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Volumn 119, Issue 45, 2015, