Reaction of [CpRu(CH3CN)3]PF6 with bidentate ligands: structural characterization of [{CpRu(CH3CN)2}2(μ-η-dppe)](PF6)2 [dppe=1,2-bis(diphenylphosphino)ethane]

The reaction of [CpRu(CH₃CN)₃]PF₆ with the bidentate ligands L-L=1,2-bis(diphenylphosphino)ethane, dppe, and (1-diphenylarsino-2-diphenylphosphino)ethane, dpadppe, affords mononuclear or dinuclear complexes of formula [CpRu(η²-L-L)(CH₃CN)]PF₆, [{CpRu(CH₃CN)₂}₂(μ-η^1:1-L-L)](PF₆)₂ and [{CpRu(CH₃CN)}₂(μ-η^1:1-L-L)₂](PF₆)₂ (L-L=dppe, dpadppe). All of the compounds are characterized by microanalysis and NMR [¹H and ³¹P{¹H}] spectroscopy. The crystal structure of [{CpRu(CH₃CN)₂}₂(μ-η^1:1-dppe)](PF₆)₂ has been determined by X-ray diffraction analysis. The complex exhibits a dppe ligand bridging two CpRu(CH₃CN)₂ fragments.     

Electropolymerization of [Ru(bpy)(CO)2Cl2] (bpy=2,2′-bipyridine: a revisited trans versus cis(Cl) isomeric influence study

The mono-bipyridine bis carbonyl complex [Ru(bpy)(CO)₂Cl₂] exists in two stereoisomeric forms having a trans(Cl)/cis(CO) (1) and cis(Cl)/cis(CO) (2) configuration. In previous work we reported that only the trans(Cl)/cis(CO) isomer 1 leads by a two-electron reduction to the formation of [Ru(bpy)(CO)₂]_n polymeric film on an electrode surface. This initial statement was overstated, as both isomers allowed the build up of polymers. A detailed comparison of the electropolymerization of both isomers is reported here, as well as the reduction into dimers of parent stereoisomer [Ru(bpy)(CO)₂(C(O)OMe)Cl] complexes 3 and 4 obtained as side products during the synthesis of 1 and 2.     

An easy electrochemical procedure for tailoring thin films containing the [Fe(bpy)2(CH3CN)2] and/or [Fe(bpy)3]-like cores (bpy=2,2-bipyridine). Application to the design of a modified electrode with a supramolecular structure

A simple electrochemical procedure to tailor thin polymeric films containing the [Fe^II(bpy)₂(CH₃CN)₂]²⁺ and/or [Fe^II(bpy)₃]²⁺-like cores have been described (bpy=2,2^′-bipyridine). The procedure is based on the electroreductive precipitation of soluble polymers prepared in situ in CH₃CN by mixing Fe³⁺ ions and a bis bipyridyl ligand, (chiragen: chir). In the resulting [Fe^II(chir)(CH₃CN)₂]_n²⁺ films, the two labile S ligands can be easily replaced by a bidentate ligand. This method has been applied with success to design a modified electrode with a supramolecular structure.     

Electrochemical behaviour of [Ru(L)(CO)2Cl2] [Ru(L)(CO)Cl3][Me4N] and [Ru(L)(CO)2(CH3CN)2][CF3SO3]2 complexes (L = 2,2′- bipyridine or 4,4′-isopropoxycarbonyl-2,2′-bipyridine)

