Synthesis and structure of Mn(II) and Zn(II) complexes containing 1,10-phenanthroline unit

The Mn(II) and Zn(II) complexes of N,N′-diisopropyl-1,10-phenanthroline-2,9-dimethanamine have been synthesised, and the structure of the two complexes have been studied by X-ray crystallography.     

Iron(II) and nickel(II) mixed-ligand complexes containing 1,10-phenanthroline and 4,7-diphenyl-1,10-phenanthroline

Two types of mixed-ligand complexes, i.e. [M(phen)2 (dip)]2+ and [M(phen)(dip)2]2+ (M = iron(II) and nickel(II); phen = 1,10-phenanthroline and dip = 4,7-diphenyl-1,10-phenanthroline) have been prepared from their related tris-complexes, [M(phen)3]2+ by ligand substitution, and isolated by semi-preparative HPLC. Elemental and chromatographic analyses confirm the purity of the isolated complexes while u.v./vis and i.r. spectra were used to identify and characterize them. 1H-n.m.r. and room temperature Mössbauer spectra of the iron(III) complexes were also measured and the results are discussed. In addition, our preliminary results on hypochromicity in the MLCT band and circular dihroism (CD) emerging in the u.v./vis region upon addition of CT(calf thymus)-DNA to the racemic complexes indicated that the iron(II) mixed-ligand complexes interact with CT-DNA.     

Cationic carbonyl complexes of ruthenium(II) and osmium(II) containing 2,2′-bipyridyl and 1,10-phenanthroline

Summary Reactions of ruthenium carbonyl complexes of the type [RuX₂(CO)(Ph₂RAs)₃] (X=Cl or Br; R=Me or Et) with 2,2-bipyridyl (bipy) and 1,10-phenanthroline (phen) in alcohol produce orange red cationic products of the formula [RuX(CO)(N-N)(Ph₂RAs)₂]ClO₄ (N-N=bipy or phen). Likewise, the hydridocarbonyls of ruthenium and osmium of the type [MHX(CO)(Ph₂RAs)₃] (M=Ru or Os) react with bipy and phen to yield yellow cationic complexes of the composition [(MH(CO)(N-N)(Ph₂RAs)₂]ClO₄. Structures have been assigned to all the complexes on the basis of i.r. and¹ H n.m.r. spectral data.     

Synthesis, structure, and substitution mechanism of new Ru(II) complexes containing 1,4,7-trithiacyclononane and 1,10-phenanthroline ligands

Two new Ru complexes containing the 1,10-phenanthroline (phen) and 1,4,7-trithiacyclononane ([9]aneS3, SCH2CH2SCH2CH2SCH2CH2) ligands of general formula [Ru(phen)(L)([9]aneS3)]2+ (L = MeCN, 3; L = pyridine (py), 4) have been prepared and thoroughly characterized. Structural characterization in the solid state has been performed by means of X-ray diffraction analyses, which show a distorted octahedral environment for a diamagnetic d6 Ru(II), as expected. 1H NMR spectroscopy provides evidence that the same structural arrangement is maintained in solution. Further spectroscopic characterization has been carried out by UV-vis spectroscopy where the higher acceptor capability of MeCN versus the py ligand is manifested in a 9-15-nm blue shift in its MLCT bands. The E1/2 redox potential of the Ru(III)/Ru(II) couple for 3 is anodically shifted with respect to its Ru-py analogue, 4, by 60 mV, which is also in agreement with a higher electron-withdrawing capacity of the former. The mechanism for the reaction Ru-py + MeCN--> Ru-MeCN + py has also been investigated at different temperatures with and without irradiation. In the absence of irradiation at 326 K, the thermal process gives kinetic constants of k2 = 1.4 x 10(-5) s(-1) (DeltaH(++) = 108 +/- 3 kJ mol(-1), DeltaS(++) = -8 +/- 9 J K(-1) mol(-1)) and k-2 = 2.9 x 10(-6) s(-1) (DeltaH(++) = 121 +/- 1 kJ mol(-1), DeltaS(++) = 18 +/- 3 J K(-1) mol(-1)). The phototriggered process is faster and consists of preequilibrium formation of an intermediate that thermally decays to the final Ru-MeCN complex with an apparent rate constant of (k1Khnu)app = 1.8 x 10(-4) s(-1) at 304 K, under the continuous irradiation experimental conditions used.     

