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1.
Four lead(II) complexes with substituted 2,2′-bipyridine adducts and β-diketonates ligands, [Pb(5,5′-dm-2,2′-bpy)(tfpb)2]21, [Pb(4,4′-dmo-2,2′-bpy)(tfpb)2]22, [Pb(4,4′-dm-2,2′-bpy)(tfnb)2]23 and [Pb(5,5′-dm-2,2′-bpy)(tfnb)2]24, (“4,4′-dm-2,2′-bpy”, “5,5′-dm-2,2′-bpy”, “4,4′-dmo-2,2′-bpy”, “Htfpb” and “Htfnb” are the abbreviations of 4,4′-dimethyl-2,2′-bipyridine, 5,5′-dimethyl-2,2′-bipyridine, 4,4′-dimethoxy-2,2′-bipyridine, 4,4,4-trifluoro-1-phenyl-1,3-butanedione and 4,4,4-trifluoro-1-(2-naphthyl)-1,3-butanedione, respectively) have been synthesized and characterized by elemental analysis, IR, 1H NMR and 13C NMR spectroscopy and also studied by thermal and electrochemical as well as X-ray crystallography. The supramolecular features in these complexes are guided/controlled by weak directional intramolecular interactions. 相似文献
2.
A series of coordination polymers have been prepared by the combination of flexible ligand 1,1′-biphenyl-2,2′-dicarboxylic acid (H2dpa) and different types of nitrogen-containing ligands, with various metal ions such as Co(II), Zn(II) and Cd(II). The single-crystal structure analyses reveal that the above complexes possess different structure features with the introduction of different nitrogen-containing ligands. When auxiliary linear ligand 4,4′-bipyridine (4,4′-bpy) is introduced, two-dimensional layered complex, [Co2(dpa)2(4,4′-bpy)2(H2O)]n (1) is formed. Whereas if chelating ligand, 1,10-phenanthroline (1,10′-phen) and 2,2′-bipyridine (2,2′-bpy) are introduced, one-dimensional complex [Zn(dpa)(1,10′-phen)]n (2) and discrete complexes [Co2(dpa)2(2,2′-bpy)2(H2O)2] (3), [Co3(dpa)3(1,10′-phen)6(H2O)2] (4), [Cd(dpa)(1,10′-phen)2][(H2dpa)2(H2O)2] (5) are synthesized. To our interest, 1 and 2 crystallize in homochiral spacegroup. Furthermore, the magnetic property of complex 1 and the fluorescent properties of complexes 2 and 5 are studied. 相似文献
3.
Reaction of [Ru(2,2′-bipyridine)(2,2′:6′,2″-terpyridine)Cl]PF6 (abbreviated to [Ru(bipy)(terpy)Cl]PF6) with 0.5 equiv of the bidentate ligand L produces the dinuclear complexes [{Ru(bipy)(terpy)}2(μ-L)](PF6)4 (L = 4,4′-bipyridine 1, 1,4-diisocyanobenzene 2 and pyrazine 3) in moderate yields. Treating [Ru(bipy)(terpy)Cl]PF6 with equal molar of 1,4-diisocyanobenzene affords [Ru(bipy)(terpy)(CNC6H4NC)](PF6)2 (2a). These new complexes have been characterized by mass, NMR, and UV-Vis spectroscopy, and the structures of 1-3 determined by an X-ray diffraction study. Cyclic voltammetric studies suggest that metal communication between the two ruthenium ions increases from 1 to 2 to 3. 相似文献
4.
Feng-Qin Wang Dan-Feng Weng Jian-Jun Zhang Lin-Pei Jin 《Inorganica chimica acta》2007,360(6):2029-2038
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. 相似文献
5.
