Paper of the month: Redox-triggerable firefly luciferin-bioinspired hydrogels as injectable and cell-encapsulating matrices

Jin et al. employ redox activated macromers to achieve precise control over the gelation onset and kinetics of a redox-triggerable, firefly luciferin-inspired hydrogel platform.

Stimuli-responsive hydrogels are porous crosslinked networks which have recently attracted tremendous interest thanks to their unique response to external stimuli allowing to tune their properties on demand. In particular, chemically-responsive hydrogels that can be actuated via mild redox reactions are quite promising for biomedical applications once biocompatible and non-cytotoxic. Despite the remarkable progress in the field, lack of precise triggering of the gelation onset and control over the rate of the gelation process of responsive hydrogels restricts a range of applications. In their current contribution, Paez and coworkers report on a novel firefly luciferin-inspired hydrogel platform endowed with redox-triggering ability and tunability of its mechanical and biological properties. To achieve this goal, protected macromers (PEG-Cys(SR)) which can be activated in the presence of a mild reductant were used as hydrogel polymeric precursors. This design allowed to in situ trigger gel formation and achieve a high degree of control. Importantly, the gelation onset and rate could be fine-tuned via altering the molecular characteristics of the precursors (e.g., structure of the protecting group, reductant type) and/or the environmental parameters of the deprotection reaction (e.g., pH, temperature). Specifically, gelation could be achieved in times spanning from seconds (CBT–Cys(SEt) / TCEP) to hours (CBT–Cys(StBu)/DTT) using precursors with good long-term stability upon storage in physiologically-relevant aqueous conditions. Furthermore, high stem cell viability was observed after 1–3 days of encapsulation in biofunctionalized CBT–Cys(SR) hydrogels. The authors anticipate that the precise control over the gelation onset and kinetics of this this redox-triggerable system, will facilitate its use for drug delivery and tissue engineering as well as inks for extrusion-based printing of soft constructs for regenerative medicine.

 

Tips/comments directly from the authors:

  •  We engineered macromers at the molecular level to achieve highly controlled gelation onset and kinetics. In the rheological characterization, it is recommended to prepare the hydrogel formulation by mixing polymer precursors solution and reductant solution in equal volume. This enables better mixing of the components and ensures good reproducibility of the rheological measurements. Two polymer precursor solutions can be mixed in advance (first half of the total volume) before adding the reductant (second half of the total volume) and loading to the rheometer.

 

  • We evaluated the cytocompatibility of the redox-triggerable hydrogels and found excellent cell viability after 1-3 days culture. Before doing 3D cell encapsulation, it is recommended to perform a preliminary experiment of gel preparation under same conditions but in the absence of cell suspension to estimate the gelation time. Cell suspension can be replaced by cell culture medium.

 

Citation to the paper: Redox-triggerable firefly luciferin-bioinspired hydrogels as injectable and cell-encapsulating matrices, Polym. Chem., 2022, 13, 5116-5126, DOI: 10.1039/D2PY00481J

Link to the paper:

https://pubs.rsc.org/en/content/articlehtml/2022/py/d2py00481j

 

The Paez laboratory at the University of Twente:

Twitter account: @PaezLab

ResearchGate account: https://www.researchgate.net/profile/Julieta-Paez

 

 

Dr. Kelly Velonia is an Advisory Board Member and a Web Writer for Polymer Chemistry. She joined the Department of Materials Science and Technology at the University of Crete in 2007. Research in her group focuses on the synthesis and applications of bioconjugates and biopolymersYou can follow Kelly on twitter @KellyVelonia


 

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Polymer Chemistry Emerging Investigator- Julieta I. Paez

 

Julieta Paez is a group leader at the University of Twente in the Netherlands. Julieta obtained her PhD in Chemistry at the National University of Córdoba, Argentina, working with Prof. Miriam Strumia on the synthesis of polymeric materials for sensing and antifouling applications. After her PhD, Julieta moved to Prof. Rainer Haag’s lab at the Freie Universität Berlin, Germany, as a Postdoctoral Researcher, to investigate biofunctional polymeric-protein surfaces. She then joined the group of Prof. Aránzazu del Campo at the Max-Planck Institute for Polymer Research in Mainz, where she developed photoactivatable peptides for cell-instructive materials and also worked with catechol-functionalized polymers for tissue gluing applications. Next, she moved to INM – Leibniz Institute for New Materials in Saarbrücken, first as Research Scientist and then as Project Leader, developing novel coupling chemistries for bioconjugation and gelation under physiological conditions. Since April 2021, Julieta is Assistant Professor at the department of Developmental Bioengineering at the University of Twente. Her main interest is the development of chemical strategies to (macro)molecularly engineer smart hydrogels that interact with living cells and tissues, for healthcare applications.