ESI-MS studies of mixed-ligand Fe(II) complexes containing 1,10-phenanthroline and 1,10-phenanthroline-5,6-dione as ligands

In order to monitor the progression of the synthesis and the separation of novel mixed-ligand iron complexes containing 1,10-phenanthroline, 1,10-phenanthroline-5,6-dione, and NCS- as ligands all products were mass analyzed by electrospray ionization ion trap MS/MS. The spectra of methanol (MeOH), acetonitrile (ACN), water, and ethanol (EtOH) solutions were collected and the results were compared. It was detected under applied electrospray ionization mass spectrometry (ESI-MS) conditions that MeOH, water, and EtOH formed solvent clusters around the free or complexed 1,10-phenanthroline-5,6-dione. Owing to the solvent-ligand hydrogen-bond formation, the solvent-ligand clusters were formed in the polar protic solvents. The number of protic solvent molecules per complex ion in cluster depended on the number of 1,10-phenanthroline-5,6-dione ligands in the complex ion. Unlike MeOH, EtOH, or water, ACN was not involved in the formation of the solvent clusters with the iron complexes containing 1,10-phenanthroline-5,6-dione as ligand. We also showed that the NCS- group under certain solvent conditions served as a bidentate ligand.     

Platinum(II) 1,10-phenanthroline complexes of acetylides containing redox-active groups

The new diimine ligand 3,8-di-n-pentyl-4,7-di(phenylethynyl)-1,10-phenanthroline (1) was used for the synthesis of a range of Pt(II) complexes, viz.[Pt(1)Cl2], [Pt(1)(C triple bond C-Ph)2], [Pt(1)(C triple bond C-Fc)2] and [Pt(1)(C triple bond C-p-C6H4-C triple bond C-Fc)2](Fc = ferrocenyl). Crystal structure analyses were performed for [Pt(1)Cl2] and [Pt(1)(C triple bond C-Ph)2] and revealed that the di(acetylide)pi-tweezer of the latter binds a molecule of chloroform through C-H...pi hydrogen bonds. The redox and optical properties of 1 and its complexes were investigated by (spectro-)electrochemistry, UV-Vis and luminescence spectroscopy, and an energy level diagram was derived for [Pt(1)(C triple bond C-Fc)2] and related compounds on the basis of the data collected. The ferrocenyl-substituted Pt(II) complexes are donor-sensitiser assemblies. Intramolecular quenching of the photoexcited Pt(II) diimine unit leads to very short luminescence lifetimes for [Pt(1)(C triple bond C-p-C(6)H(4)-C triple bond C-Fc)2](2 ns) and [Pt(1)(C triple bond C-Fc)2](0.3 ns), as opposed to [Pt(1)(C triple bond C-Ph)2](0.7 micros). Excimer formation has been observed for [Pt(1)(C triple bond C-Ph)(2)] at room temperature in dichloromethane and at low temperatures in frozen glassy dichloromethane and 2-methyltetrahydrofuran solution, but not in the solid state.     

Oligothiophene-2-yl-vinyl bridged mono- and binuclear ruthenium(II) tris-bipyridine complexes: Synthesis, photophysics, electrochemistry and electrogenerated chemiluminescence

