Synthesis, structures, spectral and electrochemical properties of copper(II) complexes of sterically hindered Schiff base ligands

The Schiff base ligands 2-(2,6-diisopropylphenyliminomethyl)phenol H(L1), 5-diethylamino-2-(2,6-diisopropylphenyliminomethyl)phenol H(L2), 2,4-di-tert-butyl-6-(2,6-diisopropylphenyliminomethyl)phenol H(L3), 3-(2,6-diisopropylphenyliminomethyl)naphthalen-2-ol H(L4) and 4-(2,6-diisopropylphenyliminomethyl)-5-hydroxymethyl-2-methylpyridin-3-ol H(L5) have been synthesized by the condensation, respectively, of salicylaldehyde, 4-(diethylamino)salicylaldehyde, 3,5-di-tert-butylsalicylaldehyde, 2-hydroxy-1-napthaldehyde and pyridoxal with 2,6-diisopropylaniline. The copper(II) bis-ligand complexes [Cu(L1)₂] 1, [Cu(L2)₂] 2, [Cu(L3)₂] 3, [Cu(L4)₂] 4 and [Cu(L5)₂] · CH₃OH 5 of these ligands have been isolated and characterized. The X-ray crystal structures of two of the complexes [Cu(L1)₂] 1 and [Cu(L5)₂] · CH₃OH 5 have been successfully determined, and the centrosymmetric complexes possess a CuN₂O₂ chromophore with square planar coordination geometry. The frozen solution EPR spectra of the complexes reveal a square-based CuN₂O₂ chromophore, and the values of g_‖ and g_‖/A_‖ index reveal enhanced electron delocalization by incorporating the strongly electron-releasing -NEt₂ group (2) and fusing a benzene ring on sal-ring (4). The Cu(II)/Cu(I) redox potentials of the Cu(II) complexes reveal that the incorporation of electron-releasing -NEt₂ group and fusion of a benzene ring lead to enhanced stabilization of Cu(II) oxidation state supporting the EPR spectral results. The hydrogen bonding interactions between the two molecules present in the unit cell of 5a generate an interesting two-dimensional hydrogen-bonded network topology.     

A family of polyamino phenolic macrocyclic ligands. Acid-base and coordination properties towards Co(II), Ni(II), Cu(II), Zn(II), Cd(II) and Pb(II) ions

The acid-base and coordination properties towards Co(II), Ni(II), Cu(II), Zn(II), Cd(II) and Pb(II) of four polyamino-phenol macrocycles 15-hydroxy-3,6,9-triazabicyclo[9.3.1]pentadeca-11,13,1¹⁵-triene L1, 18-hydroxy-3,6,9,12-tetraazabicyclo[12.3.1]octadeca-14,16,1¹⁸-triene L2, 21-hydroxy-3,6,9,12,15-pentaazabicyclo[15.3.1]enaicosa-17,19,1²¹-triene L3 and 24-hydroxy-3,6,9,12,15,18-hexaazabicyclo[18.3.1]tetraicosa-20,22,1²⁴-triene L4 are reported. The protonation and stability constants were determined by means of potentiometric measurements in 0.15 mol dm⁻³ NMe₄Cl aqueous solution at 298.1 K. L1 forms highly unsaturated Co(II), Cu(II), Zn(II) and Cd(II) mononuclear complexes that are prone to give dimeric dinuclear species with [(MH₋₁L1)₂]²⁺ stoichiometry, in solution. L2 forms stable Co(II), Ni(II), Cu(II), Zn(II), Cd(II) and Pb(II) mononuclear complexes that can coordinate external species as OH⁻ anion, giving hydroxylated complexes at alkaline pH. L3 forms stable Co(II), Ni(II), Cu(II), Zn(II), Cd(II) and Pb(II) mononuclear complexes and Co(II), Ni(II), Cu(II) and Zn(II) dinuclear [M₂H₋₁L3]³⁺ species. L4 forms stable mono- and dinuclear Co(II), Cu(II), Zn(II) and Cd(II) complexes, but only mononuclear species with Pb(II). The effect of macrocyclic size is considered in the discussion of results.     