Find out more about Julieta’s research here: https://www.researchgate.net/profile/Julieta_Paez2

You can follow Julieta on Twitter @PaezLab

Read Julieta’s Open Access Emerging Investigator article, ‘Redox-triggerable firefly luciferin-bioinspired hydrogels as injectable and cell-encapsulating matrices’

Check out our interview with Julieta below:

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

Polymer Chemistry is a top reputed journal in the field, and represents a paramount home for discussion of the state-of-the-art. I feel delighted to contribute whenever is possible!

 

2. 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 thrilled about the transversal nature of my research. My work combines tools from synthetic organic and polymer chemistry, biomaterials science, and cell biology; to engineer smart soft materials that interacts with living cells and tissues. One research line in my lab is the development of responsive hydrogels for cell encapsulation. These artificial models can be used to study the complex communication between cells and between cells and their native microenvironment. The biggest challenge is that the native cell niche is very dynamic, therefore, capturing such features in a synthetic material is complex but fascinating at the same time.

 

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

We want to better understand how cells communicate with themselves and with their environment, so we can develop novel approaches in tissue engineering and regenerative medicine. In this regard, engineered materials whose properties can be regulated on demand can help us to investigate those type of questions. I am particularly interested in the possibility of controlling matrix viscoelasticity on demand to steer cell behavior. Thereby, I believe that the polymer chemistry field has much to offer by providing inspiration towards novel mechanoresponsive polymeric tools upon which smart biomaterials can be built.

 

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

I would encourage young researchers to get involved into (and, eventually, to create their own) diverse scientific teams. I have enjoyed very much my journey so far, since it allowed me to be surrounded and get inspired by researchers from diverse disciplines, career stage, geographical background and way of thinking. This multidisciplinary and multicultural ingredient of a scientific team, which has greatly impacted my career, is in my view what makes science very creative, rewarding and fun.

 

 

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Polymer Chemistry Emerging Investigator- Quentin Michaudel

Quentin Michaudel grew up in La Rochelle, France. He received his B.Sc. (2008) and M.Sc. (2010) from the École Normale Supérieure de Lyon. He earned his Ph.D. (2015) with Professor Phil S. Baran at The Scripps Research Institute, where he explored C–H functionalization methods and their applications to the synthesis of complex molecules. Quentin then accepted a postdoctoral position at Cornell University, where he developed photocontrolled polymerizations with Professor Brett P. Fors. In 2018, Quentin started his independent career as an assistant professor at Texas A&M University. His research group focuses on the development of synthetic methods and new organic materials. Quentin is the recipient of the 2022 ACS PMSE Young Investigator Award; the 2022 ACS Organic Division Academic Young Investigator’s Symposium; and the 2021 Thieme Chemistry Journals Award.

You can follow Quentin and his lab on Twitter @q_michaudel and @MichaudelLab

Read Quentin’s Emerging Investigator article, ‘Expedient synthesis and ring-opening metathesis polymerization of pyridinonorbornenes’

 

Check out our interview with Quentin below:

 

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

Polymer Chemistry is a great venue for synthetic studies focused on new polymeric architectures, as well as for reports of polymerizations relying on catalytic processes. It is a great place for the polymer community to share impactful results.

 

2. 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 very excited about my group’s ability to precisely synthesize polymers with high structural complexity and tailored properties. Our research requires the often-difficult characterization of novel polymers, as well as the investigation of intricate reaction mechanisms, but that challenge is exciting and motivates us to push the boundaries of the field.

 

 

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Paper of the month: Microfluidic-supported synthesis of anisotropic polyvinyl methacrylate nanoparticles via interfacial agents

Visaveliya et al. combine microfluidics with bulk batch synthesis to fabricate complex (non-spherical) anisotropic polyvinyl methacrylate (PVMA) nanoparticles (NPs) in a single step.