Sliwińska U Pruchnik FP Pelińska I Ułaszewski S Wilczok A Zajdel A 《Journal of inorganic biochemistry》2008,102(10):1947-1951
The [RhCl3(N-N)(DMSO)] complexes, the N-N being 2,2′-bipyridine (1), 1,10-phenanthroline (2), 4,7-diphenyl-1,10-phenanthroline (3), 4,4′-dimethyl-2,2′-bipyridine (4) and 1,10-phenanthroline-5,6-dione (5), have been synthesized and characterized with spectroscopic methods. The compounds 2-5 adopt mer- and complex 1fac-structure. The molecular and electronic structure studies of mer- and fac-complexes with bpy and phen ligands at the DFT B3LYP level with 3-21G∗∗ basis set showed that mer-isomers are more stable. The cytostatic activity of the [RhCl3(N-N)(DMSO)] complexes against Caco-2 and A549 tumor cells have been studied. Their antibacterial activity have also been investigated. It has been found that the very promising biological activity show complexes 2, 3 and 4. 相似文献
6.
Fernando Hung-Low 《Inorganica chimica acta》2008,361(5):1298-1310
Reaction of 2-(diphenylphosphinomethyl)pyridine (PMP-21) with the silver(I) salts of tetrafluoroborate , triflate (Otf−), and trifluoroacetate (tfa−) affords dinuclear complexes (2-4), where the ligand bridges the two silver centers, and the anions interact with the metal centers to varying degrees. Further reaction of AgBF4 and AgOtf with reaction solutions containing PMP-21 and either the bidentate 5,5′-dimethyl-2,2′-bipyridine or 4,4′-bipyridine ligands produce dimeric and bridged structural motifs. The ability of 5,5′-dimethyl-2,2′-bipyridine to chelate and the 4,4′-bipyridine to serve as a connector between metal centers, allows the construction of coordinative structures where the effect of ligand ratio and either interacting or non interacting anions influence the silver coordination environment, allowing it to take on several geometries including trigonal bipyramidal, 5, both T-shaped and tetrahedral in a single structure, 6 and 8, trigonal pyramidal, 7, and trigonal planar, 9. Structures 2, 3, and 4 display comparable Ag-Ag contacts ranging from 2.7979(10) to 3.0538(4) Å, with a corresponding weakening of the metallophilic interaction when a bipyridine ligand is coordinated. Low-temperature luminescence spectra were collected for all compounds and are compared. 相似文献
7.
Hong-Yan Li Jing Xiong Qiu-Lei Xu Yun-Mei Tao Jing-Lin Zuo 《Inorganica chimica acta》2011,370(1):398-3327
Six complexes (1-6) with the type of [Ru(bpy)2L]X2 (1-3: L = L1-L3, X = Cl−; 4-6: L = L1-L3, X = PF6−) were synthesized based on 2,2′-bipyridine and three 2,2′-bipyridine derivatives L1, L2 and L3 (L1 = 5,5′-dibromo-2,2′-bipyridine, L2 = 5-bromo-5′-carbazolyl-2,2′-bipyridine, L3 = 5,5′-dicarbazolyl-2,2′-bipyridine). The complexes 1-6 were characterized by 1H NMR, MS(ESI) and IR spectra, along with the X-ray crystal structure analysis for 1, 5 and 6. Their photophysical properties and electrochemiluminescence (ECL) properties were investigated in detail. In the UV-Vis absorption spectra, all complexes 1-6 show strong intraligand (π → π∗) transitions and metal-ligand charge transfer (MLCT, dπ (Ru) → π∗) bands. Upon the excitation wavelengths at ∼508 nm, all complexes 1-6 exhibit typical MLCT emission of ruthenium(II) polypyridyl complexes. The introduction of carbazole moieties improves the MLCT absorption and emission intensity. The ruthenium(II) complexes 1-6 exhibit good electrochemiluminescence (ECL) properties in [Ru(bpy)2L]2+/tri-n-propylamine (TPrA) acetonitrile solution and the complexes with PF6− showed higher ECL emission intensity than that of the complexes with Cl− based on the same ligands. 相似文献
8.
