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{{chembox |
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{{Chembox |
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| Verifiedfields = changed |
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| verifiedrevid = 408116285 |
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| ImageFile = Perfluoropentacene.svg |
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| ImageFile = Perfluoropentacene.svg |
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| ImageSize = 200px |
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| ImageSize = 200px |
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| PIN = Tetradecafluoropentacene |
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| Section2 = {{Chembox Properties |
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| OtherNames = |
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| Formula = C<sub>22</sub>F<sub>14</sub> |
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|Section1={{Chembox Identifiers |
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| MolarMass = 530 g/mol |
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| CASNo_Ref = {{cascite|correct|??}} |
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| CASNo = 646533-88-2 |
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| UNII_Ref = {{fdacite|correct|FDA}} |
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| UNII = PXZ2S4ZY9P |
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| PubChem = 12143313 |
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| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}} |
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| ChemSpiderID = 21431394 |
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| SMILES = c12c(c(c3c(c1F)c(c4c(c3F)c(c(c(c4F)F)F)F)F)F)c(c5c(c2F)c(c(c(c5F)F)F)F)F |
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| InChI = InChI=1S/C22F14/c23-9-1-2(12(26)6-5(11(1)25)15(29)19(33)20(34)16(6)30)10(24)4-3(9)13(27)7-8(14(4)28)18(32)22(36)21(35)17(7)31 |
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| StdInChIKey = AZVQGIPHTOBHAF-UHFFFAOYSA-N |
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}} |
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|Section2={{Chembox Properties |
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| C=22 | F=14 |
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| Appearance = Dark blueish powder |
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| Appearance = Dark blueish powder |
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| Density = |
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| MeltingPt = |
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| BoilingPt = |
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| Section7 = {{Chembox Hazards |
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| Solubility = |
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|Section3={{Chembox Hazards |
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| MainHazards = |
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| MainHazards = |
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| FlashPt = |
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| FlashPt = |
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| Autoignition = |
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| AutoignitionPt = |
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Perfluoropentacene (PFP) is an n-type ], which is made by ] of the p-type ] ]. It has a blueish-black color, and is used for molecular thin film devices (like ]s or ]s). |
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'''Perfluoropentacene''' (PFP) is an n-type ], which is made by ] of the p-type ] ].<ref>{{Cite journal | last1 = Salzmann | first1 = I. | last2 = Duhm | first2 = S. | last3 = Heimel | first3 = G. | last4 = Rabe | first4 = J. P. | last5 = Koch | first5 = N. | last6 = Oehzelt | first6 = M. | last7 = Sakamoto | first7 = Y. | last8 = Suzuki | first8 = T. | title = Structural Order in Perfluoropentacene Thin Films and Heterostructures with Pentacene | journal = Langmuir | year = 2008 | volume = 24 | issue = 14 | pages = 7294–7298 | doi = 10.1021/la800606h | pmid = 18547077 }}</ref> It has a blueish-black color, and is used for molecular thin-film devices (like ]s or ]s). |
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==References== |
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{{reflist}} |
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== External links == |
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== External links == |
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* {{cite web | author1 = Suzuki, T. | author2 = Sakamoto, Y. | author3 = Okubo, K. | title = Development of Organic Semiconductors for Molecular Thin-Film Devices | work = Annual Review | year = 2008 | volume = 2008 | publisher = Research Center for Molecular Scale Nanoscience - Division of Molecular Nanoscience | pages = 66–67 | url = http://ns.ims.ac.jp/english/know_en/publications/ann_rev_2008/suzuki.pdf | url-status = dead | archive-url = https://web.archive.org/web/20110722071708/http://ns.ims.ac.jp/english/know_en/publications/ann_rev_2008/suzuki.pdf | archive-date = 2011-07-22 }} |
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*http://ns.ims.ac.jp/english/know_en/publications/ann_rev_2008/suzuki.pdf |
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] |
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== References == |
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] |
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*http://pubs.acs.org/doi/abs/10.1021/la800606h |
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] |
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{{science-stub}} |
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] |
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{{organohalide-stub}} |
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] |
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] |
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