核磁共振法(NMR)和pH法研究Zn(Ⅱ)与HEDP(1-羟基乙叉-1,1-二膦酸)的配合物

本文用核磁共振法(NMR)和pH法对Zn(Ⅱ)与1-羟基乙叉-1,1-二膦酸(1-hydroxyethylidenel,1-diphosphonic acid,简称HEDP,以H_4L表示)的配合物进行了研究,由于pH<7时溶液中有沉淀生成,故NMR的研究是在溶液pH>7时进行.测定了溶液中不同Zn(Ⅱ)/HEDP摩尔比和pH值时~(?)PNMR的化学位移。研究结果表明在pH7.5-11.0范围内生成Zn(Ⅱ)/HEDP=1(摩尔比)组成的配合物,在pH11.8-12.3范围内生成Zn(Ⅱ)/HEDP=2(摩尔比)组成的配合物,分别用pH法和NMR法测定了上述组成配合物的稳定常数.结果如下: logK_([zn(HL)~-]) logK_([znL~(2-)]) logK_([zn,L]) pH法 4.69 7.51 11.63 NMR法——6.88-7.19 12.44     

某些酸性磷(膦)酸酯-Co(Ⅱ)、Ni(Ⅱ)、VO(Ⅱ)配合物的电子光谱和ESR波谱

本文对某些酸性磷(膦)酸酯与Co(Ⅱ)、Ni(Ⅱ)、VO(Ⅱ)配合物的电子光谱进行了测定,讨论了这类配合物的构型和光谱参数对萃取性能的影响。实验测得并计算了VO(Ⅱ)配合物的ESR波谱参数和键参数,对这类配合物的成键特性进行了讨论。     

1-(对甲苯基)-2-(三对甲苯基-5-亚磷酰基)乙醛的汞(Ⅱ)配合物的X射线晶体学、光谱表征和理论计算研究

通过2-溴-1-（对甲苯基）乙醛与三（对甲苯基）膦的反应制备α-磷配体：1-（对甲苯基）-2-（三对甲苯基-5-亚磷酰基）乙醛（L）。氯化镉和溴化汞与L分别反应,生成配合物[Cd（L）Cl₂]₂（C1）和[Hg（L）（μ₂-Br）Br]₂（C2）。用IR和NMR（¹H,¹³C,³¹P）对配合物进行了表征。通过单晶X射线衍射测定了C2的结构,并在B3LYP/6-31G^*水平对C2的结构进行了DFT计算研究,以揭示C2的复合反应位点与Schiff碱等亲核基团的相互作用。     

钴的二膦酸配合物[ Co(en) 3 ] [ Co2 (Hedbbp) 2 ]· 7H2O的合成与晶体结构

水热条件下合成了一个新的有机二膦酸钴配合物[Co(en)3][Co2(Hedbbp)2].7H2O,[H4edbbp=N,N’-二(苄基膦酸)乙二胺].X射线单晶衍射结构分析表明:配合物属三斜晶系,空间群P,ī晶胞参数:a=1.505.6(3)nm,b=1.524 8(3)nm,c=1.649 7(3)nm,α=63.10(3)°,β=78.12(3)°,γ=75.62(3)°,晶胞体积为V=3.252 4(11)nm3,Z=2.配合物结构单元中包含一个二膦酸钴的二聚单元阴离子[Co2(Hedbbp)2]2-和一个三乙二胺合钴螯合阳离子单元[Co(en)3]2 和七个水分子.     

菲咯啉取代苷脲Co(Ⅱ)、Cu(Ⅱ)配合物的合成及晶体结构

以配体菲咯啉取代苷脲(L), 分别与CoCl₂·6H₂O、CuCl₂·2H₂O进行配位反应, 得到2个配合物{[Co(L)(H₂O)₃]Cl₂·2H₂O}_n(1)和[Cu₂(L)₂Cl₄]·3C₂H₅OH(2)。并用元素分析、FTIR和X-射线单晶衍射进行了表征。晶体结构表明：配合物1属于正交晶系, P2₁2₁2₁空间群, 每个Co(Ⅱ)的配位环境为扭曲的八面体, 分别与1个配体上菲咯啉单元的2个氮原子、另外1个配体的羰基氧原子和3个水分子配位, 配合物中每个配体 L 表现为三齿配体分别与2个Co(Ⅱ)离子配位桥联形成一维链状结构。配合物2属于单斜晶系,P2₁/n空间群, Cu(Ⅱ)的配位环境为扭曲的四方锥形, 分别与配体上菲咯啉单元的2个氮原子和3个氯原子配位, 3个氯原子中有2个氯原子同时和2个Cu(Ⅱ)离子配位, 从而使配合物2形成双核配合物。     

