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1.
S. S. Yarovoi Yu. V. Mironov S. V. Tkachev V. E. Fedorov 《Russian Journal of Inorganic Chemistry》2009,54(2):299-304
Phase formation in the Re-Se-Br-MBr systems (M = K, Rb, Cs) was studied by NMR spectroscopy and powder X-ray diffraction.
The reactions taking place in alkali metal halide melts were found to give, among the series of cluster anions [{Re6Se8 − n
Br
n
}Br6](4 − n)− (0 ≤ n≤ 4), polymeric complexes Re6Se8Br 2 and M2Re6Se8Br4 (M = Cs, Rb) and salts containing cluster anions [Re6Se6Br8]2− and [Re6Se7Br7]3− as the major products. The effect of the alkali metal cation on the product composition and ratio was established.
Original Russian Text ? S.S. Yarovoi, Yu.V. Mironov, S.V. Tkachev, V.E. Fyodorov, 2009, published in Zhurnal Neorganicheskoi
Khimii, 2009, Vol. 54, No. 2, pp. 344–349. 相似文献
2.
The size-specific influence of alkali metal ions in the gradual transition from cluster rearrangement to solvation dynamics is investigated by means of molecular dynamics simulations for alkali metal cation-hexafluorobenzene systems, M(+)-C(6)F(6) (M = Na, K, Rb and Cs), surrounded by Ar atoms. To analyze such transition, different small aggregates of the M(+)-C(6)F(6)-Ar(n) (n = 1, ..., 30) type and M(+)-C(6)F(6) clusters solvated by about 500 Ar atoms are considered. The Ar-C(6)F(6) interaction contribution has been described using two different formalisms, based on the interaction decomposition in atom-bond and in atom-effective atom terms, which have been applied to study the small aggregates and to investigate the Ar solvated M(+)-C(6)F(6) clusters, respectively. The selectivity of the promoted phenomena from the M(+) ion size and their dependence from the number of Ar atoms is characterized. 相似文献
3.
The polyborates Cs(2)M(2)B(10)O(17) (M = Na, K) have been prepared and their structures determined by single-crystal X-ray diffraction methods. They crystallize in the monoclinic space group C2/c (Z = 8) with unit-cell parameters a = 21.643(3) ?, b = 6.558(2) ?, c = 11.072(2) ?, beta = 105.43(1) degrees, V = 1514.8(6) ?(3) for the Na compound and a = 22.547(9) ?, b = 6.614(2) ?, c = 11.288(4) ?, beta = 103.25 degrees, V = 1638.3(8) ?(3) for the K analogue. The new structural type contains a 2-dimensional borate matrix that is built from a complete condensation of the ring system B(5)O(11). The Cs atoms reside within the borate matrix, and the Na (K) atoms are placed between the thick Cs borate sheets. 相似文献
4.
Marcelle Gaune-Escard A. Bogacz L. Rycerz W. Szczepaniak 《Journal of Thermal Analysis and Calorimetry》1995,45(5):1117-1124
Present work is a part of thermodynamic research program on the MX?LnX3 system (M=alkali metal,X=Cl, Br andLn=lanthanide). Molar enthalpies of mixing in the LiBr?NdBr3, NaBr?NdBr3 and KBr?NdBr3 liquid binary systems have been determined at temperature 1063 K by direct calorimetry in the whole range of composition. Investigated systems are generally characterized by negative enthalpies of mixing with minimum atX NdBr3≈0.3–0.4. These enthalpies decrease with decrease of ionic radii of alkali metals. Molar enthalpies of solid-solid and solid-liquid phase transitions of K3NdBr6 and Cs3NdBr6 have been also determined by differential scanning calorimetry (DSC). K3NdBr6 is formed at 689 K from KBr and K2NdBr5 with enthalpy of 44.0 kJ·mol?1 whereas Cs3NdBr6 is stable at ambient temperature and undergoes phase transition in the solid state at 731 K with enthalpy of 8.8 kJ·mol?1. Enthalpies of melting have been also determined. 相似文献
5.
L. A. Zemnukhova R. L. Davidovich V. N. Rykovanov S. I. Kuznetsov 《Russian Chemical Bulletin》1987,36(5):1051-1053
Conclusion A study of the temperature dependence of the123Sb NQR parameters for MSbClF3 complexes (M=K, Cs, NH4) at from 77 to 390K shows temperature ranges with anomalous change in the electric field gradient asymmetry parameter for the antimony atoms.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 5, pp. 1136–1139, May, 1987.The authors express their gratitude to G. K. Semin for a useful discussion of this work. 相似文献
6.
