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1.
Cobalt(II) complexes of sulfadiazine formulated as [Co(C10H9N4O2S)2(CH3OH)2] and [Co(C10H9N4S)2(H2O)2] have been synthesized and characterized by elemental analysis, infrared and UV-Vis spectroscopy and magnetic susceptibility measurements. The crystal structures of the complex [Co(C10H9N4O2S)2(CH3OH)2] and of free sulfadiazine are also reported. The cobalt complex and the sulfadiazine ligand both crystallize in the monoclinic space group, P21/c, with sulfadiazine acting as a bidentate ligand. Cobalt is coordinated to two-sulfonamide nitrogen and the pyrimidine nitrogen of the sulfadiazine. Two molecules of methanol complete the octahedral geometry around the cobalt, with interligand hydrogen bonding between methanol and sulfadiazine. Infrared spectroscopy confirmed the presence of water molecule in the coordination sphere of [Co(C10H9N4S)2(H2O)2]. The electronic spectra and magnetic moments of both complexes were similar, indicating that both complexes have similar structure. 相似文献
2.
Reactions of salicyl- and 3,5-dichlorosalicylaldehyde-S-propyl-thiosemicarbazones with salicyl- and 3,5-dichlorosalicylaldehyde in the presence of UO2(CH3COO)2 in different alcohols yielded stable solid complexes corresponding to the general formula [UO2(L)ROH] (R: propyl-, butyl-, pentyl-, and octyl-). The complexes were characterized by means of elemental analysis, IR and 1H NMR spectroscopies. The thermal stabilities of the alcohol solvated complexes were investigated in air and nitrogen atm., and determined their decomposition phases. In the crystal structure of the [UO2(L)(C4H9OH)], the U(VI) centre is seven-coordinated in a distorted pentagonal bipyramidal geometry involving O,O,N,N atoms of two phenolic and two imine groups and one oxygen atom of alcohol molecule in basal plane and two O atoms of dioxo group in apical positions. The title structure is stabilized by one intramolecular interaction of types C-H?Cl and by two intermolecular interactions of types O-H?O and C-H?π (benzene) leading to the molecular chain along the [0 1 0] direction. 相似文献
3.
The synthesis and structure of a monoperoxo vanadate(V) of the formula K2[VO(O2)NTA]·2H[2O, where NTA = C6H6NO6 3−, the nitrilotriacetate, is described. This stable compound crystallizes in the orthorhombic system (space group Pna21): a = 7.621(1), B = 13.002(3), C = 13.155(1) Å. A tetradentate NTA encloses vanadium in a distorted pentagonal bipyramid with an apical V = O group. Cis to it, in the pentagonal plane, a non-symmetrically coordinated peroxo group is located with an (O---O) bond length of 1.438(4) Å. Complex IR spectra display rich absorption due to coordinated NTA, in addition to the characteristic V = O and (O---O) stretching vibrations. Aqueous solutions of the complex show a (peroxo → V(V)) charge transfer band at γmax = 425 nm. 相似文献
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A new vanadyl oxalatophosphate compound, (C10H10N2)[(VO)(HPO4)]2(C2O4), was synthesized via the hydrothermal approach and characterised structurally using single-crystal X-ray diffraction, FT-IR and thermogravimetric analysis. The compound has two-dimensional anionic layers with occupying the interlayer spaces. 相似文献
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7.
Margaret Goodgame Steven D. Holt Brian Piggott David J. Williams 《Inorganica chimica acta》1985,107(1):49-55
Complexes are described of Cobalt(II) and Nickel- (II) salts with the title ligand L. The X-ray crystal structure is described of NiL2L′1(ClO4)1. One ligand molecule (L′) in this complex is deprotonated and the structure involves strongly hydrogen bonded dimers with OHO bonds = 2.56 Å and 2.62 Å and a NiNi bond = 4.77 Å. The corresponding Cobalt complex is thought to be similar but no other compounds containing L′ were obtained. 相似文献
8.
