Paul Friedländer (chemist)
| Paul Friedländer | |
|---|---|
 | |
| Born |
August 29, 1857 Königsberg, Prussia |
| Died |
September 4, 1923 (aged 66) Darmstadt, Germany |
| Nationality | German |
| Fields | organic chemistry |
| Institutions | Darmstadt University of Technology |
| Alma mater | University of Munich |
| Doctoral advisor | Adolf von Baeyer |
| Known for | Friedländer synthesis |
| Notable awards | Lieben Prize 1908 |
Paul Friedländer (August 29, 1857, Königsberg – September 4, 1923, Darmstadt) was a German chemist best known for his research on derivates of indigo (for example thioindigo) and isolation of Tyrian purple from Murex brandaris.
Life and work
Paul Friedländer was born as son of Ludwig Friedländer in Königsberg in 1857. The chemist Carl Gräbe was a regular guest of his father; thus after finishing the gymnasium, Friedländer studied chemistry in Königsberg in the laboratories of Gräbe. Later he studied at the Strasbourg and Munich where he assisted Adolf von Baeyer. He received his PhD for the work with Baeyer and completed his habilitation in 1883. He left the well-equipped laboratories of Baeyer in Munich in 1884 to work in the small company K. Oehler in Offenbach. In 1888, he became professor at the University of Karlsruhe.
During a visit at his parents in Königsberg, he got engaged and married Martha Kobligk; they had three daughters. Although he liked staying in Germany, Friedländer accepted a position at the Technologische Gewerbemuseum in Vienna in 1895. During that time, he discovered the thioindigo. His research on the color variations in substituted indigoes yielded numerous patents and was applied in industrial production. Friedländer isolated and analyzed the natural dyestuff of Tyrian purple. He was able to obtain 12,000 Murex brandaris from biologists working at the Mediterranean sea. In a complicated process, he isolated 1.4 g of pure Tyrian purple. Contrary to his expectations, the compound did not contain sulfur, but was a bromine substituted indigo, which had been already synthesized back in 1903.[1][2] Friedlander was awarded the Lieben Prize for this discovery.[3]
In 1911, Friedländer abandoned his position in Vienna and joined the University of Darmstadt. The University was not far from the dye factories Chemische Fabrik Kalle, Höchst and Cassella that helped Friedländer in his research on dyes. In 1911, he was awarded the Adolf-von-Baeyer-Prize.
During World War I, Friedländer worked at the Kaiser Wilhelm Institute for Physical Chemistry and Elektrochemistry together with Fritz Haber. The poor living standards after the war affected his health, and after a trip in the summer of 1923 from Darmstadt to Biebrich, Friedländer had to stay in a hospital. His health problems gradually deteriorated and on September 4, 1923, he died in Darmstadt.[4][5]
The chemical reaction of 2-aminobenzaldehydes with ketones to form quinoline derivatives, which Friedländer discovered in 1882, is today known as the Friedländer synthesis.[6][7]
References
- ↑ Friedlaender, P. (1909). "Zur Kenntnis des Farbstoffes des antiken Purpurs aus Murex brandaris". Monatshefte für Chemie 30: 247. doi:10.1007/BF01519682.
- ↑ Sachs, F. & Kempf, R. (1903). "Über p-Halogen-o-nitrobenzaldehyde". Berichte der Deutschen Chemischen Gesellschaft 36 (3): 3299–3303. doi:10.1002/cber.190303603113.
- ↑ "Ignaz Lieben-Preisträger 1908: Paul Friedlaender". Retrieved 2010-03-02.
- ↑ Schlenk, W. (1924). "Obituaries Paul Friedländer". Berichte der deutschen chemischen Gesellschaft (A and B Series) 57: A13–A28. doi:10.1002/cber.19240570436.
- ↑ "Friedlaender Paul". Österreichisches Biographisches Lexikon 1815–1950 1. Vienna: Österreichische Akademie der Wissenschaften. 1957. ISBN 3-7001-1327-7.
- ↑ Friedlaender, Paul (1882). "Ueber o-Amidobenzaldehyd". Berichte der deutschen chemischen Gesellschaft 15 (2): 2572–2575. doi:10.1002/cber.188201502219.
- ↑ Friedländer, Paul; Gohring, C. F. (1883). "Ueber eine Darstellungsmethode im Pyridinkern substituirter Chinolinderivate". Berichte der deutschen chemischen Gesellschaft 16 (2): 1833–1839. doi:10.1002/cber.18830160265.
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