9 9 dioctyl 2 7 dibromofluorene

Manufactured by Merck Group

9,9-Dioctyl-2,7-dibromofluorene is a chemical compound used as a laboratory reagent. It is a brominated fluorene derivative with two octyl substituents at the 9-position. This compound is typically utilized in various analytical and research applications, but a detailed description of its core function is not readily available while maintaining an unbiased and factual approach.

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Lab products found in correlation

2 tributylstannyl thiophene, by Merck Group (1 mentions) 2 5 bis tributylstannyl thiophene, by Merck Group (1 mentions) 9 9 dioctylfluorene 2 7 diboronic acid bis 1 3 propanediol ester, by Merck Group (1 mentions) Anhydrous sodium carbonate, by Sinopharm (1 mentions) Organic solvents, by Sinopharm (1 mentions)

2 protocols using 9 9 dioctyl 2 7 dibromofluorene

Synthesis of Organic Fluorescent Materials

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9,9-Dioctyl-2,7-dibromofluorene, 9,9-Dioctylfluorene-2,7-diboronic acid, 2,5-Bis(tributylstannyl) thiophene and 2-(Tributylstannyl)thiophene were purchased from Sigma-Aldrich, TCI, or Acros Organics. Tetrahydrofuran (THF), bromobenzene and Pd(PPh₃)₄ were purchased from SunaTech Inc. 4-Bromobenzophenone, titanium tetrachloride and Zn were purchased from Energy Chemica. The nitro explosive analytes used in experiments were purchased from Aldrich and used as received. Other chemicals were used as received unless otherwise specified.

Chu Z., Fan Z., Zhang X., Tan X., Li D., Chen G, & Zhao Q. (2018). A Comparison of ACQ, AIE and AEE-Based Polymers Loaded on Polyurethane Foams as Sensors for Explosives Detection. Sensors (Basel, Switzerland), 18(5), 1565.

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Synthesis and Characterization of Multilayer Graphene Oxide

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Organic solvents and anhydrous sodium carbonate were purchased from Sinopharm Co. Ltd. The solvents used in this work were purified, dried, and distilled in dry nitrogen. 9,9-dioctyl-2,7-dibromofluorene and 9,9-dioctylfluorene-2,7-diboronic acid bis(1,3-propanediol)ester were purchased from Sigma-Aldrich and used with no further purification. GO was prepared by the Hummers method from graphite powder, and dried for a week under vacuum.^{24 (link)} The TEM of GO is shown in Fig. 1(a); it is established from the image that the GO is multilayer.

Xin Y., Zhao X., Jiang X., Yang Q., Huang J., Wang S., Zheng R., Wang C, & Hou Y. (2018). Bistable electrical switching and nonvolatile memory effects by doping different amounts of GO in poly(9,9-dioctylfluorene-2,7-diyl). RSC Advances, 8(13), 6878-6886.

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