共查询到20条相似文献,搜索用时 93 毫秒
1.
C. Anklin P.S. Pregosin F. Bachechi P. Mura L. Zambonelli 《Journal of organometallic chemistry》1981,222(1):175-185
Platinum(II) and palladium(II) complexes containing chelating acyl ligands have been synthesized from salicylaldehyde, 2-hydroxynaphthaldehyde and 2-hydroxy-3-methoxybenzaldehyde. The platinum(II) complexes [Pt(acyl)L2], acyl OC6H4CO, OC10H6CO, O(m-CH3OC6H3CO), L tertiary phosphine, 1/2 diphenylphosphinoethane, can be isolated with both monodentate and chelating diphosphines, whereas for palladium only the compounds with chelating phosphines are readily obtainable. The reactions of [Pt(OC6H4CO)L2] with HCl afford trans-[PtCl(OHC6H4CO)L2], L monodentate tertiary phosphine and cis-[PtCl(OHC6H4CO)L2], L2 1,2-bis-diphenylphosphinoethane, in which the metal—carbon bond remains intact. The structure of [Pt(OC6H4CO)-(P(p-CH3C6H4)3)2] has been determined by X-ray diffraction methods and found to have the expected square planar structure. Some relevant bond lengths and angles are: PtP; 2.271(4) and 2.348(5) Å; PtC; 1.96(2) Å and PtO; 2.07(1) Å; PPtP 101°, CPtO 82°. 相似文献
2.
Swadhin K. Mandal Setharampattu S. Krishnamurthy Thomas Stey 《Journal of organometallic chemistry》2005,690(3):742-750
Chiral “P-N-P” ligands, (C20H12O2)PN(R)PY2 [R = CHMe2, Y = C6H5 (1), OC6H5 (2), OC6H4-4-Me (3), OC6H4-4-OMe (4) or OC6H4-4-tBu (5)] bearing the axially chiral 1,1′-binaphthyl-2,2′-dioxy moiety have been synthesised. Palladium allyl chemistry of two of these chiral ligands (1 and 2) has been investigated. The structures of isomeric η3-allyl palladium complexes, (R′ = Me or Ph; Y = C6H5 or OC6H5) have been elucidated by high field two-dimensional NMR spectroscopy. The solid state structure of [Pd(η3-1,3-Ph2-C3H3){κ2-(racemic)-(C20H12O2)PN(CHMe2)PPh2}](PF6) has been determined by X-ray crystallography. Preliminary investigations show that the diphosphazanes, 1 and 2 function as efficient auxiliary ligands for catalytic allylic alkylation but give rise to only moderate levels of enantiomeric excess. 相似文献
3.
Francisco Pérez-García José G. Alvarado-Rodríguez Carlos Andrés Galán-Vidal M. Elena Páez-Hernández Noemí Andrade-López Rafael Moreno-Esparza 《Structural chemistry》2010,21(1):191-196
Treatment of KS2P(OC6H4)2 (1) with five n-alkyl halides afforded the stable n-alkyldithiophosphate compounds RS2P(OC6H4)2 (2–6). Single crystal X-ray analysis revealed that the PS2 fragment in 1 displays an isobidentate coordination pattern; compounds 2–4 display a monodentate binding pattern. The crystal packing of title compounds is stabilized by cation-π, weak hydrogen bonding
C–H---O, as well as aromatic non-bonded interactions. 相似文献
4.
