Synthesis and Structural Characterization of Three New Tetraorganodistannoxanes

An efficient method was developed for the preparation of three tetraorganodistannoxane complexes, (C₂H₅)₈Sn₄Cl₂(CH₃O)₂O₂ (1), (CH₃)₈Sn₄(C₃H₄N₃S)₂(CH₃O)₂O₂ (2) and (C₄H₉)₈Sn₄(C₃H₄N₃S)₂(CH₃O)₂O₂ (3). All prepared complexes were characterized by infrared, ¹H, ¹³C and ¹¹⁹Sn NMR spectroscopes and elemental analysis. The molecular structure of a representative complex (1) was determined by single-crystal X-ray diffraction. Results showed that 1 is a tetranuclear, centrosymmetric dimeric, and contains two endo-cyclic five-coordinated tin atoms and two exo-cyclic five-coordinated tin atoms. Compound 1 lies about a center of inversion and the tetranuclear molecule features a three-ring-staircase Sn₄O₄ core. The asymmetric unit of 1 contains two independent Sn(IV) atoms and a 2D infinite rigid chain structure forms via C–H···Cl interactions between tetranuclear units.     

Salen Type Sandwich Triple-Decker Tri- and Di-nuclear Lanthanide Complexes

Four N,N′-bis(salicylidene)-1,2-(phenylene-ediamine) (H₂L) trinuclear lanthanide complexes, namely, [Ln₃L₃(CH₃OH)₂(NO₃)₃]·(CH₂Cl₂)·(CH₃OH)·(H₂O)₂ [Ln = Tb (1), Ho (2), Er (3) and Lu (4)], have been isolated by the reactions of H₂L and Ln(NO₃)₃·6H₂O. And one N,N′-bis(salicylidene)-1,2-(phenylene-ediamine) dinuclear neodymium complex [Nd₂L₃(CH₃OH)] (5) has been harvested from the reaction of H₂L with Nd(OAc)₃·4H₂O. X-ray crystallographic analysis reveals that complexes 1?4 are of triple-decker trinuclear sandwich structure, while complex 5 is of a triple-decker dinuclear sandwich structure, expanding upon the recent reports of the multinuclear pure lanthanide complexes.     

A Facile Access to New Polymethylmethacrylate-Anchored Ferrocene Substituted Nickel(II) Unsymmetrical Schiff Base Complexes: Synthesis and Characterization

This paper discloses two new side-chain metallopolymers containing an unsymmetrical organometallic Schiff base complex of Ni(II) linked to a polymethylmethacrylate (PMMA) matrix. The neutral ferrocene substituted Schiff base complex 1, Ni{CpFe(η⁵-C₅H₄)-C(O)CH=C(CH₃)N–o-C₆H₄N=CH-(2-O,5-OH-C₆H₃)} where (Cp = η⁵-C₅H₅), was synthesized via template reaction by condensation of the tridentate half-unit metalloligand Fc-C(O)CH=C(CH₃)-N(H)-o-C₆H₄NH₂ (Fc = ferrocenyl = CpFe(η⁵-C₅H₄)) with 2,5-dihydroxybenzaldehyde in the presence of nickel(II) acetate tetrahydrate. The binuclear Schiff base complex of Ni(II) containing an aromatic free hydroxyl group was reacted under basic conditions with PMMA to afford, upon trans-esterification reaction, metallopolymers 2 (complex 1 monomeric unit/PMMA = 1/5) and 3 (complex 1 monomeric unit/PMMA = 1/3). Elemental analysis, FT-IR, ¹H and ¹³C NMR spectroscopies, and cyclic voltammetry were utilized to characterize the newly synthetized compounds. Surface morphology of the metallopolymer film of 2 was studied using atomic force microscopy.     

Synthesis, Crystal Structure, Fluorescence and Thermostability of Ni(II), Zn(II), Cd(II) Complexes with Schiff Base 2-Acetylpyridine-d-tryptophan

Three novel transition metal coordination polymers, [Ni(C₁₈H₁₆N₃O₂)₂·2CH₃OH] _n (1), [Zn(C₁₈H₁₆N₃O₂)₂·4CH₃OH] _n (2) and [Cd(C₁₈H₁₆N₃O₂)₂·2CH₃OH] _n (3) (C₁₈H₁₆N₃O₂=2-acetylpyridine-d-tryptophan) were synthesized and characterized by elemental analysis, IR, UV, ¹H NMR and X-ray diffraction single crystal analysis. The analyses of the structures indicate that all three materials crystallize in the tetragonal crystal system, space group P4₁2₁2. They have similar structures; i.e., the Schiff base coordinates in its deprotonated form and behaves as a hexadentate (4N+2O) coordinated ligand to form a distorted octahedron geometry. On the other hand, as a result of the alternate arrangement of chains through N–H···O intermolecular hydrogen bonds interactions, 2-D layers are formed for the three complexes. Furthermore, the luminescent properties and thermal stabilities of the three complexes were investigated.     

