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Volumn 5, Issue 1, 2011, Pages

Theoretical study on the electronic, structural, properties and reactivity of a series of mono-, di-, tri- and tetrachlorothiophenes as well as corresponding radical cation forms as monomers for conducting polymers

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EID: 79952495791     PISSN: None     EISSN: 1752153X     Source Type: Journal    
DOI: 10.1186/1752-153X-5-13     Document Type: Article
Times cited : (5)

References (49)
  • 1
    • 79952455412 scopus 로고    scopus 로고
    • Theoretical study on the electronic, structural, properties and reactivity of a series of mono-, di-, tri- and tetrafluorothiophenes as well as corresponding radical cation forms
    • Jameh-Bozorghi S, Shirani ILH. Theoretical study on the electronic, structural, properties and reactivity of a series of mono-, di-, tri- and tetrafluorothiophenes as well as corresponding radical cation forms. J Fluor Chem 2011,
    • (2011) J Fluor Chem
    • Jameh-Bozorghi, S.1    Shirani, I.L.H.2
  • 2
    • 0035898341 scopus 로고    scopus 로고
    • Synthetic metals: A novel role for organic polymers
    • MacDiarmid AG. Synthetic metals: A novel role for organic polymers. Chem Int E 2001, 40:2581-2585.
    • (2001) Chem Int E , vol.40 , pp. 2581-2585
    • MacDiarmid, A.G.1
  • 3
    • 0142062490 scopus 로고    scopus 로고
    • Novel UV cured coatings and adhesives based on the photoinitiated cyclopolymerization of derivatives of diallylamine
    • Hall AW, Blackwood KM, Milne PE, Goodby JW. Novel UV cured coatings and adhesives based on the photoinitiated cyclopolymerization of derivatives of diallylamine. Chem Commun 2003, 2530-2531.
    • (2003) Chem Commun , pp. 2530-2531
    • Hall, A.W.1    Blackwood, K.M.2    Milne, P.E.3    Goodby, J.W.4
  • 5
    • 20544441907 scopus 로고    scopus 로고
    • Conducting Polymer Nanostructures
    • Los Angeles: American Scientific Publishers, Nalwa HS
    • Gangopadhyay R. Conducting Polymer Nanostructures. In Encyclopedia of Nanoscience and Nanotechnology 2004, 2:105-131. Los Angeles: American Scientific Publishers, Nalwa HS.
    • (2004) In Encyclopedia of Nanoscience and Nanotechnology , vol.2 , pp. 105-131
    • Gangopadhyay, R.1
  • 9
    • 77949538978 scopus 로고    scopus 로고
    • Synthesis of polythiophene nanoparticles by surfactant - assisted dilut polymerization method for high performance redox supercapacitors
    • Richard SP, Rajasekhar M, Subramania A. Synthesis of polythiophene nanoparticles by surfactant - assisted dilut polymerization method for high performance redox supercapacitors. Int J Electrochem Sci 2009, 4:1289-1301.
    • (2009) Int J Electrochem Sci , vol.4 , pp. 1289-1301
    • Richard, S.P.1    Rajasekhar, M.2    Subramania, A.3
  • 10
    • 34047135967 scopus 로고    scopus 로고
    • Gas sensors based on conducting polymers
    • Bai H, Shi G. Gas sensors based on conducting polymers. Sensors 2007, 7:267-307.
    • (2007) Sensors , vol.7 , pp. 267-307
    • Bai, H.1    Shi, G.2
  • 11
    • 54249146931 scopus 로고    scopus 로고
    • Toward an understanding of the formation of conducting polymer nanofibers
    • 10.1021/nn800272z, 19206423
    • Henry D, Tran YW, Julio MD, Richard BK. Toward an understanding of the formation of conducting polymer nanofibers. ACS Nano 2008, 2:1841-1848. 10.1021/nn800272z, 19206423.
    • (2008) ACS Nano , vol.2 , pp. 1841-1848
    • Henry, D.1    Tran, Y.W.2    Julio, M.D.3    Richard, B.K.4
  • 12
    • 79952820548 scopus 로고    scopus 로고
    • Polymerization in liquid crystal medium: preparation of polythiophene derivatives bearing a bulky pyrimidine substituent
    • Ohkawa S, Ohta R, Kawabata K, Goto H. Polymerization in liquid crystal medium: preparation of polythiophene derivatives bearing a bulky pyrimidine substituent. Polymers 2010, 2:393-406.