Τhe properties of polymer nanoparticles are dictated by both structure-property and structure-function relationships however, the importance of particle shape is generally overlooked due to the inherent difficulty to synthesize anisotropic nanoparticles in a single step. Anisotropic colloids are currently produced via multi-step synthesis platforms restrict scaling-up and evaluating as an alternative to the well-established spherical colloidal particles.

To address this issue, Eisele and collaborators developed a single-step, microfluidic-supported synthesis for anisotropic polyvinyl methacrylate (PVMA) nanoparticles that takes advantage of the homogeneous conditions given by microfluidics for the initial emulsification process and of the inhomogeneous conditions provided by bulk batch synthesis for the thermal polymerization. Α monomer with two active polymerization sites (vinyl methacrylate) was used and the impact of interfacial agents including a molecular surfactant (sodium dodecyl sulfate, SDS), anionic polyelectrolytes (poly(sodium 4-styrene sulfonate), PSSS and poly(4-styrene sulfonic acid) ammonium salt, PSSA), a cationic polyelectrolyte (poly(diallyldimethylammonium chloride), PDADMAC), and the non-ionic polymer (polyvinylpyrrolidone,PVP) on the shape and size of the produced nanoparticles was systematically evaluated. A direct effect of the identity and the concentration on the shape of the produced nanoparticles was observed and led to a plethora of structures varying from isotropic spherical structures (SDS) to anisotropic elongated (PSSS, PSSA) and flower-like structures (low PVP concentrations) or irregularly shaped assemblies (PDADMAC, high PVP concentrations).

In summary, this study provides a general framework to guide investigations on colloidal polymerization towards predicting nanoparticle shapes below the critical 200 nm regime.

 

Microfluidic-supported synthesis of anisotropic polyvinyl methacrylate nanoparticles via interfacial agents, Polym. Chem., 2022,13, 4625-4633

Link to the paper: https://pubs.rsc.org/en/content/articlelanding/2022/py/d1py01729b

 

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

You can follow Kelly on twitter @KellyVelonia


 

 

 

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Polymer Chemistry Emerging Investigator- Zachary Hudson

 

 

Zachary M. Hudson is an Associate Professor and Canada Research Chair in Sustainable Chemistry at the University of British Columbia. Zac completed his B.Sc. at Queen’s University in Kingston, Ontario. He remained at Queen’s to pursue a Ph.D. in Inorganic Chemistry under the supervision of Prof. Suning Wang, focusing on the development of luminescent materials for organic electronics. During his Ph.D. he also held graduate fellowships at Jilin University in China as well as Nagoya University in Japan. He then moved to the University of Bristol as a Marie Curie Postdoctoral Fellow with Prof. Ian Manners, followed by a second Postdoctoral Fellowship at the California Nanosystems Institute at the University of California, Santa Barbara with Prof. Craig Hawker. He joined the faculty at UBC in 2015, where he holds the Canada Research Chair in Sustainable Chemistry. He leads a research program in synthetic materials chemistry, studying topics ranging from solutions for energy-efficient displays and light sources to the self-assembly of electronic materials on the nanoscale. He was the recipient of the ACS Herman Mark Young Scholar Award and Polymer International-IUPAC Award in 2022.

Read Zachary’s Emerging Investigator article, ‘Donor modification of thermally activated delayed fluorescence photosensitizers for organocatalyzed atom transfer radical polymerization’

 

Check out our interview with Zachary below:

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

Polymer Chemistry is the perfect place to read about innovative techniques in polymer synthesis, and we’re excited to contribute an article with a photophysical twist.

 

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

I’m very excited about our work on luminescent polymer dots, or Pdots – nanoparticles that can be bright enough to be detected with a handheld smartphone camera. We’re collaborating with my colleague Russ Algar at UBC to develop nanoparticles for biosensing using smartphones, and translating this to technology that could be used in a healthcare setting represents a major exciting challenge.

 

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

Our current featured article uses organic photosensitizers as catalysts for controlled radical polymerization. In this space, we need to develop highly photostable sensitizers that can perform using visible light irradiation. This is a major challenge, because accessing suitably high-energy excited states using visible light is itself a contradictory requirement.

 

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

I’m a big fan of ‘white space’ in my calendar – time in which nothing is booked, so I have the space to just read or think. The hectic lifestyle of early-career academia combined with our always-connected culture makes it hard to find time to just think about science – schedule it if you have to!

