- 7,7,8,8-Tetracyanoquinodimethane - 1518-16-7, C12H4N4, density, melting . . .
7,7,8,8-Tetracyanoquinodimethane - cas 1518-16-7, synthesis, structure, density, melting point, boiling point
- Tetracyanoquinodimethane - Wikipedia
TCNQ is prepared by the condensation of 1,4-cyclohexanedione with malononitrile, followed by dehydrogenation of the resulting diene with bromine: [2] The molecule is planar, with D 2h symmetry [3] Like tetracyanoethylene (TCNE), TCNQ is easily reduced to give a blue-coloured radical anion
- Tetracyanoquinodimethane | C12H4N4 | CID 73697 - PubChem
Tetracyanoquinodimethane is an organic compound of cyanide It is an electron-acceptor that is used to prepare charge transfer salts, which are of interest in the area of molecular electronics
- 7,7,8,8-Tetracyanoquinodimethane 98 1518-16-7 - MilliporeSigma
7,7,8,8-Tetracyanoquinodimethane (TNCQ) is a strong electron acceptor as it has four cyano groups and π-conjugation bonds that form charge transferring chains and ion radical salts which are mainly used as p-dopants for the fabrication of a variety of semiconductor applications
- Optoelectronic Properties of Tetracyanoquinodimethane (TCNQ) Related . . .
Tetracyanoquinodimethane (TCNQ) and related compounds are thoroughly investigated as potential innovative organic semiconductors and singlet fission (SF) materials
- 7,7,8,8-Tetracyanoquinodimethane 1518-16-7 | TCI AMERICA
CAS RN: 1518-16-7 | Product Number: T0078 7,7,8,8-Tetracyanoquinodimethane Purity: >98 0% (HPLC) (N) Synonyms: 1,4-Bis (dicyanomethylene)cyclohexadiene TCNQ
- Tetracyanoquinodimethane - an overview | ScienceDirect Topics
Tetracyanoquinodimethane (TCNQ) is defined as a compound with four strong electron-accepting cyano groups, widely used as an electron acceptor in organic electronics due to its significant electron-accepting properties
- 7,7,8,8-Tetracyanoquinodimethane | 1518-16-7 - ChemicalBook
In 1960, the organic acceptor Tetracyanoquinodimethane (TCNQ; 7,7,8,8-Tetracyanoquinodimethane) was synthesized, as well as a great number of its conducting charge-transfer complexes and radical ion salts In the 1970s, the organic donor TTF led to the first organic metal TTF-TCNQ
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