Structural, Theoretical and Multinuclear NMR Study of a New Polymeric Mercury(II) Complex with an Ambidentate Phosphorus Ylide

The reactions of phosphorus ylides of the type Ph₃P=C(H)C(O)R [R = 2,4-dichlorophenyl (L ¹ ) and 4-isopropylphenyl (L ² )] with HgX₂ [X = Cl (1, 4), Br (2, 5) and I (3, 6)] salts using methanol as a solvent are reported. Single crystal X-ray analysis carried out on L ¹ , 2 and 3 and reveals the presence of a novel polymeric structure for 2 and a centrosymmeteric dimeric structure for 3. The complexes have been studied by elemental analyses, IR, ¹H and ³¹P NMR spectroscopy. On the basis of DFT calculations, the formation of [Hg₂Br₆]^2? anions in 2 has a key role in the formation of the polymeric structure; and, the formation of [Hg₂L₂I₄] molecule thermodynamically is about 25 kcal/mol more favorable than the corresponding [Hg₂L₂Br₄] molecule.     

Thermal and Fluorescence Properties of New Nanostructured Hg(ll) -2,2′-Bipyridine Derivative Complexes

Two new nano-structured Hg(II) supramolecular complexes, [Hg(5,5′-di-t-but-bpy)(μ-Br)Br]₂[Hg(5,5′-di-t-but-bpy)Br₂](1) and [Hg(5,5′-di-t-but-bpy)I₂] (2) were synthesized by the sonochemical method. The structures of 1 and 2 were characterized by elemental analysis, IR, ¹H-NMR, and ¹³C-NMR spectroscopy and single crystal X-ray diffraction. Their thermal stabilities were studied by thermogravimetric and differential thermal analyses. Solid-state luminescent spectra of 1 and 2 indicate a fluorescent broad emission band between 304 and 404 nm with excitation at 284 nm. These nanostructured coordination polymers were characterized by scanning electron microscopy, elemental analysis, and IR spectroscopy.     

Syntheses and Structural Analytical Studies of Two Co(II) Complexes Based on 1,4-Di(benzimidazole-1-yl)benzene

Two new Co(II) complexes of 1,4-di(benzimidazole-1-yl)benzene ligand (L) with the formulas [(CoLCl₂)(CHCl₃)(DMF)]_∞ (1) and [CoL(NO₃)₂]_∞ (2) have been synthesized by anion-directed self-assembly. Both complexes have been characterized by elemental analyses, IR, and X-ray single crystal diffraction. Complexes 1 and 2 exhibit 1D chain structures. In 1, Co(II) ions possess a distorted tetrahedral coordination environment composed of N₂Cl₂ donors from two L ligands and two chloride ions, while the Co(II) ions in 2 reveal a distorted octahedral structure defined by the N₂O₄ donors from two L ligands and two nitrate anions. These results illustrate that the anions play an important role in the self-assembly of metal–organic materials.     

Tris-Alkoxylphenylterpyridine Cobalt(II) Complexes: Synthesis, Structure, and Magnetic and Mesomorphic Behaviors

Two novel cobalt(II) complexes [Co(L1)₂](BF₄)₂·CH₃CN·0.5H₂O (1) and [Co(L2)₂](BF₄)₂ (2) (L1 = 4′-(3,4,5-trimethoxy-phenyl)-[2,2′:6′,2″]terpyridine, L2 = 4′-(3,4,5-tris-hexadecyloxy-phenyl)-[2,2′:6′,2″]terpyridine) have been synthesized, and their structural, magnetic and mesomorphic properties were characterized by single crystal X-ray diffraction (XRD) analysis, temperature-dependent magnetic susceptibility, POM, DSC, and powder XRD analysis. The molecular structure of the complex 1 with short alkyl substituents exhibited that the metal ion has an N₆ coordination sphere of distorted octahedral geometry and various intermolecular π–π interactions are important factors influencing the crystalline array. The magnetic behaviour of 1 displayed a typical of gradual spin transition for cobalt(II) terpyridine complexes. On the other hand, the complex 2 possessing linear long alkyl chains showed a gradual spin transition between low-spin and high-spin with a thermal hysteresis loop (T _1/2↑ = 338 and T _1/2↓ = 327 K) triggered by the crystal-to-mesophase transition. The powder XRD and POM analyses were indicative of the liquid crystalline lamellar phase of 2.     

