Krzysztof Matyjaszewski

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Name: Matyjaszewski, Krzysztof
Organization: Carnegie Mellon University , USA
Department: Department of Chemistry
Title: Professor(PhD)

TOPICS

Co-reporter:Krzysztof Matyjaszewski, Axel H.E. Müller
Progress in Polymer Science 2006 Volume 31(Issue 12) pp:1039-1040
Publication Date(Web):December 2006
DOI:10.1016/j.progpolymsci.2006.09.002
Co-reporter:Krzysztof Matyjaszewski
Progress in Polymer Science 2005 Volume 30(8–9) pp:858-875
Publication Date(Web):August–September 2005
DOI:10.1016/j.progpolymsci.2005.06.004
Macromolecular engineering includes: rational design of the macromolecular structure including chain size, uniformity, topology, microstructure (sequencing and tacticity), composition and functionality; precise synthesis with high selectivity at reasonable cost, both in effort and environmental impact; assembly of macromolecules to supramolecular objects via controlled processing, including temperature, pressure, solvents, mechanical stresses, etc.; detailed characterization of the prepared materials at both molecular and macroscopic level; modeling of polymerization and processing conditions to aid in the design of appropriate conditions to reach targeted properties and function, and optimization of the entire process. Some recent unprecedented advances in control over various polymerization systems, including ionic, radical, coordination and even polycondensation have enabled synthesis of many new well-defined (co)polymers and some of them are briefly discussed. Precise control of various aspects of macromolecular architecture, including topology, functionality and microstructure have been achieved both in homogeneous and heterogeneous polymerization system and applied to preparation of polymeric hybrids, conjugates and other functional materials. The well-defined (co)polymers self-assembly or can be pre-assembled to materials with precisely controlled morphologies which can be affected and fixed by processing. The final macroscopic materials properties depend on molecular structure of (co)polymers and can be rationally retro-designed.
Co-reporter:Krzysztof Matyjaszewski
Macromolecular Symposia 2002 Volume 183(Issue 1) pp:71-82
Publication Date(Web):2 AUG 2002
DOI:10.1002/1521-3900(200207)183:1<71::AID-MASY71>3.0.CO;2-Y

Fundamental mechanistic features of copper mediated atom transfer radical polymerization (ATRP) are presented together with a discussion on radical intermediates involved in atom transfer process. Rate constants of racemization of optically active methyl 2-bromopropionate, of halogen exchange, of trapping with TEMPO and with methyl methacrylate are very similar, confirming free radical intermediates. Rate constant of reaction of propionate radical with methyl methacrylate under model ATRP conditions at 22°C (k= 5.6 104mol−1 L s−1) is nearly identical to that measured by time resolved EPR (k= 6.0 104mol−1 L s−1).

Propanoic acid, 2-bromo-2-methyl-, 6-(chlorodimethylsilyl)hexyl ester
Propanoic acid, 2-bromo-2-methyl-, 10-undecen-1-yl ester
Ethanol,2-[bis(2-pyridinylmethyl)amino]-
Pyridine, 4-(phenyldithio)-