The clectrochemical behaviour of the complexes [Ru^II(L)(CO)₂Cl₂], [Ru^II(L)(CO)Cl₃][Me₄N] and [Ru^II(L)(CO)₂(CH₃CN)₂][CF₃SO₃]₂ (L = 2,2′-bipyridine or 4,4′-isopropoxycarbonyl-2,2′-bipyridine) has been investigated in CH₃CN. The oxidation of [Ru(L)(CO)₂Cl₂] produces new complexes [Ru^III(L)(CO)(CH₃CN)₂Cl]²⁺ as a consequence of the instability of the electrogenerated transient Ru^III species [Ru^III(L)(CO)₂Cl₂]⁺. In contrast, the oxidation of [Ru^II(L)(CO)Cl₃][Me₄N] produces the stable [Ru^III(L)(CO)Cl₃] complex. In contrast [Ru^II(L)(CO)₂(CH₃CN)₂][CF₃SO₃]₂ is not oxidized in the range up to the most positive potentials achievable. The reduction of [Ru^II(L)(CO)₂Cl₂] and [Ru^II(L)(CO)₂(CH₃CN)₂][CF₃SO₃]₂ results in the formation of identical dark blue strongly adherent electroactive films. These films exhibit the characteristics of a metal-metal bond dimer structure. No films are obtained on reduction of [Ru^II(L)(CO)Cl₃][Me₄N]. The effect of the substitution of the bipyridine ligand by electron-withdrawing carboxy ester groups on the electrochemical behaviour of all these complexes has also been investigated.     

Preparation and structural characterization of [RuCl2(CO)2{Te(CH2SiMe3)2}2] and [RuCl2(CO){Te(CH2SiMe3)2}3]

The objective of the present work was to synthesize mononuclear ruthenium complex [RuCl₂(CO)₂{Te(CH₂SiMe₃)₂}₂] (1) by the reaction of Te(CH₂SiMe₃)₂ and [RuCl₂(CO)₃]₂. However, the stoichiometric reaction affords a mixture of 1 and [RuCl₂(CO){Te(CH₂SiMe₃)₂}₃] (2). The X-ray structures show the formation of the cis(Cl), cis(C), trans(Te) isomer of 1 and the cis(Cl), mer(Te) isomer of 2. The ¹²⁵Te NMR spectra of the complexes are reported. The complex distribution depends on the initial molar ratio of the reactants. With an excess of [RuCl₂(CO)₃]₂ only 1 is formed. In addition to the stoichiometric reaction, a mixture of 1 and 2 is observed even when using an excess of Te(CH₂SiMe₃)₂. Complex 1 is, however, always the main product. In these cases the ¹²⁵Te NMR spectra of the reaction solution also indicates the presence of unreacted ligand.     

Crystal structures of [Ru(terpy)(HPB)(H2O)](PF6)2 and [Ru(terpy)(HPB)(2-picoline)](PF6) and the kinetics studies of the aqua ligand substitution by pyridine and substituted pyridines

The crystal structures of [Ru(terpy)(HPB)(H₂O)](PF₆)₂, 1, and [Ru(terpy)(HPB)(2-picoline)](PF₆), 2, (where terpy = 2,2′:6′,2′′-terpyridine and HPB = 2-(2′-hydroxyphenyl)-benzoxazole) have been determined. Both structures show slightly distorted octahedral coordination around the ruthenium center. In complex 1, the imine nitrogen of the HPB ligand occupies an axial position and is trans to the aqua ligand whereas in complex 2, the imine nitrogen is trans to the nitrogen of the 2-picoline ligand. The Ru-N(2-picoline) bond distance is much longer than the other Ru-N bonds in the complex due to steric effects from the methyl group of 2-picoline. In both complexes, the phenolate oxygen of the HPB ligand is in the equatorial position and trans to the center nitrogen of the terpyridine. The reaction of [Ru(terpy)(HPB)(H₂O)](PF₆)2 with pyridine and its analogs, 2-picoline and 4-picoline in dichloromethane was monitored spectrophotometrically. There is an initial reduction of the [Ru(III)-H₂O] complex to [Ru(II)-H₂O] complex prior to the substitution of the aqua ligand. The values of the activation parameters indicate that the substitution of the aqua ligand by pyridine, 2-picoline and 4-picoline follow an associative mechanism.     

