Ebbe Nordlander

Lund University, Lund, Skåne, Sweden

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Publications (144)432.69 Total impact

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    ABSTRACT: The mol-ecule of the title compound, C14H13N5O2, is approximately planar (r.m.s deviation for all non-H atoms = 0.093 Å), with the planes of the two pyridine rings inclined to one another by 5.51 (7)°. The oxime group is syn to the amide group, probably due to the formation of an intra-molecular N-H⋯N hydrogen bond that forms an S(6) ring motif. In the crystal, mol-ecules are linked by pairs of bifurcated O-H⋯(O,N) hydrogen bonds, forming inversion dimers. The latter are linked via C-H⋯O and C-H⋯N hydrogen bonds, forming sheets lying parallel to (502). The sheets are linked via π-π stacking inter-actions [inter-centroid distance = 3.7588 (9) Å], involving the pyridine rings of inversion-related mol-ecules, forming a three-dimensional structure.
    Acta Crystallographica Section E Structure Reports Online 12/2014; 70(Pt 12):584-6. · 0.35 Impact Factor
  • Debbie C. Crans, Ebbe Nordlander
    Berichte der deutschen chemischen Gesellschaft 09/2014; 2014(27). · 2.97 Impact Factor
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    ABSTRACT: Enantioselective hydrogenation of tiglic acid effected by diastereomers of the general formula [(μ-H)2Ru3(μ3-S)(CO)7(μ-P-P*)] (P-P* = chiral Walphos diphosphine ligand) strongly supports catalysis by intact Ru3 clusters. A catalytic mechanism involving Ru3 clusters has been established by DFT calculations.
    Chemical Communications 06/2014; · 6.72 Impact Factor
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    ABSTRACT: The new clusters [Ru3(CO)9(μ-dppf){P(C4H3E)3}] (E = O, S) rearrange upon heating to give cyclometalated clusters [(μ-H)Ru3(CO)7(μ-dppf){μ3-(C4H3E)2P(C4H2E)}], behavior that is in marked contrast to the analogous dppm complexes in which both carbon-hydrogen and carbon-phosphorus bond activation yields furyne- and thiophyne-capped clusters. This difference in reactivity is probed by DFT calculations.
    Journal of Organometallic Chemistry 06/2014; 760:231–239. · 2.30 Impact Factor
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    ABSTRACT: The heterodinuclear mixed-valence complex [FeMn(ICIMP)(OAc)2Cl] (1) {H2ICIMP = 2-(N-carboxylmethyl)-[N-(N-methylimidazolyl-2-methyl)aminomethyl]-[6-(N-isopropylmethyl)-[N-(N-methylimidazolyl-2-methyl)]aminomethyl-4-methylphenol], an unsymmetrical N4O2 donor ligand} has been synthesized and fully characterized by several spectroscopic techniques as well as by X-ray crystallography. The crystal structure of the complex reveals that both metal centers in 1 are six-coordinate with the chloride ion occupying the sixth coordination site of the MnII ion. The phenoxide moiety of the ICIMP ligand and both acetate ligands bridge the two metal ions of the complex. Mössbauer spectroscopy shows that the iron ion in 1 is high-spin FeIII. Two quasi-reversible redox reactions for the complex, attributed to the FeIIIMnII/FeIIMnII (at –0.67 V versus Fc/Fc+) and FeIIIMnII/FeIIIMnIII (at 0.84 V), were observed by means of cyclic voltammetry. Complex 1, with an FeIII–MnII distance of 3.58 Å, may serve as a model for the mixed-valence oxidation state of purple acid phosphatase from sweet potato. The capability of the complex to effect organophosphate hydrolysis (phosphatase activity) has been investigated at different pH levels (5.5–11) by using bis(2,4-dinitrophenyl)phosphate (BDNPP) as the substrate. Density functional theory calculations indicate that the substrate coordinates to the MnII ion. In the transition state, a hydroxide ion that bridges the two metal ions becomes terminally coordinated to the FeIII ion and acts as a nucleophile, attacking the phosphorus center of BDNPP with the concomitant dissociation of the leaving group.
