journal article·2013-09-24

Controlled Synthesis of Anisotropic Polymer Particles Templated by Porous Coordination Polymers

Takashi Uemura, Tetsuya Kaseda, Susumu Kitagawa

Chemistry of Materials· Volume 25· Issue 18
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Abstract

Nonspherical polymer particles have been efficiently prepared in different morphological crystals of porous coordination polymers (PCPs) by in situ radical polymerization of styrene and methylmethacrylate, followed by removal of the host PCP frameworks in aqueous tetrasodium ethylenediaminetetraacetate (Na-EDTA) solution. In this replication process, the isolated vinyl polymer particles retained the size and morphologies of the original PCP particles, although the polymer chains were not stabilized by cross-linking. This morphological retention of vinyl polymers after the isolation from the PCP matrixes was ensured by the rigidity and porosity of the polymers, which was confirmed by DSC and adsorption measurements. The unconventional assembly of polymer chains in the particles is of interest from the viewpoints of functional properties of the polymer particles.
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Research context

OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · Covalent Organic Framework Applications · Mesoporous Materials and Catalysis

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Katsura, Nishikyo-ku, Kyoto 615-8510, Japan

Institute for Integrated Cell-Material Sciences (WPI-iCeMS), Kyoto University, Yoshida, Sakyo-ku, Kyoto 606-8501, Japan

References (43)

Show source-provided references
1. Mittal V. · 2011
2. Arshady R. · Colloid Polym. Sci. · 1992 · 270 · 71710.1007/BF00776142 ↗
3. Rao J. P. · Prog. Polym. Sci. · 2011 · 36 · 88710.1016/j.progpolymsci.2011.01.001 ↗
4. Landfester K. · Angew. Chem., Int. Ed. · 2009 · 48 · 448810.1002/anie.200900723 ↗
5. Nie Z. · J. Am. Chem. Soc. · 2005 · 127 · 805810.1021/ja042494w ↗
6. Herlihy K. P. · Langmuir · 2008 · 24 · 842110.1021/la801250g ↗
7. Chang C.-J. · Polymer · 2006 · 47 · 59110.1016/j.polymer.2005.11.075 ↗
8. Park J.-G. · J. Am. Chem. Soc. · 2010 · 132 · 596010.1021/ja101760q ↗
9. Xu S. · Angew. Chem., Int. Ed. · 2005 · 44 · 72410.1002/anie.200462226 ↗
10. Lu Y. · Adv. Mater. · 2001 · 13 · 41510.1002/1521-4095(200103)13:6<415::AID-ADMA415>3.0.CO;2-O ↗
11. Lu Y. · Langmuir · 2002 · 18 · 772210.1021/la025946w ↗
12. Champion J. A. · J. Controlled Release · 2007 · 121 · 310.1016/j.jconrel.2007.03.022 ↗
13. Sozzani P. · Nat. Mater. · 2006 · 5 · 54510.1038/nmat1659 ↗
14. Cepak V. M. · Chem. Mater. · 1999 · 11 · 136310.1021/cm9811500 ↗
15. Moon S. I. · Macromolecules · 2003 · 36 · 425310.1021/ma0300239 ↗
16. Sada K. · Chem. Soc. Rev. · 2007 · 36 · 41510.1039/B603555H ↗
17. Yaghi O. M. · Nature · 2003 · 423 · 70510.1038/nature01650 ↗
18. Kitagawa S. · Angew. Chem., Int. Ed. · 2004 · 43 · 233410.1002/anie.200300610 ↗
19. Bradshaw D. · Acc. Chem. Res. · 2005 · 38 · 27310.1021/ar0401606 ↗
20. Ferey G. · Chem. Soc. Rev. · 2009 · 38 · 138010.1039/b804302g ↗
21. Cohen S. M. · Chem. Rev. · 2012 · 112 · 97010.1021/cr200179u ↗
22. Murray L. J. · Chem. Soc. Rev. · 2009 · 38 · 129410.1039/b802256a ↗
23. Lee J. · Chem. Soc. Rev. · 2009 · 38 · 145010.1039/b807080f ↗
24. Ma L. Q. · Chem. Soc. Rev. · 2009 · 38 · 124810.1039/b807083k ↗
25. Li J.-R. · Chem. Rev. · 2012 · 112 · 86910.1021/cr200190s ↗
26. Uemura T. · Bull. Chem. Soc. Jpn. · 2011 · 84 · 116910.1246/bcsj.20110211 ↗
27. Uemura T. · Top. Curr. Chem. · 2010 · 293 · 15510.1007/128_2009_6 ↗
28. Uemura T. · Chem. Soc. Rev. · 2009 · 38 · 122810.1039/b802583p ↗
29. Uemura T. · Chem. Mater. · 2009 · 21 · 409610.1021/cm901361m ↗
30. Uemura T. · J. Am. Chem. Soc. · 2012 · 134 · 836010.1021/ja301903x ↗
31. Ishiwata T. · J. Am. Chem. Soc. · 2013 · 135 · 542710.1021/ja3125614 ↗
32. Wang Q.-X. · Macromol. Rapid Commun. · 2011 · 32 · 161010.1002/marc.201100305 ↗
33. Spokoyny A. M. · Chem. Soc. Rev. · 2009 · 38 · 121810.1039/b807085g ↗
34. Bétard A. · Chem. Rev. · 2012 · 112 · 105510.1021/cr200167v ↗
35. Carné A. · Chem. Soc. Rev. · 2011 · 40 · 29110.1039/C0CS00042F ↗
36. Bradshaw D. · Chem. Soc. Rev. · 2012 · 41 · 234410.1039/C1CS15276A ↗
37. Dybtsev D. N. · Angew. Chem., Int. Ed. · 2004 · 43 · 503310.1002/anie.200460712 ↗
38. Chun H. · Inorg. Chem. · 2007 · 46 · 437110.1021/ic070036t ↗
39. Uemura T. · Macromolecules · 2008 · 41 · 8710.1021/ma7022217 ↗
40. Uemura T. · J. Am. Chem. Soc. · 2010 · 132 · 491710.1021/ja100406k ↗
41. Thomas A. · Chem. Mater. · 2008 · 20 · 73810.1021/cm702126j ↗
42. Johnson S. A. · Chem. Mater. · 1997 · 9 · 244810.1021/cm9703278 ↗
43. Barrett E. P. · J. Am. Chem. Soc. · 1951 · 73 · 37310.1021/ja01145a126 ↗