Effect of anionic co-ligands on structure and magnetic coupling of bis(μ-phenoxo)-bridged dinuclear copper(II) complexes

Two phenoxo bridged dinuclear Cu(II) complexes, [Cu₂L₂(NO₂)₂] (1) and [Cu₂L₂(NO₃)₂] (2) have been synthesized using the tridentate reduced Schiff-base ligand 2-[(2-dimethylamino-ethylamino)-methyl]-phenol (HL). The complexes have been characterized by X-ray structural analyses and variable-temperature magnetic susceptibility measurements. The structures of the two compounds are very similar having the same tridentate chelating ligand (L) and mono-dentate anionic ligand nitrite for 1 and nitrate for 2. In both complexes Cu(II) is penta-coordinated but the square pyramidal geometry of the copper ions is severely distorted (Addison parameter (τ) = 0.33) in 1 while the distortion is quite small (average τ = 0.11) in 2. These differences have marked effect on the magnetic properties of two compounds. Although both are antiferromagnetically coupled, the coupling constants (J = −140.8 and −614.7 cm⁻¹ for 1 and 2, respectively) show that the coupling is much stronger in 2.     

Cyanide and imidazolate bridged macrocyclic dinuclear CuII complexes: Synthesis, structure and magnetic properties

Reaction of [Cu₂L](ClO₄)₄ with CH₃CN in acetonitrile, and Him in DMF gave cyanide and imidazolate bridged macrocyclic dinuclear copper (II) complexes with the formula [Cu₂L(CN)](ClO₄)₃ (1) and [Cu₂L(im)](ClO₄)₂ · 0.7Br · 0.3Cl, (2), respectively (L = N[(CH₂)₂NHCH₂(C₆H₄-p)CH₂NH(CH₂)₂]₃N). In 2, each Cu(II) atom is coordinated with four macrocyclic nitrogen atoms and one imidazolate N atom, forming a slightly distorted square pyramidal geometry. Magnetic susceptibility measurements of 1 and 2 show that the two Cu(II) atoms of the binuclear unit are antiferromagnetically coupled with g = 2.148, J = −86.09 cm⁻¹ for 1, and g = 2.047, J = −38.20 cm⁻¹ for 2. The correlation between the structures and the J values is discussed.     

Synthesis and characterization of Cu(II) and Ni(II) complexes of a tripodal ligand containing imidazoles

Two complexes of the formula [MH₃L](ClO₄)₂ [M = Cu(II) (1), Ni(II) (2)] have been prepared by the reaction of M(ClO₄)₂ · 6H₂O with the ligand (H₃L) formed by the Schiff base condensation of tris(2-aminoethyl)amine (tren) with three molar equivalents of 4-methyl-5-imidazolecarboxaldehyde and structurally and magnetically characterized. The structures of 1 and 2 are isomorphous with each other and with the iron(II) complex of H₃L which has been reported previously. The ligand, while potentially heptadentate, forms six coordinate complexes with both metal centers forming three M-N_imine and three M-N_imidazole bonds. The tren central N atom is at a nonbonded distance from M of 3.261 Å for 1 and 3.329 Å for 2. The neutral complex CuHL 3 was prepared by reaction of H₃L with Cu(OCH₃)₂ and the ionic complex Na[NiL] 4 was prepared by deprotonation of 2 with aqueous sodium hydroxide. Magnetic measurements of 1-3 are consistent with the spin-only values expected for S = 1/2 (d⁹, Cu(II)) and S = 1 (d⁸, Ni (II)) systems.     

Structural and spectroscopic comparison of five-coordinate cobalt(II) and nickel(II) thiolato complexes with the related four-coordinate complexes

Five-coordinate thiolato complexes, [L1M(SMeIm)] (M = Co and Ni) (L1 = hydrotris(3,5-diisopropyl-1-pyrazolyl)borate anion and HSMeIm = 2-mercapto-1-methylimidazole), were synthesized. These complexes were compared with the corresponding Cu(II) and Zn(II) complexes with the same ligands and were also compared with the related four-coordinate complexes [L1M(SC₆F₅)] (HSC₆F₅ = pentafluorobenzenthiol). All the complexes were characterized by X-ray crystallography and UV-Vis absorption, IR, ¹H NMR, and other spectroscopic techniques. All five-coordinate thiolato complexes, [L1M(SMeIm)] (M = Co, Ni, and Cu), form a distorted square pyramidal structure with a high spin state, and only [L1Zn(SMeIm)] takes a four-coordinate structure with a distorted tetrahedral configuration. The N21-M-S bond angles of the obtained five-coordinate complexes were proportional to the corresponding d value, which comes from between the equatorial basal plane with N4S ligand donor sets and metal ion. These observations and M-S bond distances affect on UV-Vis and far-IR spectral behavior.     

