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Volumn 14, Issue 18, 2010, Pages 2070-2108

Synthetic chemistry of acenes and heteroacenes

Author keywords

Acene; Heteroacene; Polycyclic aromatic hydrocarbons

Indexed keywords


EID: 78649932313     PISSN: 13852728     EISSN: None     Source Type: Journal    
DOI: 10.2174/138527210793351580     Document Type: Article
Times cited : (64)

References (205)
  • 1
    • 85171974454 scopus 로고
    • Clar: Vorschlage zur nomenklatur kondensierter ringsysteme (Aromatische Kohlenwasserstoffe, XXVI. Mitteil.)
    • Clar, E. E. Clar: Vorschlage zur nomenklatur kondensierter ringsysteme (Aromatische Kohlenwasserstoffe, XXVI. Mitteil.). Chem. Ber. 1939, 72, 2137-2139.
    • (1939) Chem. Ber , vol.72 , pp. 2137-2139
    • Clar, E.E.1
  • 3
    • 0002197464 scopus 로고    scopus 로고
    • On new compounds of carbon and hydrogen, and on certain other products btained during the decomposition of oil by heat
    • London
    • Faraday, M. On new compounds of carbon and hydrogen, and on certain other products btained during the decomposition of oil by heat. Phil. Trans. Royal. Soc. London, 1825, 440-466.
    • Phil. Trans. Royal. Soc , vol.1825 , pp. 440-466
    • Faraday, M.1
  • 4
    • 40949149866 scopus 로고    scopus 로고
    • The larger acenes: Versatile organic semiconductors
    • Anthony, J. E. The larger acenes: versatile organic semiconductors. Angew. Chem. Int. Ed., 2008, 47, 452-483.
    • (2008) Angew. Chem. Int. Ed , vol.47 , pp. 452-483
    • Anthony, J.E.1
  • 5
    • 0003913040 scopus 로고
    • Academic Press: London and New York
    • Clar, E. Polycyclic Hydrocarbons; Academic Press: London and New York, 1964, Vols. 1 and 2.
    • (1964) Polycyclic Hydrocarbons , vol.1
    • Clar, E.1
  • 6
    • 34248339106 scopus 로고    scopus 로고
    • Electron and ambipolar transport in organic field-effect transistors
    • Zaumseil, J.; Sirringhaus, H. Electron and ambipolar transport in organic field-effect transistors. Chem. Rev., 2007, 107, 1296-1323.
    • (2007) Chem. Rev , vol.107 , pp. 1296-1323
    • Zaumseil, J.1    Sirringhaus, H.2
  • 7
    • 10344259627 scopus 로고    scopus 로고
    • Tetrathiafulvalenes, oligoacenenes, and their buckminsterfullerene derivatives: The brick and mortar of organic electronics
    • Bendikov, M.; Wudl, F.; Perepichka, D. F. Tetrathiafulvalenes, oligoacenenes, and their buckminsterfullerene derivatives: the brick and mortar of organic electronics. Chem. Rev., 2004, 104, 4891-4946.
    • (2004) Chem. Rev , vol.104 , pp. 4891-4946
    • Bendikov, M.1    Wudl, F.2    Perepichka, D.F.3
  • 8
    • 13244287401 scopus 로고
    • Polyacene and a new class of quasi-one-dimensional conductors
    • Kivelson, S.; Chapman O. L., Polyacene and a new class of quasi-one-dimensional conductors. Phys. Rev. B., 1983, 28, 7236-7243.
    • (1983) Phys. Rev. B , vol.28 , pp. 7236-7243
    • Kivelson, S.1    Chapman, O.L.2
  • 10
    • 33846219497 scopus 로고    scopus 로고
    • Functionalized acenes and heteroacenes for organic electronics
    • Anthony, J. E. Functionalized acenes and heteroacenes for organic electronics. Chem. Rev., 2006, 106, 5028-5048.
    • (2006) Chem. Rev , vol.106 , pp. 5028-5048
    • Anthony, J.E.1
  • 11
    • 67650493441 scopus 로고    scopus 로고
    • N-Heteroacenes
    • Bunz, H. F. N-Heteroacenes. Chem. Eur. J., 2009, 15, 6780-6789.
    • (2009) Chem. Eur. J , vol.15 , pp. 6780-6789
    • Bunz, H.F.1
  • 12
    • 85066140837 scopus 로고
    • Convenient syntheses of naphthalene-, anthracene-, and naphthacene-2,3-dicarboxaldehydes
    • Mallouli, A.; Lepage, Y. Convenient syntheses of naphthalene-, anthracene-, and naphthacene-2,3-dicarboxaldehydes. Synthesis, 1980, 9, 689.
    • (1980) Synthesis , vol.9 , pp. 689
    • Mallouli, A.1    Lepage, Y.2
  • 13
    • 0002791310 scopus 로고    scopus 로고
    • A reiterative approach to 2,3-disubstituted naphthalenes and anthracenes
    • Bowles, D. M.; Anthony, J. E. A reiterative approach to 2,3-disubstituted naphthalenes and anthracenes. Org. Lett., 2000, 2, 85-87.
    • (2000) Org. Lett , vol.2 , pp. 85-87
    • Bowles, D.M.1    Anthony, J.E.2
  • 14
    • 62949244023 scopus 로고    scopus 로고
    • Iterative synthesis of acenes via homoelongation
    • Lin, C.; Lin, K-H.; Pal, B.; Tsouz, L. Iterative synthesis of acenes via homoelongation. Chem. Commun., 2009, 803-805.
    • (2009) Chem. Commun , pp. 803-805
    • Lin, C.1    Lin, K.-H.2    Pal, B.3    Tsouz, L.4
  • 15
    • 0001494245 scopus 로고
    • Syntheses of some furans and naphtho[2,3-c] derivatives of furan, pyrrole, and thiophene
    • Haddadin, M. J.; Agha, B. J.; Tabri, R. F. Syntheses of some furans and naphtho[2,3-c] derivatives of furan, pyrrole, and thiophene. J. Org. Chem., 1979, 44, 494-497.
    • (1979) J. Org. Chem , vol.44 , pp. 494-497
    • Haddadin, M.J.1    Agha, B.J.2    Tabri, R.F.3
  • 17
    • 0141627869 scopus 로고    scopus 로고
    • Photoluminescence and electronic interaction of anthracene derivatives adsorbed on sidewalls of single-walled carbon nanotubes
    • Zhang, J.; Lee, J. K.; Wu, Y.; Murray, R. W. Photoluminescence and electronic interaction of anthracene derivatives adsorbed on sidewalls of single-walled carbon nanotubes. Nano Lett., 2003, 3, 403-407.
    • (2003) Nano Lett , vol.3 , pp. 403-407
    • Zhang, J.1    Lee, J.K.2    Wu, Y.3    Murray, R.W.4
  • 18
    • 0032783371 scopus 로고    scopus 로고
    • A new type of pi-electron donors with one dithiole unit: Substituted 7-(1,3-dithiol-2-ylidene)-7-hydrobenz[d,e]anthracenes
    • Nazario, M.; Enrique, O.; Luis, S.; Pedro, M. V.; Rafael, V. A new type of pi-electron donors with one dithiole unit: substituted 7-(1,3-dithiol-2-ylidene)-7-hydrobenz[d,e]anthracenes. Eur. J. Org. Chem., 1999, 1999, 1239-1247.
    • (1999) Eur. J. Org. Chem , vol.1999 , pp. 1239-1247
    • Nazario, M.1    Enrique, O.2    Luis, S.3    Pedro, M.V.4    Rafael, V.5
  • 19
    • 78649966235 scopus 로고
    • Optical measurements of anthracene
    • Maureen, M. J.; Bloss, F. D. Optical measurements of anthracene. Acta Cryst., 1982, A38, 167-169.
    • (1982) Acta Cryst , vol.A38 , pp. 167-169
    • Maureen, M.J.1    Bloss, F.D.2
  • 21
    • 33847086970 scopus 로고
    • Flash Vacuum Pyrolysis of 2-Methylbenzophenones and 2-Methyldiphenyl Ketimines
    • Gu, T. Y.; Weber, W. P. Flash Vacuum Pyrolysis of 2-Methylbenzophenones and 2-Methyldiphenyl Ketimines. J. Org. Chem., 1980, 45, 2541-2544.
    • (1980) J. Org. Chem , vol.45 , pp. 2541-2544
    • Gu, T.Y.1    Weber, W.P.2
  • 22
    • 37049168478 scopus 로고
    • The reduction of anthraquinone and other polycyclic quinones with aluminium alkoxides (Meerwein-Pondorff Reagent)
    • Coffey, S.; Boyd, V. The reduction of anthraquinone and other polycyclic quinones with aluminium alkoxides (Meerwein-Pondorff Reagent). Chem. Commun., 1954, 2468-2470.
    • (1954) Chem. Commun , pp. 2468-2470
    • Coffey, S.1    Boyd, V.2
  • 23
    • 0001348346 scopus 로고
    • Efficient reduction of polycyclic quinones, hydroquinones, and phenols to polycyclic aromatic hydrocarbons with hydriodic acid
    • Konieczny, M.; Harvey, R. G. Efficient reduction of polycyclic quinones, hydroquinones, and phenols to polycyclic aromatic hydrocarbons with hydriodic acid. J. Org. Chem., 1979, 44, 4813-4816.
    • (1979) J. Org. Chem , vol.44 , pp. 4813-4816
    • Konieczny, M.1    Harvey, R.G.2
  • 24
    • 0001635012 scopus 로고
    • Lithium aluminum hydride reduction of peri-alkoxy-9,l0-anthraquinones
    • Shyamasundar, N.; Caluwe, P. Lithium aluminum hydride reduction of peri-alkoxy-9,l0-anthraquinones. J. Org. Chem., 1981, 46, 1552-1557.
    • (1981) J. Org. Chem , vol.46 , pp. 1552-1557
    • Shyamasundar, N.1    Caluwe, P.2
  • 25
    • 58149302259 scopus 로고    scopus 로고
    • Preparation of sterically congested compounds: 6,7-di-t-butyl-1,4-naphthoquinone, 2,3,6,7-tetra-t-butylanthraquinone, and 2,3,6,7-tetra-t-butylanthracene
    • Iguchi, K.; Sugihara, Y.; Nakayama, J. Preparation of sterically congested compounds: 6,7-di-t-butyl-1,4-naphthoquinone, 2,3,6,7-tetra-t-butylanthraquinone, and 2,3,6,7-tetra-t-butylanthracene. Bull. Chem. Soc. Jpn., 2008, 81, 304-306.
    • (2008) Bull. Chem. Soc. Jpn , vol.81 , pp. 304-306
    • Iguchi, K.1    Sugihara, Y.2    Nakayama, J.3
  • 26
    • 0000968634 scopus 로고
    • Repetitive Diels-Alder reactions for the growth of linear polyacenequinoid derivatives
    • Thomas, A. D.; Miller, L. L. Repetitive Diels-Alder reactions for the growth of linear polyacenequinoid derivatives. J. Org. Chem., 1986, 51, 4160-4169.
    • (1986) J. Org. Chem , vol.51 , pp. 4160-4169
    • Thomas, A.D.1    Miller, L.L.2
  • 27
    • 33846635003 scopus 로고    scopus 로고
    • Synthesis of aromatic cycloketones via intramolecular Friedel-Crafts acylation catalyzed by heteropoly acids
    • Lan, K.; Fen, S.; Shan, Z. Synthesis of aromatic cycloketones via intramolecular Friedel-Crafts acylation catalyzed by heteropoly acids. Aust. J. Chem., 2007, 60, 80-82.
    • (2007) Aust. J. Chem , vol.60 , pp. 80-82
    • Lan, K.1    Fen, S.2    Shan, Z.3
  • 28
    • 84985640683 scopus 로고
    • Novel alkylanthracenes synthesis, reductive alkylation, and reductive polymerization
    • Bender, D.; Mullen, K. Novel alkylanthracenes synthesis, reductive alkylation, and reductive polymerization. Chem. Ber., 1988, 121, 1187-1197.