Effects of tris(pentafluorophenyl)borane on the activation of zerovalent-nickel complex in the addition polymerization of norbornene

The effects of B(C₆F₅)₃ on the activation of the Ni(0) and Ni(II) complexes were studied in the polymerization of norbornene. The Ni(0) complex, such as bis(1,5-cyclooctadiene)nickel (Ni(COD)₂ (1), biacetylbis(2,6-diisopropylphenylimmine)(1,3-butadiene)nickel (2), or tetrakis(triphenylphosphine)nickel (5), in combination with B(C₆F₅)₃, was determined to have high activity in the polymerization of norbornene. On the other hand, the Ni(II) complex with B(C₆F₅)₃ did not provide any activity at all under analogous conditions regardless of the structure of the Ni(II) complex. The use of other borane compounds, such as B(C₆H₅)₃, BEt₃, and BF₃ etherate, with Ni(COD)₂ (1) in place of B(C₆F₅)₃ clearly showed the main functions of B(C₆F₅)₃. The high Lewis acidity of B(C₆F₅)₃ enabled it to activate catalytic complexes, thus inducing polymerization. The study of the ¹H, ¹³C, and ¹⁹F NMR spectra of the polynorbornene produced with Ni(COD)₂ (1) and B(C₆F₅)₃, in the presence or absence of ethylene, showed that the initiation of addition polymerization occurred through the insertion of the exo face of the norbornene into the Ni-C bond of the C₆F₅ ligand. A new polymerization mechanism was proposed in norbornene polymerization, wherein the active complex formed from Ni(COD)₂ (1) and B(C₆F₅)₃ acts as a catalyst.     

The Inclusion of Organometallic Derivatives of Cyclotriphosphazenes Inside SiO2 Matrix and Their Conversion to Nanostructured Metal-Oxides and Phosphates

Organometallic derivatives of the cyclotriphosphazene N₃P₃[OC₆H₄CH₂CN·TiClCp₂]₆ (1), N₃P₃(O₆H₅)₅[OC₆H₄N·W(CO)₅] (2), N₃P₃[OC₆H₄CH₂CN·Mo(CO)₅]₆ (3), [N₃P₃(O₆H₅)₅(OC₅H₄N·CpRu(PPh₃)₂)][PF₆] (4), [N₃P₃(O₂C₁₂H₈)₂OC₅H₄N·Ag(PPh₃)][OSO₂CF₃] (5), N₃P₃[OC₆H₅]₅ [OC₅H₄N·Cu][PF₆] (6) and N₃P₃[OC₆H₄CH₂CN·CuCl]₆[PF₆]₆ (7),were incorporated inside SiO₂ through the sol–gel method. The metal–organic nanocomposites of the general formula N₃P₃[OC₆H₄CH₂CN·TiClCp₂]₆·nSiO₂ (G ₁ ), N₃P₃[OC₆H₄N·W(CO)₅]·nSiO₂ (G ₂ ), N₃P₃[OC₆H₄CH₂CN·Mo(CO)₅]₆·nSiO₂ (G ₃ ), N₃P₃(O₆H₅)₅OC₅H₄N·CpRu(PPh₃)₂][PF₆]·nSiO₂ (G ₄ ), [N₃P₃(O₂C₁₂H₈)₂OC₅H₄N·Ag(PPh₃)][OSO₂CF₃]·nSiO₂ (G ₅ ), N₃P₃[OC₆H₅]₅[OC₅H₄N·Cu][PF₆]·(SiO₂) _n (G ₆ ), and N₃P₃[OC₆H₄CH₂CN·CuCl]₆[PF₆]₆·(SiO₂) _n (G ₇ ), were characterized by IR spectroscopy; ¹²C, ³¹ P and ²⁹Si MAS NMR measurements as well as UV–Visible diffuse reflectance spectra, indicating the presence of the respective organometallic derivatives of the cyclotriphosphazene incorporated into SiO₂. Pyrolysis of these nanocomposites under air at 800 °C gives rise to nanostructured metal-oxides and metal phosphates incorporated into amorphous SiO₂, with the presence in some cases of complexes phase mixtures. From some precursors, we obtained metal-oxides/phosphates nanoparticles separated from the SiO₂ nanoparticles instead the oxides/phosphates nanoparticles inside the SiO₂ matrix. Additionally and for comparison purposes, we used the compound N₃P₃[NH(CH₂)₃Si(OEt)₃]₆ as gelator. Nanocomposites (G′ ₁ ), (G′ ₂ ) and (G′ ₃ ) exhibited mainly morphological differences while in some cases composition differences when using TEOS as gelator. Some simple metal-containing compounds as (O₃SCF₃)Ag(PPh₃)(HOC₅H₄N), [CuCl₂·NC₅H₄OH] and [CuCl₂·NCCH₂C₆H₄OH]—which are useful models of the most complexes (G ₅ ), (G ₆ ) and (G ₇ ) were also prepared and incorporated in amorphous silica. Their pyrolytic products were compared with those of more complex cyclotriphosphazene analogous. Interestingly, the pyrolysis of the nanocomposite [(O₃SCF₃)Ag(PPh₃)(HOC₅H₄N)][SiO₂] _n affords the firstly-reported materials containing Ag₂O along with SiO₂ nanoparticles.     

