New themed collection: Molecularly defined polymers

We are very pleased to announce the Polymer Chemistry special collection on Molecularly Defined Polymers: Synthesis and Function

 

This special issue presents the latest developments in the synthesis and applications of polymers with controlled, defined and/or precise molecular-scale structures. The Guest Editors for this collection are:

  • Professor Jeremiah Johnson (MIT, USA)
  • Professor Filip Du Prez (Ghent University, Belgium)
  • Professor Elizabeth Elacqua (Pennsylvania State University, USA)

 

Profile pictures of Jeremiah Johnson, Filip Du Prez and Elizabeth Elacqua

 

In their Editorial, Guest Editors Jeremiah Johnson, Filip Du Prez and Elizabeth Elacqua selected a number of manuscripts to exemplify and highlight goals and strategies for attaining sequence-defined macromolecules, synthesis of precise macromolecules, macromolecular precision and its roles in dictating the properties of bulk materials.

Button saying Click here to read the full Molecularly Defined Polymers collection

 

The full collection can be found here and we have also highlighted a selection of articles below. We hope you enjoy these, and the rest of the articles included in the collection:

 

Green light LED activated ligation of a scalable, versatile chalcone chromophore

Ishrath Mohamed Irshadeen, Kevin De Bruycker, Aaron S. Micallef, Sarah L. Walden, Hendrik Frisch and Christopher Barner-Kowollik

Polymer Chemistry, 2021,12, 4903-4909

 

Recent progress in the construction of polymers with advanced chain structures via hybrid, switchable, and cascade chain-growth polymerizations

Guang Chen, Lei Xia, Fei Wang, Ze Zhang and Ye-Zi You

Polymer Chemistry, 2021,12, 3740-3752

 

Synthesis and sequencing of informational poly(amino phosphodiester)s

Ian Roszak, Laurence Oswald, Abdelaziz Al Ouahabi, Annabelle Bertin, Eline Laurent, Olivier Felix, Isaure Carvin-Sergent, Laurence Charles and Jean-François Lutz

Polymer Chemistry, 2021,12, 5279-5282

 

Amino acid acrylamide mimics: creation of a consistent monomer library and characterization of their polymerization behaviour

Dries Wyers, Toon Goris, Yana De Smet and Tanja Junkers

Polymer Chemistry, 2021,12, 5037-5047

 

Stereocontrolled, multi-functional sequence-defined oligomers through automated synthesis

Chiel Mertens, Matthieu Soete, Marcin L. Ślęczkowski, Anja R. A. Palmans, E. W. Meijer, Nezha Badi and Filip E. Du Prez

Polymer Chemistry, 2020,11, 4271-4280

 

Mechanistic insights into the pressure-induced polymerization of aryl/perfluoroaryl co-crystals

Margaret C. Gerthoffer,  Bohan Xu,  Sikai Wu,  Jordan Cox,  Steven Huss,  Shalisa M. Oburn,  Steven A. Lopez,  Vincent H. Crespi,  John V. Badding and  Elizabeth Elacqua

Polymer Chemistry, 2022,13, 1359-1368

 

All the articles in the collection are currently FREE to read until 14 June!

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Paper of the month: Reconsidering terms for mechanisms of polymer growth: the “step-growth” and “chain-growth” dilemma

An international group of polymer scientists from the International Union of Pure and Applied Chemistry (IUPAC) Subcommittee on Polymer Terminology (SPT) convey concerns with the basic terms typically used for classifying methods of polymer synthesis and initiate a dialogue with the broader polymer community to resolve terminology shortcomings.

In 1994 the IUPAC SPT highlighted long-standing problems with the widely used terms “step-growth polymerization” and “chain-growth polymerization,” which describe two discrete mechanisms of polymer growth, and depreciated their use since they do not describe the fundamental differences in the growth of polymers by these methods and are often confusing. To address this, the 1994 SPT members recommended the terms polycondensation and polyaddition for the two variants of “step-growth polymerization”, and similarly chain polymerization and condensative chain polymerization for the two variants of “chain-growth polymerization”. However, these terms have not been widely adopted by the community, and have also created confusion.

