Biography:Hermann Staudinger

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Short description: German chemist, winner of the 1953 Nobel Prize in Chemistry (1881–1965)
Hermann Staudinger
Hermann Staudinger.jpg
Born
Worms, German Empire
Died8 September 1965(1965-09-08) (aged 84)
Freiburg, West Germany
Alma materTechnische Universität Darmstadt, University of Halle
Known forKetenes
Polymer chemistry
Staudinger coupling
Staudinger reaction
Staudinger synthesis
Spouse(s)Magda Staudinger (née Woit)
AwardsNobel Prize in Chemistry (1953)
Rudolf Diesel Medal (1962)
Scientific career
FieldsOrganic and Polymer chemistry
InstitutionsUniversity of Strasbourg
University of Karlsruhe
ETH Zürich
University of Freiburg
ThesisAnlagerung des Malonesters an ungesättigte Verbindungen (1903)
Doctoral advisorDaniel Vorländer
Doctoral studentsWerner Kern
Tadeusz Reichstein
Leopold Ružička
Rudolf Signer

Hermann Staudinger (German pronunciation: [ˈhɛʁman ˈʃtaʊ̯dɪŋɐ] (About this soundlisten); 23 March 1881 – 8 September 1965) was a German organic chemist who demonstrated the existence of macromolecules, which he characterized as polymers. For this work he received the 1953 Nobel Prize in Chemistry.

He is also known for his discovery of ketenes and of the Staudinger reaction. Staudinger, together with Leopold Ružička, also elucidated the molecular structures of pyrethrin I and II in the 1920s, enabling the development of pyrethroid insecticides in the 1960s and 1970s.

Early work

Staudinger was born in 1881 in Worms. Staudinger, who initially wanted to become a botanist, studied chemistry at the University of Halle, at the TH Darmstadt and at the LMU Munich. He received his "Verbandsexamen" (comparable to Master's degree) from TH Darmstadt. After receiving his Ph.D. from the University of Halle in 1903, Staudinger qualified as an academic lecturer at the University of Strasbourg in 1907.[1] He was supported in his work by new his wife Dora Staudinger who wrote up his lectures.[2]

Figure 1. The general structure of a ketene. R is any group.

It was here that he discovered the ketenes, a family of molecules characterized by the general form depicted in Figure 1.[3] Ketenes would prove a synthetically important intermediate for the production of yet-to-be-discovered antibiotics such as penicillin and amoxicillin.[4]

In 1907, Staudinger began an assistant professorship at the Technical University of Karlsruhe. Here, he successfully isolated a number of useful organic compounds (including a synthetic coffee flavoring) as more completely reviewed by Rolf Mülhaupt.Cite error: Closing </ref> missing for <ref> tag This reaction, commonly referred to as the Staudinger reaction, typically produces a high yield of the iminophosphorane.[5]

Figure 2. Triphenylphosphine and an azide react to form an iminophosphorane and gaseous nitrogen by the Staudinger reaction.
Nylon 6 and Nylon 6-6

World War I

While in autumn 1914 German professors joined the widespread public support of the war, Staudinger refused to sign Manifesto of the Ninety-Three and joined the few exceptions like Max Born, Otto Buek and Albert Einstein in condemning it. In 1917 he authored an essay predicting the defeat of Germany due to industrial superiority of the Entente and called for a peaceful settlement as soon as possible, and after the entrance of the US he repeated the call in a long letter to the German military leadership.[6] Fritz Haber attacked him for his essay, accusing him of harming Germany, and Staudinger in turn criticized Haber for his role in the German chemical weapons program.

Polymer chemistry

While at Karlsruhe and later, Zurich, Staudinger began research in the chemistry of rubber, for which very high molecular weights had been measured by the physical methods of Raoult and van 't Hoff. Contrary to prevailing ideas (see below), Staudinger proposed in a landmark paper published in 1920 that rubber and other polymers such as starch, cellulose and proteins are long chains of short repeating molecular units linked by covalent bonds.[7] In other words, polymers are like chains of paper clips, made up of small constituent parts linked from end to end (Figure 3).

Figure 3. A chain of paper clips (above) is a good model for a polymer such as polylactic acid (below). The polymer chain is composed of small pieces linked together in a head-to-tail fashion.

At the time, leading organic chemists such as Emil Fischer and Heinrich Wieland[8][9] believed that the measured high molecular weights were only apparent values caused by the aggregation of small molecules into colloids. At first, the majority of Staudinger’s colleagues refused to accept the possibility that small molecules could link together covalently to form high-molecular weight compounds. As Mülhaupt aptly notes, this is due in part to the fact that molecular structure and bonding theory were not fully understood in the early 20th century.[8]

In 1926, he was appointed lecturer of chemistry at the University of Freiburg at Freiburg im Breisgau (Germany), where he spent the rest of his career.[10] In 1927, he married the Latvian botanist, Magda Voita (also shown as; German: Magda Woit), who was a collaborator with him until his death and whose contributions he acknowledged in his Nobel Prize acceptance.[11] Further evidence to support his polymer hypothesis emerged in the 1930s. High molecular weights of polymers were confirmed by membrane osmometry, and also by Staudinger’s measurements of viscosity in solution. The X-ray diffraction studies of polymers by Herman Mark provided direct evidence for long chains of repeating molecular units. And the synthetic work led by Carothers demonstrated that polymers such as nylon and polyester could be prepared by well-understood organic reactions. His theory opened up the subject to further development, and helped place polymer science on a sound basis.

