Control of coordination polymerization behavior by counter-anionic effects

In coordination polymerization chemistry, the most active species are cationic transition metals which bear vacant sites for monomer coordination. The steric and electronic properties around the metal center are strongly related to the polymerization behavior. Thus, the development of the catalyst s...

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Veröffentlicht in:Progress in polymer science Jg. 142; S. 101690
Hauptverfasser: Tanaka, Ryo, Ajala, Oluwaseyi Aderemi, Nakayama, Yuushou, Shiono, Takeshi
Format: Journal Article
Sprache:Englisch
Veröffentlicht: Elsevier B.V 01.07.2023
Schlagworte:
Cocatalyst
Conjugated diene polymerization
Coordination polymerization
Olefin polymerization
XANES
DNP
EBI
EXAFS
BHT
PFG
DOSY
LDH
LMCT
DFT
MD
EDX
XPS
SBI
Conjugated diene polymerization
sMAO
CGC
GGA
Olefin polymerization
Coordination polymerization
ESR
MOF
NOE
ROESY
CPMAS
ESI-MS
MMAO
QM/MM
DRIFT
OSIP
STEM
ISIP
Cocatalyst
DP-MAS
OMTS
EXSY
MAO
SEM
TEMPO
ISSN:0079-6700
Online-Zugang:Volltext
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Abstract In coordination polymerization chemistry, the most active species are cationic transition metals which bear vacant sites for monomer coordination. The steric and electronic properties around the metal center are strongly related to the polymerization behavior. Thus, the development of the catalyst system mainly represents the design of neutral metal complex precursors, especially the structure of the ligand. On the other hand, the choice of counteranions derived from the cocatalysts sometimes plays a crucial role in the controlled coordination polymerization. Some unusual polymerization behaviors on stereospecificity, activity, and monomer reactivity ratios have been reported by designing the structure of these cocatalysts. The review summarizes these examples of polymerization controlled by cocatalysts. Various cocatalysts, such as methylaluminoxane (MAO), fluoroarylboranes, and borates with different activation mechanisms, are introduced based on their structural analysis and molecular design. Heterogeneous cocatalysts, important for industrial applications, are also mentioned with their various characterization methods. The application of these cocatalysts is discussed, along with the introduction of several techniques evaluating the relationship between cocatalysts and polymerization behavior. Moreover, the counter-anionic effect in the late-transition metal-catalyzed polymerization chemistry, which recently attracted many researchers for its versatile applicability for polar monomers, is reviewed. [Display omitted]
AbstractList In coordination polymerization chemistry, the most active species are cationic transition metals which bear vacant sites for monomer coordination. The steric and electronic properties around the metal center are strongly related to the polymerization behavior. Thus, the development of the catalyst system mainly represents the design of neutral metal complex precursors, especially the structure of the ligand. On the other hand, the choice of counteranions derived from the cocatalysts sometimes plays a crucial role in the controlled coordination polymerization. Some unusual polymerization behaviors on stereospecificity, activity, and monomer reactivity ratios have been reported by designing the structure of these cocatalysts. The review summarizes these examples of polymerization controlled by cocatalysts. Various cocatalysts, such as methylaluminoxane (MAO), fluoroarylboranes, and borates with different activation mechanisms, are introduced based on their structural analysis and molecular design. Heterogeneous cocatalysts, important for industrial applications, are also mentioned with their various characterization methods. The application of these cocatalysts is discussed, along with the introduction of several techniques evaluating the relationship between cocatalysts and polymerization behavior. Moreover, the counter-anionic effect in the late-transition metal-catalyzed polymerization chemistry, which recently attracted many researchers for its versatile applicability for polar monomers, is reviewed. [Display omitted]
ArticleNumber 101690
Author Shiono, Takeshi
Tanaka, Ryo
Ajala, Oluwaseyi Aderemi
Nakayama, Yuushou
Author_xml – sequence: 1
  givenname: Ryo
  orcidid: 0000-0002-6085-074X
  surname: Tanaka
  fullname: Tanaka, Ryo
– sequence: 2
  givenname: Oluwaseyi Aderemi
  surname: Ajala
  fullname: Ajala, Oluwaseyi Aderemi
– sequence: 3
  givenname: Yuushou
  surname: Nakayama
  fullname: Nakayama, Yuushou
– sequence: 4
  givenname: Takeshi
  surname: Shiono
  fullname: Shiono, Takeshi
  email: tshiono@hiroshima-u.ac.jp
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Keywords XANES
DNP
EBI
EXAFS
BHT
PFG
DOSY
LDH
LMCT
DFT
MD
EDX
XPS
SBI
Conjugated diene polymerization
sMAO
CGC
GGA
Olefin polymerization
Coordination polymerization
ESR
MOF
NOE
ROESY
CPMAS
ESI-MS
MMAO
QM/MM
DRIFT
OSIP
STEM
ISIP
Cocatalyst
DP-MAS
OMTS
EXSY
MAO
SEM
TEMPO
Language English
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PublicationTitle Progress in polymer science
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Snippet In coordination polymerization chemistry, the most active species are cationic transition metals which bear vacant sites for monomer coordination. The steric...
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StartPage 101690
SubjectTerms Cocatalyst
Conjugated diene polymerization
Coordination polymerization
Olefin polymerization
Title Control of coordination polymerization behavior by counter-anionic effects
URI https://dx.doi.org/10.1016/j.progpolymsci.2023.101690
Volume 142
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