journal article·2012-07-05

Tuning Growth of Low-Dimensional Organic Nanostructures for Efficient Optical Waveguide Applications

Taifeng Liu, Yongjun Li, Yongli Yan, Yuliang Li, Yanwen Yu, Nan Chen, Songhua Chen, Chao Liu, Yongsheng Zhao, Huibiao Liu

The Journal of Physical Chemistry C· Volume 116· Issue 26
Publisher page

Abstract

A novel amphiphilic porphyrin derivative DOCP-Zn has been synthesized and utilized to construct tunable nanostructures from 0D to 1D by controlling the axial coordination of zinc porphyrin with 4,4′-bipyridine. SEM images indicated that patterns between 0D nanospheres and 1D nanorods or nanoslices can be reversibly converted by the construction or destroy of the axial coordination interaction. This facile approach provided a new method for controlling the nanostructure morphologies and dimension by patterns conversion. The photoluminescence microscopy images indicated the 1D nanorods material has the potential application as nanoscale photonic elements.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Porphyrin and Phthalocyanine Chemistry · Luminescence and Fluorescent Materials · Supramolecular Self-Assembly in Materials

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

Affiliations

CAS Key Laboratory of Organic Solids and ‡CAS Key Laboratory of Photochemistry, Beijing National Laboratory for Molecular Sciences (BNLMS), Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, P. R. China

References (42)

Show source-provided references
1. Besenius P. · Science · 2010 · 328 · 100910.1126/science.1185547 ↗
2. Chen C. L. · Angew. Chem., Int. Ed. · 2010 · 49 · 192410.1002/anie.200903572 ↗
3. Tanner P. · Chem.—Eur. J. · 2011 · 17 · 455210.1002/chem.201002782 ↗
4. Ho V. · J. Am. Chem. Soc. · 2011 · 133 · 927010.1021/ja2035317 ↗
5. Yan Y. · J. Am. Chem. Soc. · 2010 · 132 · 1200610.1021/ja1036447 ↗
6. Qiao Y. · J. Phys. Chem. B · 2010 · 114 · 3610.1021/jp1047369 ↗
7. Liu H. B. · Acc. Chem. Res. · 2010 · 43 · 149610.1021/ar100084y ↗
8. Zheng H. Y. · Chem. Soc. Rev. · 2011 · 40 · 450610.1039/c0cs00222d ↗
9. Michael D. W. · Nature · 2000 · 405 · 29310.1038/35012741 ↗
10. Matsumoto A. · Nature · 2000 · 405 · 32810.1038/35012550 ↗
11. Grimsdale A. C. · Angew. Chem., Int. Ed. · 2005 · 44 · 559210.1002/anie.200500805 ↗
12. Horn D. · Angew. Chem.,Int. Ed. · 2001 · 40 · 433010.1002/1521-3773(20011203)40:23<4330::AID-ANIE4330>3.0.CO;2-W ↗
13. Jiang L. · J. Am. Chem. Soc. · 2008 · 130 · 393710.1021/ja077600j ↗
14. Zhang Y. · J. Am. Chem. Soc. · 2009 · 131 · 275610.1021/ja805891k ↗
15. Che Y. · J. Am. Chem. Soc. · 2007 · 129 · 723410.1021/ja071903w ↗
16. Balakrishnan K. · J. Am. Chem. Soc. · 2006 · 128 · 739010.1021/ja061810z ↗
17. Tang M. L. · J. Am. Chem. Soc. · 2008 · 130 · 606410.1021/ja8005918 ↗
18. Zhou Z. · Appl. Phys. Lett. · 2007 · 90 · 19311510.1063/1.2738380 ↗
19. Hoeben F. J. M. · J. Am. Chem. Soc. · 2007 · 129 · 981910.1021/ja072548c ↗
20. Xie Y. S. · Chem.Commun. · 2011 · 47 · 228510.1039/C0CC04855K ↗
21. Würthner F. · Angew. Chem., Int. Ed. · 2011 · 50 · 337610.1002/anie.201002307 ↗
22. Hofkens J. · J. Phys. Chem. B · 1997 · 101 · 1058810.1021/jp972305e ↗
23. Gust D. · Acc. Chem. Res. · 2001 · 34 · 4010.1021/ar9801301 ↗
24. Armstrong N. R. J. · J. Porphyrins Phthalocyanines · 2000 · 4 · 41410.1002/(SICI)1099-1409(200006/07)4:4<414::AID-JPP247>3.0.CO;2-B ↗
25. Wagner R. W. · J. Am. Chem. Soc. · 1996 · 118 · 399610.1021/ja9602657 ↗
26. Senthil Kumar K. · Chem.—Eur. J. · 2011 · 17 · 532710.1002/chem.201002981 ↗
27. Schwab A. D. · Nano Lett. · 2004 · 4 · 126110.1021/nl049421v ↗
28. Mbenkum B. N. · Nano Lett. · 2006 · 6 · 285210.1021/nl062057a ↗
29. Gnichwitz J. F. · J. Am. Chem. Soc. · 2008 · 130 · 849110.1021/ja8018065 ↗
30. Hu J. S. · J. Am. Chem. Soc. · 2005 · 127 · 1709010.1021/ja0553912 ↗
31. Wang Z. · J. Am. Chem. Soc. · 2004 · 126 · 1595410.1021/ja045068j ↗
32. Huang C. S. · Chem. Commun. · 2010 · 46 · 316110.1039/b927059k ↗
33. Huang C. S. · Adv. Mater. · 2009 · 21 · 172110.1002/adma.200802114 ↗
34. Charvet R. · Chem. Commun. · 2004 · 23 · 266410.1039/B409228G ↗
35. Li Y. J. · Angew. Chem., Int. Ed. · 2006 · 45 · 363910.1002/anie.200600554 ↗
36. Huang C. S. · Adv. Mater. · 2009 · 21 · 172110.1002/adma.200802114 ↗
37. Beletskaya I. · Chem. Rev. · 2009 · 109 · 165910.1021/cr800247a ↗
38. Janczak J. · Inorg. Chem. · 2002 · 41 · 505910.1021/ic020258l ↗
39. Gardberg A. S. · Inorg. Chem. · 2002 · 41 · 177810.1021/ic010994+ ↗
40. Boyd P. D. W. · Chem. Commun. · 1999 · 7 · 637
41. Zhu P. H. · Eur. J. Inorg. Chem. · 2011 · 27 · 424110.1002/ejic.201100421 ↗
42. Law M. · Science · 2004 · 305 · 126910.1126/science.1100999 ↗