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(Co)polymers and a novel polymerization process based on atom (or group) transfer radical polymerization

Patent 5763548 Issued on June 9, 1998. Estimated Expiration Date: Icon_subject June 9, 2015. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Patent References

Polymerization process and polymers produced thereby
Patent #: 4581429
Issued on: 04/08/1986
Inventor: Solomon ,   et al.

Titanium, zirconium- and hafnium containing initiators in the polymerization of acrylic monomers to "living" polymers
Patent #: 4728706
Issued on: 03/01/1988
Inventor: Farnham ,   et al.

Group Transfer Polymerization process employing supported initiators
Patent #: 4940760
Issued on: 07/10/1990
Inventor: Boettcher, et al.

Free radical polymerization process
Patent #: 5312871
Issued on: 05/17/1994
Inventor: Mardare, et al.

Free radical copper(II)-enolate polymerization initiators Patent #: 5470928
Issued on: 11/28/1995
Inventor: Harwood, et al.

Inventors

Assignee

Application

No. 414415 filed on 03/31/1995

US Classes:

526/135, With non-metal N, P, O, S, Se, Te, or halogen material other than nitrogen gas526/145, Non-metal phosphorus-containing material526/147Non-metal nitrogen-containing material

Examiners

Primary: Schofer, Joseph L.
Assistant: Cheng, Wu C.

Attorney, Agent or Firm

International Classes

C08F 004/06
C08F 004/40

Abstract

A new polymerization process (atom transfer radical polymerization, or ATRP) based on a redox reaction between a transition metal (e.g., Cu(I)/Cu(II), provides "living" or controlled radical polymerization of styrene, (meth)acrylates, and other radically polymerizable monomers. Using various simple organic halides as model halogen atom transfer precursors (initiators) and transition metal complexes as a model halogen atom transfer promoters (catalysts), a "living" radical polymerization affords (co)polymers having the predetermined number average molecular weight by Ɗ›M!/›I!0 (up to Mn >105) and a surprisingly narrow molecular weight distribution (Mw /Mn), as low as 1.15. The participation of free radical intermediates in ATRP is supported by end-group analysis and stereochemistry of the polymerization. In addition, polymers with various topologies (e.g., block, random, star, graft, hyperbranched, dendritic end-functional and in-chain functional copolymers ›for example, of styrene and methyl (meth)acrylate!) have been synthesized using the present process. The Polymeric products encompassed by the present invention can be widely used as plastics, elastomers, adhesives, emulsifiers, thermoplastic elastomers, etc.

Other References

  • O.W. Webster, Science, 251, 887 (1991)
  • Greszta et al, Macromolecules, 27, 638 (1994)
  • Georges et al, Macromolecules, 26, 2987 (1993)
  • Wayland, B. B.; Pszmik, G.; Mukerjee, S. L.; Fryd, M. J. Am. Chem. Soc., 116, 7943 (1994)
  • Mardare et al, Macromolecules, 27, 645 (1994)
  • Lee et al, J. Chem. Soc. Trans. Faraday Soc. I, 74, 1726 (1978)
  • Otsu, T.; Tashinori, T.; Yoshioka, M., Chem. Express 5(10), 801 (1990)
  • Kato, M.; Kamigaito, M.; Sawamoto, M.; Higashimura, T., Macrocmolecules, 28, 1721 (1995)
  • Bamford, in Comprehensive Polymer Science (First Supplement), Allen, G., Aggarwal, S. L., Russo, S., eds., Pergamon: Oxford, vol. 3, p. 123 (1991)
  • Curran, D. P. in Comprehensive Organic Synthesis, Trost, B. M., Fleming, I., eds., Pergamon: Oxford, vol. 4, p. 715 (1991)
  • Curran et al, J. Am. Chem. Soc., 116, 4279 (1994)
  • Curran et al, J. Org. Chem., 54, 3140 (1989)
  • Iqbal, J; Bhatia, B.; Nayyar, N. K., Chem. Rev., 94, 519 (1994)
  • Hirao et al, J. Synth. Org. Chem. (Japan), 52(3), 197 (1994)
  • Hirao et al, Syn. Lett., 217 (1990)
  • Hayes, T. K.; Villani, R.; Weinreb, S. M., J. Am. Chem. Soc. 110, 5533 (1988)
  • Nagashima, H.; Wakamatsu, H.; Ozaki, N.; Ishii, T.; Watanabe, M.; Tajima, T.; Itoh, K., J. Org. Chem. 57, 1682 (1992)
  • Seijas et al, Tetrahedron, 48(9), 1637 (1992)
  • Udding, J. H.; Tuijp, K. J. M.; van Zanden, M. N. A.; Hiemstra, H.; Speckamp, W. N., J. Org. Chem. 59, 1993 (1994)
  • Nagashima, H.; Ozaki, N.; Ishii, M.; Seki, K.; Washiyama, M.; Itoh, K., J. Org. Chem. 58, 464 (1993)
  • Bellus, D., Pure & Appl. Chem. 57, 1827 (1985)
  • Curran, D. P., Synthesis, 489 (1988)
  • Mardare et al, Polym. Prep. (ACS), 36(1), 700-701 (1995)
  • Orochov, A.; Asscher, M.; Vofsi, D., J. Chem. Soc., Perkin II., 1000 (1973)
  • Mitani, M.; Kato, L.; Koyama, K., J. Am. Chem. Soc., 105, 6719 (1983)
  • Cohen, H.; Meyerstein, D., Inorg. Chem., 13, 2434 (1974)
  • Endo et al, Macromocules, 25, 5554 (1992)
  • Bledzki et al, Makromol. Chem., 184, 745 (1983)
  • Druliner, Macromolecules, 24, 6079 (1991)
  • Gaynor et al, Polym. Prep. (Am. Chem. Soc., Polym. Chem. Div.), 36(1), 467 (1995)
  • Wang et al, Polym. Prep. (Am. Chem. Soc. Polym. Chem. Div.), 36(1), 465 (1995
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