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  • 2,2'-bis(trifluoromethyl)-[1,1'-biphenyl]-4,4'-diamine(TFDB/TFMB)

  • 2,2'-bis(trifluoromethyl)-[1,1'-biphenyl]-4,4'-diamine(TFDB/TFMB)

    Catalog Number
    ACM341582-2
    CAS Number
    341-58-2
    Product Name
    2,2'-bis(trifluoromethyl)-[1,1'-biphenyl]-4,4'-diamine(TFDB/TFMB)
    Structure
    Category
    Organic Light-Emitting Diode (OLED) Materials
    IUPAC Name
    4-[4-amino-2-(trifluoromethyl)phenyl]-3-(trifluoromethyl)aniline
    Molecular Weight
    320.23g/mol
    Molecular Formula
    C14H10F6N2
    Canonical SMILES
    C1=CC(=C(C=C1N)C(F)(F)F)C2=C(C=C(C=C2)N)C(F)(F)F
    InChI
    InChI=1S/C14H10F6N2/c15-13(16,17)11-5-7(21)1-3-9(11)10-4-2-8(22)6-12(10)14(18,19)20/h1-6H,21-22H2
    InChI Key
    NVKGJHAQGWCWDI-UHFFFAOYSA-N
    Application
    2,2'-bis(trifluoromethyl)-[1,1'-biphenyl]-4,4'-diamine (TFDB/TFMB) serves as a crucial component for developing high-strength, flexible, and transparent polyimide materials. It is a fluorinated benzidine derivative featuring trifluoromethyl groups at strategic positions, which imparts rigidity and an aromatic character beneficial for synthesizing metal-organic and covalent organic frameworks with high specific surface areas. The unique electron-withdrawal properties of the trifluoromethyl groups enhance the material's transparency by mitigating electron dispersion within the polymer's conjugated backbone. This makes TFDB/TFMB-based polyimides not only UV-resistant and effectively colorless but also ideal for optoelectronic applications such as thin films. Additionally, these polyimides are suitable for encapsulating solar cells, where they contribute to efficient light diffusion when paired with MOFs clusters.
    Complexity
    345
    Covalently-Bonded Unit Count
    1
    Exact Mass
    320.074817g/mol
    Formal Charge
    0
    Heavy Atom Count
    22
    Monoisotopic Mass
    320.074817g/mol
    Rotatable Bond Count
    1
    XLogP3
    4
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