Syntheses and Structures of Two Heteronuclear Complexes with Glycine {[CuEr(Gly)_5(H_2O)_2](ClO_4)_5·H_2O}_n and {[Cu_2Gd_2(Gly)_10 (H_2O)_4](ClO_4)_10·4H_2O}_n

Two one dimensional heterometallic coordination polymers {[CuEr(Gly) 5(H 2O) 2](ClO 4) 5·H 2O} n (1) and {[Cu 2Gd 2(Gly) 10 (H 2O) 4](ClO 4) 10 ·4H 2O} n (2) (Gly = glycine) were synthesized and structurally and characterized magnetically. Complex 1 crystallizes in a triclinic space group of P 1 with a =1.1769(2) nm, b =1 2289(3) nm, c = 1.4452(3) nm, α = 89.90(3)°, β = 71.88(3)°, γ = 62.15(3)°, and Z =2. The carboxyl groups of glycine molecules take two coordination modes. The first one acts as a bidentate bridging ligand only. The second is a tridentate bridge that coordinates to three different metal ions. Each erbium ion is eight coordinated, taking a distorted square antiprism arrangement. The copper ion has a square pyramidal coordination polyhedron. The topological structure of complex 2 is similar to complex 1, but there are some disparities in the bond lengths and bond angles. It is also triclinic space group of P 1 with a = 1.2479(3) nm, b = 1.4489(3) nm, c =2.0885(4) nm, α = 109.56(3)°, β = 93.75(3)°, γ = 93.54(3)°, and Z =2. Variable temperature susceptibility measurements show that there is a weak ferromagnetic interaction between the Gd 3+ and Cu 2+ ions in complex 2.

Nitrilotriacetate Bridged 3d-4f Heteronuclear Complex: Synthesis and Crystal Structure of ｛[GdCu(NTA)(H_2O)_6Cl]ClO_4·H_2O｝_n

The heteronuclear gadolinium copper complex was synthesized. Its crystal structure was determined by single crystal diffraction. The crystal crystallizes in triclinic, space group P 1, a=0 8483(1) nm, b =0 9642(2) nm, c =1 2838(2) nm, α =111 17(1)°, β = 93 52(1)°, γ =100 89(1)°, Z =2, D c=2 335 g·cm -3 . The complex appears as a zigzag 1D chain. Each gadolinium ion is coordinated by three carboxylic oxygen atoms and six oxygen atoms from H 2O. Each copper ion is chelated by NTA with its nitrogen atom and three oxygen atoms of three carboxyl groups, and coordinated by a chlorine ion. The ClO 4 - is located between the chains as a counter ion.

Syntheses and Structural Characterizations of η~5-2,4-Cyclopentadien-1-yl Di-carbonyliron Heteronuclear Bi-Metallic Complexes

The novel complexes, Cp(CO) 2FeTiCp 2Cl(1) and Cp(CO) 2FeSn(CH 2CMe 2Ph) 3(2), were synthesized and characterized by means of elemental analyses and IR spectra, Cp(CO) 2FeSn· (CH 2CMe 2Ph) 3 was additionally characterized by X ray crystal structure analysis. The results of the elemental analyses are in good agreement with the theoretical values. The IR spectra show the existence of η 5 2,4 cyclopentadien 1 yl, carbonyl and methyl groups in the title complexes. The above experimental results show that the M-M bond exists in Cp(CO) 2FeSn· (CH 2Me 2Ph) 3, while the existence of the M-M bond in Cp(CO) 2FeTiCp 2Cl is highly possible, too. Both the two complexes are rather stable towards air and moisture, easily soluble in tetrahydrofuran and toluene, while their solubilities are greatly different in n hexane.

Synthesis and Crystal Structure of Heteronuclear Complex of Copper and Ytrium with Glycine

The title complex [CuY(Gly) 5(H 2O) 2](ClO 4) 5H 2O was synthesized in aqueous solution and its crystal structure was determined by X ray diffraction method. The crystal is triclinic, space group P 1 with a =1 1751(3) nm, b =1 2410(3) nm, c =1 4448(3) nm, α =72 97(2)°, β =71 82(2)°, γ =60 96(2)°, V =1 7244(6) nm 3, Z =2, d c=2 08 g/cm 3. The crystal is composed of one dimensional chain of infinite length.

