共查询到20条相似文献,搜索用时 46 毫秒
1.
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
2.
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
3.
Yu. V. Rakitin V. T. Kalinnikov S. G. Khodasevich V. M. Novotortsev 《Russian Journal of Coordination Chemistry》2007,33(12):891-895
The electronic structures of the complex ions [CuCl4]2? and [CuCl5]3? were analyzed in terms of the extended angular overlap model (AOM) with consideration to sd and pd mixing. The total antibonding orbital energies of these ions show no anomalies in the transition from a tetrahedron to a planar square [CuCl4]2? and from a trigonal bipyramid to a tetragonal pyramid [CuCl5]3?. Presumably, the existence of numerous intermediate forms of these complexes is mainly due to the packing effects rather than the electronic factors. 相似文献
4.
A. V. Churakov E. A. Legurova A. A. Dutov P. V. Prikhodchenko T. A. Tripol’skaya 《Russian Journal of Inorganic Chemistry》2008,53(8):1187-1192
Peroxide derivatives of heteropoly compounds with Keggin anions [PW12O40]3? and [SiW12O40]4? are isolated in an individual state from concentrated hydrogen peroxide solutions and characterized by physicochemical methods. The structure of Ba2[SiW12O40] · 4H2O2 · 11H2O (I) is solved by X-ray crystallography. Crystals of compound I (H30Ba2O59Si1W12, FW = 3483.21) are monoclinic, space group C2/c, a = 24.981(2) Å, b = 12.2103(11) Å, c = 18.7142(17) Å, β = 122.620(2)o, V = 4808.0(8) Å3, Z = 4. The structure contains Keggin anions [SiW12O40]4?; all hydrogen peroxide molecules are coordinated to Ba2+ cations. 相似文献
5.
V. V. Sharutin I. V. Egorova N. N. Klepikov O. K. Sharutina 《Russian Journal of Inorganic Chemistry》2010,55(7):1103-1106
The complex [Ph3P] 4 + [Bi4I16]4? · 2 Me2C=O (I) was synthesized by the reaction of triphenyl(propyl)phosphonium iodide with bismuth iodide in acetone. The crystal structure of complex I was determined by X-ray crystallography. It contains, in addition to solvent molecules, two types of crystallographically independent tetrahedral tetraphenyl(propyl)phosphonium cations and tetranuclear anions [Bi4I16]4? in a chair conformation with the bismuth atoms being in an octahedral coordination. The Bi-I distances in the anion vary within 2.8768(4)–3.2524(4) Å. 相似文献
6.
7.
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
8.
É. B. Coropceanu A. P. Rija V. N. Shafranskii O. A. Bologa M. Gdaniec S. T. Malinovskii 《Journal of Structural Chemistry》2007,48(6):1110-1117
The complexes [Co(DH)2(Sam)2]2[ZrF6]·5H2O (I) and [Co(DH)2(Sam)2][BF4]·H2O (II), where DH? is the dimethylglyoxime monoanion, and Sam is para-aminobenzenesulfamide (sulfanilamide, white streptocid), were synthesized, and their crystal structures were determined by X-ray diffraction analysis. The coordination polyhedron of the Co3+ atom is an N6 octahedron formed by four nitrogen atoms of the two dimethylglyoxime residues and two nitrogen atoms of the Sam fragments. The latter are realized in virtually parallel orientation relative to the polyhedron of the metal atom and its equatorial plane; the average value of the dihedral angles is 26.8(1)°, and there is π-π interaction between the benzene rings of the Sam fragments and the π delocalized equatorial metallocycle. The deviation of the cobalt atom from the four-angle plane is up to 0.009(1) Å. The (Co-N)DH? and (Co-N)Sam distances in the [Co(DH)2(Sam)2]+ complex cations vary from 1.892(2) Å to 1.907(3) Å and from 2.000(2) Å to 2.012(2) Å, respectively. The [ZrF6]2? and [BF4]? complex anions play the major role in crystal formation; they produce a substantial effect on the formation of a complex system of hydrogen bonds. 相似文献
9.
