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1.
V. V. Sharutin V. S. Senchurin O. K. Sharutina 《Russian Journal of Inorganic Chemistry》2012,57(3):398-401
The complex [(HOCH2)3CNH3] 2 + [HgI4]2? (I) was synthesized by reacting (trioxymethyl)methylammonium iodide with mercury dioide (2: 1 mol/mol) in acetone. X-ray crystallography shows that the complex consists of two types of crystallographically independent [(HOCH2)3CNH3]+ cations and tetrahedral anions [HgI4]2? (IHgI, 106.49(2)°–113.99(4)°; Hg-I, 2.7849(8)-2.8105(8) Å. [(HOCH2)3CNH3]+ cations are linked via hydrogen bonds O…H-N and O-H…N (O…N, 2.84–2.92 Å) to form polymer chains, which are cross-linked with one another via anions (I…H, 2.81, 2.82 Å). 相似文献
2.
V. V. Sharutin O. K. Sharutina V. S. Senchurin 《Russian Journal of General Chemistry》2016,86(9):2141-2142
3.
A. I. Gubanov A. M. Danilenko A. I. Smolentsev N. V. Kuratieva A. B. Venediktov S. V. Korenev 《Journal of Structural Chemistry》2016,57(8):1606-1612
Double complex salts (DCS) α-[Pd(NH3)4][IrF6]·H2O (P21/m, a = 6.3181(3) Å, b = 10.8718(5) Å, с = 7.4526(4) Å, β = 103.568(2)°), β-[Pd(NH3)4][IrF6]·H2O (P21/с, a = 8.5773(3) Å, b = 10.8791(4) Å, с = = 12.6741(3) Å, β = 122.497(2)°), [Pd(NH3)4]3[IrF6]2Cl2·H2O (P-1, a = 7.6080(2) Å, b = 7.6274(2) Å, с = 11.8070(3) Å, β = 122.497(2)°), and [Pd(NH3)4]2[IrF6]NO3 (Fm-3m, a = 11.21210(10) Å) have been synthesized and structurally characterized for the first time. The existence of polymorphs for the DCS has been revealed. The influence of the chemical composition of the initial reagents on the reaction course and, respectively, the products, has been demonstrated. A hypothesis on the influence of the second coordination sphere on the formation of one or the other polymorph of the DCS has been suggested. It has been shown that the series α-[Pd(NH3)4][МF6]·H2O (M = Pt, Pd) exhibits isostructurality. 相似文献
4.
Evidence for the existence of primitive life forms such as lichens and fungi can be based upon the formation of oxalates.
These oxalates form as a film like deposit on rocks and other host matrices. The anhydrous oxalate mineral moolooite CuC2O4 as the natural copper(II) oxalate mineral is a classic example. Another example of a natural oxalate is the mineral wheatleyite
Na2Cu2+(C2O4)2·2H2O.
High resolution thermogravimetry coupled to evolved gas mass spectrometry shows decomposition of wheatleyite at 255°C. Two
higher temperature mass losses are observed at 324 and 349°C. Higher temperature mass losses are observed at 819, 833 and
857°C. These mass losses as confirmed by mass spectrometry are attributed to the decomposition of tennerite CuO. In comparison
the thermal decomposition of moolooite takes place at 260°C. Evolved gas mass spectrometry for moolooite shows the gas lost
at this temperature is carbon dioxide. No water evolution was observed, thus indicating the moolooite is the anhydrous copper(II)
oxalate as compared to the synthetic compound which is the dihydrate. 相似文献
5.
A. S. Kubasov E. Yu. Matveev E. S. Turyshev I. N. Polyakova K. Yu. Zhizhin N. T. Kuznetsov 《Doklady Chemistry》2017,477(1):257-260
The interaction of the [B10H10]2– and [B12H12]2– anions with aliphatic and aromatic nitro compounds (RNO2, where R = Et, n-Pr, i-Pr, tert-Bu, Ph) has been studied under irradiation with visible and UV light. It has been shown that, depending on the reaction conditions, both mono- and disubstituted nitro-closo-decaborates can be selectively obtained in yields up to 50%. 相似文献
6.
F. Bousmina L. Zayani D. Ben Hassen-Chehimi N. Kbir-Ariguib M. Trabelsi-Ayedi 《Monatshefte für Chemie / Chemical Monthly》2003,134(5):763-768
Summary. The diagram of the ternary system Mg2+/Cl−, SO4
2−–H2O was established at 15°C by means of analytical and conductimetric measurements. Three compounds were found in this diagram,
which are MgSO4·6H2O, MgSO4·7H2O, and MgCl2·6H2O. The solubility field of MgSO4·7H2O is important whereas those of MgSO4·6H2O and MgCl2·6H2O are small. The compositions (mass-%) of the two invariant points determined by the two methods are: MgSO4:MgCl2=2.73:33.80 and MgSO4: MgCl2=3.38:28.91. Both the measured and the calculated isotherm at 15°C have been used for modelling of the diagram Mg2+/Cl−, SO4
2−–H2O between 0 and 35°C. The polythermal invariant point was approximately located between 15 and 10°C.