In this contribution, current IUPAC SPT members provide detailed descriptions of these two processes and outline concerns associated with the terms “step-growth,” “chain-growth,” and related terms. By discussing in detail the historical development of these terms and analyzing their use in current textbooks, the authors underline the lack of consensus in the terminology used within the polymer community. Interestingly, they demonstrate how the similarity of these terms leads to further confusion when translating into languages other than English. Finally, examples of polymerizations that cannot be classified under the umbrella of the existing definitions and have no designated terminology are discussed.

In 2019, IUPAC recognized the need to resolve these polymer terminology shortcomings and approved a project aimed to propose new terminologies. The authors, as members of the IUPAC SPT task group studying this issue, aim to clarify the naming of polymerisation processes and invite all members of the community to contribute by emailing to polymer.terminology@iupac.org.

Tips/comments directly from the authors:

  • We, the subcommittee of polymer nomenclature (SPT), want to raise attention to a long-standing dilemma in the terms that many of us use every day: “step-growth” and “chain-growth” polymerization.
  • A number of terms have been used over the past century to describe these two fundamental mechanisms of polymer growth, and many prominent polymer chemists have noted their shortcomings in textbooks.
  • We detail here the history of the terms, current usage in textbooks, and our specific concerns.
  • In particular, we invite feedback from the broader polymer community, including from students, lecturers, researchers, and anyone who uses polymer science regularly.

 

Reconsidering terms for mechanisms of polymer growth: the “step-growth” and “chain-growth” dilemma, Polym. Chem., 2022, 13, 2262-2270.

Link to the paper: https://pubs.rsc.org/en/content/articlelanding/2022/py/d2py00086e

You can follow the authors on twitter: @IUPACPolymer

 

Dr. Kelly Velonia is an Advisory Board Member and a Web Writer for Polymer Chemistry. She joined the Department of Materials Science and Technology in 2007. Research in her group focuses on the synthesis and applications of bioconjugates and biopolymers.

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Paper of the month: The difference between photo-iniferter and conventional RAFT polymerization: high livingness enables the straightforward synthesis of multiblock copolymers

Lehnen et al. highlight the role of reversible deactivation as a key difference between photo-iniferter and conventional RAFT polymerization.

The use of light has become increasingly widespread in diverse polymerization approaches including reversible-addition fragmentation chain-transfer (RAFT) strategies. Among these, the photo-iniferter (PI)-RAFT polymerization in which light directly activates the chain transfer agent (CTA), has been shown to overcome several of the restrictions of conventional RAFT resulting in increased chain end fidelity. In this context, reversible deactivation is accepted to determine the fate of the growing radical via pathways that need to be understood to offer the means to further push the limits of PI-RAFT polymerization.  

To address this, Hartlieb and collaborators studied the PI-RAFT using an acrylamide (N-acryloyl morpholine) and a xanthate ((2-((ethoxycarbonothioyl)thio)propionic acid)). This monomer-CTA pair combination was selected on the basis of the low chain transfer capabilities (Ctr < 1) expected to result in high dispersities (>1.5). When targeting different degrees of polymerization (DP), the control over the molecular weight distribution was not found to significantly increase. However, control could be achieved through slow monomer addition that results in increasing the numbers of activation-deactivation events per monomer addition. Importantly, the high livingness associated with PI-RAFT proved to be invaluable in chain extension experiments since it was found to enable the straightforward, easy and rapid synthesis of very high molecular weight multiblock copolymers with up to 20 blocks and a high number of repeating units per block (DP = 25-100) with impressive precision.  