E. Yu. Matveev S. S. Akimov A. S. Kubasov A. I. Nichugovskii A. S. Nartov V. M. Retivov K. Yu. Zhizhin N. T. Kuznetsov 《Russian Journal of Inorganic Chemistry》2017,62(6):808-813
The reactions of 1,4-dioxane-substituted closo-decaborate anion ([B10H9O2C4H8]–) with metal acetylenides, diethyl malonate, ethyl acetoacetate, triethyl orthoformate, acetylacetone, and malonodinitrile were studied. The reactions were shown to be accompanied with substituent ring opening and attachment of the corresponding pendant functional group. The obtained compounds were characterized by various physicochemical methods (IR and polynuclear NMR spectroscopy, ESI mass spectrometry). 相似文献
10.
E. E. Karslyan D. S. Perekalin P. V. Petrovskii A. O. Borisova A. R. Kudinov 《Russian Chemical Bulletin》2009,58(3):585-588
The cation [CpRu(η6-C10H8)]+ was shown to exchange naphthalene for other arenes under visible-light irradiation to form the complexes [CpRu (η6-arene)]+ (arene = C6H6, 1,4-C6H4Me2, 1,3,5-C6H3Me3, or 1,2,4,5-C 6H2Me4) in 70–95% yields. The reaction rate of exchange decreases in the series arene = 1,4-C6H4Me2 > C6H6 > 1,3,5-C6H3Me3 > 1,2,4,5-C 6H2Me4 >> C6Me6 and increases with the coordinating ability of the solvent in the order CH2Cl2 < THF—CH2Cl2 mixture (1: 1) < acetone. 相似文献
11.
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
12.
D. S. Bolotin M. Ya. Demakova E. A. Daines M. S. Avdontseva A. P. Zhdanov K. Yu. Zhizhin N. T. Kuznetsov 《Russian Journal of General Chemistry》2017,87(1):37-43
A series of closo-decaborate anions containing an O-iminoacylamide oxime fragment were synthesized by nucleophilic addition of aromatic amide oximes to 2-propionitrilium closo-decaborate anion. The isolated compounds were characterized by IR, 1H, 13C–{1H}, and 11B–{1H} NMR, and mass spectra. The structure of (Ph4P)[2-B10H9NH=C(Et)ON=C(NH2)C6H4Me-2] was determined by single-crystal X-ray analysis. 相似文献
13.
Hongli Chen Yan Ding Enbo Wang Xinxin Xu Yanfei Qi Song Chang Yangguang Li 《Transition Metal Chemistry》2008,33(3):341-346
In this article, two compounds [H2bpy][Ln(DMF)4(H2O)3(Hbpy)][H2W12O40] (Ln = La,Ce; DMF = N,N-dimethylformamide, bpy = 4,4′-bipyridine) have been synthesized and characterized by single-crystal X-ray diffraction, IR
spectra, and TG analysis. X-Ray analysis showed that the [Ln(DMF)4(H2O)3(Hbpy)]4+ unit is supported on the α-Keggin polyoxoanion [H2W12O40]6− via the surface bridging oxygen atom. The [H2bpy][Ln(DMF)4(H2O)3(Hbpy)][H2W12O40] entity is further extended into 2D supramolecular networks with 1-D channels by hydrogen-bonding interactions, in which
4,4′-bipy ligands reside. To the best of our knowledge, these complexes represent the first examples of rare earth metal-organic
complex-decorated α-metatungstate clusters. Furthermore, the electrochemical properties of these compounds have been studied
via the method of bulk-modified carbon paste electrodes. 相似文献
14.
V. V. Sharutin O. K. Sharutina V. S. Senchurin 《Russian Journal of General Chemistry》2016,86(9):2141-2142
15.
P. Storoniak M. Kabir J. Błażejowski 《Journal of Thermal Analysis and Calorimetry》2008,93(3):727-732
The enthalpies of formation of PbCl4, PbCl5− and PbCl62−, originating from quantum mechanics, have enabled the thermodynamic behaviour of these ions with respect to Cl-detachment
to be assessed. The stability of salts containing PbCl5− and PbCl62− as a function of the dimensions of these anions and complementary cations was studied using an approach combining the Kapustinskii-Yatsimirskii
equation with basic thermochemical relationships.