    Berichte der deutschen chemischen Gesellschaft 05/2014; · 2.97 Impact Factor
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    ABSTRACT: A series of novel neutral and cationic methylpalladium complexes bearing N-alkyl-2,2′-dipyridylaldiminato ligands were prepared and characterized. In the presence of ethylene, the cationic complexes were active as dimerization catalysts, producing a mixture of 1- and 2-butenes. A Pd–ethyl π-ethylene species was identified as the catalyst resting state by low-temperature spectroscopic and DFT studies, which provided insights into the effect of both steric and electronic factors on the observed reactivity.
    Organometallics 04/2014; · 4.25 Impact Factor
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    Biswanath Das, Matti Haukka, Ebbe Nordlander
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    ABSTRACT: The binuclear title complex, [Zn2(C33H33N6O)(CH3COO2)(CH3OH)](ClO4)2, was synthesized by the reaction between 2,6-bis-({[bis-(pyridin-2-yl)meth-yl]amino}-meth-yl)-4-methyl-phenol (H-BPMP), Zn(OAc)2 and NaClO4. The two Zn(II) ions are bridged by the phenolate O atom of the octadentate ligand and the acetate group. An additional methanol ligand is terminally coordinated to one of the Zn(II) ions, rendering the whole structure unsymmetric. Other symmetric dizinc complexes of BPMP have been reported. However, to the best of our knowledge, the present structure, in which the two Zn(II) ions are distinguishable by the number of coordinating ligands and the coordination geometries (octahedral and square-pyramidal), is unique. The dizinc complex is a dication, and two perchlorate anions balance the charge. The -OH group of the coordinating methanol solvent mol-ecule forms a hydrogen bond with a perchlorate counter-anion. One of the anions is disordered over two sets of sites with an occupancy ratio of 0.734 (2):0.266 (2).
    Acta Crystallographica Section E Structure Reports Online 04/2014; 70(Pt 4):m120-1. · 0.35 Impact Factor
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    ABSTRACT: The mixed-valence triiron complexes [Fe3(CO)7-x (PPh3) x (μ-edt)2] (x = 0-2; edt = SCH2CH2S) and [Fe3(CO)5(κ(2)-diphosphine)(μ-edt)2] (diphosphine = dppv, dppe, dppb, dppn) have been prepared and structurally characterized. All adopt an anti arrangement of the dithiolate bridges, and PPh3 substitution occurs at the apical positions of the outer iron atoms, while the diphosphine complexes exist only in the dibasal form in both the solid state and solution. The carbonyl on the central iron atom is semibridging, and this leads to a rotated structure between the bridged diiron center. IR studies reveal that all complexes are inert to protonation by HBF4·Et2O, but addition of acid to the pentacarbonyl complexes results in one-electron oxidation to yield the moderately stable cations [Fe3(CO)5(PPh3)2(μ-edt)2](+) and [Fe3(CO)5(κ(2)-diphosphine)(μ-edt)2](+), species which also result upon oxidation by [Cp2Fe][PF6]. The electrochemistry of the formally Fe(I)-Fe(II)-Fe(I) complexes has been investigated. Each undergoes a quasi-reversible oxidation, the potential of which is sensitive to phosphine substitution, generally occurring between 0.15 and 0.50 V, although [Fe3(CO)5(PPh3)2(μ-edt)2] is oxidized at -0.05 V. Reduction of all complexes is irreversible and is again sensitive to phosphine substitution, varying between -1.47 V for [Fe3(CO)7(μ-edt)2] and around -1.7 V for phosphine-substituted complexes. In their one-electron-reduced states, all complexes are catalysts for the reduction of protons to hydrogen, the catalytic overpotential being increased upon successive phosphine substitution. In comparison to the diiron complex [Fe2(CO)6(μ-edt)], [Fe3(CO)7(μ-edt)2] catalyzes proton reduction at 0.36 V less negative potentials. Electronic structure calculations have been carried out in order to fully elucidate the nature of the oxidation and reduction processes. In all complexes, the HOMO comprises an iron-iron bonding orbital localized between the two iron atoms not ligated by the semibridging carbonyl, while the LUMO is highly delocalized in nature and is antibonding between both pairs of iron atoms but also contains an antibonding dithiolate interaction.