Influence of the phosphine arrangement on the reactivity of palladium(II) and platinum(II) polyphosphine complexes with copper(I) chloride

The distorted square-planar complexes [Pd(PNHP)Cl]Cl (1) (PNHP = bis[2-(diphenylphosphino)ethyl]amine), [M(P₃)Cl]Cl [P₃ = bis[2-(diphenylphosphino)ethyl]phenylphosphine; M = Pd (2), Pt (3)] and [Pt(NP₃)Cl]Cl (5) (NP₃ = tris[2-(diphenylphosphino)ethyl]amine), coexisting in the later case with a square-pyramidal arrangement, react with one equivalent of CuCl to give the mononuclear heteroionic systems [M(L)Cl](CuCl₂) [L = PNHP, M = Pd (1a); L = P₃, M = Pd (2a), Pt (3a); L = NP₃, M = Pt (5a)]. The crystal structure of 3a confirms that Pt(II) retains the distorted square-planar geometry of 3 in the cation with P₃ acting as tridentate chelating ligand, the central P atom being trans to one chloride. The counter anion is a nearly linear dichlorocuprate(I) ion. However, the five-coordinate complexes [Pd(NP₃)Cl]Cl (4), [M(PP₃)Cl]Cl (M = Pd (6), Pt (7); PP₃ = tris[2-(diphenylphosphino)ethyl] phosphine) containing three fused five-membered chelate rings undergo a ring-opening by interaction with one (4, 6, 7) and two (6, 7) equivalents of CuCl with formation of neutral MCu(L)Cl₃ [L = NP₃, M = Pd (4a); L = PP₃, M = Pd (6a), Pt (7a)] and ionic [MCu(PP₃)Cl₂](CuCl₂) [M = Pd (6b), Pt (7b)] compounds, respectively. The heteronuclear systems were shown by ³¹P NMR to have structures where the phosphines are acting as tridentate chelating ligands to M(II) and monodentate bridging to Cu(I). Further additions of CuCl to the neutral species 6a and 7a in a 1:1 ratio resulted in the achievement of the ionic complexes 6b and 7b with ions as counter anions. It was demonstrated that the formation of heterobimetallic or just mononuclear mixed salt complexes was clearly influenced by the polyphosphine arrangement with the tripodal ligands giving the former compounds. However, complexes [M(NP₃)Cl]Cl constitute one exception and the type of reaction undergone versus CuCl is a function of the d⁸ metal centre.     

3D supramolecular network assembly and thermal decomposition of new copper(II) complexes with pyrazine-2,6-dicarboxylic acid

Four new Cu(II) complexes [Cu(pzda)(2,2′-bpy)(H₂O)] · 2.5H₂O (1), [Cu(pzda)(phen)(H₂O)] · H₂O (2), [Cu(pzda)(4,4′-bpy)] · H₂O (3) and [Cu(pzda)(bpe)_0.5(H₂O)] (4) were synthesized by hydrothermal reactions of copper salt (acetate or sulphate) with pyrazine-2,6-dicarboxylic acid (H₂pzda), and 2,2′-bipyridine (2,2′-bpy), 1,10-phenanthroline (phen), 4,4′-bipyridine (4,4′-bpy) or 1,2-bis(4-pyridyl)-ethane (bpe), respectively. For 1 and 2, they are both monomeric entities which are further assembled into 3D supramolecular networks by hydrogen bonds and π-π stacking interactions. Complex 3 has a 2D metal-organic framework which is connected into 3D supramolecular network by hydrogen bonds. However, for 4, the bpe ligand bridges two Cu(II) ions into binuclear unit, and then the binuclear molecules are assembled into 3D supramolecular network by hydrogen bonds between the coordination water molecule and the carboxylate oxygen atoms. The thermal decomposition mechanism of complexes 1 and 2 cooperated with powder XRD at different temperatures is discussed. The results reveal that once liberation of water molecules takes place the supramolecular network of 1 and 2 collapses.     

