CH Activation as a Shortcut to Conjugated Polymer Synthesis. Issue 1 (10th September 2018)
- Record Type:
- Journal Article
- Title:
- CH Activation as a Shortcut to Conjugated Polymer Synthesis. Issue 1 (10th September 2018)
- Main Title:
- CH Activation as a Shortcut to Conjugated Polymer Synthesis
- Authors:
- Blaskovits, J. Terence
Leclerc, Mario - Abstract:
- Abstract: Direct (hetero)arylation polymerization exploits the palladium‐catalyzed activation of aromatic CH bonds for the atom‐economical synthesis of conjugated polymers for a wide range of applications. This account outlines how direct arylation methodologies overcome many of the limitations of contemporary polymerization techniques at both the research and production scale, and explains how monomer design and reaction conditions must be tailored to ensure high polymer molecular weight, yield, and structural integrity. Current research aims to improve further this reaction's profile as a sustainable methodology while at the same time making it competitive with the Migita–Stille and Miyaura–Suzuki polymerizations both in scope of accessible structures and synthetic efficiency. This feature article charts the recent developments and future directions of CH activation research as it moves toward becoming at once an industrially feasible, environmentally friendly, and synthetically powerful polymerization technique. Abstract : The well‐travelled paths to conjugated polymers are paved with many synthetic steps and reaction by‐products. The direct (hetero)arylation and oxidative CH arylation polymerizations streamline synthesis through the activation of aromatic CH bonds without requiring organometallic intermediates. This feature article highlights the applications of transition‐metal‐catalyzed CH arylation reactions to the environmentally friendly and industriallyAbstract: Direct (hetero)arylation polymerization exploits the palladium‐catalyzed activation of aromatic CH bonds for the atom‐economical synthesis of conjugated polymers for a wide range of applications. This account outlines how direct arylation methodologies overcome many of the limitations of contemporary polymerization techniques at both the research and production scale, and explains how monomer design and reaction conditions must be tailored to ensure high polymer molecular weight, yield, and structural integrity. Current research aims to improve further this reaction's profile as a sustainable methodology while at the same time making it competitive with the Migita–Stille and Miyaura–Suzuki polymerizations both in scope of accessible structures and synthetic efficiency. This feature article charts the recent developments and future directions of CH activation research as it moves toward becoming at once an industrially feasible, environmentally friendly, and synthetically powerful polymerization technique. Abstract : The well‐travelled paths to conjugated polymers are paved with many synthetic steps and reaction by‐products. The direct (hetero)arylation and oxidative CH arylation polymerizations streamline synthesis through the activation of aromatic CH bonds without requiring organometallic intermediates. This feature article highlights the applications of transition‐metal‐catalyzed CH arylation reactions to the environmentally friendly and industrially amenable synthesis of conjugated polymers. … (more)
- Is Part Of:
- Macromolecular rapid communications. Volume 40:Issue 1(2019)
- Journal:
- Macromolecular rapid communications
- Issue:
- Volume 40:Issue 1(2019)
- Issue Display:
- Volume 40, Issue 1 (2019)
- Year:
- 2019
- Volume:
- 40
- Issue:
- 1
- Issue Sort Value:
- 2019-0040-0001-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2018-09-10
- Subjects:
- CH activation -- conjugated polymer synthesis -- direct (hetero)arylation polymerization -- green chemistry -- palladium catalysis
Macromolecules -- Periodicals
Polymers -- Periodicals
Chemistry -- Periodicals
547.705 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/marc.201800512 ↗
- Languages:
- English
- ISSNs:
- 1022-1336
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5330.400000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 11560.xml