18870-40-1

Usage

Uses

Used in Organic Synthesis:
Tris(4-methylphenyl)(phenyl)silane is used as a cross-coupling reagent for the formation of carbon-silicon bonds. This application is crucial in the synthesis of various organic compounds that require Si-C linkages.
Used in Electronic Materials Production:
This organosilicon compound is utilized in the production of electronic materials, where its properties can contribute to the performance and functionality of these materials.
Used in Advanced Functional Polymers Synthesis:
Tris(4-methylphenyl)(phenyl)silane is also a component in the synthesis of advanced functional polymers, where its silicon-containing groups can enhance the polymers' characteristics and performance.
Used in Research and Development:
Due to its unique structure, tris(4-methylphenyl)(phenyl)silane is valuable in research and development for exploring new applications and properties of organosilicon compounds in various industries.

Upstream product

• 2417-95-0 p-tolyllithium 
• 98-13-5 Phenyltrichlorosilane 
• 106-38-7 para-bromotoluene 

Downstream Products

• 1361962-07-3 5,5',5''-((phenylsilanetriyl)tris(benzene-4,1-diyl))tris(2-phenyl-1,3,4-oxadiazole) 
• 61414-17-3 4,4′,4″-(phenylsilanetriyl)tribenzoic acid 
• 445429-82-3 4,4',4''-(phenylsilanetriyl)tribenzoyl chloride 

Relevant academic research and scientific papers

Entangled Uranyl Organic Frameworks with (10,3)-b Topology and Polythreading Network: Structure, Luminescence, and Computational Investigation

Two 3D uranyl organic frameworks (UOFs) with entangled structures, (HPhen)2[(UO2)2L2]·4.5H2O (1) and [(UO2)3(H2O)4L2]·6H2O (2), were synthesized using a rigid tripodal linker (4,4′,4″-(phenylsilanetriyl)tribenzoic acid, H3L). Compound 1 represents a 2-fold interpenetrating UOF with the unique (10,3)-b topology. Compound 2 is composed of three interlocked sets of identical singlet networks and thus exhibits a rare 3D polythreading network with (3,4)-connected topology. These two compounds have been characterized by IR, UV-vis, and photoluminescent spectroscopy. A density functional theory (DFT) study on the model compounds of 1 and 2 shows good agreement of structural parameters and U=O stretching vibrational frequencies with experimental data. The experimentally measured absorption bands were well reproduced by the time-dependent DFT calculations.

Ueber Tetraaryl-Methan-Analoga in der Gruppe 14. II. Ph4-nSi-p-Toln und Ph4-nSn-p-Toln (n = 0 bis 4): Einfluss der p-Tolyl-Substituenten auf Struktur und NMR-chemische Verschiebungen

The title compounds have been synthesized by Li and Grignard reactions.The crystal structure of Ph3Si-p-Tol has been determined.The substitution of only one phenyl by one p-tolyl group causes only a slight deviation from the ideal S4 symmetry of Ph4Si.Gra