Structural studies on supramolecular adducts of cyclodextrins with the complex [Ru([9]aneS3)(bpy)Cl]Cl

The complex [Ru([9]aneS₃)(bpy)Cl]Cl (bpy = 2,2′-bipyridine) was immobilised in plain β-cyclodextrin (β-CD) and permethylated β-CD (TRIMEB) to yield two adducts with a 1:1 host:guest stoichiometry. The adducts were studied by powder X-ray diffraction (XRD), thermogravimetric analysis (TGA), ¹³C{¹H} CP/MAS NMR and vibrational spectroscopy (FT-IR and Raman). Results support the formation of stable supramolecular adducts with a proposed geometry in which the coordinated bypiridine fragment of the guest is partially included in the host cavities, and the bulky [9]aneS₃ fragment protrudes out to the interstitial spaces. A packing mode is proposed for [Ru([9]aneS₃)(bpy)Cl]Cl · TRIMEB, obtained by Monte Carlo optimisation of the XRD data. TRIMEB molecules are stacked in tilted channels, with the voluminous part of the guest molecules in the inter-channel space. The behaviour of [Ru([9]aneS₃])(bpy)Cl]Cl upon CD encapsulation and the chloride ligand hydrolysis process in solution for all compounds were studied in detail by Raman spectroscopy.     

Synthesis and crystal structure of [Ru8(μ5-S)2(μ4-S)(μ3-S)(μ-CNMe2)2(μ-CO)(CO)15] formed via the double sulphur-carbon bond cleavage of dithiocarbamate ligands

Heating cis-[Ru(S₂CNMe₂)₂(CO)₂] and [Ru₃(CO)₁₂] in xylene affords octanuclear [Ru₈(μ₅-S)₂(μ₄-S)(μ₃-S)(μ-CNMe₂)₂(μ-CO)(CO)₁₅] resulting from the double carbon-sulfur bond cleavage of two dithiocarbamate ligands. The structure consists of a tri-edge-bridged square of ruthenium atoms with a further ruthenium atom being bound only to the central bridging atom. Studies suggest that it may be formed via the pentanuclear intermediate [Ru₅(μ₄-S)₂(μ-CNMe₂)₂(CO)₁₁] which is formed in trace amounts.     

The reactions of 2-benzoylpyridine with [RuHCl(CO)(PPh3)3] and [(C6H6)RuCl2]2

The reactions of [RuHCl(CO)(PPh₃)₃] and [(C₆H₆)RuCl₂]₂ with 2-benzoylpyridine have been examined, and two novel ruthenium(II) complexes – [RuCl(CO)(PPh₃)₂(C₅H₄NCOO)] and [RuCl₂(C₁₂H₉NO)₂] – have been obtained. The compounds have been studied by IR and UV–Vis spectroscopy, and X-ray crystallography. The molecular orbital diagrams of the complexes have been calculated with the density functional theory (DFT) method. The spin-allowed singlet–singlet electronic transitions of the compounds have been calculated with the time-dependent DFT method, and the UV–Vis spectra of the compounds have been discussed on this basis.     

Reactions of Ru3(CO)12 with Ene-yne and Alkoxy-silyl Functionalized Compounds. The Crystal Structure of (μ-H)Ru3(CO)9[μ3-η2-HC=N(CH2)3Si(OEt)3]

