have been identified by spectroelectrochemical, continuous-flow, and interrupted-flow techniques. The mechanism for electrocatalytic proton reduction suggested by these observations yields digital simulation of the voltammetry in close agreement with measurements conducted in THF over a range of acid concentrations. The mechanism for electrocatalytic proton reduction involves initial formation of the dianion, 1(2-), which is doubly protonated prior to further reduction and dihydrogen elimination. The IR spectra of the singly and doubly protonated forms of 1(2-) indicate structures corresponding to [FeH(CO)(3)(mu-PPh(2))(2)Fe(CO)(3)](-) (1H-) and FeH(CO)(3)(mu-PPh(2))(2)FeH(CO)(3) (1H(2)). The thiolato and dithiolato analogues of 1 exhibit electrocatalytic proton reduction associated with the two-electron reduction step, and this implies that the corresponding two-electron reduced doubly protonated species is unstable with respect to dihydrogen elimination. The stability of 1H(2) is most likely to be due to the weak interactions between the iron centers of the flattened [2Fe2P] core. Whereas 1H(2) is stable in the absence of a reducing potential, 1H- rearranges rapidly to a product previously described as [Fe(2)(mu-PPh(2))(mu-CO)(PHPh(2))(CO)(5)](-) (1H-(W)). Another protonation product of 1(2-), previously formulated as [Fe(2)(mu-PPh(2))(2)(mu-CO)H(CO)(5)](-), has been reformulated as [Fe(2)(mu-PPh(2))(mu-CO)(CO)(6)](-) (2) on the basis of a range of spectroscopic measurements. Solution EXAFS measurements of 1, 1(2-), 1H-(W), and 2 are reported, and these yield model-independent Fe-Fe distances of 2.61 (1), 3.58 (1(2-)), 2.58 (1H-(W)), and 2.59 A (2). The presence of an Fe-Fe bond for both 1H-(W) and 2 is a key aspect of the proposed structures, and this strongly supports the deductions based on spectroscopic evidence. The fits of the solution EXAFS to different structural models give statistics in agreement with the proposed structures. 相似文献
44.
Melina C.L. Cheah Ray L. Withers Takashi Kamiyama 《Journal of solid state chemistry》2006,179(8):2487-2494
The synthesis and crystal structures of nine members of the rock-salt ordered double perovskites Sr2−xCaxCrNbO6 is presented. The crystal structures of the end members of the series Sr2CrNbO6 and Ca2CrNbO6 were refined using powder neutron diffraction data and are cubic in and monoclinic in P21/n, respectively, in both cases there being considerable anti-site Cr-Nb mixing. Variable temperature and/or composition studies suggest a direct first-order P21/n to transition, a suggestion supported by selected area electron diffraction studies. 相似文献
45.
Abul K. Mallik Wee Keat Cheah Kaori Shingo Aika Ejzaki Makoto Takafuji Hirotaka Ihara 《Analytical and bioanalytical chemistry》2014,406(19):4585-4593
A new hydrophilic and nonionic poly(2-vinyloxazoline)-grafted silica (Sil-VOX n ) phase was synthesized and applied for the separation of nucleosides and nucleobases in hydrophilic interaction chromatography (HILIC). Polymerization and immobilization onto silica were confirmed by using characterization techniques including 1H NMR spectroscopy, elemental analysis, and diffuse reflectance infrared Fourier transform spectroscopy. The hydrophilicity or wettability of Sil-VOX n was observed by measuring the contact angle (59.9°). The chromatographic results were compared with those obtained with a conventional HILIC silica column. The Sil-VOX n phase showed much better separation of polar test analytes than the silica column, and the elution order was different. Differences in selectivity between these two columns indicate that the stationary phase cannot function merely as an inert support for a water layer into which the solutes are partitioned from the bulk mobile phase. To elucidate the interaction mechanism, the separation of dihydroxybenzene isomers was performed on both columns in normal-phase liquid chromatography. Sil-VOX n was very sensitive to the dipole moments of the positional isomers of polycyclic aromatic compounds in normal-phase liquid chromatography. The interaction mechanism for Sil-VOX n in HILIC separation is also described. Figure
Separation of nucleosides and nucleobases with Sil-VOXn (bottom) and a commercial silica column (top). Mobile phase of acetonitrile and 20 mM ammonium acetate (9:1, v/v). Flow rate 1 ml min-1, column temperature 25 °C. The analytes were as follows 5-iodouracil (1), thymine (2), uracil (3), 4,6-diaminopyrimidine (4), uridine (5), adenosine 2 (6), cytosine (7), cytidine (8), and guanosine (9) 相似文献
46.
