Polymer Chemistry issue 9 is now online!

front cover image for Polymer Chemistry, Issue 9, 2011

Polymer Chemistry issue 9 is now online.

The article highlighted on the front cover is Modular design for the controlled production of polymeric nanotubes from polymer/peptide conjugates by Robert Chapman, Katrina A. Jolliffe and Sébastien Perrier. The paper describes the preparation of nanotubes via the self assembly of well defined peptide polymer conjugates, synthesised using CuAAC chemistry.

Issue 9 contains 4 reviews:

To keep up-to-date with all the latest research, sign up for the journal’s e-alerts or RSS feeds or follow Polymer Chemistry on Twitter or Facebook.

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

Fluorescent dendrimers for the detection of explosives

Dendrimers capable of detecting TNT have been developed and tested by scientists in Australia. 

TNT and other nitroaromatic explosives are used in landmines. Current detectors for TNT are bulky and unsuitable for use in the field. Now Paul Burn, Paul Meredith and colleagues the University of Queensland have developed dendrimers that can sense nitroaromatic explosives. Burn and the team tested the performance of three generations of fluorescent carbazole dendrimers, in solution and in thin films, to identify differences in the binding between different explosives. This technology could help create portable sensors for detecting nitroaromatic explosives.

 Graphical abstract: Fluorescent carbazole dendrimers for the detection of explosives

Read the full article here (free registration required): G Tang, S S Y Chen, P E Shaw, K Hegedus, X Wang, P L Burn and P Meredith, Polym. Chem., 2011, DOI: 10.1039/c1py00222h

To keep up-to-date with all the latest research, sign up for the journal’s e-alerts or RSS feeds or follow Polymer Chemistry on Twitter or Facebook.

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

Polymer Chemistry Author of the Week-Marc Hillmyer

Marc Hillmyer received his B.S. in Chemistry from the University of Florida in 1989 and his Ph.D. in Chemistry from the California Institute of Technology in 1994. After completing a postdoctoral research position in the University of Minnesota’s Department of Chemical Engineering and Materials Science he joined the Chemistry faculty at Minnesota in 1997. He is currently a Distinguished McKnight University Professor of chemistry and leads a research group focused on the synthesis and self-assembly of multifunctional polymers. In addition to his teaching and research responsibilities, Marc also serves as an Associate Editor for the ACS journal Macromolecules and is the director of the Center for Sustainable Polymers at the University of Minnesota.

Please follow the link for further information on Marc Hillmyer’s research group and his recent paper in Polymer Chemistry.

What was your inspiration in becoming a chemist?

Since I’ve been young, I have always been attracted to math and science in school. I really enjoyed lab work in high school and trying to understanding how things worked. The turning point for me with respect to choosing the chemistry path was as a freshman in college. My first chemistry professor was an inspirational lecturer and really sparked my interest in pursing chemistry as a career.

What was the motivation behind the research in your recent Polymer Chemistry paper? (DOI: 10.1039/c1py00147g)

We had some success in related isomerization work with seed oils and were curious about application of the same catalytic isomerization chemistry applied to unsaturated polymers. Simple catalytic conversions of renewable polymers can be a powerful approach to new sustainable materials development, and we saw how the conjugation approach using polyisoprene could have some utility. The work was also motivated by recent research in the group on how to toughen polylactide using graft copolymers. Functionalized polyisoprene enabled the preparation of a new set of materials that we hoped had similar (or even better!) properties.

Why did you choose Polymer Chemistry to publish your work?

I am a strong proponent of society journals and feel that Polymer Chemistry is rapidly emerging as an important venue for advances in synthetic polymer chemistry.

In which upcoming conferences may our readers meet you?

I will be at the IUPAC 2011 World Chemistry Congress in San Juan, Puerto Rico this July/August.

How do you spend your spare time?

I do my best to spend most of my spare time with my family. Playing guitar, running, and golf take up the rest!

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

I would be a (paid) musician.

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

Announcing the 33rd Australasian Polymer Symposium

The 33rd Australasian Polymer Symposium (33APS) will be held from 12th to 15th February 2012 at Wrest Point Convention Centre in Hobart, Tasmania.  An exciting program will cover all areas of polymer science and engineering, including synthesis, characterisation, processing, modeling and materials.  Topics will range from the latest techniques in polymer synthesis to applications in materials science, medicine, energy and environment. 

Registrations are now open and abstract submissions are being excepted until 2 September 2011. Visit www.33aps.org.au for more information.

