Inter-ring η6⇌η5 haptotropic rearrangements of 18ē and 19ē (η5-pentamethylcyclopentadienyl)(η6-9-methylfluorenyl)iron complexes

New cationic complexes [(⁶-C₁₃H₁₀)Fe(⁵-Cp^*)]PF₆ and [(⁶-9-CH₃-C₁₃H₉)Fe(⁵-Cp^*)]PF₆ were obtained by the reaction of Cp^*Fe(CO)₂Br with fluorene and 9-methylfluorene, respectively. Deprotonation of these complexes byt-BuOK in THF affords zwitter-ionic compounds (⁶-C₁₃H₉)Fe(⁵-Cp^*) and (⁶-9-CH₃-C₁₃H₈)Fe(⁵-Cp^*) (A). WhenA is heated in nonane at 150 °C it undergoes ⁶⁵ inter-ring rearrangement with the formation of hexamethyldibenzoferrocene (B). The electrochemical behavior ofA andB was studied by cyclic voltammetry. One-electron reduction ofA andB to the corresponding radical anions induces inter-ring haptotropic rearrangementA ^.–B ^.–. The equilibrium in the 19 state is shifted to the ⁶-isomeric radical anionA ^.–, while in the 18 precursors, it shifts to the ⁵-isomerB.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 2, pp. 319–324, February, 1994.The authors are grateful to D. V. Zagorevskii (A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences) for recording and interpreting the mass spectra, and to A. A. Borisenko (Moscow State University) for recording the NMR spectra.This work was financially supported by the Russian Foundation for Basic Research (Grant 93-03-5209).     

Oxidation of isomeric η6- and η5-fluorenylchromiumtricarbonyl anions

The oxidation of the carbon-centered [(⁶-C₁₃H₉)Cr(CO)₃]^– anion (1 ^–) results in formation of (-⁶:⁶-9,9-bifluorenyl)bis-chromiumtricarbonyl (3) due to coupling of the intermediate carbon-centered radical (1^.). The oxidation of the metal-centered anion [(⁵-C₁₃H₉)Cr(CO)₃]^– (2 ^–), which is isomeric to the 1^– anion, gives an equilibrium mixture of the chromium-centered radical {(⁵-C₁₃H₉)Cr(CO)₃}^. (2 ^.) and its dimer [(⁵-C₁₃H₉)Cr(CO)₃]₂ (6). Radical2 ^. readily reacts with MeI and the solvent (THF); the resulting derivatives, (⁵-C₁₃H₉)Cr(CO)₃R (R=Me (10); R=H (7)), undergo fast ricochet inter-ring ⁵⁶ rearrangements into (⁶-9R-C₁₃H₉)Cr(CO)₃ (R=CH₃ (9); R=H (4)).Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 7, pp. 1354–1358, July, 1995.The authors are grateful to D. V. Zagorevskii who recorded the mass spectra. This study was financially supported by the Russian Foundation for Basic Research (Grant No. 94-03-05209) and the International Science Foundation (Grant Nos. MQ 4000 and REV 000).     

Redox-induced η5 ⇔ η3 haptotropy of the fluorenyl ligand in 9-substituted η5-fluorenylmanganesetricarbonyl complexes

It has been shown by cyclic voltammetry in THF within the –90 to 40 °C temperature range that fluorenyl (⁵-9-R-C₁₃H₈)Mn(CO)₃ complexes (R=Bu^t (3) and Ph (4)) undergo two-electron reduction to form allyl type [(³-9-R-C₁₃H₈)Mn(CO)₃]^2– dianions as final products. At low temperatures complexes3 and4 are reduced in two one-electron steps according to the EEC-scheme. The first step is reversible and corresponds to the formation of 19-radical anions 3^–. and 4^–.. TheE ⁰ values for redox pairs3 ^0/–. and4 ^0/–. are –1.88 and –1.73 V, respectively. The further reduction of radical anions3 ^–. and4 ^–. at more negative potentials is accompanied by fast ^{5 3} haptocoordination of the fluorenyl ligand to form 18-dianions [(³-9-R-C₁₃H₈)Mn(CO)₃]^2–. These dianions obtained by the reduction of complexes3 and4 by the radical anion of pyrene are stable at –80 °C and are characterized by their IR spectra. At room temperature the ^{5 3} hapticity change is a fast and reversible process occurring at the step of 19-radical anions3 ^–. and4 ^–. and leading to the electron deficient 17-species [(³-9-R-C₁₃H₈)Mn(CO)₃]^–., which are reduced easier than the initial complexes. As a result, complexes3 and4 are reduced to the corresponding dianions [(³-9-R-C₁₃H₈)Mn(CO)₃]^2– at room temperature in one reversible two-electron step according to the ECE-scheme. Reactivities of 19e^–-species of the isomeric ⁵- and ⁶-fluorenylmanganesetricarbonyl complexes are compared.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 7, pp. 1347–1353, July, 1995.The work was financially supported by the Russian Foundation for Basic Research (Project No. 93-03-05209) and the International Science Foundation (Grant No. REV 000).     

