Author of the Week: Prof. Per Zetterlund

Prof. Per Zetterlund was born in Karlskoga, Sweden, in 1968. He graduated from The Royal Institute of Technology in Stockholm (Sweden) in 1994 with an M.Sc. in Chemical Engineering, and obtained his Ph.D. in the School of Chemistry at Leeds University (UK) in 1998 with Prof. A. F. Johnson in radical crosslinking polymerizations.  He carried out postdoctoral research at Griffith University (Brisbane) with A/Prof. W. K. Busfield and Prof. I. D. Jenkins in nitroxide-mediated polymerization (NMP) and the use of nitroxides as radical traps.  In 1999, he became Assistant Professor at Osaka City University (Japan) in the group of Prof. B. Yamada, and worked on kinetics/mechanism of high conversion radical polymerization, synthesis/polymerization of macromonomers, and NMP.  In 2003, he moved to Kobe University (Japan) and joined the team of Prof. M. Okubo, where he was promoted to Associate Prof in 2005.  Since 2009, he is working as Associate Prof at The Centre for Advanced Macromolecular Design (CAMD) at The University of New South Wales (Sydney, Australia).

Current research focuses on controlled/living radical polymerization (CLRP) in aqueous and carbon dioxide based dispersed systems for synthesis of well-defined polymer and nanoparticles.  Particular attention is given to how CLRP is influenced by compartmentalization (nanoreactors), and how this can be exploited to improve control/livingness.

He has published 116 peer-reviewed papers and 2 book chapters, and is a member of the IUPAC Macromolecular Division (IV) Subcommittee on Modeling of Polymerization Kinetics and Processes, The International Polymer and Colloid Group, The American Chemical Society, The Society of Polymer Science, Japan, as well as RACI.

http://www.camd.unsw.edu.au/index.php?option=com_content&view=article&id=128&Itemid=58

What was your inspiration in becoming a chemist?

I always enjoyed science (being able to explain and understand stuff) when I was at school, and I really liked my chemistry teacher in high school (thank you Mr Kerr!).

What was the motivation to write your Polymer Chemistry article (DOI: 10.1039/C2PY20434G)?

There is extensive literature on the use of microwave irradiation in polymer synthesis, but it remains to be clarified with confidence what exact effect(s), if any, the microwave irradiation has on radical polymerization.  The term “microwave-assisted” polymerization is frequently used, but it is not clear exactly what this means.  We carried out a number of polymerizations under microwave irradiation under different conditions, trying to clarify the situation in the case of the monomer styrene.

Why did you choose Polymer Chemistry to publish your work?

Despite Polymer Chemistry being a new journal, it has already established itself as one of the major journals in the polymer chemistry field with an impressive impact factor – we therefore thought it would be a great way to gain exposure for our work.

In which upcoming conferences may our readers meet you?

In Kobe, Japan, at The 9th SPSJ International Polymer Conference, Dec 11-14 (http://www.spsj.or.jp/IPC2012.html), and at the Australasian Polymer Symposium in Darwin (Australia) 7-10 July next year (http://www.34aps.org.au/2013/), and also at the International Polymer Colloids Group Conference in Shanghai, China, in June 2013.

How do you spend your spare times?

With my family (wife and 8 year old son), playing tennis, jogging, listening to Kiss and playing the drums.

Which profession would you choose if you were not a scientist?

Not that it is very realistic, but I think I would like to try being a professional drummer in a heavy rock band.

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Paper of the week: Highly stable polymeric vesicles prepared by a simple coating method

Graphical abstract: Well-defined polymeric vesicles with high stability and modulation of cell uptake by a simple coating protocol

Amphiphilic polymers have been synthesised by controlled free radical polymerisation techniques. These polymers self-assemble into well-defined vesicles in aqueous conditions, enabling encapsulation of a model hydrophilic molecule. The polymeric vesicles show high stability against a range of aqueous conditions with marginal release of cargo, even in the presence of known cell-membrane disruptive polymers such as branched poly(ethylene imine) (b-PEI). This stability allows for inversion of the surface charge of the polymeric vesicles by a simple coating protocol leading to an enhanced uptake by mammalian cells.

Well-defined polymeric vesicles with high stability and modulation of cell uptake by a simple coating protocol Gökçen Yaşayan, Martin Redhead, Johannes P. Magnusson, Sebastian G. Spain, Stephanie Allen, Martyn Davies, Cameron Alexander and Francisco Fernández-Trillo Polym. Chem., 2012, 3, 2596-2604.