    Organometallics 03/2014; 33(6):1356-1366. · 4.25 Impact Factor
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    ABSTRACT: The reactivity of the σ,π-furyl complex [Fe2(CO)6(μ-Fu)(μ-PFu2)] (1) towards PPh3 and a range of bidentate phosphines has been studied and a number of different reaction products have been identified. With PPh3, carbonyl substitution affords [Fe2(CO)5(PPh3)(μ-Fu)(μ-PFu2)] (2) in which the new phosphine is coordinated to the iron center that is σ-coordinated by the bridging furyl moiety. With small bite-angle diphosphines – bis(diphenylphosphino)methane (dppm) and 1,8-bis(diphenylphosphino)naphthalene (dppn) – carbonyl substitution and migratory carbonyl insertion result to give the furyl–acyl complexes with bridging, [Fe2(CO)4(μ-dppm)(μ-OCFu)(μ-PFu2)] (3), or chelating, [Fe2(CO)4(κ2-dppn)(μ-OC–Fu)(μ-PFu2)] (4), diphosphines, respectively. With the more flexible diphosphines Ph2P(CH2)nPPh2 (n = 2, dppe, n = 3, dppp), the cyclometallated products [Fe2(CO)5{μ,κ2-C6H4PPh(CH2)nPPh2}(μ-PFu2)] (n = 2, 5; n = 3, 6) are isolated as a result of carbonyl substitution and furan elimination, and a similar complex [Fe2(CO)5{μ,κ2-C6H4PPh(C6H4)PPh2}(μ-PFu2)] (7) is generated from the more rigid diphosphine bis(diphenylphosphino)benzene (dppb). With bis(diphenylphosphino)-1,1-binaphthalene (1,1-BINAP) the novel tridentate phosphine complex [Fe2(CO)5{μ,κ3-C6H4P(C20H12PPh2)C6H4PFu}] (8) results from the putative coupling of cyclometallated diphosphine and difurylphosphido ligands, following elimination of two equivalents of furan. The crystal structures of 2, 3, 5 and 8 have been determined and allow a detailed insight into the overall reaction profile.
    Journal of Organometallic Chemistry 02/2014; · 2.30 Impact Factor
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    ABSTRACT: Ten rhenium carbonyl complexes—[Re(H)(CO)3(1a)], [Re3(µ-H)3(CO)10(1a)], [Re2(CO)9(2a)], [Re2(CO)8(2a)], [Re2(CO)9(2b)], [{Re2(CO)9}2(2b)], [Re2(CO)8(2b)], [Re2(CO)8(1b)], [Re2(µ-H)2(CO)6(2b)] and [Re3(µ-H)3(CO)11(2b)]—containing different bidentate chiral phosphine ligands of the Josiphos (1a, 1b) and Walphos (2a, 2b) families have been synthesized and fully characterized (1a: (R)-1-{(S P)-2-[Bis[3,5-bis(trifluoromethyl)phenyl]phosphino]ferrocenyl}ethyldi(3,5-xylyl)phosphine, 1b: (R)-1-{(S P)-2-[Di(2-furyl)phosphino]ferrocenyl}ethyldi-tert-butylphosphine, 2a: (R)-1-{(R P)-2-[2-[Bis(4-methoxy-3,5-dimethylphenyl)phosphino]phenyl]ferrocenyl}ethylbis[3,5-bis(trifluoromethyl)phenyl]phosphine and 2b: (R)-1-{(R P)-2-[2-(Diphenylphosphino)phenyl]ferrocenyl}ethyldicyclohexylphosphine). The phosphine-substituted clusters were tested for hydrogenation of tiglic acid [trans-2-methyl-2-butenoic acid]. The catalytic reactions gave reasonable conversion rates (15–88 %) under relatively mild conditions but relatively moderate enantiomeric excesses (8–57 %) were observed. The crystal structures of [ReH(CO)3(1a)], [Re2(CO)9(2a)], [{Re2(CO)9}2(2b)] and [Re2(µ-H)2(CO)6(2b)] are presented.
