57102-48-4

Upstream product

• 19264-74-5 9-(4-methoxyphenyl)-9H-carbazole 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 696-62-8 para-iodoanisole 
• 86-74-8 9H-carbazole 

Downstream Products

• 1028843-48-2 bis(9-(hydroxyphenyl)carbazol-3-yl) 

Relevant academic research and scientific papers

Synthesis of carbazole-based small organic molecule hole transport material and application of carbazole-based small organic molecule hole transport material in perovskite solar cell

The invention belongs to the field of perovskite solar cell materials, and discloses a carbazole-based small organic molecule hole transport material. According to the carbazole-based small organic molecule hole transport material, a carbazole intermediate core group fragment is synthesized by utilizing a low-temperature reaction and a bromination reaction; a target product OY1, a target product OY2 and a target product OY3 are obtained by means of synthesis from the carbazole intermediate core group fragment and peripheral triphenylamine micromolecules through an acylation reaction and a coupling reaction; the structures of the target product OY1, the target product OY2 and the target product OY3 are confirmed through a high-resolution mass spectrum characterization means, and the target product OY1, the target product OY2 and the target product OY3 are applied to a perovskite solar cell; the synthesized compound is subjected to photophysic, electrochemical, intrinsic hole mobility and thin film characteristic tests, and in addition, the photovoltaic performance of the perovskite solar cell is represented through tests of output current-voltage, incident monochromatic photon-electron conversion efficiency, long-term stability and the like of the cell device. Due to low cost, easy chemical synthesis and excellent performance, the carbazole-based small organic molecule hole transport material will become a powerful competitor.

Electrochemical and spectral characterizations of 9-phenylcarbazoles

A series of 9-phenylcarbazoles have been synthesized and characterized for their electrochemical as well as spectral properties. For 3,6-substituted carbazoles, the oxidation is reversible and the potential is affected by the substituents. For 3,6-unprotected carbazoles, on the other hand, the oxidized forms can undergo dimerization. Their corresponding dimers have been independently synthesized by chemical methods and have exhibited identical spectral properties. The para position of the 9-phenyl group is relatively insensitive for redox and chemical reactions. The amino derivatives are unstable in carbazole cation radical form compared with their triphenylamine counterparts.

BIS-CARBAZOLE MONOMERS AND POLYMERS

The invention relates to compounds of formula I wherein R1, R2, and R4 are independently at each occurrence a C1-C20 aliphatic radical, a C3- C20 aromatic radical, or a C3-C20 cycloaliphatic radical; R3 and R5 are independently at each occurrence hydrogen, a C1-C20 aliphatic radical, a C3-C20 aromatic radical, or a C3-C20 cycloaliphatic radical; and a, b and d are independently 0 or an integer ranging from 1 to 3. The invention further relates to polymers derived from compounds of formula I. The polymers may be polyesters, polyethers, polycarbonates, polyestercarbonates, polyetherketones, or polyethersulfones. Compounds and polymers of the invention find use in light emitting devices.

Carbazole Compounds as Host Materials for Triplet Emitters in Organic Light-Emitting Diodes: Tuning the HOMO Level without Influencing the Triplet Energy in Small Molecules

A series of novel carbazole compounds was synthesized and tested for their suitability as host for triplet emitters in an organic-light emitting diode (OLED). In these compounds, a carbazole unit is either connected to other carbazole units to form carbazole dimers and trimers or to fluorene and oxadiazole derivatives to form mixed compounds. The HOMO level of carbazole compounds can be tuned by substitution at the 3, 6, and/or 9 positions. Making oligomers by connecting carbazole molecules via their 3 (3′) positions shifts the HOMO level to higher energy, while replacing alkyl groups at the 9 (9′) positions by aryl groups shifts the HOMO level to lower energy. Furthermore, it has been found that the triplet energy of these compounds is determined by the presence of poly(p-phenyl) chains in the molecular structure. By identifying the longest poly(p-phenyl) chain, one can predict whether a compound will be a suitable host for a high-energy triplet emitter. An overview of HOMO levels, singlet and triplet levels, and exchange energies is given for all carbazole compounds synthesized. Finally, OLEDs employing two selected carbazole compounds as host and fac-tris(2-phenylpyridine)-iridium (Ir(ppy) 3) as guest were constructed and characterized electrically.