1 / 39

Cations

Cations. Carey & Sundberg , Part A Chapter 5, "Nucleophilic Substitution", 263-350. John D. Roberts was born in 1918, starting his career in 1922. He became Prof. at MIT and then Prof. at Caltech where he is still active. His work is centered on mechanisms of organic reactions.

Download Presentation

Cations

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Cations Carey & Sundberg, Part A Chapter 5, "Nucleophilic Substitution", 263-350 .

  2. John D. Roberts was born in 1918, starting his career in 1922. He became Prof. at MIT and then Prof. at Caltech where he is still active. His work is centered on mechanisms of organic reactions. John D. Roberts graduated from the University of California at Los Angeles where he had received A. B. (hons) degree in 1941 and the Ph. D. degree in 1944. In 1945-1946 he was a National Research Council Fellow and Instructor at Harvard. Later on, he went to MIT in 1946 as an Instructor. He had introduced the terms "nonclassical" carbocations and "benzyne" into organic chemistry. He had won numerous awards; he is a member of the National Academy of Sciences (1956) and the American Philosophical Society (1974). He received the Welch Award (1990, with W. E. Doering), the National Medal of Science (1990), and the ACS Arthur C. Cope Award (1994). Since 1939 his research has been concerned with the mechanisms of organic reactions and the chemistry of small-ring compounds. His current work involves applications of nuclear magnetic resonance spectroscopy to physical organic chemistry. Roberts made major research and pedagogic contributions to mechanistic organic chemistry. He pioneered the use of 14C and other isotopic labels to follow molecular rearrangements as, for example, in the complex and subtle solvolysis of cyclopropylcarbinyl systems. He introduced the terms "nonclassical" carbocations and "benzyne" into organic chemistry, and used isotopic labeling to establish the intermediacy of each. Roberts was early to recognize NMR's potential, and used 1H NMR to study nitrogen inversion, long-range spin-spin coupling and conformational isomerism, and later 13C and 15N NMR to study other reactions, including the active sites of certain enzymes. Roberts' superb short books on "Nuclear Magnetic Resonance" (1959), "Spin-Spin Splitting in High Resolution NMR" (1961) and "Notes on Molecular Orbital Calculations" (1961) did much to popularize and clarify these subjects for organic chemists. His highly successful text "Basic Principles of Organic Chemistry" (1964), written with Marjorie Caserio, introduced spectroscopy early to undergraduates. Roberts received many awards, including the Roger Adams (1967) and Priestley (1987) Medals. An excellent photographer, Roberts graciously supplied several of the photographs for the MSU collection. B.A., 1941, UCLA Ph.D. 1944, UCLA Instructor, Harvard, 1945-6 “One of the joys of being a professor is when an exceptional student comes along and wants to work with you”. J.D. Roberts, The Right Place at the Right Time. p. 63.

  3. Carbocations

  4. Cationic Systems

  5. Carbocation Stability

  6. Carbocation Generation

  7. Carbocation Stability

  8. Carbocations

  9. b-Si stabilization (hyperconjugation) Preparation of a vinyl cation • no good nucleophiles • prevent loss of H+ • stabilizing b-Si groups Müller T., Juhasz, M., Reed, C. A., Angew. Chem. Int. Ed., 2004, 43, 1543-1546.

  10. NMR evidence 13C and 29SiNMR chemical shifts • Only one 29Si signal • Symmetric in solution (confirms ring closure) • =C+ is far downfield • Si resonance is downfield • No solvent effect 29.1 29.1 75.3 202.4 +

  11. B-H C=C+ + CB11H6Br6- IR spectrum Typical Frequencies: C=C 1660 cm-1 C≡C 2200 cm-1 Exp. C=C+ 1987 cm-1 Calculated: 1956 cm-1

  12. Selected distances/angles C2 - C11: 1.220 Å C2-C11-C12: 178.8 ° Si1 – C2: 1.984 Å Si3 – C2: 1.946 Å Crystal Structure crystal packing Müller T., Juhasz, M., Reed, C. A., Angew. Chem. Int. Ed., 2004, 43, 1543-1546.

  13. Cyclopropyl Cations

  14. Carbocations In Bridged Systems

  15. Carbocation [1,2] Sigmatropic Rearrangements

  16. Carbocation [1,2] Sigmatropic Rearrangements

  17. Carbocation [1,2] Sigmatropic Rearrangements

  18. Carbocation [1,2] Sigmatropic Rearrangements

  19. The Prins Reaction

  20. Tandem Prins-Pinacol Reaction

  21. Overman’s Laurenyne Synthesis

  22. Overman’s trans-Kumausyne Synthesis

  23. Overman’s trans-Kumausyne Synthesis

  24. The b-Silicon Effect

  25. The b-Silicon Effect

  26. Reactions of Allylsilanes

  27. Iminium Ions

  28. Iminium Ions

  29. N-Acyliminium Ion Rearrangements

  30. Aza-Cope Manich Reactions

  31. Terpenes

  32. Isoprene : Nature's C5 Building Block

  33. Terpene Biosynthesis

  34. Terpene Biosynthesis

  35. Steriod and Squalene Oxide Cyclization

  36. Steriod Biosynthesis; Squalene Oxide Cyclization

More Related