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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
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Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Dec 17, 2015

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Page 1: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Chemistry 125: Lecture 52February 17, 2010

Additions by Radicals & Electrophilic Carbon;

Isoprenoids; andPolymer Properties This

For copyright notice see final page of this file

Page 2: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Radical PolymerizationSec 11.5 (487-489)

R

H

Occasional butyl side-chains inhibit close packing.

Page 3: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Cl CCl3R Cl

CCl3

CCl3

Controlling Polymer Chain LengthCCl4 is a “Chain-Transfer Agent”

shortens polymer molecules without terminating chain reaction

Properties like viscosity and melting point depend on

chain length.etc.

Cl

ktransfer/kpolymerization ~ 0.01 for styrene polymerization

When other termination is negligible, molecular length

~ kp[styrene] / kt[CCl4]“dispersity”

Page 4: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Alkene Oligomerization and Polymerization Using

Carbon Electrophiles

R+ (SN1)

R-L*

(SN2)

(“oligo”, a few)

Page 5: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

CH3

CH3

H2C C

H

CH3

CH3 C CH3

CH3

CH3

H2C C

R+ Electrophile in Formation of 2,2,4-Trimethylpentane, “Isooctane”

CH3

CH3

CH3 C H

CH3

CH3

H2C C

CH3

CH3

CH3 C CH2

CH3

CH3

HCH2SO4+

CH3

CH3

CH3 C+

CH3

CH3

CH3 C +

CH3

CH3

CH2 C

H+

(defined as “100 octane”)

inter molecular hydride shift(Bartlett, 1944)

chainpoly(isobutylene)

“butyl rubber” air-tight

+

CH3

CH3

CH2 C

CH3

CH3

CH3 C

CH3

CH3

CH2 Cetc. etc.

Page 6: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Sec. 12.13pp. 554-562

R-L and R+ Electrophiles in*

Terpene/Steroid Biogenesis

Page 7: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Isopentenyl Pyrophosphate

OPP

OP

OP

O

O O O O_ _

_

OPP

DimethylallylPyrophosphate

Adjacent unsaturationapparently speeds SN2

(as well as SN1)

CH2

Nu

L

Cl

I

Clbenzyl 250Cl

Clallyl 90Cl

Cln-propyl

krel for rxn with

I- in acetone

[1]Cl

Page 8: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Isopentenyl Pyrophosphate

OPP

OP

OP

O

O O O O_ _

_

OPPOPP

OPP

GeranylPyrophosphate

OPP

OPP

+

_

OPP

C5

C10

Page 9: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Geranyl Pyrophosphate

OPPcistrans

OPP

NerylPyrophosphate

+

Limonene

-H++

+

-Pinene

-H+

+

-H+

+H2OOH

[Ox]O

Camphor

"Terpene" essential oils C10

Markovnikov

anti-Markovnikov

Page 10: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Geranyl Pyrophosphate

OPP

OPP

Farnesyl Pyrophosphate

OPP

"head-to-headreductive dimerization"

PPO

Squalene (shark liver oil)

new bond

C15

“sesquiterpenes”

C30 “triterpenes”

e.g. caryophyllene(clove, hemp, rosemary)

Page 11: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

+

Squalene

H +

+

+

+

+

+

HOO

Markovnikov

Markovnikov

Anti-Markovnikov

Markovnikov

Enzyme makes “O” selective among many trisubstituted alkene groups.

Page 12: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Squalene

+

+

+

+

+

HO

HH

H

CH3

HH

CH3

H+

CH3H3C

H3C CH3

CH3

CH3

CH3H3C

Lanosterol(source of cholesterol& steroid hormones)

Not this time! (enzyme control)

C30 “triterpenes”

3°3°

Page 13: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Squalene

+

+

+

+

+

HO

HH

H

CH3

HH

CH3

H+

CH3H3C

H3C CH3

CH3

CH3

CH3H3C

Lanosterol(source of cholesterol& steroid hormones)

Not this time! (enzyme control)

C30 “triterpenes”

3°3°

Cute StoryIs it True?

(Wait for NMR)

Page 14: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

2 Isoprenes

Isoprene

HOH

Geraniol“dimer”

HOH

Page 15: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Isoprene

OH

2 Isoprenes

Menthol“dimer” OH

Page 16: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Isoprene

O

4 Isoprenes

Retinal“tetramer”

O

Page 17: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Latex“polymer”

Isoprene

30,000 Isoprenes

Page 18: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Hevea braziliensis

Page 19: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Latex to Caoutchouc

Page 20: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Gooey in heatBrittle in cold

Thomas Hancock(England -1820) “Masticator”

Goodyear

(1839)Vulcanization

Charles Macintosh(Scotland - 1823)

Sandwiched rubber between clothlayers for waterproof garments

Page 21: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Discovery of Vulcanization

1839

Page 22: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

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 Vulcanizationfrom Goodyear’s Autobiographical

“Gum-Elastic” (1855)

Page 23: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

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

Page 24: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.
Page 25: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

U.S. Pavilion Crystal Palace (1851)

Page 26: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Goodyear’s Vulcanite Court

India Rubber Desk

Mattatuck Museum, Waterbury

Page 27: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

SomehowVulcanizationjoins adjacent chainswith sulfur “cross-links”

S

Latexpolymer

Radical Addition and Allylic Substitution?

H ?

Page 28: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Vulcanization and the Physical Properties

of Polymers

Page 29: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Gough

Page 30: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

wordsworth

“No floweret bloomsThroughout the lofty range of these rough hills,Nor in the woods, that could from him concealIts birth-place; none whose figure did not liveUpon his touch.” Wordsworth “Excursion” (1813)

(1757-1825)

Page 31: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

John Gough

Heating rubber makes it expand (more than H2O).

Page 32: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.
Page 33: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Heating tightly stretched rubber makes it contract!

Page 34: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

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”).

Page 35: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Why?

Page 36: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Goodyear Plot

Page 37: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Goodyear Inventor

Page 38: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Goodyear to Gibbs

Page 39: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Gibbs Mathematical Physics

Page 40: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Gibbs to Onsager

Page 41: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Kirkwood & Onsager

Page 42: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

PolymerStatistical Mechanics

Page 43: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Statistics Contracts a Stretched Chain

etc.

only one arrangement of maximum lengthmany arrangement of shorter length

Page 44: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Near maximum extensionthere is local Crystallization

Stretching

Contributes RigidityRigidity 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.

Page 45: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Lengthwise Motion by “Reptation”

Change shape by snaking along a tunnel through the tangled neighbors.

How to make a tangle flow?

Page 46: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Sulfur Cross-Links Stop Reptation

Vulcanization

(no flow when hot)

and inhibit crystallization.(not brittle when cold)

Page 47: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

Vulcanization in theHome

Page 48: Chemistry 125: Lecture 52 February 17, 2010 Additions by Radicals & Electrophilic Carbon; Isoprenoids; and Polymer Properties This For copyright notice.

End of Lecture 52Feb. 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).

Use of this content constitutes your acceptance of the noted license and the terms and conditions of use.

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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