A series of mono- and binuclear ruthenium(II) tris-bipyridine complexes tethered to oligothienylenevinylenes have been synthesized and characterized by ¹H NMR, ¹³C NMR and TOF-MS spectrometry. Photophysics, electrochemistry and electrogenerated chemiluminescence (ECL) properties of these complexes are investigated. The electronic absorption spectra of the mononuclear ruthenium complexes show a significant red shift both at MLCT (metal-to-ligand charge transfer) and π-π^∗ transitions of oligothienylenevinylenes with increase in the number of thiophenyl-2-yl-vinyl unit. For the binuclear complexes these two absorption bands are overlapped. All the metal complexes have very weak emission compared to that of the reference complex Ru(bpy)²⁺₃. The first reduction potentials of all mononuclear ruthenium complexes are less negative than that of Ru(bpy)²⁺₃, due to the moderate electron-withdrawing effect of oligothienylenevinylenes. For binuclear ruthenium complexes, only one Ru(II/III) oxidation peak (E_1/2 = 0.96 V vs. Ag/Ag⁺) was observed, suggesting a weak interaction between two metal centers. Three successive reduction processes of bipyridine ligands are similar among all ruthenium complexes except for RuTRu, which has a very sharp peak owing to the accumulation of neutral product on the electrode surface. All these ruthenium complexes exhibited different ECL property in CH₃CN solution without any additional reductant or oxidant. For three mononuclear ruthenium complexes, the ECL intensity strengthens with increase in the number of thiophene-2-yl-vinyl unit. However, the ECL efficiency dramatically decreased in the binuclear ruthenium complexes. The ECL efficiencies of all the reported complexes do not exceed that of Ru(bpy)²⁺₃, where the ECL efficiency decreases in the order of RuTRu > Ru3T > Ru2T > RuT > Ru2TRu (RuT,bis-2,2′-bipyridyl-(4-methyl-4′-(2-thienylethenyl)-2,2′-bipyridine) ruthenium dihexafluorophosphate; Ru2T, bis-2,2′-bipyridyl-(4-methyl-4′-{(E)-2-[5-((E)-2-thienylethenyl)-thienylethenyl]}-2,2′-bipyridine) ruthenium dihexafluorophosphate; Ru3T, bis-2,2′-bipyridyl-(4-methyl-4′-{(E)-2-{(E)-2-[5-((E)-2-thienylethenyl)-thienylethenyl]}}-2,2′-bipyridine) ruthenium dihexafluorophosphate; RuTRu, bis-2,2′-bipyridyl-ruthenium-bis-[2-((E)-4′-methyl-2, 2′-bipyridinyl-4)-ethenyl]-thienyl-bis-2,2′-bipyridyl-ruthenium tetrahexafluorophosphate; Ru2TRu, bis-2,2′-bipyridyl-ruthenium-(E)-1,2-bis-{2-[2-((E)-4′-methyl-2,2′-bipyridinyl-4)-ethenyl]-thienyl}-ethenyl-bis-2,2′-bipyridyl-ruthenium tetrahexafluorophosphate).     

Synthesis,structure and luminescent properties of zinc(II) and Hg(II) complexes with substituted 1,10-phenanthroline

Two d¹⁰ group 12 metal complexes, 2-(2-methoxyphenyl)-1,10-phenanthroline zinc dichloride (2a) and 2-(2-methoxyphenyl)-1,10-phenanthroline mercury dichloride (2b) were synthesized and characterized by IR, ¹H and ¹³C NMR as well as elemental analysis. Structure of 2b in the solid state was determined by single-crystal X-ray crystallography, revealing that 2b is four-coordinate in a distorted tetrahedral geometry with the methoxy group uncoordinated. Luminescent properties of 2a and 2b in solution and the solid state were studied.     

Redox properties of bis(1,10-phenanthroline)-(pyridine)ruthenium(II) complexes

The redox properties of a series of [Ru(phen)₂(py)X]ⁿ⁺ cations (X = pyridine, NH₃, Cl, Br, I, CN, SCN, N₃ and NO₂) have been investigated in acctonitrile. Two reversible reduction steps are seen at ? 1.35 and ? 1.6 V vs Ag/AgCl; the invariance of these processes with X-group is indicative of electron addition to molecular orbitals mainly of phenanthroline ligand π^* origin. Irreversible multi-electron reductions follow below ? 2.20 V. The Ru(II)/Ru(III) couple is seen as a reversible wave near + 0.8 V vs the normal hydrogen electrode, from calibration with ferrocene, except in the cases of the NO₂ and SCN complexes, where rapid reactions involving these ligands occur.     