Salen Type Homo-multinuclear Yb3 and Yb4 Complexes and Their NIR Luminescence

Two discrete salen type homo-multinuclear Yb₃ and Yb₄ complexes, namely, [Yb₃L₃(OAc)₃]·3CH₃OH·H₂O (1) and [Yb₄L₂(OAc)₄(μ₃-OH)₂(H₂O)₂](ZnCl₄)·3CH₃OH (2) (H₂L = N,N′-bis(2-oxy-3-methoxybenzylidene)-1,2-phenylenediamine) have been synthesized by reactions of H₂L and different ytterbium salts. X-ray crystallographic analysis reveals that complex 1 exhibits a triple-decker Yb₃ sandwich structure with a ratio of H₂L:Yb = 1:1, while complex 2 exhibits a defect-dicubane Yb₄ core with a ratio of H₂L:Yb = 1:2. The NIR luminescence of complexes 1 and 2 have been investigated and discussed.     

Selective activation of metallic center in heterobinuclear cobalt and nickel complex in ethylene polymerization

Heterobinuclear cobalt and nickel complex {2-[2,6-R₂-C₆H₃NC(CH₃)-(CH₃)CN-(3,5-R₂′)C₆H₂-CH₂-(3′,5′-R₂)C₆H₂NC(CH₃)]-6-[2,6-R₂-C₆H₃NC(CH₃)] pyridine}CoCl₂NiBr₂ (R = isopropyl) (N₅CoNi) was prepared by reaction of pentadentate nitrogen ligand containing 2,6-bis(imino)-pyridine and α-diimine moieties with CoCl₂ and NiBr₂(DME) in turn. The complex was applied as catalyst for ethylene polymerization activated by AlEt₃, MMAO and AlEt₃/[PhMe₂NH] [B(C₆F₅)₄] respectively. The performance of the heterobinuclear complex in ethylene polymerization was compared with corresponding mononuclear complexes (α-diimine nickel bromide and 2,6-bis(imino)-pyridine cobalt chloride) and their equivalent mixture (binary complexes). When the complex N₅CoNi was activated by AlEt₃ or MMAO, its ethylene polymerization activity was lower than its control, the binary complexes. Both heterobinuclear complex and binary complex produced PE with bimodal molecular weight distribution. The amount of high-molecular-weight polyethylene produced by nickel center of N₅CoNi was less than the binary complexes, which reveals that productivity of nickel center of N₅CoNi is selectively suppressed. When the heterobinuclear complex N₅CoNi is activated by AlEt₃/[PhMe₂NH][B(C₆F₅)₄], the relative productivity of nickel center increased, although the total activity of catalyst decreased compared with AlEt₃ as cocatalyst. With respect to AlEt₃, [PhMe₂NH][B(C₆F₅)₄] can preferably activate nickel center of heterobinuclear complex. The results suggest that metal site in the heterobinuclear complex is selectively activated by cocatalyst.     

