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1.
1 INTRODUCTION The picoloylhydrazide compounds are close to thebiologic environment and can react with microele-ments in organism so as to have antitubercular andantineoplastic activities. However, owing to the exis-tence of amino group, this kind of compounds aretoxic to some extent[1]. In order to decrease theirtoxicity, hydrazone or hydrazide compounds synthe-sized by the condensation reaction of amino and car-bonyl groups have been well studied in recentyears[1~7]. Herein we report t… 相似文献
2.
1 INTRODUCTION In 1945, Braude[1] found for the first time that adding copper (Cu) ten times the normal requisite amount into the feed can improve the production property of the animal obviously. Therefore, from then on copper has been widely applied in pig- breeding industry as an effective growth-promoting agent, especially in the process of intensive culture, which plays an important part in improving the growth of animal and the production property. However, at the same time, the high… 相似文献
3.
IntroductionExchange coupledpolynuclearcopper(II)complex esareofspecialinterestduetotheirinvolvementinbio logicalprocessesandininorganicmaterials .1,2 Theinti materelationshipbetweenthespincouplingandthemolecularstructurehasfosteredtheemergenceofmolec ular… 相似文献
4.
IntroductionMolecularmagnetismofpolynuclearcomplexesisofconsiderableinterestfordesigningnewmagneticmaterialsandforinvestigatingtherelationshipbetweenthestructureandtheroleofthepolymetallicactivesitesinbiologicalsystems.1 4 Journauxetal .5haverecentlyprop… 相似文献
5.
1 INTRODUCTION The chemical properties of acylhydrazones Schiff bases and their complexes with some transition metal ions have been intensively investigated in several re- search areas because of their chelating capability and pharmacological applications[1~10]. Intriguingly, the copper(II) complexes are shown to be signifycantly more potent than the metal free chelate, suggesting that the metal complex is the biologically active species. Owing to the biological interest in these types … 相似文献
6.
LI Yana b WU A-Qinga b ZHENG Fa-Kuna② GUO Guo-Conga② LU Can-Zhonga HUANG Jin-Shuna a 《结构化学》2005,(11)
1 INTRODUCTION Exploration on the syntheses and properties of car- boxylate complexes, especially aromatic carboxylate complexes, has always been a fascinating and chal- lenging research field for decades either in coor- dination chemistry or in functional materials[1, 2]. Cy- anobenzoic acid (Hcba) possessing two functional coordination groups should display structural diver- sities on the formation of complexes[3~15]. In particu- lar, the copper(II) carboxylate complexes bearing spe- … 相似文献
7.
Teresa Kowalik-Jankowska Henryk Kozlowski Karol Kociolek Miroslaw T. Leplawy Giovanni Micera 《Transition Metal Chemistry》1995,20(1):23-25
Summary Potentiometric and spectroscopic measurements were used to characterize the binding ability of -hydroxy-methylserine (Hms) with copper(II) and oxovanadium(IV) ions. The ligand was found to be generally a more efficient chelating agent than serine. Both of the deprotonated hydroxyl groups of Hms can be involved in coordination to vanadyl ions, whereas copper(II) binds in the same way as with serine. 相似文献
8.
Introduction Imidazoleisofconsiderableinterestasaligandwhichpresentsinmanybiologicalsystems (forexampleinthehistidylresidueofproteins)providingapotentialbindingsiteformetalions .Imidazoleasanunidentateligandcanformcomplexeswithmetalionsthroughitstertiarynitro genatom .Somecomplexesofimidazoleanditsderivativeswithtransition metalionshavebeenreported .1 4 Thepreparationofthecomplexesofcopper(II)car boxylatewithavarietyofbasicligandsandtheirmagneticandspectralpropertieshavebeenreported .5,… 相似文献
9.
《Journal of Coordination Chemistry》2012,65(3):281-285
By using the donor ligand 2,6-diacetylpyridinebis(semicarbazone) (DAPSC), pentagonal bipyramidal complexes of Mn(II), Fe(II), Ni(II) and Cu(II) have been obtained. The structure of [MnCl2(DAPSC)]·H2O has been determined by X-ray crystallography. Further reactions of these complexes with lithium salts of 7,7',8,8'-tetracyanoquinodimethane (TCNQ) yielded their corresponding adducts. 相似文献
10.
《Journal of Coordination Chemistry》2012,65(10):1209-1217
The title compound has been synthesized and characterized by elemental analysis and conductivity studies. The crystal and molecular structure has been determined. There are two different types of molecules in the crystal: mono- and diaquadi(acetato-O)-bis(2,4'-bipyridyl) copper (II). Both copper atoms occupy special positions. The copper atoms show almost ideal square pyramidal (4 + 1) and square bipyramidal (4 + 2) coordination. Due to the Jahn-Teller effect, the axial Cu-O(water) bond distances are longer than respective equatorial Cu-O(acetate) bond distances. The bond valences of the copper were computed. An intramolecular strong hydrogen bond linking O(water) and O(acetate) atoms exists in the molecule. The differences of geometrical environment for copper in mono- and diaquadi(acetato-O)-bis(2,4'-bipyridyl) copper(II) are imposed by strong intermolecular hydrogen bonds creating a linear infinite chain structure along crystallographic x axis. Also weak intramolecular hydrogen bonds are present in the molecule. 相似文献
11.
