Literature DB >> 18776947

Design, Development and Evaluation of Monovinyl Acrylates Characterized by Secondary Functionalities as Reactive Diluents to Diacrylates.

Harini Kilambi1, Sirish K Reddy, Lauren Schneidewind, Tai Yeon Lee, Jeffrey W Stansbury, Christopher N Bowman.   

Abstract

This study focuses on the design and development of novel monovinylic (meth)acrylate monomers with enhanced polymerization kinetics and the evaluation of their performance as reactive diluents in diacrylate systems. Novel (meth)acrylic monomers characterized by several new secondary functionalities are developed in this study and are shown to exhibit reactivities 10-70 fold greater than traditional monoacrylates such as hexyl acrylate. These monomers were designed based on our understanding of interactions between monomer structure, polymerizations kinetics, and polymer properties. Performance of these monovinyl monomers as reactive diluents is also investigated in this study. Copolymerization of these monomers with diacrylates enhanced both the reactivity and the mechanical properties of the diacrylate system. Specifically, while copolymerization of a diacrylate system with traditional monoacrylates such as hexyl acrylate decreases the overall reactivity of the system, its copolymerization with the novel monomers led to comonomer mixtures, that were 30-50% more reactive than either of the individual components, with initial polymerization rates increased by as much as 2 times the more reactive component. Further, the copolymerization of these novel monovinyl systems with diacrylates also enabled formation of polymers with enhanced mechanical properties over the corresponding diacrylates including a more homogeneous network structure as indicated by a glass transition temperature that was narrowed by up to 55 % while increasing the glass transition temperature by as much as 10°C.

Entities:  

Year:  2007        PMID: 18776947      PMCID: PMC2529465          DOI: 10.1021/ma062708p

Source DB:  PubMed          Journal:  Macromolecules        ISSN: 0024-9297            Impact factor:   5.985


  3 in total

1.  Primary cyclization in the polymerization of bis-GMA and TEGDMA: a modeling approach to understanding the cure of dental resins.

Authors:  J E Elliott; L G Lovell; C N Bowman
Journal:  Dent Mater       Date:  2001-05       Impact factor: 5.304

2.  Robust polymer microfluidic device fabrication via contact liquid photolithographic polymerization (CLiPP).

Authors:  J Brian Hutchison; K Tommy Haraldsson; Brian T Good; Robert P Sebra; Ning Luo; Kristi S Anseth; Christopher N Bowman
Journal:  Lab Chip       Date:  2004-09-24       Impact factor: 6.799

3.  Monomers with low oxygen inhibition as enamel/dentin adhesives.

Authors:  W J Finger; K S Lee; W Podszun
Journal:  Dent Mater       Date:  1996-07       Impact factor: 5.304

  3 in total
  2 in total

1.  Reactivity of Monovinyl (Meth)Acrylates Containing Cyclic Carbonates.

Authors:  Kathryn A Berchtold; Jun Nie; Jeffrey W Stansbury; Christopher N Bowman
Journal:  Macromolecules       Date:  2008-12-09       Impact factor: 5.985

2.  Tris(trimethylsilyl)silane as a co-initiator for dental adhesive: Photo-polymerization kinetics and dynamic mechanical property.

Authors:  Linyong Song; Qiang Ye; Xueping Ge; Anil Misra; Paulette Spencer
Journal:  Dent Mater       Date:  2015-11-27       Impact factor: 5.304

  2 in total

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