Literature DB >> 23288304

N-Heterocyclic carbenes (NHCs) as organocatalysts and structural components in metal-free polymer synthesis.

Maréva Fèvre1, Julien Pinaud, Yves Gnanou, Joan Vignolle, Daniel Taton.   

Abstract

The chemistry of N-heterocyclic carbenes (NHCs) has witnessed tremendous development in the past two decades: NHCs have not only become versatile ligands for transition metals, but have also emerged as powerful organic catalysts in molecular chemistry and, more recently, in metal-free polymer synthesis. To understand the success of NHCs, this review first presents the electronic properties of NHCs, their main synthetic methods, their handling, and their reactivity. Their ability to activate key functional groups (e.g. aldehydes, esters, heterocycles, silyl ketene acetals, alcohols) is then discussed in the context of molecular chemistry. Focus has been placed on the activation of substrates finding analogies with monomers (e.g. bis-aldehydes, multi-isocyanates, cyclic esters, epoxides, N-carboxyanhydrides, etc.) and/or initiators (e.g. hydroxy- or trimethylsilyl-containing reagents) employed in such "organopolymerisation" reactions utilizing NHCs. A variety of metal-free polymers, including aliphatic polyesters and polyethers, poly(α-peptoid)s, poly(meth)acrylates, polyurethanes, or polysiloxanes can be obtained in this way. The last section covers the use of NHCs as structural components of the polymer chain. Indeed, NHC-based photoinitiators, chain transfer agents or functionalizing agents, as well as bifunctional NHC monomer substrates, can also serve for metal-free polymer synthesis.

Entities:  

Year:  2013        PMID: 23288304     DOI: 10.1039/c2cs35383k

Source DB:  PubMed          Journal:  Chem Soc Rev        ISSN: 0306-0012            Impact factor:   54.564


  27 in total

1.  Cyclopropenimine Superbases: Competitive Initiation Processes in Lactide Polymerization.

Authors:  Tyler S Stukenbroeker; Jeff S Bandar; Xiangyi Zhang; Tristan H Lambert; Robert M Waymouth
Journal:  ACS Macro Lett       Date:  2015-07-30       Impact factor: 6.903

2.  Chemoselective Lewis pair polymerization of renewable multivinyl-functionalized γ-butyrolactones.

Authors:  Ravikumar R Gowda; Eugene Y-X Chen
Journal:  Philos Trans A Math Phys Eng Sci       Date:  2017-08-28       Impact factor: 4.226

3.  Fast and selective ring-opening polymerizations by alkoxides and thioureas.

Authors:  Xiangyi Zhang; Gavin O Jones; James L Hedrick; Robert M Waymouth
Journal:  Nat Chem       Date:  2016-07-25       Impact factor: 24.427

4.  An overview of N-heterocyclic carbenes.

Authors:  Matthew N Hopkinson; Christian Richter; Michael Schedler; Frank Glorius
Journal:  Nature       Date:  2014-06-26       Impact factor: 49.962

Review 5.  N-Heterocyclic Carbene Complexes in C-H Activation Reactions.

Authors:  Qun Zhao; Guangrong Meng; Steven P Nolan; Michal Szostak
Journal:  Chem Rev       Date:  2020-01-22       Impact factor: 60.622

6.  Bio-inspired NHC-organocatalyzed Stetter reaction in aqueous conditions.

Authors:  Mégane Debiais; Aladin Hamoud; Reihana Drain; Philippe Barthélémy; Valérie Desvergnes
Journal:  RSC Adv       Date:  2020-11-09       Impact factor: 4.036

7.  N-Heterocyclic Olefins as Organocatalysts for Polymerization: Preparation of Well-Defined Poly(propylene oxide).

Authors:  Stefan Naumann; Anthony W Thomas; Andrew P Dove
Journal:  Angew Chem Int Ed Engl       Date:  2015-07-01       Impact factor: 15.336

8.  Crystal structure of di-μ-iodido-bis-{[1,3-bis-(2,6-diiso-propyl-phen-yl)imidazol-2-yl-idene]lithium}.

Authors:  Hui-Da Wan; Jian-Quan Hong
Journal:  Acta Crystallogr E Crystallogr Commun       Date:  2015-05-28

Review 9.  BIAN-NHC Ligands in Transition-Metal-Catalysis: A Perfect Union of Sterically Encumbered, Electronically Tunable N-Heterocyclic Carbenes?

Authors:  Changpeng Chen; Feng-Shou Liu; Michal Szostak
Journal:  Chemistry       Date:  2021-01-18       Impact factor: 5.236

10.  Efficient synthetic protocols for the preparation of common N-heterocyclic carbene precursors.

Authors:  Morgan Hans; Jan Lorkowski; Albert Demonceau; Lionel Delaude
Journal:  Beilstein J Org Chem       Date:  2015-11-25       Impact factor: 2.883

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