To keep up-to-date with all the latest research, sign up for the journal’s e-alerts or RSS feeds or follow Polymer Chemistryon Twitter or Facebook.
To keep up-to-date with all the latest research, sign up for the journal’s e-alerts or RSS feeds or follow Polymer Chemistryon Twitter or Facebook.
Join us for a selection of stimulating lectures on synthetic and biological macromolecules, delivered by a collection of internationally recognised researchers and local speakers
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.
Synthesis and post-polymerization modification of poly(pentafluorophenyl methacrylate) brushes by Kemal Arda Günay, Nicolas Schüwer and Harm-Anton Klok Polym. Chem. 2012, 3, 2186-2192.
To keep up-to-date with all the latest research, sign up for the journal’s e-alerts or RSS feeds or follow Polymer Chemistryon Twitter or Facebook.
This month sees the following articles in Polymer Chemistry that are in the top ten most accessed for June:
Thiol-ene “click” reactions and recent applications in polymer and materials synthesis
Prof. Andrew Brian Lowe
Polym. Chem., 2010, 1, 17-36
DOI: 10.1039/B9PY00216B
New methods of polymer synthesis
Christopher Barner-Kowollik, Jean-François Lutz and Sébastien Perrier
Polym. Chem., 2012, 3, 1677-1679
DOI: 10.1039/C2PY90007F
2-(2,3,4,5,6-Pentafluorophenyl)-1H-benzo[d]imidazole, a fluorine-rich building block for the preparation of conjugated polymer donors for organic solar cell applications
Marios Neophytou, Heraklidia A. Ioannidou, Theodosia A. Ioannou, Christos L. Chochos, Solon P. Economopoulos, Panayiotis A. Koutentis, Grigorios Itskos and Stelios A. Choulis
Polym. Chem., 2012, 3, 2236-2243
DOI: 10.1039/C2PY20198D
Supramolecular three-armed star polymers via cyclodextrin host–guest self-assembly
Bernhard V. K. J. Schmidt, Tobias Rudolph, Martin Hetzer, Helmut Ritter, Felix H. Schacher and Christopher Barner-Kowollik
Polym. Chem., 2012, Advance Article
DOI: 10.1039/C2PY20293J
UCST-driven self-assembly and crosslinking of diblock copolymer micelles
Peter J. Roth, Thomas P. Davis and Andrew B. Lowe
Polym. Chem., 2012, 3, 2228-2235
DOI: 10.1039/C2PY20204B
Three new conjugated polymers based on benzo[2,1-b:3,4-b′]dithiophene: synthesis, characterization, photoinduced charge transfer and theoretical calculation studies
Shaojie Chen, Qiuyu Zhang, Hepeng Zhang, Junwei Gu, Mingliang Ma, Tiejun Xin, Yanyang Zhou, Jian Zhou and Qing Liu
Polym. Chem., 2012, 3, 2244-2253
DOI: 10.1039/C2PY20122D
Diels–Alder “click” reactions: recent applications in polymer and material science
Mehmet Atilla Tasdelen
Polym. Chem., 2011, 2, 2133-2145
DOI: 10.1039/C1PY00041A
Single-chain polymer nanoparticles via reversible disulfide bridges
Bryan T. Tuten, Danming Chao, Christopher K. Lyon and Erik B. Berda
Polym. Chem., 2012, Advance Article
DOI: 10.1039/C2PY20308A
Fluorescence resonance energy transfer in recognition-mediated polymer-quantum dot assemblies
Vikas Nandwana, Brian Fitzpatrick, Qian Liu, Kyril M. Solntsev, Xi Yu, Gülen Yesilbag Tonga, Serkan Eymur, Murat Tonga, Graeme Cooke and Vincent M. Rotello
Polym. Chem., 2012, Advance Article
DOI: 10.1039/C2PY20353G
Photo-responsive systems and biomaterials: photochromic polymers, light-triggered self-assembly, surface modification, fluorescence modulation and beyond
Francesca Ercole, Thomas P. Davis and Richard A. Evans
Polym. Chem., 2010, 1, 37-54
DOI: 10.1039/B9PY00300B
Why not take a look at the articles today and blog your thoughts and comments below.
Fancy submitting an article to Polymer Chemistry? Then why not submit to us today!
Synthesis and charge-transporting properties of electron-deficient CN2–fluorene based D–A copolymers by Jianhua Huang, Yan Zhao, Xunlei Ding, Hui Jia, Bo Jiang, Zhiguo Zhang, Chuanlang Zhan, Shenggui He, Qibing Pei, Yongfang Li, Yunqi Liu and Jiannian Yao Polym. Chem. 2012, 3, 2170-2177.