Naokazu Yoshikawa Shinichi Yamabe Yasushi Kai Keiichi Tsukahara 《Inorganica chimica acta》2006,359(14):4585-4593
A series of mononuclear acetonitrile complexes of the type [Ru(CH3CN)(L)(terpy)]2+ {L = phen (1), dpbpy (3), and bpm (5)}, and their reference complexes [RuCl(L)(terpy)]+ {L = phen (2), dpbpy (4), and dpphen (6)} were prepared and characterized by electrospray ionization mass spectrometry, UV-vis spectroscopy, and cyclic voltammograms (CV). Abbreviations of the ligands (Ls) are phen = 1,10-phenanthroline, dpbpy = 4,4′-diphenyl-2,2′-bipyridine, bpm = 2,2′-bipyrimidine, dpphen = 4,7-diphenyl-1,10-phenanthroline, bpy = 2,2′-bipyridine, and terpy = 2,2′:6′,2″-terpyridine. The X-ray structures of the two complexes 2 and 3 were newly obtained. The metal-to-ligand charge transfer (MLCT) bands in the visible region for 1, 3, and 5 in acetonitrile were blue shifted relative to those of the reference complexes [RuCl(L)(terpy)]+. CV for all the [Ru(CH3CN)(L)(terpy)]2+ complexes showed the first oxidation wave at around 0.95 V, being more positive than those of [RuCl(L)(terpy)]+. The time-dependent-density-functional-theory approach (TDDFT) was used to interpret the absorption spectra of 1 and 2. Good agreement between computed and experimental absorption spectra was obtained. The DFT approach also revealed the orbital interactions between Ru(phen)(terpy) and CH3CN or Cl−. It is demonstrated that the HOMO-LUMO energy gap of the acetonitrile ligand is larger than that of the Cl− one. 相似文献
9.
Interaction of [Cp*RuCl(μ-Cl)]2 with 2,2′-bipyridine (2,2′-bipy) in the presence of Na[PF6] gave a chloride bridging dinuclear complex [{Cp*Ru(2,2′-bipy)}2(μ-Cl)][PF6] (1). In the crystal structure, the cation [{Cp*Ru(2,2′-bipy)}2(μ-Cl)]+ contains a bent Ru-Cl-Ru linkage with an angle of 141.87(12)°. The tris(μ-hydroxo)diruthenium complex [{(η6-p-cymene)Ru}2(μ-OH)3][BF4] in acetone solution was treated by 4,4′-bipyridine (4,4′-bipy) to give a hydroxo-bridged tetranuclear complex [{(η6-p-cymene)Ru}2(μ-OH)2(μ-4,4′-bipy)]2[BF4]4 (2). Complex 2 consists of four (η6-p-cymene)Ru moieties connected by two 4,4′-bipy and four hydroxo-bridging groups, forming a novel metallomacrocycle with alternating hydroxyl and 4,4′-bipy bridges between the ruthenium atoms. Spectroscopic properties along with electrochemistry of two organoruthenium (II) complexes 1 and 2 are reported. 相似文献
10.
Montserrat Barquín Nerea Cocera Liher Larrínaga José M. Seco 《Inorganica chimica acta》2010,363(1):127-133
By the reactions of Cu(AcO)2·H2O and Cu(HCOO)2·4H2O with 4,4′-dimethyl-2,2′-bipyridine and 5,5′-dimethyl-2,2′-bipyridine the compounds [Cu(AcO)2(4,4′-Me2-2,2′-bipy)]·1/2H2O (1), [Cu(AcO)2(5,5′-Me2-2,2′-bipy)(H2O)] (2), [Cu(HCOO)(μ-HCOO)(4,4′-Me2-2,2′-bipy)]n·nH2O (3) and [Cu(HCOO)(μ-HCOO)(5,5′-Me2-2,2′-bipy)]n·2nH2O (4) were obtained. In the acetate complexes, 1 and 2, the geometry around copper is distorted octahedral and square pyramidal, respectively. Dimeric units of different geometry are formed in both cases through hydrogen bonds in which non-coordinated (in 1) and coordinated (in 2) water molecules are involved. The structures of 3 and 4 consist of polymeric monodimensional chains of square pyramidal copper units linked by axial-equatorial syn-anti (3) or anti-anti (4) bridging formate groups. Water molecules form hydrogen bonds with formate groups of the same chain in compound 3. In compound 4 the water molecules link the polymeric contiguous chains of complex through hydrogen bonds with oxygen atoms of formate groups and they are also linked between them, forming monodimensional water chains which run parallel to the complex chains. Sheets parallel to the ac plane are formed by alternating chains of water and polymeric complex. Magnetic properties and EPR spectra for these compounds have been studied. 相似文献
11.
