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1.
XIE  Yong-Shu ZHU  Yu 等 《中国化学》2002,20(3):292-295
A mixed-ligand copper(Ⅱ) complex[Cu2(phen)2(HL^1)2]-(ClO4)2(1) was synthesized.X-ray analyses reveal that 1 has a bis(μ2-phenoxo)-bridged dicopper(Ⅱ) structure.2D hydrogen-bonded network is formed utilizing the N-H,O-H and C-H groups of the (HL^1) ligands (H2L^1=N-(2-hydroxybenzyl)ethanolamine),the C-H groups of the phenanthrolines and the perchlorate anions.Variable temperature magnetic properties of 1 have shown comparatively weak antiferromagnetic interactions with respect to the bridge angles, which have been ascribed to the unfavorable overlaps of the magnetic orbitals fo the highly distorted copper coordination polyhedra and the pyramidal distortions at the phenoxo oxygen atoms.  相似文献   

2.
1 INTRODUCTIONRecently,bridgedbinuclearcomplexesoffirstrowtransitionmetalshavereceivedmuchattentiononaccountoftheirbiologicalrelevanceandcondensedphasemagneticproperties[1,2].Intheseresearches,manybridgedligandswhichplayimportantroleshavebeenusedasuseful…  相似文献   

3.
1 INTRODUCTION Transition metal complexes with ferrocene are of considerable interest in the past fifty years because of their novel structures and special properties[1, 2]. The chemistry of ferrocene and its derivatives has become richer and richer in the last decade. Many complexes containing ferrocenyl have been synthesized and characterized[3~5]. Recently we have reported the synthesis and crystal structure of dibromo[1,1?bis(diphenylphosphino)- ferrocene]cadmium (Ⅱ)[6]. Herein we…  相似文献   

4.
王庆伦  廖代正  阎世平  姜宗慧  程鹏 《中国化学》2002,20(11):1249-1255
IntroductionMolecularmagnetismofpolynuclearcomplexesisofconsiderableinterestfordesigningnewmagneticmaterialsandforinvestigatingtherelationshipbetweenthestructureandtheroleofthepolymetallicactivesitesinbiologicalsystems.1 4 Journauxetal .5haverecentlyprop…  相似文献   

5.
A new complex [Zn(NIT-1'-MeBzIm)Cl2(H2O)] (NIT-1'-MeBzIm = 2-{2'-[(l'- methyl)benzimidazolyl]}-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide) has been prepared and structurally characterized by X-ray diffraction method. Crystal data: monoclinic, space group P21/n, Z = 4, C15H21Cl2N4O3Zn, Mr = 441.63, a = 7.2225(10), b = 30.849(4), c = 8.8758(13) , β = 103.904(2)°, V = 1919.6(5) 3, Dc = 1.528 g/cm3, μ(MoKα) = 1.579 mm1, F(000) = 908, R = 0.0436 and wR = 0.1029 for 2456 observed reflections with I > 2σ(I). X-ray analysis reveals that the Zn(II) ion is four-coordinated with a distorted tetrahedron. There also exist H-bonds, π-π piling interactions and weak intermolecular contacts between the NO groups which form a mutual stagger 3-D network configuration. Magnetic investigation reveals that there exists intermolecular antiferro- and ferromagnetic interactions in the title complex.  相似文献   

6.
1 INTRODUCTION The synthesis and study of transition metal com-plexes incorporating organic free radicals have arou-sed great interest in the field of molecular magne-tism[1]. Nitronyl nitroxide radicals (NITR), stable or-ganic radicals, have been widely used as molecularunits in the design and construction of magnetic ma-terials[2~5]. These radicals are especially attractivedue to that their donor atoms can assemble an exten-ded coordination geometry with changing magneticcoupling. A…  相似文献   

7.
A new dinuclear Cu(II) complex, [Cu2L(N3)2](ClO4)1.5 (OH)4.5 · 2H2O 0.5C2H5OH (1), of a bis‐macrocyclic ligand, 2,6‐bis(l,4,7,10‐tetraazacyclododecan‐10‐ylmethyl)‐methoxybenzene (L), has been synthesized, characterized and structurally determined by X‐ray diffraction analysis. Complex 1 crystallizes in orthorhombic crystal system, Pca2(l) space group with a = 1.5371(3), b = 1.6641(3), c = 3.0950(6) nm, V = 7.917(3) nm3, Fw = 904.62, Z=8, Dc= 1.529 g/cm3 and final R = 0.0568, wR = 0.1406 for 10410 observed reflections with I≥2σ (I). Both Cu(II) centers in the structure are coordinated by four nitrogen atoms of 1,4,7, 10‐tetraazacyclododecane (cyclen) and a nitrogen donor of the axial azide anion. Each Cu(II) center is in a square‐pyramidal coordination environment, and the intra‐and nearest inter‐molecular Cu? Cu nonbonding distances are 0.9855 and 0.7298 nm, respectively. Variable temperature magnetic susceptibility measurements in the range of 4.2–300 K indicate mat there exists weak intra‐ and inter‐molecular antiferromagnetic coupling between the Cu(II) centers with 27= ?4.2 cm?1 and Θ = ?0.47 K.  相似文献   

