journal article·2013

Perylene diimide functionalized polynorbornene: a macromolecular scaffold for supramolecular self-assembly

Micah S. Glaz, Joshua D. Biberdorf, Minh T. Nguyen, Jonathon J. Travis, Bradley J. Holliday, David A. Vanden Bout

Journal of Materials Chemistry C· Volume 1· Issue 48
Publisher page

Abstract

We have synthesized and characterized a polymer comprising a polynorbornene backbone with perylene diimide (PDI) pendant groups. The polymer exhibits intramolecular self-assembly into molecular aggregates that can be controlled via solvent quality. In a medium that solvates the polymer backbone well the PDI chromophores self-assemble into characteristic H-type aggregates aligned along the polymer backbone. In contrast, in a solvent medium that does not solvate the polymer well the polynorbornene backbone collapses into a globular conformation preventing the aggregation of the PDI chromophores, which display monomer-like photophysics. The polymer photophysics are recorded under a variety of conditions, including lifetimes and relative quantum yields. Furthermore, we utilize the weakly coupled H-aggregate model to quantify the exciton bandwidth of the polymer structure and demonstrate that polymer thin films can retain the same chromophore aggregated morphology as the fully solvated polymer.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Organic Electronics and Photovoltaics · Luminescence and Fluorescent Materials · Analytical Chemistry and Sensors

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

References (29)

Show source-provided references
1. Tour · Acc. Chem. Res. · 2000 · 33 · 79110.1021/ar0000612 ↗
2. Chesterfield · J. Phys. Chem. B · 2004 · 108 · 1928110.1021/jp046246y ↗
3. Riede · Nanotechnology · 2008 · 19 · 42400110.1088/0957-4484/19/42/424001 ↗
4. Rajaram · Chem. Mater. · 2009 · 21 · 177510.1021/cm900911x ↗
5. Hutchison · J. Am. Chem. Soc. · 2005 · 127 · 1686610.1021/ja0533996 ↗
6. Kline · Macromolecules · 2007 · 40 · 796010.1021/ma0709001 ↗
7. Shin · J. Mater. Chem. · 2006 · 16 · 38410.1039/B512983D ↗
8. Balakrishnan · J. Am. Chem. Soc. · 2006 · 128 · 739010.1021/ja061810z ↗
9. Tauber · J. Am. Chem. Soc. · 2006 · 128 · 178210.1021/ja057031k ↗
10. Tang · Langmuir · 2005 · 22 · 2610.1021/la052766o ↗
11. Clark · J. Am. Chem. Soc. · 2007 · 129 · 758610.1021/ja0687724 ↗
12. Liu · J. Phys. Chem. B · 2002 · 106 · 130710.1021/jp013254v ↗
13. Struijk · J. Am. Chem. Soc. · 2000 · 122 · 1105710.1021/ja000991g ↗
14. Ahrens · J. Am. Chem. Soc. · 2004 · 126 · 828410.1021/ja039820c ↗
15. Kaiser · Angew. Chem., Int. Ed. · 2007 · 46 · 554110.1002/anie.200701139 ↗
16. Spano · Acc. Chem. Res. · 2010 · 43 · 42910.1021/ar900233v ↗
17. Schwartz · Chem.–Eur. J. · 2009 · 15 · 253610.1002/chem.200801746 ↗
18. Vougioukalakis · Chem. Rev. · 2009 · 110 · 174610.1021/cr9002424 ↗
19. Davies · J. Chem. Soc., Perkin Trans. 1 · 1973 · 43310.1039/p19730000433 ↗
20. Pochas · J. Am. Chem. Soc. · 2013 · 135 · 305610.1021/ja3087449 ↗
21. Spano · J. Am. Chem. Soc. · 2009 · 131 · 426710.1021/ja806853v ↗
22. Ries · BioEssays · 2012 · 34 · 36110.1002/bies.201100111 ↗
23. Huang · Proc. R. Soc. London, Ser. A · 1950 · 204 · 40610.1098/rspa.1950.0184 ↗
24. Spano · J. Chem. Phys. · 2005 · 122 · 23470110.1063/1.1914768 ↗
25. Spano · Chem. Phys. · 2006 · 325 · 2210.1016/j.chemphys.2005.08.019 ↗
26. Ford · J. Phys. Chem. · 1987 · 91 · 637310.1021/j100309a012 ↗
27. Bisht · Chem. Phys. Lett. · 1996 · 258 · 7110.1016/0009-2614(96)00641-0 ↗
28. Holden · Macromolecules · 1980 · 13 · 28910.1021/ma60074a016 ↗
29. Holden · Macromolecules · 1980 · 13 · 29510.1021/ma60074a017 ↗