Organometallic chemistry

study of chemical compounds containing at least one bond between a carbon atom of an organic compound and a metal

Organometallic chemistry is the study of chemical compounds containing bonds between carbon and a metal.[1][2] It combines aspects of inorganic chemistry (the study of non-carbon bonds) and organic chemistry (the study of carbon bonds).

n-Butyllithium, an organometallic compound. Four lithium atoms are shown in purple in a tetrahedron, and each lithium atom is bound to a butyl group (carbon is black, hydrogen is white)

An example of an organometallic compounds is tetraethyllead; it was used as a fuel (leaded gasoline) additive in the past. Methylcobalamin (Vitamin B12) is a common organometallic compound.

Organometallic compounds

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The Fe (red) metal binds two organic rings together. In the ring structures each point represents a carbon atom. So ferrocene has 10 carbon atoms, 5 in the ring above the iron and 5 in the ring below

Organometallic compounds are compounds that have chemical bonds between an one or more metal atoms and one or more carbon atoms of an organyl group (an organic ligand). They have the prefix "organo-" (for example, organopalladium compounds). Organometallic compounds include subgroups like the metalloproteins such as haemoglobin.

The term "metalorganics" usually refers to metal-containing compounds lacking direct metal-carbon bonds but which contain organic ligands which bind them to an organic compound. Metal beta-diketonates, alkoxides, and dialkylamides are members of this class.

In addition to the traditional metals, elements such as boron, silicon, arsenic, and selenium form organometallic compounds.

Coordination compounds with organic ligands

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Heme group of hemoglobin

Many complexes have coordination bonds between a metal and organic ligands. The organic ligands often bind the metal through a heteroatom such as oxygen or nitrogen, in which case such compounds are called "coordination compounds".

Many organic coordination compounds occur in nature. For example, hemoglobin and myoglobin contain an iron center coordinated to the nitrogen atoms of a porphyrin ring; magnesium is the center of a chlorin ring in chlorophyll. The field of such inorganic compounds is known as bioinorganic chemistry. However, methylcobalamin (a form of Vitamin B12), with a cobalt-methyl bond, is a true organometallic complex, one of the few known in biology.

Structure and properties

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The metal-carbon bond in organometallic compounds is half way between being ionic and covalent. Organometallic compounds with bonds that have characters in between ionic and covalent are very important in industry. They are both relatively stable in solutions but ionic enough to undergo reactions. Two important classes are organolithium and Grignard reagents.

Organometallics find practical uses in stoichiometric and catalytic processes, especially processes involving carbon monoxide and alkene-derived polymers. All the world's polyethylene and polypropylene are produced with organometallic catalysts. Acetic acid is produced using metal carbonyl catalysts in the Monsanto process and Cativa process. The bulk of the synthetic alcohols, at least those larger than ethanol, are produced by hydrogenation of hydroformylation-derived aldehydes. The Wacker process is used in the oxidation of ethylene to acetaldehyde.

Organomettalics are highly basic and highly reducing. They catalyze many polymerization reactions. They are also useful stoichiometrically.

Organometallic compounds may be found in the environment. Environmentalists worry about organo-lead and organo-mercury compounds. They are toxic hazards.[3]

Research is underway using organometallic catalysis. The energy crisis has increased interest in more efficient ways of working with the fossil fuels we have left. The new interest in “green” technologies has also helped increase research. Many examples of organometallic research can be found in the petrochemical and pharmaceutical industries. Some current methods of chemical production are wasteful and produce toxic waste, while many organometallic catalysts show promise to change that.

History

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Louis Claude Cadet synthesized methyl arsenic compounds related to cacodyl. William Christopher Zeise[4] made platinum-ethylene complex.[5] Edward Frankland discovered dimethyl zinc. Ludwig Mond discovered Ni(CO)4.[6] Victor Grignard worked with organomagnesium compounds. The abundant and diverse products from coal and petroleum led to Ziegler-Natta, Fischer-Tropsch, hydroformylation catalysis which employ CO, H2, and alkenes as feedstocks and ligands.

Years ago, Tetraethyllead was added to gasoline as an antiknock agent. Because lead is toxic, it is no longer used in gasoline. Instead, other organometallic compounds such as ferrocene and methylcyclopentadienyl manganese tricarbonyl are now added to gasoline to prevent knocking.

The 1973 Nobel Prizes to Ernst Fischer and Geoffrey Wilkinson for work on metallocenes made organometallic chemistry more popular. In 2005, Yves Chauvin, Robert H. Grubbs and Richard R. Schrock shared the Nobel Prize for metal-catalyzed olefin metathesis.

Organometallic chemistry timeline

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References

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  1. Robert H. Crabtree (2005). The organometallic chemistry of the transition metals. Wiley. p. 560. ISBN 978-0-471-66256-3. Archived from the original on 2009-02-14. Retrieved 2011-08-21.
  2. Toreki R. (2003). "Organometallics defined". Interactive Learning Paradigms.
  3. Organometallics in environment and toxicology. Cambridge, UK: RSC Publishing. 2010. ISBN 978-1-84973-082-2. OCLC 642690101.
  4. Hunt L.B. (1984). "The First Organometallic Compounds: WILLIAM CHRISTOPHER ZEISE AND HIS PLATINUM COMPLEXES" (PDF). Platinum Metals Rev. 28 (2): 76–83. Archived from the original (PDF) on 2015-09-24. Retrieved 2011-08-21.
  5. Zeise, W.C. (1831). "Von der Wirkung zwischen Platinchlorid und Alkohol, und von den dabei entstehenden neuen Substanzen". Ann. Der Physik. 97 (4): 497–541. Bibcode:1831AnP....97..497Z. doi:10.1002/andp.18310970402.
  6. Crabtree R.H. (2009). The Organometallic Chemistry of the Transition Metals. Wiley. p. 2. ISBN 9780470257623.

Other websites

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