    Journal of Cluster Science 01/2014; · 1.36 Impact Factor
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    ABSTRACT: A new iron complex mediates stereospecific hydroxylation of alkyl C-H bonds with hydrogen peroxide, exhibiting excellent efficiency. Isotope labelling studies provide evidence that the relative reactivity of tautomerically related oxo-iron species responsible for the C-H hydroxylation reaction is dominated by steric factors.
    Chemical Communications 11/2013; · 6.38 Impact Factor
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    ABSTRACT: The dinuclear complex [Zn2(DPCPMP)(pivalate)](ClO4), where DPCPMP is the new unsymmetrical ligand [2-(N-(3-((bis((pyridin-2-yl)methyl)amino)methyl)-2-hydroxy-5-methylbenzyl)-N-((pyridin-2-yl)methyl)amino)acetic acid], has been synthesized and characterized. The complex is a functional model for zinc phosphoesterases with dinuclear active sites. The hydrolytic efficacy of the complex has been investigated using bis-(2,4-dinitrophenyl)phosphate (BDNPP), a DNA analog, as substrate. Speciation studies using potentiometric titrations have been performed for both the ligand and the corresponding dizinc complex to elucidate the formation of the active hydrolysis catalyst; it reveals that the dinuclear zinc(II) complexes, [Zn2(DPCPMP)](2+) and [Zn2(DPCPMP)(OH)](+) predominate the solution above pH4. The relatively high pKa of 8.38 for water deprotonation suggests that a terminal hydroxide complex is formed. Kinetic investigations of BDNPP hydrolysis over the pH range 5.5-11.0 and with varying metal to ligand ratio (metal salt:ligand=0.5:1 to 3:1) have been performed. Variable temperature studies gave the activation parameters ΔH(‡)=95.59kJmol(-1), ΔS(‡)=-44.82Jmol(-1)K(-1), and ΔG(‡)=108.00kJmol(-1). The cumulative results indicate the hydroxido-bridged dinuclear Zn(II) complex [Zn2(DPCPMP)(μ-OH)](+) as the effective catalyst. The mechanism of hydrolysis has been probed by computational modeling using density functional theory (DFT). Calculations show that the reaction goes through one concerted step (SN2 type) in which the bridging hydroxide in the transition state becomes terminal and performs a nucleophilic attack on the BDNPP phosphorus; leaving group dissociates simultaneously in an overall inner sphere type activation. Calculated free energy barrier is in good agreement with the experimentally determined activation parameters.
    Journal of inorganic biochemistry 08/2013; · 3.25 Impact Factor
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    ABSTRACT: The dinuclear complex [Zn2(papy)2]·2CH3OH [H2papy = N-(2-hydroxybenzyl)-N-(2-picolyl)glycine] was synthesized and characterized. The crystal structure of the complex reveals that both ZnII ions are pentacoordinate with distorted pentagonal bipyramidal coordination arrangements. The phenoxyl groups of each ligand bridge the two metal atoms, whereas each carboxylate of the ligand is terminally bound to one ZnII ion. Potentiometric studies of the ZnII:H2papy system in a methanol/water mixture show the existence of a mononuclear species at lower pH; but at a pH above 5, a dimeric species starts to dominate and transforms further into a bis(μ-phenoxo) bridged dizinc complex by deprotonation of phenolic hydrogen. A kinetic study of the hydrolysis of bis(2, 4-dinitrophenyl)phosphate at different pH, catalyzed by complex 1, indicates a maximum rate at pH 9, where the bis(μ-phenoxo)-bridged dizinc species corresponding to 1 dominates in solution.