Ru₃(CO)₁₂ has been reacted with the compounds hex-1-en-3-yne [EtC≡CCH=CH₂], 2-methyl-hex-1-en-3-yne [EtC≡CC(=CH₂)CH₃] and with 3(ethoxy-silyl)propyl isocyanate [(EtO)₃Si(CH₂)₃NCO] and the compound tb [(EtO)₃Si(CH₂)₃NHC(=O)OCH₂C≡CCH₂OC(=O)NH(CH₂)₃Si(OEt)₃] in hydrocarbon solution. Some reactions in CH₃OH/KOH solution (followed by acidification) have also been performed. The main products of the reactions with ene-ynes are the clusters Ru₃(CO)₆(μ-CO)₂L₂ (L = C₆H₈, C₇H₁₀) and their demolition products, the “ferrole” Ru₂(CO)₆L₂ complexes. One of the isomers of Ru₃(CO)₆(μ-CO)₂L₂, and Ru₂(CO)₆L₂ (L = C₇H₁₀) have been reacted with vinyl-triethoxysilane [(EtO)₃SiCH=CH₂]: these reactions did not afford complexes containing new carbon–carbon bonds or triethoxy-silyl groups. Only polymerization of vinyl-triethoxysilane occurred. The reactions of Ru₃(CO)₁₂ with triethoxysilyl-propyl-isocyanate and tb (in the presence of Me₃NO) lead to the same products, that is the isomeric complexes (μ-H)Ru₃(CO)₉[C=N(H)(CH₂)₃Si(OEt)₃] with a “perpendicular” ligand (complex 3, as proposed on the basis of spectroscopic results) and (μ-H)Ru₃(CO)₉[HC=N(CH₂)₃Si(OEt)₃] with a “parallel” ligand (complex 4, as confirmed by a X-ray analysis). The reaction pathways leading to these products are discussed. Complex 4 has been reacted with tetraethyl orthosilicate and the resulting material has been characterized. These reactions are part of a study on the synthesis of inorganic-organometallic materials through sol–gel techniques. This paper is dedicated to Prof. Gunther Schmid in the occasion of his 70th birthday.     

Trifluoroacetylacetonate rhodium(III) methyl complexes, cis-[Rh(TFA)(PPh3)2(CH3)(L)][BPh4] and cis-[Rh(TFA)(PPh3)2(CH3)(I)] (L = CH3CN, NH3, pyridine), in comparison with their acetylacetonate analogs

The oxidative addition of CH₃I to planar rhodium(I) complex [Rh(TFA)(PPh₃)₂] in acetonitrile (TFA is trifluoroacetylacetonate) leads to the formation of cationic, cis-[Rh(TFA)(PPh₃)₂(CH₃)(CH₃CN)][BPh₄] (1), or neutral, cis-[Rh(TFA)(PPh₃)₂(CH₃)(I)] (4), rhodium(III) methyl complexes depending on the reaction conditions. 1 reacts readily with NH₃ and pyridine to form cationic complexes, cis-[Rh(TFA)(PPh₃)₂(CH₃)(NH₃)][BPh₄] (2) and cis-[Rh(TFA)(PPh₃)₂(CH₃)(Py)][BPh₄] (3), respectively. Acetylacetonate methyl complex of rhodium(III), cis-[Rh(Acac)(PPh₃)₂(CH₃)(I)] (5), was obtained by the action of NaI on cis-[Rh(Acac)(PPh₃)₂(CH₃)(CH₃CN)][BPh₄] in acetone at −15 °C. Complexes 1-5 were characterized by elemental analysis, ³¹P{¹H}, ¹H and ¹⁹F NMR. For complexes 2, 3, 4 conductivity data in acetone solutions are reported. The crystal structures of 2 and 3 were determined. NMR parameters of 1-5 and related complexes are discussed from the viewpoint of their isomerism.     

Cyclometalated N,N-dimethylbenzylamine ruthenium(II) complexes [Ru(C6HRRR-o-CH2NMe2)(bpy)(RCN)2]PF6 for bioapplications: synthesis, characterization, crystal structures, redox properties, and reactivity toward PQQ-dependent glucose dehydrogenase