    • (1988) Chem. Ber , vol.121 , pp. 1187-1197
    • Bender, D.1    Mullen, K.2
  • 29
    • 1442275477 scopus 로고    scopus 로고
    • Molecular crystals with moving parts: Synthesis, characterization, and crystal packing of molecular gyroscopes with methyl-substituted triptycyl frames
    • Godinez, C. E.; Zepeda, G.; Mortko, C. J.; Dang, H.; Garcia-Garibay, M. A. Molecular crystals with moving parts: synthesis, characterization, and crystal packing of molecular gyroscopes with methyl-substituted triptycyl frames. J. Org. Chem., 2004, 69, 1652-1662.
    • (2004) J. Org. Chem , vol.69 , pp. 1652-1662
    • Godinez, C.E.1    Zepeda, G.2    Mortko, C.J.3    Dang, H.4    Garcia-Garibay, M.A.5
  • 30
    • 17444392875 scopus 로고    scopus 로고
    • Synthesis and activity of substituted anthraquinones against a human filarial parasite, Brugia malayi
    • Dhananjeyan, M. R.; Milev, Y. P.; Kron, M. A.; Nair, M. G. Synthesis and activity of substituted anthraquinones against a human filarial parasite, Brugia malayi. J. Med. Chem., 2005, 48, 2822-2830.
    • (2005) J. Med. Chem , vol.48 , pp. 2822-2830
    • Dhananjeyan, M.R.1    Milev, Y.P.2    Kron, M.A.3    Nair, M.G.4
  • 31
    • 34247604971 scopus 로고    scopus 로고
    • A new InCl3-catalyzed reduction of anthrones and anthraquinones by using aluminum powder in aqueous media
    • Wang, C.; Wan, J.; Zheng, Z.; Pan, Y. A new InCl3-catalyzed reduction of anthrones and anthraquinones by using aluminum powder in aqueous media. Tetrahedron, 2007, 63, 5071-5075.
    • (2007) Tetrahedron , vol.63 , pp. 5071-5075
    • Wang, C.1    Wan, J.2    Zheng, Z.3    Pan, Y.4
  • 32
    • 0021933217 scopus 로고
    • Chinon-Amin-Reaktionen, 13. Mitt. Synthesen von Chinoxalinonen und Naphthochinoxalinon zum Farbvergleich mit Benzochinoxalinonen
    • Kallmayer, H. J.; Karlheinz, S. Chinon-Amin-Reaktionen, 13. Mitt. Synthesen von Chinoxalinonen und Naphthochinoxalinon zum Farbvergleich mit Benzochinoxalinonen. Archiv. Pharm., 1985, 318, 607-614.
    • (1985) Archiv. Pharm , vol.318 , pp. 607-614
    • Kallmayer, H.J.1    Karlheinz, S.2
  • 33
    • 33947591471 scopus 로고    scopus 로고
    • Synthesis and characterization of fluorescent acenequinones as dyes for guest-host liquid crystal displays
    • Chen, Z.; Swager, T. M. Synthesis and characterization of fluorescent acenequinones as dyes for guest-host liquid crystal displays. Org. Lett., 2007, 9, 997-1000.
    • (2007) Org. Lett , vol.9 , pp. 997-1000
    • Chen, Z.1    Swager, T.M.2
  • 34
    • 20444430141 scopus 로고    scopus 로고
    • Functionalized higher acenes: Hexacene and heptacene
    • Referring to the Supporting Information: Payne, M. M.; Parkin, S. R.; Anthony, J. E
    • Referring to the Supporting Information: Payne, M. M.; Parkin, S. R.; Anthony, J. E. Functionalized higher acenes: hexacene and heptacene. J. Am. Chem. Soc., 2005, 127, 8028-8029.
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 8028-8029
  • 35
    • 27644487544 scopus 로고
    • Chlorination of aromatic hydrocarbons by cupric chloride
    • Ware, J. C.; Borchert, E. E. Chlorination of aromatic hydrocarbons by cupric chloride. I. anthracene. J. Org. Chem., 1961, 26, 2263-2267.
    • (1961) I. Anthracene. J. Org. Chem , vol.26 , pp. 2263-2267
    • Ware, J.C.1    Borchert, E.E.2
  • 36
    • 55549101993 scopus 로고
    • Copper(II) halides as halogenating agents
    • Nonhebel, D. C. Copper(II) halides as halogenating agents. J. Chem. Soc., 1963, 1216-1220.
    • (1963) J. Chem. Soc , pp. 1216-1220
    • Nonhebel, D.C.1
  • 37
    • 0000842432 scopus 로고
    • Reaction of cupric halides with organic compounds-II
    • Mosnaim, D.; Nonhebel, D. C. Reaction of cupric halides with organic compounds-II. Tetrahedron, 1969, 25, 1591-1595.
    • (1969) Tetrahedron , vol.25 , pp. 1591-1595
    • Mosnaim, D.1    Nonhebel, D.C.2
  • 38
    • 33644643078 scopus 로고    scopus 로고
    • Synthesis of new anthracene derivatives
    • Cakmak, O.; Erenler, R.; Tutar, A.; Celik, N. Synthesis of new anthracene derivatives. J. Org. Chem., 2006, 71, 1795-1801.
    • (2006) J. Org. Chem , vol.71 , pp. 1795-1801
    • Cakmak, O.1    Erenler, R.2    Tutar, A.3    Celik, N.4
  • 39
    • 78649950275 scopus 로고    scopus 로고
    • Highly brominated anthracenes as precursors for the convenient synthesis of 2,9,10-trisubstituted anthracene derivatives. Beilstein
    • DOI:10.3762/bjoc.4.50
    • akmak, O.; Aydogan, L.; Berkil, K.; Gulcin, I.; Buyukgungor, O. Highly brominated anthracenes as precursors for the convenient synthesis of 2,9,10-trisubstituted anthracene derivatives. Beilstein J. Org. Chem., 2008, 4, No. 50, DOI:10.3762/bjoc.4.50.
    • (2008) J. Org. Chem , vol.4 , Issue.50
    • Akmak, O.1    Aydogan, L.2    Berkil, K.3    Gulcin, I.4    Buyukgungor, O.5
  • 41
    • 24944529982 scopus 로고    scopus 로고
    • Enantioselective preparation and structural and conformational analysis of the chiral solvating agent α,α'-bis(trifluoromethyl)-1,8-anthra--cenedimethanol
    • Perez-Trujillo, M.; Maestre, I.; Jaime, C.; Alvarez-Larena, A.; Piniella, J. F.; Virgili, A. Enantioselective preparation and structural and conformational analysis of the chiral solvating agent α,α'-bis(trifluoromethyl)-1,8-anthra--cenedimethanol. Tetrahedron Asymmetry, 2005, 16, 3084-3093.
    • (2005) Tetrahedron Asymmetry , vol.16 , pp. 3084-3093
    • Perez-Trujillo, M.1    Maestre, I.2    Jaime, C.3    Alvarez-Larena, A.4    Piniella, J.F.5    Virgili, A.6
  • 43
    • 0003422565 scopus 로고    scopus 로고
    • Completely regioselective, highly stereoselective syntheses of cis-bisfullerene[60] adducts of 6,13-disubstituted pentacenes
    • Miller, G. P.; Mack, J. Completely regioselective, highly stereoselective syntheses of cis-bisfullerene[60] adducts of 6,13-disubstituted pentacenes. Org. Lett., 2000, 2, 3979-3982.
    • (2000) Org. Lett , vol.2 , pp. 3979-3982
    • Miller, G.P.1    Mack, J.2
  • 44
    • 0142062437 scopus 로고    scopus 로고
    • 2,6-Bis(styryl)anthracene derivatives with large two-photon cross-sections
    • Yang, W. J.; Kim, D. Y.; Jeong, M.-Y.; Kim, H. M.; Jeon, S.-J.; Cho, B. R. 2,6-Bis(styryl)anthracene derivatives with large two-photon cross-sections. Chem. Commun., 2003, 2618-2619.
    • (2003) Chem. Commun , pp. 2618-2619
    • Yang, W.J.1    Kim, D.Y.2    Jeong, M.-Y.3    Kim, H.M.4    Jeon, S.-J.5    Cho, B.R.6
  • 45
    • 22044447261 scopus 로고    scopus 로고
    • Two-photon absorption properties of 2,6-bis(styryl)anthracene derivatives: Effects of donor-acceptor substituents and the pi center
    • Yang, W. J.; Kim, D. Y.; Jeong, M.-Y.; Kim, H. M.; Lee, Y. K.; Fang, X.; Jeon, S.-J.; Cho, B. R. Two-photon absorption properties of 2,6-bis(styryl)anthracene derivatives: effects of donor-acceptor substituents and the pi center. Chem. Eur. J., 2005, 11, 4191-4198.
    • (2005) Chem. Eur. J , vol.11 , pp. 4191-4198
    • Yang, W.J.1    Kim, D.Y.2    Jeong, M.-Y.3    Kim, H.M.4    Lee, Y.K.5    Fang, X.6    Jeon, S.-J.7    Cho, B.R.8
  • 46
    • 33947464259 scopus 로고
    • Some meso-substituted anthracenes. I. 9,10-bis-(chloromethyl)-anthracene as a synthetic intermediate
    • Miller, M. W.; Amidon, R. W.; Tawney, P. O. Some meso-substituted anthracenes. I. 9,10-bis-(chloromethyl)-anthracene as a synthetic intermediate. J. Am. Chem. Soc., 1955, 77, 2845-2848.
    • (1955) J. Am. Chem. Soc , vol.77 , pp. 2845-2848
    • Miller, M.W.1    Amidon, R.W.2    Tawney, P.O.3
  • 47
    • 0013942017 scopus 로고
    • Aldehyde Synthesis. A study of the preparation of 9,l0-anthracenedicarbox-aldehyde and other aromatic dialdehydes
    • Klanderman, B. H. Aldehyde Synthesis. A study of the preparation of 9,l0-anthracenedicarbox-aldehyde and other aromatic dialdehydes. J. Org. Chem., 1966, 31, 2618-2620.
    • (1966) J. Org. Chem , vol.31 , pp. 2618-2620
    • Klanderman, B.H.1
  • 49
    • 33845375520 scopus 로고
    • Synthesis of 1,5-diamino-1,5-dihydrobenzo[1, 2-d:4,5-d']bistriazo(DABT) and its use as a 1,4-benzadiyne equivalent
    • Hart, H.; Ok, D. Synthesis of 1,5-diamino-1,5-dihydrobenzo[1, 2-d:4,5-d']bistriazo(DABT) and its use as a 1,4-benzadiyne equivalent. J. Org. Chem., 1986, 51, 979-986.
    • (1986) J. Org. Chem , vol.51 , pp. 979-986
    • Hart, H.1    Ok, D.2
  • 50
    • 37749034421 scopus 로고    scopus 로고
    • Influence of alkyl chain length on the solid-state packing and fluorescence of 1,4,5,8-tetra(alkyl)anthracenes
    • Kitamura, C.; Abe, Y.; Kawatsuki, N.; Yoneda, A.; Asada, K.; Kobayashi, T.; Naito, H. Influence of alkyl chain length on the solid-state packing and fluorescence of 1,4,5,8-tetra(alkyl)anthracenes. Mol. Cryst. Liq. Cryst., 2007, 474, 119-135.
