Organometallics is the branch of chemical science studying the chemistry of molecules that have direct carbon-metal bonds.
Main group organometallic chemistryEdit
Alkali and akaline earths organometallicEdit
- Li, Na, K organyls
- Be organyls
- Mg organyls
- Si organyls
- Ga organyls
Pb, Sb, Sn, HgEdit
Transition-metal organometallic chemistryEdit
The organometallic chemistry of the transition elements is quite different from the main-group ones due to the availability for bonding of the n d orbitals with consequent ability for the central atom to change geometry and expand the octet.
- σ *→dσ
- dπ→π *
These interactions are synergicin increading the M-CO bond strength. In fact, the second interaction, as known as pi backbonding increases the available electron density on the CO.
The partial filling of the π* orbital leads to a weakened C-O triple bond, as showed from the stretching frequencies (in cm-1) of CO free and in M/CO complexes.
Carbenes and carbynes compoundsEdit
Catalysis by organometallic compoundsEdit
It occurs via the carbene species nowaday known as Schrock's carbenes
- ^ Grubbs, Olefin metathesis, Tetrahedron
Ziegler-Natta catalyst Ziegler in the 40's worked on the oligomerisation of ethylene by aluminium alkyls via the reaction HAl-R + CH2=CH2 -> HAl-CH2CH2-R
Hydroformylation Hydroformylation is the process that transforms an alkene into an aldehyde by reaction with CO.
Fischer-Tropsch synthesis is the heterogeneously-catalysed formation of hydrocarbons (alkanes and alkenes) from CO and hydrogen (synthesis gas). It can be seen as the inverse of synthesis gas preparation (although this is usually from methane and lighter hydrocarbons). It is the heart of the gas-to-liquids processes developed commercially by big petrochemical firms in the 90's.
Organometallics in living systemsEdit
The only example of a biological molecule containing direct carbon-metal bonds is cobalamin, as known as vitamin B12