Wilhelm Rudolph Fittig

Wilhelm Rudolph Fittig

Infobox Scientist
name = PAGENAME
box_width =


image_size =150px
caption = PAGENAME
birth_date = December 6, 1835
birth_place = Hamburg, Germany
death_date = November 19, 1910
death_place =
residence = |citizenship =
nationality = German
ethnicity =
field = chemistry
work_institutions =
alma_mater =
doctoral_advisor =
doctoral_students =
known_for = Fittig reaction
author_abbrev_bot =|author_abbrev_zoo =
influences =
influenced =
prizes =
religion = |footnotes = |

Wilhelm Rudolph Fittig (b. December 6, 1835, Hamburg, GermanyNovember 19, 1910) was a German chemist. Fittig was responsible for discovery of the pinacol coupling reaction, mesitylene, diacetyl and biphenyl. He studied the action of sodium on ketones and
hydrocarbons. He discovered the Fittig reaction or Wurtz-Fittig reaction for the synthesis of alkylbenzenes, he proposed a diketone structure for benzoquinone and isolated phenanthrene from coal tar. He discovered andsynthesized the first lactones and investigated structures of piperine
naphthalene and fluorene.

Career

Fittig studied chemistry at Göttingen, graduating as Ph.D. with a dissertation on acetone in 1858, under the supervision of Heinrich Limpricht and Friedrich Wöhler. He subsequently held several appointments at Göttingen, being "privat dozent" (1860), and extraordinary professor (1870). In 1870 he obtained the chair at Tübingen, and in 1876 that at Strassburg, where the laboratories were erected from his designs. Fittig's researches are entirely in organic chemistry, and cover an exceptionally wide field. The aldehydes and ketones provided material for his earlier work. He observed that aldehydes and ketones may suffer reduction in neutral, alkaline, and sometimes acid solution to secondary and tertiary glycols, substances which he named pinacones; and also that certain pinacones when distilled with dilute sulphuric acid gave compounds, which he named pinacolines. The unsaturated acids also received much attention, and he discovered the internal anhydrides of oxyacids, termed lactones. In 1863 he introduced the reaction known by his name. In 1855 Adolph Wurtz had shown that when sodium acted upon alkyl iodides, the alkyl residues combined to form more complex hydrocarbons; Fittig developed this method by showing that a mixture of an aromatic and alkyl haloid, under similar treatment, yielded homologues of benzene. His investigations on Perkins reaction led him to an explanation of its mechanism which appeared to be more in accordance with the facts. The question, however, is one of much difficulty, and the exact course of the reaction appears to await solution. These researches incidentally solved the constitution of coumarin, the odoriferous principle of woodruff. Fittig and Erdmann's observation that phenyl isocrotonic acid readily yielded α-naphthol by loss of water was of much importance, since it afforded valuable evidence as to the constitution of raphthalene. They also investigated certain hydrocarbons occurring in the high boiling point fraction of the coal tar distillate and solved the constitution of phenanthrene. We also owe much of our knowledge of the alkaloid piperine to Fittig, who in collaboration with Ira Remsen established its constitution in 1871. Fittig has published two widely used textbooks; be edited several editions of Wohler's "Grundriss der organischen Chemie" (11th ed., 1887) and wrote an "Unorganische Chemie" (1st ed., 1872; 3rd, 1882). His researches have been recognized by many scientific societies and institutions, the Royal Society awarding him the Davy medal in 1906.

References

*1911

External links

* [http://www.scs.uiuc.edu/~mainzv/Web_Genealogy/Info/fittigwr.pdf Genealogy database entry, University of Illinois]


Wikimedia Foundation. 2010.

Игры ⚽ Поможем решить контрольную работу

Look at other dictionaries:

  • Rudolph Fittig — Wilhelm Rudolph Fittig (* …   Deutsch Wikipedia

  • Fittig — Rudolph Fittig Wilhelm Rudolph Fittig (* 6. Dezember 1835 in Hamburg; † 19. November 1910 in Straßburg) war ein deutscher Chemiker. Leben und Wirken Nach dem Studium der Chemie an der Universität Göttingen promovierte …   Deutsch Wikipedia

  • Wilhelm Friedrich Philipp Pfeffer — 230px Nacimiento 9 de marzo 1845 Grebenstein, Kassel Fallecimiento 31 de enero 1920 Leptzig Nacionalidad …   Wikipedia Español

  • Wilhelm Pfeffer — Wilhelm Friedrich Philipp Pfeffer (9 March 1845 31 January 1920) was a German botanist and plant physiologist who was born in Grebenstein. He studied botany, physics and pharmacology at the University of Goettingen under Friedrich Wöhler (1800… …   Wikipedia

  • Wilhelm Pfeffer — Wilhelm Friedrich Philipp Pfeffer (* 9. März 1845 in Grebenstein bei Kassel; † 31. Januar 1920 in Leipzig) war ein deutscher Botaniker und Pflanzenphysiologe. Sein offizielles botanisches Autorenkürzel lautet „Pfeff.“ …   Deutsch Wikipedia

  • Pinacol rearrangement — The pinacol rearrangement or pinacol pinacolone rearrangement is a method for converting a 1,2 diol to a carbonyl compound in organic chemistry. This rearrangement takes place under acidic conditions. The name of the reaction comes from the… …   Wikipedia

  • Фиттиг, Вильгельм Рудольф — Вильгельм Рудольф Фиттиг Wilhelm Rudolph Fittig Дата рождения …   Википедия

  • William Ramsay — Infobox Scientist name = William Ramsay image size = 180px birth date = birth date|1852|10|2|df=y birth place = Glasgow, Scotland nationality = Scotland death date = death date and age|1916|7|23|1852|10|2|df=y death place = High Wycombe, Bucks.,… …   Wikipedia

  • Heinrich Limpricht — Infobox Scientist name = Heinrich Limpricht |300px image width = 300px caption = Heinrich Limpricht birth date = 21 April 1827 birth place = Eutin, Duchy of Oldenburg death date = 13 May 1909 death place = Greifswald, German Empire residence =… …   Wikipedia

  • Pinacol coupling reaction — A pinacol coupling reaction is an organic reaction in which a carbon carbon covalent bond is formed between the carbonyl groups of an aldehyde or a ketone in presence of an electron donor in a free radical process Ref|1. The reaction product is a …   Wikipedia

Share the article and excerpts

Direct link
Do a right-click on the link above
and select “Copy Link”