Copper complexes with new oxaaza-pendant-armed macrocyclic ligands: X-ray crystal structure of a macrocyclic copper(II) complex

The synthesis of new oxaaza macrocyclic ligands (2-4) derived from O¹,O⁷-bis(2-formylphenyl)-1,4,7-trioxaheptane and functionalized tris(2-aminoethyl)amine are described. Mononuclear copper(II) complexes were isolated in the reaction of the corresponding macrocyclic ligand and copper(II) perchlorate. The structure of the [Cu(2)](ClO₄)₂ complex was determined by X-ray diffraction analysis. The copper(II) ion is five-coordinated by all N₅ donor atoms, efficiently encapsulated by the amine terminal pendant-arm, with a trigonal-bipyramidal geometry. The complexes are further characterized by UV-Vis, IR and EPR studies. The electronic reflectance spectra evidence that the coordination geometry for the Cu(II) complexes is trigonal-bipyramidal with the ligands 1 and 2 or distorted square-pyramidal with the ligands 3 and 4. The electronic spectra in MeCN solutions are different from those in the solid state, which suggest that some structural modification may occur in solution. The EPR spectrum of powder samples of the copper complex with 2 presents axial symmetry with hyperfine split at g_// with the copper nuclei (I = 3/2), which is characteristic of weakly exchange coupled extended systems. The EPR parameters (g_// = 2.230, A_// = 156 × 10⁻⁴ cm⁻¹ and g_⊥ = 2.085) indicate a d_x²-y² ground state. The EPR spectra of the complexes with ligands 3 and 4 show EPR spectra with a poorly resolved hyperfine structure at g_//. In contrast, the complex with ligand 2 shows no hyperfine split and a line shape which was simulated assuming rhombic g-tensor (g₁ = 2.030, g₂ = 2.115 and g₃ = 2.190).     

Synthesis and characterization of imidazolate-bridged polynuclear copper complexes

Copper(II) complexes of N4-donor ligands containing imidazole moieties, 4-[bis(1-methylimidazole-2-yl-methyl)aminomethyl]imidazole (Him-im₂) and 4-[bis(1-methylimidazole-2-yl-methyl)aminoethyl]imidazole (Hhis-im₂), were prepared, and [Cu(Him-im₂)Cl]ClO₄ (1) and [Cu(Hhis-im₂)Cl]ClO₄ (2) were structurally characterized by the X-ray diffraction method. Complexes 1 and 2 have a mononuclear structure with a coordinated chloride ion. The geometry of the Cu(II) center in 1 was found to be 5-coordinate trigonal-bipyramidal, whereas that of 2 was square-pyramidal. Complexes 1 and 2 showed different absorption and EPR spectra in MeOH, indicating that these compounds in solution maintain the structures revealed in the solid state. On the other hand, the reaction of Him-im₂ with Cu(ClO₄)₂ · 6H₂O under basic conditions gave a tetranuclear Cu(II) complex, [Cu₄(im-im₂)₄](ClO₄)₄ (3), whereas using the ligand Hhis-im₂ gave two kinds of polynuclear complexes [Cu₄(his-im₂)₄](ClO₄)₄ (4) and [Cu₆(his-im₂)₆](ClO₄)₆ (5) exhibiting discretely different structures. X-ray crystal structure analysis of the polynuclear complexes revealed their cyclic structures bridged by the imidazolate moiety. The geometry difference of the Cu(II) centers between 1 and 2 is thus concluded to determine the structures of tetranuclear complexes 3 and 4, respectively. Temperature dependent magnetic susceptibility measurements of complexes 3, 4, and 5 have shown an antiferromagnetic exchange interaction with a coupling constant of J = −32.5, −27.1 and −22.8 cm⁻¹, respectively.     