Four novel metal coordination polymers, [Cd(dpa)(H2O)]n (1), [Cd(dpa)(2,2′-bipy)]n (2), {[Cd2(dpa)2(4,4′-bipy)3](4,4′-bipy)(H2O)2}n (3) and [Cd(dpa)(bim)2(H2O)]}n (4) (H2dpa = 2,4′-biphenyl-dicarboxylic acid, 2,2′-bipy = 2,2′-bipyridine, 4,4′-bipy = 4,4′-bipyridine, bim = benzimidazole), have been synthesized and structurally characterized by elemental analysis, IR and X-ray diffraction. Single-crystal X-ray analyses reveal that the 2,4′-diphenic acids acts as bridging ligands, exhibiting rich coordination modes to link metal ions: bis-monodentate, bidentate chelating, chelating/bridging, monoatomic bridging and monodentate modes. In addition, the luminescent properties for compound 1-4 are also investigated in this work. 相似文献
12.
Six antimony adducts with N-donor neutral ligands (1,10-phenanthroline, 4,4′-bipyridine) have been obtained following the reaction of antimony halides with phenanthroline and 4,4′-bipyridine. By changing the solvent and stoichiometry, we obtained six different complexes, Sb(phen)Cl3 (1), Sb(phen)Br3 (2), Sb2(phen)4Br8 (3) and Sb(bpy)Cl3 (4), Sb(bpy)2Cl3 (5), Sb(bpyH · bpyH2)Br6 (6) (where phen = 1,10-phenanthroline, bpy = 4,4′-bipyridine). All the complexes have been characterized via elemental analysis, FT-IR and NMR (1H, 13C) spectroscopy. The crystal structures of complexes 2, 3 and 6 have been determined by X-ray single crystal diffraction.The structural analysis show that the coordination sphere around antimony atom in complex 2 is a distorted square pyramid, coordinated by three bromine atoms and two nitrogen atoms from phen. In complex 3, the central antimony atom is six-coordinated through four bromine atoms and two nitrogen atoms forming a distorted octahedral geometry. Besides that, there are also uncoordinated 1,10-phenanthroline bonded by hydrogen bonds and π-π stacking interactions, which is rarely observed in previous reports. The crystal structure of complex 6 consists of bpyH · bpyH2 trications and hexabromoantimonate trianions. The antimony atom in the anion has a distorted octahedral environment. Additionally, all complexes present a 3D framework built up by N-H?Br, C-H?Br and C-H?Cl weak hydrogen bonds interactions. 相似文献
13.
A new series of amphiphilic heteroleptic ruthenium(II) sensitizers [Ru(H2dcbpy)(dhbpy)(NCS)2] (C1), [Ru(H2dcbpy)(bccbpy)(NCS)2] (C2), [Ru(H2dcbpy)(mpubpy)(NCS)2] (C3), [Ru(H2dcbpy)(bhcbpy)(NCS)2] (C4) have been synthesized and fully characterized by UV-Vis, emission, NMR and cyclic voltammetric studies (where dhbpy = 4,4′-dihexyl-2,2′-bipyridine, bccbpy = 4,4′-bis(cholesteroxycarbonyl)-2,2′-bipyridine, mpubpy = 4-methyl-4′-perfluoro-1H,1H,2H,2H,3H,3H-undecyl-2,2′-bipyridine, bhcbpy = 4,4′-Bis(hexylcarboxamido)-2,2′-bipyridine). The amphiphilic amide heteroleptic ruthenium(II) sensitizers, self-assembled on TiO2 surface from ethanol solution, reveal efficient sensitization in the visible window range yielding ≈80% incident photon-to-current efficiencies (IPCE). Under standard AM 1.5 sunlight, the C4 sensitizer gave 15 mA/cm2 short circuit photocurrent density, 0.66 fill factor and an open circuit voltage of 0.75 V, corresponding to an overall conversion efficiency of 7.4%. 相似文献
14.
