7,7-Dimethyl-4,10-dinaphthalen-2-yl-3,11-dithia-7-silatricyclo[6.3.0.02,6]undeca-1(8),2(6),4,9-tetraene | 1231544-28-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: 7,7-Dimethyl-4,10-dinaphthalen-2-yl-3,11-dithia-7-silatricyclo[6.3.0.02,6]undeca-1(8),2(6),4,9-tetraene
• 英文别名: 7,7-dimethyl-4,10-dinaphthalen-2-yl-3,11-dithia-7-silatricyclo[6.3.0.02,6]undeca-1(8),2(6),4,9-tetraene
• CAS: 1231544-28-7
• 化学式: C₃₀H₂₂S₂Si
• 分子量: 474.722
• InChiKey: PHQAXPCWQCEAQN-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  8.25
• 重原子数：
  33
• 可旋转键数：
  2
• 环数：
  7.0
• sp3杂化的碳原子比例：
  0.07
• 拓扑面积：
  56.5
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  2-溴萘 、 4,10-Diiodo-7,7-dimethyl-3,11-dithia-7-silatricyclo[6.3.0.02,6]undeca-1(8),2(6),4,9-tetraene 在 正丁基锂 、 indium(III) chloride 、 (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride 作用下， 以 正己烷 、 四氢呋喃 、 乙醚 为溶剂， 反应 10.0h， 以49%的产率得到7,7-Dimethyl-4,10-dinaphthalen-2-yl-3,11-dithia-7-silatricyclo[6.3.0.02,6]undeca-1(8),2(6),4,9-tetraene
  参考文献：
  名称：

  Palladium-Catalyzed Cross-Coupling Reactions of Dithienosilole with Indium Reagents: Synthesis and Characterization of Dithienosilole Derivatives and Their Application to Organic Light-Emitting Diodes

  摘要：

  Three dithienosilole (DTS) derivatives bearing naphthyl segments, 5,5'-dinaphthyl-1,1-dimethyldithienosilol (1), 5,5'-dinaphthyl-l-methyl-l-phenyldithienosilole (2), and 5,5'-dinaphthyl-1,1-diphenyldithienosilol (3), are prepared through Pd(II)-catalyzed cross-coupling using an organoindium reagent as a nucleophile. The molecular structure of 3 is confirmed by single-crystal X-ray analysis. In addition, thermal, photophysical, and electrochemical properties for all three compounds are systematically investigated. The introduction of naphthyl segments into the DTS framework leads to an excellent enhancement of thermal stability with relatively high glass transition (T(g): 87 degrees C) and decomposition temperatures (T(d): 320-380 degrees C). A red shift in both absorption and emission is observed in the DTS series as the 1,1-substituents on the ring silicon atom become more electronegative. On the basis of absorption spectra and DFT/TDDFT calculations, intense green photoluminescence observed for all compounds can be attributed to the effective pi-pi* transition of the DTS and naphthyl group with a small contribution of the sigma* orbital of the exocyclic Si-C bond. The electron-transporting properties of 1, 2, and 3 were evaluated by the performance of organic light-emitting diodes (OLEDs), comprising 4,4',4 ''-tris(N-(2-naphthyl)-N-phenylamino)triphenylamine (2-TNA-TA) as hole-injection layer, 4,4'-bis(N-phenyl-1-naphthylamino)biphenyl (NPB) as hole-transport layer, 10-(2-benzothiazolyl)-1,1,7,7-tetramethyl-2,3,6,7-tetrahydro-1H,5H,11H-benzo[l]pyrano[678-ij]quinolizin]-11-one(C545T)/tris(8-quinolinato)aluminum (Alq(3)) as emitting layer, and the DTS series as electron-transporting layer, respectively. The device shows intense green emission with a high efficiency of 8.0 cd/A at 1000 cd/m(2).

  DOI：

  10.1021/om100222b

文献信息

• Palladium-Catalyzed Cross-Coupling Reactions of Dithienosilole with Indium Reagents: Synthesis and Characterization of Dithienosilole Derivatives and Their Application to Organic Light-Emitting Diodes
  作者：Hwasoon Jung、Hyonseok Hwang、Ki-Min Park、Jinho Kim、Dong-Ha Kim、Youngjin Kang

  DOI：10.1021/om100222b

  日期：2010.6.28

  Three dithienosilole (DTS) derivatives bearing naphthyl segments, 5,5'-dinaphthyl-1,1-dimethyldithienosilol (1), 5,5'-dinaphthyl-l-methyl-l-phenyldithienosilole (2), and 5,5'-dinaphthyl-1,1-diphenyldithienosilol (3), are prepared through Pd(II)-catalyzed cross-coupling using an organoindium reagent as a nucleophile. The molecular structure of 3 is confirmed by single-crystal X-ray analysis. In addition, thermal, photophysical, and electrochemical properties for all three compounds are systematically investigated. The introduction of naphthyl segments into the DTS framework leads to an excellent enhancement of thermal stability with relatively high glass transition (T(g): 87 degrees C) and decomposition temperatures (T(d): 320-380 degrees C). A red shift in both absorption and emission is observed in the DTS series as the 1,1-substituents on the ring silicon atom become more electronegative. On the basis of absorption spectra and DFT/TDDFT calculations, intense green photoluminescence observed for all compounds can be attributed to the effective pi-pi* transition of the DTS and naphthyl group with a small contribution of the sigma* orbital of the exocyclic Si-C bond. The electron-transporting properties of 1, 2, and 3 were evaluated by the performance of organic light-emitting diodes (OLEDs), comprising 4,4',4 ''-tris(N-(2-naphthyl)-N-phenylamino)triphenylamine (2-TNA-TA) as hole-injection layer, 4,4'-bis(N-phenyl-1-naphthylamino)biphenyl (NPB) as hole-transport layer, 10-(2-benzothiazolyl)-1,1,7,7-tetramethyl-2,3,6,7-tetrahydro-1H,5H,11H-benzo[l]pyrano[678-ij]quinolizin]-11-one(C545T)/tris(8-quinolinato)aluminum (Alq(3)) as emitting layer, and the DTS series as electron-transporting layer, respectively. The device shows intense green emission with a high efficiency of 8.0 cd/A at 1000 cd/m(2).