    • (2007) Mol. Cryst. Liq. Cryst , vol.474 , pp. 119-135
    • Kitamura, C.1    Abe, Y.2    Kawatsuki, N.3    Yoneda, A.4    Asada, K.5    Kobayashi, T.6    Naito, H.7
  • 51
    • 33644678298 scopus 로고    scopus 로고
    • Hierarchic supramolecular interactions within assemblies in solution and in the crystal of 2,3,6,7-tetrasubstituted 5,5'-(anthracene-9,10-diyl) bis[pyrimidin-2-amines])
    • Balaban, T. S.; Eichhoefer, A.; Krische, M. J.; Lehn, J.-M. Hierarchic supramolecular interactions within assemblies in solution and in the crystal of 2,3,6,7-tetrasubstituted 5,5'-(anthracene-9,10-diyl) bis[pyrimidin-2-amines]). Helv. Chim. Acta, 2006, 89, 333-351.
    • (2006) Helv. Chim. Acta , vol.89 , pp. 333-351
    • Balaban, T.S.1    Eichhoefer, A.2    Krische, M.J.3    Lehn, J.-M.4
  • 52
    • 57649183702 scopus 로고    scopus 로고
    • 9,10-diarylanthracenes as molecular switches: Syntheses, properties, isomerisations and their reactions with singlet oxygen
    • Daniel, Z.; Werner, F.; Melanie, H.; Uwe, S.; Alexandra, K.; Torsten, L. 9,10-diarylanthracenes as molecular switches: syntheses, properties, isomerisations and their reactions with singlet oxygen. Chem. Eur. J., 2008, 14, 11429-11441.
    • (2008) Chem. Eur. J , vol.14 , pp. 11429-11441
    • Daniel, Z.1    Werner, F.2    Melanie, H.3    Uwe, S.4    Alexandra, K.5    Torsten, L.6
  • 54
    • 0027768754 scopus 로고
    • Unsymmetrically substituted 2,7-dimethyl-1,8-diarylanthracenes
    • House, H. O.; Holt, J. T.; VanDerveer, D. Unsymmetrically substituted 2,7-dimethyl-1,8-diarylanthracenes. J. Org. Chem., 1993, 58, 7516-7523.
    • (1993) J. Org. Chem , vol.58 , pp. 7516-7523
    • House, H.O.1    Holt, J.T.2    Vanderveer, D.3
  • 56
    • 66149117066 scopus 로고    scopus 로고
    • Convenient synthesis of tetra-and hexaarylanthracenes by means of RuH2(CO)(PPh3)3-catalyzed C-H arylation of anthraquinone with arylboronates
    • Kitazawa, K.; Kochi, T.; Sato, M.; Kakiuchi, F. Convenient synthesis of tetra-and hexaarylanthracenes by means of RuH2(CO)(PPh3)3-catalyzed C-H arylation of anthraquinone with arylboronates. Org. Lett., 2009, 11, 1951-1954.
    • (2009) Org. Lett , vol.11 , pp. 1951-1954
    • Kitazawa, K.1    Kochi, T.2    Sato, M.3    Kakiuchi, F.4
  • 57
    • 0037429889 scopus 로고    scopus 로고
    • Oligo(2,6-anthrylene)s: Acene-oligomer approach for organic field-effect transistors
    • Ito, K.; Suzuki, T.; Sakamoto, Y.; Kubota, D.; Inoue, Y.; Sato, F.; Tokito, S. Oligo(2,6-anthrylene)s: acene-oligomer approach for organic field-effect transistors. Angew. Chem. Int. Ed., 2003, 42, 1159-1162.
    • (2003) Angew. Chem. Int. Ed , vol.42 , pp. 1159-1162
    • Ito, K.1    Suzuki, T.2    Sakamoto, Y.3    Kubota, D.4    Inoue, Y.5    Sato, F.6    Tokito, S.7
  • 59
    • 34250004403 scopus 로고    scopus 로고
    • A cyclodextrin-insulated anthracene rotaxane with enhanced fluorescence and photostability
    • Stone, M. T.; Anderson, H. L. A cyclodextrin-insulated anthracene rotaxane with enhanced fluorescence and photostability. Chem. Commun., 2007, 2387-2389.
    • (2007) Chem. Commun , pp. 2387-2389
    • Stone, M.T.1    Anderson, H.L.2
  • 60
    • 14744270761 scopus 로고    scopus 로고
    • High-performance, stable organic thin-film field-effect transistors based on bis-5'-alkylthiophen-2'-yl-2,6-anthracene semiconductors
    • Meng, H.; Sun, F.; Goldfinger, M. B.; Jaycox, G. D.; Li, Z.; Marshall, W. J.; Blackman, G. S. High-performance, stable organic thin-film field-effect transistors based on bis-5'-alkylthiophen-2'-yl-2,6-anthracene semiconductors. J. Am. Chem. Soc., 2005, 127, 2406-2407.
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 2406-2407
    • Meng, H.1    Sun, F.2    Goldfinger, M.B.3    Jaycox, G.D.4    Li, Z.5    Marshall, W.J.6    Blackman, G.S.7
  • 63
    • 58149314178 scopus 로고    scopus 로고
    • Organic single-nanofiber transistors from organogels
    • Hong, J. P.; Um, M. C.; Nam, S. R.; Hong, J. I.; Lee, S. Organic single-nanofiber transistors from organogels. Chem. Commun., 2009, 310-312.
    • (2009) Chem. Commun , pp. 310-312
    • Hong, J.P.1    Um, M.C.2    Nam, S.R.3    Hong, J.I.4    Lee, S.5
  • 64
    • 70350733736 scopus 로고    scopus 로고
    • Pi-Conjugated oligothiophene-anthracene co-oligomers: Synthesis, physical properties, and self-assembly
    • Luo, J.; Qu, H.; Yin, J.; Zhang, X.; Huang, K.-W.; Chi, C. pi-Conjugated oligothiophene-anthracene co-oligomers: synthesis, physical properties, and self-assembly. J. Mater. Chem., 2009, 19, 8202-8211.
    • (2009) J. Mater. Chem , vol.19 , pp. 8202-8211
    • Luo, J.1    Qu, H.2    Yin, J.3    Zhang, X.4    Huang, K.-W.5    Chi, C.6
  • 65
    • 67650699262 scopus 로고    scopus 로고
    • Low-dimensional arylacetylenes for solution-processable organic field-effect transistors
    • Marrocchi, A.; Seri, M.; Kim, C.; Facchetti, A.; Taticchi, A.; Marks, T. J. Low-dimensional arylacetylenes for solution-processable organic field-effect transistors. Chem. Mater., 2009, 21, 2592-2594.
    • (2009) Chem. Mater , vol.21 , pp. 2592-2594
    • Marrocchi, A.1    Seri, M.2    Kim, C.3    Facchetti, A.4    Taticchi, A.5    Marks, T.J.6
  • 66
    • 61849095725 scopus 로고    scopus 로고
    • Conjugated anthracene derivatives as donor materials for bulk heterojunction solar cells: Olefinic versus acetylenic spacers
    • Marrocchi, A.; Silvestri, F.; Seri, M.; Facchetti, A.; Taticchi, A.; Marks, T. J. Conjugated anthracene derivatives as donor materials for bulk heterojunction solar cells: olefinic versus acetylenic spacers. Chem. Commun., 2009, 1380-1382.
    • (2009) Chem. Commun , pp. 1380-1382
    • Marrocchi, A.1    Silvestri, F.2    Seri, M.3    Facchetti, A.4    Taticchi, A.5    Marks, T.J.6
  • 67
    • 19544381074 scopus 로고    scopus 로고
    • Synthesis, electronic properties, and electrochemiluminescence of donor-substituted phenylethynylanthronitriles
    • Elangovan, A.; Kao, K.-M.; Yang, S.-W.; Chen, Y.-L.; Ho, T.-I.; Su, Y. O. Synthesis, electronic properties, and electrochemiluminescence of donor-substituted phenylethynylanthronitriles. J. Org. Chem., 2005, 70, 4460-4469.
    • (2005) J. Org. Chem , vol.70 , pp. 4460-4469
    • Elangovan, A.1    Kao, K.-M.2    Yang, S.-W.3    Chen, Y.-L.4    Ho, T.-I.5    Su, Y.O.6
  • 68
    • 38849133492 scopus 로고    scopus 로고
    • 9,10-Ter-anthrylene-ethynylene: A new molecular architecture for solution processed anthracene-based thin film transistors
    • Dell'Aquila, A.; Marinelli, F.; Tey, J., Keg, P.; Lam Y.-M. 9,10-Ter-anthrylene-ethynylene: a new molecular architecture for solution processed anthracene-based thin film transistors. J. Mater. Chem., 2008, 786-791.
    • (2008) J. Mater. Chem , pp. 786-791
    • Dell'Aquila, A.1    Marinelli, F.2    Tey, J.3    Keg, P.4    Lam, Y.-M.5
  • 69
    • 52649180041 scopus 로고    scopus 로고
    • Transistors from a conjugated macrocycle molecule: Field and photo effects
    • Zhao, W.; Tang, Q.; Chan, H. S.; Xu, J.; Lo, K. Y.; Miao, Q. Transistors from a conjugated macrocycle molecule: field and photo effects. Chem. Commun., 2008, 4324-4326.
    • (2008) Chem. Commun , pp. 4324-4326
    • Zhao, W.1    Tang, Q.2    Chan, H.S.3    Xu, J.4    Lo, K.Y.5    Miao, Q.6
  • 70
    • 23944495533 scopus 로고    scopus 로고
    • Silylethynylated anthracene derivatives for use in organic light-emitting diodes
    • Landis, C. A.; Parkin, S. R.; Anthony, J. E. Silylethynylated anthracene derivatives for use in organic light-emitting diodes. Jpn. J. Appl. Phys. Part 1, 2005, 44, 3921-3922.
    • (2005) Jpn. J. Appl. Phys. Part , vol.1 , Issue.44 , pp. 3921-3922
    • Landis, C.A.1    Parkin, S.R.2    Anthony, J.E.3
  • 71
    • 22144456353 scopus 로고    scopus 로고
    • A simple palladium-free synthesis of phenyleneethynylene-based molecular materials revisited
    • Lydon, D. P.; Porres, L.; Beeby, A.; Marder, T. B.; Low, P. J. A simple palladium-free synthesis of phenyleneethynylene-based molecular materials revisited. New J. Chem., 2005, 29, 972-976.
    • (2005) New J. Chem , vol.29 , pp. 972-976
    • Lydon, D.P.1    Porres, L.2    Beeby, A.3    Marder, T.B.4    Low, P.J.5
  • 72
    • 35948935913 scopus 로고    scopus 로고
    • Anthracenedicarboximides as air-stable n-channel semiconductors for thin-film transistors with remarkable current on-off ratios
    • Wang, Z.; Kim, C.; Facchetti, A.; Marks, T. J. Anthracenedicarboximides as air-stable n-channel semiconductors for thin-film transistors with remarkable current on-off ratios. J. Am. Chem. Soc., 2007, 129, 13362-13363.
    • (2007) J. Am. Chem. Soc , vol.129 , pp. 13362-13363
    • Wang, Z.1    Kim, C.2    Facchetti, A.3    Marks, T.J.4
  • 73
    • 53849120254 scopus 로고    scopus 로고
    • 9,10-Disubstituted octafluoroanthracene derivatives via palladium-catalyzed cross-coupling
    • Tannaci, J. F.; Noji, M.; McBee, J. L.; Tilley, T. D. 9,10-Disubstituted octafluoroanthracene derivatives via palladium-catalyzed cross-coupling. J. Org. Chem., 2008, 73, 7895-7900.
    • (2008) J. Org. Chem , vol.73 , pp. 7895-7900
    • Tannaci, J.F.1    Noji, M.2    McBee, J.L.3    Tilley, T.D.4
  • 74
    • 33644770052 scopus 로고    scopus 로고
    • Synthesis and characterization of soluble oligo(9,10-bisalkynylanthrylene) s
    • Cui, W.; Zhang, X.; Jiang, X.; Tian, H.; Yan, D.; Geng, Y.; Jing, X.; Wang, F. Synthesis and characterization of soluble oligo(9,10-bisalkynylanthrylene) s. Org. Lett., 2006, 8, 785-788.