Structural investigation of mM Ni(II) complex isomers using transmission XAFS: the significance of model development
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M. Tauhidul Islam Christopher T. Chantler Mun Hon Cheah Lachlan J. Tantau Chanh Q. Tran Stephen P. Best 《Journal of synchrotron radiation》2015,22(6):1475-1491
High‐accuracy transmission XAFS determined using the hybrid technique has been used to refine the geometries of bis(N‐n‐propyl‐salicylaldiminato) nickel(II) (n‐pr Ni) and bis(N‐i‐propyl‐salicylaldiminato) nickel(II) (i‐pr Ni) complexes which have approximately square planar and tetrahedral metal coordination. Multiple‐scattering formalisms embedded in FEFF were used for XAFS modelling of the complexes. Here it is shown that an IFEFFIT‐like package using weighting from experimental uncertainty converges to a well defined XAFS model. Structural refinement of (i‐pr Ni) was found to yield a distorted tetrahedral geometry providing an excellent fit, χr2 = 2.94. The structure of (n‐pr Ni) is best modelled with a distorted square planar geometry, χr2 = 3.27. This study demonstrates the insight that can be obtained from the propagation of uncertainty in XAFS analysis and the consequent confidence which can be obtained in hypothesis testing and in analysis of alternate structures ab initio. It also demonstrates the limitations of this (or any other) data set by defining the point at which signal becomes embedded in noise or amplified uncertainty, and hence can justify the use of a particular k‐range for one data set or a different range for another. It is demonstrated that, with careful attention to data collection, including the correction of systematic errors with statistical analysis of uncertainty (the hybrid method), it is possible to obtain reliable structural information from dilute solutions using transmission XAFS data. 相似文献
47.
High‐accuracy X‐ray absorption spectra from mM solutions of nickel (II) complexes with multiple solutions using transmission XAS
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Christopher T. Chantler M. Tauhidul Islam Stephen P. Best Lachlan J. Tantau Chanh Q. Tran Mun Hon Cheah Andrew T. Payne 《Journal of synchrotron radiation》2015,22(4):1008-1021
A new approach is introduced for determining X‐ray absorption spectroscopy (XAS) spectra on absolute and relative scales using multiple solutions with different concentrations by the characterization and correction of experimental systematics. This hybrid technique is a development of standard X‐ray absorption fine structure (XAFS) along the lines of the high‐accuracy X‐ray extended range technique (XERT) but with applicability to solutions, dilute systems and cold cell environments. This methodology has been applied to determining absolute XAS of bis(N‐n‐propyl‐salicylaldiminato) nickel(II) and bis(N‐i‐propyl‐salicylaldiminato) nickel(II) complexes with square planar and tetrahedral structures in 15 mM and 1.5 mM dilute solutions. It is demonstrated that transmission XAS from dilute systems can provide excellent X‐ray absorption near‐edge structure (XANES) and XAFS spectra, and that transmission measurements can provide accurate measurement of subtle differences including coordination geometries. For the first time, (transmission) XAS of the isomers have been determined from low‐concentration solutions on an absolute scale with a 1–5% accuracy, and with relative precision of 0.1% to 0.2% in the active XANES and XAFS regions after inclusion of systematic corrections. 相似文献
48.