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Reversible addition–fragmentation chain transfer (RAFT) polymerization was used to generate well-defined pH-responsive biofunctional polymers as potential ‘smart’ gene delivery systems. A series of five poly(dimethylamino ethyl methacrylate-co-cholesteryl methacrylate) P(DMAEMA-co-CMA) statistical copolymers, with similar molecular weights and varying cholesterol content, were prepared. The syntheses, compositions and molecular weight distributions for P(DMAEMA-co-CMA) were monitored by nuclear magnetic resonance (NMR), solid-state NMR and gel permeation chromatography (GPC) evidencing well-defined polymeric structures with narrow polydispersities. Aqueous solution properties of the copolymers were investigated using turbidimetry and light scattering to determine hydrodynamic diameters and zeta potentials associated with the phase transition behaviour of P(DMAEMA-co-CMA) copolymers. UV-Visible spectroscopy was used to investigate the pH-responsive behaviour of copolymers. Hydrodynamic radii were measured in the range 10–30 nm (pH, temperature dependent) by dynamic light scattering (DLS). Charge studies indicated that P(DMAEMA-co-CMA) polymers have an overall cationic charge, mediated by pH. Potentiometric studies revealed that the buffering capacity and pKa values of polymers were dependent on cholesterol content as well as on cationic charge. The buffering capacity increased with increasing charge ratio, overall demonstrating transitions in the pH endosomal region for all five copolymeric structures. Cell viability assay showed that the copolymers displayed increasing cytotoxicity with decreasing number of cholesterol moieties. These preliminary results show the potential of these well-defined P(DMAEMA-co-CMA) polymers as in vitro siRNA delivery agents.
Synthesis, self-assembly and stimuli responsive properties of cholesterol conjugated polymers by Sema Sevimli, Sharon Sagnella, Maria Kavallaris, Volga Bulmus and Thomas P. Davis Polym. Chem. 2012, 3, 2057-2069.
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Polymer Chemistry is delighted to welcome Professor Brent S. Sumerlin as an Associate Editor.
“It is an honor to become an Associate Editor for Polymer Chemistry. Since it’s original launch in 2010, I have been an avid supporter of the journal in various capacities, most importantly as an author. The rapid success of the journal and its acceptance by polymer chemists worldwide is exciting. The editors, Editorial Board, Editorial Advisory Board, authors, and referees have worked hard to make this one of the top polymer journals. I look forward to contributing to the continued success and growth of Polymer Chemistry in the years to come.”
If you’d like to learn more about Professor Sumerlin’s own research you can find a few of his recent papers below. He’s also been featured as an ‘Author of the Week’ in 2011 and in video interview in earlier in the year.
Recent papers:
Professor Brent S. Sumerlin, Associate Editor Prof. Brent S. Sumerlin graduated with a B.S. from North Carolina State University (1998) and obtained a Ph.D. in Polymer Science and Engineering at the University of Southern Mississippi (2003) under the direction of Prof. Charles L. McCormick. After serving as a Visiting Assistant Professor at Carnegie Mellon University under the direction of Prof. Krzysztof Matyjaszewski (2003-2005), he joined the Department of Chemistry at Southern Methodist University (Dallas, Texas, USA) as an assistant professor in 2005 and was promoted to associate professor in 2009. Prof. Sumerlin joined the Department of Chemistry, the George and Josephine Butler Polymer Research Laboratory, and the Center for Macromolecular Science and Engineering at the University of Florida as an associate professor in the fall of 2012. He has received several awards, including an Oak Ridge Associated Universities Ralph E. Powe Award (2007), an NSF CAREER Award (2009), an ACS Leadership Development Award (2010), and an Alfred P. Sloan Research Fellowship (2010). He is a member of the editorial advisory boards for several journals and is now an Associate Editor of Polymer Chemistry. Current research in his group involves the synthesis of functional macromolecules, responsive polymer systems, polymer-protein bioconjugates, and dynamic covalent macromolecular assemblies.
Fast and scalable production of hyperbranched polythioether-ynes was achieved by applying sequential click chemistry (SCC) via couple-monomer methodology (CMM). As a typical example, thiol-halogen click-like reaction employing strong base, KOH and thiol-yne click reaction via UV irradiation were used for precursor preparation and polymerization, respectively. Two series of hyperbranched polythioether-ynes employing two kinds of di-thiols with different reactivity have been prepared within 10 h and characterized with 1H NMR spectroscopy and gel permeation chromatography. The hyperbranched polymers (HPs) derived from 1,6-hexanedithiol reached high weight-average molecular weight (Mw) of 230500, high weight-average degree of polymerization (DPw) of 1224 and high degree of branching (DB) of 0.82–0.68. Postmodification of abundant alkyne terminal groups afford HPs with a greatly enhanced DB of 0.96. Heat-initiated polymerization was also attempted. The present study clearly demonstrates the robustness of application of SCC technique in the CMM strategy for fast, scalable preparation of multifunctional HPs.
Fast and scalable production of hyperbranched polythioether-ynes by a combination of thiol-halogen click-like coupling and thiol-yne click polymerization by Jin Han, Bo Zhao, Aijin Tang, Yanqin Gao and Chao Gao Polym. Chem., 2012, 3, 1918-1925
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