In summary this study highlights the role of reversible deactivation and employs the high livingness of PI-RAFT to demonstrate its enormous potential for the synthesis of polymeric materials and more specifically segmented macromolecules.

Tips/comments directly from the authors:

  • We want to emphasize how fast and easy polymerization reactions can be performed using this technique as the shown xanthate is an extremely powerful iniferter
  • The shown multiblocks were produced in a very straight forward way; no rigorously clean or inert conditions or specialized equipment.
  • The photo-iniferter process is older than RAFT polymerization but its full potential isn’t used yet.  

 

The difference between photo-iniferter and conventional RAFT polymerization: high livingness enables the straightforward synthesis of multiblock copolymers, Polym. Chem., 2022, 13, 1537-1546

Link to the paper: https://pubs.rsc.org/en/content/articlelanding/2022/py/d1py01530c

Link to Dr Matthias Hartlieb’s group website: https://www.uni-potsdam.de/polybio

You can follow Dr Matthias Hartlieb on Twitter: @PolyBioPotsdam

 

Dr. Kelly Velonia is an Advisory Board Member and a Web Writer for Polymer Chemistry. She joined the Department of Materials Science and Technology in 2007. Research in her group focuses on the synthesis and applications of bioconjugates and biopolymers.

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Polymer Chemistry Emerging Investigator – Nicholas Warren

Profile picture of Nicholas WarrenNick Warren is an Associate Professor at School of Chemical and Process Engineering at the University of Leeds. He was awarded an Masters in Chemistry from the University of Bristol in 2005 following which he conducted two years industrial research. He then moved to the University of Sheffield where he obtained a PhD in Polymer Chemistry. He continued as a postdoctoral researcher in Sheffield working in the area of polymerisation-induced self-assembly (PISA) until 2016, when he moved to Leeds to start his independent research career. His research group aims to design a new generation of sustainable and functional polymer materials by exploiting the latest advances in both polymer chemistry and self-optimising reactor technologies equipped with advanced online monitoring and computer control. He can be found on Twitter @njwarren1.

 

 

 

Read Nick’s Emerging Investigator article ‘Autonomous polymer synthesis delivered by multi-objective closed-loop optimisation’.

 

How do you feel about Polymer Chemistry as a place to publish research on this topic?

The vision of our research group is to develop technologies which aim to enhance precision and reproducibility in polymer synthesis and it is therefore vital that we target polymer chemists directly. Polymer Chemistry is the ideal avenue for this, and we hope it encourages adoption of new technologies in polymer synthesis labs around the world. Hopefully over the next few years, we can work with others to discover new materials with our platforms by implementing them for more technically demanding polymerisation processes.

 

What aspect of your work are you most excited about at the moment and what do you find most challenging about your research?

The ability to control our systems remotely, means we anticipate that networks of reactors in different labs around the world can communicate via cloud computing to optimise and discover new polymers. We are really excited by the fact that this is bringing artificially intelligent approaches to polymer discovery one step closer!

There are many advantages that flow chemistry affords here, but the challenges associated with polymer solutions in flow means a lot of work is required to optimise the reactor geometries and to provide consistent mixing. However, by working with fluid dynamics experts we are beginning to address these problems, which have traditionally been a major barrier. We are also keen to enable multi-step processes, without human intervention with each characterised in real-time. This includes post-polymerisation processing, and purification. There are also significant challenges in dealing with all sorts of data, which means we’re going to need to tailor our machine learning algorithms to accept this – essentially teaching robots how to do polymer synthesis!

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New themed collection: Sustainable polymers

We are very pleased to announce the Polymer Chemistry special collection on Sustainable Polymers

 

This special issue presents the most important developments in these fields in novel synthetic methodology and making use of modern methods such as continuous flow chemistry or energy-efficient photochemical reactions for sustainable polymer synthesis. The Guest Editors for this collection are:

  • Professor Antoine Buchard (University of Bath, Belgium)
  • Professor Tanja Junkers (Monash University, Australia)

 

In their Editorial, Guest Editors Antoine Buchard and Tanja Junkers discuss the importance of sustainability in polymers including in areas such as renewable polymers, green synthetic methods, improving polymer properties, degradability, chemical recycling, toxicology impact and design.

