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2,7-Dibromo-9,9'-spiro-bifluorene

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2,7-Dibromo-9,9'-spiro-bifluorene Basic information

Product Name:
2,7-Dibromo-9,9'-spiro-bifluorene
Synonyms:
  • 9,9′-Spirobi[9H-fluorene],2,7-dibromo
  • 2,7-DIBROMO-9,9''-SPIRO-BIFLUOROENE
  • 2,7-Dibromo-9,9-spriobifluorene
  • 2,7-Dibromo-9,9'-sp
  • 2,7-DibroMo-9,9'-spirobi[9H-fluorene]
  • 2,7-dibroMo-9,9'-Spirobi[9H]-fluorene (DBSBF)
  • 2,7-dibroMo -9,9-screwtwo fluorene
  • 2,7-Dibromo-9,9'-spirofluorene
CAS:
171408-84-7
MF:
C25H14Br2
MW:
474.19
EINECS:
805-788-7
Product Categories:
  • Fluorene Derivatives
  • Fluorene Series
  • OLED
Mol File:
171408-84-7.mol
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2,7-Dibromo-9,9'-spiro-bifluorene Chemical Properties

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
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Safety Information

WGK Germany 
3
HS Code 
2903.99.8001
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2,7-Dibromo-9,9'-spiro-bifluorene Usage And Synthesis

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

171408-85-8

171408-84-7

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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