    • (2006) Org. Lett , vol.8 , pp. 785-788
    • Cui, W.1    Zhang, X.2    Jiang, X.3    Tian, H.4    Yan, D.5    Geng, Y.6    Jing, X.7    Wang, F.8
  • 75
    • 54249099705 scopus 로고    scopus 로고
    • Poly(anthrylenebutadiynylene)s: Precursor-based synthesis and band-gap tuning
    • Taylor M. S.; Swager, T. M. Poly(anthrylenebutadiynylene)s: precursor-based synthesis and band-gap tuning. Angew. Chem., Int. Ed., 2007, 119, 8632-8635.
    • (2007) Angew. Chem., Int. Ed , vol.119 , pp. 8632-8635
    • Taylor, M.S.1    Swager, T.M.2
  • 76
    • 0344927987 scopus 로고    scopus 로고
    • Tetracene derivatives as potential red emitters for organic LEDs
    • Odom, S. A.; Parkin, S. R.; Anthony, J. E. Tetracene derivatives as potential red emitters for organic LEDs. Org. Lett., 2003, 5, 4245-4248.
    • (2003) Org. Lett , vol.5 , pp. 4245-4248
    • Odom, S.A.1    Parkin, S.R.2    Anthony, J.E.3
  • 77
    • 0001658183 scopus 로고
    • The crystal and molecular structure of tetracene
    • Robertson, M., Sinclair, V. C.; Trotter, J. The crystal and molecular structure of tetracene. Acta Cryst., 1961, 14, 697-704.
    • (1961) Acta Cryst , vol.14 , pp. 697-704
    • Robertson, M.1    Sinclair, V.C.2    Trotter, J.3
  • 78
    • 33646910771 scopus 로고    scopus 로고
    • Synthesis and photophysical properties of dihydroheptacenes: New blue-emitting materials
    • Mondal, R.; Shah, B. K.; Neckers, D. C. Synthesis and photophysical properties of dihydroheptacenes: new blue-emitting materials. J. Org. Chem., 2006, 71, 4085-4091.
    • (2006) J. Org. Chem , vol.71 , pp. 4085-4091
    • Mondal, R.1    Shah, B.K.2    Neckers, D.C.3
  • 80
    • 33947093318 scopus 로고
    • Diels-Alder approach to naphthocyclobutenes and anthrocyclobutenes
    • Thummel, R.P.; Cravey, W. E.; Nutakul, W. Diels-Alder approach to naphthocyclobutenes and anthrocyclobutenes. J. Org. Chem., 1978, 43, 2473-2477.
    • (1978) J. Org. Chem , vol.43 , pp. 2473-2477
    • Thummel, R.P.1    Cravey, W.E.2    Nutakul, W.3
  • 81
    • 0011209423 scopus 로고
    • A convenient generation of 2,3-naphthalyne. Linear annulation of naphthalene and a new naphthacene synthesis
    • LeHoullier, C.S.; Gribble, G.W. A convenient generation of 2,3-naphthalyne. Linear annulation of naphthalene and a new naphthacene synthesis. J. Org. Chem., 1983, 48, 2364-2366.
    • (1983) J. Org. Chem , vol.48 , pp. 2364-2366
    • Lehoullier, C.S.1    Gribble, G.W.2
  • 83
    • 0001970474 scopus 로고
    • Capture du paradimethoxyorthoquinodimethane: Syntheses de quinones et d'un intermediaire de la daunomycinone
    • Laduranty, J.; Lepage, L.; Lepage, Y. Capture du paradimethoxyorthoquinodimethane: syntheses de quinones et d'un intermediaire de la daunomycinone. Can. J. Chem., 1980, 58, 1161-1167.
    • (1980) Can. J. Chem , vol.58 , pp. 1161-1167
    • Laduranty, J.1    Lepage, L.2    Lepage, Y.3
  • 85
    • 0000505621 scopus 로고
    • Synthesis of 2,3-norbornadienonaphthacene
    • Patney, H.K. Synthesis of 2,3-norbornadienonaphthacene. J. Org. Chem., 1988, 53, 6106-6109.
    • (1988) J. Org. Chem , vol.53 , pp. 6106-6109
    • Patney, H.K.1
  • 87
    • 0010942365 scopus 로고
    • Naphthaceno[1,12-cd: 4,5-c'd']bis[1,2]diselenole as a new electron donor
    • Miyamoto, H.; Aso, Y.; Otsubo, T.; Ogura, F. Naphthaceno[1,12-cd: 4,5-c'd']bis[1,2]diselenole as a new electron donor. Bull. Chem. Soc. Jpn., 1990, 63, 2441-2443.
    • (1990) Bull. Chem. Soc. Jpn , vol.63 , pp. 2441-2443
    • Miyamoto, H.1    Aso, Y.2    Otsubo, T.3    Ogura, F.4
  • 89
    • 0000360473 scopus 로고
    • Linear acene derivatives. new routes to pentacene and naphthacene and the first synthesis of a triptycene with two anthracene moieties
    • Luo, J.; Hart, H. Linear acene derivatives. new routes to pentacene and naphthacene and the first synthesis of a triptycene with two anthracene moieties. J. Org. Chem., 1987, 52, 4833-4836.
    • (1987) J. Org. Chem , vol.52 , pp. 4833-4836
    • Luo, J.1    Hart, H.2
  • 90
    • 15744364080 scopus 로고
    • Production of tetracenes by reduction Of 6,11-dihydroxy-5,12-tetracenequinones, phthalide derivatives, with aluminum cyclohexanolate
    • Medne, R. S.; Livdane, A. D.; Neiland, O. Y. Production of tetracenes by reduction Of 6,11-dihydroxy-5,12-tetracenequinones, phthalide derivatives, with aluminum cyclohexanolate. J. Org. Chem. USSR (Engl. Transl.), 1977, 13, 572.
    • (1977) J. Org. Chem. USSR (Engl. Transl.) , vol.13 , pp. 572
    • Medne, R.S.1    Livdane, A.D.2    Neiland, O.Y.3
  • 91
    • 68949111608 scopus 로고    scopus 로고
    • 2,8-and 2,9-Diboryltetracenes as useful building blocks for extended pi-conjugated tetracenes
    • Kimoto, T.; Tanaka, K.; Sakai, Y.; Ohno, A.; Yoza, K.; Kobayashi, K. 2,8-and 2,9-Diboryltetracenes as useful building blocks for extended pi-conjugated tetracenes. Org. Lett., 2009, 11, 3658-3661.
    • (2009) Org. Lett , vol.11 , pp. 3658-3661
    • Kimoto, T.1    Tanaka, K.2    Sakai, Y.3    Ohno, A.4    Yoza, K.5    Kobayashi, K.6
  • 92
    • 37049167688 scopus 로고
    • Homologues of naphthacene. Part I. 2:6-dimethylnaphthacene
    • Coulson, E. A. Homologues of naphthacene. Part I. 2:6-dimethylnaphthacene. J. Chem. Soc. 1934, 1406-1412.
    • (1934) J. Chem. Soc , pp. 1406-1412
    • Coulson, E.A.1
  • 93
    • 37049175919 scopus 로고
    • Homologues of naphthacene. Part II
    • 2-Methyl-and 2:7-Dimethylnaphthacene: Synthetic applications of 2:6-and 2:7-dimethyl-1:2:3:4-tetrahydronaphthalene
    • Coulson, E. A. Homologues of naphthacene. Part II. 2-Methyl-and 2:7-Dimethylnaphthacene: synthetic applications of 2:6-and 2:7-dimethyl-1:2:3:4-tetrahydronaphthalene. J. Chem. Soc., 1935, 77-83.
    • (1935) J. Chem. Soc , pp. 77-83
    • Coulson, E.A.1
  • 94
    • 0007033149 scopus 로고
    • Twin benzoannulation of naphthalene via 1,3-,1,6-, and 2,6-naphthodiyne synthetic equivalents
    • Gribble, G. W.; Perni, R. B.; Onan, K. D. Twin benzoannulation of naphthalene via 1,3-,1,6-, and 2,6-naphthodiyne synthetic equivalents. J. Org. Chem., 1985, 50, 2934-2939.
    • (1985) J. Org. Chem , vol.50 , pp. 2934-2939
    • Gribble, G.W.1    Perni, R.B.2    Onan, K.D.3
  • 95
    • 75249083902 scopus 로고    scopus 로고
    • Synthesis and crystallochromy of 1,4,7,10-tetraalkyltetracenes: Tuning of solid-state optical properties of tetracenes by alkyl side-chain length
    • Chitoshi, K.; Yasushi, A.; Takuya, O.; Akio, Y.; Takeshi, K.; Takashi, K.; Hiroyoshi, N.; Toshiki, K. Synthesis and crystallochromy of 1,4,7,10-tetraalkyltetracenes: tuning of solid-state optical properties of tetracenes by alkyl side-chain length. Chem. Eur. J., 2010, 16, 890-898.
    • (2010) Chem. Eur. J , vol.16 , pp. 890-898
    • Chitoshi, K.1    Yasushi, A.2    Takuya, O.3    Akio, Y.4    Takeshi, K.5    Takashi, K.6    Hiroyoshi, N.7    Toshiki, K.8
  • 96
    • 0008288651 scopus 로고
    • Synthesis of new cyclopenta-fused PAH isomers of cata-annelated benzenoid systems
    • Sangaiah, R.; Gold, A. Synthesis of new cyclopenta-fused PAH isomers of cata-annelated benzenoid systems. J. Org. Chem., 1987, 52, 3205-3211.
    • (1987) J. Org. Chem , vol.52 , pp. 3205-3211
    • Sangaiah, R.1    Gold, A.2
  • 97
    • 58149178492 scopus 로고    scopus 로고
    • Unexpected photooxidation of H-bonded tetracene
    • Liang, Z.; Zhao, W.; Wang, S.; Tang, Q.; Lam, S.-C.; Miao, Q. Unexpected photooxidation of H-bonded tetracene. Org. Lett., 2008, 10, 2007-2010.
    • (2008) Org. Lett , vol.10 , pp. 2007-2010
    • Liang, Z.1    Zhao, W.2    Wang, S.3    Tang, Q.4    Lam, S.-C.5    Miao, Q.6
  • 98
    • 18244408507 scopus 로고    scopus 로고
    • Synthesis of 2,3-substituted tetracenes and evaluation of their self-assembling properties in organic solvents
    • Reichwagen, J.; Hopf, H.; Del Guerzo, A.; Belin, C.; Bouas-Laurent, H.; Desvergne, J. P. Synthesis of 2,3-substituted tetracenes and evaluation of their self-assembling properties in organic solvents. Org. Lett., 2005, 7, 971-974.
    • (2005) Org. Lett , vol.7 , pp. 971-974
    • Reichwagen, J.1    Hopf, H.2    Del Guerzo, A.3    Belin, C.4    Bouas-Laurent, H.5    Desvergne, J.P.6
  • 99
    • 3042833040 scopus 로고    scopus 로고
    • Photodimers of a soluble tetracene derivative. excimer fluorescence from the head-to-head isomer
    • Reichwagen, J.; Hopf, H.; Del Guerzo, A.; Desvergne, J. P.; Bouas-Laurent, H. Photodimers of a soluble tetracene derivative. excimer fluorescence from the head-to-head isomer. Org. Lett., 2004, 6, 1899-1902.
    • (2004) Org. Lett , vol.6 , pp. 1899-1902
    • Reichwagen, J.1    Hopf, H.2    Del Guerzo, A.3    Desvergne, J.P.4    Bouas-Laurent, H.5
  • 100
    • 0343258598 scopus 로고
    • Regioselective synthesis of substituted rubrenes
    • Dodge, J. A.; Bain, J. D.; Chamberlin, A. R. Regioselective synthesis of substituted rubrenes. J. Org. Chem., 1990, 55, 4190-4198.
