Facile Synthesis of π-Conjugated Polymers via Direct Arylation Polycondensation DOI Open Access
Junpei Kuwabara, Takaki Kanbara

Bulletin of the Chemical Society of Japan, Год журнала: 2018, Номер 92(1), С. 152 - 161

Опубликована: Окт. 4, 2018

Abstract In this paper, we summarize recent developments made by our group in direct arylation polycondensation. The method under optimal conditions affords a high-molecular-weight polymer with high purity through simple purification process. high-quality polymers have been used as active materials for optoelectronic applications and show equivalent or superior performance to the same prepared conventional methods. development of facile synthetic protocols could increase their practical applications. Recent C-H/C-H coupling polycondensation are also described.

Язык: Английский

Sustainable protocols for direct C–H bond arylation of (hetero)arenes DOI
Gianluigi Albano, Angela Punzi, Maria Annunziata M. Capozzi

и другие.

Green Chemistry, Год журнала: 2022, Номер 24(5), С. 1809 - 1894

Опубликована: Янв. 1, 2022

A comprehensive and critical overview of the sustainable strategies for direct C–H bond arylation (hetero)arenes, based on use recoverable catalysts, solvents non-conventional energy sources, has been performed.

Язык: Английский

Процитировано

72

Direct arylation polymerization: A guide to optimal conditions for effective conjugated polymers DOI Creative Commons

Nemal S. Gobalasingham,

Barry C. Thompson

Progress in Polymer Science, Год журнала: 2018, Номер 83, С. 135 - 201

Опубликована: Июнь 12, 2018

Язык: Английский

Процитировано

136

Mesopolymer synthesis by ligand-modulated direct arylation polycondensation towards n-type and ambipolar conjugated systems DOI
Zhenjie Ni, Hanlin Wang,

Huanli Dong

и другие.

Nature Chemistry, Год журнала: 2019, Номер 11(3), С. 271 - 277

Опубликована: Янв. 28, 2019

Язык: Английский

Процитировано

131

The sustainable materials roadmap DOI Creative Commons
Maria‐Magdalena Titirici, Sterling G. Baird, Taylor D. Sparks

и другие.

Journal of Physics Materials, Год журнала: 2022, Номер 5(3), С. 032001 - 032001

Опубликована: Янв. 25, 2022

Abstract Over the past 150 years, our ability to produce and transform engineered materials has been responsible for current high standards of living, especially in developed economies. However, we must carefully think effects addiction creating using at this fast rate will have on future generations. The way currently make use detrimentally affects planet Earth, many severe environmental problems. It next generations by putting danger economy, energy, climate. We are point where something drastically change, it change now. create more sustainable alternatives natural raw inspiration from nature while making sure not deplete important resources, i.e. competition with food chain supply. less materials, eliminate toxic a circular economy reuse recycle priorities. develop methods recycling encourage design disassembly. look across whole life cycle resources till end apply thorough assessments (LCAs) based reliable relevant data quantify sustainability. need seriously start thinking come how could track them, given that confronted resource scarcity geographical constrains. This is particularly development new energy technologies, key transition net zero. Currently ‘critical materials’ central components systems because they best performing. A few examples include permanent magnets rare earth metals (Dy, Nd, Pr) used wind turbines, Li Co Li-ion batteries, Pt Ir fuel cells electrolysers, Si solar just mention few. These classified as ‘critical’ European Union Department Energy. Except also packaging, construction, textile industry along other industrial sectors. roadmap authored prominent researchers working disciplines very field intended highlight outstanding issues be addressed provide an insight into pathways towards solving them adopted community. In compiling roadmap, hope aid wider research community, providing guide academia, industry, government, funding agencies critically rapidly developing space which

Язык: Английский

Процитировано

57

Highly Efficient Catalysts for Direct Arylation Polymerization (DArP) DOI
Masayuki Wakioka, Fumiyuki Ozawa

Asian Journal of Organic Chemistry, Год журнала: 2018, Номер 7(7), С. 1206 - 1216