Bruno Therrien Ludovic Vieille-Petit Georg Süss-Fink 《Inorganica chimica acta》2004,357(11):3289-3294
The trinuclear arene-ruthenium cluster cation [H3Ru3(C6H6)(C6Me6)2(O)]+, containing a μ3-oxo cap and three arene ligands that span a hydrophobic pocket above the metal skeleton, has been crystallised as tetrafluoroborate salt in the presence of various guest molecules. The host-guest complexes have been characterised by single-crystal X-ray structure analysis. With chloroform as the guest molecule, a CHCl3 molecule sits perfectly in the hydrophobic pocket, the hydrogen atom being encapsulated inside the cavity. When dioxane is added during the crystallisation process, the cluster forms infinite chains which are connected by a complex network of hydrogen bonds involving the μ3-oxo ligand, water and dioxane molecules. Interestingly, in the presence of phenol, a water molecule is hydrogen-bonded between the μ3-oxo ligand and the phenol molecule, forming a one-dimensional μ3-O ? H2O ? HO hydrogen-bonded chain. Finally, with benzoic acid, a head-to-tail host-guest chain is obtained, the phenyl ring being incorporated in the hydrophobic pocket, while the acid group is hydrogen-bonded to the μ3-oxo ligand. 相似文献
9.
M.S Papadopoulos P Bouziotis I.C Pirmettis C.P Raptopoulou A Terzis E Chiotellis 《Inorganica chimica acta》1999,290(2):2808-250
A novel five-coordinate rhenium(III)-thiolato complex, Re(SCH2C6H4OCH3-p)3(PPh3)2 has been isolated during the reaction of trans-ReOCl3(PPh3)2 with p-methoxybenzyl mercaptan. In the unexpected structure that was acquired, the central metal has undergone a reduction from Re(V) to Re(III). The five-coordinate Re(III) complex has been characterized by spectroscopic methods, elemental analysis and X-ray crystallography. X-ray crystallographic studies showed the coordination geometry around rhenium to be that of a trigonal bipyramid. The basal plane is defined by three sulfur atoms of the monodentate ligand, while the two apical positions are occupied by two phosphines of the precursor. 相似文献
10.
Terrence L. Nicholson Ashfaq Mahmood Alan Davison Alun G. Jones 《Inorganica chimica acta》2011,365(1):484-486
The reaction of the Tc(I) complex [Tc(NO)Cl2(HOMe)(PPh3)2] with stoichiometric amounts of 2-mercatopyridine and a proton scavenger yields [Tc(NO)Cl(Spy)(PPh3)2] or [Tc(NO)(Spy)2(PPh3)], depending upon quantities of ligands employed. These two complexes have been structurally characterized. The small bite angles of the bidentate mercaptopyridine ligands cause significant deviation from octahedral coordination geometry. 相似文献
11.
Alma Itzel Olivos-Surez Gustavo Ríos-Moreno Simn Hernndez-Ortega Rubn A. Toscano Juventino J. García David Morales-Morales 《Inorganica chimica acta》2007,360(15):4133-4141
The fluorinated thioether compounds [C6H4Br-2-(CH2SRF)] (SRF = SC6F5 (1), SC6F4-4-H (2), SC6H4-2-F (3), SC6H4-3-F (4), SC6H4-4-F (5)) were synthesized and the reactivity of (1) was explored with transition metal complexes of the group 10. The results obtained indicate that the reactivity of these ligands is strongly dependent on the oxidation state of the metal center on the complex. Thus, products of the coordination of Pd(II) and Pt(II) to the sulfur moiety were obtained and unequivocally characterized by single crystal X-ray diffraction analyses. While spectroscopic evidence indicates that reaction of the Pt(0) compound [Pt(PEt3)3] leads to the formation of C–Br activation products, it is worth noting that similar reactions with Ni(0) and Pd(0) compounds only afford complex mixtures that in most of the cases indicate desulfurization of the ligands and decomposition of the metallic starting materials. 相似文献
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Valente Gómez-Benítez 《Inorganica chimica acta》2007,360(6):2128-2138
A series of palladium complexes of the type [Pd(phPS2)(PAr3)] (phPS2) = [PhP(C6H4-2-S)2]2− have been synthesized in good yields and their crystal structures determined. Heck coupling reactions were carried out using the [Pd(phPS2)(PPh3)] (1), [Pd(phPS2){P(C6H4-4-Cl)3}] (2), [Pd(phPS2){P(C6H4-4-F)3}] (3), [Pd(phPS2){P(C6H4-4-CF3)3}] (4), [Pd(phPS2){P(C6H4-4-Me)3}] (5) and [Pd(phPS2){P(C6H4-4-OMe)3}] (6) complexes as catalyst precursors in order to examine the potential effect of the para-substituted triarylphosphines in the reaction of bromobenzene and styrene. 相似文献
14.