Corresponding author. E-mail: ariguib@planet.tn
Received October 16, 2002; accepted (revised) December 3, 2002
Published online April 24, 2003
RID="a"
ID="a" Dedicated to Prof. Dr. Heinz Gamsj?ger on the occasion of his 70th birthday 相似文献
7.
S. Menecier S. Valette P. Denoirjean P. Lefort 《Journal of Thermal Analysis and Calorimetry》2012,107(2):607-616
In this article, corrosion of Invar® in a static carbon dioxide atmosphere \( 2\times 1 0^{4} \le P_{{{\text{CO}}_{ 2} }} \le 10^{5} \,{\text{Pa}} \) has been studied between 1163 and 1263 K. At the beginning, after a short initial deceleration for weight gains Δm/S <0.5 mg cm?2, oxidation kinetics were linear up to weight gains of about 4.0 mg cm?2, and only wüstite Fe1?x O was formed with a constant rate r (mg cm?2 s?1) \( r = \frac{{{\text{d}}\left( {\frac{\Updelta m}{S}} \right)}}{{{\text{d}}t}} = 0.41 \times P_{{{\text{CO}}_{ 2} }} \exp \left( {\frac{ - 198000}{RT}} \right) \) where R is the gas constant and t the time (s). Reaction mechanism is similar to that of the pure iron in analogous conditions, with the same rate limiting step i.e. external reaction of CO2 with wüstite and outward diffusion of ions Fe2+ (not limiting). For weight gains Δm/S higher than 4 mg cm?2, the limiting step changes, with an increase of the reaction rate and an internal oxidation. The origin of this mechanism change lies in the microcracks appearing in the oxide during its growth. Then, wüstite is no longer bound to the substrate; outward diffusion of ions Fe2+ stops and a topotactic transformation converts wüstite into magnetite. 相似文献
8.
S. A. Gromilov I. A. Baidina T. A. Denisova L. G. Maksimova 《Journal of Structural Chemistry》2005,46(1):116-121
Synthesis of a mixed complex compound Pb2[Fe(CN)6]NO3·5.5H2O is described. The results of its X-ray structural investigation are presented. Crystal data: C6H11FeN7O8.50Pb2: a = 7.2582(6) Å, b = 21.838(3) Å, c = 11.612(1) Å; β = 107.91(1)°, V = 1751.4(3) Å3, Z = 4, dcalc = 2.986 g/cm3, space group P21/m, R = 0.038. The compound has a framework polymer structure. 相似文献
9.
L. A. Zemnukhova R. L. Davidovich A. A. Udovenko E. V. Kovaleva 《Russian Journal of Coordination Chemistry》2005,31(2):115-120
Preparative method in combination with X-ray diffraction and IR spectroscopy is used to study reaction of Sb(III) fluoride with -aminoisovaleric acid (DL-valine) in an aqueous solution in the range of the molar ratios of components (0.25–2) : 1 in the presence of hydrofluoric acid. The molecular complex of Sb(III) fluoride with valine (1 : 1) of the composition SbF3{(CH3)2CHCH(+NH3)COO–}(I) and valinium tetrafluoro-antimonate(III) monohydrate {(CH3)2CHCH(+NH3)COOH}SbF4· H2O (II) are synthesized for the first time. Crystal structure was determined for the molecular complex I consisting of SbF3 groups and valine molecules united into polymer chains through bidentate bridging carboxylate groups of amino acid molecules.Translated from Koordinatsionnaya Khimiya, Vol. 31, No. 2, 2005, pp. 125–131.Original Russian Text Copyright © 2005 by Zemnukhova, Davidovich, Udovenko, Kovaleva. 相似文献
10.
11.
T. V. Koksharova V. S. Sergienko M. D. Surazhskaya T. V. Mandzii Yu. N. Mikhailov 《Russian Journal of Inorganic Chemistry》2017,62(12):1568-1575
The synthesis, IR and Raman spectroscopic study, and X-ray diffraction analysis of [Ni(HL1)3](L2)2 · 4H2O (I), where HL1 is phenylacetic acid hydrazide and L2 is the benzoate monoanion, have been performed. The structural units of a crystal of complex I are complex [Ni(HL1)3]2+ cations, (L2)– anions, and crystallization water molecules. The nickel atom is coordinated to the three oxygen atoms at octahedron apices and the three nitrogen atoms of three bidentate chelate (О, N) ligands HL1 in cis,trans-meredianal (fac) conformation. The structural units of a crystal of complex I are bonded by a branched network of О–Н···О and N–H···O hydrogen bonds. 相似文献
12.