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

Top Ten most-read Polymer Chemistry articles in June

Read the most-read Journal of Materials Chemistry articles of June 2011, listed below:

Diels–Alder “click” reactions: recent applications in polymer and material science
Mehmet Atilla Tasdelen
Polym. Chem., 2011, Advance Article, DOI: 10.1039/C1PY00041A

Thiol-ene “click” reactions and recent applications in polymer and materials synthesis        
Andrew B. Lowe
Polym. Chem., 2010, 1, 17-36

Controlled polymerizations for the synthesis of semiconducting conjugated polymers 
Ken Okamoto and Christine K. Luscombe
Polym. Chem., 2011, Advance Article, DOI: 10.1039/C1PY00171J        

Multiresponsive polymers: nano-sized assemblies, stimuli-sensitive gels and smart surfaces
George Pasparakis and Maria Vamvakaki
Polym. Chem., 2011, 2, 1234-1248

Polymer bioconjugates           
Jan van Hest and Brent Sumerlin
Polym. Chem., 2011, 2, 1427-142

Synthesis and characterization of well-defined thermo- and light-responsive diblock copolymers by atom transfer radical polymerization and click chemistry      
Xiangdong Tao, Zhengguo Gao, Toshifumi Satoh, Yuan Cui, Toyoji Kakuchi and Qian Duan
Polym. Chem., 2011, Advance Article, DOI: 10.1039/C1PY00165E7

Recognition of polymer side chains by cyclodextrins 
Akihito Hashidzume and Akira Harada
Polym. Chem., 2011, Advance Article, DOI: 10.1039/C1PY00162K

Facile, modular transformations of RAFT block copolymers via sequential isocyanate and thiol-ene reactions      
Joel D. Flores, Nicolas J. Treat, Adam W. York and Charles L. McCormick
Polym. Chem., 2011, Advance Article, DOI: 10.1039/C1PY00182E

Synthesis of thermo-responsive glycopolymers via copper catalysed azide?alkyne ?click? chemistry for inhibition of ricin: the effect of spacer between polymer backbone and galactose           
Jatin Kumar, Lyndal McDowall, Gaojian Chen and Martina H. Stenzel
Polym. Chem., 2011, 2, 1879-1886

Construction and application of pH-triggered cleavable hyperbranched polyacylhydrazone for drug delivery  
Lijuan Zhu, Chunlai Tu, Bangshang Zhu, Yue Su, Yan Pang, Deyue Yan, Jieli Wu and Xinyuan Zhu
Polym. Chem., 2011, 2, 1761-1768

To keep up-to-date with all the latest research, sign up for the journal’s e-alerts or RSS feeds or follow Polymer Chemistry on Twitter or Facebook.

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

Polymer Chemistry Author of the Week-Richard Hoogenboom

Richard Hoogenboom was born in 1978 in Rotterdam (Netherlands) and studied chemical engineering at the Eindhoven University of Technology (TU/e; Netherlands). In 2005, he obtained his PhD under the supervision of Ulrich S. Schubert (TU/e) and continued working as project leader for the Dutch Polymer Institute. The final two years of this appointment were combined with a part-time position as senior product developer at Dophys Medical BV. After postdoctoral training with Martin Möller at the RWTH Aachen (Humboldt fellowship; 2008-2009) and Roeland J. M. Nolte at the Radboud University Nijmegen (NWO veni-grant; 2009-2010), he was appointed as associate professor at Ghent University mid 2010 where he currently heads a research group on Supramolecular Chemistry. His research interests include stimuli-responsive polymers, supramolecular polymers, and poly(2-oxazoline)s.

Please follow the link for further information on Richard’s research group and his recent paper in Polymer Chemistry.

What was your inspiration in becoming a chemist?

My decision to study chemical engineering was a trade off between my love for maths, physics and chemistry at high school. In the end I choose a study that combined all these topics. During my studies I was greatly attracted by organic chemistry inspired by the courses given by Bert Meijer and, despite being at a technical university, I ended up graduating in organic and polymer chemistry.

 

What was the motivation behind the research in your recent Polymer Chemistry paper?

The Polymer Chemistry paper reports cloud point tuning of biocompatible poly(2-oxazoline)s by attaching glucose substituents to the side chains via thiol-ene addition. This work was motivated by my interest in developing novel methods for the synthesis of functional poly(2-oxazoline)s as well as my interest in adaptive materials. In addition, the resulting glycopolymers are attractive biomaterials for interaction with sugar-binding proteins, namely lectins. The beauty of this work lies in the unexpected lowering of the water-solubility of the copolymers upon incorporation of hydrophilic sugar moieties. This once more shows how little we actually understand about adaptive materials that are not only governed by hydrophilicity, but also by non-covalent interactions, such as hydrogen bonding in this work.

 

Why did you choose Polymer Chemistry to publish your work?