8.
A new complex [Cu(phen)3][(C6H5)2C(OH)COO]2·6H2O was prepared by self-assembly of benzilic acid, 1,10-phenanthroline (phen), and copper perchlorate. It crystallizes in triclinic, space group P1, with a = 1.14661(17), b = 1.6455(2), c = 1.6457(2) nm, α = 74.779(2), β = 74.904(3), γ = 84.424(3)o, V = 2.8914(7) nm3, Dc = 1.340 g/cm3, Z = 2, F(000) = 1218, GOOF = 1.018, the final R = 0.0643 and wR = 0.1633. The crystal structure shows that the copper ion is coordinated with six nitrogen atoms from six 1,10-phenanthroline molecules, forming a distorted octahedral coordination geometry.  相似文献   

9.
Schiff碱双核Mn配合物的合成、结构和性能研究   总被引:3,自引:0,他引:3  
Five manganese complexes of Schiff base were synthesized: [MnⅣ,Ⅳ(μ-O)(Salen)]2·DMF·H2O (1), [MnⅣ,Ⅳ(μ-O)(5-BrSalen)]2·DMF·0.5H2O (2), {MnⅣ,Ⅳ(μ-O)[Sal(1,2-pn)]}2·H2O (3), {MnⅣ,Ⅳ(μ-O)[5-Br-Sal(1,2-pn)]}2·H2O (4), {MnⅣ,Ⅳ(μ-O)[5-CH3-Sal(1,2-pn)]}2·2H2O (5), and were characterized by element analysis, IR and UV-Vis spectra. The results of cyclic voltammogram show that Schiff base ligands can drop the potential of manganese and steady high oxide state of manganese. The magnetic properties of 1 and 3 have also been studied. The results show that there is a weak ferromagnetically coupling of Mn2 pair at room and low temperature, and the interactions of complex 3 are weaker than complex 1.  相似文献   

10.
A new cadmium(II) complex Cd(OBBA)2(2,2A-bipy)2 with 2-benzoylbenzoic acid(HOBBA) and 2,2-bipyridine(2,2A-bipy) as ligands has been synthesized. Crystal data for the complex are as follows: monoclinic, space group P21/c with a = 16.402(3), b = 10.4191(18), c = 23.395(4) A, β = 91.765(2)o, V = 3996.2(12) A3, Dc = 1.455 gAcm-3, Z = 4, μ(Mo Kα) = 0.603 mm-1, F(000) = 1784, the final R = 0.0218 and w R = 0.0558. In the electrode reaction, its electron transfer is quasi reversible and the electrode reaction corresponds to Cd(II)/Cd(0). Under 618 nm radiation, the title complex shows a strong fluorescent band at around 326 nm. In addition, in the range of 2~300 K, this complex displays diamagnetic property.  相似文献   

11.
合成了双核铜配合物 [Cu(TSSB) (H2 O) ] 2 ·2H2 O (TSSB =牛磺酸缩水杨醛席夫碱 ) ,通过元素分析、红外光谱对配合物进行了表征 ,并利用X射线法测定其结构 .晶体属三斜晶系 ,空间群P1- ,其晶胞参数为 :a =0 .69613 ( 19)nm ,b =0 .93 0 7( 3 )nm ,c=1.0 43 9( 3 )nm ;α =10 8.796( 5 )° ,β =10 1.2 71( 5 )° ,γ =10 5 .617( 5 )° ,V =0 .5 869( 3 )nm3 ,Z =1,Dcald=1.849g/cm3 ,μ =2 .0 5 8mm-1,F( 0 0 0 ) =3 3 4,Gof =1.0 79,Δρ =3 79~ -4 0 6e·nm-3 .两个铜原子配位数各为五 ,处于变形四方锥的配位环境中 .并对配合物进行了的生物活性试验 ,结果表明 ,配合物抗菌活性与青霉素接近 ,肿瘤抑制率达 63 .5 % .半数致死量为 10 0 0mg/kg .有可能成为一种新的抗菌、抗肿瘤药物  相似文献   

12.
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   

13.
双吡唑桥联的大环状钯(Ⅱ)配合物的合成与结构(英)   总被引:2,自引:0,他引:2  
A dipyrazol-bridged macrocyclic palladium(Ⅱ) complex [{Pd(en)}4L4](NO3)8 (en=ethylenediamine, L=3,3′,5,5′-tetramethyldipyrazol) 1 was prepared in water through a [4+4] macrocyclization of cis-(ethylenediamine)Pd(Ⅱ) nitrate and the neutral form of the dipyrazol ligand 3,3′,5,5′-tetramethyldipyrazol. This cationic palladium macrocycle is highly distorted rather than a planar macrocycle and can hold eight nitrate anions around the macrocyclic framework through both hydrogen bonding and electrostatic interactions. CCDC: 192017.  相似文献   

14.