Crystal Structure of a Heteronuclear Complex of Erbium-Yttrium and Glycine [ErY(GIy)_6(H_2O)_4] (ClO_4)_6·5H_2O

The title complex [ErY(Gly)_6(H_2O)4](ClO_4)_6·51H_2O has been synthesized.Its crystal structure has been determined by X-ray diffraction method.The crystal is triclinic with space group P.The unit cell parameters are as follows:a=1.1518(4) nm,b=1.4105(7) nm,c=1.5530(6) nm,α=96.61(3)°,β=102.74(3)°, γ=105.70(3)°,V=2.3277(17) nm^3,Z=2,D_(calc)=2.091 g/cm^3.The structure has been refined to a final R of 0.0785.The crystal-is an infinite chain complex,in which four carboxyl groups from glycine molecules bridge the Er^(3+) and Y^(3+) ions,and the other two carboxyl groups bridge two adjacent Er^(3+) or Y^(3+) ions.

Synthesis and Crystal Structure of a Heteronuclear Complex［MnSc（DTPA）（H_2O）_2］·2H_2O

The title complex, [MnSc (DTPA) (H2O)2]·2H2O (DTPA is diethylenetriaminepentaacetic acid). has been synthesized in aqueous solution. Its crystal structure has been determined by four-circle X-ray diffractometer. The crystal is monoclinic with space group P21/n. The cell parameters are as follows:α=0.7886 (3) nm, b=1.5094 (5) nm. c=1. 8162(6) nm; β=100. 32(2)°, V= 2. 121 (2) nm3 , Z= 4 , Dc =1. 75 g/cm3. In the crystal,Sc3+ ion is coordinated by five oxygen atoms and three nitrogen atoms of DTPA with coordination number eight. taking a trigondodecahedron arrangement. Mn2+ ion is coordinated by four oxygen atoms from different DTPA and two oxygen atoms from H2O molecules with coordination number six, forming an octahedron. Each Sc(DTPA) is further connected with Mn2+ ions through four carboxyl groups of DPTA serving as bridges to form a three dimensional network.

CRYSTAL STRUCTURE OF A HETERONUCLEAR LANTHANIDE COMPLEX OF ERBIUM-YTTRIUM AND GLYCINE[ErY(GlY)_6(H_2O)_4](ClO_4)_65H_2O

The title complex [ErY(Gly)_6(H_2O)_4](ClO_4)_6 5H_2O has been synthesized.Its crystal structure has been determined by X-ray diffraction method.The crystal is triclinic with space group P1.The unit cell parameters are as follows:a=11.518(4),b=14.105(7),c=15.530(6) ,α=96.61(3), β=102.74(3),γ=105.70(3)°,V=2327.7(17) ~3,Z=2,Dc=2.091g/cm^3.The structure has been refined to a final R of 0.0785.The crystal is an infinite chain complex,in which four carboxyl groups from glycine molecules bridge the Er(Ⅲ)and Y(Ⅲ)ion,other two carboxyl groups bridge two adjacent Er(Ⅲ)or two Y(Ⅲ)ions.

Synthesis,Structure and Photophysical Properties of Heteronuclear Pt_2Cu Alkynyl Complexes

Two luminescent hetero-trinuclear complexes [Pt2Cu（μ-dpppy）2（C≡CC6H4R-4）4]（Cl O4）（R = H,1;R = CH3,2;dpppy = 2,6-bis（diphenylphosphino）pyridine） have been synthesized and characterized by elemental analyses,ESI-MS,^1H and ^31P{^1H} NMR spectroscopy,and X-ray crystallography for 2.Their photophysical properties in the solid state and in solutions at room temperature and in frozen glasses at 77 K were studied.Both complexes 1 and 2 show strong orange-red emission in the solid state at room temperature and in frozen glasses at 77 K,and weak emission in solutions.