Sevagapandian Sankarapandian Rajagopal Gurusamy Nehru Kasi Athappan Periakaruppan 《Transition Metal Chemistry》2000,25(4):388-393
Complexes of the general formula, ML2 [M = CuII, NiII, CoII and OVIV; L = 1,2,3,5,6,7,8,8a-octahydro-3-hydroxyimino-N-(4-X-phenyl)-l-phenyl-5-(phenylmethylene)-2-naphthalenecarboxamide (X =
H, Me, OMe, Cl)] have been prepared and characterized on the basis of elemental analysis, magnetic moments and i.r., e.p.r.
and electronic spectra. These metal complexes contain the N4 chromophore with the ligand coordinating through nitrogens of the azomethine and deprotonated anilide functions. C.v. measurements
indicate that the copper(II) complexes are quasi-reversible in acetonitrile solution. Square planar and square pyramidal structures
are assigned respectively to the copper(II) and oxovanadium(IV) complexes, whereas tetrahedral geometry is assigned to the
nickel(II) and cobalt(II) complexes. Deprotonated anilide nitrogen is involved in coordination and the presence of an electron-donating
group para to the anilide function decreases the ΔE values of the d–d transitions while the value is found to increase when electron-withdrawing groups are substituted. Line
spacing in the e.p.r. spectra of the copper(II) and oxovanadium(IV) complexes increases when methyl group is para to the anilide group, and decreases when this group is replaced by methoxy or chloro. The ν(C–N) of the anilide group and
the ν(C-N) of the azomethine function of the oxime metal complexes are metal-sensitive and the blue shift for the above stretching
frequencies follows the order: copper(II) > oxovanadium(IV) > nickel(II) ≈ cobalt(II).
This revised version was published online in June 2006 with corrections to the Cover Date. 相似文献
12.
Andrea Preuß Marcus Korb Tobias Rüffer Jörn Bankwitz Colin Georgi Alexander Jakob Stefan E. Schulz Heinrich Lang 《无机化学与普通化学杂志》2020,646(13):670-680
The template synthesis of ethylenediamine ( 1 ) with 2-acetylcyclopentanone ( 2 ) and [Cu(OAc)2 · H2O] ( 5 ) produced [Cu(1-(2-cC5H6(O))C(Me)NCH2)2)] ( 6 ) in 82 % yield. Reaction of 5 with bis(benzoylacetone)diethylenetriamine ( 7 , = L H)[1] gave [Cu(μ-OAc)( L )(H2O)]2 ( 8 ). The solid-state structures of 6 and 8 were determined confirming that 8 possesses intra- and intermolecular hydrogen bonds resulting in a dimer formation. The thermal behavior of 6 – 8 was studied by TG and TG-MS. Under oxygen CuO was formed, whereas under Ar Cu/Cu2O ( 6 ) or Cu ( 8 ) was obtained. Complex 6 was used as CVD precursor for Cu and Cu-oxide deposition (substrate temp., 400–500 °C, N2, 60 mL · min–1; O2, 60 mL · min–1; pressure, 0.87–1.5 mbar). The as-obtained deposits show separated particles of different appearance at the substrate surface as evidenced by SEM. Non-volatile 8 was applied as spin-coating precursor for Cu and CuO formation [conc. 0.25 mol · L–1; volume 0.2 mL; 3000 rpm; depos. time 2 min; heating rate 50 K · min–1; holding time 60 min (Ar), 120 min (air) at 800 °C]. The samples on silicon consist of granulated particles (Ar) or are non-dense with a grainy topography (air). EDX and XPS measurements confirmed the formation of Cu (Ar) or CuO (O2) with up to 13 mol-% C impurity. 相似文献
13.