Platinum(II) oxalato complexes with adenine-based carrier ligands showing significant in vitro antitumor activity

[Pt(L)₂(ox)] (1), [Pt(2-OMeL)₂(ox)] (2), [Pt(3-OMeL)₂(ox)] (3), [Pt(2,3-diOMeL)₂(ox)] (4), [Pt(2,4-diOMeL)₂(ox)] (5), [Pt(3,4-diOMeL)₂(ox)] (6) and [Pt(3,5-diOMeL)₂(ox)]·4H₂O (7) platinum(II) oxalato (ox) complexes were synthesized using the reaction of potassium bis(oxalato)platinate(II) dihydrate with 2-chloro-N6-(benzyl)-9-isopropyladenine or its benzyl-substituted analogues (nL). The complexes 1-7, which represent the first platinum(II) oxalato complexes involving adenine-based ligands, were fully characterized by various physical methods including multinuclear and two dimensional NMR spectroscopy. A single-crystal X-ray analysis of [Pt(2,4-diOMeL)₂(ox)]·2DMF (5·2DMF; DMF = N,N′-dimethylformamide), proved the slightly distorted square-planar geometry in the vicinity of the Pt(II) ion with one bidentate-coordinated oxalate dianion and two adenine derivatives (nL) coordinated to the Pt(II) centre through the N7 atom of an adenine moiety, thereby giving a PtN₂O₂ donor set. In vitro cytotoxicity of the prepared complexes was tested by an MTT assay against osteosarcoma (HOS) and breast adenocarcinoma (MCF7) human cancer cell lines. The best results were achieved for the complexes 2 and 5 in the case of both cell lines, whose IC₅₀ values equalled 3.6 ± 1.0, and 4.3 ± 2.1 μM (for 2), and 5.4 ± 3.8, and 3.6 ± 2.1 μM (for 5), respectively. The IC₅₀ equals 9.2 ± 1.5 μM against MCF7 cells in the case of 1. The in vitro cytotoxicity of the mentioned complexes significantly exceeded commercially used platinum-based anticancer drugs cisplatin (34.2 ± 6.4 μM and 19.6 ± 4.3 μM) and oxaliplatin (> 50.0 μM for both cancer cell lines).     

From “naked” copper(II) ions and asymmetric macrocyclic complex linkers with a monodentate top and a bidentate top to molecular rectangle and infinite molecular rectangle strands

A molecular rectangle [Cu{CuL¹(NO₃)}(H₂O)(NO₃)]₂ (1) and two infinite molecular rectangle strands {[Cu{CuL¹(NO₃)}₂] · 2H₂O}_∞ (2) and [Cu{CuL²(ClO₄)}₂]_∞ (3) were prepared by reaction of “naked” Cu(II) ions with macrocyclic complex ligands CuL¹ for 1 and 2 and CuL² for 3 in metal-to-ligand molar ratios of 1:1, 1:2 and 1:2, respectively. L¹ and L² denote the dianions of diethyl 5,6,7,8,15,16-hexahydro-6,7-dioxodibenzo[1,4,8,11]tetraazacyclotetradecine-13,18-dicarboxylate and diethyl 5,6,7,8,15,16-hexahydro-15-methyl-6,7-dioxodibenzo[1,4,8,11]tetraazacyclotetradecine-13,18-dicarboxylate, respectively. The structures of 1-3 were determined by X-ray single-crystal analyses. CuL¹ in 1 and 2 and CuL² in 3 act as angular linkers with a monodentate coordination top and a bidentate one between two Cu(II) nodes to enclose the molecular rectangle of 1 and the rectangular subunits of 2 and 3. The angular shape, the monodentate top plus bidentate top coordination mode and the self-complementarity for π?π interactions of the macrocyclic complex linkers, the ratio between the reactants and the octahedral coordination geometry of the naked Cu(II) ions jointly determined the interesting structures of metallocyclophane 1 and 1D double chain coordination polymers 2 and 3. The cavities of the rectangular molecules of 1 are arranged into infinite strands so that parallel channels occur in the crystal. The molecules of 2 and 3 all pack parallel in the crystals.     

