64394-47-4 Usage
Uses
Used in Coordination Chemistry:
BIS(CARBONYLDITHIO)TETRATHIAFULVALENE is used as a ligand for forming stable complexes with transition metal ions. Its ability to coordinate with metals is crucial in the development of new materials and catalysts.
Used in Materials Science:
In the field of materials science, BIS(CARBONYLDITHIO)TETRATHIAFULVALENE is utilized as a building block for the synthesis of various organic compounds. Its unique structure and reactivity contribute to the creation of advanced materials with specific properties.
Used in Catalysis:
BIS(CARBONYLDITHIO)TETRATHIAFULVALENE is employed as a catalyst or a catalyst component in various chemical reactions. Its interaction with transition metal ions enhances the catalytic activity and selectivity of the reactions it is involved in.
Used in Organic Electronics:
BIS(CARBONYLDITHIO)TETRATHIAFULVALENE is used in organic electronics due to its interesting electronic properties. Its incorporation into electronic devices can potentially improve their performance and efficiency.
Used in Molecular Electronics:
BIS(CARBONYLDITHIO)TETRATHIAFULVALENE also has potential applications in molecular electronics, where its unique electronic characteristics can be harnessed for the development of molecular-scale electronic components and systems.
Check Digit Verification of cas no
The CAS Registry Mumber 64394-47-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,3,9 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 64394-47:
(7*6)+(6*4)+(5*3)+(4*9)+(3*4)+(2*4)+(1*7)=144
144 % 10 = 4
So 64394-47-4 is a valid CAS Registry Number.
InChI:InChI=1/C8O2S8/c9-7-15-3-4(16-7)12-1(11-3)2-13-5-6(14-2)18-8(10)17-5
64394-47-4Relevant academic research and scientific papers
Tetrathiafulvalenes. XIX. Synthesis and Properties of Electron Conducting Poly-Dithiolene Complexes with Ethylene Tetrathiolat and Tetrathiafulvalene Tetrathiolat as Bridge Ligands
Poleschner, H.,John, W.,Hoppe, F.,Fanghaenel, E.
, p. 957 - 975 (2007/10/02)
-Dithiolo-1,3-dithiol-2,5-dione 7 and 5-(5-oxo-dithiolo-1,3-dithiole-2-ylidene)-dithiolo-1,3-dithiol-2-one 8 were synthesized from 1,3-dithiole-2-thione-4,5-dithiolat.The ligands react with salts of iron, cobalt, nickel
ELECTROCHEMICAL REDUCTION OF CARBON DISULFIDE. SYNTHESIS OF CARBON SULFIDE HETEROCYCLES
Hurley, Michael F.,Chambers, James Q.
, p. 775 - 778 (2007/10/02)
Detailed procedures for the electrochemical reduction of carbon disulfide in N,N-dimethylformamide and acetonitrile are given.The synthetic utility of the method is demonstrated by the preparation of several thio-substituted derivatives of tetrathiafulvalene.Cyclic voltammograms of the tetrapotassium salt of the tetrathio anion of tetrathiofulvalene indicate four successive electron-transfer steps and in situ formation of a C6S8 species.Oxidation of the CS2 electrolysis solutions produces a compound which is tentatively identified as dithiolo-1,2,3-trithiole-5-thione.
Tetrathiapentalene and tetraselenapentalene compounds
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, (2008/06/13)
This application is concerned with tetrathiapentalene and tetraselenapentalene compounds. Specifically, it is concerned with 1, 3, 4, 6-tetrathia-2, 5-dihetero-pentalene and 1, 3, 4, 6-tetraselena-2,5-dihetero-pentalene compounds having the formula STR1 w