《Journal of Coordination Chemistry》2012,65(2):235-251
Abstract The stoichiometric reaction of copper(II) hydroxycarbonate, N-(2-hydroxyethyl)iminodiacetic acid [H2heida?HOCH2CH2N(CH2CO2H)2)] and 2,2′-bipyridine (bipy) in water yields crystalline (2,2′-bipyridine)(N-(2-hydroxyethyl)iminodiacetato)copper(II) tetrahydrate, [Cu(heida)-(bipy)] · 4H2O (compound I). This was studied by TG analysis (with FT-IR study of evolved gases), IR, electronic and ESR spectra, magnetic susceptibility data and single crystal X-ray diffraction methods. The compound crystallises in the triclinic system, space group P1, a = 7.011(2), b = 12.586(3), c = 13.052(3) Å, α = 62.14(1), β = 80.51(2), γ = 77.09(2)°, Z = 2, final R 1 = 0.051 for 3900 independent reflections. The Cu(II) atom exhibits an asymmetric, elongated, octahedral coordination (type 4+1 + 1), and bipy acts as an N,N-bidentate ligand supplying two among the four closest donor atoms of the metal (Cu-N bond lengths of 1.994(2) and 2.053(2) Å); heida plays an N,O,O′,O″-tetradentate chelating role (bond lengths Cu?N = 2.075(2), Cu-O(carboxyl) = 1.958(2), Cu-O′(carboxyl) = 2.337(2) and Cu-O″(hydroxyl) = 2.459(2) Å). The effective bidentate chelation of bipy imposes fac-chelation to the iminodiace-tate moiety of heida in I, as previously reported in mixed-ligand complexes having a 1:1:2 Cu(II)/IDA/N(heterocyclic) or a 1/1/(1 + 1) Cu/IDA/(N-heterocyclic + N-aliphatic) donor ratio. The tetradentate role of heida in I reveals its noticeable conformational flexibility. The crystal features a hydrogen bond network forming supra-molecular chains extending along the a axis. These are linked by two symmetry-related hydrogen bonds of the type O(hydroxyl)-H…O′(carboxyl) between two adjacent complex units (symmetry code i=-x, -y+1, -z+1), related to each other by an inversion centre. 相似文献
14.
Using Cu(Ⅱ) as the template, a complex {[Cu2L2(H2O)2] 4H2O}n (L = N-acetoxyl-
picolinamide) has been successfully synthesized and characterized by single-crystal X-ray diffrac
tion. The crystal is of monoclinic, space group C2/c, with a = 24.144(5), b = 7.1622(14), c =
17.283(4) (A), C16H24Cu2N4O12, Mr = 591.47, β = 131.73(3)°, V = 2230.3(8) (A)3, Z = 4, Dc= 1.761
g/cm3, F(000) = 1208,μ = 1.978 mm-1, R = 0.0400 and wR = 0.1099. The copper (Ⅱ) ion is five
coordinated with a distorted square pyramidal geometry. The complex can be viewed as a one
dimensional chain structure by carboxylic bridges among copper atoms. In the complex there exist
hydrogen bonding interactions to stabilize the structure. 相似文献
15.
IntroductionDimericcopper(II)carboxylatescontainingavarietyofoxygenandnitrogen donorligandshavebeenextensivelyinvestigatedandtheirpreparations ,magneticandspectralpropertieshavebeenreviewed .1 5Differentkindsofcopper(II)carboxylateadductshavebeensynthesizedandalsodinuclearcopper(II)complexeshavebeenearlystud iedasusefulmodelstoestablishmagneto structuralcorre lationsforspinexchangebetweenmetalions .Inparticu lar,theoccurrenceofdicopperionsattheactivesiteofthevariousformsoftheoxygencarrierpro… 相似文献
16.
Antsyshkina A. S. Sadikov G. G. Korshunov O. Yu. Anpilova E. L. Bicherov A. S. Sergienko V. S. Uflyand I. E. Garnovskii A. D. 《Russian Journal of Coordination Chemistry》2003,29(10):724-731
Heterocyclic -aminovinyl ketones (HL) and the copper complex CuL2 are synthesized and studied by IR and 1H NMR spectroscopies. The crystal structure of one of the tautomeric HL molecules is determined by X-ray diffraction analysis. The crystals are triclinic: a = 9.261(6) Å, b = 9.448(6) Å, c = 11.310(5) Å, = 96.74(5)°, = 99.46(5)°, = 93.60(5)°, space group P
. The compound has the form of a ketoamine tautomer. The structure contains intramolecular and intermolecular hydrogen bonds. The latter link the molecules into the center-symmetric dimers. 相似文献
17.
18.
IntroductionThecrystalengineeringofone ,two ,andthree di mensionalcoordinationpolymerswas ,inthenearpastyears ,ofgreatinterestandarapidlydevelopingareaofresearchthathasimplicationsfortherationaldesignofnewfunctionalmaterials .1Thisareahasadvancedtoastageat… 相似文献
19.
1 INTRODUCTION Galactose oxidase is a monomeric enzyme that catalyzes the stereospecific oxidation of a broad range of primary alcohol substrates and possesses a unique mononuclear copper site essential for catalyzing a two-electron transfer reaction during the oxidation of primary alcohol to corresponding aldehydes[1]. The catalytic reaction is shown in Eq. 1. RCH2OH + O2 RCHO + H2O2 (1) A recent report on the crystal structure of galactose oxidase reveals a unique mo… 相似文献
20.
LI Hao-Honga CHEN Zhi-Ronga② REN Yong-Gang LI Jun-Qiana b HUANG Chang-Canga ZHAO Bina a 《结构化学》2005,(12)
1 INTRODUCTION terested in the unique effects associated with substituents at 4- and 7-positions of the phenan- The coordination chemistry of 1,l0-phenanthroline throline ring. Thus, when phenyl groups are present, and its derivatives has captured the attention of che- the absorptivities of the CT transitions are increased mists for years. The reports on biological importance[1~4], markedly due to the extension of the dipole moment supramolecular chemistry[5], electronic spectra[6], conne… 相似文献