F. Charbonnier 《Thermochimica Acta》1974,10(3):285-298
Two new salts of malonic acid have been prepared: the copper(II) malonate tetrahydrate and the copper(II)-ammonium double malonate. Their study by thermal analysis (TG and DTA) leads to the following results:Cu(C3H2O4)·4H2O: the dehydration is rather complex and it is only under careful conditions that an intermediate hydrate Cu(C3H2O4)·3H2O could be traced. At about 170°C the dehydration is not ended (the salt holds yet about 0.15H2O) and the anhydrous salt occurs only at about 240°C. It decomposes immediately leading to residues the composition of which depends upon the surrounding atmosphere; the part played by the gas given off is discussed.Cu(NH4)2(C3H2O4)2: this salt melts and decomposes simultaneously at about 190°C. During the decomposition the copper nitride Cu3N forms as intermediate compound (as well as copper metal). Concerning the final residues of the decomposition the results and the conclusions are the same as the ones of the previous case. 相似文献
5.
A novel trinuclear manganese(II) complex, Mn3(C12H8N2)2(C10H11O5)6 (I), has been hydrothermally synthesized and characterized by single-crystal X-ray diffraction. The crystal belongs to the monoclinic
system, space group P21/n, with cell parameters a = 12.1935(7), b = 19.0249(11), c = 18.0515(10)?, β = 105.0430(10)°, V = 4044.1(4)?3, Z = 2. Two of the three manganese atoms in the crystal structure are crystallographically equivalent and adopt N2O4 coordination mode, whereas the remaining manganese atom adopts O6 coordination mode, which forms a nearly regular octahedron. The experimental result of thermal analysis shows that complex
I remains stable below 300°C. 相似文献
6.
D. V. Pushkin E. V. Peresypkina L. B. Serezhkina A. V. Savchenkov A. V. Virovets V. N. Serezhkin 《Russian Journal of Inorganic Chemistry》2012,57(2):175-180
Single crystals of (CN3H6)2[(UO2)2(C2O4)(SeO3)2] were synthesized and studied by IR spectroscopy and X-ray diffraction. The compound crystallizes in the triclinic system
with the unit cell parameters a = 7.1169(12) ?, b = 7.4874(10) ?, c = 8.9748(14) ?, α = 88.243(6)°, β = 74.546(6)°, γ = 81.445(6)°, space group P[`1]P\bar 1, Z = 1, R = 0.0304. The main structural units of the crystals are layers of the [(UO2)2(C2O4)(SeO3)2]2− composition; the layers belong to the crystal chemical group A
2
K
02
T
23 (A = UO22+
K
02 = C2O42−, T
3 = SeO3–) of uranyl complexes. Uranium-containing complex groups are linked by electrostatic interactions and a network of hydrogen
bonds with CN3H6+ guanidinium ions to form a three-dimensional framework. 相似文献
7.
Crystal and molecular structure of tricyclopentadienyltetrahydrofuranuranium(III), (η5-C5H5)3U·OC4H8
H.J. Wasserman A.J. Zozulin D.C. Moody R.R. Ryan K.V. Salazar 《Journal of organometallic chemistry》1983,254(3):305-311
Tricyclopentadienyltetrahydrofuranuranium(III), (η5-C5H5)3U·OC4H8, crystallizes in the centrosymmetric monoclinic space group P21/n with a 8.248(3), b 24.322(17), c 8.357(4) Å, β 101.29(5)°, V 1644.0 Å3 and ρ(calc) 2.04 g cm?1 for Z = 4 and mol.wt. 595.0. Diffraction data (Mo-Kα, 2θ(max) 45°) were collected on an Enraf-Nonius CAD4 diffractometer and the structure was refined to Rw(F) 4.7% for those 1530 reflections having I > 2σ(I). The molecule consists of a distorted tetrahedral arrangement of THF and (η5-C5H5) ligands with CpUCp angles in the range 110.4–122.4° and CpUO angles between 90.2 and 106.0°. Individual uranium-carbon distances range from 2.76(2) to 2.82(2) Å and average 2.79[1] Å. The uranium-oxygen distance of 2.551(10) Å suggests a 10-coordinate U3+ radius of 1.20 Å in this class of compounds. 相似文献
8.