HETERONUCLEAR COMPLEX CONTAINING COPPER-LANTHANIDE ARRAYS: THE SYNTHESIS AND CRYSTAL STRUCTURE OF Ln_2Cu_4L_8 (HL)_4(OH)_2(CIO_4)_4(H_2O)_(10)·2CH_3COCH_3 (Ln = Tb (1), Y (2); HL = 2-Pyridone C_5H_5NO)

Reaction of 2-pyridone, copper acetate and terbium(or yttrium) perchlorate in acetone with the mole ratio 6: 2: 1 results in the formation of heteronuclear complex Ln_2Cu_4L_8 (HL)_4 (OH)_2 (ClO_4)_4 (H_20)_(10) 2CH_3COCH_3(Ln = Tb (1), Y (2)). By recrystallizing (1) in CHCl_3 single crystals were obtained and the structure was determined by four-circle diffractometer. Data showed that the crystal is in space group C2/m with a=27. 454(9)A, b=13, 608A, c=30. 556(11)A, β=99. 89(3)°, v=11245. 7(7. 5)A^3. The structure was solved by a combination of Patterson method and Fourier technique. The final R value is 0. 103. In the structure, four copper and two terbium ions are bridged by 2-pyridone anions to form an essentially octahedral Cu_4Tb_2 core. The terbium atoms are each eight-coordinate and the copper atoms are five-coordinate.

Synthesis and Crystal Structure of a Heteronuclear Erbium and Yttrium Complex with Proline: [ErY(pro)_6(H_2O)_6] (ClO_4)_6

The title complex was synthesized in an aqueous solution at pH=3. 5,and its crystal structure was determined by X-ray diffraction methods. The com-plex is triclinic with space group P1, formula C30H66O42N6Cl6ErY, Mr,= 1651. 76, a=9. 860(2), b=13. 020(5), c= 13. 632(5) A ; a= 109. 32(3), β=110. 19(2), γ=100. 96(2)°, V= 1456(1 ) A3, Dc= 1. 884 g/cm3, Z= 1, F(000) =833, P= 2. 812mm-1 ;R=0. 046, wR(F2) =0. 123 for 4897 reflections with I>2(I). The complexis of an infinite chain structure with the neibouring metal ions connected by two bridging carboxyl groups from two different proline molecules. The erbium ion and the yttrium ion statistically lies at the position of the metal ion with M=1/2(Er+Y).

Structure and Fluorescence Emission of Hetero-Nuclear Complexes of Europium-Lanthanum Nitrates with N,N′-Substituted Adipamide

A europium lanthanum hetero nuclear complex with new ligand N, N′ dimethyl N, N′ diphenyladipamide (MPAA) was prepared. The one dimensional chain structure of [La 0.5 Eu 0.5 (MPAA) 2(NO 3) 3] was determined crystallographicaly. The europium ion and lanthanum ion statistically lie at the position of the metal ion with M=1/2(La+Eu). Each Ln 3+ ion is nine coordinated including three bidentate nitrates, three carboxyl groups from three MPAA molecules, in which two MPAA are act as bridge ligand. The intensity of fluorescence of La 3+ Eu 3+ heteronuclear complex A was obviously higher than that of pure Eu 3+ complex B both in solution and in solid state.

Synthesis and Structure of Vanadium-barium Complex of 2,4,6-Tripicolinato with 20-Member Macrocyclic Cavities

A new heteronuclear complex, dimer [(2-OH2)2Ba2(H2O)4][VO2(tpa)]24H2O (tpa: 2,4,6-tripicolinate trianion), was synthesized and structurally determined by X-ray diffraction technique where all hydrogen atoms have been located directly. The coordination geometry of V(V) ion is a distorted trigonal bipyrimid and that of Ba(II) ion is a capped square antiprism. One 2-O bridging bond and two hydrogen bonds act between the coordination geometries. A 1-D extended porous construction containing 20-member cavities is observed in the crystal.