 

 

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Paper of the month: Donor modification of thermally activated delayed fluorescence photosensitizers for organocatalyzed atom transfer radical polymerization

Polgar et al. use donor-modified thermally activated delayed fluorescence (TADF) emitters as photocatalysts for O-ATRP.

O-ATRP has emerged as an attractive alternative to conventional metal-catalyzed ATRP that uses organic compounds that catalyze polymerization under light irradiation instead of the well-studied metal catalysts. Specifically, O-ATRP using thermally activated delayed fluorescence (TADF) emitters as photocatalysts takes advantage of the unique ability of TADFs to interconvert singlet and triplet excited states and has been more recently implemented in diverse fields including organic electronics, photocatalysis, biological imaging, and chemical sensing. TADF emitters mostly contain a twisted donor–π–acceptor (D–π–A) motif which results in a prolonged excited state lifetime and facilitates singlet and triplet energy and electron transfer. Nevertheless, the coexistence of both electron donors and acceptors in photoredox catalysis results in unwanted excited state side reactivity that limits initiator efficiency and might also deactivate the catalyst.

To address this issue, Hudson and collaborators use donor-modified TADF emitters as photocatalysts for O-ATRP. More specifically, TADF photosensitizers based on 9,10-dihydro-9,9-dimethylacridine/2,4,6-triphenylpyrimidine conjugates exhibiting strong visible absorption, large excited state reduction potentials, and long-lived triplet excited states were employed to evaluate catalyst structure–activity relationships. The stability of the radical cation was found to be determining for controlled polymerization, however, significant differences were observed among donor-modified catalysts which were also related to variation in the rates of photoinduced electron transfer (PET). Time-resolved photoluminescence studies of the catalysts supported initiation by electron transfer from both singlet and triplet states while, the functionalized donors possessed the higher driving forces for PET. Through this study, the donor-modified TADF photocatalyst PymDMDMA -bearing a methoxyphenyl substituent- was identified to yield methacrylic polymers with Đ below 1.3 at low catalyst loadings (50 ppm) while also being able to catalyze the controlled synthesis of block copolymers in contrast to the unmodified TADF.

This study explores the ability to design more efficient catalysts by merely altering the types of donors, acceptors and their derivatives and proposes that more efficient catalysts can be designed through theoretical modeling.

Tips/comments directly from the authors:

  • ppm-levels of catalyst are sufficient for the synthesis of polymers with well-defined size, composition, and topology by O-ATRP, potentially obviating the need for post-polymerization purification.
  • Donor-acceptor fluorophores can exhibit thermally activated delayed fluorescence (TADF), a phenomenon that prolongs the excited state lifetime. The ability to control the lifetime and excited-state reduction potential of TADF emitters makes them versatile photocatalysts for O-ATRP, particularly at low catalyst loadings.
  • A donor-modification strategy was used in this study to mitigate deleterious excited-state side-reactivity associated with the electron-rich donors used in TADF. Rational design of modifying groups can not only enhance the photostability of these dyes, but also provide an extra dimension of control over the excited state reduction potentials and rates of electron transfer in O-ATRP.

 

Donor modification of thermally activated delayed fluorescence photosensitizers for organocatalyzed atom transfer radical polymerization, Polym. Chem., 2022, 13, 3892-3903. 

 

Link to the paper: https://pubs.rsc.org/en/content/articlelanding/2022/py/d2py00470d

 

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- Myungwoong Kim

Myungwoong Kim received his B.S. in Chemistry (2002) and M.S. in Physical Chemistry (2004) from Hanyang University under supervision of Prof. Daewon Sohn, then worked for several years in photopatterning materials industry. He completed his Ph.D. in Materials Science (2013) at University of Wisconsin – Madison under supervision of Prof. Padma Gopalan. He then conducted his postdoctoral research in Prof. Christopher K. Ober’s group at Cornell University. In 2015, he joined the Department of Chemistry at Inha University to begin his independent research career. His current research interests include precision polymer synthesis for desired structures and properties, surface and interface engineering, polymeric material designs for micro/nanofabrications, for functional gels, and for understanding polymer dynamics.