Despite being a very young journal, in my opinion Polymer Chemistry has already evolved into a well-established polymer journal that is well-recognized by the community. Therefore, publishing our work in Polymer Chemistry ensures wide exposure of our work. In addition, publication in Polymer Chemistry is accompanied by a fast and smooth evaluation and publication process.

 

In which upcoming conferences may our readers meet you?

In September I will attend the APME 2011 (IUPAC 9th International Conference on Advanced Polymers via Macromolecular Engineering) in Cappadocia, Turkey.

At the 2012 ACS Spring Meeting in San Diego, CA, I will organize a symposium on ‘Poly(2-oxazoline)s and related pseudo-polypeptide structures’ together with Helmut Schlaad and Scott Grayson, where our just published work on glyco-poly(2-oxazoline)s also will be presented.

 

How do you spend your spare times?

My spare time is mostly spent with my family. It is great to play with my kids of 1 and 3 years and to see how they discover the world around them. To stay a bit in shape after too much time spend behind a computer in the office, you will find me at least one time a week on the tennis court.

 

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

This is a very difficult one. I guess I would still be a scientist, but in a different discipline.

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

Polymer Chemistry Author of the Week-Yasuyuki Tezuka

Yasuyuki Tezuka is Professor of Tokyo Institute of Technology.  He is a graduate of The University of Tokyo, and received his doctorate degree from Ghent University (Belgium) in 1982.  He then joined Nagaoka University of Technology (Japan) as an assistant professor.  In 1994, he moved to the Tokyo Institute of Technology, and has been a professor since 2003 in the Department of Organic and Polymeric Materials.  He received Tokyo Tech Award of Best Teacher, 2004, and The Award of the Society of Polymer Science, Japan (2010).  He has served as an Asian Editor of Reactive and Functional Polymers since 2006.  His current research is focused on topological polymer chemistry, in particular on the design of topologically unique macromolecular architectures, and of novel polymer materials by their topology effects.

Please follow the link to get more information of Yasuyuki’s research group and his recent paper in Polymer Chemistry.


What attracted you to follow a life-course to become a chemist?

Almost 30 years ago in 1979, I left Tokyo to join in a lab in a Belgian university as a doctorate student.  That time was still good-old-days for university research in Europe.  I was fascinated by and decided to pursue academic course.  Therefore, I was not smart enough to anticipate a rapid change of university researches into a hungry-business.  I feel now, however, that I was lucky to go with chemistry, in particular synthetic polymer chemistry, offering excitement to create something so small and invisible but convincingly proved and eventually testable in macroscopically.  I am also thankful for my respectful mentors to encourage me to follow chemistry as a life-long amusing business.  Thus, I gratefully acknowledge Professors, Teiji Tsuruta, Shohei Inoue and Eric Goethals.

What was the motivation behind the research in your recent Polymer Chemistry paper? (DOI: 10.1039/C1PY00088H)

A class of macromolecular constructions having single-cyclic (ring) or multi-cyclic polymer units has been a synthetic challenge, though they are regarded geometrically primitive due to their small junction and terminus numbers.  For more than a decade we have been fascinated and involved in a project to make them smartly despite their immediate applications unforeseeable.  In our review in Polymer Chemistry, we have shown recent synthetic breakthroughs and I am happy to include our own, namely an electrostatic self-assembly and covalent conversion (ESA-CF) process among such developments.  Topological Polymer Chemistry has now provided innovative opportunities, not only to bring new insights in the frontier of basic polymer chemistry and physics, but also to disclose unusual properties and functions based on their cyclic topologies, i.e., topology effects, unattainable either by linear or branched counterparts.

Why did you choose Polymer Chemistry to publish your work?

I am thankful to Prof. Barner-Kowollik, an editorial board member of the journal to offer us a valuable opportunity to summarize recent achievements in Topological Polymer Chemistry.  Also, I am impressed by a variety of competitive measures continuously introduced by the journal, through which this relatively young journal has promoted quickly into the leading position.

In which upcoming opportunities may our readers meet you or catch up your work ?

We are still experiencing prolonging aftermath of rare disasters caused not only by natural but also by human origins.  We are now rebuilding ourselves quickly back to normal university life, to welcome overseas colleagues for scientific visits to us in Tokyo.  Meanwhile, I am now working to edit a book, which hopefully becomes a follow-up of a seminal work of the late Dr. Semlyen (Cyclic Polymers, 2nd Ed).  The title of the Book will be; Topological Polymer Chemistry / The progress in cyclic polymers: Synthesis, Properties and Functions.

How do you spend your spare times?

Taking care of, and hoping to better communicate with B – -, a selfish cat at home, with only occasional success.

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

A teenager, at the student-riot period of 1960-70s in Japan, was likely a follower of such now-passed stars like, Shuji Terayama (an avant-garde artist, as well as a haiku- and tanka-poet writer), Yasujiro Odzu (movie director) in addition to Che Guevara, Leon Trotsky, – –

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

Polymer Chemistry Author of the Week – Milan Maric

Milan Maric studied Chemistry (B.Sc.) and Chemical Engineering and Management (B.Eng.&Mgmt.) at McMaster University in Hamilton, Ontario, Canada. He then pursued graduate studies working with Chris Macosko at the University of Minnesota-Twin-Cities in the area of compatibilization of thermoplastic/silicone blends, earning his Ph.D. in 1999. He then worked in the Scale-up Engineering Group at the Xerox Research Centre of Canada (XRCC) from 1999-2003 and subsequently joined McGill University in 2003 as an Assistant Professor in the Department of Chemical Engineering. In 2009, he was promoted to Associate Professor. Maric’s research group principally focuses on the application of nitroxide mediated polymerization to develop functional materials for a wide range of applications such as block copolymer surfactants, membrane/barrier materials, conductive copolymers and stimuli-responsive polymers.

Please follow the link for further information on Milan Maric’s research group and his recent paper in Polymer Chemistry.

What was your inspiration in becoming a chemist?

I thank my high school teachers and the professors at my undergraduate university for providing me with the stimulus. I liked the ability to creatively transform materials and to do it in a methodical and disciplined manner.

What was the motivation behind the research in your recent Polymer Chemistry paper? (DOI: 10.1039/C1PY00190F)

The main thrust of my research group is to use nitroxide mediated polymerization (NMP) for functional materials. Specifically, we have been trying to show that NMP can be used for a wider range of monomers than has been traditionally associated with NMP, such as methacrylates. In this particular case, we have been trying to make epoxy functional block copolymers with glycidyl methacrylate and our paper describes how we can do that with the BlocBuilder family of nitroxides.

Why did you choose Polymer Chemistry to publish your work?

Polymer Chemistry, since its inception, has provided an excellent forum to disseminate the latest developments in polymer synthesis techniques. We thought the results of our work were aligned well with the aims of the journal and we felt it would be an interesting venue to communicate our work with our peers.

In which upcoming conferences may our readers meet you?

I will be at the ACS fall meeting in Denver at the end of August and after that, I will attend the CSChE meeting in London, Ontario in October.

How do you spend your spare time?

I try to keep active with athletics and I am trying to stay in shape by weight training and swimming.

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

Growing up in Canada, I dreamed of being an ice hockey player, naturally, although soccer was the only sport I was allowed to put school in a subordinate position. More realistically, I think I would still be involved in teaching in some kind of capacity.

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

Hot Article: Block copolymer conjugates prepared by sequentially grafting from proteins via RAFT

Scientists at Southern Methodist University, USA, have shown that retaining the active end group functionality during grafting-from RAFT polymerizations from model proteins can give thermoresponsive diblock copolymer–protein conjugates. The team behind the research claim that the reduced steric limitations of this method could help create a wide variety of block copolymer bioconjugates with high molecular weight synthetic components.

Graphical abstract: Block copolymer conjugates prepared by sequentially grafting from proteins via RAFT

Interested to know more? Why not read the full paper: Hongmei Li, Ming Li, Xiao Yu, Abhijeet P. Bapat and Brent S. Sumerlin, Polym. Chem., 2011, 2, 1531-1535

To keep up-to-date with all the latest research, sign up for the journal’s e-alerts or RSS feeds or follow Polymer Chemistry on Twitter or Facebook.

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)

Hot Article: Multi-functionalization of helical block copoly(alpha-peptide)s by orthogonal chemistry

A method for preparing block copolypeptides with side-chain groups capable of orthogonal functionalisation via “click” chemistry has been developed by polymer chemists at Louisiana State University, USA. All the block copoly(α-peptide)s adopt α-helical conformations both in solid state and in solution. The team say that this methodology provides a convenient and modular approach towards helical block copoly(α-peptides) with diverse structures by side-chain conjugation, allowing control over polymer bioactivity, solubility and self-assembly properties.

Graphical abstract: Multi-functionalization of helical block copoly(α-peptide)s by orthogonal chemistry

Read the full paper: Haoyu Tang and Donghui Zhang, Polym. Chem., 2011, 2, 1542-1551

 

To keep up-to-date with all the latest research, sign up for the journal’s e-alerts or RSS feeds or follow Polymer Chemistry on Twitter or Facebook.

Digg This
Reddit This
Stumble Now!
Share on Facebook
Bookmark this on Delicious
Share on LinkedIn
Bookmark this on Technorati
Post on Twitter
Google Buzz (aka. Google Reader)