Characterisation of anodic oxide films on zirconium formed in sulphuric acid: XPS and corrosion resistance investigations

Present work describes investigations of a two-step process consisting of galvanostatic anodising in a 1 M H₂SO₄ solution at 100 mA cm⁻² up to the limiting voltages of 20, 60, 80, 100 and 120 V, directly after which potentiostatic regime was employed and the current was allowed to drop. The total treatment time (5 min) was held constant for all samples. The treatment was carried out to improve the corrosion resistance of zirconium in physiological conditions, which was determined by electrochemical evaluation in Ringer’s solution. XPS studies revealed that after anodising sulphur was incorporated into the oxide film in the form of sulphated zirconia. The maximum content of sulphate in the oxide layer was observed after anodising at 80 V. Anodising at higher voltages resulted in formation of coatings with decreasing amount of sulphur. It was found that there is a strong correlation between the sulphur content in the oxide layers and the measured corrosion current density. On the other hand, the pitting corrosion resistance seemed to be unaffected by the presence of S and it was improving with the increasing limiting voltage of the treatment.

     

Reduction of acetylene by zinc amalgam catalyzed by molybdenum cyclopentadienylcarbonyl complexes

Conclusions The products of the reduction of Cp₂Mo₂(CO)₆, Cp₂Mo₂(CO)₄, and Cp₂Mo₂(CO)₄(C₂H₂) are mononuclear CpMo(CO)_3-xL_x anions (x=0-2). These anions catalyze the reduction of acetylene by zinc amalgam with a quantitative yield of ethane and ethylene relative to amalgam consumedTranslated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 2, pp. 464–466, February, 1988.     

Cu-Site Disorder in CuAl2O4 as Studied by XPS Spectroscopy

JETP Letters - The results of full study of X-ray photoelectron spectra (XPS) of spin-liquid candidate CuAl2O4 including the measurements of high-energy resolved core level (Cu $$2p$$ , Al $$3p$$ ,...     

Bifurcation of resonance during flutter of the blades of a turbocompressor rotor

Bifurcation of the trajectory of the resonance of rotor blades of an axial turbocompressor leading to flutter of the blade cascade is investigated. The investigation is based on spectral analysis of the records of the transient process of the blades. It is shown that in contrast to the resonance, which has a constant phase difference between the excitation and forced oscillations of the blades, the phase shift of collective synchronous vibrations of the blades during the flutter depends on their number and the form of the diametral mode of the blade cascade. It is formed by one of the pulsation modes of the pressure of air flow.     

Kinetic Theory of a Weakly‐Nonideal Spatially Nonuniform Polarizable Plasma

A nonmarkovian and nonlocal kinetic equation, which is a generalization of the (nonlinear) Balescu‐Lenard equation, is derived for a weakly nonuniform multicomponent polarizable plasma. A specific expansion of the plasma resolvent, which allow to separate the dymamic, kinetic and hydrodynamic scales, is proposed. Explicit expressions of the collision integral and of the nonequilibrium pair correlation function are given in an approximation which take into account the effect of patial and temporal nonlocality a well as of the polarization. Balance equation for the momentum and energy densitie are calculated in the first order in nonlocality, and potential contributions to the fluxes due to polarization are obtained.