Electrochemical behaviour of dicyanobis(2,2′-bipyridine) ruthenium(II) and dicyanobis(1,10-phenanthroline) ruthenium(II) complexes

The electrochemical behaviour of Ru(bipy)₂(CN)₂ and Ru(phen)₂(CN)₂ (bipy=2,2′-bipyridine; phen=1,10-phenanthroline) has been investigated in dimethylformamide. Both complexes exhibit one oxidation wave and three reduction waves. In the case of Ru(bipy)₂-(CN)₂ the anodic process and the first two cathodic processes involve one electron and are reversible in the time scale of polarographic and cyclic voltammetric experiments. The third reduction step is irreversible and has been attributed to the addition of three electrons to Ru(bipy)₂(CN)₂ followed by liberation of one or more ligands and reduction of liberated bipyridine. The features of the redox processes for the Ru(phen)₂(CN)₂ are similar to those found for the bipy complex except for the first reduction wave, which is complicated by adsorption phenomena. A qualitative MO discussion of the redox processes is also reported.     

Synthesis, characterization and photophysics of bimetallic manganese(I) and ruthenium(II) complexes

A series of new manganese(I) and ruthenium(II) monometallic and bimetallic complexes made of 2,2′-bipyridine and 1,10-phenanthroline ligands, [Mn(CO)₃(NN)(4,4′-bpy)]⁺, [{(CO)₃(NN)Mn}₂(4,4′-bpy)]²⁺ and [(CO)₃(NN)Mn(4,4′-bpy)Ru(NN)₂Cl]²⁺ (NN = 2,2′-bipyridine, 1,10-phenanthroline; 4,4′-bpy = 4,4′-bipyridine) are synthesized and characterized, in addition to already known ruthenium(II) complexes [Ru(NN)₂Cl(4,4′-bpy)]⁺ and [Cl(NN)₂Ru(4,4′-bpy)Ru(NN)₂Cl]²⁺. The electrochemical properties show that there is a weak interaction between two metal centers in Mn–Ru heterobimetallic complexes. The photophysical behavior of all the complexes is studied. The Mn(I) monometallic and homobimetallic complexes have no detectable emission. In Mn–Ru heterobimetallic complexes, the attachment of Mn(I) with Ru(II) provides interesting photophysical properties.     

Synthesis,characterization, electrochemistry,catalytic, and antimicrobial studies of ruthenium(III) complexes containing ONO donor ligands

A series of ruthenium(III) complexes [RuX(EPh₃)₂L] (where X = Cl or Br; E = P or As; L = deprotonated dibasic tridentate ligand) were prepared by the reaction of [RuX₃(EPh₃)₃] with Schiff bases (H₂L¹–H₂L⁴). The ligands were prepared by the condensation of N-4 phenyl/methyl semicarbazide with o-vanillin/o-hydroxy acetophenone. The complexes were characterized by elemental, physico-chemical, and electrochemical methods. Catalytic studies of these complexes for the oxidation of alcohols and aryl–aryl coupling were carried out. Antimicrobial experiments were also carried out.     

Cobalt(III), nickel(II) and ruthenium(II) complexes of 1,10-phenanthroline family of ligands: DNA binding and photocleavage studies

DNA binding and photocleavage characteristics of a series of mixed-ligand complexes of the type [M(phen)₂LL]ⁿ⁺ (where M = Co(III), Ni(II) or Ru(II), LL = 1,10-phenanthroline (phen), phenanthroline-dione (phen-dione) or dipyridophenazine (dppz) andn = 3 or 2) have been investigated in detail. Various physico-chemical and biochemical techniques including UV/Visible, fluorescence and viscometric titration, thermal denaturation, and differential pulse voltammetry have been employed to probe the details of DNA binding by these complexes; intrinsic binding constants (K _b) have been estimated under a similar set of experimental conditions. Analysis of the results suggests that intercalative ability of the coordinated ligands varies as dppz>phen>phen-dione in this series of complexes. While the Co(II) and Ru(II) complexes investigated in this study effect photocleavage of the supercoiled pBR 322 DNA, the corresponding Ni(II) complexes are found to be inactive under similar experimental conditions. Results of detailed investigations carried out inquiring into the mechanistic aspects of DNA photocleavage by [Co(phen)₂(dppz)]³⁺ have also been reported.     

