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・ Pentagonal trapezohedron
・ Pentacalia todziae
・ Pentacalia zakii
・ Pentacalia zamorana
・ Pentacarbon dioxide
・ Pentacarbonylhydridomanganese
・ Pentacarbonylhydridorhenium
・ Pentace
・ Pentace acuta
・ Pentace excelsa
・ Pentace exima
・ Pentace grandiflora
・ Pentace microlepidota
・ Pentace perakensis
・ Pentace strychnoidea
Pentacene
・ Pentaceras australis
・ Pentaceraster
・ Pentaceraster cumingi
・ Pentaceratops
・ Pentaceros
・ Pentachaeta
・ Pentachaeta alsinoides
・ Pentachaeta aurea
・ Pentachaeta bellidiflora
・ Pentachaeta exilis
・ Pentachaeta lyonii
・ Pentachlaena
・ Pentachloride
・ Pentachlorobenzene


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Pentacene : ウィキペディア英語版
Pentacene

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Pentacene is a polycyclic aromatic hydrocarbon consisting of five linearly-fused benzene rings. This highly conjugated compound is an organic semiconductor. The compound generates excitons upon absorption of ultra-violet (UV) or visible light; this makes it very sensitive to oxidation. For this reason, this compound, which is a purple powder, slowly degrades upon exposure to air and light.
Structurally, pentacene is one of the linear acenes, the previous one being tetracene (four fused benzene rings) and the next one being hexacene (six fused benzene rings). In August 2009, a group of researchers from IBM published experimental results of imaging a single molecule of pentacene using an atomic force microscope. In July 2011, they used a modification of scanning tunneling microscopy to experimentally determine the shapes of the highest occupied and lowest unoccupied molecular orbitals.
In 2012, pentacene-doped p-terphenyl was shown to be effective as the amplifier medium for a room-temperature maser.
In February 2014, NASA announced a (greatly upgraded database ) for tracking polycyclic aromatic hydrocarbons (PAHs), including Pentacene, in the universe. According to scientists, more than 20% of the carbon in the universe may be associated with PAHs, possible starting materials for the formation of life. PAHs seem to have been formed shortly after the Big Bang, are widespread throughout the universe, and are associated with new stars and exoplanets.
==Synthesis==

A classic method for pentacene synthesis is by the Elbs reaction. Pentacenes can also be prepared in the laboratory by extrusion of a small volatile component. In one such experimental procedure carbon monoxide is liberated from a precursor at 150 °C. The precursor is reported to have some solubility in chloroform and is therefore amenable to spin coating. Pentacene is soluble in hot chlorinated benzenes, such as 1,2,4-trichlorobenzene, from which it can be recrystallized to form platelets.
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抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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