 

Click here to read the full collection

 

The full collection can be found here and we have also highlighted a selection of articles below. We hope you enjoy these, and the rest of the articles included in the collection.

 

A guide towards safe, functional and renewable BPA alternatives by rational molecular design: structure–property and structure–toxicity relationships
L. Trullemans, S.-F. Koelewijn, I. Scodeller, T. Hendrickx, P. Van Puyvelde and B. F. Sels

Polymer Chemistry, 2021, 12, 5870-5901

 

Recent developments towards performance-enchancing lignin-based polymers
Garrett F. Bass and Thomas H. Epps, III
Polymer Chemistry, 2021, 12, 4130-4158

 

Sustainable synthesis of CO2-derived polycarbonates from ᴅ-xylose
David K. Tran, Ahmed Z. Rashad, Donald J. Darensbourg and Karen L. Wooley

Polymer Chemistry, 2021, 12, 5271-5278

 

Access to high-molecular-weight poly(γ-butyrolactone) by using simple commercial catalysts
Yihuan Liu, Xin Yuan, Jiaqi Wu, Xin Hu, Ning Zhu and Kai Guo

Polymer Chemistry, 2022, 13, 439-445

 

Novel imino- and aryl-sulfonate based photoacid generators for the cationic ring-opening polymerizarion of ε-caprolactone
Xabier Lopez de Pariza, Erick Cordero Jara, Nicolas Zivic, Fernando Ruipérez, Timothy E. Long and Haritz Sardon
Polymer Chemistry, 2021, 12, 4035-4042

 

Renewable and recyclable covalent adaptable networks based on bio-derived lipoic acid
Maher A. Alraddadi, Viviane Chiaradia, Connor J. Stubbs, Joshua C. Worch and Andrew P. Dove

Polymer Chemistry, 2021, 12, 5796-5802

 

All the articles in the collection are currently FREE to read until 2 May 2022!

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Paper of the month: Iron-containing poly(ionic liquid) membranes: a heterogeneous Fenton reaction and enhanced anti-fouling ability

Guan et al. develop iron-containing poly(ionic liquid) (Fe-PIL) membranes with anti-fouling properties enhanced by a heterogeneous Fenton reaction.

The life span of membranes used in various separation technologies is often limited by fouling causing decreased performance and large economic costs. Recently, poly(ionic liquid)s (PILs) have been employed to prepare membranes with a large range of applications due to their unique material properties including excellent stability, processability and flexibility. Although PIL membranes are less prone to fouling and easier to clean due to their charged nature, the problem of irreversible pollutant deposition can limit their efficiency.  

To address this, Zhang and collaborators developed iron-containing PIL (Fe-PIL) membranes and used them as catalysts for heterogenous Fenton reaction. Poly(4-vinylpyridine)-b-polysulfone-b-poly(4-vinylpyridine) (PSF-b-P4VP) blend membranes were synthesized via Cu(0)-RDRP. The pore size and hydrophilicity of the membranes fabricated via NIPS, were found to depend on the block ratio of the polymer. A quaternization reaction followed by coordination with Fe(II) bromide was employed to generate the Fe-PILs on the surface of the polysulfone blends.  The membranes were shown to possess low surface roughness, increased hydrophilicity, anti-fouling properties and scalability. The dispersibility of the catalyst and the catalytic efficiency in heterogeneous Fenton reactions were shown to be excellent in a broad pH range from acidic to neutral and basic conditions. More importantly, the Fe-PIL membranes exhibited superior synergistic performance with filtration in the dynamic heterogeneous Fenton reaction and excellent reusability as they could be maintained well after five cycles.