Theoretical study of the reactive intermediate Si2Me4[(η5-C5H4) Fe(CO)2] 2 2−

In two previous papers (Kinget al., J. Organomet. Chem. 19, 327, 1969; Pannellet al., Organometallics 9, 859, 1990), the synthesis and X-ray structure of the two tetramethyl disilyl complexes [(η⁵-C₅H₅) Fe(CO)₂]₂Si₂Me₄ (I) and Si₂Me₄[(η⁵-C₅H₄) Fe(CO)₂CH₃]₂ (II) were reported. ComplexII is obtained fromI [2]. However, attempts to form other derivatives fromI have generally failed. In the chemical process to getII fromI, an intermediate complex, Si₂Me₄[(η⁵-C₅H₄) Fe(CO)₂] ₂ ^2? (III), is probably formed. This is similar to complexII without the two methyl groups bonded to the Fe atoms. Therefore, a theoretical study that may shed some light on the intermediate structure, stability, and reactivity is justified. We have developed theoretical studies consisting of extended Huckel electronic structure calculations on the simulated intermediate geometry. The results obtained from these calculations suggest that it might be stable enough to form during reactions of complexI. The more reactive sites, which suggest reaction alternatives, are pointed out.     

Synthesis and Structures of Two Triorganotin(IV) Polymers R3Sn{O2CC6H4[N=C(H)}{C(CH3)CH(CH3)-3-OH]-p} n (R = Me and Ph) Containing a 4-[(2Z)-(3-Hydroxy-1-methyl-2-butenylidene)amino] benzoic Acid Framework

Two new polymeric triorganotin(IV) complexes R₃Sn{O₂CC₆H₄[N=C(H)}{C(CH₃)CH(CH₃)-3-OH]-p} _n ([Me₃Sn(LH)] _n : 1) and ([Ph₃Sn(LH)] _n : 2) containing a 4-[(2Z)-(3-hydroxy-1-methyl-2-butenylidene)amino]benzoate (LH) framework were prepared. Both compounds have been characterized by ¹H, ¹³C, ¹¹⁹Sn NMR, IR and ¹¹⁹Sn Mössbauer spectroscopic techniques in combination with elemental analyses. The crystal structures of complexes 1 and 2 reveal that they exist as polymeric zig-zag chains in which the LH-bridged Sn-atoms adopt a trans-R₃SnO₂ trigonal bipyramidal configuration with R groups in the equatorial positions and the axial sites occupied by an oxygen atom from the carboxylate ligand and the alcoholic oxygen atom of the next carboxylate ligand in the chain. The carboxylate ligands coordinate in the zwitterionic form with the alcoholic proton moved to the nearby nitrogen atom.     

Supramolecular Chemistry of Organoplatinum(IV) Complexes Bearing Ligands with Remote Carboxylic Acid Substituents

The oxidative addition of compounds RBr to [PtMe₂(bpox)], 1, bpox = 2,5-bis(2-pyridyl)-1,3,4-oxadiazole gave the corresponding organoplatinum(IV) complexes [PtBrMe₂(R)(bpox)], 2, R = CH₂CO₂H; 3, R = CH₂-4-C₆H₄CO₂H; 4, R = CH₂-4-C₆H₄CH₂CO₂H, whereas the reaction with BrCH₂CH₂CO₂H gave only the platinum(II) complex [PtBrMe(bpox)], 5. The organoplatinum(IV) complexes with carboxylic acid substituents form unusual supramolecular structures in the solid state through hydrogen bonding interactions, some of which are supramolecular polymers.     

Ionic Liquids Promoted the C-Acylation of Acetals in Solvent-free Conditions

The synthesis of a series of fourteen 4-alkoxy-1,1,1-trihalo-3-alken-2-ones (2,3) [CX₃COC(R²)=C(R¹)OMe, where X = Cl, F; R¹/R² = Me/H, Bu/H, i-Bu/H, Ph/H, Thien-2-yl/H, –(CH₂)₄–, –CH(CH₂)₄CH(CH₂)₂–] from the acylation reactions of acetals (1) with trichloroacetyl chloride or trifluoroacetic anhydride in the presence of equimolar amounts of pyridine and imidazolium based ionic liquid ([BMIM][BF₄] or [BMIM][PF₆]) is reported. The reaction time, yields and IL recyclation are also investigated and this method showed advantages over the methods described in the literature.     