    • (2010) Polymers , vol.2 , pp. 393-406
    • Ohkawa, S.1    Ohta, R.2    Kawabata, K.3    Goto, H.4
  • 13
    • 0038399846 scopus 로고    scopus 로고
    • Phosphonic acid derivatized polythiophene: A building block for metal phosphonate and polyelectrolyte multilayers
    • Viinikanoja A, Lukkari J, Aaritalo T, Laiho T, Kankare J. Phosphonic acid derivatized polythiophene: A building block for metal phosphonate and polyelectrolyte multilayers. Langmuir 2003, 19:2768-2775.
    • (2003) Langmuir , vol.19 , pp. 2768-2775
    • Viinikanoja, A.1    Lukkari, J.2    Aaritalo, T.3    Laiho, T.4    Kankare, J.5
  • 14
    • 3342885384 scopus 로고    scopus 로고
    • Electrochemistry: Arrays of polymer nanowires
    • 10.1038/nmat1173, 15286749
    • Grevin B, Rannou P. Electrochemistry: Arrays of polymer nanowires. Nature Materials 2004, 3:503-504. 10.1038/nmat1173, 15286749.
    • (2004) Nature Materials , vol.3 , pp. 503-504
    • Grevin, B.1    Rannou, P.2
  • 15
    • 78650412786 scopus 로고    scopus 로고
    • Synthesis and properties of octithiophene dication sterically segregated by annelation with bicycle [2.2.2]octene units
    • Nishinaga T, Yamazaki D, Tateno M, Iyoda M, Komatsu K. Synthesis and properties of octithiophene dication sterically segregated by annelation with bicycle [2.2.2]octene units. Materials 2010, 3:2037-2052.
    • (2010) Materials , vol.3 , pp. 2037-2052
    • Nishinaga, T.1    Yamazaki, D.2    Tateno, M.3    Iyoda, M.4    Komatsu, K.5
  • 16
    • 77954939832 scopus 로고    scopus 로고
    • Step-by-step growth of epitaxially aligned polythiophene by surface-confined reaction
    • 10.1073/pnas.1000726107, 2895091, 20534511
    • Lipton-Duffin JA, Miwa JA, Kondratenko M, Cicoira FB, Sumpter G, Meunier V, Perepichka DF, Rosei F. Step-by-step growth of epitaxially aligned polythiophene by surface-confined reaction. PNAS 2010, 107:11200-11204. 10.1073/pnas.1000726107, 2895091, 20534511.
    • (2010) PNAS , vol.107 , pp. 11200-11204
    • Lipton-Duffin, J.A.1    Miwa, J.A.2    Kondratenko, M.3    Cicoira, F.B.4    Sumpter, G.5    Meunier, V.6    Perepichka, D.F.7    Rosei, F.8
  • 17
    • 12944324733 scopus 로고    scopus 로고
    • Bioaffinity sensing using biologically functionalized conducting-polymer nanowire
    • 10.1021/ja044486l, 15643853
    • Ramanathan K, Bangar M, Yun M, Chen W, Myung N, Mulchandani A. Bioaffinity sensing using biologically functionalized conducting-polymer nanowire. J Am Chem Soc 2005, 127:496-497. 10.1021/ja044486l, 15643853.
    • (2005) J Am Chem Soc , vol.127 , pp. 496-497
    • Ramanathan, K.1    Bangar, M.2    Yun, M.3    Chen, W.4    Myung, N.5    Mulchandani, A.6
  • 18
    • 84855331285 scopus 로고    scopus 로고
    • Electrically and thermally conducting nanocomposites for electronic applications
    • Wayne E, Jones J, Chiguma J, Johnson E, Pachamuthu A, Santos D. Electrically and thermally conducting nanocomposites for electronic applications. Materials 2010, 3:1478-1496.
    • (2010) Materials , vol.3 , pp. 1478-1496
    • Wayne, E.1    Jones, J.2    Chiguma, J.3    Johnson, E.4    Pachamuthu, A.5    Santos, D.6
  • 19
    • 15344344562 scopus 로고    scopus 로고
    • Conducting Polymer Nanotubes
    • Los Angeles, American Scientific Publishers, Nalwa HS
    • Wan MX. Conducting Polymer Nanotubes. In Encyclopedia of Nanoscience and Nanotechnology 2004, 2:153-169. Los Angeles, American Scientific Publishers, Nalwa HS.