V. V. Sharutin I. V. Egorova O. K. Sharutina A. P. Pakusina M. A. Pushilin 《Russian Journal of Coordination Chemistry》2007,33(1):12-19
Triphenylbismuth diaroxides Ph3Bi(OAr)2 (Ar = C6H3(Br2-2,4) (I), C6H2(Br2-2,6)(NO2-4) (II), and C6H2[(NO2)3-2,4,6] (III) are synthesized in yields up to 74% by the reaction of triphenylbismuth with phenols in the presence of hydrogen peroxide
(taken at a molar ratio 1: 2: 1, respectively) in ether. According to X-ray diffraction data, the bismuth atoms in compounds
I-III have distorted trigonal-bipyramidal coordination with the aroxyl substituents in the axial positions; the Bi-C, Bi-O bond
lengths and the OBiO, CBiC angles vary in the intervals 2.162–2.204, 2.150–2.299 ? and 172.4°–176.1°, 109.6°–139.9°, respectively.
Compound II exhibits intramolecular contacts between the central atom and ortho-Br atoms (3.924, 4.101 ?), and compound III has similar contacts of the Bi atom with the O atoms of the ortho-nitro groups (3.114, 3.313 ?).
Original Russian Text ? V.V. Sharutin, I.V. Egorova, O.K. Sharutina, A.P. Pakusina, M.A. Pushilin, 2007, published in Koordinatsionnaya
Khimiya, 2007, Vol. 33, No. 1, pp. 14–21. 相似文献
9.
The reaction of MoO2Cl2(OPMePh2)2 with t-butylhydroperoxide (TBHP) in the presence of cis-cyclooctene yields the tetrameric complex Mo4O6(O2)2(μ3-O)2{(μ2-O,μ3-OC8H14}2(OPMePh2)2, (1). Additionally in the absence of cis-cyclooctene MoO(O2)Cl2(OPMePh2)2, MoO(O2)2(H2O)(OPMePh2), (2), and two novel yellow compounds can be isolated depending on the quantity of TBHP used and the reaction conditions. Both the starting material MoO2Cl2(OPMePh2)2 and tetramer 1 are capable of accomplishing the epoxidation of cis-cyclooctene as catalysts. The single crystal X-ray determined structures of complexes 1 and 2 are reported.Dedicated to Professor F. A. “Chief” Cotton on the occasion of his 75th birthday 相似文献
10.
P. A. Abramov S. A. Adonin E. V. Peresypkina M. N. Sokolov V. P. Fedin 《Journal of Structural Chemistry》2010,51(4):731-736
Adducts of cucurbit[6]uril with Ca2+ and trinuclear cluster chloroaquacomplexes (H9O4)2(H7O3)2[(Ca(H2O)5)2(C36H36N24O12)]Cl8·0.67H2O (1) and [(Ca(H2O)5)2(C36H36N24O12)]× [Mo3O2S2Cl6(H2O)3]2·13H2O (2) are obtained and structurally characterized. The structures of both compounds contain polymeric [Ca(H2O)
n
]22 CB[6]∞ cations that form infinite columns; the space between them is filled with Cls- (1) and [Mo3O2S2Cl6(H2O)3]2s- (2). A new (H7O3)2(H5O2)× [Mo3S4Cl6.25Br0.25(H2O)2](C36H36N24O12)·CH2Cl2·6H2O complex (3) is also obtained and structurally characterized. 相似文献
11.
V.A. Bhirud P.W. Kletnieks J.F. Haw M.M. Olmstead 《Journal of organometallic chemistry》2007,692(10):2107-2113
We report a new synthesis and characterization of Ir(C2H4)2(C5H7O2) [(acetylacetonato)-bis(η2-ethene)iridium(I)], prepared from (NH4)3IrCl6 · H2O in a yield of about 45%. The compound has been characterized by X-ray diffraction crystallography, infrared, Raman, and NMR spectroscopies and calculations at the level of density functional theory. Ir(C2H4)2(C5H7O2) is isostructural with Rh(C2H4)2(C5H7O2), but there is a substantial difference in the ethylene binding energies, with Ir-ethylene having a stronger interaction than Rh-ethylene; two ethylenes are bound to Ir with a binding energy of 94 kcal/mol and to Rh with a binding energy of 70 kcal/mol. 相似文献
12.
