1. Dramatic Tunability of the Glass Transition Temperature and Fragility of Low Molecular Weight Polystyrene by Initiator Fragments Located at Chain Ends
- Author
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Lanhe Zhang, John A. Marsiglio, Tian Lan, and John M. Torkelson
- Subjects
Kinetic chain length ,Nitroxide mediated radical polymerization ,Polymers and Plastics ,Chemistry ,Organic Chemistry ,Radical polymerization ,02 engineering and technology ,010402 general chemistry ,021001 nanoscience & nanotechnology ,01 natural sciences ,0104 chemical sciences ,Isobutyric acid ,Inorganic Chemistry ,chemistry.chemical_compound ,Fragility ,Polymerization ,Polymer chemistry ,Materials Chemistry ,Polystyrene ,0210 nano-technology ,Glass transition - Abstract
Important, yet unexplored effects of chemically distinct initiator fragments incorporated at chain ends in linear polymer are investigated in depth. Polystyrene (PS) samples of a wide range of molecular weight (MW) were synthesized by conventional free radical polymerization and controlled radical polymerization using seven different initiators and compared with anionically polymerized PS. The initiator fragments incorporated during polymerization have major consequences on the glass transition temperature (Tg) and dynamic fragility of low MW PS. For example, with ∼4 kg/mol PS, the Tg onset value and fragility can be tuned from ∼334 K and ∼65, respectively, with dodecanethiol and hydrogen atom chain ends to ∼367 K and ∼130, respectively, with cyanopentanoic acid chain ends. A similar high Tg and high fragility were measured with isobutyric acid/SG1 nitroxide chain ends. These remarkable effects, with a greater than 30 K difference in Tg and a factor of 2 difference in fragility, indicate that chain ends i...
- Published
- 2016
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