    • (2004) In Encyclopedia of Nanoscience and Nanotechnology , vol.2 , pp. 153-169
    • Wan, M.X.1
  • 20
    • 77955721107 scopus 로고    scopus 로고
    • Doping kinetics of organic Semiconductors investigated by field-effect transistors
    • Maddalena F, Meijer EJ, Asadi K, Leeuw DM, Blom PWM. Doping kinetics of organic Semiconductors investigated by field-effect transistors. Appl Phys Lett 2010, 97:0433021-0433023.
    • (2010) Appl Phys Lett , vol.97 , pp. 433021-433023
    • Maddalena, F.1    Meijer, E.J.2    Asadi, K.3    Leeuw, D.M.4    Blom, P.W.M.5
  • 21
    • 13444267557 scopus 로고    scopus 로고
    • Direct synthesis, characterization and catalytic application of SBA-15 containing heteropolyacid
    • Yang L, Qi Y, Yuan X, Shen J, Kim J. Direct synthesis, characterization and catalytic application of SBA-15 containing heteropolyacid. Journal of Molecular Catalysis A: Chemical 2005, 229:199-205.
    • (2005) Journal of Molecular Catalysis A: Chemical , vol.229 , pp. 199-205
    • Yang, L.1    Qi, Y.2    Yuan, X.3    Shen, J.4    Kim, J.5
  • 23
    • 0034615995 scopus 로고    scopus 로고
    • Oxidation induced variation in polyelectrolyte multilayers prepared from sulfonated self-dopable poly(alkoxythiophene)
    • Lukkari J, Viinikanoja A, Paukkunen J, Salomaki M, Mervi J, Aaritalo T, Kankare J. Oxidation induced variation in polyelectrolyte multilayers prepared from sulfonated self-dopable poly(alkoxythiophene). Chem Commun 2000, 571-572.
    • (2000) Chem Commun , pp. 571-572
    • Lukkari, J.1    Viinikanoja, A.2    Paukkunen, J.3    Salomaki, M.4    Mervi, J.5    Aaritalo, T.6    Kankare, J.7
  • 24
    • 33846146696 scopus 로고    scopus 로고
    • Development of a novel environmentally friendly electropolymerization of water-insoluble monomers in aqueous electrolytes using acoustic emulsification
    • Asami R, Fuchigami T, Atobe M. Development of a novel environmentally friendly electropolymerization of water-insoluble monomers in aqueous electrolytes using acoustic emulsification. Langmuir 2006, 22:0258-10263.
    • (2006) Langmuir , vol.22 , pp. 258-10263
    • Asami, R.1    Fuchigami, T.2    Atobe, M.3
  • 26
    • 77951883486 scopus 로고    scopus 로고
    • Acetylene-Based materials in organic photovoltaics
    • 10.3390/ijms11041471, 2871127, 20480031
    • Silvestri F, Marrocchi A. Acetylene-Based materials in organic photovoltaics. Int J Mol Sci 2010, 11:1471-1508. 10.3390/ijms11041471, 2871127, 20480031.
    • (2010) Int J Mol Sci , vol.11 , pp. 1471-1508
    • Silvestri, F.1    Marrocchi, A.2
  • 27
    • 79952443417 scopus 로고
    • Synthesis and properties of polythiophenes
    • Oterom TF, Azelain EL. Synthesis and properties of polythiophenes. Polym Comm 1988, 29:21-50.
    • (1988) Polym Comm , vol.29 , pp. 21-50
    • Oterom, T.F.1    Azelain, E.L.2
  • 28
    • 67249095363 scopus 로고    scopus 로고
    • Study of kinetic formation and the electrochemical behavior of polypyrrole films
    • Alvaro AA, Rosa LT. Study of kinetic formation and the electrochemical behavior of polypyrrole films. J Chil Chem Soc 2009, 54:14-19.
    • (2009) J Chil Chem Soc , vol.54 , pp. 14-19
    • Alvaro, A.A.1    Rosa, L.T.2
  • 33
    • 17244367197 scopus 로고    scopus 로고
    • New scale factors for harmonic vibrational frequencies using the B3LYP density functional method with the triple- Basis Set 6-311+G(d,p)
    • 10.1021/jp045733a, 16833612
    • Andersson MP, Uvdal P. New scale factors for harmonic vibrational frequencies using the B3LYP density functional method with the triple- Basis Set 6-311+G(d,p). J Phys Chem A 2005, 109:2937-2941. 10.1021/jp045733a, 16833612.