1-Allyl-4-aminopyridinium chloride reacts with Cu(NO3)2 · 3H2O in an ethanolic solution under the conditions of ac electrochemical synthesis at copper electrodes to form crystals of compound
[(NH2C5H4N(C3H5))2Cu3Cl3(NO3)2] (I). The crystals of compound I are monoclinic: space group P21/c, Z = 4, a = 25.770(7), b = 7.230(4), c = 12.505(5) ?, β = 92.58(3)°, V = 2328(2) ?3. The direct interaction of 1-allylquinolinium nitrate with Cu(NO3)2 · 3H2O in a methanolic solution in the presence of metallic copper yields crystals of compound [C9H7N(C3H5)Cu(NO3)2] (II). The crystals of compound II are triclinic: space group P
, a = 6.756(3), b = 8.391(4), c = 12.489(5) ?, α = 77.18(3)°, β = 89.48(4)°, γ = 73.32(3)°, V = 662.0(5) ?3. The structure of compound I is built of infinite linear anions: polymeric fragments {(NH2C5H4N(C3H5))2Cu3Cl3(NO3)2}
n
. Each of two copper atoms (Cu(1) and Cu(2)) π-coordinates the C=C bonds of the allyl groups of the 1-allyl-4-aminopyridinium
cations, the oxygen atom of the nitrate ions, and two chlorine atoms. The third copper atom Cu(3) is linearly linked with
two chlorine atoms. Particular polymeric fragments are additionally joined by the N-H…O, C-H…O, C-H…Cl hydrogen bonds. The
crystal structure of compound II is built-up of the isolated L2Cu2(NO3)4 fragments (L is the 1-allylquinolinium cation). The metal atom is localized in the trigonal pyramidal coordination environment
of three oxygen atoms of the nitrate ions and of the C=C bond of the allyl group of the cation. The particular L2Cu2(NO3)4 fragments are additionally joined by the C-H…O hydrogen bonds.
Original Russian Text ? A.V. Pavlyuk, T. Lis, M.G. Mys’kiv, 2009, published in Koordinatsionnaya Khimiya, 2009, Vol. 35, No.
6, pp. 458–462. 相似文献
13.
Chelladurai Ganesamoorthy Maravanji S. Balakrishna Joel T. Mague 《Journal of organometallic chemistry》2009,694(21):3390-3394
The stoichiometric reaction of phenylene-1,4-diaminotetra(phosphonite), p-C6H4[N{P(OC6H4OMe-o)2}2]2 (P2NФNP2) (1) with [RuCl2(p-cymene)]2 in acetonitrile produces cis,cis-[{RuCl2(CH3CN)2}2(P2NФNP2)] (2), whereas the similar reaction of 1 with [RuCl2(p-cymene)]2 in THF medium affords a tri-chloro-bridged tetrametallic complex, [{(η6-p-cymene)Ru2(μ2-Cl)3Cl}2(P2NФNP2)] (3) irrespective of the stoichiometry and reaction conditions. The formation and structure of complexes 2 and 3 are assigned through various spectroscopic and micro analysis data. The molecular structure of 2 is confirmed by single crystal X-ray diffraction study. The catalytic activities of complexes 2 and 3 have been investigated in transfer hydrogenation reactions. 相似文献
14.
D. P. Domonov S. I. Pechenyuk N. L. Mikhailova A. T. Belyaevskii 《Russian Journal of Inorganic Chemistry》2007,52(7):1027-1032
The thermolysis of the complexes [Co(NH3)6]2C2O4[Cu(C2O4)2]2 (I) and [Co(NH3)6]Cl[Cu(C7H4O3)2] (II) in air and hydrogen at 200, 350, and 500°C and the composition and properties of the thermolysis products are considered.
