Polymers with multiple hydrogen-bonded end groups and their blends

K. Feldman; M.J. Kade; T.F.A. Greef, de; E.W. Meijer; G.J. Kramer; C.J. Hawker

doi:10.1021/ma800375r

Polymers with multiple hydrogen-bonded end groups and their blends

K. Feldman, M.J. Kade, T.F.A. Greef, de, E.W. Meijer, G.J. Kramer, C.J. Hawker

Research output: Contribution to journal › Article › Academic › peer-review

163 Citations (Scopus)

Abstract

A new strategy for synthesizing well-defined, chain-end-functionalized polymers containing multiple hydrogen-bonding (MHB) groups capable of heterodimerization in both solution and the melt has been developed. Two complementary MHB systems were chosen for initial studies: 2-ureido-4[1H]-pyrimidinone (UPy) and 2,7-diamido-1,8-naphthyridine (Napy) and ATRP initiators containing either UPy or Napy were prepared and shown to produce well-defined (meth)acrylic polymers with the desired MHB functionality present at the chain end. To characterize the effectiveness of the MHB interaction in the melt, blends of chain-end-functionalized linear polymers were cast into films, annealed at various temperatures above Tg, and then quenched, and their structures were analyzed by transmission electron microscopy (TEM) and differential scanning calorimetry (DSC). It was shown that the nature of the hydrogen-bonding group(s) present in the blend has a significant effect on bulk microstructure and thermal behavior, in particular for blends of UPy- and Napy-functional chains.

Original language	English
Pages (from-to)	4694-4700
Journal	Macromolecules
Volume	41
Issue number	13
DOIs	https://doi.org/10.1021/ma800375r
Publication status	Published - 2008

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title = "Polymers with multiple hydrogen-bonded end groups and their blends",

abstract = "A new strategy for synthesizing well-defined, chain-end-functionalized polymers containing multiple hydrogen-bonding (MHB) groups capable of heterodimerization in both solution and the melt has been developed. Two complementary MHB systems were chosen for initial studies: 2-ureido-4[1H]-pyrimidinone (UPy) and 2,7-diamido-1,8-naphthyridine (Napy) and ATRP initiators containing either UPy or Napy were prepared and shown to produce well-defined (meth)acrylic polymers with the desired MHB functionality present at the chain end. To characterize the effectiveness of the MHB interaction in the melt, blends of chain-end-functionalized linear polymers were cast into films, annealed at various temperatures above Tg, and then quenched, and their structures were analyzed by transmission electron microscopy (TEM) and differential scanning calorimetry (DSC). It was shown that the nature of the hydrogen-bonding group(s) present in the blend has a significant effect on bulk microstructure and thermal behavior, in particular for blends of UPy- and Napy-functional chains.",

author = "K. Feldman and M.J. Kade and {Greef, de}, T.F.A. and E.W. Meijer and G.J. Kramer and C.J. Hawker",

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doi = "10.1021/ma800375r",

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T1 - Polymers with multiple hydrogen-bonded end groups and their blends

AU - Feldman, K.

AU - Kade, M.J.

AU - Greef, de, T.F.A.

AU - Meijer, E.W.

AU - Kramer, G.J.

AU - Hawker, C.J.

PY - 2008

Y1 - 2008

N2 - A new strategy for synthesizing well-defined, chain-end-functionalized polymers containing multiple hydrogen-bonding (MHB) groups capable of heterodimerization in both solution and the melt has been developed. Two complementary MHB systems were chosen for initial studies: 2-ureido-4[1H]-pyrimidinone (UPy) and 2,7-diamido-1,8-naphthyridine (Napy) and ATRP initiators containing either UPy or Napy were prepared and shown to produce well-defined (meth)acrylic polymers with the desired MHB functionality present at the chain end. To characterize the effectiveness of the MHB interaction in the melt, blends of chain-end-functionalized linear polymers were cast into films, annealed at various temperatures above Tg, and then quenched, and their structures were analyzed by transmission electron microscopy (TEM) and differential scanning calorimetry (DSC). It was shown that the nature of the hydrogen-bonding group(s) present in the blend has a significant effect on bulk microstructure and thermal behavior, in particular for blends of UPy- and Napy-functional chains.

AB - A new strategy for synthesizing well-defined, chain-end-functionalized polymers containing multiple hydrogen-bonding (MHB) groups capable of heterodimerization in both solution and the melt has been developed. Two complementary MHB systems were chosen for initial studies: 2-ureido-4[1H]-pyrimidinone (UPy) and 2,7-diamido-1,8-naphthyridine (Napy) and ATRP initiators containing either UPy or Napy were prepared and shown to produce well-defined (meth)acrylic polymers with the desired MHB functionality present at the chain end. To characterize the effectiveness of the MHB interaction in the melt, blends of chain-end-functionalized linear polymers were cast into films, annealed at various temperatures above Tg, and then quenched, and their structures were analyzed by transmission electron microscopy (TEM) and differential scanning calorimetry (DSC). It was shown that the nature of the hydrogen-bonding group(s) present in the blend has a significant effect on bulk microstructure and thermal behavior, in particular for blends of UPy- and Napy-functional chains.

U2 - 10.1021/ma800375r

DO - 10.1021/ma800375r

M3 - Article

VL - 41

SP - 4694

EP - 4700

JO - Macromolecules

JF - Macromolecules

SN - 0024-9297

IS - 13

ER -

Polymers with multiple hydrogen-bonded end groups and their blends

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