    • (2005) J Phys Chem A , vol.109 , pp. 2937-2941
    • Andersson, M.P.1    Uvdal, P.2
  • 34
    • 26844490119 scopus 로고    scopus 로고
    • Theoretical study of chloropyrroles as monomers for new conductive Polymers
    • 10.1021/jp0518310, 16834291
    • Omrani A, Sabzyan H. Theoretical study of chloropyrroles as monomers for new conductive Polymers. J Phys Chem A 2005, 109:8874-8879. 10.1021/jp0518310, 16834291.
    • (2005) J Phys Chem A , vol.109 , pp. 8874-8879
    • Omrani, A.1    Sabzyan, H.2
  • 35
    • 0042879719 scopus 로고    scopus 로고
    • Ab initio and DFT study of all Mono-, Di-, Tri- and Tetrafluoropyrroles and their cations: predicting structural, spectroscopic, electropolymerization and electrochemical properties
    • Sabzyan H, Omrani A. Ab initio and DFT study of all Mono-, Di-, Tri- and Tetrafluoropyrroles and their cations: predicting structural, spectroscopic, electropolymerization and electrochemical properties. J Phys Chem A 2003, 107:6476-6482.
    • (2003) J Phys Chem A , vol.107 , pp. 6476-6482
    • Sabzyan, H.1    Omrani, A.2
  • 37
    • 34248364799 scopus 로고    scopus 로고
    • DFT study of molecular structure and electronic properties of fluoromethylpyrrole oligomers including di-, tri- and tetramer
    • Nikoofard H, Sabzyan H. DFT study of molecular structure and electronic properties of fluoromethylpyrrole oligomers including di-, tri- and tetramer. Journal of Fluorine Chemistry 2007, 128:668-673.
    • (2007) Journal of Fluorine Chemistry , vol.128 , pp. 668-673
    • Nikoofard, H.1    Sabzyan, H.2
  • 38
    • 0035528892 scopus 로고    scopus 로고
    • Ab initio calculation of the anisotropy effect of multiple bonds and the ring current effect of arenes-application in conformational and configurational analysis
    • Kleinpeter E, Klod S. Ab initio calculation of the anisotropy effect of multiple bonds and the ring current effect of arenes-application in conformational and configurational analysis. J Chem Soc Perkin Trans 2001, 2:1893-1898.
    • (2001) J Chem Soc Perkin Trans , vol.2 , pp. 1893-1898
    • Kleinpeter, E.1    Klod, S.2
  • 39
    • 58949097520 scopus 로고    scopus 로고
    • Ab initio calculation of through-space magnetic shielding of linear polycyclic aromatic hydrocarbons (acenes): Extent of aromaticity
    • 10.1016/j.jmgm.2008.10.007, 19081276
    • Martin NH, Caldwell BC, Carlson KP, Teague MR. Ab initio calculation of through-space magnetic shielding of linear polycyclic aromatic hydrocarbons (acenes): Extent of aromaticity. J Mol Graph Model 2009, 27:689-692. 10.1016/j.jmgm.2008.10.007, 19081276.
    • (2009) J Mol Graph Model , vol.27 , pp. 689-692
    • Martin, N.H.1    Caldwell, B.C.2    Carlson, K.P.3    Teague, M.R.4
  • 40
    • 27744530363 scopus 로고    scopus 로고
    • Nucleus-Independent Chemical Shifts (NICS) as an Aromaticity Criterion
    • 10.1021/cr030088+, 16218569
    • Chen Z, Wannere CS, Corminboeuf C, Puchta R, Schleyer PVR. Nucleus-Independent Chemical Shifts (NICS) as an Aromaticity Criterion. Chem Rev 2005, 105:3842-3888. 10.1021/cr030088+, 16218569.
    • (2005) Chem Rev , vol.105 , pp. 3842-3888
    • Chen, Z.1    Wannere, C.S.2    Corminboeuf, C.3    Puchta, R.4    Schleyer, P.V.R.5
  • 41
    • 0000967157 scopus 로고    scopus 로고
    • Correlation of empirical (TMS) and absolute NMR chemical shifts predicted by ab initio computations
    • Baldridge KK, Siegel JS. Correlation of empirical (TMS) and absolute NMR chemical shifts predicted by ab initio computations. J Phys Chem A 1999, 103:4038-4042.
