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C18H8S4*2C12H4N4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

42439-34-9

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42439-34-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42439-34-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,4,3 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 42439-34:
(7*4)+(6*2)+(5*4)+(4*3)+(3*9)+(2*3)+(1*4)=109
109 % 10 = 9
So 42439-34-9 is a valid CAS Registry Number.

42439-34-9Downstream Products

42439-34-9Relevant academic research and scientific papers

Tamperature Dependence of Magnetic Susceptibilities of (TTT)(TCNQ) and (TTT)(TCNQ)2

Takahashi, Masashi,Sugano, Tadashi,Kinoshita, Minoru

, p. 26 - 35 (1984)

Static magnetic susceptibility and ESR studies of 1:1 and 1:2 charge-transfer complexes of naphthacenobisdithiole and 2,2'-(2,5-cyclohexadiene-1,4-diylidene)bis(propanedinitrile) in the temperature region of 2-310 K are described. (TTT)(TCNQ)2 exhibits a temperature dependent spin susceptibility, while the spin susceptibility of (TTT)(TCNQ) is almost independent of temperature.Spin susceptibilities of the TTT and TCNQ chains, which are evaluated with a g-value decomposition technique, are interpreted in terms of aone-dimensional Hubbard model.In both complexes, the on-site Coulomb repulsion is comparable with or larger than the band width on the TCNQ chains and is smaller on the TTT chains.Two magnetic phase transitions are observed in (TTT)(TCNQ)2.The transition is driven in each chain independently by the Peierls instability.The amount of charge transfer in (TTT)(TCNQ) is determined to be 0.73+/-0.05 from an X-ray photoelectron spectroscopic study.

Electrochemical Behavior of Donor-Tetracyanoquinodimethane Electrodes in Aqueous Media

Jaeger, Calvin D.,Bard, Allen J.

, p. 5435 - 5442 (2007/10/02)

Electrodes prepared as compacted pellets from conductive donor-acceptor complexes of tetraquinodimethane (TCNQ) with several donors (D) (tetrathiotetracene, acridine, quinoline, N-methylphenazine, 2,2'- and 4,4'-bipyridine) were investigated in aqueous solutions.The results were compared to those of a previous investigation of TTF-TCNQ pellets (TTF = tetrathiafulvalene) and to results on single crystals of TTF-TCNQ reported here.The electrodes are stable over a potential region in which they could be employed as inert electrodes.The potential limits depended upon the stabilization gained upon complexation and the relative electrode potentials of the constituent compounds.Upon exceeding the potential limits of stability of the electrode, the electrode was reduced or oxidized.Subsequent voltammograms showed peaks attributable to insoluble compounds formed on the electrode surface.The potentials observed for the redox processes could be correlated to the degree of charge transfer, ρ, as well as gas-transfer ionization potentials and electron affinities.

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