Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Tetraselenafulvalene

Tetraselenafulvalene, tetramethyl-, hexafluorophosphate-, TCNQ salt X-ray, 1, 355 <79AX(B)772>... [Pg.59]

Tetraselenafulvalene, hexamethylene— see A-2,2 -Bi-4,5-trimethylene-1,3-diselenolylidene Tetraselenafulvalenes H NMR, 6, 958 mass spectra, 6, 955 PE spectra, 6, 953 Raman spectra, 6, 954, 955 synthesis, 6, 971 UV spectra, 6, 952 vertical ionization potential, 6, 953 Tetraselenafulvalenes, diphenyl-synthesis, 6, 963... [Pg.850]

Tetraselenafulvalenes, tetramethyl-Raman spectra, 6, 954, 955 structure, 6, 950 UV spectra, 6, 952 Tetraselenafulvalenes, tetraphenyl-synthesis, 6, 963 1,3,5,7-T etrasilaadamantane formation, 1, 622 Tetrasilabicyclo[3.3. l]octane synthesis, I, 622 T etratellurafulvalenes IR spectra, 6, 954... [Pg.850]

Tetrathia- and tetraselenafulvalenes, polythiophenes and related compounds, polypyridines as organic electronic conductors 97YGK410. [Pg.218]

A series of papers describing detailed studies on dibromo- and diiodo-dithiadiselenafulvalene and tetraselenafulvalene derivatives has appeared including examples such as 54 <06JMAC4110>, 55 <06JMAC3381>, 56 and 57 <06JMAC162> and 58... [Pg.281]

The following compounds are the most popular donors for organic metals (see Scheme 8.9) TTF, tetraselenafulvalene (TSeF), tetrathiatetracene (TTT), tetraselenatetracene (TSeT), tetra-methyl tetraselenafulvalene (TMeTSeF), bis(thiadimethylene) tetrathiafulvalene (BTDM-TTF), bis(ethylenedithia) tetrathiafulvalene (BEDT TTF or ET), tetrakis(methyltelluro) tetrathiafulvalene (TTeCj-TTF), tetramethylbis(ethylenedithia) tetrathiafulvalene (TMET), 2,2 -(2,6-naphthalenediy-lydene) bis(l,3-dithiole) (NBDT). All the abbreviations are those used in the current literature. [Pg.410]

Tables 1.1 and 1.2 show the most relevant organic and hybrid organic-inorganic molecules used throughout the body of the book in alphabetical order. The schemes of the molecules go hand in hand with their most commonly accepted acronyms as well as reduced chemical names. Instead of using the well-established International Union of Pure and Applied Chemistry (lUPAC) convention for unequivocally identifying the molecules, we follow a reduced formulation, thinking more of the non-chemist communities. For instance, 7,7,8,8-tetracyano-/ -quinodimethane will be simplified to tetracyano-quinodimethane and 2,3,6,7-tetramethyl-l,4,5,8-tetraselenafulvalene to tetramethyl-tetraselenaful-valene. In general the reduction will consist in removing the numeric locators. This modification should not affect the comprehension of the issues described in the hook. In case of douht it is recommended to consult the schemes in the mentioned tables. The molecules will be classified in the next sections... Tables 1.1 and 1.2 show the most relevant organic and hybrid organic-inorganic molecules used throughout the body of the book in alphabetical order. The schemes of the molecules go hand in hand with their most commonly accepted acronyms as well as reduced chemical names. Instead of using the well-established International Union of Pure and Applied Chemistry (lUPAC) convention for unequivocally identifying the molecules, we follow a reduced formulation, thinking more of the non-chemist communities. For instance, 7,7,8,8-tetracyano-/ -quinodimethane will be simplified to tetracyano-quinodimethane and 2,3,6,7-tetramethyl-l,4,5,8-tetraselenafulvalene to tetramethyl-tetraselenaful-valene. In general the reduction will consist in removing the numeric locators. This modification should not affect the comprehension of the issues described in the hook. In case of douht it is recommended to consult the schemes in the mentioned tables. The molecules will be classified in the next sections...
Kobayashi H, Kobayashi A, Cassoux P (2000) BETS as a source of molecular magnetic superconductors (BETS = bis(ethylenedithio)tetraselenafulvalene). Chem Soc Rev 29 325-333... [Pg.120]

Kato R, Aonuma S, Okano Y, Sawa H, Tamura M, Kinoshita M, Oshima K, Kobayashi A, Bun K, Kobayashi H (1993) Metallic and supCTConducting salts based on an unsymmetrical Tt-donor dimethyl(ethylenedithio)tetraselenafulvalene (DMET-TSeF). Synth Met 61 199-206... [Pg.121]

Tanaka H, Ojima E, Eujiwara H, Nakazawa Y, Kobayashi H, Kobayashi A (2000) A new K-type organic superconductor based on BETS molecules, K-(BETS)2GaBr4 [BETS = bis (ethylenedithio)tetraselenafulvalene]. J Mater Chem 10 245-247... [Pg.122]

See other pages where Tetraselenafulvalene is mentioned: [Pg.977]    [Pg.999]    [Pg.59]    [Pg.59]    [Pg.59]    [Pg.59]    [Pg.275]    [Pg.192]    [Pg.207]    [Pg.785]    [Pg.787]    [Pg.3]    [Pg.3]    [Pg.57]    [Pg.79]    [Pg.716]    [Pg.523]    [Pg.7]    [Pg.8]    [Pg.8]    [Pg.9]    [Pg.123]    [Pg.87]    [Pg.348]    [Pg.59]    [Pg.59]    [Pg.59]    [Pg.59]    [Pg.238]   
See also in sourсe #XX -- [ Pg.201 ]

See also in sourсe #XX -- [ Pg.118 , Pg.126 , Pg.129 ]

See also in sourсe #XX -- [ Pg.256 , Pg.258 ]

See also in sourсe #XX -- [ Pg.201 ]

See also in sourсe #XX -- [ Pg.215 ]

See also in sourсe #XX -- [ Pg.280 ]



SEARCH



Bis tetraselenafulvalene

Dimethyl -tetraselenafulvalene

Reactivity of Tetraselenafulvalenes

Tetraselenafulvalene cation-radicals

Tetraselenafulvalene complexes

Tetraselenafulvalene derivative

Tetraselenafulvalene ionization potential

Tetraselenafulvalene structure

Tetraselenafulvalene, tetramethyl

Tetraselenafulvalenes

Tetrathia- and Tetraselenafulvalenes, reactivity

Tetrathia- and tetraselenafulvalenes

© 2024 chempedia.info