Poly(methyl methacrylate)-Supported Polydiacetylene Films: Unique Chromatic Transitions and Molecular Sensing
Source abstract
Abstract
Polydiacetylenes (PDAs) constitute a family of conjugated polymers exhibiting unique colorimetric and fluorescence transitions, and have attracted significant interest as chemo- and biosensing materials. We spin-coated PDA films upon poly(methyl methacrylate) (PMMA), and investigated the photophysical properties and sensing applications of the new PDA configuration. Specifically, the as-polymerized blue PDA layer underwent distinct transformations to purple, red, and yellow phases, which could be quantified through conventional color scanning combined with application of image analysis algorithms. Furthermore, we recorded a reversible red-purple PDA transition that was induced by ultraviolet irradiation, a phenomenon that had not been reported previously in PDA film systems. We show that distinct color and fluorescence transitions were induced in the PMMA-supported PDA films by amphiphilic substances-surfactants and ionic liquids-and that the chromatic transformations were correlated to the analyte structures and properties. Overall, this study presents a new chromatic PDA film system in which noncovalent interactions between the PMMA substrate and spin-coated PDA give rise to distinct chromatic properties and molecular sensing capabilities.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Polydiacetylene-based materials and applications · Ocular Surface and Contact Lens · Supramolecular Self-Assembly in Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Biomedical Engineering and Computational Science, Aalto University, Helsinki, Finland
Interdipartimental Center for Industrial research (CIRI) Energy & Environment, University of Bologna, via S. Alberto 163, 48123 Ravenna, Italy
Department of Chemistry “G. Ciamician”, University of Bologna, via Selmi 2, 40126 Bologna, Italy
References (47)
Show source-provided references
1. Wegner G. · Z. Naturoforsch. B · 1969 · 24 · 82410.1515/znb-1969-0708 ↗
2. Sun X. · Chem. Soc. Rev. · 2010 · 39 · 424410.1039/c001151g ↗
3. Dong J. A. · Acc. Chem. Res. · 2008 · 41 · 80510.1021/ar7002489 ↗
4. Jelinek R. · RSC Adv. · 2013 · 3 · 2119210.1039/c3ra42639d ↗
5. Yarimaga O. · Chem. Commun. · 2012 · 48 · 246910.1039/c2cc17441c ↗
6. Diegelmann S. R. · J. Am. Chem. Soc. · 2012 · 134 · 202810.1021/ja211539j ↗
7. Reppy M. A. · Chem. Commun. · 2007 · 42 · 431710.1039/b703691d ↗
8. Zou G. · J. Mater. Chem. · 2010 · 20 · 28510.1039/B913764E ↗
9. Lee J. · J. Am. Chem. Soc. · 2008 · 130 · 501010.1021/ja709996c ↗
10. Park C. H. · Adv. Funct. Mater. · 2009 · 19 · 370310.1002/adfm.200900393 ↗
11. Wu J. · J. Am. Chem. Soc. · 2011 · 133 · 972010.1021/ja204013u ↗
12. Gravel E. · Chem. - Eur. J. · 2012 · 18 · 40010.1002/chem.201102769 ↗
13. MacKiewicz N. · Small · 2011 · 7 · 278610.1002/smll.201100212 ↗
14. Wacharasindhu S. · Macromolecules · 2010 · 43 · 71610.1021/ma902282c ↗
15. Kolusheva S. · Anal. Chem. · 2012 · 84 · 592510.1021/ac300449u ↗
16. Xu Q. · J. Am. Chem. Soc. · 2013 · 135 · 1775110.1021/ja410557x ↗
17. Wang X. · Adv. Funct. Mater. · 2013 · 23 · 604410.1002/adfm.201301044 ↗
18. Yoon J. · J. Am. Chem. Soc. · 2007 · 129 · 303810.1021/ja067856+ ↗
19. Choi H. · J. Nanosci. Nanotechnol. · 2011 · 11 · 620310.1166/jnn.2011.4403 ↗
20. Ye Q. · J. Mater. Chem. · 2008 · 18 · 277510.1039/b803333a ↗
21. Chen X. · Angew. Chem., Int. Ed. · 2010 · 49 · 142210.1002/anie.200905041 ↗
22. Dei S. · Macromolecules · 2008 · 41 · 246710.1021/ma702789f ↗
23. Lee S. · ACS Appl. Mater. Interfaces · 2013 · 5 · 452110.1021/am3030245 ↗
24. Lee J. · Adv. Funct. Mater. · 2011 · 21 · 103210.1002/adfm.201002042 ↗
25. Carpick R. W. · J. Phys.: Condens. Matter. · 2004 · 16 · R679
26. Jiang H. · J. Mater. Chem. · 2011 · 21 · 451810.1039/c0jm03174g ↗
27. Ritenberg M. · ChemPlusChem. · 2012 · 77 · 75210.1002/cplu.201200088 ↗
28. You X. · J. Mater. Chem. · 2008 · 18 · 470410.1039/b806458j ↗
29. Jiang H. · Chem. Phys. Lett. · 2010 · 500 · 10010.1016/j.cplett.2010.10.022 ↗
30. Tariq M. · Chem. Soc. Rev. · 2012 · 41 · 82910.1039/C1CS15146K ↗
31. Gal N. · Biochim. Biophys. Acta, Biomembr. · 2012 · 1818 · 296710.1016/j.bbamem.2012.07.025 ↗
32. Nockemann P. · Chem. Phys. Lett. · 2005 · 415 · 13110.1016/j.cplett.2005.08.128 ↗
33. Earle M. J. · Anal. Chem. · 2007 · 79 · 75810.1021/ac061481t ↗
34. Paytash P. L. · J. Am. Chem. Soc. · 1950 · 72 · 141510.1021/ja01159a520 ↗
35. Galletti P. · Green Chem. · 2007 · 9 · 98710.1039/b702031g ↗
36. Volinsky R. · Biosens. Bioelectron. · 2007 · 22 · 324710.1016/j.bios.2006.12.024 ↗
37. Pevzner A. · Adv. Funct. Mater. · 2008 · 18 · 24210.1002/adfm.200700726 ↗
38. Giorgetti E. · Langmuir · 2006 · 22 · 112910.1021/la0514157 ↗
39. Xu Y. · J. Colloid Interface Sci. · 2013 · 400 · 11610.1016/j.jcis.2013.02.049 ↗
40. Cui C. · J. Nanosci. Nanotechnol. · 2011 · 11 · 575410.1166/jnn.2011.4405 ↗
41. Seo S. · Macromol. Rapid Commun. · 2013 · 34 · 74310.1002/marc.201200819 ↗
42. Cho Y.-S. · Chem.—Asian J. · 2013 · 8 · 75510.1002/asia.201201139 ↗
43. Foley P. · Chem. Soc. Rev. · 2012 · 41 · 149910.1039/C1CS15217C ↗
44. Franklin, R.InSurfactants from Renewable Resources;Kjellin, M.; Johansson, I., Eds;John Wiley and Sons:West Sussex, U.K., 2010; Chapter 2, pp21–43.
45. Willke T. · Appl. Microbiol. Biotechnol. · 2004 · 66 · 13110.1007/s00253-004-1733-0 ↗
46. Shafizadeh F. · J. Appl. Polym. Sci. · 1979 · 23 · 352510.1002/app.1979.070231209 ↗
47. Potisatityuenyong A. · Langmuir · 2008 · 24 · 446110.1021/la800354q ↗