62608-15-5

Basic information

• Product Name: 3,3'-(1,4-Phenylenedi-2,1-ethenediyl)bis(9-ethyl-9H-carbazole)
• Synonyms: BCzVB;3,3'-(1,4-Phenylenedi-2,1-ethenediyl)bis(9-ethyl-9H-carbazole);1,4-Bis(9-ethyl-3-carbazovinylene)benzene;1,4-Bis[2-(3-N-ethylcarbazoryl)vinyl]benzene;3,3'-(1,4-Phenylened;BCzVB , 3,3'-(1,4-Phenylenedi-2,1-ethenediyl)bis(9-ethyl;BCZVB, 1,4-bis[2-(3-N-ethylcarbazoryl)vinyl]benzene;1,4-Bis[2-(9-ethylcarbazol-3-yl)vinyl]benzene
• CAS NO: 62608-15-5
• Molecular Formula: C38H32N2
• Molecular Weight: 516.67
• Product Categories: OLED
• Mol File: 62608-15-5.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 744.9±60.0 °C(Predicted)
• Appearance: /
• Density: 1.11
• CAS DataBase Reference: 3,3'-(1,4-Phenylenedi-2,1-ethenediyl)bis(9-ethyl-9H-carbazole)(CAS DataBase Reference)
• NIST Chemistry Reference: 3,3'-(1,4-Phenylenedi-2,1-ethenediyl)bis(9-ethyl-9H-carbazole)(62608-15-5)
• EPA Substance Registry System: 3,3'-(1,4-Phenylenedi-2,1-ethenediyl)bis(9-ethyl-9H-carbazole)(62608-15-5)

Safety Data

• Hazardous Substances Data: 62608-15-5(Hazardous Substances Data)

Usage

Uses

Used in Display Industry:
3,3'-(1,4-Phenylenedi-2,1-ethenediyl)bis(9-ethyl-9H-carbazole) is used as a blue emitter for full color displays. Its ability to emit blue light makes it a valuable component in creating vibrant and high-quality color displays.
Used in Organic Light Emitting Diodes (OLEDs) Industry:
3,3'-(1,4-Phenylenedi-2,1-ethenediyl)bis(9-ethyl-9H-carbazole) is used as a blue emitter in double emitting layers for white OLEDs (WOLEDs). This application takes advantage of the compound's blue light emission properties to create white light, which is essential for various lighting and display applications. The use of this compound in WOLEDs can lead to improved energy efficiency and longer device lifetimes.

Upstream product

• 7570-45-8 N-ethyl-3-carbazolealdehyde 
• 106-42-3 para-xylene 

Relevant articles and documents

Four new two-photon polymerization initiators with varying donor and conjugated bridge: Synthesis and two-photon activity

A specific series of dumbbell-shaped bis-carbazoles or bis-phenothiazines dyes (1, 2, 3 and 4) constructed with styrene or biphenylethyne as the π-bridge have been synthesized and characterized. Detailed spectral properties including linear absorption, one and two-photon fluorescence properties were investigated. The results show that extending conjugated chain and introducing donors have substantial effect on their photophysical properties. Among them, two-photon absorption cross sections (σ) of the four dyes in DMF determined by the Z-scan technique are successively increased from 1 to 4 with enhancing electron-donating ability and extending conjugated chain, but electron-donating ability has larger contribution to the σ values than extending conjugated chain based on the comparison of small molecules (D-π-D). Two-photon initiation polymerization (TPIP) microfabrication experiments have been carried out using compound 4 as an initiator under irradiation of 200 fs, 76 MHz femtosecond laser at 760 nm. The results confirm that the four dyes can be effectively used as organic two-photon photopolymerization initiators.

Ruthenium-Sulfonamide-Catalyzed Direct Dehydrative Condensation of Benzylic C-H Bonds with Aromatic Aldehydes

The first catalytic dehydrative condensation of the benzylic C-H bonds of toluene and p-xylene with aromatic aldehydes is reported herein. This protocol provides highly atom-economical access to stilbene and p-distyrylbenzene derivatives, whereby water is the sole byproduct. The reaction is based on the deprotonation-functionalization of benzylic C-H bonds through η6-complexation of the arenes, which is realized for the first time using a catalytic amount of a transition metal activator. The key to the success of this method is the use of a sulfonamide anion as a catalyst component, which appears to facilitate not only the deprotonation of the benzylic C-H bonds but also the formation of a C-C bonds via an electrophilic tosylimine intermediate.