In summary this study combines PIL membrane technology with dynamic heterogeneous catalysis (Fenton reaction) to create reusable PILs that address the issue of membrane fouling.

 

Iron-containing poly(ionic liquid) membranes: a heterogeneous Fenton reaction and enhanced anti-fouling ability, Polym. Chem., 2022,13, 130-138

Link to the paper: https://pubs.rsc.org/en/content/articlelanding/2022/py/d1py01345a

 

Dr. Kelly Velonia is an Advisory Board Member and a Web Writer for Polymer Chemistry. She joined the Department of Materials Science and Technology in 2007. Research in her group focuses on the synthesis and applications of bioconjugates and biopolymers.

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New themed collection: Synthetic methodologies for complex macromolecular structures

We are very pleased to announce the Polymer Chemistry special collection on Synthetic methodologies for complex macromolecular structures, in honour of Professor Yusuf Yağci’s 70th birthday

 

Professor Yusuf Yağci has worked on various aspects of polymer synthesis during his long research career and has developed several new synthetic methodologies to create functional macromolecules. He has benefited from ionic polymerizations, photo-initiated polymerizations, as well as controlled or living radical polymerization techniques. This collection is not just limited to these topics but also aims to reflect the inspiring, creative and entertaining character of Yusuf. The Guest Editors for this collection are:

  • Dr Hatice Mutlu (Karlsruhe Institute of Technology, Germany)
  • Professor Filip Du Prez (Ghent University, Belgium)
  • Professor Remzi Becer (University of Warwick, UK)

 

In their Editorial, Guest Editors Hatice, Filip and Remzi, discuss the impact that Professor Yağci has had on the advancement of many fields, his commitment to the polymer chemistry community and his entertaining character.

 

Click here to read the full collcetion

 

The full collection can be found here and we have also highlighted a selection of articles below. We hope you enjoy these, and the rest of the articles included in the collection.

 

Synthesis of core-crosslinked star polymers via organocatalyzed living radical polymerization
Yichao Zheng, Jit Sarkar, Hiroshi Niino, Shunsuke Chatani, Shu Yao Hsu and Atsushi Goto

Polymer Chemistry, 2021, 12, 4043-4051

 

Trehalose coated nanocellulose to inhibit the infections by S. aureus
Yimeng Li, Małgorzata Milewska, Yee Yee Khine, Nicholas Ariotti and Martina Stenzel
Polymer Chemistry, 2022, 10.1039/D1PY01422F

 

Bromoform-assisted aqueous free radical polymerisation: a simple, inexpensive route for the preparation of block copolymers
Helena Hutchins-Crawford, Padarat Ninjiaranai, Matthew Derry, Robert Molloy, Brian Tighe and Paul Topham

Polymer Chemistry, 2021, 12, 4317-4325

 

Redox-sensitive ferrocene functionalised double cross-linked supramolecular hydrogels
Nikolai Liubimtsev, Tom Kösterke, Yunjiao Che, Dietmar Appelhans, Jens Gaitzsch and Brigitte Voit

Polymer Chemistry, 2022, 13, 427-438

 

Effect of halogen and solvent on iron-catalyzed atom transfer radical polymerization
Sajjad Dadashi-Silab, Khidong Kim, Francesca Lorandi, Dirk Schild, Marco Fantin and Krzysztof Matyjaszewski
Polymer Chemistry, 2022, 13, 1059-1066

 

Upconversion nanoparticle-assisted cationic and radical/cationic hybrid photopolymerization using sulfonium salts
Xiaoyan Meng, Longji Li, Yaoxin Huang, Xin Deng, Xiaoxuan Liu and Zhiquan Li

Polymer Chemistry, 2021, 12, 7005-7009

 

All the articles in the collection are currently FREE to read until 17 April 2022!

