| Identification | Back Directory | [Name]
2,7-Dibromo-9,9'-spiro-bifluorene | [CAS]
171408-84-7 | [Synonyms]
M8917
2,7-Dibromo-9,9'-sp
2,7-Dibromo-9,9'-spirobifL
2,7-Dibromo-9,9'-spirofluorene
2,7-Dibromo-9,9-spriobifluorene
2,7-DIBROMO-9,9'-SPIROBIFLUORENE
2,7-dibroMo -9,9-screwtwo fluorene
2,7-DIBROMO-9,9''-SPIRO-BIFLUOROENE
9,9′-Spirobi[9H-fluorene],2,7-dibromo
2,7-DibroMo-9,9'-spirobi[9H-fluorene]
2,7-Dibromo-9,9'-spirobi[9H-fluorene]>
2,7-dibroMo-9,9'-Spirobi[9H]-fluorene
(DBSBF)
2,7-Dibromo-9,9'-spiro-bifluorene ISO 9001：2015 REACH | [EINECS(EC#)]
805-788-7 | [Molecular Formula]
C25H14Br2 | [MDL Number]
MFCD08704218 | [MOL File]
171408-84-7.mol | [Molecular Weight]
474.19 |
| Chemical Properties | Back Directory | [Melting point ]
334-336°C | [Boiling point ]
557.4±50.0 °C(Predicted) | [density ]
1.74±0.1 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Inert atmosphere,Room temperature | [form ]
powder to crystal | [color ]
White to Almost white | [InChI]
InChI=1S/C25H14Br2/c26-15-9-11-19-20-12-10-16(27)14-24(20)25(23(19)13-15)21-7-3-1-5-17(21)18-6-2-4-8-22(18)25/h1-14H | [InChIKey]
UPJLZKCEPFAKSH-UHFFFAOYSA-N | [SMILES]
C12(C3=C(C=CC=C3)C3=C1C=CC=C3)C1=C(C=CC(Br)=C1)C1=C2C=C(Br)C=C1 |
| Hazard Information | Back Directory | [Chemical Properties]
white powder | [Uses]
2,7-Dibromo-9,9′-spirobifluorene can be used in the preparation of 9,9′-spirobifluorene-based small molecules, which can further be utilized as host materials in organic light emitting diodes (OLEDs). | [General Description]
2,7-Dibromo-9,9′-spirobifluorene is a 9,9 substituted poly(2,7-fluorene) that is synthesized from 2,7-dribromo-9-fluorenone by reacting with a Grignard reagent of 2-bromobiphenyl. It has high photoluminescence and electroluminescent quantum efficiency that make it useful in the development of organic electronic devices. | [Synthesis]
General procedure for the synthesis of 2,7-dibromo-9,9'-spirobifluorene from the compound (CAS: 171408-85-8): to a toluene solution containing 180 g of 9-(2-biphenylyl)-2,7-dibromo-9-fluorenol (the product of Example 3), the reaction was initiated by the slow addition of 18.0 g (0.180 mol, 2.00 M) of concentrated sulfuric acid. The reaction mixture was stirred at room temperature for 2 hours. Upon completion of the reaction, aqueous caustic soda solution was added dropwise to the mixture until neutral, followed by the addition of toluene to promote crystallization. The precipitated white crystals were collected by filtration and washed with an appropriate amount of toluene and dried to afford 35.9 g of 2,7-dibromo-9,9'-spirobifluorene (yield: 80%, based on Example 3 the total yield was 72%, HPLC purity ≥95%). | [References]
[1] Patent: EP1777227, 2007, A1. Location in patent: Page/Page column 6-7
[2] Macromolecules, 2010, vol. 43, # 24, p. 10355 - 10365
[3] Patent: CN108863694, 2018, A. Location in patent: Paragraph 0039; 0040
[4] Patent: KR101555155, 2015, B1. Location in patent: Paragraph 0119; 0120; 0121; 0122
[5] Patent: JP6257340, 2018, B2. Location in patent: Paragraph 0050 |
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