    Zeitschrift für anorganische Chemie 07/2013; 639(8‐9). · 1.25 Impact Factor
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    ABSTRACT: The title compound, C14H16N6O2, is a second monoclinic polymorph of 2-[1-(3,5-dimeth-yl)pyrazol-yl]-2-hy-droxy-imino-N'-[1-(2-pyrid-yl)ethyl-idene] acetohydrazide, with two crystallographically independent mol-ecules per asymmetric unit. The non-planar mol-ecules are chemically equal having similar geometric parameters. The previously reported polymorph [Plutenko et al. (2012 ▶). Acta Cryst. E68, o3281] was described in space group Cc (Z = 4). The oxime group and the O atom of the amide group are anti with respect to the C-C bond. In the crystal, mol-ecules are connected by N-H⋯N hydrogen bonds into zigzag chains extending along the b axis.
    Acta Crystallographica Section E Structure Reports Online 05/2013; 69(Pt 5):o765-6. · 0.35 Impact Factor
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    ABSTRACT: Reaction of [Os3(CO)11(NCMe)] with bis-diphenylphosphanylethylene sulfide, {Ph2PCH2CH2}2S (PSP), leads to the formation of [Os3(CO)11(PSP)] and [{Os3(CO)11}2(μ-PSP)] in good yield. Similarly, treatment of [Os3(CO)10(NCMe)2] with PSP affords the cluster [Os3(CO)10(μ-PSP)], in which the two phosphanes of the PSP ligand coordinate to different osmium atoms of the same triosmium unit. Reaction of [Os3(CO)11(PSP)] with [Os3(CO)10(NCMe)2] yields the compound 1,2-[{Os3(CO)11}(μ3-PSP){Os3(CO)10}] in which the thioether moiety and one of the phosphane groups of the PSP ligand are coordinated equatorially to the {Os3(CO)10} subunit. The cluster 1,2-[{Os3(CO)11}(μ3-PSP){Os3(CO)10}] is also formed when [Os3(CO)11(PSP)] is oxidatively decarbonylated by reaction with trimethylamine N-oxide. The metastable cluster 1,2-[{Os3(CO)11}(μ3-PSP){Os3(CO)10}] undergoes slow isomerisation at room temperature to form 1,1-[{Os3(CO)11}(μ3-PSP){Os3(CO)10}] in which the thioether and phosphane moieties coordinate in a chelating mode to one of the {Os3(CO)10} subunits with the thioether moiety in an axial position. The dynamic behaviour of these clusters has been investigated by variable-temperature 13C{1H} and 13P{1H} NMR spectroscopy. The solid-state structures of [{Os3(CO)11}2(μ-PSP)] and [Os3(CO)10(μ-PSP)] are reported.
    Berichte der deutschen chemischen Gesellschaft 05/2013; 2013(13). · 2.97 Impact Factor
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    ABSTRACT: In the title compound, CHNO, the dihedral angles formed by the mean plane of the acetohydrazide group [maximum deviation 0.0629 (12) Å] with the pyrazole and pyridine rings are 81.62 (6) and 38.38 (4)° respectively. In the crystal, mol-ecules are connected by N-H⋯O and O-H⋯N hydrogen bonds into supra-molecular chains extending parallel to the -axis direction.