Private life

He married in 1906 to Dora Förster and they remained together until their divorce in 1926. They had four children including Eva Lezzi (1907-1993) and Klar (Klara) Kaufmann who were active in resisting the rise of fascism. Dora married again and became a leading peace activist.[2]

In 1935 Staudinger became a Patron Member of the SS.[12][13][14]

Legacy

Staudinger's groundbreaking elucidation of the nature of the high-molecular weight compounds he termed Makromoleküle paved the way for the birth of the field of polymer chemistry.[15] Staudinger himself saw the potential for this science long before it was fully realized. "It is not improbable," Staudinger commented in 1936, "that sooner or later a way will be discovered to prepare artificial fibers from synthetic high-molecular products, because the strength and elasticity of natural fibers depend exclusively on their macro-molecular structure – i.e., on their long thread-shaped molecules."[16] Staudinger founded the first polymer chemistry journal in 1940,[17] and in 1953 received the Nobel Prize in Chemistry for "his discoveries in the field of macromolecular chemistry."[18] In 1999, the American Chemical Society and Gesellschaft Deutscher Chemiker designated Staudinger's work as an International Historic Chemical Landmark.[19] His pioneering research has afforded the world myriad plastics, textiles, and other polymeric materials which make consumer products more affordable, attractive and enjoyable, while helping engineers develop lighter and more durable structures.

See also

Notes

  1. ↑ "Hermann Staudinger - Biographical". 1953. https://www.nobelprize.org/nobel_prizes/chemistry/laureates/1953/staudinger-bio.html. 
  2. ↑ 2.0 2.1 "Staudinger, Dora" (in de). https://hls-dhs-dss.ch/articles/028319/2021-03-26/. 
  3. ↑ Hermann Staudinger (1905). "Ketene, eine neue Körperklasse". Berichte der Deutschen Chemischen Gesellschaft 38 (2): 1735–1739. doi:10.1002/cber.19050380283. https://zenodo.org/record/1426156. 
  4. ↑ Tidwell, Thomas T. (2017). "Beta-Lactams from ketene- Imine Cycloadditins: An Update". in Banik, Bimal K. (in en). Beta-Lactams: Novel Synthetic Pathways and Applications. Edinburg, Texas: Springer. pp. 105. ISBN 978-3-319-55621-5. https://books.google.com/books?id=VDXbDgAAQBAJ&q=Ampicillin/flucloxacillin&pg=PA106. 
  5. ↑ Breinbauer, R.; Kohn, M. (2004). "The Staudinger Ligation – A Gift to Chemical Biology". Angew. Chem. Int. Ed. 43 (24): 3106–3116. doi:10.1002/anie.200401744. PMID 15199557. 
  6. ↑ "Life and work of Hermann Staudinger". https://www.k-online.com/en/Press/News/Dezember_2019_The_life_and_work_of_Hermann_Staudinger/Life_and_work_of_Hermann_Staudinger. 
  7. ↑ Staudinger, H. (1920). "Über Polymerisation". Ber. Dtsch. Chem. Ges. 53 (6): 1073–1085. doi:10.1002/cber.19200530627. https://zenodo.org/record/1426679. 
  8. ↑ 8.0 8.1 Cite error: Invalid <ref> tag; no text was provided for refs named mul
  9. ↑ Feldman, S. D.; Tauber, A. I. (1997). "Sickle Cell Anemia: Reexamining the First "Molecular Disease"". Bulletin of the History of Medicine 17 (4): 623–650. doi:10.1353/bhm.1997.0178. PMID 9431738. 
  10. ↑ Biography on Nobel prize website
  11. ↑ Ogilvie & Harvey 2000, p. 1223.
  12. ↑ Bernd Martin: Die Entlassung der jüdischen Lehrkräfte an der Freiburger Universität und die Bemühungen um ihre Wiedereingliederung nach 1945. In: Freiburger Universitätsblätter. H. 129, September 1995, pp. 7–46.
  13. ↑ Guido Deußing, Markus Weber, Das Leben des Hermann Staudinger, k-online, 2012, Teil 3.
  14. ↑ Uta Deichmann, Flüchten, Mitmachen, Vergessen. Chemiker und Biochemiker in der NS-Zeit. Weinheim: Wiley-VCH 2001.
  15. ↑ Staudinger, H. (1933). "Viscosity investigations for the examination of the constitution of natural products of high molecular weight and of rubber and cellulose". Trans. Faraday Soc. 29 (140): 18–32. doi:10.1039/tf9332900018. 
  16. ↑ Staudinger, H.; Heuer, W.; Husemann, E.; Rabinovitch, I. J. (1936). "The insoluble polystyrene". Trans. Faraday Soc. 32: 323–335. doi:10.1039/tf9363200323. 
  17. ↑ Meisel, I.; Mülhaupt, R. (2003). "The 60th Anniversary of the First Polymer Journal ("Die Makromolekulare Chemie"): Moving to New Horizons". Macromolecular Chemistry and Physics 204 (2): 199. doi:10.1002/macp.200290078. 
  18. ↑ The Nobel Prize in Chemistry 1953 (accessed Mar 2006).
  19. ↑ "Hermann Staudinger and the Foundation of Polymer Science". International Historic Chemical Landmarks. American Chemical Society. https://www.acs.org/content/acs/en/education/whatischemistry/landmarks/staudingerpolymerscience.html. 

References

External links



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