Cyclometalated derivatives of ring-substituted N,N-dimethylbenzylamines with controlled redox potentials as potent mediators of bioelectrochemical electron transport are reported. The cycloruthenation of R¹R²R³C₆H₂CH₂NMe₂ (R¹, R², R³ = H, Me, ^tBuO, MeO, NMe₂, F, CF₃, CN, NO₂) by [(η⁶-C₆H₆)RuCl(μ-Cl)]₂ in the presence of NaOH/KPF₆ in acetonitrile or pivalonitrile affords cyclometalated complexes [(η⁶-C₆H₆)Ru(C₆HR¹R²R³-o-CH₂NMe₂)(RCN)]PF₆ [R = Me (1) and R = CMe₃ (2)] in good yields. Reactions of complexes 1 and 2 with 2,2′-bipyridine (bpy) in acetonitrile or pivalonitrile result in dissociation of η⁶-bound benzene and the formation of [Ru(C₆HR¹R²R³-o-CH₂NMe₂)(bpy)(RCN)₂]PF₆ [R = Me (3) and R = CMe₃ (4)]. All new compounds have been fully characterized by mass spectrometry, ¹H/¹³C NMR, and IR spectroscopy. An X-ray crystal structural investigation of complex 1 (R¹/R²/R³ = H/H/H) and two complexes of type 3 (R¹/R²/R³ = MeO/H/H, MeO/MeO/H) has been performed. Acetonitrile ligands of 3 are mutually cis and the σ-bound carbon is trans to one of the bpy nitrogens. Measured by the cyclic voltammetry in MeOH as solvent, the redox potentials of complexes 3 for the Ru^II/III feature cover the range 320-720 mV (versus Ag/AgCl) and correlate linearly with the Hammett constants. Complexes 3 mediate efficiently the electron transport between the active site of PQQ-dependent glucose dehydrogenase (PQQ = pyrroloquinoline quinone) and a glassy carbon electrode. Determined by cyclic voltammetry the second order rate constant for the oxidation of the reduced (by d-glucose) enzyme active site by Ru^III derivative of 3 (R¹/R²/R³ = H) (generated electrochemically) is as high as 4.8 × 10⁷ M⁻¹ s⁻¹ at 25 °C and pH 7.     

The reactions between [RuHCl(CO)(PPh3)3] and quinoline carboxylic acids

The reactions of [RuHCl(CO)(PPh₃)₃] with 8-hydroxy-2-methyl-quinoline-7-carboxylic acid and quinoline-2-carboxylic acid have been examined, and two novel ruthenium(II) complexes – [(PPh₃)₂RuH(CO)(C₁₀H₈NO₃)] and [(PPh₃)₂RuCl(CO)(C₉H₆O₂)] – have been obtained. The compounds have been studied by IR and UV–Vis spectroscopy, and X-ray crystallography. The molecular orbital diagrams of the complexes have been calculated with the density functional theory (DFT) method. The spin-allowed singlet–singlet electronic transitions of the compounds have been calculated with the time-dependent DFT method, and the UV–Vis spectra of the compounds have been discussed on this basis.     

Protonolysis of the PtC bond in trans-[PtH(CH2CN)(PPh3)2]

The protonolysis of the PtC bond in trans-[PtH(CH₂CN)(PPh₃₂] in methanol/1,2- dichloroethane is shown to take place by a two step mechanism involving oxidative addition to the metal center followed by reductive elimination of CH₃CN to give trans-[PtHCl(PPh₃)₂].     

Synthesis and Structural Characterization of Manganese Carbonyl Incorporated Polyoxomolybdate （n-Bu4N）2 [Mo6O16（OCH3）2 {HOCH2C（CH2O）3}2 {Mn（CO）3}2]

The polyoxoanion incorporated {Mn（CO）3^＋} complex, （n-Bu4N）2[Mo6O16（OCH3）2{HOCH2C（CH2O）3}2·{Mn（CO）3}2]（1）, has been synthesized by the reaction of （n-Bu4N）4[Mo8O26] with Mn（CO）5Br in methanol, in the presence of C（CH2OH）4. The complex 1 has been characterized by IR, UV-Vis, X-ray single crystal diffraction, and TG. Crystal data for the complex 1：C25H48MnMo3NO16 （1）, Triclinic Pi, a=0.9405（3） nm, b=1.3351（4） nm, c=1.5455（4） nm, α=103.206（5）°, β=102.165（5）°, γ=100.784（5）°, V=1.7896（9） nm^3, Z=2, R1=0.0703, wR2= 0.1495. The structure analysis of complex 1 shows that the complex consists of two tetrabutylammonium cations and a polyoxomolybdate anion that incorporates two fac-Mn（CO）3^＋ units. The anion of complex 1 can be considered as the dimer of two rhomb-like anions by sharing of two comers.     