    Acta Crystallographica Section E Structure Reports Online 12/2012; 68(Pt 12):o3381. · 0.35 Impact Factor
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    ABSTRACT: The zinc(II) coordination chemistry of the bioinspired bis(tetradentate) ligand 3,5-bis{bis[2-(1-methylimidazolyl)methyl]aminomethyl}pyrazole (L) was studied in detail both in solution and in the solid state. Six different species were determined in aqueous solution by means of potentiometry within the pH range 2–11, namely mononuclear [ZnH2L]4+, dinuclear [Zn2L]4+, [Zn2H–1L]3+ and [Zn2H–2L]2+, as well as tetranuclear [Zn4H–5L2]3+ and [Zn4H–6L2]2+. Complexes representing the protonation state of four of these species could be isolated and structurally characterized by X-ray diffraction, namely [ZnH2L(MeCN)](ClO4)4 (1), [Zn2H–1L](SO3CF3)3 (4), [Zn2H–1L(MeOHOMe)](ClO4)2 (5a), [Zn2H–1L(OMe)](ClO4)2 (5b), and [(Zn2H–1L)2(μ-O)(μ-OH)](ClO4)3 (6). In addition, a bis(pyrazolato)-bridged complex, [(ZnH–1L)2](ClO4)2 (2), was obtained and structurally characterized, and it was found to exhibit ligand dynamics in solution. Both 5a and 5b are likely present in solution, which requires significant plasticity of the Zn···Zn distance (4.21 Å in 5a vs. 3.38 Å in 5b). Interconversion of 5a and 5b is proposed to be a facile process, supporting the idea that the Zn–O2H3–Zn moiety is a functionally relevant hydrolytic zinc–aqua structure in oligozinc metalloenzymes. The tetranuclear complex 6 that features two {Zn2H–1L} subunits connected by a central μ-oxido-μ-hydroxido moiety is unprecedented in zinc(II) chemistry. Combining X-ray crystallography with potentiometry, ESI mass spectrometry, as well as NMR and EXAFS spectroscopy has provided a comprehensive picture of the multitude of species present in this rather complex system.
    Berichte der deutschen chemischen Gesellschaft 10/2012; 2012(29). · 2.97 Impact Factor
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    ABSTRACT: 5-Acetyl-substituted pyrazole-3-carboxylic acid (H2L) forms [2×2] grid-like tetranuclear Cu(II) complexes with four five-coordinated copper(II) ions bridged by pyrazolate groups. Despite a significant dissociation of [Cu4L4(H2O)4]·4H2O (1) in aqueous solution1, it was possible to substitute the coordinated water molecules by pyridine ligands or azide anions. The resulting tetranuclear complexes [Cu4L4Py4]·2H2O (2) and Na4[Cu4L4(N3)4]·7MeOH (3) were isolated and studied by X-ray diffraction analysis. In 2 and 3 the azide anions or pyridine molecules complete the distorted square-pyramidal coordination of each copper(II) center. Magnetic susceptibilities of the obtained compounds have been measured by SQUID techniques. Simulation of the data using a Heisenberg spin Hamiltonian approach showed that the bridges between the metals mediate weak intramolecular antiferromagnetic coupling (J in the range −13.3 to −17.1 cm−1) and lead to a singlet ground state in all cases.
    Inorganica Chimica Acta 09/2012; 392:322–330. · 2.04 Impact Factor
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    ABSTRACT: Reaction of tris[6-(2-hydroxymethyl)pyridylmethyl]amine, tpa(OH)(3), with (VOSO4)-O-IV center dot 5H(2)O resulted in an unexpected redox reaction producing [(VLH)-L-III][(VLH2)-L-III][PF6](3)center dot 1.5H(2)O (where H3L is bis(2-hydroxymethylpyridyl)(2-carboxypyridylmethyl)amine). This reaction is interesting in the light of the ability of ascidians to accumulate V-III by reduction of V-V from sea water. It also provides additional proof to the susceptibility of pyridylmethylamines to oxidation by certain metal ions. (C) 2012 Elsevier B. V. All rights reserved.