A series of novel heterobimetallic group 1/strontium and group 1/calcium aryloxo complexes having the composition [MAe(Odpp)3] [Ae=Sr and M=Na (1), K (2, 3), Cs (4); Ae=Ca and M=Na (5), K (6), Cs (7)] or [M2Ae(Odpp)4] [M=Li and Ae=Sr (9), Ca (10)] have been prepared using 2,6-diphenylphenol (HOdpp) as the ligand. Through the use of solid-state direct metalation, these compounds were obtained either directly from the reaction vessel or after workup in toluene. The Lewis base adduct [KCa(Odpp)3(thf)] (8) was obtained by treatment of [KCa(Odpp)3] (6) with tetrahydrofuran (thf). All of the compounds displayed extensive metal-pi-arene interactions, which provide significant stabilization in these reactive species. The thermal stabilities and volatilities of representative heterobimetallic strontium and calcium complexes were investigated using thermogravimetric analysis. 相似文献
7.
Pet'kov V. I. Kir'yanov K. V. Orlova A. I. Kitaev D. B. 《Journal of Thermal Analysis and Calorimetry》2001,65(2):381-389
The enthalpies of the solution of MZr2(PO4)3(M=Na, K, Rb or Cs) compounds have been measured by the help of a differential automatic isothermal Calvet calorimeter and the
standard enthalpies of formation have been derived. The temperature dependencies of the standard heat capacity of the samples
of crystalline NaZr2(PO4)3 and CsZr2(PO4)3 were studied between 7 and 340 K in an automatic adiabatic vacuum calorimeter. The main thermodynamic functions H
0(T)–H
0(0), S
0(T) andG
0(T)–H
0(0) have been determined. The Gibbs energies of formation of the NaZr2(PO4)3and CsZr2(PO4)3 at 298.15 K were calculated on the basis of these experimental data and the enthalpy of formation data. Qualitative explanations
for the results observed were presented.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
8.
用水热晶化法合成了MZr_2(ASO_4)_3(M=Na,K,Rb,Cs)系列化合物。研究了反应物浓度、配比及不同砷源等水热晶化条件对产物物相的影响。用XRD、IR和Raman光谱对产物进行了表征。4种晶体的振动光谱由钠到铯呈现出规律性变化。 相似文献
9.
Single-walled carbon nanotubes filled with M OH (M = K, Cs) and then washed and refilled with clusters and molecules 总被引:1,自引:0,他引:1
Thamavaranukup N Hoppe HA Ruiz-Gonzalez L Costa PM Sloan J Kirkland A Green ML 《Chemical communications (Cambridge, England)》2004,(15):1686-1687
Heating single-walled carbon nanotubes (SWNTs) with molten hydroxides MOH (M = K, Cs) gave MOH@SWNT in good yield; high resolution transmission electron microscopy (HRTEM) indicated that CsOH in CsOH@SWNT often adopts twisted 1D crystal structures inside SWNTs; treating MOH@SWNT with water at room temperature removes the soluble hydroxide filling and the resulting SWNTs may then be filled using aqueous solutions of uranyl acetate or uranyl nitrate at rt giving SWNTs filled with UO(2) clusters and uranyl acetate molecules. 相似文献
10.
11.
Y Kado CY Lee K Lee J Müller M Moll E Spiecker P Schmuki 《Chemical communications (Cambridge, England)》2012,48(69):8685-8687
We use a highly aligned Ta(2)O(5) nanochannel structure to fabricate alkali metal ion (Na, K, Rb or Cs) doped Ta(3)N(5)via solution seeding and thermal conversion in NH(3). Under optimized conditions the resulting doped structures show a strongly enhanced visible light water splitting performance in comparison to undoped Ta(3)N(5). 相似文献
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13.
O. A. Gapurenko T. N. Gribanova R. M. Minyaev V. I. Minkin 《Russian Journal of Inorganic Chemistry》2008,53(10):1605-1613
The electronic and geometric structures of M4NO 4 + compounds (M = Li, Na, K) in classical and nonclassical isomeric forms were studied by the ab initio (MP2(full)/6-311+G**) and density functional theory (B3LYP/6-311+G**) methods. For all M atoms, structurally stable nonclassical isomers were found with octacoordinated nitrogen atoms and tetracoordinated oxygen atoms. For Li4NO 4 + , the classical structure with the tetracoordinated nitrogen atom is energetically more stable, whereas nonclassical structures with the octacoordinated nitrogen center are more stable for Na4NO 4 + and K4NO 4 + . 相似文献
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15.