Synthesis,Structure and Luminescence of Zn_(4.5)Cu_3 Heteronuclear Coordination Polymer Comprising Macrocyclic Oxamide and 5-Sulfosalicylic Ion

The complex [Zn4.5（SSA）3（CuL）3（H2O）6]n was synthesized and structurally determined, where SSA is fully deprotonated 5-sulfosalicylic acid（CuL, H2L=2,3-dioxo-5,6,14,15-dibenzo-1,4,8,12-tetraazacyclo-pentadeca- 7,13-dien）. The title complex crystallized in the triclinic system with space group P1^-, a=1.19788（17） nm, b=1.4253（2） nm, c=2.2890（4） nm, α=90.211（2）°, ,β=93.076（2）°, γ=90.600（2）°. The complex displayed a 1D ladderlike chain. All these 1D chains were further interlinked via hydrogen bonds, resulting in a 2D architecture. The luminescent property of the compound was also discussed.

A Three-dimensional Tm(Ⅲ)-Zn(Ⅱ)Heteronuclear Metalorganic Framework Based on Imidazole-dicarboxylate Ligand:Synthesis,Crystal Structure and Luminescence Property

A d-f heteronuclear metal-organic framework（MOF）,{[Tm3Zn6（bipy2）2（mimda）7（H2O）3]·（H2O）5}n（1,H3 mimda = 2-methyl-1-H-imidazole-4,5-dicarboxylic acid,and bipy = 4,4？-bipyridine）,has been synthesized under solvothermal conditions,and structurally characterized by elemental analysis,IR spectra and X-ray single-crystal diffraction.It crystallizes in orthorhombic system,space group Pnma with a = 16.1102（9）,b = 33.5805（19）,c = 16.8593（10） ？,β = 97.344（11）°,V = 9120.7（9） ？-3,Z = 4,F（000） = 5184,the final R = 0.0530 and w R = 0.1306.In complex 1,the Tm（Ⅲ） ions adopt two types of coordination fashions.Complex 1 shows onedimensional（1-D） Tm-Zn heteronuclear zigzag chains,and these chains are further linked by H3 mimda ligands into Tm-Zn heteronuclear 2-D lattice-like arrays.The 2-D heteronuclear units were connected through [Zn6（mimda）6] rings to give rise to the Tm-Zn heteronuclear cages.Finally,H3 mimda ligands connected the cages into a 3-D heterometallic framework by the combination of [TmO7]n and Tm-Zn heteronuclear cages.In addition,the thermal stability and luminescent property have been investigated.

钕钇异核谷氨酸配合物的合成及晶体结构

在水溶液中合成发钕钇异核谷氨酸配合物［（Ｎｄ４／３Ｙ２／３（Ｇｌｕ）２（Ｈ２Ｏ）８）４］（ＣｌＯ４）１６．１０Ｈ２Ｏ的单晶，并测定其结构。晶体属单斜晶系，Ｐ２１空间群，晶胞参数：ａ＝１．１０３７（５）ｎｍ，ｂ＝１．６７１０（５）ｎｍ，ｃ＝２．００８６（１０）ｎｍ，β＝１０２．８０（４）°，Ｖ＝３．６１２（３）ｎｍ＾３，Ｚ＝１，Ｄｃ＝２．０７９ｇ／ｃｍ＾３。最终偏差因子Ｒ＝０．０５８。

新型二维异核配位聚合物{[NdBi(cydta)(NO3)2(H2O)4]·2．5H2O}n的晶体结构与热分解

由Bi(Hcydta).5H2O和Nd(NO3).6H2O按1︰1的物质的量比,在水溶液中合成了含Bi(III)-Nd(III)的异核配位聚合物{[(NO3)Nd(H2O)4(μ3-cydta)Bi(μ-ONO2)].2.5H2O}n.用元素分析、红外光谱、热重-差热和X射线单晶衍射等手段对标题配合物的组成和结构进行了表征.该配合物属三斜晶系,空间群P1,晶胞参数:a=0.9235(3)nm,b=1.0902(4)nm,c=1.4253(5)nm,α=71.840(4)°,β=86.877(4)°,γ=76.991(4)°,Z=2,Mr=936.65,V=1.3284(8)nm3,Dc=2.342g.cm-3,μ=8.646mm-1,F(000)=900,最终偏离因子R1=0.0406,wR2=0.1124.在该配合物中,铋(III)与配体cydta4-的4O2N和1个硝酸根中1个O原子以及邻位分子的硝酸根形成8配位的畸变双帽三棱柱.钕(III)与4个水分子的O,1个硝酸根中2个O以及来自3个不同配体cydta4-的桥联羧基O结合,形成9配位的三帽三棱柱构型.羧酸根在Bi—Nd和硝酸根在Bi—Bi间的桥联作用,使得整个配合物分子连接成无限二维框架结构.热分析以及分解产物的红外光谱表明配合物热分解经历脱水、配体热分解、硝酸盐转变成氧化物等多步连续分解过程,最后在625℃失重恒定.