The oxidative thermolysis of the complexes yields mixtures of cobalt and copper oxides, including mixed ones. The reductive
thermolysis of the complexes yields a Co + Cu bimetallic powder in the case of compound I and a Co + Cu + C powder in the
case of compound II. The thermal behavior of the complexes is governed by the nature of the ligand coordinated to the copper
atom. The observed data are explicable in terms of the properties of this ligand. The chemistry of the oxidative and reductive
thermolysis is discussed.
Original Russian Text ? D.P. Domonov, S.I. Pechenyuk, N.L. Mikhailova, A.T. Belyaevskii, 2007, published in Zhurnal Neorganicheskoi
Khimii, 2007, Vol. 52, No. 7, pp. 1104–1110. 相似文献
15.
Mohamed Ali Saada Annie Hémon-Ribaud Vincent Maisonneuve 《Journal of fluorine chemistry》2005,126(7):1072-1077
Tren amine cations [(C2H4NH3)3N]3+ and zirconate or tantalate anions adopt a ternary symmetry in two hydrates, [H3tren]2·(ZrF7)2·9H2O and [H3tren]6·(ZrF7)2·(TaOF6)4·3H2O, which crystallise in R32 space group with aH = 8.871 (2) Å, cH = 38.16 (1) Å and aH = 8.758 (2) Å, cH = 30.112 (9) Å, respectively. Similar [H3tren]2·(MX7)2·H2O (M = Zr, Ta; X = F, O) sheets are found in both structures; they are separated by a water layer (Ow(2)-Ow(3)) in [H3tren]2·(ZrF7)2·9H2O. Dehydration of [H3tren]2·(ZrF7)2·9H2O starts at room temperature and ends at 90 °C to give [H3tren]2·(ZrF7)2·H2O. [H3tren]2·(ZrF7)2·H2O layers remain probably unchanged during this dehydration and the existence of one intermediate [H3tren]2·(ZrF7)2·3H2O hydrate is assumed. Ow(1) molecules are tightly hydrogen bonded with -NH3+ groups and decomposition of [H3tren]2·(ZrF7)2·H2O occurs from 210 °C to 500 °C to give successively [H3tren]2·(ZrF6)·(Zr2F12) (285 °C), an intermediate unknown phase (320 °C) and ZrF4. 相似文献
16.
The crystal structure of a double salt of sodium and cesium with 2-diphenylacetyl-1,3-indandione of the composition [Cs2Na(H2O)2(C23H16O3)(C23H15O3)3] (I) was studied by X-ray crystallography. The crystals of I are monoclinic, Z = 2, space group P21/n, a = 10.212(2) ?, b = 23.479(5) ?, c = 15.638(3) ?, β = 98.30(03)°. The compound contains [Cs2NaO10] trimers, in which the central Na atom shares two edges with two Cs atoms through deprotonated bridging ligands. The trimers
are connected to adjacent trimers by paired C-H...O contacts to form layers. The layers form an infinite open framework via
hydrogen bonds between the oxygen atoms of keto groups of noncoordinated indandione moieties and water molecules that enter
the cesium coordination sphere in trimers of the adjacent layers. 相似文献
17.