Read Myungwoong’s Emerging Investigator article, ‘Comprehensive studies of continuous flow reversible addition–fragmentation chain transfer copolymerization and its application for photoimaging materials’

Check out our interview with Myungwoong below:

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

I have enjoyed reading the articles in Polymer Chemistry. I have been impressed by the journal scope, especially respecting and embracing conventional, but fundamental and significant polymer chemistry topics, for example, polymerization kinetics and photopolymer chemistry. However, the journal has also been enthusiastic to publish high quality articles dealing with cutting edge topics. This unique balancing makes me keep following every day and considering Polymer Chemistry as a place to publish.

 

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

For the patterns in single-digit nanometer dimension, the size becomes equivalent to less than ten copolymer chains. In this limit, the homogeneity of the copolymer system gets important to improve the pattern quality, such as line edge roughness. The continuous flow process shown in our work can address this issue; however, it also gave us an important message: the compositional drift due to unequal reactivity between monomers results in an intrinsic compositional inhomogeneity in copolymer samples. This is further related to the fundamental challenging question: “can we precisely control the structure and composition of complex polymers?”.

 

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

How do we precisely control compositional and structural parameters of polymers, for example, sequence, desired chemical functionalities, molecular weight, and its distribution, while the high complexity is attained? Can we produce this elegantly shaped polymer in a large quantity? How are the parameters correlated with the resulting properties, for example, the position of developable unit in the chain vs. the quality of photopattern? Can we expand these challenges to more complex polymeric systems such as crosslinked polymer networks and polymer thin films?

 

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

We all experience failure. No one can become always successful. This should be the case especially for early career scientists including me. I have thought of an inspirational quote that was personally given to me by Prof. Hyuk Yu, Emeritus Professor of Chemistry at University of Wisconsin at Madison, and now I am so happy to share this with other early career polymer scientists: “Life and hope are viscoelastic. Failure should take time to restore, but never yield to or break by it. Bend and recover!!!”. This may be the advice given to us by polymer, our lifelong friend, as well.

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Polymer Chemistry Emerging Investigator- Athina Anastasaki

Athina Anastasaki was born and raised in Athens, Greece and obtained her B.S. in Chemistry at the University of Athens. She then commenced her PhD studies at the University of Warwick under the supervision of Prof. Dave Haddleton and graduated in late 2014 with the Jon Weaver award for the best PhD in polymer chemistry in the UK. In early 2015, she accepted a Monash-Warwick research fellow position between the Pharmaceutical department at Monash University and the University of Warwick, jointly supervised by Prof. Thomas Davis and Prof. Dave Haddleton. She then received an Elings Fellowship, followed by a Global Marie Curie Fellowship, to conduct research alongside Prof. Craig Hawker at the University of California, Santa Barbara. Since January 2019, she is an Assistant Professor at ETH and her group focuses on fundamental polymer synthesis and self-assembly predominantly in the area of controlled radical polymerisation. Athina has co-authored over 100 peer-reviewed publications and has been the recipient of the ERC starting Grant, the Hanwha-Total IUPAC Young Scientist Award, the Polymers Young Investigator Award and the Golden Owl award, which is in recognition of outstanding faculty teaching. Athina also currently serves as an Associate Editor for Polymer Chemistry. More details about Athina’s lab can be found here https://polymeric.mat.ethz.ch/

You can follow Athina on Twitter @AthinaAnastasa1 and her lab group @AnastasakiLab

Read Athina’s Emerging Investigator article, ‘The effect of surface-active statistical copolymers in low-energy miniemulsion and RAFT polymerization’ 

Check out our interview with Athina below:

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

I am very excited about publishing our work in Polymer Chemistry and it has always been a very pleasant experience as, even for the negative decisions, the Editors always treat you with respect and professionalism.

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

What has helped me a lot is asking for support every time I need it without worrying about appearing weak. Finding one (or two) mentors and/or an academic friend makes a huge difference.

