|Born||December 12, 1866|
|Died||November 15 1919 (aged 52)|
|Institutions||University of Zurich|
|Alma mater||University of Zurich|
|Doctoral advisor||Arthur Rudolf Hantzsch, Marcellin Berthelot|
|Known for||configuration of transition metal complexes|
|Notable awards||Nobel Prize for Chemistry (1913)|
Alfred Werner (December 12, 1866 - November 15, 1919) was a Swiss chemist who was a professor at the University of Zurich. He won the Nobel Prize in Chemistry in 1913 for proposing the octahedral configuration of transition metal complexes. Werner developed the basis for modern coordination chemistry. He was the first inorganic chemist to win the Nobel prize, and the only one prior to 1973.
He was born in 1866 in Mulhouse, Alsace (which was then part of France, but which was annexed by Germany in 1871). He went to Switzerland to study chemistry at Zurich where he obtained his doctorate in 1890. After postdoctoral study in Paris, he returned to Zurich to teach in 1892, and became a professor as well a Swiss citizen in 1895.
For example, it was known that cobalt forms a "complex" with formula CoCl3•6NH3, but the nature of the association indicated by the dot was mysterious. Werner proposed the structure [Co(NH3)6]Cl3, with the Co3+ ion surrounded by six NH3 at the vertices of an octahedron. The three Cl- are dissociated as free ions, which Werner confirmed by measuring the electrical conductivity of the compound in aqueous solution, and also by chloride anion analysis using precipitation with silver nitrate. Later, magnetic susceptibility analysis was also used to confirm Werner's proposal for the chemical nature of CoCl3•6NH3.
For complexes with more than one type of ligand, Werner succeeded in explaining the number of isomers observed. For example, he explained the existence of two isomers of "Co(NH3)4Cl3", one green and one purple. Werner proposed that these are two geometric isomers of formula [Co(NH3)4Cl2]Cl, with one Cl- ion dissociated as confirmed by conductivity measurements. The Co atom is surrounded by four NH3 and two Cl ligands at the vertices of an octahedron. The green isomer is "trans" with the two Cl ligands at opposite vertices, and the purple is "cis" with the two Cl at adjacent vertices.
Nature of valence
Before Werner, chemists defined the valence of an element as the number of its bonds without distinguishing different types of bond. However in complexes such as [Co(NH3)6]Cl3 for example, Werner considered that the Co-Cl bonds correspond to a "primary" valence of 3 at long distance, while the Co-NH3 bonds which correspond to a "secondary" or weaker valence of 6 at shorter distance. This secondary valence of 6 he referred to as the coordination number which he defined as the number of molecules (here of NH3) directly linked to the central metal atom. In other complexes he found coordination numbers of 4 or 8.
On these views, and other similar views, in 1904 Richard Abegg formulated what is now known as Abegg's rule which states that that the difference between the maximum positive and negative valence of an element is frequently eight. This rule was used later in 1916 when Gilbert N. Lewis formulated the “octet rule” in his cubical atom theory.
Today Werner's primary valence corresponds to the oxidation state, and the secondary valence is always called coordination number. The Co-Cl bonds (in the above example) are now classed as ionic, and each Co-N bond is a coordinate covalent bond between the Lewis acid Co3+ and the Lewis base NH3.
- Biography at Nobelprize.org
- The Nobel Prize in Chemistry 1913 - short article about his work on the linkage of atoms in molecules by which he has thrown new light on earlier investigations and opened up new fields of research especially in inorganic chemistry.
- Alfred Werner – Biography.
- W. Gregory Jackson, Josephine A. McKeon, Silvia Cortez (2004). "Alfred Werner's Inorganic Counterparts of Racemic and Mesomeric Tartaric Acid: A Milestone Revisited". Inorg. Chem. 43 (20): 6249–6254. doi:10.1021/ic040042e.
- Kristin Bowman-James (2005). "Alfred Werner Revisited: The Coordination Chemistry of Anions". Acc. Chem. Res. 38 (8): 671–678. doi:10.1021/ar040071t S0001-4842(04)00071-8 Check
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