Synthesis and characterization of nickel(II) complexes bearing 2-(imidazol-2-yl)pyridines or 2-(pyridin-2-yl)phenanthroimidazoles/oxazoles and their polymerization of norbornene

Series of 2-R₁-6-(1-R₂-4,5-diphenyl-1H-imidazol-2-yl)pyridine (R₁ = R₂ = H, L1; R₁ = Me, R₂ = H, L2; R₁ = H, R₂ = Me, L3; R₁ = R₂ = Me, L4), 2-(6-R₁-pyridin-2-yl)-1H-phenanthro[9,10-d]imidazole (R₁ = H, L5; R₁ = Me, L6) and 2-(pyridin-2-yl)phenanthro[9,10-d]oxazole (L7) were synthesized and used to prepare their corresponding dihalonickel complexes (C1-C9). All organic compounds and nickel complexes were characterized by elemental and spectroscopic analyses. Molecular structures of C1, C4, C5 and C8 were confirmed by the single-crystal X-ray diffraction analysis. The single-crystal X-ray analysis revealed complex C1 as a distorted octahedral geometry, complex C4 as a distorted square pyramidal geometry, complex C5 as a distorted trigonal bipyramidal configuration, and complex C8 as a tetrahedral geometry. Upon activation with methylaluminoxane (MAO), the nickel complexes showed good activity towards norbornene polymerization through main additional and minor ring-opening metathesis. The reaction parameters such as norbornene concentration, reaction temperature and different coordinate environments caused by the ligands affected their catalytic performances.     

Luminescent probes for indole-binding proteins derived from ruthenium(II) polypyridine complexes

We report here the synthesis, characterisation, electrochemical, photophysical and protein-binding properties of four luminescent ruthenium(II) polypyridine indole complexes [Ru(bpy)₂(L1)](PF₆)₂ (1), [Ru(bpy)₂(L2)](PF₆)₂ (2), [Ru(L1)₃](PF₆)₂ (1a), and [Ru(L2)₃](PF₆)₂ (2a) (bpy = 2,2′-bipyridine; L1 = 4-(N-(2-indol-3-ylethyl)amido)-4′-methyl-2,2′-bipyridine; L2 = 4-(N-(6-N-(2-indol-3-ylethyl)hexanamidyl)amido)-4′-methyl-2,2′-bipyridine). Their indole-free counterparts, [Ru(bpy)₂(L3)](PF₆)₂ (3) and [Ru(L3)₃](PF₆)₂ (3a) (L3 = 4-(N-(ethyl)amido)-4′-methyl-2,2′-bipyridine), have also been synthesised for comparison purposes. Cyclic voltammetric studies revealed ruthenium-based oxidation at ca. +1.3 V versus SCE and diimine-based reductions at ca. −1.20 to −2.28 V. The indole moieties of complexes 1, 2, 1a and 2a displayed an irreversible wave at ca. +1.1 V versus SCE. All the ruthenium(II) complexes exhibited intense and long-lived orange-red triplet metal-to-ligand charge-transfer ³MLCT (dπ(Ru) → π*(L1-L3)) luminescence upon visible-light irradiation in fluid solutions at 298 K and in alcohol glass at 77 K. The binding of the indole-containing complexes to bovine serum album (BSA) has been studied by quenching experiments and emission titrations.     

Synthesis, characterization, interaction with DNA and cytotoxicity in vitro of dinuclear Pd(II) and Pt(II) complexes dibridged by 2,2'-azanediyldibenzoic acid

The dinuclear complexes [Pd₂(L)₂(bipy)₂] (1), [Pd₂(L)₂(phen)₂] (2), [Pt₂(L)₂(bipy)₂] (3) and [Pt₂(L)₂(phen)₂] (4), where bipy = 2,2′-bipyridine, phen = 1,10-phenanthroline and L = 2,2′-azanediyldibenzoic dianion) dibridged by H₂L ligands have been synthesized and characterized. The binding of the complexes with fish sperm DNA (FS-DNA) were investigated by fluorescence spectroscopy. The results indicate that the four complexes bound to DNA with different binding affinity, in the order complex 4 > complex 3 > complex 2 > complex 1, and the complex 3 binds to DNA in both coordination and intercalative mode. Gel electrophoresis assay demonstrates the ability of the complexes to cleave the pBR 322 plasmid DNA. The cytotoxic activity of the complexes was tested against four different cancer cell lines. The four complexes exhibited cytotoxic specificity and significant cancer cell inhibitory rate.     