Ln(Ⅲ)-Co(Ⅱ)与双水杨醛缩乙二胺Schiff碱异核配合物的合成与波谱性质

合成了双水杨醛缩乙二胺Ｓｃｈｉｆ碱（ＳＡＬＥＮ）与钴的配合物Ｃｏ（ＳＡＬＥＮ）（ＮＯ３）２·３Ｈ２Ｏ及镧系－钴的异核配合物ＬｎＣｏ（ＳＡＬＥＮ）２（ＮＯ３）５·２Ｈ２Ｏ（Ｌｎ＝Ｌａ，Ｎｄ，Ｓｍ，Ｇｄ，Ｙｂ，Ｙ）．以紫外、红外光谱，特别是１ＨＮＭＲ及ＥＰＲ波谱等方法研究了它们在组成、结构和配位等方面的异同．文中讨论了配合物ＥＰＲ谱在不同溶剂中峰宽的相对关系、配合物晶体场强度及Ｇｄ３＋周围局部对称性等问题．

异核稀土双亚砜配合物的合成、表征和荧光性质

合成得到一系列异核稀土双（苯基亚砜）乙烷（bphse）配合物和异核稀土双（苯基亚砜）乙烷与1，10-啡咯啉的配合物，通过元素分析、电感耦合等离子体法、电导、红外和紫外光谱对配合物进行了表征，并研究了这些配合物的固体和溶液的荧光光谱。荧光光谱说明这些配合物均有较强的荧光，其中三元配合物Eu(3+)的荧光强于二元配合物。在同系列异核配合物中Eu(3+)的荧光强度次序为：Eu－Y配合物＞Eu-Gd配合物＞Eu－Tb配合物＞Eu配合物＞Eu-La配合物。

Ln(Ⅲ)-Ni(Ⅱ)与双水杨醛缩乙二胺席夫碱异核配合物的合成与波谱

合成了双水杨醛缩乙二胺席夫碱（ＳＡＬＥＮ）与镍的配合物Ｎｉ３（ＳＡＬＥＮ）２（ＮＯ３）６·Ｈ２Ｏ及镧系镍的异核配合物Ｌｎ２Ｎｉ３（ＳＡＬＥＮ）６（ＮＯ３）１２·Ｈ２Ｏ（Ｌｎ＝Ｌａ，Ｎｄ，Ｓｍ，Ｇｄ，Ｙｂ，Ｙ）．以紫外、红外光谱、磁化率，特别是１ＨＮＭＲ及ＥＰＲ波谱等方法研究了它们在组成、结构和配位等方面的异同．ＧｄＮｉＳＡＬＥＮ配合物的ＥＰＲ谱表明其在低温ＴＨＦ中呈“单峰效应”．文中讨论了配合物在不同溶剂中峰宽的相对关系。

镧掺杂铕发光材料的合成、结构及光学性能

以2-羟基-6-甲基尼古丁酸(HA)、1,10-菲咯啉(phen)为配体,合成了五种新型镧掺杂铕的四元异核配合物,并对其进行元素分析、红外光谱测试以及荧光分析。结果表明:配合物的组成为(EuxLay)A3phen.3H2O(x∶y=0.10∶0.90,0.30∶0.70,0.50∶0.50,0.70∶0.30,0.90∶0.10),配体的羧基与稀土离子以螯合双齿配位;镧对铕的配合物有荧光浓聚效应,且随镧离子浓度的增加而加强;五种配合物的荧光寿命比较接近,均在1ms左右。