He was born in Yelisavetgrad, Russian Empire to a Jewish merchant family. His father was Hershko (Hirsh) Gomberg and his mother was Maryam-Ethel Reznikova. In 1884, the family emigrated to Chicago to escape the pogroms following the assassination of Czar Alexander II. In Chicago he worked at the stockyards 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.[5]
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.
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.[7][8]
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.[9] 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.[10] 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).[11] However this structure was later disproven in favor of the quinoid dimer (3).[12][13][14][15]
At the end of his first report of trivalent carbon "On Trivalent Carbon"[11] 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.[16]
References
^Schoepfle, C.; Bachmann, W. (2004-05-19). "Moses Gomberg 1866-1947". Journal of the American Chemical Society. 69 (12): 2921–2925. doi:10.1021/ja01204a641.
^Gomberg, American Chemical Journal (1892) 14 611-19.
^Gomberg, M.; Bachmann, W. E. (2002-05-01). "The synthesis of biaryl compounds by means of the diazo reaction". Journal of the American Chemical Society. 46 (10): 2339–2343. doi:10.1021/ja01675a026.
^Lankamp, H.; Nauta, W. Th.; MacLean, C. (1968-01-01). "A new interpretation of the monomer-dimer equilibrium of triphenylmethyl- and alkylsubstituted-diphenyl methyl-radicals in solution". Tetrahedron Letters. 9 (2): 249–254. doi:10.1016/S0040-4039(00)75598-5.