Luciana Naldini Maria Antonietta Cabras Maria Antonietta Zoroddu Francesco Demartin Mario Manassero Mirella Sansoni 《Inorganica chimica acta》1984,88(1):45-50
The reaction of [Cu2(O2CCH3)4·2H2O] with trimethoprim is reported. In methanol a green solution was obtained, which, on adding benzene, yielded tetrakis(μ-acetato)bis(trimethoprim)dicopper(II) di-benzene methanol solvate. The compound crystallizes with four molecules per cell in the monoclinic space group C2/c, with a = 24.109(5), b = 15.256(3), c = 16.532(3) Å, β = 116.89(2) for λ(Mo-Kα) = 0.71073 Å. The copper atoms are bridged by four acetate groups to form the binuclear molecule [Cu2-(O2CCH3)4(TMP)2]·2C6H6·CH3OH. The TMP ligand acts as a donor molecule through one pyrimidinic nitrogen atom. 相似文献
15.
Reaction between a mixture of cis-trans-[PtCl2(SMe2)2] and 1 equiv. AsPh3 in chloroform gives cis-[PtCl2(SMe2)(AsPh3)] crystallizing in P21/n with a=10.397(2), b=14.876(3), c=13.956(3) Å, β=90.86(3)° and Z=4. Selected geometrical parameters are PtAs 2.3531(10), PtS 2.262(2), PtCl (trans to S) 2.301(2), PtCl (trans to As) 2.328(2) Å and SPtAs 88.85(6), SPtCl(2) 90.77(8), AsPtCl(1) 91.07(6) and ClPtCl 89.42(7)°. cis-[PtCl2(AsPh3)2]·CHCl3 crystallizes in P21/c with a=20.557(4), b=9.5951(19), c=20.147(4) Å, β=96.77(3)° and Z=4. Selected geometrical parameters are PtAs(1) 2.3599(9), PtAs(2) 2.3770(9), PtCl(1) (trans to As(1)) 2.3515(18), PtCl(2) (trans to As(2)) 2.3251(18) Å and AsPtAs 97.87(3), As(1)PtCl(2) 88.67(5), As(2)PtCl(1) 84.30(5) and ClPtCl 89.32(7)°. By comparison with related structures from the literature the following trans influence series was established PMe2Ph>PPh3>AsPh3≈SbPh3>Me2SO≈SMe2≈SPh2>NH3≈olefin>Cl−>MeCN. 相似文献
16.
The hydrothermal reactions of (Ph4P)[VO2Cl2] and H2C2O4 at 150 and 125°C yield (Ph4P)2[V2O2(H2O)2(C2O4)3]·4H2O (1) and (Ph4P)[VOCl(C2O4)] (2), respectively. The structure of the molecular anion of 1 consists of a binuclear unit of oxovanadium(IV) octahedra bridged by a bisbidentate oxalate group. The VO6 coordination geometry at each vanadium site is defined by a terminal oxo group, an aquo ligand, and four oxygen donors — two from the bisbidentate bridging oxalate and two from the terminal bidentate oxalate. The structure of 2 consists of discrete Ph4P+ cations occupying regions between [VOCl(C2O4)]−∞ spiral chains. The structure of the one-dimensional anionic chain exhibits V(IV) octahedra bridged by bisbidentate oxalate groups. Crystal data: 1·4H2O, monoclinic P21/n, A = 12.694(3), B = 12.531(3), C = 17.17(3) Å, β = 106.32(2)°, V = 2621.3(13) Å3, Z = 2, Dcalc = 1.501 g cm−3, structure solution and refinement converged at a conventional residual of 0.0518; 2, tetragonal P43, A = 12.145(2), C = 15.991(3) Å, V = 2358.7(12) Å3, Z = 4, R = 0.0452. 相似文献
17.