钴的二膦酸配合物[ Co(en) 3 ] [ Co2 (Hedbbp) 2 ]· 7H2O的合成与晶体结构

水热条件下合成了一个新的有机二膦酸钴配合物[Co(en)3][Co2(Hedbbp)2]·7H2O,[H4edbbp=N,N'-二(苄基膦酸)乙二胺].X射线单晶衍射结构分析表明配合物属三斜晶系,空间群P-1,晶胞参数a=1.505.6(3)nm,b=1.524 8(3)nm,c=1.649 7(3)nm,α=63.10(3)°,β=78.12(3)°,γ=75.62(3)°,晶胞 体积为V=3.2524(11)nm3,Z=2.配合物结构单元中包含一个二膦酸钴的二聚单元阴离子[Co2(Hedbbp)2]2-和一个三乙二胺合钴螯合阳离子单元[Co(en)3]2+和七个水分子.     

菲咯啉取代苷脲的Co(Ⅱ)、Cu(Ⅱ)配合物的合成及晶体结构

以配体菲咯啉取代苷脲(L), 分别与CoCl₂·6H₂O、CuCl₂·2H₂O进行配位反应, 得到2个配合物{[Co(L)(H₂O)₃]Cl₂·2H₂O}_n(1)和[Cu₂(L)₂Cl₄]·3C₂H₅OH(2)。并用元素分析、FTIR和X-射线单晶衍射进行了表征。晶体结构表明:配合物1属于正交晶系, P2₁2₁2₁空间群, 每个Co(Ⅱ)的配位环境为扭曲的八面体, 分别与1个配体上菲咯啉单元的2个氮原子、另外1个配体的羰基氧原子和3个水分子配位, 配合物中每个配体 L 表现为三齿配体分别与2个Co(Ⅱ)离子配位桥联形成一维链状结构。配合物2属于单斜晶系, P2₁/_n空间群, Cu(Ⅱ)的配位环境为扭曲的四方锥形, 分别与配体上菲咯啉单元的2个氮原子和3个氯原子配位, 3个氯原子中有2个氯原子同时和2个Cu(Ⅱ)离子配位, 从而使配合物2形成双核配合物。     

新型Zn(Ⅱ)和Co(Ⅱ)配合物的合成、表征及性能

以4,4'-联苯二羧酸（H₂BPDC）和4,4'-联吡啶（BPY）作为混合有机配体,Zn(II)或Co(II)作为中心金属离子,通过溶剂热法合成了两种新型配合物[Zn₃(bpdc)₃bpy]_n（1, CCDC: 1843824）和[Co₃(bpdc)₃bpy]_n（2, CCDC: 1887332）,其结构和性能经X-射线单晶衍射、红外光谱（FT-IR）、粉末X-射线衍射（PXRD）、热重分析（TG）和N₂吸附/脱附测试表征。结果表明:两种配合物具有相似的三维孔状结构,由Zn(II)或Co(II)以四配位和六配位呈现四面体和八面体空间几何构型;1和2均具有较好的热稳定性;在77 K,氮气吸附条件下,配合物1的BET比表面积为5.584 m²/g,吸附总孔体积为0.024 cm³/g,吸附平均孔径为13.932 nm。      

Tb(Ⅲ)-氨基多膦酸-邻菲咯啉三元配合物的溶液荧光

氨基多膦酸类配体如乙二胺四甲基次膦酸(EDTP)等与氨基多羧酸类配体具有相似的骨架结构 ,只是后者分子中的羧酸根-COOH被前者的膦酸根-PO3H2所取代.     

