journal article·2017

Self-assembly of single amino acid/pyrene conjugates with unique structure–morphology relationship

Srinivasa Rao Nelli, Rajan Deepan Chakravarthy, Yue-Ming Xing, Jen-Po Weng, Hsin-Chieh Lin

Soft Matter· Volume 13· Issue 45
Publisher page

Abstract

This article describes the self-assembly of π-conjugated building blocks composed of single amino acid and pyrene (Py) moieties. In aqueous conditions, the Py-capped amino acids undergo self-assembly through various non-covalent interactions such as hydrogen-bonding, π-π stacking as well as electrostatic interactions to form supramolecular nanostructures in acidic and basic conditions. Interestingly, we found that the blend of different Py-gelators with oppositely charged amino acids (Py-Glu and Py-Lys) displays unique nano-structural morphologies and gelation properties of the resulting hydrogels at physiological pH when compared with single Py conjugates, which was attributed to additional electrostatic interactions. Overall, this report illustrates the importance of two-component supramolecular co-assembled hydrogels and their structure-morphology relationship, improved mechanical properties, and biocompatibility and thus provides a new insight into the design of self-assembled nanomaterials.
Source: openalex_inverted_index · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Supramolecular Self-Assembly in Materials · Lipid Membrane Structure and Behavior · Supramolecular Chemistry and Complexes

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

Affiliations

Department of Materials Science and Engineering

National Chiao Tung University

Hsinchu

Republic of China

Funding

Ministry of Science and Technology, Taiwan

References (47)

Show source-provided references
1. Fleming · Chem. Soc. Rev. · 2014 · 43 · 815010.1039/C4CS00247D ↗
2. Tomasini · Chem. Soc. Rev. · 2013 · 42 · 15610.1039/C2CS35284B ↗
3. Raeburn · Chem. Soc. Rev. · 2013 · 42 · 514310.1039/c3cs60030k ↗
4. Babu · Chem. Rev. · 2014 · 114 · 197310.1021/cr400195e ↗
5. Weiss · J. Am. Chem. Soc. · 2014 · 136 · 751910.1021/ja503363v ↗
6. Javid · Biomacromolecules · 2013 · 14 · 436810.1021/bm401319c ↗
7. Bhattacharya · Langmuir · 2009 · 25 · 837810.1021/la901017u ↗
8. Edwards · J. Am. Chem. Soc. · 2013 · 135 · 591110.1021/ja4017107 ↗
9. Edwards · J. Am. Chem. Soc. · 2014 · 136 · 111610.1021/ja411724r ↗
10. Castelletto · Biomater. Sci. · 2014 · 2 · 86710.1039/C4BM00001C ↗
11. Basak · J. Mater. Chem. · 2012 · 22 · 1165810.1039/c2jm30711a ↗
12. Basak · Chem. Commun. · 2014 · 50 · 691710.1039/c4cc02300e ↗
13. Jiang · Nanoscale · 2015 · 7 · 1916010.1039/C5NR05233E ↗
14. Yang · J. Controlled Release · 2012 · 162 · 61210.1016/j.jconrel.2012.08.002 ↗
15. Tokuda · Biomaterials · 2014 · 35 · 431010.1016/j.biomaterials.2014.01.063 ↗
16. Ghobril · Chem. Soc. Rev. · 2015 · 44 · 182010.1039/C4CS00332B ↗
17. Sun · Nature · 2012 · 489 · 13310.1038/nature11409 ↗
18. Martin · Soft Matter · 2016 · 12 · 270010.1039/C6SM00025H ↗
19. Baral · Soft Matter · 2015 · 11 · 494410.1039/C5SM00808E ↗
20. Suzuki · Chem. Soc. Rev. · 2009 · 38 · 96710.1039/b816192e ↗
21. Terech · Chem. Rev. · 1997 · 97 · 313310.1021/cr9700282 ↗
22. de Loos · Eur. J. Org. Chem. · 2005 · 361510.1002/ejoc.200400723 ↗
23. Skilling · Soft Matter · 2014 · 10 · 23710.1039/C3SM52244J ↗
24. Cheng · Langmuir · 2010 · 26 · 499010.1021/la903678e ↗
25. Nelli · New J. Chem. · 2017 · 41 · 122910.1039/C6NJ02820A ↗
26. Gujrati · Langmuir · 2011 · 27 · 655410.1021/la2012809 ↗
27. Sivakova · Chem. Soc. Rev. · 2005 · 34 · 910.1039/b304608g ↗
28. Meyer · Angew. Chem., Int. Ed. · 2003 · 42 · 121010.1002/anie.200390319 ↗
29. King · Soft Matter · 2016 · 12 · 191510.1039/C5SM02039E ↗
30. Yan · Langmuir · 2013 · 29 · 79310.1021/la304957n ↗
31. Zhang · J. Am. Chem. Soc. · 2004 · 126 · 1502810.1021/ja044401g ↗
32. Yan · J. Am. Chem. Soc. · 2013 · 135 · 898910.1021/ja402560n ↗
33. Berdugo · ACS Appl. Mater. Interfaces · 2015 · 7 · 2594610.1021/acsami.5b08968 ↗
34. Niko · RSC Adv. · 2014 · 4 · 3648010.1039/C4RA06282E ↗
35. Adhikari · Soft Matter · 2011 · 7 · 891310.1039/c1sm05907f ↗
36. Fleming · Biomacromolecules · 2014 · 15 · 117110.1021/bm401720z ↗
37. Kameta · Chem. Commun. · 2015 · 51 · 1110410.1039/C5CC03843J ↗
38. Du · Chem. Rev. · 2015 · 115 · 1316510.1021/acs.chemrev.5b00299 ↗
39. Nanda · Soft Matter · 2013 · 9 · 419810.1039/c3sm27050e ↗
40. Tao · Chem. Soc. Rev. · 2016 · 45 · 393510.1039/C5CS00889A ↗
41. Zhu · Chem. – Eur. J. · 2010 · 16 · 803410.1002/chem.201000595 ↗
42. Mutaf · Macromol. Rapid Commun. · 2015 · 36 · 195810.1002/marc.201500368 ↗
43. Wu · Soft Matter · 2012 · 8 · 1045710.1039/c2sm25668a ↗
44. Haedler · ChemPhysChem · 2013 · 14 · 181810.1002/cphc.201300242 ↗
45. Goormaghtigh · Biophys. J. · 2006 · 90 · 294610.1529/biophysj.105.072017 ↗
46. Adochitei · Rev. Roum. Chim. · 2011 · 56 · 783
47. Palui · Chem. – Eur. J. · 2009 · 15 · 690210.1002/chem.200900149 ↗