journal article·2018

A general approach for encapsulating organic crystals in a polyaniline shell

Miao Yan, Neng Wang, Bingju Zhong, Xuejun Cheng, Hong Wang, Hongyu Chen

Nanoscale· Volume 10· Issue 45
Publisher page

Abstract

The hydrophobicity and instability of organic crystals restrict their further applications. Here, we present a general and scalable method to encapsulate different organic crystals in a conductive polyaniline (PANI) shell. The shell significantly improves the stability and dispersity of the nanocrystals, without compromising their luminescence intensity.
Source: openalex_inverted_index · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Conducting polymers and applications · Photochromic and Fluorescence Chemistry · Luminescence and Fluorescent Materials

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

Affiliations

Institute of Advanced Synthesis

School of Chemistry and Molecular Engineering

Jiangsu National Synergetic Innovation Center for Advanced Materials

Nanjing Tech University

Nanjing 211816

Funding

National Natural Science Foundation of China · Recruitment Program of Global Experts · Nanjing Tech University

References (31)

Show source-provided references
1. Gong · ACS Appl. Mater. Interfaces · 2014 · 6 · 1101810.1021/am502060y ↗
2. Li · Acc. Chem. Res. · 2010 · 43 · 52910.1021/ar900228v ↗
3. Kim · Nano Lett. · 2010 · 10 · 288410.1021/nl1009662 ↗
4. Bertorelle · Langmuir · 2006 · 22 · 852310.1021/la060239e ↗
5. D'Addio · Mol. Pharm. · 2010 · 7 · 55710.1021/mp900260q ↗
6. Yimin · Nanotechnology · 2015 · 26 · 37400210.1088/0957-4484/26/37/374002 ↗
7. Takeda · Mol. Pharm. · 2017 · 14 · 79110.1021/acs.molpharmaceut.6b01048 ↗
8. Zhao · ACS Appl. Mater. Interfaces · 2017 · 9 · 3288710.1021/acsami.7b09659 ↗
9. Hu · J. Mater. Chem. · 2012 · 22 · 23210.1039/C1JM13556B ↗
10. Shen · J. Phys. Chem. C · 2013 · 117 · 733410.1021/jp311360p ↗
11. Helmut · Angew. Chem., Int. Ed. · 1999 · 38 · 218810.1002/(SICI)1521-3773(19990802)38:15<2188::AID-ANIE2188>3.0.CO;2-# ↗
12. Misra · Chem. Commun. · 2014 · 50 · 907610.1039/C4CC02824D ↗
13. Kulkarni · Chem. Mater. · 2004 · 16 · 455610.1021/cm049473l ↗
14. Zhang · ACS Nano · 2015 · 9 · 1190910.1021/acsnano.5b04427 ↗
15. Hovers · Mol. Membr. Biol. · 2011 · 28 · 17110.3109/09687688.2011.552440 ↗
16. Birch · Org. Process Res. Dev. · 2013 · 17 · 135910.1021/op4000972 ↗
17. Ito · ACS Nano · 2014 · 8 · 6410.1021/nn401888h ↗
18. Xu · Chem. Rev. · 2018 · 118 · 320910.1021/acs.chemrev.7b00208 ↗
19. Xing · J. Mater. Chem. · 2009 · 19 · 328610.1039/b900993k ↗
20. Tan · J. Am. Chem. Soc. · 2016 · 138 · 519010.1021/jacs.6b00594 ↗
21. Janković · ACS Nano · 2013 · 7 · 381510.1021/nn400246q ↗
22. Liu · J. Am. Chem. Soc. · 2012 · 134 · 1879710.1021/ja3088218 ↗
23. Kamata · J. Am. Chem. Soc. · 2003 · 125 · 238410.1021/ja0292849 ↗
24. Wang · Acc. Chem. Res. · 2013 · 46 · 163610.1021/ar400020j ↗
25. Sindoro · Angew. Chem., Int. Ed. · 2011 · 50 · 989810.1002/anie.201102994 ↗
26. Tarver · Chem. Mater. · 2009 · 21 · 28010.1021/cm802314h ↗
27. Kim · Langmuir · 2000 · 16 · 584110.1021/la9915320 ↗
28. Marcolongo · J. Chem. Educ. · 2011 · 88 · 62910.1021/ed900019u ↗
29. Chauhan · J. Surfactants Deterg. · 2013 · 17 · 16910.1007/s11743-013-1532-7 ↗
30. Sulthana · J. Phys. Chem. B · 1998 · 102 · 965310.1021/jp982060l ↗
31. Wang · Angew. Chem., Int. Ed. · 2010 · 49 · 842610.1002/anie.201001065 ↗