Poly(9,9-di-n-hexylfluorenyl-2,7-diyl)

Product Information

Molecular Formula:
(C27H34)n
Molecular Weight:
492.3
Description
PHF is majorly used in the fabrication of organic light emitting diodes for display applications.
Conjugated, light-emitting polymer. Exhibits blue photo- and electroluminescence.
Synonyms
9,9-Dihexyl-2,7-dibromofluorene; 2,7-dibromo-9,9-dihexyl-9H-fluorene; 2,7-Dibromo-9,9-dihexylfluorene; 9H-Fluorene, 2,7-dibromo-9,9-dihexyl-; 2,7-dibromo-9,9-di-n-hexylfluorene; 9,9-Dihexyl-2,7-dibr; 9,9-Di-n-hexyl-2,7-dibromofluorene
IUPAC Name
2,7-dibromo-9,9-dihexylfluorene
Canonical SMILES
CCCCCCC1(C2=C(C=CC(=C2)Br)C3=C1C=C(C=C3)Br)CCCCCC
InChI
InChI=1S/C25H32Br2/c1-3-5-7-9-15-25(16-10-8-6-4-2)23-17-19(26)11-13-21(23)22-14-12-20(27)18-24(22)25/h11-14,17-18H,3-10,15-16H2,1-2H3
InChI Key
OXFFIMLCSVJMHA-UHFFFAOYSA-N
Flash Point
Not applicable
Solubility
soluble in THF
Application
PHF is majorly used in the fabrication of organic light emitting diodes for display applications.

Computed Properties

XLogP3
11.2
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
0
Rotatable Bond Count
10
Exact Mass
492.08503 g/mol
Monoisotopic Mass
490.08708 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
27
Formal Charge
0
Complexity
394
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-114149568-A Preparation method of polyfluorene material and obtained polyfluorene material 2021-11-01
CN-114149405-A Method for synthesizing aromatic thioether through aromatic exchange bimetallic catalysis and application 2021-10-27
CN-113717352-A Main chain type alkaline anion exchange membrane based on ether bond-free polyfluorene and preparation method thereof 2021-08-06
CN-113178539-A Organic electroluminescence circular polarization light-emitting device based on achiral polymer 2021-04-27
KR-20220001952-A Novel polymer and organic light emitting device comprising the same 2020-06-30
CN-111607082-A Preparation method of polyimide film with low thermal expansion coefficient 2020-06-05
CN-111574691-A Fluorescent star polymer and preparation method and application thereof 2020-04-01
CN-111574691-B Fluorescent star polymer and preparation method and application thereof 2020-04-01
JP-2021138915-A Arylamine-fluorene alternating copolymer, and electroluminescence element materials and electroluminescence elements using the copolymer. 2020-03-05
KR-20210113556-A Arylamine-fluorene alternating copolymer including silicone, and electroluminescence device material and electroluminescence device using the polymer 2020-03-05

Literatures

PMID Publication Date Title Journal
19719231 2009-08-18 Poly(9,9-dihexylfluorene) layers grown via surface-directed Ni(0) condensation polymerization Langmuir : the ACS journal of surfaces and colloids
16519429 2006-03-14 Patterned polyfluorene surfaces by functionalization of nanoimprinted polymeric features Langmuir : the ACS journal of surfaces and colloids
14518131 2003-09-07 New pyrimidine- and fluorene-containing oligo(arylene)s: synthesis, crystal structures, optoelectronic properties and a theoretical study Organic & biomolecular chemistry
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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