    Inorganica Chimica Acta 09/2012; 392:490-493. · 2.04 Impact Factor
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    ABSTRACT: The new clusters [H(4) Ru(4) (CO)(10) (μ-1,2-P-P)], [H(4) Ru(4) (CO)(10) (1,1-P-P)] and [H(4) Ru(4) (CO)(11) (P-P)] (P-P=chiral diphosphine of the ferrocene-based Josiphos or Walphos ligand families) have been synthesised and characterised. The crystal and molecular structures of eleven clusters reveal that the coordination modes of the diphosphine in the [H(4) Ru(4) (CO)(10) (μ-1,2-P-P)] clusters are different for the Josiphos and the Walphos ligands. The Josiphos ligands bridge a metal-metal bond of the ruthenium tetrahedron in the "conventional" manner, that is, with both phosphine moieties coordinated in equatorial positions relative to a triangular face of the tetrahedron, whereas the phosphine moieties of the Walphos ligands coordinate in one axial and one equatorial position. The differences in the ligand size and the coordination mode between the two types of ligands appear to be reflected in a relative propensity for isomerisation; in solution, the [H(4) Ru(4) (CO)(10) (1,1-Walphos)] clusters isomerise to the corresponding [H(4) Ru(4) (CO)(10) (μ-1,2-Walphos)] clusters, whereas the Josiphos-containing clusters show no tendency to isomerisation in solution. The clusters have been tested as catalysts for asymmetric hydrogenation of four prochiral α-unsaturated carboxylic acids and the prochiral methyl ester (E)-methyl 2-methylbut-2-enoate. High conversion rates (>94 %) and selectivities of product formation were observed for almost all catalysts/catalyst precursors. The observed enantioselectivities were low or nonexistent for the Josiphos-containing clusters and catalyst (cluster) recovery was low, suggesting that cluster fragmentation takes place. On the other hand, excellent conversion rates (99-100 %), product selectivities (99-100 % in most cases) and good enantioselectivities, reaching 90 % enantiomeric excess (ee) in certain cases, were observed for the Walphos-containing clusters, and the clusters could be recovered in good yield after completed catalysis. Results from high-pressure NMR and IR studies, catalyst poisoning tests and comparison of catalytic properties of two [H(4) Ru(4) (CO)(10) (μ-1,2-P-P)] clusters (P-P=Walphos ligands) with the analogous mononuclear catalysts [Ru(P-P)(carboxylato)(2) ] suggest that these clusters may be the active catalytic species, or direct precursors of an active catalytic cluster species.
    Chemistry - A European Journal 08/2012; 18(39):12458-78. · 5.93 Impact Factor

Publication Stats

739 Citations
432.69 Total Impact Points

Institutions

  • 1996–2014
    • Lund University
      • • Department of Physical Chemistry
      • • Department of Organic Chemistry
      • • Department of Chemistry
      Lund, Skåne, Sweden
  • 2012–2013
    • National Taras Shevchenko University of Kyiv
      • Department of Inorganic Chemistry
      Kievo, Kyiv City, Ukraine
    • Universidad Nacional Autónoma de México
      • Institute of Chemistry
      Mexico City, The Federal District, Mexico
  • 2010
    • University of Colorado at Boulder
      • Department of Chemistry and Biochemistry
      Boulder, CO, United States
  • 2004–2010
    • University College London
      • Department of Chemistry
      London, ENG, United Kingdom
  • 2001–2010
    • Saint-Petersburg State Institute of Technology
      Sankt-Peterburg, St.-Petersburg, Russia
  • 2006–2008
    • Jahangirnagar University
      • Department of Chemistry
      Dhaka, Dhaka Division, Bangladesh
  • 1995–2008
    • University of Cambridge
      • Department of Chemistry
      Cambridge, England, United Kingdom
  • 2007
    • University of Joensuu
      • Department of Chemistry
      Yoensu, Eastern Finland Province, Finland
  • 2002
    • Russian Academy of Sciences
      • Institute of the Problems of Chemical Physics
      Moskva, Moscow, Russia