(11bS)-4,4-Dibutyl-2,6-bis(3,4,5-trifluorophenyl)-4,5-dihydro-3H-dinaphtho[2,1-c:1',2'-e]azepinium bromide

≥98%

Reagent Code: #237548
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CAS Number 851942-89-7

science Other reagents with same CAS 851942-89-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 748.64 g/mol
Formula C₄₂H₃₆BrF₆N
badge Registry Numbers
MDL Number MFCD09264271
thermostat Physical Properties
Melting Point 224-229 °C
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used in organic electronics as a dopant to enhance charge transport in semiconductor materials. Its fluorinated aromatic structure improves stability and electron affinity, making it suitable for use in organic field-effect transistors (OFETs) and perovskite solar cells. The compound acts as a p-type dopant, increasing conductivity by generating free holes in the host material. It is also explored in photovoltaic devices for its ability to modify work function of electrodes and improve device efficiency. Due to its thermal stability and solubility in nonpolar solvents, it is compatible with solution-processing techniques used in large-area electronics.

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inventory 50mg
10-20 days ฿28,360.00

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(11bS)-4,4-Dibutyl-2,6-bis(3,4,5-trifluorophenyl)-4,5-dihydro-3H-dinaphtho[2,1-c:1',2'-e]azepinium bromide
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Used in organic electronics as a dopant to enhance charge transport in semiconductor materials. Its fluorinated aromatic structure improves stability and electron affinity, making it suitable for use in organic field-effect transistors (OFETs) and perovskite solar cells. The compound acts as a p-type dopant, increasing conductivity by generating free holes in the host material. It is also explored in photovoltaic devices for its ability to modify work function of electrodes and improve device efficiency.

Used in organic electronics as a dopant to enhance charge transport in semiconductor materials. Its fluorinated aromatic structure improves stability and electron affinity, making it suitable for use in organic field-effect transistors (OFETs) and perovskite solar cells. The compound acts as a p-type dopant, increasing conductivity by generating free holes in the host material. It is also explored in photovoltaic devices for its ability to modify work function of electrodes and improve device efficiency. Due to its thermal stability and solubility in nonpolar solvents, it is compatible with solution-processing techniques used in large-area electronics.

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