It was found that hexachloroplumbates of monovalent metal cations will not dissociate into metal chlorides and PbCl4, provided the complementary cations are suitably large in size. Hexachloroplumbates of divalent metal cations have not yet
been synthesised since no known metal cations attain the requisite large size. Such salts will not dissociate if the divalent
metal cations are able to complex suitably large electron-donating ligands. The pentachloroplumbates of both monovalent and
divalent metal cations are unstable, since no known metal cations have appropriately large ionic radii. The approach adopted
appears to be useful for the examination of the thermal behaviour, stability and reactivity of chloroplumbates. 相似文献
16.
Zongxiao Li Chunlan Yuan 《Russian Journal of Physical Chemistry A, Focus on Chemistry》2011,85(8):1332-1335
With the help of the kinetic parameters (the rate constant (k
in
k
p) and the apparent activation energy (E
in
E
p) of the oscillatory induction period and oscillation period) of the oscillating reaction using thirteen amino acids, leucine
(Leu), threonine (Thr), arginine (Arg), lysine (Lys), histidine (His), alanine (Ala), glutamine (Glu), glycine (Gly), methionine
(Met), cystine (Cys), tryptophan (Trp), serine (Ser) and tyrosine (Tyr), as organic substrates in amino acid-BrO3−-Mn2+-H2SO4-acetone system, then based on the Oregonator model and the thermodynamics theory on irreversible process, the thermodynamic
function (ΔH
in, ΔG
in, ΔS
in and ΔH
p, ΔG
p, ΔS
p) of these oscillating system are studied. The results indicate the entropy ΔS of these oscillating reaction are negative, thereby it is proved that the oscillating reaction is a noequilibrium system
with dissipation structure in agreement with the character of the oscillating reaction from disorder to order in irreversible
thermodynamics. These are satisfactorily to explain the experimental phenomena. 相似文献
17.
E. E. Karslyan D. S. Perekalin P. V. Petrovskii K. A. Lyssenko A. R. Kudinov 《Russian Chemical Bulletin》2008,57(10):2201-2203
Naphthalene in the [CpRu(6−C10H8)]+ complex (1) is substituted for other arenes under reflux in 1,2-dichloroethane to form the [CpRu(6-arene)]+ cations (arene = C6H6, 1,2-C6H4Me2, 1,2,4,5-C6H2Me4, or C6Me6) in 70–80% yields. The reaction is accelerated in the presence of a catalytic amount of acetonitrile. The structure of [1]PF6 was established by X-ray diffraction. 相似文献
18.
V. A. Nadolinnyi T. M. Polyanskaya M. K. Drozdova O. V. Antonova A. A. Ryadun V. V. Volkov 《Russian Journal of Coordination Chemistry》2010,36(5):370-377
The influence of specific features of the structure and nature of the cations (Ph4P+, H(Phen)+, Cs+, and (CH3)4N+) on the ERP spectra of the nickel ions in salts with the dicarbollylnickelate anion [Ni(B9C2H11)2]− is studied. It is shown that the change in the cation type in these compounds results in the electron density redistribution,
which affects the change in the main and average values of the g factor. The g
av value increases over that observed in frozen solutions upon the localization of the positive charge of the cation on one
atom and in the absence of the screening effect of the solvent and large functional groups of the cation. The exception is
the compound (Ph4P+)NiCb2− (Cb is B9C2H11) with solvated CCl4 molecules. For all compounds studied, the temperature dependence of the linewidths in the EPR spectra is described by the
equation ΔH = αT + βT7 with different α and β values and is defined by the temperature dependence of the relaxation process caused by the Raman
interaction. 相似文献
19.
A. Yu. Bykov G. A. Razgonyaeva N. N. Mal’tseva K. Yu. Zhizhin N. T. Kuznetsov 《Russian Journal of Inorganic Chemistry》2012,57(4):471-473
A new method of synthesis of the B3H8− anion has been suggested. The method uses the reaction of some metal halides (CuCl, SnCl2, CrCl3, PbF2, PbCl2, PbBr2, and BiCl3) with sodium tetrahydroborate. It is characterized by high (up to quantitative) yields and simplicity of isolation of the
target products ((n-C4H9)4N)[B3H8] and Cs[B3H8]. 相似文献
20.
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