REPARATION AND CHARACTERIZATION OF NEW SUPROFEN COMPLEXES OF Fe(III), Co(II) AND Ni(II)

Abstract

The preparation and properties of new complexes containing the biometals Fe(III), Co(II) and Ni(II) coordinated to the anti-inflammatory drug Suprofen are reported. The elemental analyses, together with the magnetic and thermal behavior and electronic, IR and Raman spectra, indicated the following stoichiometries for the latter two complexes: [M(Sup)₂(H₂O)₄]. For the Fe(III) complex, the generation of a dinuclear species may be proposed on the basis of ⁵⁷Fe Mössbauer measurements.     

假四面体(C2v)钴(Ⅱ)配合物电子光谱的强场处理

钴(Ⅱ)的假四面体(C_(2v))配合物 CoL_2X_2的配体场光谱一般显示出两组谱带,分别对应于基态~4A_2对两个~4T_1谱项的三个低对称性分量~4B_1,~4A_2和~4B_2的跃迁。前人对这类光谱的处理多采用弱场近似,模型多采用点电荷模型,结果得到的跃迁能和实测值相差较大。Menzel等指出:简单点电荷模型的固有弊病使得它不可能对此类共价配合物的光谱作出理想的处理。他们对点电荷模型作了适当的修改,应用弱场近似取得了满意的结果。本文应用强场近似处理这类配合物的光谱,和修改的点电荷模型相比较我们的结果更为满意。     

SYNTHESIS AND ELECTROCHEMICAL PROPERTIES OF CYCLOPENTADIENYLIRON(II) COMPLEXES WITH BIS(DIPHENYLPHOSPHINO)AMINE AS LIGAND

Abstract

The synthesis and properties of new cationic iron(II) complexes of general formula [(η⁵-C₅H₅)FeL(η²-dppa)]A [A=I^?, L = CO(1); A = BF₄, L = CO(2) CH₃CN(4), η¹-dppa(5); dppa = NH(PPh₂)₂] are described. The carbonyl complex [(η⁵-C₅H₅)Fe(CO)(η²-dppa)]BF₄ is deprotonated to give the neutral complex [(η⁵-C₅H₅)Fe(CO){η²-(PPh₂)₂N}](3). All complexes have been characterized by elemental analysis and IR and NMR spectroscopies. Cyclic voltammetry of complexes 1–5 shows a diverse redox chemistry in acetonitrile solution. While the reduction of 1 and 2 leads to the formation of a dinuclear Fe(I) complex, 4 and 5 form mononuclear species of Fe(I); oxidation of metal centers of 1 and 2 is not observed and in complexes 3 and 4 the metal centers are oxidized at potentials < 1. Complex 5 in acetonitrile solution is transformed into complex 4.     

COMPLEXES OF AMINOPHOSPHONATES PART 9.1 COPPER(II) COMPLEXES OF CIT RIC ACID DERIVATIVES

Abstract

Complex formation between copper(II) and 3-amino-3-phosphonoglutaric acid (Apga), an ambidentate aminophosphonate or citric acid derivative, was studied in aqueous solution by pH-potentiometry and EPR and electronic spectroscopy. Complexation with the parent molecules citric acid and tricarballylic acid was reinvestigated. The stoichiometries and stability constants of the complexes formed in these systems were determined at 25°C at an ionic strength of 0.20 mol dm^?3 (KCl). Stability constant data and spectroscopic results revealed that in the acidic pH range Apga behaves as a citric acid derivative, forming the phosphonate-bridged dimeric species Cu₂A₂H₂, while in the basic pH range, with decreasing proton competition at the amino binding site, it rearranges to yield mononuclear complexes involving aminophosphonate-like (NH₂, PO₃ ^2-, CO₂) coordination.     

Coordination compounds of Co(II), Ni(II) and Cu(II) with capric acid hydrazide

The reaction of aquo-ethanolic solutions of Co(II), Ni(II) and Cu(II) salts and ethanolic solution of capric acid hydrazide (L) yielded paramagnetic, high-spin bis- and tris(ligand) chelate complexes. The tris(ligand) complexes, [ML ₃]X ₂·nH₂O [M=Co(II), Ni(II);X=NO ₃ ^– , ClO ₄ ^– , 1/2SO ₄ ^2– ], have an octahedral structure formed on account of the bidentate (NO) coordination of three neutral hydrazide molecules. In the bis(ligand) complexes,ML ₂(NCS)₂ [M=Co(II), Ni(II)] and CuL ₂ X ₂·nH₂O (X=NO ₃ ^– , ClO ₄ ^– and 1/2SO ₄ ^2– ), the oxoanions and NCS^– take also part in coordination. The complexes have been characterized by elemental analysis, IR spectra, magnetic measurements, molar conductivity and TG analysis.

