Robert Robinson (chemist)
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Sir Robert Robinson
|President of the Royal Society|
|Preceded by||Sir Henry Harrett Dale|
|Succeeded by||Edgar Adrian|
|Born||13 September 1886|
|Died||8 February 1975 (aged 88)|
Great Missenden, Buckinghamshire, England
|Alma mater||University of Manchester|
|Known for||Development of Organic synthesis|
|Spouse(s)||Gertrude Maud Robinson|
|Awards||Davy Medal (1930)|
Royal Medal (1932)
Copley Medal (1942)
Nobel Prize for Chemistry (1947)
Franklin Medal (1947)
Albert Medal (1947)
|Institutions||University of Sydney|
University of Liverpool
British Dyestuffs Corporation
University of Manchester
University of London
University of Oxford
|Doctoral advisor||William Henry Perkin, Jr.|
|Doctoral students||Arthur John Birch|
William Sage Rapson
Sir Robert Robinson OM PRS FRSE (13 September 1886 – 8 February 1975) was an English organic chemist and Nobel laureate recognised in 1947 for his research on plant dyestuffs (anthocyanins) and alkaloids. In 1947, he also received the Medal of Freedom with Silver Palm.
Born at Rufford Farm, near Chesterfield, Derbyshire, Robinson went to school at the Chesterfield Grammar School, the private Fulneck School and the University of Manchester. In 1907 he was awarded an 1851 Research Fellowship from the Royal Commission for the Exhibition of 1851 to continue his research at the University of Manchester. He was appointed as the first Professor of Pure and Applied Organic Chemistry in the School of Chemistry at the University of Sydney in 1912. He was the Waynflete Professor of Chemistry at Oxford University from 1930 and a Fellow of Magdalen College, Oxford.
Robinson Close in the Science Area at Oxford is named after him, as is the Robert Robinson Laboratory at the University of Liverpool, the Sir Robert Robinson Laboratory of Organic Chemistry at the University of Manchester and the Robinson and Cornforth Laboratories at The University of Sydney.
Robinson was a strong amateur chess player. He represented Oxford University in a friendly match with a team from Bletchley Park in December 1944; he lost his game to pioneering computer scientist I. J. Good. He was president of the British Chess Federation from 1950–53, and with Raymond Edwards he co-authored the book The Art and Science of Chess (Batsford, 1972).
His synthesis of tropinone, a precursor of cocaine, in 1917 was not only a big step in alkaloid chemistry but also showed that tandem reactions in a one-pot synthesis are capable of forming bicyclic molecules. 
He invented the symbol for benzene having a circle in the middle whilst working at St Andrews University in 1923. He is known for inventing the use of the curly arrow to represent electron movement, and he is also known for discovering the molecular structures of morphine and penicillin.
- Saltzman, M. D. (1987). "The development of Sir Robert Robinson's contributions to theoretical organic chemistry". Natural Product Reports. 4: 53–20. doi:10.1039/NP9870400053.
- Todd, L.; Cornforth, J. W. (1976). "Robert Robinson. 13 September 1886 – 8 February 1975". Biographical Memoirs of Fellows of the Royal Society. 22: 414. doi:10.1098/rsbm.1976.0018. JSTOR 769748.
- "Former RSE Fellows 1783–2002" (PDF). Royal Society of Edinburgh. Retrieved 31 March 2010.
- 1851 Royal Commission Archives
- "Science Area". www.ox.ac.uk. Retrieved 12 June 2009.
- Nicholas Metropolis (ed.), History of Computing in the Twentieth Century; chapter Pioneering Work on Computers at Bletchley (I. J. Good), p38
- British Chess magazine, February 1945, p36
- Nobel Prize bio
- Chemical and Engineering news
- Robinson, R. (1917). "LXIII. A Synthesis of Tropinone". Journal of the Chemical Society, Transactions. 111: 762–768. doi:10.1039/CT9171100762.
- Birch, A. J. (1993). "Investigating a Scientific Legend: The Tropinone Synthesis of Sir Robert Robinson, F.R.S". Notes and Records of the Royal Society of London (1938–1996). 47 (2): 277–226. doi:10.1098/rsnr.1993.0034. JSTOR 531792.
- Abraham, E. P. (1987). "Sir Robert Robinson and the early history of penicillin". Natural Product Reports. 4 (1): 41–46. doi:10.1039/np9870400041. PMID 3302773.