    • (1990) J. Org. Chem , vol.55 , pp. 4190-4198
    • Dodge, J.A.1    Bain, J.D.2    Chamberlin, A.R.3
  • 101
    • 1642403575 scopus 로고
    • A colored hydrocarbon: Rubrene
    • Charles, M.; Charles, D.; Dean, P. M. A colored hydrocarbon: rubrene. Compt. Rend. 1926, 182, 1440-1443.
    • (1926) Compt. Rend , vol.182 , pp. 1440-1443
    • Charles, M.1    Charles, D.2    Dean, P.M.3
  • 103
    • 0000361469 scopus 로고
    • 5,6:11,12-Bis(ditelluro)tetracene: Synthesis, molecula, and supramolecular properties
    • Sandman, D. J.; Stark, J. C.; Foxman, B. M. 5,6:11,12-Bis(ditelluro)tetracene: synthesis, molecula, and supramolecular properties. Organometallics, 1982, 1, 739-742.
    • (1982) Organometallics , vol.1 , pp. 739-742
    • Sandman, D.J.1    Stark, J.C.2    Foxman, B.M.3
  • 104
    • 10344243379 scopus 로고
    • The structural problem of the tetracene series
    • Marshalk, C.; Stumm, C. The structural problem of the tetracene series. Bull. Soc. Chim. Fr., 1948, 418.
    • (1948) Bull. Soc. Chim. Fr , pp. 418
    • Marshalk, C.1    Stumm, C.2
  • 105
  • 106
    • 0010942365 scopus 로고
    • Naphthaceno [1,12-cd:4,5-c'd']bis[1,2]diseleole as a new electron donor
    • Miyamoto, H.; Aso, Y.; Otsubo, T.; Ogura, F. Naphthaceno [1,12-cd:4,5-c'd']bis[1,2]diseleole as a new electron donor. Bull. Chem. Soc. Jpn., 1990, 63, 2441-2443.
    • (1990) Bull. Chem. Soc. Jpn , vol.63 , pp. 2441-2443
    • Miyamoto, H.1    Aso, Y.2    Otsubo, T.3    Ogura, F.4
  • 107
    • 33744990854 scopus 로고    scopus 로고
    • Perfluoropentacene and perfluorotetracene: Syntheses, crystal structures, and FET characteristics
    • Sakamoto, Y.; Suzuki, T.; Kobayashi, M.; Gao, Y.; Inoue, Y.; Tokito, S. Perfluoropentacene and perfluorotetracene: syntheses, crystal structures, and FET characteristics. Mol. Cryst. Liq. Cryst., 2006, 444, 225-232.
    • (2006) Mol. Cryst. Liq. Cryst , vol.444 , pp. 225-232
    • Sakamoto, Y.1    Suzuki, T.2    Kobayashi, M.3    Gao, Y.4    Inoue, Y.5    Tokito, S.6
  • 108
    • 31544461755 scopus 로고    scopus 로고
    • Syntheses of soluble, pi-stacking tetracene derivatives
    • Chen, Z.; Muller, P.; Swager, T. M. Syntheses of soluble, pi-stacking tetracene derivatives. Org. Lett., 2006, 8, 273-276.
    • (2006) Org. Lett , vol.8 , pp. 273-276
    • Chen, Z.1    Muller, P.2    Swager, T.M.3
  • 110
    • 65249123392 scopus 로고    scopus 로고
    • A Meaningful analogue of pentacene: Charge transport, polymorphs, and electronic structures of dihydrodiazapentacene
    • Tang, Q.; Zhang, D.; Wang, S.; Ke, N.; Xu, J.; Yu, J. C.; Miao, Q. A Meaningful analogue of pentacene: charge transport, polymorphs, and electronic structures of dihydrodiazapentacene. Chem. Mater., 2009, 21, 1400-1405.
    • (2009) Chem. Mater , vol.21 , pp. 1400-1405
    • Tang, Q.1    Zhang, D.2    Wang, S.3    Ke, N.4    Xu, J.5    Yu, J.C.6    Miao, Q.7
  • 111
    • 85162681095 scopus 로고
    • Zur Kenntnis mehrkerniger aromatischer Kohlenwasserstoffeund ihrer Abkommlinge, V. Mitteil: Naphtho-anthracene, ihre O xydationsprodukte und eine neue Klasse tiefgefarbter Kohlenwasserstoffe
    • Clar, E.; John, F. Zur Kenntnis mehrkerniger aromatischer Kohlenwasserstoffeund ihrer Abkommlinge, V. Mitteil: Naphtho-anthracene, ihre O xydationsprodukte und eine neue Klasse tiefgefarbter Kohlenwasserstoffe. Chem. Ber., 1929, 62, 3021-3029.
    • (1929) Chem. Ber , vol.62 , pp. 3021-3029
    • Clar, E.1    John, F.2
  • 112
    • 78649956812 scopus 로고
    • Kondensationsprodukte des Anthrafuchsons
    • Clar, E.; Muller, W. Kondensationsprodukte des Anthrafuchsons. Chem. Ber., 1930, 63,869-873.
    • (1930) Chem. Ber , vol.63 , pp. 869-873
    • Clar, E.1    Muller, W.2
  • 113
    • 0038988852 scopus 로고
    • Zur Kenntnis mehrkerniger
    • Clar, E.; John, F. Zur Kenntnis mehrkerniger. Chem. Ber., 1931, 64, 2194-2200.
    • (1931) Chem. Ber , vol.64 , pp. 2194-2200
    • Clar, E.1    John, F.2
  • 114
    • 0042875649 scopus 로고
    • Cyclic Dienes. II. A new synthesis of pentacene
    • Bailey, W. J.; Madoff, M. Cyclic Dienes. II. A new synthesis of pentacene. J. Am. Chem. Soc., 1953, 75, 5603-5604.
    • (1953) J. Am. Chem. Soc , vol.75 , pp. 5603-5604
    • Bailey, W.J.1    Madoff, M.2
  • 115
    • 0000123990 scopus 로고
    • Isobenzofuran-aryne cycloadducts: Formation and regioselective conversion to anthrones and substituted polycyclic aromatics
    • Netka, J.; Crump, S. L.; Rickborn, B. Isobenzofuran-aryne cycloadducts: formation and regioselective conversion to anthrones and substituted polycyclic aromatics. J. Org. Chem., 1986, 51, 1189-1199.
    • (1986) J. Org. Chem , vol.51 , pp. 1189-1199
    • Netka, J.1    Crump, S.L.2    Rickborn, B.3
  • 116
    • 33845184269 scopus 로고
    • Syntheses and electrochemical properties of tetracyano-p-quinodimethane derivatives containing fused aromatic rings
    • Martin, N.; Behnisch, R.; Hanack, M. Syntheses and electrochemical properties of tetracyano-p-quinodimethane derivatives containing fused aromatic rings. J. Org. Chem., 1989, 54, 2563-2568.
    • (1989) J. Org. Chem , vol.54 , pp. 2563-2568
    • Martin, N.1    Behnisch, R.2    Hanack, M.3
  • 118
    • 0345685445 scopus 로고    scopus 로고
    • A soluble pentacene precursor: Synthesis, solid-state conversion into pentacene and application in a field-effect transistor
    • Peter, T. H.; Klaus, M. A soluble pentacene precursor: synthesis, solid-state conversion into pentacene and application in a field-effect transistor. Adv. Mater., 1999, 11, 480-483.
    • (1999) Adv. Mater , vol.11 , pp. 480-483
    • Peter, T.H.1    Klaus, M.2
  • 119
    • 0037205851 scopus 로고    scopus 로고
    • High-performance, solution-processed organic thin film transistors from a novel pentacene precursor
    • Afzali, A.; Dimitrakopoulos, C. D.; Breen, T. L. High-performance, solution-processed organic thin film transistors from a novel pentacene precursor. J. Am. Chem. Soc., 2002, 124, 8812-8813.
    • (2002) J. Am. Chem. Soc , vol.124 , pp. 8812-8813
    • Afzali, A.1    Dimitrakopoulos, C.D.2    Breen, T.L.3
  • 120
    • 0346500474 scopus 로고    scopus 로고
    • Photosensitive pentacene precursor: Synthesis, photothermal patterning, and application in thin-film transistors. Adv
    • Afzali, A.; Dimitrakopoulos, C. D.; Graham, T. O. Photosensitive pentacene precursor: synthesis, photothermal patterning, and application in thin-film transistors. Adv. Mater., 2003, 15, 2066-2069.
    • (2003) Mater , vol.15 , pp. 2066-2069
    • Afzali, A.1    Dimitrakopoulos, C.D.2    Graham, T.O.3
  • 121
    • 5744244910 scopus 로고    scopus 로고
    • A photopatternable pentacene precursor for use in organic thin-film transistors
    • Weidkamp, K. P.; Afzali, A.; Tromp, R. M.; Hamers, R. J. A photopatternable pentacene precursor for use in organic thin-film transistors. J. Am. Chem. Soc., 2004, 126, 12740-12741.
    • (2004) J. Am. Chem. Soc , vol.126 , pp. 12740-12741
    • Weidkamp, K.P.1    Afzali, A.2    Tromp, R.M.3    Hamers, R.J.4
  • 123
    • 33845375277 scopus 로고
    • The preparation and reactions of naphtho[1,2-c]furan and naphtho[2,3-c]furan
    • Smith, J. G.; Dibble, P. W.; Sandborn, R. E. The preparation and reactions of naphtho[1,2-c]furan and naphtho[2,3-c]furan. J. Org. Chem., 1986, 51, 3762-3768.
    • (1986) J. Org. Chem , vol.51 , pp. 3762-3768
    • Smith, J.G.1    Dibble, P.W.2    Sandborn, R.E.3
  • 124
    • 78649976830 scopus 로고
    • Synthesen in der Pentacen-Reihe (Aromatische Kohlenwasserstoffe und ihre Derivate, Xxxl. Mitteil.)
    • Clar, E. Synthesen in der Pentacen-Reihe (Aromatische Kohlenwasserstoffe und ihre Derivate, Xxxl. Mitteil.) Chem. Ber., 1940, 73, 409-415.
    • (1940) Chem. Ber , vol.73 , pp. 409-415
    • Clar, E.1
  • 125
    • 78649926883 scopus 로고
    • Les dibenzoyl-xylenes et les dinaphtanthracenediquinones
    • Henri de, D. Les dibenzoyl-xylenes et les dinaphtanthracenediquinones. Helv. Chim. Acta, 1923, 6, 539-548.
    • (1923) Helv. Chim. Acta , vol.6 , pp. 539-548
    • de Henri, D.1
  • 126
    • 29444441861 scopus 로고
    • The synthetical production of derivatives of dinaphthanthracene
    • Mills, W. H.; Miller, M. The synthetical production of derivatives of dinaphthanthracene. J. Chem. Soc., Trans., 1912, 101, 2194-2208.
    • (1912) J. Chem. Soc., Trans , vol.101 , pp. 2194-2208
    • Mills, W.H.1    Miller, M.2
  • 127
    • 34548749744 scopus 로고    scopus 로고
    • Double Diels-Alder strategies to soluble 2,9-and 2,9,6,13-tetraethynylpentacenes, photolytic [4+4] cycloadditions, and pentacene crystal packing
    • Benard, C. P.; Geng, Z.; Heuft, M. A.; VanCrey, K.; Fallis, A. G. Double Diels-Alder strategies to soluble 2,9-and 2,9,6,13-tetraethynylpentacenes, photolytic [4+4] cycloadditions, and pentacene crystal packing. J. Org. Chem., 2007, 72, 7229-7236.
    • (2007) J. Org. Chem , vol.72 , pp. 7229-7236
    • Benard, C.P.1    Geng, Z.2    Heuft, M.A.3    Vancrey, K.4    Fallis, A.G.5
  • 128
    • 34548258799 scopus 로고    scopus 로고
    • Synthesis of solution-soluble pentacene-containing conjugated copolymers
    • Okamoto, T.; Bao, Z. Synthesis of solution-soluble pentacene-containing conjugated copolymers. J. Am. Chem. Soc., 2007, 129, 10308-10309.
