Neighboring Group Participation and Internal Catalysis Effects on Exchangeable Covalent Bonds: Application to the Thriving Field of Vitrimer Chemistry DOI
Florian Cuminet, Sylvain Caillol, Éric Dantras

и другие.

Macromolecules, Год журнала: 2021, Номер 54(9), С. 3927 - 3961

Опубликована: Апрель 19, 2021

Vitrimers constitute a fascinating class of polymer materials that make the link between historically opposed 3D networks (thermosets) and linear polymers (thermoplastics). Their chemical resistance, reshaping ability, unique rheological behavior upon heating them promising for future applications in industry. However, many vitrimers require use high catalyst loadings, which raises concerns their durability limits potential applications. To cope with this issue, internal catalysis neighboring group participation (NGP) can be used to enhance ability such materials. A few studies report effect activating groups on exchange reactions vitrimers. Nevertheless, knowledge topic remains scarce, although research would greatly benefit from NGP already known organic chemistry. The present Perspective presents different types exchangeable bonds implemented discusses have or potentially capable an enhancing reactions. This analysis is underpinned by thorough mechanistic discussion various presented.

Язык: Английский

Dynamic Covalent Polymer Networks: A Molecular Platform for Designing Functions beyond Chemical Recycling and Self-Healing DOI
Ning Zheng, Yang Xu, Qian Zhao

и другие.

Chemical Reviews, Год журнала: 2021, Номер 121(3), С. 1716 - 1745

Опубликована: Янв. 4, 2021

Dynamic covalent polymer networks (DCPN) have historically attracted attention for their unique roles in chemical recycling and self-healing, which are both relevant sustainable societal development. Efforts these directions intensified the past decade with notable progress newly discovered dynamic chemistry, fundamental material concepts, extension toward emerging applications including energy electronic devices. Beyond that, values of DCPN discovering/designing functional properties not offered by classical thermoplastic thermoset polymers recently gained traction. In particular, bond exchangeability has shown unparalleled design versatility various areas shape-shifting materials/devices, artificial muscles, microfabrication. Going beyond this basic exchangeability, molecular mechanisms to manipulate network topologies (topological transformation) led opportunities program polymers, concepts such as living topological isomerization. review, we provide an overview above particular focuses on strategies exploitation properties. Based this, point out remaining issues offer perspectives how class materials can shape future ways that complementary polymers.

Язык: Английский

Процитировано

916

Translational Applications of Hydrogels DOI Creative Commons
Santiago Correa, Abigail K. Grosskopf, Hector Lopez Hernandez

и другие.

Chemical Reviews, Год журнала: 2021, Номер 121(18), С. 11385 - 11457

Опубликована: Май 3, 2021

Advances in hydrogel technology have unlocked unique and valuable capabilities that are being applied to a diverse set of translational applications. Hydrogels perform functions relevant range biomedical purposes-they can deliver drugs or cells, regenerate hard soft tissues, adhere wet prevent bleeding, provide contrast during imaging, protect tissues organs radiotherapy, improve the biocompatibility medical implants. These make hydrogels useful for many distinct pressing diseases conditions even less conventional areas such as environmental engineering. In this review, we cover major hydrogels, with focus on novel benefits injectable how they relate applications medicine environment. We pay close attention development contemporary requires extensive interdisciplinary collaboration accomplish highly specific complex biological tasks from cancer immunotherapy tissue engineering vaccination. complement our discussion preclinical clinical mechanical design considerations needed scaling technologies application. anticipate readers will gain more complete picture expansive possibilities practical impactful differences across numerous fields

Язык: Английский

Процитировано

719

Vitrimers: Permanently crosslinked polymers with dynamic network topology DOI Creative Commons
Nathan J. Van Zee, Renaud Nicolaÿ

Progress in Polymer Science, Год журнала: 2020, Номер 104, С. 101233 - 101233

Опубликована: Март 15, 2020

Язык: Английский

Процитировано

544

Bio-based polymers with performance-advantaged properties DOI
Robin M. Cywar, Nicholas A. Rorrer, Caroline B. Hoyt

и другие.

Nature Reviews Materials, Год журнала: 2021, Номер 7(2), С. 83 - 103

Опубликована: Сен. 23, 2021

Язык: Английский

Процитировано

487

Vitrimers: directing chemical reactivity to control material properties DOI Creative Commons
Marc Guerre, Christian Taplan, Johan M. Winne

и другие.

