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Upstream product

• 61676-62-8 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 601454-33-5 9-(4-bromophenyl)-3,6-bis(1,1-dimethylethyl)-9H-carbazole 
• 73183-34-3 bis(pinacol)diborane 
• 106-37-6 1.4-dibromobenzene 
• 255829-32-4 3,6-di-tert-butyl-9-(4-iodophenyl)-9H-carbazole 
• 589-87-7 1,4-bromoiodobenzene 
• 37500-95-1 3,6-di(tert-butyl)-9H-carbazole 

Relevant academic research and scientific papers

Alkylated indolo[3,2,1-jk]carbazoles as new building blocks for solution processable organic electronics

A facile strategy for the introduction of tert-butyl and hexyl chains to the indolo[3,2,1-jk]carbazole scaffold is presented. With these building blocks six materials based on three different 4,4′-bis(N-carbazolyl)-1,1-biphenyl derivatives with varying degree of planarization were prepared. Characterization of the materials showed that the alkyl chains have only minor effects on the photophysical properties of the compounds. In contrast, thermal robustness towards decomposition and electrochemical stability are increased by the introduced alkyl chains. Detailed investigation of the solubility in five different solvents revealed that the incorporation of the alkyl chains increases the solubility significantly. The increased solubility of the materials allowed the application as host materials in red, green and sky-blue solution processed phosphorescent organic light emitting diodes. Hence, this work presents the first solution processed light emitting devices based on the indolo[3,2,1-jk]carbazole scaffold.

A solution-processable hybridized local and charge-transfer (HLCT) phenanthroimidazole as a deep-blue emitter for efficient solution-processed non-doped electroluminescence device

Most highly efficient hybridized local and charge-transfer (HLCT)-based organic light‐emitting diodes (OLEDs) are multi-layer devices fabricated by thermal vacuum evaporation techniques, which are inappropriate for the simplified device fabrication process. However, there are only a couple of reported examples of solution-processed HLCT OLEDs, particularly deep-blue OLEDs. Herein, we design and synthesize a solution-processable HLCT emitter, CPPI, in which 1,2-diphenyl-phenanthroimidazole (PI) as an acceptor core is substituted by three 3,6-di-tert-butyl-N-phenyl-carbazole (CP) moieties as a donor and hole-transporting/solubilizing unit. The HLCT and photophysical properties are thoroughly examined by theoretical and experimental methods. CPPI exhibits HLCT characteristics with intense deep-blue color emission, high thermal and electrochemical stability, and decent hole-transporting ability. The molecule is successfully fabricated as a solution-processed non-doped emitter in organic light-emitting diodes (OLED). The solution-processed OLED retains efficient and stable deep-blue color emission (CIE coordinates of (0.157, 0.089)) with a narrow FWHM of 66 nm, an EQEmax of 3.39% and a high exciton utilization efficiency of 42.4%. Crucially, this result signifies an advance in developing a solution-processable HLCT molecule as an emitter for solution-processed non-doped OLEDs.

Organic light-emitting material containing benzo[c][1,2,5]thiadiazole derivative receptor structural unit and application

The invention provides an organic light-emitting material based on a donor-receptor structure of a benzo[c][1,2,5]thiadiazole-4-aldehyde group receptor and a 2-(benzo[c][1,2,5]thiadiazole-4-methylene)malononitrile receptor and application thereof. The organic light-emitting material is a receptor-donor separation system, wherein the receptor is benzo[c][1,2,5]thiadiazole-4-aldehyde or 2-(benzo[c][1,2,5]thiadiazole-4-methylene) malononitrile, and a donor is carbazole and a derivative or benzoxazine and the like. The lowest unoccupied molecular orbital (LUMO) in the material is located in the receptor, and the highest occupied molecular orbital (HOMO) in the material is located in the donor, so that the molecular orbital energy level of the luminescent material can be effectively regulated and controlled through electrical regulation of the receptor structure and the donor. By regulating and controlling the structure of the light-emitting material or the electron donating capability of the donor, the light-emitting color of material molecules can be conveniently regulated. The organic light-emitting material has the characteristic that the light-emitting color is easy to adjust, andcan be used as a light-emitting material for preparing an OLED device.

NARROW ABSORPTION POLYMER NANOPARTICLES AND RELATED METHODS

Polymers, monomers, narrow-band absorbing polymers, narrow-band absorbing monomers, absorbing units, polymer dots, and related methods are provided. Bright, luminescent polymer nanoparticles with narrow-band absorptions are provided. Methods for synthesizing absorbing monomers, methods for synthesizing the polymers, preparation methods for forming the polymer nanoparticles, and applications for using the polymer nanoparticles are also provided.