Опубликована: Май 24, 2018

Abstract Recently, the palladium‐catalyzed direct arylation polymerization (DArP) has emerged as a viable alternative to conventional synthetic means of making π‐conjugated polymers based on catalytic cross‐coupling reactions. The DArP, which proceeds through C−H bond activation, distinct advantage over in terms fewer reaction steps and higher functional group tolerance. We have developed novel catalysts for DArP by using P(2‐MeOC 6 H 4 ) 3 ( L1 P(2‐Me 2 NC L2 ligands. Although common require use strongly coordinating solvents such DMA DMF, our exhibit high activity THF toluene, are good polymers. Thus, we could realize precise synthesis highly head‐to‐tail regioregular poly(3‐hexylthiophene) (HT‐P3HT) donor–acceptor type alternating copolymers (DA polymers) with well‐controlled structures DArP.

Язык: Английский

Процитировано

69

Metal-catalyzed C H activation for polymer synthesis and functionalization DOI
Yang Yang, Masayoshi Nishiura, Haobing Wang

и другие.

Coordination Chemistry Reviews, Год журнала: 2018, Номер 376, С. 506 - 532

Опубликована: Сен. 5, 2018

Язык: Английский

Процитировано

66

Eco-friendly semiconducting polymers: from greener synthesis to greener processability DOI

Madison Mooney,

Audithya Nyayachavadi,

Simon Rondeau‐Gagné

и другие.

Journal of Materials Chemistry C, Год журнала: 2020, Номер 8(42), С. 14645 - 14664

Опубликована: Янв. 1, 2020

This review presents emerging strategies for materials scientists to design, prepare and process semiconducting polymers in a more sustainable eco-friendly manner.

Язык: Английский

Процитировано

58

Direct (Hetero)arylation: A Tool for Low-Cost and Eco-Friendly Organic Photovoltaics DOI

Mathieu Mainville,

Mario Leclerc

ACS Applied Polymer Materials, Год журнала: 2020, Номер 3(1), С. 2 - 13

Опубликована: Сен. 30, 2020

Organic photovoltaics have attracted much attention in the past few years, mainly due to their ability be fully printed at low cost and large scale. However, organic semiconductors utilized as active layer are typically synthesized using Migita–Stille or Suzuki–Miyaura cross-coupling, which is not efficient may bring toxicity concerns. In search for atom-economical synthesis, direct (hetero)arylation polymerization (DHAP) enables activation of aromatic C–H bonds, both reducing synthetic steps monomers toxic reaction byproducts. this issue, we will discuss recent contributions on synthesis toward mass production photovoltaic materials. The impact DHAP material efficiency addressed compared conventional coupling methods. ongoing improvements discussed, becomes more sustainable higher scale materials observed having quality.

Язык: Английский

Процитировано

55

Precise control of conjugated polymer synthesis from step-growth polymerization to iterative synthesis DOI Creative Commons
Chaoran Xu, Jinxiang Dong,

Congze He

и другие.

Giant, Год журнала: 2023, Номер 14, С. 100154 - 100154

Опубликована: Апрель 14, 2023

Conjugated polymers with excellent optoelectronic properties, easy processability, and flexible physical properties are versatile in various applications. In recent years, the precise synthesis of conjugated has attracted much attention due to close relationship between structure property. From perspective polymerization mechanism, synthetic methods can be classified into step-growth polymerization, chain-growth iterative synthesis. synthesis, polymer becomes more controllable. this review, we introduce these three approaches prepare controllable structures based on transition metal-catalyzed cross-coupling reactions further reveal control over chemical structures, including length, regioregularity, sequence, topology. The is great significance for functional a specific structure, which paves way fabricating high-performance devices.

Язык: Английский

Процитировано

19

Pd-Catalyzed Thiophene–Aryl Coupling Reaction via C–H Bond Activation in Deep Eutectic Solvents DOI
Angela Punzi, Donato Ivan Coppi, Sergio Matera

и другие.

Organic Letters, Год журнала: 2017, Номер 19(18), С. 4754 - 4757

Опубликована: Сен. 6, 2017

Direct arylation of 5-octylthieno[3,4-c]pyrrole-4,6-dione with a series functionalized aryl iodides via C–H bond activation is demonstrated in deep eutectic solvent made choline chloride and urea non-anhydrous conditions without exclusion air. This the first demonstration thiophene–aryl coupling direct solvents.

Язык: Английский

Процитировано

58