Baoling Wang Liuzheng Sun Haidong Ju Shilong Zhao Degang Deng Huanping Wang Shiqing Xu 《Journal of Sol-Gel Science and Technology》2009,50(3):368-371
CaAl2Si2O8: Eu2+, Mn2+ phosphors have been prepared by a sol–gel method. X-ray diffractometer, spectrofluorometer and UV–Vis spectrometer were used
to characterize structural and optical properties of the samples. The results indicate that anorthite (CaAl2Si2O8) directly crystallizes at 1000 °C in the sol–gel process. CaAl2Si2O8: Eu2+, Mn2+ phosphors show two emission bands excited by ultraviolet light. Blue (around 415 nm) and yellow (around 575 nm) emissions
originate from Eu2+ and Mn2+, respectively. With appropriate tuning of Mn2+ content, CaAl2Si2O8: Eu2+, Mn2+ phosphors exhibit different hues and relative color temperatures. 相似文献
13.
Pavel A. Abramov Anton A. Ivanov Michael A. Shestopalov Mhamad A. Moussawi Emmanuel Cadot Sébastien Floquet Mohamed Haouas Maxim N. Sokolov 《Journal of Cluster Science》2018,29(1):9-13
Slow evaporation of water solution of [{Re6S8}(H2O)6]2+ generated in situ from [{Re6S8}(OH)6]4– in presence of γ-cyclodextrin (CD) leads to crystallization of {[{Re6S8}(H2O)6] ? [γ-CD]}(NO3)2·12H2O (1·12H2O) supramolecular complex, which was characterized by single-crystal X-ray diffraction crystallography, IR-spectroscopy, thermogravimetric and elemental analyses. X-ray analysis confirms the formation of 1:1 {[{Re6S8}(H2O)6] ? [γ-CD]}2+ inclusion compound in the solid state. However, no adduct formation was detected between [{Re6S8}(H2O)6]2+ and γ-cyclodextrin in solution, according to 1H NMR spectroscopy. In the case of in situ generated [{Re6Se8}(H2O)6]2+ the reaction solution with γ-cyclodextrin is unstable and during the crystallization only amorphous precipitate has been obtained. 相似文献
14.
E. G. Il’in A. S. Parshakov G. G. Aleksandrov V. G. Yarzhemskii V. V. Danilov G. V. Bodrin E. I. Goryunov E. E. Nifantev 《Doklady Chemistry》2016,470(1):255-259
The crystal structure of TiF4[(Ph2P(O)CH2CH2C(O)NMe2)] chelate (I) was studied by X-ray crystallography, which revealed four crystallographically independent complex molecules of similar structure (1–4). It was found that the molecules are only slightly different in the bond lengths between the coordinated atoms and the central titanium ion and considerably different in the geometry of the seven-membered TiOPCCCO chelate ring. The geometry of the chelate rings was found to be almost identical in each pair of complexes 1, 2 (A) and 3, 4 (B), and a conclusion was drawn on the presence of two conformational isomers (A and B) of the chelate complex. Quantum chemical calculations of the relative thermodynamic stability of molecules 1–4 were performed, and their geometry optimization led to one theoretical structure. The comparison of the chelate ring geometry in the theoretical structure and in conformers A and B revealed that the conformation of the theoretical chelate ring coincides with that of conformer A. 相似文献
15.
A. B. Azlarov Kh. M. Polvonov M. K. Askarova S. Tukhtaev 《Russian Journal of Inorganic Chemistry》2011,56(1):124-127
The solubility in the 2Na+,Mg2+‖2Cl−, 2ClO3−-H2O system was studied at 20 and 100°C and the solubility diagrams were plotted. New compounds were not found to form in the
title quaternary reciprocal system. The sodium chloride field was observed to expand with rising temperature. 相似文献
16.
Richard D. Adams Erin M. Boswell Burjor Captain Lei Zhu 《Journal of Cluster Science》2008,19(1):121-132
Three new platinum–ruthenium complexes: Pt3Ru3(PBut
3)3(CO)12, 8, Pt5Ru3(PBut
3)3(CO)12, 9 and PtRu3(PBut
3)2(CO)8(μ3-PBut)(μ-H)2, 10 were obtained from the reaction of Ru3(CO)12 with Pt(PBut
3)2. Compound 8 was obtained from this reaction when conducted at 25 °C. Compounds 9 and 10 were obtained when the reaction was conducted at 68 °C. The structure of 8 consists of a central triangular cluster of three ruthenium atoms with one Pt(PBut
3) group bridging each of the three Ru–Ru bonds. The structure of 9 consists of a capped pentagonal bipyramidal cluster of eight metal atoms that is formed formally by the addition of two platinum
atoms to 8. The structure of 10 contains a triangular cluster of three ruthenium atoms with a Pt(PBut
3) group bridging one of the Ru–Ru bonds. A t-butyl phosphido ligand formed by degradation of a molecule of PBut
3 bridges the three ruthenium atoms.