B. P. Burylev E. B. Kritskaya V. E. Kritskii 《Russian Journal of Physical Chemistry A, Focus on Chemistry》2006,80(12):1883-1886
Our own experimental studies of vapor pressure and surface tension were used to analyze isotherms of various types of the properties under consideration. The data obtained were processed using a mathematical model to calculate the molar surface and excess molar Gibbs energy, which clearly indicated that the surface properties obeyed the general rules that governed changes in these properties of solutions according to the position of alkali metals in the periodic table of the elements. The data on various physicochemical properties of the cesium chloride-manganese chloride system are evidence of the presence of singular extremum points on concentration dependence isotherms. 相似文献
16.
The Hartree–Fock (HF) approximation and the Single‐excitation configuration interaction (single‐CI) method are used, with sum‐over‐state (SOS) approach, in order to determine the static (ω = 0) and frequency dependent linear and non linear optical (NLO) properties of the M @ C60 endohedrals (M = Cs, Li, and Na). We discuss the effects of displacement, movement direction, and type of atom on the (hyper) polarizability of the M at C60 endohedrals. A HF‐single‐CI model yields the (hyper) polarizability magnitudes and spectra, which are in agreement with experiment. Our results indicate that the movement of the atom (M) effect on the NLO spectra of M @ C60 endohedrals is dramatic. These results may provide new means to design some new types of NLO materials. © 2009 Wiley Periodicals, Inc. Int J Quantum Chem, 2011 相似文献
17.
Miao Yan Hai-Ru Li Xin-Xin Tian Yue-Wen Mu Hai-Gang Lu Si-Dian Li 《Journal of computational chemistry》2019,40(11):1227-1232
Detailed molecular orbital and bonding analyses reveal the existence of both fluxional σ- and π-bonds in the global minima Cs ( 1 ) and Cs MB18 ( 3 ) and transition states Cs ( 2 ) and Cs ( 4 ) of dianion and monoanions (M = K, Rb, and Cs). It is the fluxional bonds that facilitate the fluxional behaviors of the quasi-planar and half-sandwich which possess energy barriers smaller than the difference of the corresponding zero-point corrections. © 2019 Wiley Periodicals, Inc. 相似文献
18.
Chaoyong Mang Caiping Liu Kechen Wu 《International journal of quantum chemistry》2010,110(5):1127-1135
The researches of all‐metal aromatic clusters have been a thermic theme in inorganic aromaticity domain both experimentally and theoretically since the Al4L? (L = Li, Na, Cu) clusters were created by laser vaporization. In systemic determination of the lowest structures of 20 gaseous all‐metal aromatic clusters M4L2 (M = Al, Ga, In, Tl; L = Li, Na, K, Rb, Cs), the isomer energy differences of four low‐lying structures of each cluster were evaluated at high‐quality quantum chemistry levels. Single point calculations at the coupled cluster level were performed at geometries optimized at the MP2, B3LYP, and B3PW91 levels, and harmonic frequency calculations and zero point energy corrections were implemented following optimizations at the B3LYP and B3PW91 levels. In addition to Li‐ and Na‐containing species, theoretical investigations came down to those new clusters including K, Rb, and Cs. For many clusters, the most convincing theoretical evidences indicate that the lowest structures are a square bipyramidal isomer rather than an edge‐caped square pyramidal species. A few discrepancies were addressed at the MP2, B3LYP, and B3PW91 levels in comparison with the coupled cluster results. These findings are significant because some clusters were generated by laser vaporization and served as theoretical prototypes to test the new means for assessing aromaticity. © 2009 Wiley Periodicals, Inc. Int J Quantum Chem, 2010 相似文献
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20.
Ko YJ Shakya A Wang H Grubisic A Zheng W Götz M Ganteför G Bowen KH Jena P Kiran B 《The Journal of chemical physics》2010,133(12):124308
The equilibrium structure, stability, and electronic properties of the Al(13)X (X=H,Au,Li,Na,K,Rb,Cs) clusters have been studied using a combination of photoelectron spectroscopy experiment and density functional theory. All these clusters constitute 40 electron systems with 39 electrons contributed by the 13 Al atoms and 1 electron contributed by each of the X (X=H,Au,Li,Na,K,Rb,Cs) atom. A systematic study allows us to investigate whether all electrons contributed by the X atoms are alike and whether the structure, stability, and properties of all the magic clusters are similar. Furthermore, quantitative agreement between the calculated and the measured electron affinities and vertical detachment energies enable us to identify the ground state geometries of these clusters both in neutral and anionic configurations. 相似文献