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Polymer Chemistry Emerging Investigator – Runhui Liu

Professor Runhui Liu obtained Ph.D in organic chemistry 2009 at Purdue University. Afterward, he took postdoctoral trainings at California Institute of Technology and University of Wisconsin-Madison during 2010-2014. At the end of 2014, he took a professor position in the School of Materials Science and Engineering at East China University of Science and Technology (ECUST). His current research focuses on peptide polymer-based biomaterials for antimicrobial and tissue engineering applications.

 

 

 

Read Runhui’s article ‘Facile Synthesis of Polypeptoid Bearing Bulky Sidechains via Urea Accelerated Ring-Opening Polymerization of a-Amino Acid N-Substituted N-Carboxyanhydrides’.

 

How do you feel about Polymer Chemistry as a place to publish research on this topic?

Polymer Chemistry is a wonderful place to publish our work on polymer synthesis.

 

What aspect of your work are you most excited about at the moment and what do you find most challenging about your research?

I am most excited in exploring new chemistry for polymer synthesis, especially to tackle the long-lasting challenges.

The most challenging things for me as a professor are in two folds: keeping the lab running efficiently and productively with minimum amount of funding; inspiring/encouraging students to work on long-standing challenges but not hot topics, and persuading students to give up results that look interesting and publishable at first glance.

 

Can you share one piece of career-related advice or wisdom with other early career scientists?

As long as the start-up funding can support the lab for the first 3-4 years, focus on science is more productive eventually; as long as the PI and students can survive, no rush to publish or publish a lot at the first 3 years.

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Polymer Chemistry Emerging Investigator – Matthias Hartlieb

Matthias Hartlieb received his PhD in Chemistry in 2015 at the Friedrich Schiller-University in Jena. He proceeded to work as a DFG-funded postdoctoral research fellow at the University of Warwick followed by a research position at the Helmholtz Zentrum Geesthacht. He joined the University of Potsdam in 2019 as an Open-Topic Postdoc and, since 2021, he leads an Emmy Noether research group at Potsdam. His research interests are the design of functional polymeric (bio)materials, specifically in the areas of antimicrobial polymers and supramolecular polymers, using tools such as (photo)-RAFT polymerization or solid phase synthesis. More information can be found on his group website and on Twitter @PolyBioPotsdam.

 

 

Read Matthias’ article ‘The role of reversible deactivation in photo-iniferter RAFT polymerization: high livingness enables the straightforward synthesis of multiblock copolymers’.

 

How do you feel about Polymer Chemistry as a place to publish research on this topic?

A significant share of my publications are in Polymer Chemistry and there are reasons for that. Of course, it is one of the leading journals in macromolecular chemistry, and in my opinion, it presents the broadest overview in this area. So, it’s a great journal for researchers to see and be seen. I am also in favor of the uncomplicated and open reviewing process. Waiting times are relatively short and usually feedback is extremely constructive. It might also be a result of my time in the UK, but for me Polymer Chemistry is the journal where I feel most “at home” with my research.

 

What aspect of your work are you most excited about at the moment and what do you find most challenging about your research?

There are actually at least two aspects I am currently equally excited about. On the one hand there is photo-iniferter RAFT polymerization, which is also the topic of the publication in the special issue. This method has a tremendous potential, both for polymer synthesis as well as for material design. On the other hand, I am very keen on developing new antimicrobial polymers. At some point in the future antibiotics might fail us and then we need to have something to replace them to avoid a drastic decrease in health care quality and life expectancy.

We are looking at the impact of polymer architecture and on the membrane interaction of these polymers, among other things in order to get closer to an application. For the development of new antimicrobial polymers, we are currently implementing PI-RAFT as well.

 

In your opinion, what are the most important questions to be asked/answered in this field of research?

When it comes to antimicrobial polymers, the most important question is how we can improve their properties to bring them closer to an actual clinical application. However, this contains a lot of other questions, as there are many parameters, influencing the bioactivity of these polymers. Overall, their selectivity (targeting bacterial cells over mammalian cells) requires improvement but its not entirely clear how to achieve optimal performance.

