Georg Wittig

Georg Wittig

Infobox_Scientist
name = Georg Wittig



birth_date = birth date|1897|6|16
birth_place = Berlin, Germany
death_date = death date and age|1987|8|26|1897|6|16
death_place =
nationality = Germany
field = Chemistry
work_institution = University of Marburg
Technical University at Brunswick
University of Freiburg
University of Tübingen
alma_mater = University of Marburg
doctoral_advisor = Karl von Auwers
doctoral_students = Ulrich Schöllkopf
known_for = Wittig reaction
1,2-Wittig rearrangement
2,3-Wittig rearrangement
Potassium tetraphenylborate
prizes = Nobel Prize in Chemistry (1979)
footnotes =

Georg Wittig (June 16, 1897 – August 26 1987) was a German chemist who reported a method for synthesis of alkenes from aldehydes and ketones using compounds called phosphonium ylides in the Wittig reaction. He shared the Nobel Prize in Chemistry with Herbert C. Brown in 1979.

Biography

Wittig was born in Berlin, Germany and shortly after his birth he moved with his family to Kassel, where his father was professor at the applied arts high school. He attended school in Kassel and started studying chemistry at the University of Tübingen 1916. He was drafted and became a lieutenant in the cavallery of Hesse-Kassel (or Hesse-Cassel). After being a English prisoner of war from 1918 till 1919 the restart of his chemistry studies was complicated, due to the overcrowded universities. By a direct plea to Karl von Auwers, who was professor for organic chemistry at the University of Marburg at time, he was able rejoin a university. After 3 years he was rewarded his PhD in organic chemistry. Karl von Auwers was able to convince him to start an academic career, which yielded his habilitation in 1926. He became a close friend to Karl Ziegler, who was also doing his habilitation with Auwers during that time. The successor of Karl von Auwers Hans Meerwein assumed Wittig as lecturer, partly because he was impressed by the new 400 page book on stereochemistry that Wittig had written. In 1931 he married Waltraud Ernst, a colleague from the Auwers working group. The invitation of Karl Fries brought him as professor to the Technical University at Brunswick in 1932. The time in Brunswick became more and more problematic as the Nazis tried to get rid of Karl Fries and Wittig showed solidarity with him. After forced emeritation of Fries, in 1937 Hermann Staudinger offered Wittig a position at the University of Freiburg, partly because he knew Wittig from his book on stereochemistry in which he supported the highly criticized theory on macromolecules of Staudinger. The foundations of the carbanion chemistry was laid during the time in Freiburg. In 1944 Wittig succeeded the head of the organic department Wilhelm Schlenk at the University of Tübingen. Most of the scientific work like the Wittig reaction was done during the time at the University of Thübingen. The 1956 appointment of the nearly sixty year old Wittig as head of the organics department at the University of Heidelberg as successor of Karl Freudenberg was exceptional even at that time. The newly built department and the close connection to the BASF convinced Wittig to take this opportunity. He worked at the University of Heidelberg even after his emeritation in 1967 and published papers until 1980. Most of his awards were presented in the time in Heidelberg, such as the honorary doctor of the Sorbonne in 1956 and the Nobel Prize in Chemistry in 1979.

Work

Wittig's contributions also include the preparation of phenyllithium and the discovery of the 1,2-Wittig rearrangement and the 2,3-Wittig rearrangement.

Wittig was well known in the chemistry community for being a consummate experimenter and observer of chemical transformations, while caring very little for the theoretical and mechanistic underpinnings of the work he produced.

References

*cite journal | author=Werner Tochtermann | title=Obituary: Georg Wittig (1897-1987) | journal=Liebigs Annalen | volume=vol. 1997 | issue=no. 3 | pages=I | year=1997 | doi=10.1002/jlac.199719970303
*Citation
id = PMID:389768
url= http://www.ncbi.nlm.nih.gov/pubmed/389768
last=Gericke
first=D
publication-date=1979 Nov 15
year=1979
title= [Nobel prize for chemistry 1979 for the Wittig reaction as a basis for many-sided syntheses. Georg Wittig, 60th German Nobel laureate]
volume=97
issue=43
periodical=Fortschr. Med.
pages=1958, 1964

External links

* [http://uk.geocities.com/hertouyt/qsd/wittig-cv.html The development of the use of boron- and phosphorus-containing compounds, respectively, into important reagents in organic synthesis.]


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  • Georg Wittig — (Georg Friedrich Karl Wittig; * 16. Juni 1897 in Berlin; † 26. August 1987 in Heidelberg) war ein deutscher Chemiker und Träger des Nobelpreises für Chemie 1979. Wittig fand einen Weg, die Carbonylgruppe einer organischen Verbindung in eine… …   Deutsch Wikipedia

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  • Georg Wittig — Pour les articles homonymes, voir Wittig. Georg Wittig Naissance 16 juin 1897 Berlin (Allemagne) Décès 26 août 1987 …   Wikipédia en Français

  • Chemienobelpreis 1979: Herbert Charles Brown — Georg Wittig —   Der amerikanische und der deutsche Wissenschaftler erhielten den Nobelpreis für ihre Entwicklung von Bor beziehungsweise Phosphorverbindungen in wichtigen Reagenzien innerhalb organischer Synthesen.    Biografien   Herbert Charles Brown, *… …   Universal-Lexikon

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  • Wittig reaction — The Wittig reaction is a chemical reaction of an aldehyde or ketone with a triphenyl phosphonium ylide (often called a Wittig reagent) to give an alkene and triphenylphosphine oxide. [cite journal author = Georg Wittig, Ulrich Schöllkopf journal …   Wikipedia

  • Wittig-Synthese — Die Wittig Reaktion ist eine wichtige Reaktion der organischen Chemie. Als Namensreaktion ist sie nach ihrem Entdecker Georg Wittig benannt. Bei ihr werden Phosphorylide mit Carbonylverbindungen unter Bildung eines Alkens umgesetzt: Die Wittig… …   Deutsch Wikipedia

  • Wittig Reaktion — Die Wittig Reaktion ist eine wichtige Reaktion der organischen Chemie. Als Namensreaktion ist sie nach ihrem Entdecker Georg Wittig benannt. Bei ihr werden Phosphorylide mit Carbonylverbindungen unter Bildung eines Alkens umgesetzt: Die Wittig… …   Deutsch Wikipedia

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