稀土配合物[Nd(o-NO2-C6H4COO)3(DMF)2]2的合成及其晶体结构 总被引:2,自引:0,他引:2
合成了一种新的双核倒反中心的稀土钕配合物[Nd(o-NO2-C6H4COO)3(DMF)2]2. 通过元素分析, 核磁共振谱和红外光谱对配合物的组成和结构进行了表征, 用热重分析研究了该配合物的热稳定性, 用X射线单晶衍射法测定了其晶体的结构. 钕配合物[Nd(o- NO2-C6H4COO)3(DMF)2]2晶体属三斜晶系, 空间群P-1, 晶胞参数a=1.18652(12) nm, b=1.24784(13) nm, c=1.29958(13) nm, α=64.220 (1)°, β=66.306 (1)°, γ=71.825 (1)°, V=1.5645 (3) nm3, Dc=2.167 mg/m3, Z=2, μ=3.415 mm-1, F(000)=986. 配合物中每个Nd(Ш)被4个邻硝基苯甲酸根桥联, Nd(Ш)的配位数为8, 配位原子分别来自于5个邻硝基苯甲酸羧酸根的6个氧原子和2个DMF的羰基氧原子. 配合物中的氢键和π…π 堆积作用使其成为三维立体结构. 同时发现了标题配合物固体具有光致发光现象, 发光性能测试表明该配合物具有很好的荧光性质. 相似文献
18.
在pH=7.5的水溶液中, Na2WO4•2H2O, NaAsO2, CoCl2•6H2O与对氨基吡啶反应, 得到了一种新的夹心型杂多钨酸盐Na6(C5H7N2){[Na(H2O)2]3Co(H2O)5[Co(H2O)]3(AsW9O33)2}•27H2O单晶, 用X射线单晶衍射法及元素分析确定了其结构, 晶体属三斜晶系, P 空间群, 其晶胞参数为: a=1.3276(8) nm, b=1.7581(10) nm, c=2.4381(14) nm, α=70.954(9)°, β=86.663(9)°, γ=72.885(9)°, V=5.136(5) nm3, Z=2, R1=0.0608, wR2=0.0848 [I>2σ(I)]. 在{[Na(H2O)2]3Co(H2O)5[Co(H2O)]3(AsW9O33)2}7-阴离子中, 一个Co2+与聚阴离子{[Na(H2O)2]3[Co(H2O)]3(AsW9O33)2}9-的一个端基氧共价连接, Co2+呈现出5和6两种配位数, 质子化的氨基吡啶正离子作为抗衡离子存在于晶体之中. 对标题化合物进行了IR, UV-Vis, TG-DSC表征. 对该化合物、Na2WO4•2H2O及CoCl2•6H2O催化H2O2氧化乙醛的活性进行了比较研究, 该化合物的催化活性远优于简单化合物Na2WO4•2H2O和CoCl2•6H2O. 相似文献
19.
Michael Laing Magriet J. Nolte Eric Singleton Erwin van der Stok 《Journal of organometallic chemistry》1978,146(1):77-86
The crystal structure of [(C8H12)6H3Me)(OC6H4Me)2} {P(OCH2)3CMe}] has been determined. a 18.32, b 18.98, c 9.35 Å, U 3251 Å3, Pn21a, Z = 4, R = 0.048, 2541 observed data.The coordination about the iridium atom is distorted trigonal bipyramidal; the two phosphorus atoms are equatorial, the σ-bonded carbon is axial, and the bidentate cyclooctadiene is bonded axialequatorial. The IrC(axial) bonds are longer than the IrC(equatorial) bonds: 2.22, 2.26; 2.17, 2.19 Å. The IrC(σ) bond length is 2.19 Å, not significantly different from the formally π-bonded C to Ir distances. The IrP lengths of 2.201 and 2.240 Å and the PIrP angle of 108.7° are normal. The longer IrP bond is in the five-membered chelate ring. The inertness to substitution is discussed. 相似文献
20.
R. Schwesinger K. Piontek W. Littke O. Schweikert H. Prinzbach C. Krüger Y.-H. Tsay 《Tetrahedron letters》1982,23(24):2427-2430
According to X-ray crystal structure analyses “cis-benzenetrisimine” () and “cis-benzenetrioxide” () act as tridentate ligands in their 2:1- and 4:1-complexes (Co(C6H9N3)2(NO3)3) and (Ba(C6H6O3)4(ClO4)2), resp. The latter is the rare example of an organic complex with the (approximate) T-symmetry. 相似文献