    • (2007) J. Am. Chem. Soc , vol.129 , pp. 10308-10309
    • Okamoto, T.1    Bao, Z.2
  • 130
    • 12844259591 scopus 로고    scopus 로고
    • A soluble pentacene: Synthesis, EPR and electrochemical studies of 2,3,9,10-tetrakis(trimethylsilyl)pentacene
    • Chan, S. H.; Lee, H. K.; Wang, Y. M.; Fu, N. Y.; Chen, X. M.; Cai, Z. W.; Wong, H. N. C. A soluble pentacene: synthesis, EPR and electrochemical studies of 2,3,9,10-tetrakis(trimethylsilyl)pentacene. Chem. Commun., 2005, 66-68.
    • (2005) Chem. Commun , pp. 66-68
    • Chan, S.H.1    Lee, H.K.2    Wang, Y.M.3    Fu, N.Y.4    Chen, X.M.5    Cai, Z.W.6    Wong, H.N.C.7
  • 132
    • 33644548645 scopus 로고    scopus 로고
    • Asymmetric pentacene derivatives for organic light-emitting diodes
    • Jang, B. B.; Lee, S. H.; Kafafi, Z. H. Asymmetric pentacene derivatives for organic light-emitting diodes. Chem. Mater., 2006, 18, 449-457.
    • (2006) Chem. Mater , vol.18 , pp. 449-457
    • Jang, B.B.1    Lee, S.H.2    Kafafi, Z.H.3
  • 134
    • 2442701630 scopus 로고    scopus 로고
    • Functionalized pentacene derivatives for use as red emitters in organic light-emitting diodes
    • Wolak, M. A.; Jang, B. B.; Palilis, L. C.; Kafafi, Z. H. Functionalized pentacene derivatives for use as red emitters in organic light-emitting diodes. J. Phys. Chem. B, 2004, 108, 5492-5499.
    • (2004) J. Phys. Chem. B , vol.108 , pp. 5492-5499
    • Wolak, M.A.1    Jang, B.B.2    Palilis, L.C.3    Kafafi, Z.H.4
  • 135
    • 31544455540 scopus 로고    scopus 로고
    • Synthesis and luminescent properties of pentacene derivatives having a chromophore
    • Hwang, E. J.; Kim, Y. E.; Lee, C. J.; Park, J. W. Synthesis and luminescent properties of pentacene derivatives having a chromophore. Thin Solid Films, 2006, 499, 185-191.
    • (2006) Thin Solid Films , vol.499 , pp. 185-191
    • Hwang, E.J.1    Kim, Y.E.2    Lee, C.J.3    Park, J.W.4
  • 136
    • 0035955152 scopus 로고    scopus 로고
    • Functionalized pentacene: Improved electronic properties from control of solid-state order
    • Anthony, J. E.; Brooks, J. S.; Eaton, D. L.; Parkin, S. R. Functionalized pentacene: improved electronic properties from control of solid-state order. J. Am. Chem. Soc., 2001, 123, 9482-9483.
    • (2001) J. Am. Chem. Soc , vol.123 , pp. 9482-9483
    • Anthony, J.E.1    Brooks, J.S.2    Eaton, D.L.3    Parkin, S.R.4
  • 137
    • 33947299299 scopus 로고
    • Electronic absorption and fluorescence of phenylethynyl-substituted acenes
    • Maulding, D. R.; Roberts, B. G. Electronic absorption and fluorescence of phenylethynyl-substituted acenes. J. Org. Chem., 1969, 34, 1734-1736.
    • (1969) J. Org. Chem , vol.34 , pp. 1734-1736
    • Maulding, D.R.1    Roberts, B.G.2
  • 138
    • 0009784459 scopus 로고    scopus 로고
    • A road map to stable, soluble, easily crystallized pentacene derivatives
    • Anthony, J. E.; Eaton, D. L.; Parkin, S. R. A road map to stable, soluble, easily crystallized pentacene derivatives. Org. Lett., 2002, 4, 15-18.
    • (2002) Org. Lett , vol.4 , pp. 15-18
    • Anthony, J.E.1    Eaton, D.L.2    Parkin, S.R.3
  • 139
    • 0346937202 scopus 로고    scopus 로고
    • Funcationalized pentacene active layer organic thin-film transistor
    • Sheraw, C. D.; Jackson, T. N.; Eaton, D. L.; Anthony, J. E. Funcationalized pentacene active layer organic thin-film transistor. Adv. Mater., 2003, 15, 2009-2011.
    • (2003) Adv. Mater , vol.15 , pp. 2009-2011
    • Sheraw, C.D.1    Jackson, T.N.2    Eaton, D.L.3    Anthony, J.E.4
  • 140
    • 35948943412 scopus 로고    scopus 로고
    • Pentacene oligomers and polymers: Functionalization of pentacene to afford mono-, di-, tri-, and polymeric materials
    • Lehnherr, D.; Tykwinski, R. R. Pentacene oligomers and polymers: functionalization of pentacene to afford mono-, di-, tri-, and polymeric materials. Org. Lett., 2007, 9, 4583-4586.
    • (2007) Org. Lett , vol.9 , pp. 4583-4586
    • Lehnherr, D.1    Tykwinski, R.R.2
  • 141
    • 34547927062 scopus 로고    scopus 로고
    • Synthesis of highly soluble and oxidatively stable tetraceno[2,3-b]thiophenes and pentacenes
    • Palayangoda, S. S.; Mondal, R.; Shah, B. K.; Neckers, D. C. Synthesis of highly soluble and oxidatively stable tetraceno[2,3-b]thiophenes and pentacenes. J. Org. Chem., 2007, 72, 6584-6587.
    • (2007) J. Org. Chem , vol.72 , pp. 6584-6587
    • Palayangoda, S.S.1    Mondal, R.2    Shah, B.K.3    Neckers, D.C.4
  • 143
    • 33644651426 scopus 로고    scopus 로고
    • High performance, acene-based organic thin film transistors
    • Jiang, J.; Kaafarani, B. R.; Neckers, D. C. High performance, acene-based organic thin film transistors. J. Org. Chem., 2006, 71, 2155-2158.
    • (2006) J. Org. Chem , vol.71 , pp. 2155-2158
    • Jiang, J.1    Kaafarani, B.R.2    Neckers, D.C.3
  • 145
    • 65249092698 scopus 로고    scopus 로고
    • Synthesis, crystal structure, and physical properties of 7,14-disubstituted pentacene-5,12-diones containing a methylenequinoid structure
    • Nishida, J.-i.; Fujiwara, Y.; Yamashita, Y. Synthesis, crystal structure, and physical properties of 7,14-disubstituted pentacene-5,12-diones containing a methylenequinoid structure. Org. Lett., 2009, 11, 1813-1816.
    • (2009) Org. Lett , vol.11 , pp. 1813-1816
    • Nishida, J.-I.1    Fujiwara, Y.2    Yamashita, Y.3
  • 146
    • 55049139067 scopus 로고    scopus 로고
    • Exploring electronically polarized pentacenes
    • Lehnherr, D.; McDonald, R.; Tykwinski, R. R. Exploring electronically polarized pentacenes. Org. Lett., 2008, 10, 4163-4166.
    • (2008) Org. Lett , vol.10 , pp. 4163-4166
    • Lehnherr, D.1    McDonald, R.2    Tykwinski, R.R.3
  • 147
    • 60949102830 scopus 로고    scopus 로고
    • Synthesis and electronic properties of conjugated pentacene dimers
    • Lehnherr, D.; Gao, J.; Hegmann, F. A.; Tykwinski, R. R. Synthesis and electronic properties of conjugated pentacene dimers. Org. Lett., 2008, 10, 4779-4782.
    • (2008) Org. Lett , vol.10 , pp. 4779-4782
    • Lehnherr, D.1    Gao, J.2    Hegmann, F.A.3    Tykwinski, R.R.4
  • 148
    • 75649128701 scopus 로고    scopus 로고
    • A Cruciform 6, 6'-dipentacenyl: Synthesis, solid-state packing and applications in thin-film transistors
    • Zhang, X.; Jiang, X.; Li, J.; Chi C.; Chen, H.; Wu, J. A Cruciform 6, 6'-dipentacenyl: synthesis, solid-state packing and applications in thin-film transistors. Chem. Eur. J., 2009, 16, 464-468.
    • (2009) Chem. Eur. J , vol.16 , pp. 464-468
    • Zhang, X.1    Jiang, X.2    Li, J.3    Chi, C.4    Chen, H.5    Wu, J.6
  • 149
    • 37049126146 scopus 로고
    • Synthesis, structure, and electrical properties of naphthacene, pentacene, and hexacene sulphides
    • Goodings, E. P.; Mitchard, D. A.; Owen, G. Synthesis, structure, and electrical properties of naphthacene, pentacene, and hexacene sulphides. J. Chem. Soc., Perkin Trans. 1, 1972, 1310-1314.
    • (1972) J. Chem. Soc., Perkin Trans , vol.1 , pp. 1310-1314
    • Goodings, E.P.1    Mitchard, D.A.2    Owen, G.3
  • 150
    • 33845430762 scopus 로고    scopus 로고
    • Hexathiapentacene: Structure, molecular packing, and thin-film transistors
    • Briseno, A. L.; Miao, Q.; Ling, M.-M.; Reese, C.; Meng, H.; Bao, Z.; Wudl, F. Hexathiapentacene: structure, molecular packing, and thin-film transistors. J. Am. Chem. Soc., 2006, 128, 15576-15577.
    • (2006) J. Am. Chem. Soc , vol.128 , pp. 15576-15577
    • Briseno, A.L.1    Miao, Q.2    Ling, M.-M.3    Reese, C.4    Meng, H.5    Bao, Z.6    Wudl, F.7
  • 151
    • 33745697775 scopus 로고    scopus 로고
    • Synthesis and cofacial pi-stacked packing arrangement of 6,13-bis(alkylthio)pentacene
    • Kobayashi, K.; Shimaoka, R.; Kawahata, M.; Yamanaka, M.; Yamaguchi, K. Synthesis and cofacial pi-stacked packing arrangement of 6,13-bis(alkylthio)pentacene. Org. Lett., 2006, 8, 2385-2388.
    • (2006) Org. Lett , vol.8 , pp. 2385-2388
    • Kobayashi, K.1    Shimaoka, R.2    Kawahata, M.3    Yamanaka, M.4    Yamaguchi, K.5
  • 153
    • 33244467710 scopus 로고    scopus 로고
    • Chemical complementarity in the contacts for nanoscale organic field-effect transistors
    • Tulevski, G. S.; Miao, Q.; Afzali, A.; Graham, T. O.; Kagan, C. R.; Nuckolls, C. Chemical complementarity in the contacts for nanoscale organic field-effect transistors. J. Am. Chem. Soc., 2006, 128, 1788-1789.
    • (2006) J. Am. Chem. Soc , vol.128 , pp. 1788-1789
    • Tulevski, G.S.1    Miao, Q.2    Afzali, A.3    Graham, T.O.4    Kagan, C.R.5    Nuckolls, C.6
  • 155
    • 35748937636 scopus 로고    scopus 로고
    • Synthesis, characterization, and field-effect transistor performance of pentacene derivatives
    • Okamoto, T.; Senatore, M.; Ling, M. M.; Mallik, A.; Tang, M.; Bao, Z. Synthesis, characterization, and field-effect transistor performance of pentacene derivatives. Adv. Mater., 2007, 19, 3381-3384.