Putta Venkat Reddy Mallepally Rajender Reddy Srishailam Avudoddi Yata Praveen Kumar Chintakuntla Nagamani Nancherla Deepika K Nagasuryaprasad Surya Satyanarayana Singh Sirasani Satyanarayana 《Analytical biochemistry》2015
A novel polypyridyl ligand CNPFIP (CNPFIP = 2-(5(4-chloro-2-nitrophenyl)furan-2-yl)-1H-imidazo[4,5f][1,10]phenanthroline) and its mononuclear Ru(II) polypyridyl complexes of [Ru(phen)2CNPFIP]2+(1) (phen = 1,10-phenanthroline), [Ru(bpy)2CNPFIP]2+(2) (bpy = 2,2′-bipyridine), and [Ru(dmb)2CNPFIP]2+(3) (dmb = 4,4′-dimethyl-2,2′-bipyridine) have been synthesized successfully and characterized thoroughly by elemental analysis, UV/Vis, IR, NMR, and ESI-MS. The interaction of the Ru(II) complexes with calf thymus DNA (CT-DNA) was investigated by absorption titration, fluorescence, viscosity measurements. The experimental results suggest that three complexes bind to CT-DNA through an intercalative mode and the DNA-binding affinity of complex 1 is greater than that of complexes 2 and 3. The photocleavage of plasmid pBR322 DNA by ruthenium complexes 1, 2, and 3 was investigated. We have also tested three complexes for their antimicrobial activity against Escherichia coli (Gram-negative) and Staphylococcus aureus (Gram-positive) bacteria. The in vitro cytotoxicity of these complexes was evaluated by MTT assay, and complex 1 shows higher cytotoxicity than 2 and 3 on HeLa cells. The induced apoptosis and cell cycle arrest of HeLa cells were investigated by flow cytometry for 24 h. The molecular docking of ruthenium complexes 1, 2, and 3 with the active site pocket residues of human DNA TOP1 was performed using LibDock. 相似文献
15.
Mairéad E. Kelly Ralph Kluge Dirk Steinborn Harry Schmidt 《Inorganica chimica acta》2009,362(4):1323-4211
A number of complexes of the types [PtBr2Me2(N?N)] (N?N = 4,4′-di-Me-2,2′-bpy (1); 4,4′-di-t-Bu-2,2′-bpy (2); 2,2′-bpz (3); bpym (4)) and [PtBr2Me2(L)2] (L = H-pz (5); 4-Me-H-pz (6); H-idz (7); H-im (8); H-bim (9); quaz (10)) are reported. Characterization by NMR (1H, 13C and 195Pt), IR and EI-MS is given. In addition, crystal structures of several of these complexes are described. Furthermore, interactions within these structures including intramolecular hydrogen bonding and π-π stacking interactions are reported. The reactivity of selected mononuclear complexes was investigated and yielded two dinuclear complexes [PPh4][(PtBrMe2)2(μ-Br)(μ-pz)2] (11) and [(PtBr2Me2)2(μ-bpym)] (12), respectively. The latter complex is accompanied by a solid-state structure. Finally, the thermal stability of all complexes is reported. 相似文献
16.
Kenneth Kam-Wing Lo Terence Kwok-Ming Lee Kenneth Yin Zhang 《Inorganica chimica acta》2006,359(6):1845-1854
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. 相似文献
17.
The bidentate ligand benzylacetylacetone was used to synthesize the Cu(II) complexes 1 and 2 without and with 4,4′-bipyridine ligand, respectively. The complexes were characterized by analytical and spectroscopic studies. The mononuclear complex [Cu(C10H9O2)2] (1) has been synthesized by the reaction of copper acetate with the ligand whereas the tetranuclear complex [Cu4(4,4′-bpy)4(C10H9O2)4(C2H3O2)4] (2) has been synthesized by the reaction of copper acetate with the ligand followed by the addition of 4,4′-bipyridine. The X-ray analysis shows that the complex 1 has square planar geometry and the complex 2 has square pyramidal geometry around the metal centers. The thermogravimetric studies showed that the complexes undergo decomposition in multiple steps. 相似文献
18.
