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Jianhui Xia

Bio: Jianhui Xia is an academic researcher from Carnegie Mellon University. The author has contributed to research in topics: Radical polymerization & Atom-transfer radical-polymerization. The author has an hindex of 22, co-authored 28 publications receiving 12059 citations. Previous affiliations of Jianhui Xia include University of North Carolina at Chapel Hill.

Papers
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Journal ArticleDOI
TL;DR: The homogeneous atom transfer radical polymerization (ATRP) of styrene using solubilizing 4,4'dialkyl substituted 2,2'bipyridines yielded well-defined polymers with Mw/Mn ≤ 1.10 as mentioned in this paper.
Abstract: The homogeneous atom transfer radical polymerization (ATRP) of styrene using solubilizing 4,4‘-dialkyl substituted 2,2‘-bipyridines yielded well-defined polymers with Mw/Mn ≤ 1.10. The polymerizations exhibited an increase in molecular weight in direct proportion to the ratio of the monomer consumed to the initial initiator concentration and also exhibited internal first-order kinetics with respect to monomer concentration. The optimum ratio of ligand-to-copper(I) halide for these polymerizations was found to be 2:1, which tentatively indicates that the coordination sphere of the active copper(I) center contains two bipyridine ligands. The exclusive role for this copper(I) complex in ATRP is atom transfer, since at typical concentrations that occur for these polymerizations (≈10-7−10-8 M), polymeric radicals were found not to react with the copper(I) center in any manner that enhanced or detracted from the observed control. ATRP also exhibited first-order kinetics with respect to both initiator and copper...

852 citations

Journal ArticleDOI
10 May 1996-Science
TL;DR: A radical polymerization process that yields well-defined polymers normally obtained only through anionic polymerizations is reported, and has all of the characteristics of a living polymerization.
Abstract: A radical polymerization process that yields well-defined polymers normally obtained only through anionic polymerizations is reported. Atom transfer radical polymerizations of styrene were conducted with several solubilizing ligands for the copper(I) halides: 4,4′-di-tert-butyl, 4,4′-di-n-heptyl, and 4,4′-di-(5-nonyl)-2,2′-dipyridyl. The resulting polymerizations have all of the characteristics of a living polymerization and displayed linear semilogarithmic kinetic plots, a linear correlation between the number-average molecular weight and the monomer conversion, and low polydispersities (ratio of the weight-average to number-average molecular weights of 1.04 to 1.05). Similar results were obtained for the polymerization of acrylates.

837 citations

Journal ArticleDOI
TL;DR: In this article, three multidentate amines, tetramethylethylenediamine (TMEDA), N,N,NN, N',N' and N'N' were used as new ligands in the copper mediated atom transfer radical polymerization (ATRP) of styrene, methyl acrylate and methyl methacrylate.
Abstract: Three multidentate amines, tetramethylethylenediamine (TMEDA), N,N,N‘,N‘,N‘‘-pentamethyldiethylenetriamine (PMDETA) and 1,1,4,7,10,10-hexamethyltriethylenetetramine (HMTETA) have been successfully used as new ligands in the copper mediated atom transfer radical polymerization (ATRP) of styrene, methyl acrylate and methyl methacrylate. All the polymerizations were well controlled with a linear increase of molecular weights (Mn) with conversion and relatively low polydispersities throughout the reactions. Compared to the 2,2‘-bipyridine (bipy) based ligands, most multidentate amines are less expensive and the polymerization mixtures are less colored. In particular, the use of the tridentate PMDETA and the tetradentate HMTETA as the ligands resulted in faster polymerization rates for styrene and methyl acrylate than those using bipy as the ligand. This may be in part attributed to the fact that the coordination complexes between copper and the simple amines have lower redox potentials than the copper−bipy co...

428 citations

Patent
15 Nov 1996
TL;DR: Improved processes for atom (or group) transfer radical polymerization (ATRP) and novel polymers have been developed and described in this paper, where novel copolymers comprising a least one polymeric branch or polymeric block with a predominantly alternating monomer sequence are described.
Abstract: Improved processes for atom (or group) transfer radical polymerization (ATRP) and novel polymers have been developed and are described. In certain embodiments, novel copolymers comprising a least one polymeric branch or polymeric block with a predominantly alternating monomer sequence are described. Novel copolymers comprising a least one polymeric branch or polymeric block with a gradient monomer structure are described. Additionally, novel copolymers comprising a least one polymeric branch or polymeric block with a predominantly periodic monomer sequence are also described. Novel copolymers having a water soluble backbone and at least two hydrophobic polymeric branches grafted to the water soluble backbone are also described.

391 citations


Cited by
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Journal ArticleDOI
TL;DR: In this article, a review of recent mechanistic developments in the field of controlled/living radical polymerization (CRP) is presented, with particular emphasis on structure-reactivity correlations and "rules" for catalyst selection in ATRP, for chain transfer agent selection in reversible addition-fragmentation chain transfer (RAFT) polymerization, and for the selection of an appropriate mediating agent in stable free radical polymerisation (SFRP), including organic and transition metal persistent radicals.

2,869 citations

Journal ArticleDOI
TL;DR: In this article, the authors focused on temperature and pH responsive polymer systems and additionally the other stimuli-based responsive polymers will be assessed, which is more helpful to design new approaches because the basic concepts and mechanisms are systematically connected.

2,233 citations

Journal ArticleDOI
TL;DR: The current status and future perspectives in atom transfer radical polymerization (ATRP) are presented in this paper, with a special emphasis on mechanistic understanding of ATRP, recent synthetic and process development, and new controlled polymer architectures enabled by ATRP.
Abstract: Current status and future perspectives in atom transfer radical polymerization (ATRP) are presented. Special emphasis is placed on mechanistic understanding of ATRP, recent synthetic and process development, and new controlled polymer architectures enabled by ATRP. New hybrid materials based on organic/inorganic systems and natural/synthetic polymers are presented. Some current and forthcoming applications are described.

2,188 citations