1263774-65-7

Usage

Chemical structure

The compound consists of two units of 1,2-diphenylethene linked together by a central ethynyl group with trimethylsilyl substituents.

Derivative

It is a derivative of ethynylbenzene and diphenylethene.

Application

Commonly used in organic synthesis and material science.

Structural features

Known for its unique structural features.

Building block

Often employed as a building block for the construction of novel organic molecules and materials with specific properties.

Trimethylsilyl groups

The presence of trimethylsilyl groups contributes to the compound's stability and reactivity.

Versatility

It is a versatile tool for various applications in chemistry and material science.

Stability

The trimethylsilyl groups enhance the stability of the compound.

Reactivity

The trimethylsilyl groups also increase the reactivity of the compound, making it suitable for various chemical reactions.

Organic synthesis

The compound is used in the synthesis of complex organic molecules.

Material science

It is also used in the development of new materials with specific properties.

Novel organic molecules

The compound can be used to create novel organic molecules with unique properties.

Specific properties

The compound can be used to create materials with specific properties, such as optical, electronic, or mechanical properties.

Chemical reactions

The compound can participate in various chemical reactions due to its reactivity.

Building block for materials

The compound can be used as a building block for the construction of materials with specific properties.

Upstream product

• 184239-35-8 1,2-bis(4-bromophenyl)-1,2-diphenylethylene 
• 1066-54-2 trimethylsilylacetylene 
• 90-90-4 (4-bromophenyl)(phenyl)methanone 
• 586-76-5 4-Bromobenzoic acid 
• 71-43-2 benzene 

Downstream Products

• 1380324-43-5 1,2-bis{4-[1-(6-phenoxyhexyl)-1,2,3-triazol-4-yl]phenyl}-1,2-diphenylethene 
• 1240785-42-5 1,2-bis(4-ethynylphenyl)-1,2-diphenyl-ethene 

Relevant academic research and scientific papers

Halogen Bonding Tetraphenylethene Anion Receptors: Anion-Induced Emissive Aggregates and Photoswitchable Recognition

A series of tetraphenylethene (TPE) derivatives functionalized with highly potent electron-deficient perfluoroaryl iodo-triazole halogen bond (XB) donors for anion recognition are reported. 1H NMR titration experiments, fluorescence spectroscopy, dynamic light scattering measurements, TEM imaging and X-ray crystal structure analysis reveal that the tetra-substituted halogen bonding receptor forms luminescent nanoscale aggregates, the formation of which is driven by XB-mediated anion coordination. This anion-coordination-induced aggregation effect serves as a powerful sensory mechanism, capable of luminescence chloride sensing at parts per billion concentration. Furthermore, the doubly substituted geometric isomers act as unprecedented photoswitchable XB donor anion receptors, where the composition of the photostationary state can be modulated by the presence of a coordinating halide anion.

Fluorescence responsive conjugated poly(tetraphenylethene) and its morphological transition from micelle to vesicle

A crown ether-functionalized poly(tetraphenylethene) (AP-TPE) is synthesized and the rotation of the TPE group is successfully restricted via the complexation of crown ether and organic ammonium salts, leading to a stepwise enhanced fluorescence accompani

Luminogenic materials constructed from tetraphenylethene building blocks: Synthesis, aggregation-induced emission, two-photon absorption, light refraction, and explosive detection

Luminogenic molecules [(TPE)3 (1), TPE-C = C-TPE-C = C-TPE (2), and TPE-C≡C-TPE-C≡C-TPE (3)] and their polymers P1-P3 are constructed from tetraphenylethene (TPE) building blocks in high yields by Suzuki, Witting, and Sonogashira coupling react

High solid-state efficiency fluorescent main chain liquid crystalline polytriazoles with aggregation-induced emission characteristics

Fluorescent liquid crystals (LCs) have wide applications in optoelectronic devices. However, the synthesis of high solid-state emission efficiency LCs is difficult. On one hand, impeding the aggregation of traditional luminogens is the prerequisite for hi

Hyperbranched polytriazoles with high molecular compressibility: Aggregation-induced emission and superamplified explosive detection

Hyperbranched polytriazoles with spring-like architectures exhibit the feature of aggregation-induced emission (AIE) due to the high compressibility of polymer spheres from solution to aggregate. Thanks to their AIE effect, the polymer nanoaggregates can