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Usage

Uses

Used in Pharmaceutical Industry:
(4-(dip-tolylamino)phenyl)Methanol is used as a building block for the synthesis of pharmaceuticals, due to its versatile chemical structure and potential antiviral and anti-inflammatory properties.
Used in Agrochemical Industry:
(4-(dip-tolylamino)phenyl)Methanol is used as a building block for the synthesis of agrochemicals, contributing to the development of new and effective products for agricultural applications.
Used in Dye Industry:
(4-(dip-tolylamino)phenyl)Methanol is used as a building block for the synthesis of dyes, due to its ability to form various colored compounds.
Used in Organic Electronic Materials:
(4-(dip-tolylamino)phenyl)Methanol is used as a component in the development of organic electronic materials, such as organic light-emitting diodes (OLEDs) and organic solar cells, due to its potential electronic properties.
Used in Coordination Chemistry:
(4-(dip-tolylamino)phenyl)Methanol is used as a ligand in coordination chemistry, enabling the formation of coordination complexes with various metal ions for applications in catalysis, sensing, and other areas.
Used in Medicinal Chemistry Research:
(4-(dip-tolylamino)phenyl)Methanol is used in medicinal chemistry research for the development of new drugs and therapeutic agents, given its antiviral and anti-inflammatory properties.

Upstream product

• 42906-19-4 4-[N,N-di(p-tolyl)amino]benzaldehyde 

Downstream Products

• 1049014-88-1 4-[N,N'-di-(p-tolyl)amino]benzyl(triphenyl)phosphonium bromide 
• 160064-57-3 4-[N,N-di(p-tolyl)amino]benzylphosphonic acid diethyl ester 

Relevant academic research and scientific papers

Evidence that ?"S? Controls Interfacial Electron Transfer Dynamics from Anatase TiO2 to Molecular Acceptors

Recombination of electrons injected into TiO2 with molecular acceptors present at the interface represents an important loss mechanism in dye-sensitized water oxidation and electrical power generation. Herein, the kinetics for this interfacial

Triphenylamine-Appended Half-Sandwich Iridium(III) Complexes and Their Biological Applications

Organometallic half-sandwich IrIII complexes of the type [(η5-Cpx)Ir(N^N)Cl]PF6 (Cpx: Cp* or its phenyl Cpxph or biphenyl Cpxbiph derivatives; N^N: triphenylamine (TPA)-substitut

Investigation of benzo(1,2-b:4,5-b′)dithiophene as a spacer in organic dyes for high efficient dye-sensitized solar cell

Two benzo(1,2-b:4,5-b′)dithiophene (denoted as BDT) based organic dyes, Dye 1 and Dye 2, containing triphenylamine and carbazole in the molecular frameworks respectively, were synthesized, characterized and applied in dye-sensitized solar cells (DSSCs). The photo-physical, photovoltaic, and electrochemical properties of the two dyes were analyzed in this work. The two dyes exhibit strong charge transfer absorption bands in the visible region. The dyes were applied in dye sensitized solar cells obtaining 11.34 mA/cm2, 0.75 V and 0.74, for the short-circuit photocurrent density (Jsc), open-circuit voltage (Voc), and fill factor (FF) respectively, corresponding to an overall power conversion efficiency of 6.3%. These results revealed that BDT-based dyes are promising dyes for DSSCs.

Synthesis and properties of novel hole-transporting materials with triphenylamine units

Two novel organic hole-transporting materials have been synthesized by combination of triphenylamines (TPA) via π-conjugated bonds using Wittig reaction. The structures were characterized by NMR, FT-IR and HRMS. The optical, electrochemical and thermal properties of the materials were studied in detail. The results show that these two compounds have blue emission, proper HOMO levels and high thermal stability. Furthermore, a quantum chemical calculation on electron distribution of the two compounds was performed, which suggests the current synthesized materials would be promising candidates for hole-transporting materials.

Synthesis and properties of new luminescent hole transporting materials containing triphenylamine and carbazole units

Two new blue luminescent hole transporting materials (HTM) containing triphenylamine, carbazole units and olefinic linkers (TM1 and TM2) were synthesized via Wittig reaction and characterized by 1H NMR, FT-IR, and HRMS. The compounds show good solubility in common organic solvents such as dichloromethane, chloroform, tetrahydrofuran and dimethyl formamide. Their optical, electrochemical and crystalline properties were investigated by using UV-Vis, photoluminescence (PL) spectra, cyclic voltammetry (CV) and differential scanning calorimetry (DSC), respectively. Quantum-chemical calculation was performed to obtain their optimized structures and the electron distribution of the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO) energy levels. The UV-Vis absorption and PL spectra of the two compounds in solid state were found to be similar to that when they were in dilute THF, which suggests that these compounds remain as an amorphous state in solid films. CV measurements show that the two compounds embody suitable HOMO levels (in a range of -5.28 to -5.23 eV) for hole injection, which is consistent with the calculation consequence. Two compounds possess high glass-transition temperature (Tg) at 96.61 and 90.74 °C for TM1 and TM2, respectively, suggesting the two compounds could form stable amorphous glassy states. The experimental results show that the synthesized compounds have great potential for application in organic light-emitting devices (OLEDs).