    • (1999) J Phys Chem A , vol.103 , pp. 4038-4042
    • Baldridge, K.K.1    Siegel, J.S.2
  • 42
    • 35148897846 scopus 로고    scopus 로고
    • Geometric dependence of the B3LYP-Predicted magnetic shielding and chemical shifts
    • 10.1021/jp0740503, 17696331
    • Zhang Y, Wu A, Xu X, Yan Y. Geometric dependence of the B3LYP-Predicted magnetic shielding and chemical shifts. J Phys Chem A 2007, 111:9431-9437. 10.1021/jp0740503, 17696331.
    • (2007) J Phys Chem A , vol.111 , pp. 9431-9437
    • Zhang, Y.1    Wu, A.2    Xu, X.3    Yan, Y.4
  • 43
    • 84876480206 scopus 로고    scopus 로고
    • Gaussian 03 Online Manual
    • Gaussian 03 Online Manual. , http://www.nd.edu/~wschnei1/courses/CBE_547/g03_man/g_ur/k_nmr.htm
  • 44
    • 10644233957 scopus 로고    scopus 로고
    • Ab initio and density functional study of electrical and thermochemical properties of mono-, di-, tri- and tetrafluoropyrroles and their cations and anions
    • Sabzyan H, Omrani A. Ab initio and density functional study of electrical and thermochemical properties of mono-, di-, tri- and tetrafluoropyrroles and their cations and anions. J THEOCHEM 2005, 713:43-49.
    • (2005) J THEOCHEM , vol.713 , pp. 43-49
    • Sabzyan, H.1    Omrani, A.2
  • 45
    • 0042888578 scopus 로고    scopus 로고
    • Dissected Nucleus-Independent Chemical Shift analysis of π-aromaticity and antiaromaticity
    • 10.1021/ol016217v, 11483036
    • Schleyer PVR, Manoharan M, Wang Z-X, Kiran B, Jiao H, Puchta R, Hommes NJRVE. Dissected Nucleus-Independent Chemical Shift analysis of π-aromaticity and antiaromaticity. Org Lett 2001, 3:2465-2468. 10.1021/ol016217v, 11483036.
    • (2001) Org Lett , vol.3 , pp. 2465-2468
    • Schleyer, P.V.R.1    Manoharan, M.2    Wang, Z.-X.3    Kiran, B.4    Jiao, H.5    Puchta, R.6    Hommes, N.J.R.V.E.7
  • 46
    • 0942279537 scopus 로고    scopus 로고
    • Induced magnetic fields in aromatic [n]-annulenẽsinterpretation of NICS tensor components
    • Corminboeuf C, Heine T, Seifert G, Schleyer PVR, Weber J. Induced magnetic fields in aromatic [n]-annulenẽsinterpretation of NICS tensor components. Phys Chem Chem Phys 2004, 6:273-276.
    • (2004) Phys Chem Chem Phys , vol.6 , pp. 273-276
    • Corminboeuf, C.1    Heine, T.2    Seifert, G.3    Schleyer, P.V.R.4    Weber, J.5
  • 47
    • 0035833044 scopus 로고    scopus 로고
    • An ab initio study of the NMR properties (absolute shielding and NICS) of a series of significant aromatic and antiaromatic compounds
    • Alkorta I, Rozas I, Elguero J. An ab initio study of the NMR properties (absolute shielding and NICS) of a series of significant aromatic and antiaromatic compounds. Tetrahedron 2001, 57:6043-6049.
    • (2001) Tetrahedron , vol.57 , pp. 6043-6049
    • Alkorta, I.1    Rozas, I.2    Elguero, J.3
  • 48
    • 32144434172 scopus 로고    scopus 로고
    • Nucleus-Independent Chemical Shifts (NICS): Distance Dependence and Revised Criteria for Aromaticity and Antiaromaticity
    • 10.1021/jo051746o, 16438497
    • Stanger A. Nucleus-Independent Chemical Shifts (NICS): Distance Dependence and Revised Criteria for Aromaticity and Antiaromaticity. J Org Chem 2006, 71:883-893. 10.1021/jo051746o, 16438497.
    • (2006) J Org Chem , vol.71 , pp. 883-893
    • Stanger, A.1


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