Further study of the effect of macrocyclic pendant groups on the supramolecular architecture: Synthesis and structures of macrocyclic nickel (II) complexes with trans-butene dicarboxylate

Two nickel (II) complexes with the formula [NiL(H₂O)₂] · 6H₂O (1 · 6H₂O) and [NiH₂L(BDC)]_n (2), where L = 3,10-bis(3-propylcarboxyl)-1,3,5,8,10,12-hexaazacyclo-tetradecane, BDC = trans-butene dicarboxylate, have been synthesized and characterized by elemental analyses, IR spectra and single-crystal X-ray analyses. In 1, the Ni(II) ion is six-coordinated with four nitrogen atoms from the macrocyclic ligand in the equatorial plane and two water molecules in axial position. In 2, the structure is made up of one-dimensional chain of [NiH₂L]²⁺ units with BDC²⁻ anions, in which the Ni(II) ion is also six-coordinated with four nitrogen atoms from the macrocyclic ligand in the equatorial plane and two carboxylate oxygen atoms from the BDC²⁻ group in axial position. In 2, the 1D chains are aligned in a parallel mode.     

Spectral properties and bio-activity of copper(II) clofibriates, part III: crystal structure of Cu(clofibriate)2(2-pyridylmethanol)2, Cu(clofibriate)2(4-pyridylmethanol)2(H2O) dihydrate, and Cu2(clofibriate)4(N,N-diethylnicotinamide)2

New copper(II) clofibriates (clof, {2-(4-chlorophenoxy)-2-methylpropionic or 2-(4-chlorophenoxy)isobutyric acid}) of composition Cu(clof)₂L₂ (where L=2-pyridylmethanol (2-pymeth) (1), N-methylnicotinamide (Menia) (4), N,N-diethylnicotinamide (Et₂nia) (5), isonicotinamide (isonia) (7) or methyl-3-pyridylcarbamate (mpc) (8)), [Cu(clof)₂(4-pymeth)₂(H₂O)] · 2H₂O (4-pymeth=4-pyridylmethanol) (2 · 2H₂O) and Cu(clof)₂L (where L=4-pymeth (3) or Et₂nia (6)) have been prepared and spectroscopically characterized. All the Cu(clof)₂L₂ compounds seem to possess distorted octahedral copper(II) stereochemistry with differing tetragonal distortions. An X-ray analysis of 1 was carried out and it featured a tetragonal-bipyramidal geometry around the copper(II) atom. X-ray analysis of 2 · 2H₂O featured a square-pyramidal geometry around copper(II) atom. Both the Cu(clof)₂L compounds seem to consist of a binuclear unit of tetracarboxylate type bridging. An X-ray analysis of 6 revealed typical binuclear paddle-wheel type structure, consisting of two copper(II) atoms in square-pyramidal geometry bridged by four carboxylate anions in the xy-plane. All complexes under study were characterized by EPR and electronic spectroscopy. The antimicrobial effects have been tested on various strains of bacteria, yeasts and filamentous fungi.     

Cleavage of a RNA analog containing uridine by a bifunctional dinuclear Zn(II) catalyst

The macrocyclic ligand, 1,4-bis((1-oxa-4,7,10-triazacyclododecan-7-yl)methyl)benzene (L1) is prepared. L1 binds two Zn(II) ions at neutral pH to form Zn₂(L1) as studied by using pH-potentiometric titrations. Zn₂(L1) binds two uridines at pH 7.0, I = 0.100 M (NaCl) and the mononuclear analog Zn(L2) (L2 = 1-oxa-4,7,10-triazacyclododecane) binds a single uridine; dissociation constants for both complexes are in the millimolar range. Both complexes promote the cleavage of a simple RNA analog lacking a nucleobase (HpPNP = 2-hydroxypropyl-4-nitrophenylphosphate), and a uridine containing RNA analog UpPNP (uridine-3′-4-nitrophenylphosphate). Plots of the first-order rate constant for cleavage of HpPNP as a function of Zn(L2) concentration from 0.5 mM to 20.0 mM are linear, consistent with weak complexation to substrate K_d > 20 mM. In contrast, first-order rate constants for cleavage of UpPNP by Zn(L2) or Zn₂(L1) over similar concentration ranges exhibit a downward curvature, consistent with the formation of a complex between catalyst and UpPNP. Comparison of second-order rate constants (k₂ = k_cat/K_d) shows that the dinuclear complex Zn₂(L1) is a better catalyst than Zn(L2) for both HpPNP and UpPNP cleavage.     