A new set of supramolecular complexes, [Ni(DPAP-SHZ)(2,2′-bipy)CH3OH] (1), [Zn(DPAP-SHZ)(2,2′-bipy)CH3OH] (2) and [Cu(DPAP-SHZ)(2,2′-bipy)] · 2CH2Cl2 (3) (DPAP-SHZ = 1,3-diphenyl-4-(salicylidene hydrazide)-acetyl-pyrazolone-5, 2,2′-bipy = 2,2′-bipyridine) have been synthesized and characterized by elemental analysis, TG-DTA, IR spectroscopy and X-ray crystallography. The X-ray diffraction analyses of the complexes show that the Ni(II) ion and Zn(II) ion centers are six-coordinated while the Cu(II) ion center is five-coordinated. The three supramolecular complexes contain the same ligands, namely DPAP-SHZ and 2,2′-bipy. However, their hydrogen bonds are significantly different, and this variation apparently is responsible for the dissimilar structures of the three supramolecular complexes. 相似文献
19.
Two new binuclear copper complexes, [Cu2(oxpn)(bpy)(pic)(H2O)](pic) (1) and [Cu2(oxpn)(Me2bpy)(pic)](pic) (2) [H2oxpn = N,N′-bis(3-aminopropyl)oxamide; Hpic = 2,4,6-trinitrophenol; bpy = 2,2′-bipyridine; Me2bpy = 4,4′-dimethyl-2,2′-bipyridine], have been synthesized and characterized by elemental analyses, conductivity measurements, IR, UV-visible spectroscopy and single crystal X-ray analyses. Both complexes have similar molecular structures. In complex 1, the central two Cu(II) atoms are bridged by cis-oxpn2− with the Cu1-Cu2 separation of 5.221 Å and the polyhedron of each copper atom is a square-pyramid. Similarly, complex 2 is a cis-oxpn2−-bridged binuclear complex with the Cu1-Cu2 separation of 5.196 Å. Cu1(II) central atom situated in a tetrahedral geometry is four-coordinated and Cu(II) atom situated in a square-pyramidal geometry is five-coordinated. Hydrogen bonding interactions and π-π stacking interactions link the binuclear copper complex 1 or 2 into a 2D infinite network. The antibacterial assays indicate that the two complexes showed better activities than their ligands. The interactions of the two binuclear complexes with herring sperm DNA (HS-DNA) have been studied by UV absorption titration, fluorescence titration and viscosity measurements. The results suggest that the two binuclear complexes bind to HS-DNA via an intercalative mode. 相似文献
20.
Two new organic-inorganic hybrid compounds, {[Cu(2,2′-bipy)2]2(Hbpy)[α-AlW12O40]}·H2O (1) and {[H2en][CuI(4,4′-bipy)]3(α-AlW12O40)}·4H2O (2) (2,2′-bipy = 2,2′-bipyridine, 4,4′-bipy = 4,4′-bipyridine, py = pyridine, en = ethylene dimine) based on Keggin-type α-[AlW12O40]5− polyoxoaions and transition-metal organoamine subunits, have been hydrothermally synthesized and characterized by elemental analysis, IR spectroscopy, thermal gravimetric analysis (TG), and single-crystal X-ray diffraction. In addition, the electrochemical properties and photocatalytic activity of compound 1 were studied. The structural analysis reveals that 1 shows a 1D infinite chain structure constructed from [α-AlW12O40]5− polyoxoanions and {[CuII(2,2′-bipy)2][CuII(2,2′-bipy)(py)]}4+ fragments, in which the remarkable aspect is that [α-AlW12O40]5− polyoxoanion is modified in a fascinating symmetrical mode. Compound 2 displays an unprecedented 2D extended structure constructed from [α-AlW12O40]5− polyoxoanions and 4,4′-bipy-CuI-4,4′-bipy linear chains, in which three - chain belts formed by three linear chains arranged Cu parallel connect alternately with [α-AlW12O40]5− polyoxoanions. As far as we know, compounds 1 and 2 represent the first 1D and 2D extended hybrid materials constructed from 3d transition metals and polyoxotungstoaluminates linked through covalent bonds. 相似文献