Synthesis, characterization and photophysics of alkyne bridged bimetallic rhenium(I) and ruthenium(II) complexes

Six new homobimetallic and heterobimetallic complexes of rhenium(I) and ruthenium(II) bridged by ethynylene spacer [(CO)₃(bpy)Re(BL)Re(bpy)(CO)₃]²⁺ [Cl(bpy)₂Ru(BL)Ru(bpy)₂Cl]²⁺ and [(CO)₃(bpy)Re(BL)Ru(bpy)₂Cl]²⁺ (bpy = 2,2′-bipyridine, BL = 1,2-bis(4-pyridyl)acetylene (bpa) and 1,4-bis(4-pyridyl)butadiyne (bpb) are synthesized and characterized. The electrochemical and photophysical properties of all the complexes show a weak interaction between two metal centers in heterobimetallic complexes. The excited state lifetime of the complexes is increased upon introduction of ethynylene spacer and the transient spectra show that this is due to delocalization of electron in the bridging ligand. Also, intramolecular energy transfer from *Re(I) to Ru(II) in Re–Ru heterobimetallic complexes occurs with a rate constant 4 × 10⁷ s⁻¹.     

Synthesis,structure, and luminescent properties of lanthanide complexes containing 1,10-phenanthroline and perfluorinated 2-mercaptobenzothiazolate ligands

Mononuclear terbium and erbium complexes of the composition Ln(mbt^F)₃phen and the dinuclear complex Tb₂(mbt^F)₄(OH)₂(phen)₂ (mbt^F is 4,5,6,7-tetrafluoro-2-mercaptobenzothiazolate, phen is 1,10-phenanthroline) were synthesized. The structures of the complexes Er(mbt^F)₃phen and Tb₂(mbt^F)₄(OH)₂(phen)₂ were determined by X-ray diffraction. In the solid state, the terbium and erbium complexes exhibit intense metal-centered photoluminescence. Based on the complexes Ln(mbt^F)₃phen, double-layer organic light-emitting diodes (OLEDs) were assembled. These OLEDs exhibit electroplex emission with a band maximum at 630 nm.     

Synthesis and magnetic properties of novel containing 1,10-phenanthroline polymeric complexes

The polymer (DAPcTPA) was synthesized by polycondensation of 5,6-diamine-1,10-phenanthroline (DAP) with terephthaldehyde (TPA). Three polymeric complexes were first prepared from polymer (DAPcTPA) and NiSO₄, CoCl₂ or FeSO₄, respectively. The structures of polymer and complexes were characterized by IR, ¹H NMR spectra and elemental analysis. The magnetic behavior of these complexes was measured as a function of magnetic field strength (0-50 kOe) at 5 K and as a function of temperature (5-300 K) at a magnetic field strength of 30 kOe. The results show that DAPcTPA-Ni²⁺ and DAPcTPA-Co²⁺ are soft ferromagnets, while DAPcTPA-Fe²⁺ exhibits features of an antiferromagnet.     

Synthesis,characterization and biocidal studies of ruthenium(II) carbonyl complexes containing tetradentate Schiff bases

Stable ruthenium(II) complexes of Schiff bases have been prepared by reacting [RuHCl(CO)(PPh₃)₂(B)] (B = PPh₃, pyridine or piperidine) with bis(o-vanillin)ethylenediimine (valen), bis(o-vanillin)propylene-diimine (valpn), bis(o-vanillin)tetramethylenediimine (valtn), bis(o-vanillin)o-phenylenediimine (valphn), bis(salicylaldehyde)tetramethylenediimine (saltn) and bis(salicylaldehyde)o-phenylenediimine (salphn). These complexes have been characterised by elemental analyses, i.r., electronic, ¹H- and ³¹P{¹H}-n.m.r. spectral studies. In all the above reactions, the Schiff bases replace two molecules of Ph₃P, a hydride and a halide ion from the starting complexes, indicating that the Ru–N bonds present in the complexes containing heterocyclic nitrogen bases are stronger than the Ru–P bond to Ph₃P. The new complexes of the general formula [Ru(CO)(B)(L)] (B = PPh₃, py or pip; L = tetradentate Schiff bases) have been assigned an octahedral structure. Some of the Schiff bases and the new complexes have been tested against the pathogenic fungus Fusarium sp.