Exploring the Fascinating World of Grignard Reagent in Organometallic Chemistry

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Delve into the significance of the Grignard Reagent, a pivotal discovery honored with the Nobel Prize in Chemistry in 1912 for its transformative impact on organic chemistry. Unveil the versatile applications and reactions of this essential reagent, showcasing its ability to react with various substrates including alkyl, vinyl, alkynyl, and aryl compounds, thus playing a crucial role in advancing the field of organometallics.


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  1. Organometallics Sections 12.4 and 12.5

  2. The Grignard Reagent

  3. The Grignard Reagent The Nobel Prize in Chemistry 1912 "for the discovery of the so-called Grignard reagent, which in recent years has greatly advanced the progress of organic chemistry" Victor Grignard

  4. The Grignard Reagent

  5. The Grignard Reagent X = Cl, Br, I R = methyl 1 , 2 , 3 alkyl vinyl alkynyl aryl

  6. The Grignard Reagent d+ X = Cl, Br, I R = methyl 1 , 2 , 3 alkyl vinyl alkynyl aryl

  7. The Grignard Reagent d+ +2 X = Cl, Br, I R = methyl 1 , 2 , 3 alkyl vinyl alkynyl aryl

  8. The Grignard Reagent d+ +2 -1 X = Cl, Br, I R = methyl 1 , 2 , 3 alkyl vinyl alkynyl aryl

  9. The Grignard Reagent d+ +2 -1 -1 X = Cl, Br, I R = methyl 1 , 2 , 3 alkyl vinyl alkynyl aryl

  10. The Grignard Reagent d+ X = Cl, Br, I R = methyl 1 , 2 , 3 alkyl vinyl alkynyl aryl

  11. The Grignard Reagent X = Cl, Br, I R = methyl 1 , 2 , 3 alkyl vinyl alkynyl aryl

  12. The Grignard Reagent X = Cl, Br, I R = methyl 1 , 2 , 3 alkyl vinyl alkynyl aryl

  13. The Grignard Reagent X = Cl, Br, I R = methyl 1 , 2 , 3 alkyl vinyl alkynyl aryl

  14. The Grignard Reagent X = Cl, Br, I R = methyl 1 , 2 , 3 alkyl vinyl alkynyl aryl

  15. The Grignard Reagent d+

  16. The Grignard Reagent

  17. The Grignard Reagent

  18. The Grignard Reagent

  19. The Gilman Reagent

  20. Professor Henry Gilman (May 9, 1893 Nov 7, 1986). Born in Boston, Massachusetts, he received his B. S. (1915), an M. S. (1916), and a Ph.D. (1918) in Chemistry from Harvard University. For his pre-doctoral work he studied in Europe at Zurich Polytechnikum, the Sorbonne in Paris, and at Oxford in London. Dr. Gilman began his career at the University of Illinois as an Instructor of Chemistry in 1919. Later that year, he accepted the position of Assistant Professor (1919 - 1920) at Iowa State College (University). By 1923 Dr. Gilman had been promoted to full Professor teaching all the Organic Chemistry courses at Iowa State College. His main area of research was in the Organometallic Chemistry area of Grignard reagents where he developed numerous Organometallic reagents, including the dialkyllithium reagent which bears his name. http://www.lib.iastate.edu/spcl/exhibits/150/template/gilman.html

  21. The Gilman Reagent

  22. The Gilman Reagent

  23. The Gilman Reagent

  24. The Gilman Reagent

  25. The Gilman Reagent

  26. The Suzuzi Miyaura Cross Coupling The Nobel Prize in Chemistry 2010 The Nobel Prize in Chemistry 2010 "for palladium-catalyzed cross couplings in organic synthesis" Richard F. Heck Ei-ichi Negishi Akira Suzuki

  27. The Suzuzi Miyaura Cross Coupling Used in preparation of biaryls

  28. The Suzuzi Miyaura Cross Coupling Used in preparation of biaryls

  29. The Suzuzi Miyaura Cross Coupling Used in preparation of biaryls

  30. The Suzuzi Miyaura Cross Coupling

  31. The Suzuzi Miyaura Cross Coupling

  32. The Suzuzi Miyaura Cross Coupling

  33. The Suzuzi Miyaura Cross Coupling

  34. The Suzuzi Miyaura Cross Coupling

  35. The Suzuzi Miyaura Cross Coupling

  36. The Suzuzi Miyaura Cross Coupling

  37. The Suzuzi Miyaura Cross Coupling

  38. The Suzuzi Miyaura Cross Coupling

  39. The Sonogashira Cross Coupling Used in preparation of arylalkynes

  40. The Sonogashira Cross Coupling Used in preparation of arylalkynes

  41. The Sonogashira Cross Coupling Used in preparation of arylalkynes

  42. The Sonogashira Cross Coupling Used in preparation of arylalkynes

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