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Caprinsäurehydrazid-Komplexe von Co(II), Ni(II) und Cu(II)

Zusammenfassung Durch die Reaktion von wäßrig-ethanolischen Lösungen von Co(II)-, Ni(II)-und Cu(II)-Salzen mit einer ethanolischen Lösung von Caprinsäurehydrazid (L) wurden paramagnetische high-spin Bis- und Tris-Ligand-Chelatkomplexe erhalten. Tris-Ligand-Komplexe des Typs [ML ₃ X ₂·nH₂O [M=Co(II), Ni(II);X=NO ₃ ^– , ClO ₄ ^– , 1/2SO ₄ ^2– ], die eine oktaedrische Struktur besitzen, entstehen durch die Koordination von drei neutralen zweizähnigen (NO)-Hydrazidmolekülen. Bei den Bis-Ligand-KomplexenML ₂(NCS)₂ [M=Co(II), Ni(II)], sowie bei den Bis-Ligand-Komplexen CuL ₂ X ₂·nH₂O (X=NO ₃ ^– , ClO ₄ ^– , 1/2SO ₄ ^2– ) nehmen bei der Koordination außer Hydrazid auch die Säurereste teil. Die Komplexe wurden durch Elementaranalyse, IR-Spektren, magnetische Messungen, molare Leitfähigkeit und TG-Analysen charakterisiert.

     

SYNTHESIS AND STRUCTURE OF Pd(II) COMPLEXES OF 1,2,3-TRIPHENYLGUANIDINE

Abstract

The formation of two complexes by reaction of [PdCl₄]^2- with 1,2,3-triphenylguanidine (PhNH)₂C=NPh under different metal/ligand ratios has been observed and the structure of the complex [(1,2,3-triphenylguanidine)₂PdCl₂] has been determined by X-ray diffraction methods. The ligands are coordinated as neutral monodentate molecules to the metal centre through their imine nitrogen atoms. The second Pd(II) complex is [Pd(1,2,3-triphenylguanidine)₄]²⁺ and was isolated by precipitation with ClO^? ₄.     

SYNTHESIS AND CHARACTERIZATION OF TRIS(ALKYLISOCYANIDE) BIS(TRIARYL-PHOSPHINE)COBALT(II) COMPLEXES

Abstract

A series of complexes having the general formula, [Co(CNR)₃(PR₃)₂]X₂, X = ClO₄, BF₄ with CNR = CNCMe₃, CNCHMe₂, CNC₆H₁₁. CNCH₂Ph and PR₃ = PPh₃, P(C₆H₄Me-p)₃, P(C₆H₄OMe-p)₃ has been synthesized and characterized. Synthesis can be achieved by reaction of [Co(CNR)₄(AsPh₃)₂]X₂ complexes with controlled excess of PR₃ ligands, and by AgClO₄/AgBF₄ oxidation of the [Co(CNR)₃(PR₃)₂]X complexes. The latter procedure is preferable. Alternate syntheses of the [Co(CNR)₃(PR₃)₂]X complexes have also been employed. Five-coordinate Co(II) complexes have not been obtained using CNCMe₃ with P(C₆H₄Me-p)₃ ligands, CNCH₂Ph with P(C₆H₄OMe-p)₃ ligands, or CNC₄H_9-n with PPh₃ ligands. [Co(CNC-Me₃)₃{P(C₆H₄Cl-p)₃}₂]ClO₄ produced only [Co{CNCMe₃)₄H₂O](ClO₄)₂ upon forced oxidation with excess AgClO₄. [Co(CNR)₃(PR₃)₂]X₂ complexes appear to undergo varying degrees of distortion from regular (i.e., D _3h symmetry) axially-disubstituted trigonal bipyramidal coordination in the solid state, as evidenced by v(-N°C) IR patterns, but to assume regular trigonal bipyramidal coordination in solution. Effective magnetic moments indicate one-electron paramagnetism, and solution electronic spectra are compatible with trigonal bipyramidal coordination.