Nicolas Bucher Steffen Hartung Irina Gocheva Yan L. Cheah Madhavi Srinivasan Harry E. Hoster 《Journal of Solid State Electrochemistry》2013,17(7):1923-1929
We report on the electrochemical properties of layered manganese oxides, with and without cobalt substituents, as cathodes in sodium ion batteries. We fabricated sub-micrometre-sized particles of Na0.7MnO2?+?z and Na0.7Co0.11Mn0.89O2?+?z via combustion synthesis. X-ray diffraction revealed the same layered hexagonal P2-type bronze structure with high crystallinity for both materials. Potentiostatic and galvanostatic charge/discharge cycles in the range 1.5–3.8 V vs. Na | Na+ were performed to identify potential-dependent phase transitions, capacity, and capacity retention. After charging to 3.8 V, both materials had an initial discharge capacity of 138 mA?h?g?1 at a rate of 0.3 C. For the 20th cycle, those values reduced to 75 and 92 mA?h?g?1 for Co-free and Co-doped samples, respectively. Our findings indicate that earlier works probably underestimated the potential of (doped) P2-type Na0.7MnO2?+?z as cathode material for sodium ion batteries in terms of capacity and cycle stability. Apart from doping, a simple optimization parameter seems to be the particle size of the active material. 相似文献
49.
Li Liu Wai‐Yeung Wong Jian‐Xin Shi Kok‐Wai Cheah 《Journal of polymer science. Part A, Polymer chemistry》2006,44(19):5588-5607
A new series of organic‐soluble and thermally stable group 10 platinum(II) polyyne polymers functionalized with 9‐arylcarbazole moiety trans‐[? Pt(PBu3)2C?CRC?C? ]n (R = 9‐arylcarbazole‐3,6‐diyl; aryl = phenyl, p‐methylphenyl, p‐fluorophenyl) were prepared in good yields by Hagihara's dehydrohalogenative polymerization of trans‐[PtCl2(PBu3)2] with HC?CRC?CH under ambient conditions. The regiochemical structures of the polymers were characterized by multinuclear NMR spectroscopy. We discuss the optical spectroscopy of these polymetallaynes and compare the results with their bimetallic molecular model complexes trans‐[Pt(Ph)(PEt3)2C?CRC?CPt(Ph)(PEt3)2] as well as its group 11 gold(I) and group 12 mercury(II) congeners [(PPh3)AuC?CRC?CAu(PPh3)] and [MeHgC?CRC?CHgMe]. The structural properties of several model complexes were studied by X‐ray crystallography. The influence of the heavy metal atom and the 9‐aryl substituent of carbazole on the phosphorescence behavior and the spatial distribution of the lowest singlet (S1) and triplet (T1) excitons in these metalated alkynyl systems are comprehensively elucidated. The present work indicates that the efficiency of organic triplet emissions harnessed through the heavy‐atom effect of group 10–12 transition metals in the main chain generally follows the order Pt > Au > Hg but the optical properties of the materials are relatively insensitive to the nature of the 9‐aryl group on the carbazolyl ring. All of these metallaynyl‐carbazole materials with high‐energy T1 states of 2.68 eV or higher show high phosphorescence efficiencies at low temperatures. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 5588–5607, 2006 相似文献
50.
Xin Jiang Feng Po Lam Wu Hoi Lam Tam Dr. King Fai Li Dr. Man Shing Wong Prof. Kok Wai Cheah Prof. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2009,15(43):11681-11691
A novel series of diphenylamino‐ and 1,2,4‐triazole‐end‐capped, fluorene‐based, π‐conjugated oligomers that includes extended oligofluorenes and oligothienylfluorenes has been synthesized by means of the palladium‐catalyzed Suzuki cross‐coupling of 9,9‐dibutyl‐7‐(diphenylamino)‐2‐fluorenylboronic acid and the corresponding 1,2,4,‐triazole‐based aryl halide as a key step. It was demonstrated that efficient two‐ and three‐photon excited photoluminescence and lasing in the blue region are obtained by pumping near‐infrared femtosecond lasers on these materials. Although the absorption and emission maxima of the highly fluorescent and extended oligofluorenes reach a saturation limit, there exists an effective conjugation length for an optimum three‐photon absorption cross section in the homologous oligofluorene series. On the other hand, the multiphoton excited emission spectrum and lasing wavelength can easily be modified or tuned by an incorporation of thienyl unit(s) into the fluorene‐based π‐conjugated core with which exceptionally large three‐photon absorption cross sections up to 3.59×10?77 cm6 s2 in the femtosecond regime have been obtained, thereby highlighting the potential of this series of photonic materials. The optimized full width at half‐maximum of the cavityless three‐photon upconverted blue lasing spectra are sharply narrowed to approximately 6 nm with an efficiency of up to 0.013 %. 相似文献