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Usage

Uses

Used in Heat Transfer Fluids:
3',5'-diphenylbiphenyl-4-aMine is used as a component in heat transfer fluids for its thermal stability and ability to efficiently transfer heat in various industrial processes.
Used in Plant Growth Regulation:
In the agricultural sector, 3',5'-diphenylbiphenyl-4-aMine is used as a plant growth regulator, potentially influencing the growth and development of plants to enhance crop yields or quality.
Used in Pharmaceutical Synthesis:
3',5'-diphenylbiphenyl-4-aMine serves as an intermediate or building block in the synthesis of various pharmaceuticals, contributing to the development of new drugs and medications.

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Downstream Products

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Relevant academic research and scientific papers

Quantitative treatment of surface potentials in Langmuir films from aromatic amphiphiles

It is shown that the surface potentials of Langmuir monolayers from aromatic compounds can be interpreted using the three-layer capacitor model of Demchak and Fort, with the same local dielectric constants employed for aliphatic compounds. Based on new da

Organic Mixed Valence Systems. II. Two-Centers and Three-Centers Compounds with Meta Connections around a Central Phenylene Ring

This paper is devoted to two new aromatic polyamines derived from p-EFTP (5'-(4-(bis(4-ethylphenyl)amino)phenyl-N,N,N',N'-tetrakis(4-ethylphenyl)-1,1':3',1"-terphenyl-4,4"-diamine) and exhibiting meta connections around a central phenylene ring.In p-EFDP (5'-phenyl-(N,N,N',N'-tetrakis(4-ethylphenyl)-1,1':3',1"-terphenyl-4,4"-diamine) there are only two redox sites instead of three.Upon partial oxidation, an intervalence transition is observed from which an electronic coupling very similar to the one of p-EFTP is obtained.In p-FADP (N,N,N',N',N",N"-hexakis(4-ethylphenyl)- 1,1':3',1"-terphenyl-4,4",5'-triamine) one finds two redox sites of the N,N'-bis(4-ethylphenyl)-4-aminobiphenyl type, and one redox site of the triphenylamine type.The analysis of the electrochemical behavior and of the intervalence transitions in the mono- and dioxidized species allows the distinction among the different types of electron transfer.

Azo bond formation on metal surfaces

The formation of azo compounds via redox cross-coupling of nitroarenes and arylamines, challenging in solution phase chemistry, is achieved by on-surface chemistry. Reaction products are analyzed with a cryogenic scanning tunneling microscope (STM) and X-ray photoelectron spectroscopy (XPS). By using well-designed precursors containing both an amino and a nitro functionality, azo polymers are prepared on surface via highly efficient nitro-amino cross-coupling. Experiments conducted on other substrates and surface orientations reveal that the metal surface has a significant effect on the reaction efficiency. The reaction was further found to proceed from partially oxidized/reduced precursors in dimerization reactions, shedding light on the mechanism that was studied by DFT calculations.

A halogen substituted of compounds of preparation method

The invention discloses a type 1 shown of compounds of halogen substituted preparation method, comprises the following steps: (1) condensation reaction: (2) Cyclization reaction: (3) The substitution reaction: (4) Coupling reaction: (5) Reduction reaction: (6) The diazotization reaction: Wherein X is selected from F, Cl, Br, I.

A halogen substituted of compounds of preparation method

The invention discloses a type 1 shown compound preparation method, comprises the following steps: (1) condensation reaction: (2) Cyclization reaction: (3) The substitution reaction: (4) Coupling reaction: (5) Reduction reaction: (6) The diazotization reaction: Wherein X is selected from F, Cl, Br, I.

COMPOUND, MATERIAL FOR ORGANIC ELECTROLUMINESCENT ELEMENTS, ORGANIC ELECTROLUMINESCENT ELEMENT AND ELECTRONIC DEVICE

A compound represented by formula (1) provides a high performance organic electroluminescence device and a novel material for realizing such an organic electroluminescence device: wherein R1 to R6, a to f, L1 to L3, and Ar are as defined in the description.