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1,3,5-tris(4-biphenyl-4'-carbonitrile)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

685114-67-4

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685114-67-4 Usage

Molecular structure

Three 4-biphenyl-4'-carbonitrile units linked to a central benzene ring

Shape

Rigid rod-shaped molecule

Thermal stability

High

Chemical stability

High

Applications

Organic semiconductors, liquid crystals, molecular electronics

Field of interest

Materials science

Potential use

Developing advanced electronic devices and materials

Check Digit Verification of cas no

The CAS Registry Mumber 685114-67-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,5,1,1 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 685114-67:
(8*6)+(7*8)+(6*5)+(5*1)+(4*1)+(3*4)+(2*6)+(1*7)=174
174 % 10 = 4
So 685114-67-4 is a valid CAS Registry Number.

685114-67-4Downstream Products

685114-67-4Relevant academic research and scientific papers

Control of intermolecular bonds by deposition rates at room temperature: Hydrogen bonds versus metal coordination in trinitrile monolayers

Sirtl, Thomas,Schloegl, Stefan,Rastgoo-Lahrood, Atena,Jelic, Jelena,Neogi, Subhadip,Schmittel, Michael,Heckl, Wolfgang M.,Reuter, Karsten,Lackinger, Markus

, p. 691 - 695 (2013)

Self-assembled monolayers of 1,3,5-tris(4′-biphenyl-4″- carbonitrile)benzene, a large functional trinitrile molecule, on the (111) surfaces of copper and silver under ultrahigh vacuum conditions were studied by scanning tunneling microscopy and low-energy electron diffraction. A densely packed hydrogen-bonded polymorph was equally observed on both surfaces. Additionally, deposition onto Cu(111) yielded a well-ordered metal-coordinated porous polymorph that coexisted with the hydrogen-bonded structure. The required coordination centers were supplied by the adatom gas of the Cu(111) surface. On Ag(111), however, the well-ordered metal-coordinated network was not observed. Differences between the adatom reactivities on copper and silver and the resulting bond strengths of the respective coordination bonds are held responsible for this substrate dependence. By utilizing ultralow deposition rates, we demonstrate that on Cu(111) the adatom kinetics plays a decisive role in the expression of intermolecular bonds and hence structure selection.

Pure Deep Blue Light-Emitting Diodes from Alternating Fluorene/Carbazole Copolymers by Using Suitable Hole-Blocking Materials

Lu, Jianping,Tao, Ye,D'iorio, Marie,Li, Yuning,Ding, Jianfu,Day, Michael

, p. 2442 - 2449 (2007/10/03)

The influences of the carbazole content on the photophysical, electrochemical, and electroluminescent properties of alternating fluorene/carbazole copolymers PFnCz (n = 1, 2, 3) with well-defined chemical structures have been systematically investigated. The incorporation of carbazole units into the polyfluorene (PF) backbone resulted in a blue shift of both the absorption and photoluminescence (PL) emission peaks, improved PL thermal stability, raised HOMO energy levels, and thus facilitated hole injection into the copolymers. Pure deep blue electroluminescence (EL) with narrow with (full width at the half-maximum) (39-52 nm) and negligible low-energy emission bands was successfully achieved from the PFnCz copolymers by using l,3,5-tris(4′-fluorobiphenyl-4-yl)benzene (F-TBB) as a hole-blocking layer and Alq3 as an electron injection/transporting layer. This device configuration stabilized the blue emission from the PF derivatives. An efficiency of 0.72 cd/A at a luminance of 100 cd/m2 was obtained even with aluminum metal as the cathode.

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