We are looking into the polymer architecture, a parameter that hasn’t received much attention. We are also probing different targeting strategies and want to understand the mechanism of membrane interaction of these polymers in more detail.

 

Can you share one piece of career-related advice or wisdom with other early career scientists?

I am happy to forward something that has helped me staying on track: a fellow early career researcher did show me his folder with failed grant applications from the last few years, which had well over 30 items in it. However, he also had one successful one, and that was enough to kick start his career. The same thing happened to me. A lot of failed grant applications, not always with helpful feedback, sometimes without any feedback at all. It is easy to get frustrated at this stage but its important to continue trying. For me eventually, the DFG (Deutsche Forschungsgemeinschaft) thought my ideas regarding antimicrobial polymers were worth funding, which was the start of my independent research group. The lesson seems to be: don’t get discouraged by failure, because there will be a lot of that. Have a plan B but stay on track and try everything you can to follow your goal. Persistence is key (among other things like good mentoring, a supportive family, etc.).

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Polymer Chemistry Emerging Investigator – Wen-Ming Wan

Dr. Wen-Ming Wan is a Professor at Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences. He received his B.E. degree in Polymer Material and Engineering from Harbin Institute of Technology. He received a Ph.D. degree in Polymer Chemistry and Physics from University of Science and Technology of China, where he developed polymerization-induced self-assembly (PISA) method under the supervision of Prof. Cai-Yuan Pan. He completed postdocs at UT Southwestern Medical Center (Dallas) with Prof. Wen-Hong Li, The University of Southern Mississippi with Prof. Charles L. McCormick, and Rutgers University (Newark) with Prof. Frieder Jäkle. He started his independent research career as an Assistant Professor at Centre for Bioengineering and Biotechnology at China University of Petroleum (East China) in 2014, and then moved to Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences in 2018. His current research interests focus on the development of novel polymerization methodologies, including but not limited to Barbier polymerization, living polymerization, polymerization-induced emission (PIE), single-atom polymerization (SAP) and PISA.

 

Read Wen-Ming’s article ‘Room-temperature Barbier single-atom polymerization induced emission as a versatile approach for the utilization of monofunctional carboxylic acid resources’.

 

How do you feel about Polymer Chemistry as a place to publish research on this topic?

Polymer chemistry is of significance in polymer science. So, Polymer Chemistry journal is a significant platform to publish important research work in polymer science, including synthesis, functionality and applications of polymers.

 

What aspect of your work are you most excited about at the moment and what do you find most challenging about your research?

Carbonyl chemistry is fundamental and plays cornerstone roles in synthetic chemistry. Meanwhile, carbonyl compounds are widely and readily available from fossil fuels and biomass, which are important resources on Earth. However, corresponding carbonyl polymerization is rarely investigated. My most excited work at the moment is Barbier polymerization, which successfully realizes the utilization of a varieties of carbonyls as polymerizable groups for the molecular design of nonconjugated luminescent polymers through polymerization-induced emission (PIE) strategy. Currently, the most challenging about my research is to demonstrate the advantages and importance of carbonyl polymerization in both scientific and industrial aspects, which will ultimately allow us to exploit Earth’s carbonyl resources more efficiently and functionally.

 

In your opinion, what are the most important questions to be asked/answered in this field of research?

Since Staudinger proposed the concept of polymerization in 1920, generations of polymer chemists have spent considerable efforts to develop different kinds of polymerization methods, resulting in prosperous polymer science with abundant synthetic polymer materials in the forms of plastics, fibers, rubbers, etc. In comparison with previous polymerization methods, whether can Barbier polymerization survive throughout the history of polymer chemistry? How far can Barbier polymerization go? Whether can the prepared polymers via Barbier polymerization be recyclable? Whether is the concept of PIE applicable to other polymerization methods?

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