55035-42-2 Usage
Uses
Used in Organic Semiconductors:
4,4'-((1E,1'E)-1,4-phenylenebis(ethene-2,1-diyl))bis(N,N-diphenylaniline) is used as a dopant in organic semiconductors for enhancing their electrical and optical properties.
Used in Organic Light-Emitting Diodes (OLEDs):
In the Electronics Industry, 4,4'-((1E,1'E)-1,4-phenylenebis(ethene-2,1-diyl))bis(N,N-diphenylaniline) is used as a component in the production of OLEDs for its high charge carrier mobility and good thermal stability, contributing to improved device performance and reliability.
Used in Organic Photovoltaic Cells:
In the Renewable Energy Industry, 4,4'-((1E,1'E)-1,4-phenylenebis(ethene-2,1-diyl))bis(N,N-diphenylaniline) is used as a component in the production of organic photovoltaic cells to improve their efficiency and stability due to its desirable electronic properties.
It is important to handle and use 4,4'-((1E,1'E)-1,4-phenylenebis(ethene-2,1-diyl))bis(N,N-diphenylaniline) with caution, as it may pose some health and environmental risks if not properly managed.
Check Digit Verification of cas no
The CAS Registry Mumber 55035-42-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,0,3 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 55035-42:
(7*5)+(6*5)+(5*0)+(4*3)+(3*5)+(2*4)+(1*2)=102
102 % 10 = 2
So 55035-42-2 is a valid CAS Registry Number.
55035-42-2Relevant academic research and scientific papers
TPA-active D-π-D fluorophores with rigid, planar cores from phenylene to indenofluorene and indolocarbazole
Liu, Zhiqiang,Cao, Duxia,Chen, Ying,Fang, Qi
experimental part, p. 63 - 67 (2010/11/04)
A series of D-π-D quadrupolar fluorophores with systematically varied π-conjugated cores were prepared using the Heck reaction and their single- and two-photon photophysical properties were examined. Introduction of extended π-conjugated cores such as indenofluorene/indolocarbazole was found to induce only small shifts in the absorption and emission maxima versus the phenylene linked fluorophore but greatly enhance their single- and two-photon absorption cross-sections. The effects of positional substitution on the properties of the indolocarbazole derivatives were also investigated.
