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六溴三聚吲哚在不同溶剂中的可控自组装结构

Tunable Self-assemble Structures of Hexabromotriindole in Different Solvents
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摘要 研究了六溴三聚吲哚在不同溶剂中的自组装行为,并通过改变溶剂的极性和沸点调控自组装结构。结果表明,通过向六溴三聚吲哚的N,N′-二甲基甲酰胺(DMF)溶液中添加不同极性的第2种溶剂(添加后六溴三聚吲哚为1×10-3 mol·L-1),其自组装结构可以进行调控。降低六溴三聚吲哚溶液的浓度(0.5×10-3 mol·L-1)发现,分子可自组装成岛状结构。表明分子自身间相互作用较强,分子首先堆积成较小的核,然后以此为中心向四周生长。添加极性较强的溶剂有利于分子的重组,形成较长的纳米线;添加非极性溶剂时分子容易团聚,生长的纳米线的长度较短。 A solution-processed hexabromotriindole self-assembly behavior on substrate have been investigated.The experimental results showed that the molecules closely stacked with each other and self-assembly into well-ordered nanostructure in protonic solvent(dimethylformamide) could be controlled through adding second solvent to different polarities with the evapoation of the solvents(hexabromotriindole 1×10-3 mol·L-1).The addition of a higher polarity solvent facilitates the assembly of the molecules into longer and well-defined nanowires.The low polarity solvent will lead to shorter nanowires.The solution with a lower concentration(hexabromotriindole 0.5×10-3 mol·L-1) will assembly into well-identified "islands" on the substrate surface.This revealed that the intermolecular interactions are stranger than those of the interactions between molecules and substrate.
出处 《青岛科技大学学报(自然科学版)》 CAS 北大核心 2012年第6期575-578,共4页 Journal of Qingdao University of Science and Technology:Natural Science Edition
基金 国家自然科学基金资助项目(21176259)
关键词 超分子自组装 稠环芳烃 纳米线 三聚吲哚 溶剂诱导 supramolecular self-assemble polyaromatic hydrocarbon nanowire triindole solvent induce
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  • 1Weiss D S, Abkowitz M. Advances in orgaaic photoconduc tor technology[J]. ChemRev, 2010, 110(1): 479-526.
  • 2Gabor N M, Zhong Z, Bosnick K, et al. Extremely efficient multiple electron-hole pair generation in carbon nanotube photodiodes[J]. Science, 2009, 325(5946): 1367-1371.
  • 3Arnold M S, Zimmerman J D, Renshaw C K, et al. Broad spectral response using carbon nanotube/organie semiconduc- tor/C60 photodetectors[J]. Nano Lett, 2009, 9 (9) : 3354- 3358.
  • 4Aguirre C M, Ternon C, Paillet M, et al. Carbon nanotubes as injection electrodes for organic thin film transistors[J]. Nano Lett, 2009, 9(4): 1457-1461.
  • 5MathiissenSGJ, SmitsECP, Van HalPA, et al. Mono layer coverage and channel length set the mobility in self as- sembled monolayer field-effect transistors[J]. Nat Nanotech nol, 2009, 4(10): 674-680.
  • 6Granstr m M, Petritseh K, Arias A C, et al. Laminated fab rieation of polymeric photovoltaic diodes[J]. Nature, 1998, 395(6699) : 257-260.
  • 7Kwon O P, Lee S H, Montemezzani G, et al. Highly efficient photorefractive composites based on layered photoconductive pol-ymers[J]. J Opt Soc Am B, 2003, 20(11) :2307-2312.
  • 8Cohen Y S, Xiao S X, Steigerwald M L, et al. Enforced one dimensional photoeonductivity in core-cladding hexabenzocor onenes[J]. Nano Lett, 2006, 6(12): 2838-2841.
  • 9Percec V, Glodde M, Bera T K, et al. Self organization of supramolecular helical dendrimers into complex electronic materials[J]. Nature, 2002, 419(4905): 384-387.
  • 10Schwab A D, Smith D E, Bond-Watts B, et al. Photocon ductivity of self-assembled porphyrin nanorods [J]. Nano Lett, 2004, 4(7): 1261-1265.

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