 

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Polymer Chemistry Emerging Investigator- Louis Pitet

 

 

Louis M. Pitet is currently an assistant professor at Hasselt University, working in the Institute for Materials Research (IMO), located in Hasselt, Belgium. Louis’ research interests are broadly concerned with understanding processing–structure–property relationships in complex functional polymer constructs. The group has a keen interest in applying the fundamental relationships that are uncovered to global challenges in polymer science, including reutilizing plastic waste streams, creating smart scaffolds for tissue engineering, and improving processing–manufacturing efficiency with advanced reactors. Louis obtained his Bachelor’s degree in Chemistry from the Colorado School of Mines working with Prof. Daniel Knauss. He went on to obtain a PhD in 2011 in the Chemistry department at the University of Minnesota under the supervision of Prof. Marc Hillmyer, exploring the utility of ring-opening metathesis polymerization in creating functional materials. Louis moved to the Netherlands for a post-doctoral fellowship in the Institute for Complex Molecular Systems at the Eindhoven University of Technology, working with Prof. Bert Meijer. In Eindhoven, Louis helped build a program applying dynamic bonding strategies for the construction of well-defined block polymers. Since 2018, Louis has been leading his research group in Hasselt working with a diverse team currently consisting of 6 PhD students and 1 post-doctoral researcher. More details about the group and research topics can be found at www.uhasselt.be/en/onderzoeksgroepen-en/imo-imomec-afp/people/prof-dr-louis-pitet

You can follow Louis Pitet on Twitter @PitetGroup

Read Louis’s Emerging Investigator article ‘Fully biobased triblock copolymers generated using an unconventional oscillatory plug flow reactor’

Check out our interview with Louis below:

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

I think Polymer Chemistry is a premier journal, well-respected by everyone involved in polymer research. Polymer Chemistry consistently publishes works at the forefront of polymer science, across its diverse range of related topics, and is one of the only journals I routinely browse. The interactions with the editorial board during submission and publication have always been among the best in the publishing world. The speed and professionalism with which our manuscripts are handled is unique and refreshing.

 

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

Polymer scientists currently face a grand challenge to adapt to a global plastic-pollution crisis, with far-reaching implications related to the health of our planet and its diverse communities. Our research is helping to advance polymer materials themselves, and transform the way we make polymers to address these challenges head-on. We do this primarily by developing innovative synthetic technology. This is tremendously challenging, considering the vast diversity of topics and expertise that are involved in polymer science – from synthesis to molecular and physical characterization to processing and reactor design. However, this is also an amazing opportunity to collaborate with an inspiring community of experts across the globe – this is one of the most rewarding parts of the job.

 

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

Try to find a topic that is not only high impact, but will also hold your interest for a long time. Also, finding activities that energize you outside the lab/office has been invaluable for me in maintaining efficiency and staying engaged with both colleagues and students.

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Polymer Chemistry Emerging Investigator- Junpeng Zhao

Junpeng Zhao received his B.S. (2005) and Ph.D. (2010) from University of Science and Technology of China under the supervision of Prof. Guangzhao Zhang. From 2007 to 2009, he undertook a joint Ph.D. appointment, supported by China Scholarship Council, in National Hellenic Research Foundation (Greece) under the supervision of Prof. Stergios Pispas. Afterwards, he was a postdoctoral researcher first at Max-Planck Institute of Colloids and Interfaces (Germany) with Prof. Helmut Schlaad and Prof. Markus Antonietti (2011-2012), and then at King Abdullah University of Science and Technology (Saudi Arabia) with Prof. Nikos Hadjichristidis (2012-2014). In early 2015, he joined South China University of Technology and began his professorship. His main research interest is synthetic polymer chemistry, with special focus on anionic polymerization, organocatalytic/metal-free polymerization, and synthesis of polymers from renewable resources. He has been the coauthor of 70 peer-reviewed papers and 15 patents, and the (co)supervisor of 25 master/Ph.D. students.

 

Read Junpeng Zhao’s Emerging Investigator’s article, ‘ Selective ring-opening polymerization of glycidyl esters: a versatile synthetic platform for glycerol-based (co)polyethers

Read our interview with Junpeng below.

 

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

Submitting my work to Polymer Chemistry ensures a pleasant reviewing process as well as timely publication.

 

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

What I am most excited about at the moment is the strict but readily tunable chemoselectivity of two-component organocatalysts which enables precise and convenient synthesis of an increasingly large variety of functional and/or complex polymers. What I have found most challenging is understanding polymerization mechanism, without disproving it soon after.

 

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

How can we avoid major side effects when trying to make the world a better place using synthetic polymers? What can we learn from nature about designing and tailoring polymer structures and functions?

 

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

New successes may hide in experiments which seem to have failed at first glance.

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