Dendritic organometallic complexes as well as preparation method and application thereof

The present invention provides a preparation method of dendritic organometallic complexes. The method comprises the following step: performing a Suzuki reaction on one dendrimer unit containing boricacid or borate represented by a formula (I) and one meta

Solution processable red iridium dendrimers containing oligocarbazole dendrons for efficient nondoped and doped phosphorescent OLEDs

Solution processable red Ir dendrimers named R-D1, R-D2 and R-D3, which contain a quinoline-based homoleptic complex as the core and oligocarbazole as the dendron, have been facilely and successfully designed and synthesized via a post-dendronization procedure. With the increasing dendron generation from R-D1 to R-D3, the intermolecular interactions and luminescence quenching in solid states are found to be effectively prevented because of encapsulation from the outer dendrons. As a result, the third-generation dendrimer R-D3 achieves the best nondoped device performance, revealing a promising EQE of 10.5% (9.2 cd A-1, 7.0 lm W-1) with CIE coordinates of (0.67, 0.33). Furthermore, the doped devices of R-D3 show a wide doping concentration window in the range of 5-30 wt%, and a maximum EQE as high as 18.3% (25.7 cd A-1, 33.0 lm W-1) is realized at about a 10 wt% doping content. The results can compete well with vacuum-deposited small molecular red phosphors, representing important progress on solution processable phosphorescent dendrimers with red emission.

Multicomponent reaction comprising one-pot installation of bidentate directing group and Pd(II)-catalyzed direct β-arylation of C(sp3)[sbnd]H bond of aliphatic and alicyclic carboxamides

In this paper, we report a step-economical one-pot multicomponent reaction protocol comprising the installation of the bidentate directing group (auxiliary) followed by Pd(II)-catalyzed sp3C[sbnd]H activation and β-arylation of various aliphatic/alicyclic carboxamides. Accordingly, the reaction of a mixture of an aliphatic/alicyclic acid chloride, bidentate directing auxiliary (e.g., 8-aminoquinoline) and an aryl iodide in the presence of the Pd(OAc)2catalyst and Ag2CO3additive directly afforded the corresponding β-C[sbnd]H-arylated N-(quinolin-8-yl)carboxamide derivative. To demonstrate the efficiency of the process, various bidentate directing auxiliaries were used and 8-Aminoquinoline was found to be the best directing group for accomplishing the one-pot Pd(II)-catalyzed, sp3C[sbnd]H activation and β-arylation of aliphatic/alicyclic carboxamides. A variety of aliphatic/alicyclic acid chlorides and aryl iodides were used as the substrates and several β-C[sbnd]H arylated carboxamide derivatives were synthesized in moderate to high yields via the multicomponent reaction strategy.

Simultaneously enhancement of quantum efficiency and color purity by molecular design in star-shaped solution-processed blue emitters

A series of fluorene-free bipolar star-shaped molecules, Sn-Cz-OXD (n = 1-5), with increasing conjugated length in branches were synthesized as high efficient blue emitters for OLEDs. With the extension of conjugated branches, the solid PL quantum efficiency and external quantum efficiency of Sn-Cz-OXD significantly increased with longer spacer, while the emission spectrum of these materials exhibited a blue-shift with enhanced color purity due to the unique molecular design. All materials maintained exceptionally high thermal stability after prolonged heat treatment at 150 °C in air. The photophysical, electrochemical, thermal properties of these emitters were studied in relation to the molecular structure. Nondoped device based on S4-Cz-OXD with structure ITO/PEDOT:PSS/EML/TPBI/LiF/Al emitted stable pure blue light with CIE coordinates of (0.157, 0.146). It exhibited high current efficiency and external quantum efficiency of 4.96 cd A-1 and 4.20%, respectively. These values are among the best results for solution-processed non-doped blue device based on fluorene-free materials, indicating its potential for commercial applications.

Starburst-Type Carbazole Trimers as Host Materials for Solution-Processed Phosphorescent OLEDs

Novel starburst-type carbazole trimers SB-1 and SB-2 were developed as hole-transporting host materials for phosphorescent organic light-emitting diodes (PhOLEDs). The triplet levels (T1s) of SB-1 and SB-2 were determined as at 2.81 and 2.73 eV

Starburst 4,4′,4′′-tris(carbazol-9-yl)-triphenylamine-based deep-blue fluorescent emitters with tunable oligophenyl length for solution-processed undoped organic light-emitting diodes

On the basis of a well-known hole transporting material, namely 4,4′,4′′-tris(carbazol-9-yl)-triphenylamine (TCTA), a series of star-shaped deep-blue fluorescent emitters (2P-TCTA, 3P-TCTA, 4P-TCTA and 5P-TCTA) have been successfully developed via a simpl