This report is dedicated to the memory of Professor F. A. Cotton for his many pioneering contributions to inorganic and metal
cluster chemistry. 相似文献
17.
S. Hosein Mousavipour Fatemeh Keshavarz Sara Soleimanzadegan 《Journal of the Iranian Chemical Society》2016,13(6):1115-1124
Quasi-classical trajectory calculations and stochastic one-dimensional chemical master equation simulation methods are used to study the dynamics of the reaction of amidogen radical [NH2(2B1)] with hydroperoxyl radical [HO2(2A″)] on the lowest singlet electronic state. The title complex reaction takes place on a multi-well multichannel potential energy surface consisting of three deep potential wells and one van der Waals complex. In quasi-classical trajectory calculations a new analytical potential energy surface based on CCSD(T)/aug-cc-pVTZ//MPW1K/6-31+G(d,p) ab initio method was driven and used to study the dynamics of the title reaction. In quasi-classical trajectory calculations, the reactive cross sections and reaction probabilities are determined for 200–2000 K relative translational energies to calculate the rate constants. The same ab initio method was used to have the necessary data for solving the one-dimensional chemical master equation to calculate the rate constants of different channels. In solving the master equation, the Lennard-Jones potential model was used to form the collision between the collider gases. The fractional populations of different intermediates and products in the early stages of the reaction were examined to determine the role of the energized intermediates and the van der Waals complex on the dynamics of the title reaction. Although the calculated total rate constants from both methods are in good agreement with the reported experimental values in the literature, the quasi-classical trajectory simulation predicts the formation of NH2O + OH as the major channel in the title reaction in accordance with the previous studies (Sumathi and Peyerimhoff, Chem. Phys. Lett., 263:742–748, 1996), while the stochastic master equation simulation predicts the formation of HNO + H2O as the major products. 相似文献
18.
The dynamic structure of hydrogen sublattice in lawsonite, CaAl2[Si2O7](OH)2·H2O is studied by the solidstate proton magnetic resonance (1H NMR) spectroscopy of single crystal at room temperature. It is shown that both encapsulated water molecules, and hydroxyl OH-groups undergoes the rocking librations of the amplitudes of ~20° for H2O, and ~40° for hydroxyls. 相似文献
19.
M. S. Tarasenko A. Yu. Ledneva N. V. Kurat’eva D. Yu. Naumov Sung-Jin Kim V. E. Fedorov N. G. Naumov 《Russian Journal of Coordination Chemistry》2007,33(12):876-885
The reactions of SnMe3Cl with salts of the cluster anionic complexes [Re6Q8(CN)6]4? (Q = S, Se) gave novel complexes [{(SnMe3)2(OH)}2{SnMe3}2{Re6S8(CN)6}] (I), (Me4N)2[{SnMe3(H2O)}2{Re6Se8(CN)6}] (II), [{(SnMe2)4(μ3-O)}2{Re6Se8(CN)6}] (III), and [(SnMe2)4(μ3-O)2(μ2-OH)2(H2O)2][{SnMe3 2{Re6Se8(CN)6}] (IV). The structures of I–IV were determined by X-ray diffraction. Compounds I, IV have the chain structures with the CN-SnMe3-NC bridges between the cluster anions [Re6Q8(CN)6]4?. Compound II contains isolated fragments {SnMe3(H2O)}2{Re6Se8(CN)6}2?. In the polymer framework of compound III, the cluster anionic complexes [Re6Se8(CN)6]4? are bound by the complex cations [(SnMe2)4(μ3-O)2]4+ formed due to the hydrolysis of the initial (SnMe3)Cl. 相似文献
20.
N. A. Selivanov A. Yu. Bykov M. S. Grigor’ev K. Yu. Zhizhin N. T. Kuznetsov 《Doklady Chemistry》2016,467(1):64-68
Methods of synthesis have been developed for new types of promising precursors of metal borides, coordination compounds [ML3]B{3H8{2 (M = Fe2+, Ni2+; L = bipy, phen), using modified procedures of synthesis of octahydrotriborate anion. Compounds [Ni(bipy)3]B{3H8}2, [Ni (phen)3]B{3H8}2 and [Fe(phen)3]B{3H8}2 were prepared and characterized by single-crystal X-ray diffraction. 相似文献