    • (2007) Adv. Mater , vol.19 , pp. 3381-3384
    • Okamoto, T.1    Senatore, M.2    Ling, M.M.3    Mallik, A.4    Tang, M.5    Bao, Z.6
  • 157
    • 58149313613 scopus 로고    scopus 로고
    • Synthesis and characterization of 2,9-bis(perfluorobutyl)pentacene as an n-type organic field-effect transistor
    • Okamoto, K.; Ogino, K.; Ikari, M.; Kunugi, Y. Synthesis and characterization of 2,9-bis(perfluorobutyl)pentacene as an n-type organic field-effect transistor. Bull. Chem. Soc. Jpn., 2008, 81, 530-535.
    • (2008) Bull. Chem. Soc. Jpn , vol.81 , pp. 530-535
    • Okamoto, K.1    Ogino, K.2    Ikari, M.3    Kunugi, Y.4
  • 158
  • 159
    • 10344257104 scopus 로고
    • Linear hexacenes
    • Marschalk, Ch. Linear hexacenes. Bull. Soc. Chim., 1939, 6, 1112-1121.
    • (1939) Bull. Soc. Chim , vol.6 , pp. 1112-1121
    • Marschalk, C.1
  • 160
    • 85171974454 scopus 로고
    • Vorschlage zur Nomenklatur kondensierter Ringsysteme (Aromatische Kohlenwasserstoffe, XXVI. Mitteil.)
    • Clar, E. Vorschlage zur Nomenklatur kondensierter Ringsysteme (Aromatische Kohlenwasserstoffe, XXVI. Mitteil.). Chem. Ber., 1939, 72B, 2137-2139.
    • (1939) Chem. Ber , vol.72 B , pp. 2137-2139
    • Clar, E.1
  • 161
    • 10344248572 scopus 로고
    • Eine neue Synthese des Hexacens (Aromatische Kohlenwasserstoffe, XXXIV. Mitteil.)
    • Clar, E. Eine neue Synthese des Hexacens (Aromatische Kohlenwasserstoffe, XXXIV. Mitteil.). Chem. Ber., 1942, 75B, 1283-1287.
    • (1942) Chem. Ber , vol.75 B , pp. 1283-1287
    • Clar, E.1
  • 163
    • 33746660263 scopus 로고    scopus 로고
    • Photogeneration of heptacene in a polymer matrix
    • Mondal, R.; Shah, B. K.; Neckers, D. C. Photogeneration of heptacene in a polymer matrix. J. Am. Chem. Soc., 2006, 128, 9612-9613.
    • (2006) J. Am. Chem. Soc , vol.128 , pp. 9612-9613
    • Mondal, R.1    Shah, B.K.2    Neckers, D.C.3
  • 164
    • 70349901108 scopus 로고    scopus 로고
    • Synthesis, stability, and photochemistry of pentacene, hexacene, and heptacene: A matrix isolation study
    • Mondal, R.; Tonshoff, C.; Khon, D.; Neckers, D. C.; Bettinger, H. F. Synthesis, stability, and photochemistry of pentacene, hexacene, and heptacene: a matrix isolation study. J. Am. Chem. Soc., 2009, 131, 14281-14289.
    • (2009) J. Am. Chem. Soc , vol.131 , pp. 14281-14289
    • Mondal, R.1    Tonshoff, C.2    Khon, D.3    Neckers, D.C.4    Bettinger, H.F.5
  • 165
    • 85171975413 scopus 로고
    • Heptacen ein einfacher
    • Clar, E. Heptacen ein einfacher. Chem. Ber., 1942, 75B, 1330-1338.
    • (1942) Chem. Ber , vol.75 B , pp. 1330-1338
    • Clar, E.1
  • 166
    • 0039143678 scopus 로고
    • Cyclic Dienes. XI. New syntheses of hexacene and heptacene
    • Bailey, W. J.; Liao, C. W. Cyclic Dienes. XI. New syntheses of hexacene and heptacene. J. Am. Chem. Soc., 1955, 77, 992-993.
    • (1955) J. Am. Chem. Soc , vol.77 , pp. 992-993
    • Bailey, W.J.1    Liao, C.W.2
  • 167
    • 11644322213 scopus 로고
    • Synthesis of linear aromatic polynuclear derivatives of heptacene and octacene
    • Marschalk, C. Synthesis of linear aromatic polynuclear derivatives of heptacene and octacene. Bull. Soc. Chim. Fr., 1941, 8, 354-369.
    • (1941) Bull. Soc. Chim. Fr , vol.8 , pp. 354-369
    • Marschalk, C.1
  • 168
    • 10344234080 scopus 로고
    • Note on the article by E. Clar entitled Heptacene, an ultragreen hydrocarbon
    • Marschalk, C. Note on the article by E. Clar entitled Heptacene, an ultragreen hydrocarbon. Bull. Soc. Chim. Fr., 1943, 10, 511-512.
    • (1943) Bull. Soc. Chim. Fr , vol.10 , pp. 511-512
    • Marschalk, C.1
  • 169
    • 78649948630 scopus 로고    scopus 로고
    • For a whole story on the synthesis of heptacene, referring to: Duong, H. M., Phd Thesis, University of California, Los Angeles, USA
    • For a whole story on the synthesis of heptacene, referring to: Duong, H. M. Synthetic Strategies and Building Blocks for the Assembly of Heteroacenes, Polyacenes and Twistacenes. Phd Thesis, University of California, Los Angeles, USA. 2003, pp. 15-17.
    • (2003) Synthetic Strategies and Building Blocks For the Assembly of Heteroacenes, Polyacenes and Twistacenes , pp. 15-17
  • 170
    • 37049050411 scopus 로고
    • Four higher annellated pyrenes with acene character
    • Boggiano, B.; Clar, E. Four higher annellated pyrenes with acene character. J. Chem. Soc., 1957, 2681-2689.
    • (1957) J. Chem. Soc , pp. 2681-2689
    • Boggiano, B.1    Clar, E.2
  • 171
    • 0040056568 scopus 로고
    • Correlations between photoelectron and ultraviolet absorption spectra of polycyclic hydrocarbons and the number of aroatic sextets
    • Clar, E.; Schmidt, W. Correlations between photoelectron and ultraviolet absorption spectra of polycyclic hydrocarbons and the number of aroatic sextets. Tetrahedron, 1975, 31, 2263-2271.
    • (1975) Tetrahedron , vol.31 , pp. 2263-2271
    • Clar, E.1    Schmidt, W.2
  • 173
    • 20444430141 scopus 로고    scopus 로고
    • Functionalized higher acenes: Hexacene and heptacene
    • Payne, M. M.; Parkin, S. R.; Anthony, J. E. Functionalized higher acenes: hexacene and heptacene. J. Am. Chem. Soc., 2005, 127, 8028-8029.
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 8028-8029
    • Payne, M.M.1    Parkin, S.R.2    Anthony, J.E.3
  • 174
    • 54249130646 scopus 로고    scopus 로고
    • The most stable and fully characterized functionalized heptacene
    • Chun, D.; Cheng, Y.; Wudl, F. The most stable and fully characterized functionalized heptacene. Angew. Chem., Int. Ed., 2008, 47, 8380-8385.
    • (2008) Angew. Chem., Int. Ed , pp. 8380-8385
    • Chun, D.1    Cheng, Y.2    Wudl, F.3
  • 175
    • 67749093231 scopus 로고    scopus 로고
    • Exploiting substituent effects for the synthesis of a photooxidatively resistant heptacene derivative
    • Kaur, I.; Stein, N. N.; Kopreski, R. P.; Miller, G. P. Exploiting substituent effects for the synthesis of a photooxidatively resistant heptacene derivative. J. Am. Chem. Soc., 2009, 131, 3424-3425.
    • (2009) J. Am. Chem. Soc , vol.131 , pp. 3424-3425
    • Kaur, I.1    Stein, N.N.2    Kopreski, R.P.3    Miller, G.P.4
  • 176
    • 0035908561 scopus 로고    scopus 로고
    • Interchain interactions in organic pi-conjugated materials: Impact on electronic structure, optical response, and charge transport
    • Cornil, J.; Beljonne, D.; Calbert, J. P.; Breas, J. L. Interchain interactions in organic pi-conjugated materials: impact on electronic structure, optical response, and charge transport. Adv. Mater., 2001, 13, 1053-1067.
    • (2001) Adv. Mater , vol.13 , pp. 1053-1067
    • Cornil, J.1    Beljonne, D.2    Calbert, J.P.3    Breas, J.L.4
  • 177
    • 23044439062 scopus 로고    scopus 로고
    • Synthesis and structure of fused α-oligothiophenes with up to seven rings
    • Zhang, X.; Cote, A. P.; Matzger, A. J. Synthesis and structure of fused α-oligothiophenes with up to seven rings. J. Am. Chem. Soc., 2005, 127, 10502-10503.
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 10502-10503
    • Zhang, X.1    Cote, A.P.2    Matzger, A.J.3
  • 178
    • 36248993379 scopus 로고    scopus 로고
    • Polycyclic aromatic compounds for organic field-effect transistors: Molecular design and syntheses
    • Wu, J. S. Polycyclic aromatic compounds for organic field-effect transistors: molecular design and syntheses. Curr. Org. Chem., 2007, 11, 1220-1240.
    • (2007) Curr. Org. Chem , vol.11 , pp. 1220-1240
    • Wu, J.S.1
  • 180
    • 62149101480 scopus 로고    scopus 로고
    • Synthesis, characterization, and field-effect transistor performance of thieno[3,2-b]thieno[2',3':4,5]thieno[2,3-d]thiophene Derivatives
    • Liu, Y.; Wang, Y.; Wu, W.; Liu, Y.; Xi, H.; Wang, L.; Qiu, W.; Lu, K.; Du, C.; Yu, G. Synthesis, characterization, and field-effect transistor performance of thieno[3,2-b]thieno[2',3':4,5]thieno[2,3-d]thiophene Derivatives. Adv. Funct. Mater., 2009, 19, 772-778.
    • (2009) Adv. Funct. Mater , vol.19 , pp. 772-778
    • Liu, Y.1    Wang, Y.2    Wu, W.3    Liu, Y.4    Xi, H.5    Wang, L.6    Qiu, W.7    Lu, K.8    Du, C.9    Yu, G.10
  • 181
    • 0000437584 scopus 로고
    • Synthesis of tetrathieno-acene and pentathieno-acene: UV-spectral trend in a homologous series of thieno-acenes
    • Mazaki, Y.; Kobayashi, K. Synthesis of tetrathieno-acene and pentathieno-acene: UV-spectral trend in a homologous series of thieno-acenes. Tetrahedron Lett. 1989, 30, 3315-3318.
    • (1989) Tetrahedron Lett , vol.30 , pp. 3315-3318
    • Mazaki, Y.1    Kobayashi, K.2
  • 184
    • 33846259818 scopus 로고    scopus 로고
    • General synthesis of extended fused oligothiophenes consisting of an even number of thiophene rings
    • Okamoto, T.; Kudoh, K.; Wakamiya, A.; Yamaguchi, S. General synthesis of extended fused oligothiophenes consisting of an even number of thiophene rings. Chem. Eur. J., 2007, 13, 548-556.
    • (2007) Chem. Eur. J , vol.13 , pp. 548-556
    • Okamoto, T.1    Kudoh, K.2    Wakamiya, A.3    Yamaguchi, S.4
  • 185
    • 1942489279 scopus 로고    scopus 로고
    • 2,6-Diphenylbenzo[1,2-b:4,5-b']dichalcogenophenes: A new class of high-performance semiconductors for organic field-effect transistors
    • Takimiya, K.; Kunugi, Y.; Konda, Y.; Niihara, N.; Otsubo, T. 2,6-Diphenylbenzo[1,2-b:4,5-b']dichalcogenophenes: a new class of high-performance semiconductors for organic field-effect transistors. J. Am. Chem. Soc., 2004, 126, 5084-5085.