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Author of the Week: Prof. Yu-Zhong Wang

Prof. Yu-Zhong Wang received his PhD degree from the Sichuan University in 1994. He joined Sichuan University in 1994, and was promoted to professor in 1995. He was a visiting professor of Max-Planck Institute for Polymer Research with the support of DAAD in 1999, and in the University of Nottingham (UK) in 2002 with the support of the Royal Society, respectively. He was awarded the National Science Fund for Distinguished Young Scholars, Cheung Kong Scholar of Ministry of Education of China, Younger Prize of Guanghua Engineering Science and Technology of Chinese Engineering Academy, Excellent Postgraduate’s Advisor of Sichuan Province, Outstanding Younger Innovation Prize of Sichuan Province and over 10 governmental Science & Technology Awards such as National Technology Invention Prize, National Science and Technology Progress Prize, etc. He has published more that 300 peer reviewed research papers and 73 patents. His current research interests are the Bio-Based and Biodegradable Polymeric Materials, Halogen-Free Flame-Retardant Polymeric Materials, etc.

web site: http://chem.scu.edu.cn/polymer/yzwang/index_e.htm

What was your inspiration in becoming a chemist?

Chemistry is “the central science”. When I was young, I though that Chemistry was very magical, and could produce countless new substances, so I began to like Chemistry. In the national university entrance exam, my Chemistry test scores were almost full marks, only losing 1 point. From then on, I began my chemical career, especially the research of polymer materials.

What was the motivation to write your Polymer Chemistry article? (DOI:10.1039/C2PY20331F)

One of the most interesting phenomena in the miscible crystalline/crystalline systems is the formation of interpenetrating spherulites (IPS), where a spherulite of one component continues growing inside that of the other component when they are crystallized from a homogeneous melt. Interestingly, when we researched a novel polymer blend of branched PLA-PPDO copolymer and linear PPDO homopolymer, interpenetrating spherulites morphology was observed. Since the PLA and PPDO blocks are immiscible in the blends, understanding the special IPS crystallization mechanism, which was generally considered occurring only in those miscible polymer blends, will be of particular important and valuable.

Why did you choose Polymer Chemistry to publish your work?

Polymer Chemistry is an excellent new journal in polymer science. Moreover, the review and publishing process of this journal is very fair and fast.

In which upcoming conferences may our readers meet you?

2012 BioEnvironmental Polymer Society (BEPS) Annual Meeting, September 18th-21st in Denton, Texas, USA.

I am organizing an international conference entitled “The 2nd International Symposium on Flame-Retardant Materials & Technologies” (ISFRMT 2012), which will be held in Chengdu, China on September 17-20, 2012. Website: http://www.isfrmt.org/

How do you spend your spare times?

I like to watch TV programs and access internet for news.

Which profession would you choose if you were not a scientist?

I would be a navigator.

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Paper of the week: Nanoassemblies of surfactant-like peptide-amphiphiles

Graphical abstract: Controlled peptide coated nanostructures via the self-assembly of functional peptide building blocks

Molecular self-assembly mediated by noncovalent interactions, such as hydrogen bonding, hydrophobic and p-stacking interactions, provides important guidance for the construction of a new generation of biomaterials with various functions. Arising from the abundant examples of protein self-assembly existing in nature, peptide-based building blocks with the unique properties of good biocompatibility, chemical versatility and biological recognition abilities have been widely used to prepare a variety of functional biomaterials. In this paper, Zhang and co-workers designed and prepared a functional peptide sequence with membrane penetrating (eight continuous arginine residues) and tumor-targeting functions (GRGDS). Self-assembled GRGDS-based micelles loaded with the anti-tumor drug DOX and incubated with HeLa and COS-7 cells demonstrated tumor-targeting and membrane-penetrating abilities and delivered the drug into HeLa cells. The strategy reported in this study presents potential for the construction of biocompatible peptide-based biomaterials with favorable bioactivity.

Controlled peptide coated nanostructures via the self-assembly of functional peptide building blocks by Xiao-Ding Xu , Jing-Xiao Chen , Han Cheng , Xian-Zheng Zhang and Ren-Xi Zhuo Polym. Chem20123, 2479-2486.

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Author of the Week: Prof. Zesheng An

Zesheng An obtained his BS and MS degrees from Shandong University in 1997 and 2000, respectively. He then went to the University of Arizona to pursue his PhD degree and spent three years there from 2000 to 2003. After moving to Georgia Institute of Technology and spending two years from 2003 to 2005, he got his PhD in Chemistry with Prof. Seth R. Marder. His PhD thesis was focused on the synthesis and characterization of organic semiconductors, especially discotic liquid crystals with high charge-carrier mobility, for applications in optoelectronics. From 2005 to 2008, he was a postdoc at the University of California, Santa Barbara with Prof. Galen D. Stucky and Prof. Craig J. Hawker, working on the synthesis of polymer nanoparticles. In 2008, he joined the Institute of Nanochemistry and Nanobiology, Shanghai University, where he is now a Professor of Special Appointment (Eastern Scholar) at Shanghai Institutions of Higher Learning. His current research is focused on RAFT heterogeneous polymerization in water, which in turn serves as a platform for designing interesting materials such as nanogels and core cross-linked star polymers. Applications of these materials in emulsion and biotechnology are being investigated within the group and through collaboration with other groups within the Institute.

