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Perylene conductivity

Perylene-3,4,9,10-bis(dicarbonamide) electrical conductivity, 1, 358 Perylene hexafluoroarsenate conductors, 1, 355 Perylene vat dyes, 1, 336-337 Pestalotin synthesis, 3, 841 Pethidine... [Pg.739]

Since the discovery of the first organic semiconductor perylene-bromine complex in 1954 [1], a large number of molecular conductors, including more than 100 molecular superconductors, have been prepared. Conducting molecular materials are characterized by the following features ... [Pg.37]

It has been reported that the electrical properties of single molecules incorporating redox groups (e.g. viologens [114, 119, 120, 123, 124], oligophenylene ethynylenes [122, 123], porphyrins [111, 126], oligo-anilines and thiophenes [116, 127], metal transition complexes [118,128-132], carotenes [133], ferrocenes [134,135],perylene tetracarboxylic bisimide [93, 136, 137] and redox-active proteins [138-143]), can be switched electrochemically. Such experiments, typically performed by STM on redox-active molecules tethered via Au-S bonds between a gold substrate and a tip under potential control, allow the possibility to examine directly the correlation between redox state and the conductance of individual molecules. [Pg.96]

Chemically Controlled Conductance of Perylene Bisimide Derivatives. 167... [Pg.122]

Redox molecules are particularly interesting for an electrochemical approach, because they offer addressable (functional) energy states in an electrochemically accessible potential window, which can be tuned upon polarization between oxidized and reduced states. The difference in the junction conductance of the oxidized and the reduced forms of redox molecules may span several orders of magnitude. Examples of functional molecules used in these studies include porphyrins [31,153], viologens [33, 34,110,114,154,155], aniline and thiophene oligomers [113, 146, 156, 157], metal-organic terpyridine complexes [46, 158-163], carotenes [164], nitro derivatives of OPE (OPV) [165, 166], ferrocene [150, 167, 168], perylene tetracarboxylic bisimide [141, 169, 170], tetrathia-fulvalenes [155], fullerene derivatives [171], redox-active proteins [109, 172-174], and hydroxyquinones [175]. [Pg.133]

Fig. 5 Main contamination sources identified by PCA for sediments, fish, and suface water in the Ebro River basin, and explained variances for each principal component. Variable identification. Organic compounds in sediments 1, summatory of hexachlorocyclohexanes (HCHs) 2, summa-tory of DDTs (DDTs) 3, hexachlorobenzene (HCB) 4, hexachlorobutadiene (HCBu) 5, summatory of trichlorobenzenes (TCBs) 6, naphthalene 7, fluoranthene 8, benzo(a)pyrene 9, benzo(b) fluoranthene 10, benzo(g,h,i)perylene 11, benzo(k)fluoranthene 12, indene(l,2,3-cd)pyrene. Organic compounds in fish 1, hexachlorobenzene (HCB) 2, summatory of hexachlorocyclohexanes (HCHs) 3, o,p-DDD 4, o,p-DDE 5, o,p-DDT 6, p,p-DDD 7, />,/>DDE 8, />,/>DDT 9, summatory of DDTs (DDTs) 10, summatory of trichlorobenzenes (TCBs) 11, hexachlorobutadiene (HCBu) 12, fish length. Physico-chemical parameters in water 1, alkalinity 2, chlorides 3, cyanides 4, total coliforms 5, conductivity at 20°C 6, biological oxygen demand 7, chemical oxygen demand 8, fluorides 9, suspended matter 10, total ammonium 11, nitrates 12, dissolved oxygen 13, phosphates 14, sulfates 15, water temperature 16, air temperature... Fig. 5 Main contamination sources identified by PCA for sediments, fish, and suface water in the Ebro River basin, and explained variances for each principal component. Variable identification. Organic compounds in sediments 1, summatory of hexachlorocyclohexanes (HCHs) 2, summa-tory of DDTs (DDTs) 3, hexachlorobenzene (HCB) 4, hexachlorobutadiene (HCBu) 5, summatory of trichlorobenzenes (TCBs) 6, naphthalene 7, fluoranthene 8, benzo(a)pyrene 9, benzo(b) fluoranthene 10, benzo(g,h,i)perylene 11, benzo(k)fluoranthene 12, indene(l,2,3-cd)pyrene. Organic compounds in fish 1, hexachlorobenzene (HCB) 2, summatory of hexachlorocyclohexanes (HCHs) 3, o,p-DDD 4, o,p-DDE 5, o,p-DDT 6, p,p-DDD 7, />,/>DDE 8, />,/>DDT 9, summatory of DDTs (DDTs) 10, summatory of trichlorobenzenes (TCBs) 11, hexachlorobutadiene (HCBu) 12, fish length. Physico-chemical parameters in water 1, alkalinity 2, chlorides 3, cyanides 4, total coliforms 5, conductivity at 20°C 6, biological oxygen demand 7, chemical oxygen demand 8, fluorides 9, suspended matter 10, total ammonium 11, nitrates 12, dissolved oxygen 13, phosphates 14, sulfates 15, water temperature 16, air temperature...
The complex [perylene]2[Ni(mnt)2] showed the largest electrical conductivity among the nickel dithiolate complexes (a = 50 Q-1 cm-1 at room temperature on single crystals) but it has not yet been structurally characterized.2218,3219... [Pg.299]

Several examples of the use of microelectrodes in highly resistive media exist. The first reported measurements were an examination of the reduction of aromatic hydrocarbons such as perylene in benzene containing tetrahexylammonium perchlorate [57]. Although this electrolyte is presumably in a quite associated state in benzene (or toluene [58]), it does impart sufficient conductivity for electrochemistry to be observed. In subsequent work, this result was confirmed and extended to other low-dielectric-constant solvents [59]. Even voltammetry in hexane has been shown to be possible with a microelectrode [60]. In this sol-... [Pg.388]

Gregg et at.si) examined photosensitization of perylene pigments (Dye 15-17) on a porous Sn02 thin film instead of Ti02 film as DSC, in view of energy matching with conduction band of semiconductors and LUMO of the sensitizers. When perylene-3,4-dicarboxylic acid-9,10-(5-phenanthroline) carboximide (Dye 15) was used, Jsc of 3.26 mA-cm 2, of 0.45 V, and a photoelectric conversion efficiency of 0.89% were observed under AM 1.5 irradiation. IPCE achieves close to 40% at 460 nm. [Pg.177]

The crystalline composites obtained between poly(3-alkylthiophene) and polystyrene showed an enhanced conductivity (07MM6579). The preparation of regioregular poly(3-alkylthiophene) and perylene diimide derivatives composites have been reported (06MI384). The photoluminescence spectra of this type of composites exhibit a significant photoluminescence quenching of the perylene diimide derivative. This result implies that the light absorbed by the perylene diimide units could also contribute to the generation of current at the photovoltaic device. [Pg.287]

Wakayama, N., Hirooka, T. Effect of Chemisorption of Hydrogen on Electrical Conductivity of Perylene-Cesium Charge-Transfer Complexes. J. Catalysis <9, 383 (1967) ... [Pg.33]


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See also in sourсe #XX -- [ Pg.16 , Pg.300 ]




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