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The system most often studied for the cis effect is an octahedral complex M(CO) 5 X where X is the ligand that will labilize a CO ligand cis to it. Unlike the trans effect, which is most often observed in 4-coordinate square planar complexes, the cis effect is observed in 6-coordinate octahedral transition metal complexes.
The insertion of carbon monoxide into a metal-carbon bond to form an acyl group is the basis of carbonylation reactions, which provides many commercially useful products. Mechanistic studies reveal that the alkyl group migrates intramolecularly to an adjacent CO ligand. [2] [3] CO Insertion reaction pathway for an octahedral complex
In organic structural chemistry, the configuration of a double bond can be described with cis and trans, in case it has a simple substitution pattern with only two residues. The position of two residues relative to one another at different points in a ring system or a larger molecule can also be described with cis and trans if the structure's ...
For octahedral mono- and dicationic aquo complexes, these exchange processes occur via an interchange pathway that has more or less dissociative character. [4] Rates vary by a factor of 10 18, [Ir(H 2 O) 6] 3+ being the slowest and [Na(H 2 O) 6] + being one of the fastest for octahedral complexes. Charge has a significant influence on these ...
Organoiridium compounds share many characteristics with those of rhodium, but less so with cobalt. Iridium can exist in oxidation states of -III to +V, but iridium(I) and iridium(III) are the more common. iridium(I) compounds (d 8 configuration) usually occur with square planar or trigonal bipyramidal geometries, whereas iridium(III) compounds (d 6 configuration) typically have an octahedral ...
Methanesulfonamide (CH 3 SO 2 NH 2) has been identified as a catalyst to accelerate this step of the catalytic cycle and if frequently used as an additive to allow non-terminal alkene substrates to react efficiently at 0 °C. [8] Finally, the stoichiometric oxidant regenerates the osmium tetroxide – ligand complex (2).
Cis-dichlorobis(ethylenediamine)cobalt(III) chloride is obtained by heating a solution of trans-dichlorobis(ethylenediamine)cobalt(III) chloride, e.g. using a steam bath. The racemate can be resolved into two enantiomers (Λ and Δ) by the formation of the d-α-bromocamphor-π-sulfonate salt. The diastereomeric salts are separated by ...
The catalytic cycle of the Monsanto process. The catalytically active species is the anion cis-[Rh(CO) 2 I 2] − (top of scheme). [3] The first organometallic step is the oxidative addition of methyl iodide to cis-[Rh(CO) 2 I 2] − to form the hexacoordinate species [(CH 3)Rh(CO) 2 I 3] −.