What was your inspiration in becoming a chemist?

I have to confess that I was very much interested and did pretty well in chemistry in high school, it was however not until I met Prof. Marder at the University of Arizona that I decided to make a career out of it. Indeed, Prof. Marder was and has always been a successful career model for me.

What was the motivation to write your Polymer Chemistry article? (DOI:10.1039/C2PY20442H)

RAFT polymerization has become mature and has been widely used in the synthesis of well-defined polymers. Over the past several years, RAFT polymerization in heterogeneous polymerization media, especially in water, has witnessed significant development, which often combines polymerization and self-assembly of the produced polymers in the same system. This polymerization-induced self-assembly process has been used for the synthesis of colloids of various morphologies such as spheres, fibers and vesicles. Significantly, not only the synthesized polymers are controlled by RAFT, but also can the nano-objects of various morphologies be synthesized at high solid content (>10%). We have exploited such polymerization-induced self-assembly process to synthesize core cross-linked star (CCS) polymers via both RAFT emulsion and dispersion polymerization (Chem. Commun. 2011, 47, 12685-12687; 2012, 48, 7389-7391). This robust strategy features high concentration, high efficiency, high star yield and high star quality. In the current work, we directly polymerized polyPEGMA in aqueous solution up to complete monomer conversion and used it as the arm without separation/purification to synthesize CCS in RAFT heterogeneous polymerization in water. We also investigated the effect of various parameters on the formation of CCS.

Why did you choose Polymer Chemistry to publish your work?

Number one, Polymer Chemistry publishes high quality papers in my research area, so it is a nice place to publish my own work. Number two, through the submission experience of my previous paper published in Polymer Chemistry, I highly appreciate the way that the editors handle the review process, being highly efficient and with great fairness. Number three, Polymer Chemistry is becoming one of the leading journals in polymer science, so it is exciting to publish papers in such an excellent journal.

In which upcoming conferences may our readers meet you?

Well, I do not have plans to attend any conference at the moment. I guess I will attend more conferences in the following years.

How do you spend your spare times?

I used to play soccer but quit after an injury of my tibia. Now, I am trying to spend more time with my family, making dinner, playing Go with my daughter, walking my dog…

Which profession would you choose if you were not a scientist?

Aha, I have not realized anything that I could do better than making polymers. If I were not a scientist, I guess I might end up as a journalist.

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Paper of the week: Carbon nanotube-incorporated polymer hydrogels

Graphical abstract: Synthesis of single-walled carbon nanotube-incorporated polymer hydrogels via click chemistry

Electrically conductive hydrogels are soft, polymeric networks that combine hydrogels’ unique properties with electroactive polymers’ inherent conductivity. With this in mind, Changsik Song and co-workers reported the design of single-walled carbon nanotubes (SWNTs) incorporated into polyvinyl alcohol (PVA) hydrogels by Cu-catalyzed azide–alkyne cycloaddition reaction. This efficient and modular reaction allowed the production of hydrogels with cross-linker molecules of various properties such as hydrophilic or hydrophobic character. Control of cross-linking density and molecular transport inside the click hydrogels was demonstrated by measuring degrees of swelling and the electrochemical diffusion coefficient of an ionic solute. In addition, incorporation of single-walled carbon nanotubes into the click hydrogels aided the growth of poly(3,4-ethylenedioxythiophene), presumably due to their enhancement of electrical conductivity. SWNT-incorporated PVA hydrogels synthesized by click chemistry may be of great interest for use as electrically conductive hydrogels in biomedical applications.

Synthesis of single-walled carbon nanotube-incorporated polymer hydrogels via click chemistry by Rebecca Eunji Lee, Jiyoung Park, Sung Gap Im and Changsik Song Polym. Chem20123, 2451-2455.

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Paper of the week: Degradable copolymers by ring-opening and reverse addition–fragmentation chain transfer polymerization

Graphical abstract: Degradable graft copolymers by ring-opening and reverse addition–fragmentation chain transfer polymerization

Polymers with a diverse range of properties and applications can be prepared by tailoring polymer topology and composition. Among these polymer architectures, the preparation of graft copolymers has been intensely investigated. In this context, researchers at Warwick University reported on the synthesis and controlled ring-opening polymerization (ROP) of a six membered cyclic carbonate monomer with pendant reversible addition–fragmentation chain transfer (RAFT) functionality. The growth of fast propagating monomers (methyl acrylate, tetrahydropyran acrylate and N-isopropylacrylamide) from the obtained RAFT-functional poly(carbonate)s resulted in the formation of well-defined graft copolymers with a biodegradable backbone. Importantly, control of solution and thermal properties was achieved through variation of graft length, grafting density and grafting monomer. In addition, the preparation and self-assembly of a PNiPAm graft copolymer provided a convenient route to novel thermoresponsive biodegradable micelles.

