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  • kinetics  (3)
  • AM1  (1)
  • Cyclizations  (1)
  • Dinuclear complex  (1)
  • 1
    ISSN: 0948-5023
    Schlagwort(e): Keywords Human Carbonic Anhydrase II ; Semiempirical MO Theory ; AM1 ; Enzyme Catalysis
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract The approach of CO2 to a series of active site model complexes of human carbonic anhydrase   II (HCAII) and its catalytic hydration to bicarbonate anion have been investigated using semiempirical MO theory (AM1). The results show that direct nucleophilic attack of zinc-bound hydroxide to the substrate carbon occurs in each model system. Further rearrangement of the bicarbonate complex thus formed via a rotation-like movement of the bicarbonate ligand can only be found in active site model systems that include at least one additional water molecule. Further refinement of the model complex by adding a methanol molecule to mimic Thr-199 makes this process almost activationless. The formation of the final bicarbonate complex by an internal (intramolecular) proton transfer is only possible in the simplest of all model systems, namely {[Im3Zn(OH)]+·CO2}. The energy of activation for this process, however, is 36.8 kcal·mol−1 and thus too high for enzymatic catalysis. Therefore, we conclude that within the limitations of the model systems presented and the level of theory employed, the overall mechanism for the formation of the bicarbonate complex comprises an initial direct nucleophilic attack of zinc-bound hydroxide to carbon dioxide followed by a rotation-like rearrangement of the bicarbonate ligand via a penta-coordinate Zn2+ transition state structure, including the participation of an extra active site water molecule.
    Materialart: Digitale Medien
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  • 2
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1998 (1998), S. 389-396 
    ISSN: 1434-1948
    Schlagwort(e): Substitution mechanism ; Platinum ; Pressure dependence ; Kinetics ; Dinuclear complex ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Both reaction steps observed for the substitution of water by thiourea in the complexes [Pt(en)(OH2)2]2+ and [Pt(phen)(OH2)2]2+ (en = ethylenediamine, phen = 1,10-phenanthroline) were investigated under pseudo-first-order conditions using the stopped-flow technique. The substitution of the second water molecule in each complex was also studied under high pressure. The observed pseudo-first-order rate constants kobs (s-1) obeyed the equation k1,2obs= k1,2[tu] (tu = thiourea), where “1” and “2” refer to the first and the second substitution reactions, respectively. Kinetic parameters associated with the substitution process are: k1en (25.0°C, pH = 3.0, I = 0.1 M) = 25.6 M-1 s-1, ΔH# = 51 kJ mol-1, ΔS# = -48 J K-1 mol-1; k2en (same conditions) = 12.1 M-1 s-1, ΔH# = 30 kJ mol-1, ΔS# = -124 J K-1 mol-1, ΔV# = -7 cm3 mol-1; k1phen (25.0°C, pH = 1.0, I = 0.1 M) = 2900 M-1 s-1, ΔH# = 41 kJ mol-1, ΔS# = -41 J K-1 mol-1; k2phen (same conditions) = 1170 M-1 s-1, ΔH# = 37 kJ mol-1, ΔS#= -61 J K-1 mol-1, ΔV# = -5 cm3 mol-1. The temperature and pressure dependence of all the processes studied suggest an associative substitution mechanism. The hydroxo-bridged dinuclear complex [{Pt(phen)(μ-OH)}2]2+ is formed from [Pt(phen)(OH2)2]2+ in aqueous solution unless the solution is very dilute and highly acidic. The X-ray structure of [{Pt(phen)(μ-OH)}2](F3CSO3)2 · 2 H2O was determined. It belongs to the triclinic space group P1­ and has one formula unit in the unit cell. The unit cell dimensions are a = 7.126(5), b = 9.665(5), c = 12.774(7) Å; α = 71.85(5), β = 85.52(5), γ = 73.12(5) deg; V = 799.9(8) Å3. The structure was solved with the Patterson method and refined to R = 0.061. A square planar coordination of the platinum centers is observed, with no deviations from planarity but distortions due to the small bite angle of phen and the four-membered ring. No significant lengthening of the Pt-O bond [mean value: 2.03(1) Å] is observed in comparison with [{Pt(NH3)2(μ-OH)}2]2+.
    Materialart: Digitale Medien
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  • 3
    ISSN: 1434-193X
    Schlagwort(e): Cyclizations ; Electron transfer ; High-pressure effects ; Radical cations ; Silyl enol ethers ; Solvent effects ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Oxidative photoinduced electron transfer (PET) reactions have been performed with various silyl enol ethers and silyloxy-2H-chromones bearing an olefinic or silylacetylenic side chain. The reactions result in regioselective ring closure with the formation of bi- to tetracyclic ring systems with a well-defined ring juncture, e.g. perhydrophenanthrenones 13 or benzo-annellated xanthenones 24. Our investigations have focussed on the optimization of this cyclization method with regard to irradiation time and product yield. The irradiation times could be reduced by using the cosensitized PET method. Modifying the substrate at the silyl group led to enhanced yields. In addition, we found that solvent and pressure dependences are important tools, allowing control of the regiochemistry. Both the synthesis of 6-endo products by radical cationic reaction pathways, as well as 5-exo ring closure by radical intermediates was achieved. Mechanistic details, including findings from deuterium labelling experiments, are discussed.
    Materialart: Digitale Medien
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  • 4
    ISSN: 0947-6539
    Schlagwort(e): cobalt ; cytochrome c ; electron transfer ; kinetics ; volume profile ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The Kinetics and Thermodynamics of the Reversible Outer-Sphere Electron-Transfer Reactions between Horse Heart Cytochrome cII/III and [Co(phen)3]3+/2+ and [Co(bpy)3]3+/2+ were studied in detail, in particular as a function of temperature and pressure. It was possible to construct a volume profile for both reactions from the pressure data. The transition state was found to be halfway between the reactant and product states on a volume basis in all studied systems. This is in agreement with the λ≠ parameter estimated from the Marcus theory. For all the systems investigated, the differences in the activation volumes are in good agreement with the reaction volumes determined from spectrophotometric and electrochemical measurements at elevated pressure, and from the difference in the partial molar volumes of the metal complexes. The activation and reaction volumes of the bipyridine system are significantly smaller than those of the corresponding phenanthroline and terpyridine systems. A detailed mechanistic analysis is presented. The results show that the different kinetic and thermodynamic techniques employed complement one another.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
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  • 5
    ISSN: 0894-3230
    Schlagwort(e): cyclic sulfamates ; nucleophiles ; reactivity ; kinetics ; mechanism ; Chemistry ; Theoretical, Physical and Computational Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: ---The kinetics of the reaction of four X-3-(p-tolylsulfonyl)-1,2,3-benzoxathiazole 2,2-dioxides (X=5-Cl, 5-Br, 5-NO2 and 6-NO2) with hydroxide ion and imidazole in aqueous acetonitrile and aqueous ethanol solutions were investigated at various pressures. The volumes of activation were all found to be negative and consistent with a bimolecular reaction involving considerable solvent electrostriction. No significant dependence on the solvent composition was found. © 1997 by John Wiley & Sons, Ltd.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
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  • 6
    ISSN: 0570-0833
    Schlagwort(e): kinetics ; reaction mechanisms ; rhodium compounds ; substitutions ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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