A New Paramagnetic Pd(dmit)2 Salt: Tris(2,2′-Bipyridine)Nickel(II) Bis(1,3-Dithiole-2-Thione-4,5-Dithiolato)Palladate(II) Mono-Acetonitrile; [Ni(bpy)3][Pd(dmit)2]·CH3CN

Combination of the [Ni(bpy)₃]²⁺ cation complex and the [Pd(dmit)₂]⁻ anion (dmit=C₃S₅²⁻=1,3-dithiole-2thione-4,5-dithiolate) has resulted in the paramagnetic [Ni(bpy)₃][Pd(dmit)₂]·CH₃CN compound, a suitable precursor for a molecular magnetic conductor. Its crystal structure consists of a Pd(dmit)₂ anion arrangement that is quite different from segregated stack layers often found for M(dmit)₂−based compounds. The reduction of the [Pd(dmit)₂]^- to the 2− charged anion in the title compound most probably is the result of a charge disproportionation between Pd(dmit)₂ anions.     

Synthesis of [Ru(CO)2(PPh3)(SP)] and [Ru(CO)(PPh3)2(SP)] and their catalytic activities for the hydroamination of phenylacetylene

The reaction of [Ru(CO)₂(PPh₃)₃] (1) with o-styryldiphenylphophine (SP) (2) gave [Ru(CO)₂(PPh₃)(SP)] (3) in 83% yield. This styrylphosphine ruthenium complex 3 can also be synthesized by the reaction of [Ru(p-MeOC₆H₄NN)(CO)₂(PPh₃)₂]BF₄ (4) with NaBH₄ and 2 in 50% yield. When “Ru(CO)(PPh₃)₃” generated by the reaction of [RuH₂(CO)(PPh₃)₃] (8) with trimethylvinylsilane reacted with 2, [Ru(CO)(PPh₃)₂(SP)] (10) was produced in moderate yield as an air sensitive solid. The spectral and X-ray data of these complexes revealed that the coordination geometries around the ruthenium center of both complexes corresponded to a distorted trigonal bipyramid with the olefin occupying the equatorial position and the C-C bonding in the olefin moiety in 3 and 10 contained a significant contribution from a ruthenacyclopropane limiting structure. Complexes 3 and 10 showed catalytic activity for the hydroamination of phenylacetylene 11 with aniline 12. Ruthenium complex 3 in the co-presence of NH₄PF₆ or H₃PW₁₂O₄₀ proves to be a superior catalyst system for this hydroamination reaction. In the case of the reaction using H₃PW₁₂O₄₀ as an additive, ketimines (13) was obtained in 99% yield at a ruthenium-catalyst loading of 0.1 mol%. Some aniline derivatives such as 4-methoxy, 4-trifluoromethyl-, and 4-bromoanilines can also be used in this hydroamination reaction.     

Complete investigation on the synthesis of [Ru(bpydip)Cl2]: the nonformation of cis isomer

Complexation between the Schiff base N₄-tetradentate N,N′-bis(7-methyl-2-pyridylmethylene)-1,3-diiminopropane (bpydip) and ion Ru(II) occurs only in trans geometry. However, it is known that the most complex of these ligands with ruthenium present predominantly cis geometry. In order to clarify the effects that drive the formation of the complex [Ru(bpydip)Cl₂], we performed a new experimental study of the reaction and a complete theoretical investigation of their transition states. The results showed that nonformation of the cis isomer could be explained by the difference in relative stability of the reaction products and the transition states proposed.     

Dual luminescences in [W(Cp)(CO)3]2 and [Mo(Cp)(CO)3]2

Cyclohexane solutions of [W(Cp)(CO)₃]₂ and [Mo(Cp)(CO)₃]₂ exhibit weak bimodal emission spectra when excited With 354 nm picosecond pulses, but do not luminesce when pumped at 530 nm. Picosecond lifetimes characterize the short-wavelength, emission bands, which may originate from metal-cyclopentadienyl CT excited states.