Facilely and efficiently tuning metal–organic nanostructures of a charge-transfer complex based on a water controlled nanoreaction and the chemistry of 7,7,8,8-tetracyanoquinodimethane (TCNQ)
Source abstract
Abstract
Metal-organic charge-transfer complexes based on 7,7,8,8-tetracyanoquinodimethane (TCNQ) have received considerable attention because of their unique solid-state physical properties for potential applications in nanoscale opto-electronic devices. To address the challenge in preparing novel metal-TCNQ (MTCNQ) nanostructures, here we introduce a facile and efficient way for synthesizing MTCNQ, taking Ni[TCNQ]2(H2O)2 as an example. By finely tuning the amount of water added into TCNQ solution, well-ordered and large-scale patterns of Ni[TCNQ]2(H2O)2 were successfully obtained in a controllable manner. This facile method will not only be beneficial for the tailored preparation of nanoscale MTCNQ complexes, but also enrich the chemistry of TCNQ.
Source: openalex_inverted_index · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Organic and Molecular Conductors Research · Organic Electronics and Photovoltaics · Perovskite Materials and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Orthodontics
School and Hospital of Stomatology
Peking University
Beijing 100081, China
Beijing National Laboratory for Molecular Sciences
Institute of Microelectronics
Chinese Academy of Sciences
Beijing 100029, China
Institute of Chemistry
Beijing 100190, China
References (23)
Show source-provided references
1. Acker · J. Am. Chem. Soc. · 1960 · 82 · 640810.1021/ja01509a052 ↗
2. Wheland · J. Am. Chem. Soc. · 1976 · 98 · 391610.1021/ja00429a030 ↗
3. Potember · Appl. Phys. Lett. · 1979 · 34 · 40510.1063/1.90814 ↗
4. Potember · J. Am. Chem. Soc. · 1980 · 102 · 365910.1021/ja00530a075 ↗
5. Xiao · Adv. Mater. · 2006 · 18 · 218410.1002/adma.200600621 ↗
6. Xiao · Angew. Chem., Int. Ed. · 2007 · 46 · 265010.1002/anie.200604397 ↗
7. Xiao · J. Am. Chem. Soc. · 2012 · 134 · 1435310.1021/ja301456p ↗
8. Liu · Adv. Mater. · 2005 · 17 · 295310.1002/adma.200500809 ↗
9. Liu · J. Am. Chem. Soc. · 2006 · 128 · 1291710.1021/ja0636183 ↗
10. Liu · Small · 2011 · 7 · 141210.1002/smll.201002261 ↗
11. Liu · Small · 2012 · 8 · 55710.1002/smll.201101940 ↗
12. Siedle · Inorg. Chim. Acta · 1979 · 35 · 12510.1016/S0020-1693(00)93428-5 ↗
13. Heintz · Inorg. Chem. · 1999 · 38 · 14410.1021/ic9812095 ↗
14. Ji · Nano Res. · 2009 · 2 · 85710.1007/s12274-009-9084-x ↗
15. Melby · J. Am. Chem. Soc. · 1962 · 84 · 337410.1021/ja00876a029 ↗
16. Jeanmaire · J. Am. Chem. Soc. · 1976 · 98 · 402910.1021/ja00430a001 ↗
17. Liu · Chem. Mater. · 1996 · 8 · 277910.1021/cm9602656 ↗
18. Bolinger · Organometallics · 1986 · 5 · 238610.1021/om00142a039 ↗
19. Murthy · Anal. Chim. Acta · 1994 · 289 · 4310.1016/0003-2670(94)80006-5 ↗
20. Clerac · Chem. Mater. · 2003 · 15 · 184010.1021/cm021053d ↗
21. Wang · Chem. Rev. · 2012 · 112 · 220810.1021/cr100380z ↗
22. Wen · Chem. Rev. · 2011 · 111 · 335810.1021/cr1001904 ↗
23. Li · Acc. Chem. Res. · 2010 · 43 · 52910.1021/ar900228v ↗