110230-97-2 Usage
Uses
Used in Organic Electronics:
[2,2':5',2''-Terthiophene]-5-carbonitrile is used as a semiconductor material for its potential application in organic field-effect transistors (OFETs) due to its electronic properties that allow for efficient charge transport and manipulation.
Used in Optoelectronics:
In the optoelectronics industry, [2,2':5',2''-Terthiophene]-5-carbonitrile is used as a light-emitting material for its potential application in organic light-emitting diodes (OLEDs), taking advantage of its optical properties to create efficient and versatile light sources.
Used in Material Development:
[2,2':5',2''-Terthiophene]-5-carbonitrile is utilized as a building block in the development of new materials for sensing applications, energy storage, and other technological advancements, thanks to its specific chemical reactivity and functionality imparted by the carbonitrile group.
Used in Synthetic Processes:
[2,2':5',2''-Terthiophene]-5-carbonitrile may also find use in various synthetic processes, where its unique structure and reactivity can be exploited to create novel molecules and materials with tailored properties for specific applications.
Check Digit Verification of cas no
The CAS Registry Mumber 110230-97-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,2,3 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 110230-97:
(8*1)+(7*1)+(6*0)+(5*2)+(4*3)+(3*0)+(2*9)+(1*7)=62
62 % 10 = 2
So 110230-97-2 is a valid CAS Registry Number.
110230-97-2Relevant academic research and scientific papers
Photochemical generation of radical cations from α-terthienyl and related thiophenes: Kinetic behavior and magnetic field effects on radical-ion pairs in micellar solution
Evans, Christopher H.,Scaiano
, p. 2694 - 2701 (2007/10/02)
The photochemistry of α-terthienyl (αT) and related compounds has been examined in homogeneous solution and in anionic micelles in the presence of electron acceptors. The absorption spectra of the radical cations from four thiophenic substrates have been characterized; for example, those derived from α-bithienyl (αB) and αT show absorption maxima at 420 and 530 nm, respectively. Triplet quenching by acceptors such as methyl viologen (MV2+) and tetracyanoethylene approaches diffusion control (k > 5 × 109 M-1 s-1). Quenching by oxygen, which is known to be dominated by singlet oxygen sensitization, involves electron transfer only to a minor extent; the highest efficiency, for αB, was only 6%. In micellar systems the behavior of the radical-ion pairs produced via electron transfer involves the competition of geminate and exit processes which occurs in the 10-7-10-6 s time domain. Both processes are slower in the larger micelles. Geminate processes are dramatically affected by magnetic fields. A model is proposed where the rate of geminate processes is suggested to depend upon the intramicellar reencounter frequency for the pair and the degree of singlet character in the triplet-derived radical-ion pair. The magnetic field effects observed are consistent with such a model.
