Hydroformylation of olefins produced in the Fischer—Tropsch synthesis
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M. N. Mikhailov | G. Korneeva | D. A. Grigor’ev | T. Kron | S. Rush | D. V. Marochkin | Y. G. Noskov | O. G. Karchevskaya | I. M. Bedrina | A. Bessudnov
[1] Magn. , 2020, Catalysis from A to Z.
[2] N. Hales,et al. The application of polymer-bound carbonylcobalt(0) species in linker chemistry and catalysis. , 2003, Organic & biomolecular chemistry.
[3] J. Schraml,et al. 31P and 13C NMR spectra of cyclohexylphenylphosphines, tricyclohexylphosphine and triphenylphosphine , 1992 .
[4] J. Kochi,et al. Oxidation-reduction of carbonylcobalt cation-anion pairs in coupling to dimeric cobalt carbonyls , 1989 .
[5] E. J. Moore,et al. Kinetic and thermodynamic acidity of hydrido transition-metal complexes. 3. Thermodynamic acidity of common mononuclear carbonyl hydrides. , 1986, Journal of the American Chemical Society.
[6] T. Allman,et al. The basicity of phosphines , 1982 .
[7] J. Atwood,et al. The mechanism of substitution of dicobalt octacarbonyl , 1980 .
[8] C. A. Tolman,et al. Steric effects of phosphorus ligands in organometallic chemistry and homogeneous catalysis , 1977 .
[9] P. Szabó,et al. Phosphorus-containing cobalt carbonyls III. Monosubstituted derivatives of dicobalt octacarbonyl with phosphines and phosphites , 1968 .
[10] C. A. Streuli,et al. The Basicity of Phosphines , 1960 .
[11] O. Kühl. Phosphoros-31 NMR spectroscopy : a concise introduction for the synthetic organic and organometallic chemist , 2008 .
[12] Thomas J. Meyer,et al. Comprehensive coordination chemistry II : from biology to nanotechnology , 2004 .
[13] A. R. Manning. Infrared spectra of some derivatives of octacarbonyldicobalt , 1968 .