Dinuclear fumarato- and terephthalato-bridged copper(II) complexes: Structural characterization and magnetic properties

The dinuclear dicarboxylato-bridged copper(II) complexes [Cu₂(TPA)₂(μ-tp)](ClO₄)₂ · H₂O (1), [Cu₂(TPA)₂(μ-fum)](ClO₄)₂ · 2H₂O (2) and [Cu₂(pmedien)₂(μ-fum)(H₂O)₂](ClO₄)₂ (3) (tp = terephthalate dianion, fum = fumarate dianion, TPA = tris(2-pyridylmethyl)amine and pmedien = N,N,N′,N″,N″-pentamethyldiethylenetriamine) were synthesized and structurally characterized by X-ray crystallography. The structures of the TPA complexes 1 and 2 consist of μ-tp or μ-fum bridging two Cu(II) centers in a bis(monodentate) bonding fashion. The coordination geometry around the Cu(II) ions in these compounds has a distorted trigonal bipyamidal geometry, TBP with four nitrogen atoms from the TPA ligand and a coordinated oxygen atom supplied by the carboxylate group of the bridged dicarboxylato ligand. Complex 3 has a distorted square pyramidal geometry achieved by the three N-atoms of the pmedien, one fum-carboxylate-oxygen and by an oxygen atom from a coordinated water molecule. The intradimer Cu…Cu distances in these complexes are 11.078(3), 8.663(4) and 9.520(3) Å for 1, 2 and 3, respectively. The electronic spectra of the complexes in aqueous solutions are in complete agreement with the assigned X-ray geometry around the Cu(II) centers. Also, analysis of the infrared spectral data for the ν(COO⁻) stretching frequencies of the tp-carboxalato groups reveals the existence of the bis(mondentate) coordination mode for the bridged dicarboxylato ligands in compounds 1 and 2. The susceptibility measurements at variable temperature over the 2-300 K range are reported. For 1-3, it has been observed slight antiferromagnetic coupling with J values of −0.8, −3.0 and −2.9 cm⁻¹, respectively.     

Structures and magnetic properties of one-dimensional polymers constructed with copper(II) salts and pyridinecarboxamide-type ligands

Three complexes of the composition {[Cu(μ_1,5-dca)₂(mppca)₂] · H₂O}_n (1), [Cu(μ_1,5-dca)₂(nppca)₂]_n (2) and [Cu(μ-Cl)₂(mppca)₂]_n (3) (dca = dicyanamide, ; mppca = N-(4′-methylphenyl)-4-pyridinecarboxamide; nppca = N-(4′-nitrophenyl)-4-pyridinecarboxamide) have been synthesized and characterized by single crystal X-ray crystallography and magnetic susceptibility studies. Different supramolecular structures of the complexes have been constructed by different non-covalent motifs in the crystalline solids. In complex 1, adjacent copper(II) atoms are connected by double μ_1,5-dca(end-to-end) bridges to form a chain-like structure. The chains are linked by π-π interactions and hydrogen bonds between the ligands and water molecules to form a 3D network. In complex 2, copper(II) atom has a coordination environment similar to 1, but water molecules have not been found. Weak C-H?N hydrogen bonding and π-π interaction yield a 3D supramolecular network which is different from that of complex 1. Complex 3 is a 1D polymeric chain in which Cu(II) ions are bridged by Cl⁻, and only CH/π interactions had been found. Magnetic measurements revealed antiferromagnetic properties of 1, 3 and ferromagnetic behavior of 2.