1. Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice see final page of this file

2. Radical Polymerization Sec 11.5 (487-489) R H Occasional butyl side-chains inhibit close packing.

3. ClCCl 3 RCl CCl 3 Controlling Polymer Chain Length CCl 4 is a “Chain-Transfer Agent” shortens polymer molecules without terminating chain reaction Properties like viscosity and melting point depend on chain length. etc. Cl k transfer /k polymerization ~ 0.01 for styrene polymerization        When other termination is negligible, molecular length ~ k p [styrene] / k t [CCl 4 ] “dispersity”

4. Alkene Oligomerization and Polymerization Using Carbon Electrophiles R+R+ (S N 1) R-LR-L ** (S N 2) (“oligo”, a few)

5. CH 3 H2CH2CC H C H2CH2CC R + Electrophile in Formation of 2,2,4-Trimethylpentane, “Isooctane” CH 3 CH H2CH2CC CCH 2 CH 3 HC H 2 SO 4 + CH 3 C + C + CH 2 C H + (defined as “100 octane”) inter molecular hydride shift (Bartlett, 1944) chain poly(isobutylene) “butyl rubber” air-tight + CH 3 CH 2 C CH 3 C CH 2 C etc.

6. Sec. 12.13 pp. 554-562 R-L and R + Electrophiles in ** Terpene/Steroid Biogenesis

7. Isopentenyl Pyrophosphate Dimethylallyl Pyrophosphate Adjacent unsaturation apparently speeds S N 2 (as well as S N 1) Cl I benzyl 250 Cl allyl 90 Cl n-propyl k rel for rxn with I - in acetone [1] Cl

8. Isopentenyl Pyrophosphate Geranyl Pyrophosphate C5C5 C 10

9. Geranyl Pyrophosphate cis trans Neryl Pyrophosphate Limonene -H +  -Pinene -H + +H 2 O [Ox] Camphor "Terpene" essential oils C 10 Markovnikov anti-Markovnikov

10. Geranyl Pyrophosphate Farnesyl Pyrophosphate "head-to-head reductive dimerization" Squalene (shark liver oil) new bond C 15 “sesquiterpenes” C 30 “triterpenes” e.g. caryophyllene (clove, hemp, rosemary)

11. + Squalene H + + + + + + HO O Markovnikov Anti- Markovnikov Enzyme makes “O” selective among many trisubstituted alkene groups.

12. Squalene + + + + + HO H H H CH 3 H H H + H3CH3C H3CH3C H3CH3C Lanosterol (source of cholesterol & steroid hormones) Not this time! (enzyme control) C 30 “triterpenes” 3°

13. Squalene + + + + + HO H H H CH 3 H H H + H3CH3C H3CH3C H3CH3C Lanosterol (source of cholesterol & steroid hormones) Not this time! (enzyme control) C 30 “triterpenes” 3° Cute Story Is it True? (Wait for NMR)

14. 2 Isoprenes Isoprene H OH Geraniol “dimer” H OH

15. Isoprene OH 2 Isoprenes Menthol “dimer” OH

16. Isoprene O 4 Isoprenes Retinal “tetramer” O

17. Latex “polymer” Isoprene 30,000 Isoprenes

18. Hevea braziliensis

19. Latex to Caoutchouc

20. Gooey in heat Brittle in cold Thomas Hancock (England -1820) “Masticator” Goodyear (1839) Vulcanization Charles Macintosh (Scotland - 1823) Sandwiched rubber between cloth layers for waterproof garments

21. Discovery of Vulcanization 1839

22. The occurrence did not at the time seem to them to be worthy of notice; it was considered as one of the frequent appeals that he was in the habit of making, in behalf of some new experiment.” He endeavoured to call the attention of his brother, as well as some other individuals who were present, and who were acquainted with the manufacture of gum-elastic, to this effect, as remarkable, and unlike any before known, since gum-elastic always melted when exposed to a high degree of heat. “He was surprised to find that the specimen, being carelessly brought into contact with a hot stove, charred like leather. Discovery of Vulcanization from Goodyear’s Autobiographical “Gum-Elastic” (1855)

23. Silliman consult “Having seen experiments made, and also performed them myself, with the India rubber prepared by Mr. Charles Goodyear, I can state that it does not melt, but rather chars, by heat, and that it does not stiffen by cold, but retains its flexibility with cold, even when laid between cakes of ice.” B. Silliman October 14, 1839

25. U.S. Pavilion Crystal Palace (1851)

26. Goodyear’s Vulcanite Court India Rubber Desk Mattatuck Museum, Waterbury

27. Somehow Vulcanization joins adjacent chains with sulfur “cross-links” S Latex polymer Radical Addition and Allylic Substitution? H ?

28. Vulcanization and the Physical Properties of Polymers

29. Gough

30. wordsworth “ No floweret blooms Throughout the lofty range of these rough hills, Nor in the woods, that could from him conceal Its birth-place; none whose figure did not live Upon his touch.” Wordsworth “Excursion” (1813) (1757-1825)

31. John Gough Heating rubber makes it expand (more than H 2 O).

33. Heating tightly stretched rubber makes it contract !

34. If stretching rubber generates heat, what should letting it contract do? A) If heat comes from internal friction, contraction should also cause friction and generate heat. B) If heat comes from some other cause, contraction may do the opposite and absorb heat (“generate cold”).

35. Why?

36. Goodyear Plot

37. Goodyear Inventor

38. Goodyear to Gibbs

39. Gibbs Mathematical Physics

40. Gibbs to Onsager

41. Kirkwood & Onsager

42. Polymer Statistical Mechanics

43. Statistics Contracts a Stretched Chain etc. only one arrangement of maximum lengthmany arrangement of shorter length

44. Near maximum extension there is local Crystallization Stretching Rigidity Contributes Rigidity Releases Heat Fixed, irregular cross-links between adjacent chains prevents crystallization (and brittleness) in the cold. Warming “melts” the crystalline regions, and allows statistics to make the material contract. Absorbing heat “melts” the crystalline regions, and allows statistics to make the material contract.

45. Lengthwise Motion by “Reptation” Change shape by snaking along a tunnel through the tangled neighbors. How to make a tangle flow?

46. Sulfur Cross-Links Stop Reptation Vulcanization (no flow when hot) and inhibit crystallization. (not brittle when cold)

47. Vulcanization in the Home

48. End of Lecture 52 Feb. 17, 2010 Copyright © J. M. McBride 2010. Some rights reserved. Except for cited third-party materials, and those used by visiting speakers, all content is licensed under a Creative Commons License (Attribution-NonCommercial-ShareAlike 3.0).Creative Commons License (Attribution-NonCommercial-ShareAlike 3.0) Use of this content constitutes your acceptance of the noted license and the terms and conditions of use. Materials from Wikimedia Commons are denoted by the symbol. Third party materials may be subject to additional intellectual property notices, information, or restrictions. The following attribution may be used when reusing material that is not identified as third-party content: J. M. McBride, Chem 125. License: Creative Commons BY-NC-SA 3.0