    • (2004) J. Am. Chem. Soc , vol.126 , pp. 5084-5085
    • Takimiya, K.1    Kunugi, Y.2    Konda, Y.3    Niihara, N.4    Otsubo, T.5
  • 186
    • 35948981512 scopus 로고    scopus 로고
    • Synthesis, properties, and structures of benzo[1,2-b:4,5-b']bis[b]benzothiophene and benzo [1,2-b:4,5-b']bis[b]benzoselenophene
    • Ebata, H.; Miyazaki, E.; Yamamoto, T.; Takimiya, K. Synthesis, properties, and structures of benzo[1,2-b:4,5-b']bis[b]benzothiophene and benzo [1,2-b:4,5-b']bis[b]benzoselenophene. Org. Lett., 2007, 9, 4499-4502.
    • (2007) Org. Lett , vol.9 , pp. 4499-4502
    • Ebata, H.1    Miyazaki, E.2    Yamamoto, T.3    Takimiya, K.4
  • 187
    • 63549139199 scopus 로고    scopus 로고
    • 2,6-Bis(tributyltin)benzo [1,2-b:5,4-b']dithiophene: A new synthon for organic semiconductors
    • Boone, M. P.; Dienes, Y.; Baumgartner, T. 2,6-Bis(tributyltin)benzo [1,2-b:5,4-b']dithiophene: a new synthon for organic semiconductors. Arkivoc, 2009, 90-101.
    • (2009) Arkivoc , pp. 90-101
    • Boone, M.P.1    Dienes, Y.2    Baumgartner, T.3
  • 188
    • 42049117919 scopus 로고    scopus 로고
    • 2,6-Dialkylbenzo[1,2-b:4,5-b'] dithiophenes (Cn-BDTs) as soluble organic semiconductors for solution-processed organic field-effect transistors
    • Kashiki, T.; Miyazaki, E.; Takimiya, K. 2,6-Dialkylbenzo[1,2-b:4,5-b'] dithiophenes (Cn-BDTs) as soluble organic semiconductors for solution-processed organic field-effect transistors. Chem. Lett., 2008, 37, 284-285.
    • (2008) Chem. Lett , vol.37 , pp. 284-285
    • Kashiki, T.1    Miyazaki, E.2    Takimiya, K.3
  • 190
    • 33749514976 scopus 로고    scopus 로고
    • 2,7-Diphenyl[1]benzothieno[3,2-b]benzothiophene, A new organic semiconductor for air-stable organic field-effect transistors with mobilities up to 2.0 cm2V-1s-1
    • Takimiya, K.; Ebata, H.; Sakamoto, K.; Izawa, T.; Otsubo, T.; Kunugi, Y. 2,7-Diphenyl[1]benzothieno[3,2-b]benzothiophene, A new organic semiconductor for air-stable organic field-effect transistors with mobilities up to 2.0 cm2V-1s-1 J. Am. Chem. Soc., 2006, 128, 12604-12605.
    • (2006) J. Am. Chem. Soc , vol.128 , pp. 12604-12605
    • Takimiya, K.1    Ebata, H.2    Sakamoto, K.3    Izawa, T.4    Otsubo, T.5    Kunugi, Y.6
  • 191
    • 54949117149 scopus 로고    scopus 로고
    • Molecular ordering of high-performance soluble molecular semiconductors and re-evaluation of their field-effect transistor characteristics
    • Takafumi, I.; Eigo, M.; Kazuo, T. Molecular ordering of high-performance soluble molecular semiconductors and re-evaluation of their field-effect transistor characteristics. Adv. Mater., 2008, 20, 3388-3392.
    • (2008) Adv. Mater , vol.20 , pp. 3388-3392
    • Takafumi, I.1    Eigo, M.2    Kazuo, T.3
  • 192
    • 47749086663 scopus 로고    scopus 로고
    • Anthra[2,3-b]benzo[d]thiophene: An air-stable asymmetric organic semiconductor with high mobility at room temperature
    • Du, C.; Guo, Y.; Liu, Y.; Qiu, W.; Zhang, H.; Gao, X.; Liu, Y.; Qi, T.; Lu, K.; Yu, G. Anthra[2,3-b]benzo[d]thiophene: an air-stable asymmetric organic semiconductor with high mobility at room temperature. Chem. Mater., 2008, 20, 4188-4190.
    • (2008) Chem. Mater , vol.20 , pp. 4188-4190
    • Du, C.1    Guo, Y.2    Liu, Y.3    Qiu, W.4    Zhang, H.5    Gao, X.6    Liu, Y.7    Qi, T.8    Lu, K.9    Yu, G.10
  • 193
    • 84986524530 scopus 로고
    • The synthesis of benzo[b]--phenanthro[d]thiophenes and anthra[b]benzo[d]thiophenes
    • Tedjamulia, M. L.; Tominaga, Y.; Castle, R. N. The synthesis of benzo[b]--phenanthro[d]thiophenes and anthra[b]benzo[d]thiophenes. J. Heterocycl. Chem., 1983, 20, 861-866.
    • (1983) J. Heterocycl. Chem , vol.20 , pp. 861-866
    • Tedjamulia, M.L.1    Tominaga, Y.2    Castle, R.N.3
  • 194
    • 19544383064 scopus 로고    scopus 로고
    • Synthesis of the anti and syn isomers of thieno[f,f']bis[1]benzothiophene. Comparison of the optical and electrochemical properties of the anti and syn isomers
    • Wex, B.; Kaafarani, B. R.; Kirschbaum, K.; Neckers, D. C. Synthesis of the anti and syn isomers of thieno[f,f']bis[1]benzothiophene. Comparison of the optical and electrochemical properties of the anti and syn isomers. J. Org. Chem., 2005, 70, 4502-4505
    • (2005) J. Org. Chem , vol.70 , pp. 4502-4505
    • Wex, B.1    Kaafarani, B.R.2    Kirschbaum, K.3    Neckers, D.C.4
  • 196
    • 0001343690 scopus 로고
    • Action of sulfur on organic compounds
    • Szperl, L. Action of sulfur on organic compounds. Rocz. Chem., 1938, 18, 804-811.
    • (1938) Rocz. Chem , vol.18 , pp. 804-811
    • Szperl, L.1
  • 197
    • 35348998520 scopus 로고    scopus 로고
    • High-performance field-effect transistor based on dibenzo[d,d']thieno[3,2-b;4,5-b']dithiophene, an easily synthesized semiconductor with high ionization potential
    • Gao, J.; Li, R.; Li, L.; Meng, Q.; Jiang, H.; Li, H.; Hu, W. High-performance field-effect transistor based on dibenzo[d,d']thieno[3,2-b;4,5-b']dithiophene, an easily synthesized semiconductor with high ionization potential. Adv. Mater., 2007, 19, 3008-3011.
    • (2007) Adv. Mater , vol.19 , pp. 3008-3011
    • Gao, J.1    Li, R.2    Li, L.3    Meng, Q.4    Jiang, H.5    Li, H.6    Hu, W.7
  • 198
    • 41049106047 scopus 로고    scopus 로고
    • Benzo[1,2-b:4,5-b']bis[b]benzothiophene as solution processible organic semiconductor for field-effect transistors
    • Gao, P.; Beckmann, D.; Tsao, H. N.; Feng, X.; Enkelmann, V.; Pisula, W.; Mullen, K. Benzo[1,2-b:4,5-b']bis[b]benzothiophene as solution processible organic semiconductor for field-effect transistors. Chem. Commun., 2008, 1548-1550.
    • (2008) Chem. Commun , pp. 1548-1550
    • Gao, P.1    Beckmann, D.2    Tsao, H.N.3    Feng, X.4    Enkelmann, V.5    Pisula, W.6    Mullen, K.7
  • 199
    • 0032481337 scopus 로고    scopus 로고
    • Synthesis, morphology, and field-effect mobility of anthradithiophenes
    • Laquindanum, J. G.; Katz, H. E.; Lovinger, A. J. Synthesis, morphology, and field-effect mobility of anthradithiophenes. J. Am. Chem. Soc., 1998, 120, 664-672.
    • (1998) J. Am. Chem. Soc , vol.120 , pp. 664-672
    • Laquindanum, J.G.1    Katz, H.E.2    Lovinger, A.J.3
  • 200
    • 0034873221 scopus 로고    scopus 로고
    • Synthetic chemistry for ultrapure, processable, and high-mobility organic transistor semiconductors
    • Katz, H. E.; Bao, Z.; Gilat, S. L. Synthetic chemistry for ultrapure, processable, and high-mobility organic transistor semiconductors. Acc. Chem. Res., 2001, 34, 359-369.
    • (2001) Acc. Chem. Res , vol.34 , pp. 359-369
    • Katz, H.E.1    Bao, Z.2    Gilat, S.L.3
  • 201
    • 33847689723 scopus 로고    scopus 로고
    • Facile synthesis of highly pi-extended heteroarenes, dinaphtho[2,3-b:2,3'-f]chalcogenopheno[3,2-b]chalcogenophenes, and their application to field-effect transistors
    • Yamamoto, T.; Takimiya, K. Facile synthesis of highly pi-extended heteroarenes, dinaphtho[2,3-b:2,3'-f]chalcogenopheno[3,2-b]chalcogenophenes, and their application to field-effect transistors. J. Am. Chem. Soc., 2007, 129, 2224-2225.
    • (2007) J. Am. Chem. Soc , vol.129 , pp. 2224-2225
    • Yamamoto, T.1    Takimiya, K.2
  • 202
    • 67749110114 scopus 로고    scopus 로고
    • Pentaceno[ 2,3-b]thiophene, a hexacene analogue for organic thin film transistors
    • Tang, M. L.; Mannsfeld, S. C. B.; Sun, Y.-S.; Becerril, H. A.; Bao, Z. Pentaceno[ 2,3-b]thiophene, a hexacene analogue for organic thin film transistors. J. Am. Chem. Soc., 2009, 131, 882-883.
    • (2009) J. Am. Chem. Soc , vol.131 , pp. 882-883
    • Tang, M.L.1    Mannsfeld, S.C.B.2    Sun, Y.-S.3    Becerril, H.A.4    Bao, Z.5
  • 203
    • 4644247573 scopus 로고    scopus 로고
    • Stable, crystalline acenedithiophenes with up to seven linearly fused rings
    • Payne, M. M.; Odom, S. A.; Parkin, S. R.; Anthony, J. E. Stable, crystalline acenedithiophenes with up to seven linearly fused rings. Org. Lett., 2004, 6, 3325-3328.
    • (2004) Org. Lett , vol.6 , pp. 3325-3328
    • Payne, M.M.1    Odom, S.A.2    Parkin, S.R.3    Anthony, J.E.4
  • 204
    • 40949096935 scopus 로고    scopus 로고
    • Chromophore fluorination enhances crystallization and stability of soluble anthradithiophene semiconductors
    • Subramanian, S.; Park, S. K.; Parkin, S. R.; Podzorov, V.; Jackson, T. N.; Anthony, J. E. Chromophore fluorination enhances crystallization and stability of soluble anthradithiophene semiconductors. J. Am. Chem. Soc., 2008, 130, 2706-2707.
    • (2008) J. Am. Chem. Soc , vol.130 , pp. 2706-2707
    • Subramanian, S.1    Park, S.K.2    Parkin, S.R.3    Podzorov, V.4    Jackson, T.N.5    Anthony, J.E.6
  • 205
    • 0035838876 scopus 로고    scopus 로고
    • Polyacene and cyclacene geometries and electronic structures: Bond equalization, vanishing band gaps, and triplet ground states contrast with polyacetylene
    • Houk, K. N.; Lee, P. S.; Nendel, M. Polyacene and cyclacene geometries and electronic structures: bond equalization, vanishing band gaps, and triplet ground states contrast with polyacetylene. J. Org. Chem., 2001, 66, 5517-5521.
    • (2001) J. Org. Chem , vol.66 , pp. 5517-5521
    • Houk, K.N.1    Lee, P.S.2    Nendel, M.3


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