Chemical Science, Год журнала: 2020, Номер 11(19), С. 4855 - 4870

Опубликована: Янв. 1, 2020

In this minireview, we survey recent advances in the development of vitrimer materials. Focus on how to chemically control their material properties is used highlight challenges for boosting potential emerging class polymer

Язык: Английский

Процитировано

451

Toward Stimuli‐Responsive Dynamic Thermosets through Continuous Development and Improvements in Covalent Adaptable Networks (CANs) DOI
Maciej Podgórski,

Benjamin D. Fairbanks,

Bruce E. Kirkpatrick

и другие.

Advanced Materials, Год журнала: 2020, Номер 32(20)

Опубликована: Фев. 14, 2020

Abstract Covalent adaptable networks (CANs), unlike typical thermosets or other covalently crosslinked networks, possess a unique, often dormant ability to activate one more forms of stimuli‐responsive, dynamic covalent chemistries as means transition their behavior from that viscoelastic solid material with fluid‐like plastic flow. Upon application stimulus, such light irradiation, temperature, even distinct chemical signal, the CAN responds by transforming state temporal plasticity through activation either reversible addition bond exchange, which allows essentially re‐equilibrate an altered set conditions are those in original network is formed, simultaneously enabling new and shape, function, characteristics. As such, CANs span divide between thermoplastics, thus offering unprecedented possibilities for innovation polymer materials science. Without attempting comprehensively review literature, recent developments discussed here emphasis on most effective render these be stimuli responsive, features make broadly applicable.

Язык: Английский

Процитировано

417

Cleavable comonomers enable degradable, recyclable thermoset plastics DOI
Peyton Shieh, Wenxu Zhang, Keith E. L. Husted

и другие.

Nature, Год журнала: 2020, Номер 583(7817), С. 542 - 547

Опубликована: Июль 22, 2020

Язык: Английский

Процитировано

372

Advances in sustainable thermosetting resins: From renewable feedstock to high performance and recyclability DOI
Jingkai Liu, Shuaipeng Wang,

Yunyan Peng

и другие.

Progress in Polymer Science, Год журнала: 2020, Номер 113, С. 101353 - 101353

Опубликована: Дек. 29, 2020

Язык: Английский

Процитировано

300

Reprocessable Cross-Linked Polymer Networks: Are Associative Exchange Mechanisms Desirable? DOI Creative Commons
Benjamin R. Elling, William R. Dichtel

ACS Central Science, Год журнала: 2020, Номер 6(9), С. 1488 - 1496

Опубликована: Июль 29, 2020

Covalent adaptable networks (CANs) are covalently cross-linked polymers that may be reshaped via cross-linking and/or strand exchange at elevated temperatures. They represent an exciting and rapidly developing frontier in polymer science for their potential as stimuli-responsive materials to make traditionally nonrecyclable thermosets more sustainable. CANs whose cross-links undergo associative intermediates rather than dissociating separate reactive groups termed vitrimers. Vitrimers were postulated attractive subset of CANs, because cross-link mechanisms maintain the original density network throughout process. As a result, demonstrate gradual, Arrhenius-like reduction viscosity temperatures while maintaining mechanical integrity. In contrast, reprocessed by dissociation reformation have been exhibit rapid decrease with increasing temperature. Here, we survey stress relaxation behavior all dissociative which variable temperature or data reported date. All Arrhenius relationship between viscosity, only small percentage broken instantaneously under typical reprocessing conditions. such, show nearly identical over broad ranges typically used reprocessing. Given term vitrimer was coined highlight temperature, analogy vitreous glasses, discourage its continued use describe CANs. The realization mechanism does not greatly influence practical most suggests chemistries can considered fewer constraints, focusing instead on activation parameters, synthetic convenience, application-specific considerations.

Язык: Английский

Процитировано

280

Disulfide-Mediated Reversible Polymerization toward Intrinsically Dynamic Smart Materials DOI
Qi Zhang, Da‐Hui Qu, Ben L. Feringa

и другие.

Journal of the American Chemical Society, Год журнала: 2022, Номер 144(5), С. 2022 - 2033

Опубликована: Янв. 6, 2022

The development of a dynamic chemistry toolbox to endow materials behavior has been key the rational design future smart materials. rise supramolecular and covalent offers many approaches construction polymers that can adapt, respond, repair, recycle. Within this toolbox, building blocks based on 1,2-dithiolanes have become an important scaffold, featuring their reversible polymerization mediated by disulfide bonds, which enables unique class at intersection adaptable networks. This Perspective aims explore as versatile structural unit for summarizing state art well providing overview fundamental challenges involved in research area its potential directions.

Язык: Английский

Процитировано

249