1601465-06-8

Usage

Uses

Used in Organic Electronics:
1,1-diphenyl-2,2-di(4-formylphenyl)ethylene is used as a building block in the synthesis of organic molecules and materials for its potential applications in the field of organic electronics. Its unique structure and reactivity make it a valuable component in the development of organic light-emitting diodes (OLEDs), which are widely used in display and lighting technologies.
Used in Photoresponsive Materials and Sensors:
1,1-diphenyl-2,2-di(4-formylphenyl)ethylene is also utilized in the design of photoresponsive materials and sensors due to its light-sensitive properties. Its ability to undergo structural changes upon exposure to light makes it a promising candidate for applications in optoelectronics and molecular switches.
Used in Pharmaceutical Research:
1,1-diphenyl-2,2-di(4-formylphenyl)ethylene has been investigated for its potential biological activities, including its potential as an antitumor agent. Its unique structure and reactivity may contribute to its ability to interact with biological targets, making it a candidate for further research in the development of novel therapeutic agents.
Used in Cellular Function Studies:
Additionally, 1,1-diphenyl-2,2-di(4-formylphenyl)ethylene has been studied for its effects on cellular function. Understanding its interactions with cells and biological systems can provide insights into its potential applications in the field of cell biology and may lead to the discovery of new mechanisms of action for therapeutic intervention.

Upstream product

• 2592-73-6 1,1-dibromo-2,2-diphenylethylene 
• 87199-17-5 4-formylphenylboronic acid, 
• 1122-91-4 4-bromo-benzaldehyde 
• 119-61-9 benzophenone 

Relevant academic research and scientific papers

Opposite mechanoluminescence behavior of two isomers with different linkage positions

Two isomers of mm-TPE(PI)2 and pp-TPE(PI)2, constructed by the two same aromatic blocks of tetraphenylethene and phenanthro[9,10-d]imidazole, exhibit totally different mechanoluminescence, as a result of the ignorable different linkage positions on the tetraphenylethene moiety. Detailed analysis and theoretical calculations demonstrate the structure-packing-property relationship of organic mechanoluminescent luminogens, with the emphasis on the important role of molecular packing in the solid state.

Photo-activated I-type photosensitizer as well as preparation method and application thereof

The invention belongs to the technical field of biological imaging treatment materials, and discloses a photo-activated I-type photosensitizer as well as a preparation method and application thereof. The photo-activated I-type photosensitizer has a struct

Photoinduced crystallization isoquinoline salt compound, preparation method and application thereof, and preparation method of nanocrystal

The invention belongs to the technical field of photoresponse materials, and discloses a photoinduced crystallization isoquinoline salt compound, a preparation method and application thereof, and a preparation method of nanocrystals, and the preparation m

Divergent and Stereoselective Synthesis of Tetraarylethylenes from Vinylboronates

The synthesis of a new tetraborylethylene (TBE) is reported, and its application in the preparation of [4+0]-tetraarylethenes (TAEs) is elucidated. TAEs have widespread applications in material science and supramolecular chemistry due to their aggregation-induced emission (AIE) properties. The divergent and stereoselective synthesis of [3+1]-, [2+2]-, and [2+1+1]-TAEs via multiple couplings of vinylboronates with aryl bromides is demonstrated. These couplings feature a broad substrate scope and excellent functional group compatibility due to mild reaction conditions. Facile access to various tetraarylethenes is provided. This strategy represents an important complement to the conventional methods employed for the synthesis of TAEs, and would be a valuable tool for synthesizing TAE-based molecules useful in functional materials, biological imaging and chemical sensing.