Polymerization of propylene catalyzed by α-diimine nickel complexes/methylaluminoxane: catalytic behavior and polymer properties

α-Diimine nickel dibromide complexes of dibromo[N,N’-bis(2,6-diisopropylphenyl)-2,3-butanediimine]nickel(II) (A) and dibromo[N,N’-(phenanthrene-9,10-diylidene)bis(2,6-diisopropylaniline)]nickel(II) (B) were synthesized under controlled conditions. The catalysts A, B and mixed of 1:1 weight ratio of them (C) were activated by methylaluminoxane and were used for propylene polymerization in a semi-batch reactor. In study of the catalytic systems behavior, activities, glass transition temperature (T _g) and viscosity average molecular weight (M _v) values related to the catalyst C were between those related to the catalysts A and B under same conditions. The highest and the lowest molecular weights of the obtained polymers were produced by the catalysts B and A which were about 80,000 and 70,000 (g/mol) under same conditions, respectively. The T _g of polypropylenes produced by the catalysts was about ?34 °C. The resulting polymers had similar behavior with ethylene-propylene copolymer which it could be due to formation of ethylene-type units in the polymer chain.     

Syntheses and Characterization of Two New M(II)-5,5′-dimethyl-2,2′-bipyridine (M = Cd and Pb) Coordination Polymers and Study of Their Thermal and Electrochemical Properties

Two new cadmium(II) and lead(II)-thiocyanato coordination polymers with 5,5′-dimethyl-2,2′-bipyridine (5,5′-dm-2,2′-bpy) as chelating ligands were synthesized and characterized by elemental analysis, IR and ¹H NMR spectroscopy and by X-ray crystallography. Thermal and electrochemical properties were also studied as well. These complexes have formed formula [Cd(5,5′-dm-2,2′-bpy)(NCS)₂]_n (1) and [Pb(5,5′-dm-2,2′-bpy)(CH₃COO)(NCS)]_n (2). The coordination numbers of Cd^II in 1 and Pb^II in 2 are six (CdN₄S₂) and seven (PbN₃O₃S₂), respectively. In 2, “stereo-chemically active” electron lone pairs and the coordination spheres were hemidirected. Bridging properties of thiocyanato anions in 1 and 2 created one- and two-dimensional coordination polymers, respectively. The supramolecular features in these complexes were guided and controlled by weak directional intermolecular interactions.     

Synthesis and Crystal Structure of Two Coordination Polymers Assembled from a Versatile 4-(4-Hydroxypyridinium-1-yl)phthalic Acid

Two coordination polymers, namely, [Ni(L)(C₂H₃N)(H₂O)₅] _n (1), and [Mn(L)(H₂O)₂] _n (2) have been hydro(solvo)thermally synthesized through the reaction of 4-(4-hydroxypyridinium-1-yl)phthalic acid (H₂L) with divalent nickel and manganese salts. As a result of various coordination modes of the versatile 4-(4-hydroxypyridinium-1-yl)phthalic acid, these compounds exhibit structural diversity. Complex 1 exhibits a 3D coordination framework through the rich hydrogen bond. Complex 2 exhibits a 3D coordination network based on layers. These complexes have been characterized by powder X-ray diffractions (PXRD), IR spectroscopy, elemental analysis, thermogravimetry, single-crystal X-ray crystallography and solid UV spectroscopy.     

Three-Dimensional Structure of Barium–Cupric Nitrilotriacetate and One-Dimensional Structure of Cobalt–Cupric Nitrilotriacetate: Template Effect of Cations on the Formation of Coordination Polymers

Three mixed-metal nitrilotriacetates [Ba(H₂O)₃Co(nta)Cl]_n (1), [Ba(H₂O)₃Ni(nta)Cl]_n (2), and [Ba(H₂O)₃Cu(nta)Cl]_n (3) (H₃nta = nitrilotriacetic acid) were prepared by the reaction of M²⁺ ions (M = Co, Ni, and Cu), K₃nta, and Ba²⁺ ions in water. The reaction of complexes 1 and 2 with CuSO₄·5H₂O afforded [Co(H₂O)₆]_n[Cu₂(nta)₂]_n·2nH₂O (4) and [Ni(H₂O)₆]_n[Cu₂(nta)₂]_n·2nH₂O (5), respectively. The reaction mechanism was elucidated. The crystal structure analyses indicate that the Ba²⁺ ions formed one-dimensional (1D) zigzag chains in complex 3, and the chains were connected by Cu(nta)^? anions to form a three-dimensional network. On the other hand, in complexes 4 and 5, the Cu(nta)^? anions formed 1D zigzag chains, and the [Co(H₂O)₆]²⁺ (or [Ni(H₂O)₆]²⁺) cations existed as isolated units.