Stefan Köcher Anthony L. Spek Rajendra Prasad Gerard van Koten 《Inorganica chimica acta》2006,359(14):4454-4462
The meta-diaminoaryl ferrocenes Fc-NCN-H (3) and Fc-CC-NCN-H (5) (Fc = (η5-C5H5)(η5-C5H4)Fe, NCN-H = C6H3(CH2NMe2)2-3,5) can be used as precursors in the preparation of heterobimetallic transition metal complexes of structural type Fc-NCN-MX (NCN = [C6H2(CH2NMe2)2-2,6]−; MX = PdCl (7), PtCl (8), PtI (9)) and Fc-CC-NCN-MX (MX = PdCl (11), PdI (12), PtCl (13)), respectively. They are accessible by applying different synthesis procedures, including oxidative addition and metallation-transmetallation processes.Cyclovoltammetric studies show that the ferrocene moieties in 3, 5, 7-9 and 11-13 can reversibly be oxidised. The potential of the Fe(II)/Fe(III) redox couple decreases with increasing electron density at the NCN pincer unit. The use of 8 as a possible (electro)chemical sensor in the detection of SO2 is discussed as well.The solid-state structures of 8 and 13 are reported. The crystals of 8 contain two molecules of 8 in the asymmetric unit. The plane of the C6H2 moiety is with 27.2(3)° and 38.2(3)° tilted towards the C5H4 entity, while in 13 an angle of 45.9(3)° can be found. The d8-electron configured platinum atoms possess a somewhat distorted square-planar surrounding, setup by two Me2NCH2ortho-substituents, the NCN Cipso carbon atom and the chloride ligand. 相似文献
18.
Two new zincophosphites [C6H14N2]0.5[Zn(H2PO3)2] 1 and [C4H12N2]0.5[(CH3)2NH2][Zn2(HPO3)3] 2 have been solvothermally synthesized in mixed solvents of N,N-dimethylformamide (DMF) and 1,4-dioxane (DOA), respectively. Single-crystal X-ray diffraction analysis reveals that compound 1 exhibits a neutral inorganic chain formed by ZnO4 and HPO2(OH) units. Interestingly, the left- and right-handed hydrogen-bonded helical chains are alternately formed via the hydrogen-bonds between two adjacent chains. Compound 2 exhibits a layer structure with 4- and 12-MRs formed by ZnO4 and HPO3 units, in which two kinds of organic amine molecules both act as countercations to compensate the overall negative electrostatic charge of the anionic network. 相似文献
19.
A novel organic-inorganic hybrid pentaborate [Ni(C4H10N2)(C2H8N2)2][B5O6(OH)4]2 has been synthesized by hydrothermal reaction and characterized by FT-IR, Raman spectroscopy, elemental analyses and DTA-TGA. Its crystal structure was determined from single crystal X-ray diffraction. The structure consists of isolated polyborate anion [B5O6(OH)4]− and nickel complex cation of [Ni(C4H10N2)(C2H8N2)2]2+, in which the two kinds of ligands come from the decomposition of triethylenetriamine material. The [B5O6(OH)4]− units are connected to one another through hydrogen bonds, forming a three-dimensional framework with large channel along the a and c axes, in which the templating [Ni(C4H10N2)(C2H8N2)2]2+ cations are located. The assignments of the record FT-IR absorption frequencies and Raman shifts were given. 相似文献
20.
Vito Di Noto Roberto Zannetti Silvano Bresadola Antonio Marigo Carla Marega 《Inorganica chimica acta》1991,190(2)
The reaction of α-MgCl2 with boiling ethyl acetate affords MgCI2(CH3COOC2H5)2·
(CH3COOC2H5), which is obtained as crystals suitable for X-ray analysis only from the mother liquor. M=315.5, orthorhombic, space group P21221 (No. 18), a=25.077(3), b=8.616(1), c=7.345(1) Å, V=1587.0(3) Å3, Z=4, Dx=1.32 g cm−3,λ A(Mo Kα)=0.71069 Å, μ=4.17 cm−1, F(000)=664, T=298 K, observed reflections: 1667, R=0.059 and Rw=0.069. The structure is composed of polymeric chains of MgCl2(CH3COOC2H5)2 and the ethyl acetate molecules occupy a mutually trans position. 相似文献