A new terephthalato-bridged binuclear nickel(II) complex with a tetraazamacrocyclic compound as the terminal ligand, [Ni 2 (cth) 2 (µ-TPHA)](ClO 4 ) 2 (1) [cth= rac -5,7,7,12,14,14-hexamethyl-1,4,8,11-tetraazacyclotetradecane] has been synthesized and characterized. According to X-ray crystallographic studies on the solvated species 1·2CH 3 OH, each Ni(II) ion lies in a distorted octahedral environment, and the terephthalato ligand bridges two Ni(II) ions in a bis bidentate fashion. Cryomagnetic measurements revealed Curie-Weiss behaviour with è = m 1.4 K. Such behaviour may be due to a very weak intramolecular superexchange interaction through the extended bridge, a weak intermolecular exchange interaction or the local zero-field splitting of Ni(II) ions.  相似文献   

15.
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   

16.
The pentanuclear complex, Cu5(SIP)2(HSIP)2(H2O)18(H2O)5(H3SIP = 5-sulfoi-sophthalic acid), has been synthesized by the hydrothermal reaction of CuCl2 with NaH2SIP at 160 ℃, and characterized by single-crystal X-ray diffraction and IR spectrum.The crystal of the complex crystallizes in a triclinic system, space group P1-, with a = 7.0018(5), b = 11.9725(8), c = 19.0424(13) , α = 78.8540(10), β = 85.1710(10), γ = 83.6080(10)o, V = 1553.24(19) 3, Z = 1, C32H60O51S4Cu5, Mr = 1706.74, Dc = 1.825 g/cm3, μ = 1.937 mm-1, F(000) = 869, the final R = 0.0709 and wR = 0.1503 for 4235 observed reflections with I > 2σ(I).The five Cu2+ ions are connected by two symmetry-related tridentate SIP3-ligands and charge-balanced by two monodentate HSIP2-ligands, giving a discrete pentanuclear structure.The pentanuclear copper molecules are linked by hydrogen bonds to form a three-dimensional supramolecular structure.The temperature-dependent magnetic susceptibility data revealed weak ferromagnetic magnetic interactions between the Cu2+ ions.  相似文献   

17.
1INTRODUCTIONCoppercomplexeshavealargevarietyofstericstructuresandplayanimportantroleincatalysingtheenzymaticactivities,which...  相似文献   

18.
Introduction Many examples of complexes containing the eight-membered ring M(-dppm)M' are known with a variety of metals, oxidation states and stereochemis-tries.1-4 In general, they contain trans-bound, bridging dppm ligands to give a planar M2P4 core structure with the two metal atoms held in close proximity to each other (regardless of whether a metal-metal bond is pre-sent or not). This feature is presumably one of the chief reasons for the unusual bonding, reactivity and catalytic prope…  相似文献   

19.
IntroductionDimericcopper(II)carboxylatescontainingavarietyofoxygenandnitrogen donorligandshavebeenextensivelyinvestigatedandtheirpreparations ,magneticandspectralpropertieshavebeenreviewed .1 5Differentkindsofcopper(II)carboxylateadductshavebeensynthesizedandalsodinuclearcopper(II)complexeshavebeenearlystud iedasusefulmodelstoestablishmagneto structuralcorre lationsforspinexchangebetweenmetalions .Inparticu lar,theoccurrenceofdicopperionsattheactivesiteofthevariousformsoftheoxygencarrierpro…  相似文献   

20.
在自然界中,α-羟基羧酸广泛的存在于动植物体内,在羧酸循环、碳水化合物代谢和氨基酸的合成中起到重要的作用。Tapscott等详细总结了有关羟基羧酸及其金属配合物的合成化学[1]。芴的9位上2个氢原子被羟基和羧基取代可生成9-羟基-芴-9-羧酸(简称芴酸),它是α-羟基乙酸的衍生物,是一种具有生理活性的植物生长整形素,它能够延缓植株生长,影响植株根的向地性和茎的向光性[2]。由于芴酸含有羟基和羧基两种不同的氧配位原子,使其又可以作为一种潜在的构筑配合物的组织基元。目前有关芴酸与金属离子的合成与结构化学研究相对较少,仅见铜、镉的单…  相似文献   

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