Moses Gomberg

Moses Gomberg

Moses Gomberg, the father of radical chemistry
Born (1866-02-08)February 8, 1866
Yelizavetgrad, Russian Empire [now Kirovograd, Ukraine]
Died February 12, 1947(1947-02-12) (aged 81)
Ann Arbor, Michigan, United States
Fields chemistry
Institutions University of Michigan
Alma mater University of Michigan
Doctoral advisor A. B. Prescott
Known for radical chemistry
Notable awards Willard Gibbs Award (1925)

Moses Gomberg (February 8, 1866 – February 12, 1947) was a chemistry professor at the University of Michigan.[1]

Early life and education

He was born in Yelisavetgrad, Russian Empire. In 1884, the family emigrated to Chicago to escape the pogroms following the assassination of Czar Alexander II. In Chicago he worked at the Stock Yards while attending Lake High School. In 1886, Moses entered the University of Michigan, where he obtained his B.Sc in 1890 and his doctorate in 1894 under the supervision of A. B. Prescott. His thesis, titled "Trimethylxanthine and Some of its Derivatives", dealt with the derivatization of caffeine.[2]

Career

Appointed an instructor in 1893, Gomberg worked at the University of Michigan for the duration of his professional academic career, becoming chair of the Department of Chemistry from 1927 until his retirement in 1936. Dr. Gomberg served as President of the American Chemical Society in 1931.

In 1896–1897, he took a year's leave to work as a postdoctoral researcher with Baeyer and Thiele in Munich and with Victor Meyer in Heidelberg, where he successfully prepared the long-elusive tetraphenylmethane.

During attempts to prepare the even more sterically congested hydrocarbon hexaphenylethane, he correctly identified the triphenylmethyl radical, the first persistent radical to be discovered, and is thus known as the founder of radical chemistry. The work was later followed up by Wilhelm Schlenk. Gomberg was a mentor to Werner Emmanuel Bachmann who also carried on his work and together they discovered the Gomberg-Bachmann reaction.[3] In 1923, he claimed to have synthesized chlorine tetroxide via the reaction of silver perchlorate with iodine, but was later shown to have been mistaken.

Synthesis of tetraphenylmethane

Gomberg was the first to successfully synthesize tetraphenylmethane. This was accomplished by the thermal decomposition of 1-phenyl-2-trityldiazene to the desired product in 2-5% yield.[4][5]

Discovery of persistent radicals

Seeking to prepare hexaphenylethane (5), Gomberg attempted a Wurtz coupling of triphenylmethyl chloride (1). Elemental analysis of the resultant white crystalline solid, however, uncovered discrepancies with the predicted molecular formula:

calculated for (5) found
% Carbon 93.83 87.93
% Hydrogen 6.17 6.04

Hypothesizing that (1) had combined with molecular oxygen to form the peroxide (4), Gomberg found that treatment of (1) with sodium peroxide was another means of synthesizing (4).

By performing the reaction of triphenylchloromethane with zinc under an atmosphere of carbon dioxide Gomberg obtained the free radical (2). This compound reacted readily with air, chlorine, bromine and iodine. On the basis of his experimental evidence Gomberg concluded that he had discovered the first instance of a persistent radical and trivalent carbon. This was a controversial conclusion for many years as molecular weight determinations of (2) found a value that was double that of the free radical. Gomberg postulated that some non-tetravalent carbon structure existed in solution because of the observed activity towards oxygen and the halogens.[6] Gomberg and Bachmann later found that treatment of "hexaphenylethane" with magnesium resulted in a Grignard reagent, the first instance of the formation of such a compound from a hydrocarbon.[7] Studies of other triarylmethyl compounds gave results similar to Gomberg's, and it was hypothesized that (2) existed in equilibrium with its dimer hexaphenylethane (5).[8] However this structure was later disproven in favor of the quinoid dimer (3).[9][10][11][12]

At the end of his first report of trivalent carbon "On Trivalent Carbon"reference 5 Gomberg wrote "This work will be continued and I wish to reserve the field for myself." While nineteenth-century chemists respected such claims Gomberg found that the field of chemistry he founded was too rich to reserve for himself.

Legacy

Upon his death in 1947 Moses Gomberg bequeathed his estate to the Chemistry Department of the University of Michigan for the creation of student fellowships. In 2000, the centennial of his paper "Triphenylmethyl, a Case of Trivalent Carbon", a symposium was held in his memory and a plaque was installed in the Chemistry Building at the University of Michigan designating a National Historic Chemical Landmark.

In 1993, the Chemistry Department of the University of Michigan instituted the Moses Gomberg Lecture series to provide assistant professors an opportunity to invite distinguished scientists to the Chemistry department.

Personal life

Gomberg never married, living with his sister Sophia in Ann Arbor for his adult life.

External links

References

  1. ↑ C. S. Schoepple and W. E. Bachmann (1947). "Moses Gomberg 1866-1947". Journal of the American Chemical Society 69 (12): 2921–5,. doi:10.1021/ja01204a641.
  2. ↑ Gomberg, American Chemical Journal (1892) 14 611-19.
  3. ↑ M. Gomberg, W. E. Bachmann (1924). "The Synthesis of Biaryl Compounds by Means of the Diazo Reaction". Journal of the American Chemical Society 42 (10): 2339–2343. doi:10.1021/ja01675a026.
  4. ↑ Gomberg, Berichte der Deutschen Chemischen Gesellschaft (1897) 30 2043
  5. ↑ Gomberg, Journal of the American Chemical Society, 1898, 20 pg 773 DOI 0.1021/ja02072a009
  6. ↑ Gomberg, Journal of the American Chemical Society (1900) 22 pg 757 DOI 10.1021/ja02049a006
  7. ↑ Gomberg, Bachmann Journal of the American Chemical Society (1930) 52 2455
  8. ↑ Gomberg, Journal of the American Chemical Society, (1901) 23 496 DOI 10.1021/ja02033a015
  9. ↑ Gomberg, Journal of the American Chemical Society (1903) 25, pg 1274 DOI 10.1021/ja02014a009
  10. ↑ Gomberg, Journal of Chemical Education (1932) 9, 439
  11. ↑ H. Lankamp, W. Th. Nauta and C. MacLean Tetrahedron Letters (1968) 9 249–254 doi 10.1016/S0040-4039(00)75598-5
  12. ↑ March, Advanced Organic Chemistry 4ed, 1992 pg189


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