Literature DB >> 15382937

Living copolymerization of ethylene with norbornene catalyzed by bis(pyrrolide-imine) titanium complexes with MAO.

Yasunori Yoshida1, Jun-ichi Mohri, Sei-ichi Ishii, Makoto Mitani, Junji Saito, Shigekazu Matsui, Haruyuki Makio, Takashi Nakano, Hidetsugu Tanaka, Mitsuhiko Onda, Yukari Yamamoto, Akira Mizuno, Terunori Fujita.   

Abstract

Bis(pyrrolide-imine) Ti complexes in conjunction with methylalumoxane (MAO) were found to work as efficient catalysts for the copolymerization of ethylene and norbornene to afford unique copolymers via an addition-type polymerization mechanism. The catalysts exhibited very high norbornene incorporation, superior to that obtained with Me(2)Si(Me(4)Cp)(N-tert-Bu)TiCl(2) (CGC). The sterically open and highly electrophilic nature of the catalysts is probably responsible for the excellent norbornene incorporation. The catalysts displayed a marked tendency to produce alternating copolymers, which have stereoirregular structures despite the C(2) symmetric nature of the catalysts. The norbornene/ethylene molar ratio in the polymerization medium had a profound influence on the molecular weight distribution of the resulting copolymer. At norbornene/ethylene ratios larger than ca. 1, the catalysts mediated room-temperature living copolymerization of ethylene and norbornene to form high molecular weight monodisperse copolymers (M(n) > 500,000, M(w)/M(n) < 1.20). (13)C NMR spectroscopic analysis of a copolymer, produced under conditions that gave low molecular weight, demonstrated that the copolymerization is initiated by norbornene insertion and that the catalyst mostly exists as a norbornene-last-inserted species under living conditions. Polymerization behavior coupled with DFT calculations suggested that the highly controlled living polymerization stems from the fact that the catalysts possess high affinity and high incorporation ability for norbornene as well as the characteristics of a living ethylene polymerization though under limited conditions (M(n) 225,000, M(w)/M(n) 1.15, 10-s polymerization, 25 degrees C). With the catalyst, unique block copolymers [i.e., poly(ethylene-co-norbornene)(1)-b-poly(ethylene-co-norbornene)(2), PE-b-poly(ethylene-co-norbornene)] were successfully synthesized from ethylene and norbornene. Transmission electron microscopy (TEM) indicated that the PE-b-poly(ethylene-co-norbornene) possesses high potential as a new material consisting of crystalline and amorphous segments which are chemically linked.

Entities:  

Year:  2004        PMID: 15382937     DOI: 10.1021/ja048357g

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  4 in total

1.  Kinetics and thermodynamics of living copolymerization processes.

Authors:  Pierre Gaspard
Journal:  Philos Trans A Math Phys Eng Sci       Date:  2016-11-13       Impact factor: 4.226

2.  Alternating ROMP copolymers containing charge-transfer units.

Authors:  Joy Romulus; Li Tan; Marcus Weck; Nicole S Sampson
Journal:  ACS Macro Lett       Date:  2013-08-20       Impact factor: 6.903

3.  Kinetics, Mechanism and Theoretical Studies of Norbornene-Ethylene Alternating Copolymerization Catalyzed by Organopalladium(II) Complexes Bearing Hemilabile α-Amino-pyridine.

Authors:  Kuo-Hsuan Yu; Shou-Ling Huang; Yi-Hung Liu; Yu Wang; Shiuh-Tzung Liu; Yuan-Chung Cheng; Ya-Fan Lin; Jwu-Ting Chen
Journal:  Molecules       Date:  2017-06-30       Impact factor: 4.411

4.  Early Metal Di(pyridyl) Pyrrolide Complexes with Second Coordination Sphere Arene-π Interactions: Ligand Binding and Ethylene Polymerization.

Authors:  Jessica Sampson; Gyeongshin Choi; Muhammed Naseem Akhtar; E A Jaseer; Rajesh Theravalappil; Nestor Garcia; Theodor Agapie
Journal:  ACS Omega       Date:  2019-09-19
  4 in total

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