Degradable graft copolymers by ring-opening and reverseaddition–fragmentation chain transfer polymerization by Rebecca J. Williams, Rachel K. O’Reilly and Andrew P. Dove Polym. Chem20123, 2156-2164.

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Paper of the week: water-dispersible silver-decorated polymer vesicles and micelles with antibacterial efficacy

Graphical abstract: Preparation of water-dispersible silver-decorated polymer vesicles and micelles with excellent antibacterial efficacy

It is well known that silver nanoparticles have excellent antibacterial activities. However, to prepare well-defined, water-dispersible and long-term stable silver nanoparticles still remains a challenge. Presented in this paper are the design and preparation of new water-dispersible silver-decorated polymer vesicles and micelles based on a new kind of amphiphilic block-statistical copolymer synthesized by ATRP: poly(ethylene oxide)-block-poly(2-(dimethylamino)ethyl methacrylate-stat-t-butyl acrylate) (PEO-b-P(DMA-stat-tBA)) and its partially hydrolyzed derivative, poly(ethylene oxide)-block-poly(2-(dimethylamino)ethyl methacrylate-stat-acrylic acid) (PEO-b-P(DMA-stat-AA)). Poly(DMA) is introduced for the coordination of Ag+ ions to form silver nanoparticles in situ upon reduction, whereas poly(AA) is designed to serve the scaffold for the silver nanoparticle formation in the micelle core by electrostatic interactions with Ag+ ions. Those water-dispersible silver-decorated polymer micelles and vesicles showed excellent antibacterial efficacy against Escherichia coli (E. coli) with quite low minimum inhibitory concentration and minimum bactericidal concentration.

Preparation of water-dispersible silver-decorated polymer vesicles and micelles with excellent antibacterial efficacy by Hang Lu, Lang Fan, Qiuming Liu, Jingren Wei, Tianbin Renand Jianzhong Du Polym. Chem. 2012, 3, 2217-2227.

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1st Polymer Chemistry International Symposium

Join us for a selection of stimulating lectures on synthetic and biological macromolecules, delivered by a collection of internationally recognised researchers and local speakers

1st Polymer Chemistry International Symposium

The 1st Polymer Chemistry International Symposium will take place in China this year. The purpose of RSC journal symposia is to bring together scientists in a stimulating and friendly environment that will foster collaborations between the researchers and the universities involved in the meetings.

The symposium will comprise of three one-day meetings held at three separate institutions. Each one day meeting will feature talks by Polymer Chemistry international speakers from the journal’s Editorial Board, in addition to a collection of local speakers. The symposium is organised by Polymer Chemistry, the Royal Society of Chemistry and the local host organisations. The meetings will take place at Tsinghua University (Beijing), Suzhou University and Fudan University (Shanghai). 

The symposium will appeal to academic and industrial scientists with an interest in all aspects of synthetic and biological macromolecules. Attendance at the symposium is free of charge and student participation is strongly encouraged. 

See list of speakers…

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Paper of the Week: Design of a platform for the preparation of libraries of functional polymer brushes

Graphical abstract: Synthesis and post-polymerization modification of poly(pentafluorophenyl methacrylate) brushes

Post-polymerization modification is a powerful strategy to endow polymers with functional groups that cannot be incorporated via direct polymerization. In this paper, Klok and co-workers explored the reversible addition–fragmentation chain transfer polymerization (RAFT) of pentafluorophenyl methacrylate (PFMA) to prepare active ester containing polymer brushes and investigated the feasibility and versatility of these reactive thin polymer films towards post-polymerization modification with a variety of amines. Except for the secondary amine diisopropylamine, the sterically demanding aminomethylanthracene and aniline, post-polymerization modification with all other investigated amines proceeded with near to quantitative conversion within 2–20 hours. The high reactivity towards a broad range of amines, combined with a good hydrolytic stability and solubility/swellability in a range of organic solvents makes the PPFMA brushes a very attractive platform for the rapid synthesis of diverse libraries of functional polymer brushes via post-polymerization modification.

Synthesis and post-polymerization modification of poly(pentafluorophenyl methacrylate) brushes by Kemal Arda Günay, Nicolas Schüwer and Harm-Anton Klok Polym. Chem. 20123, 2186-2192.

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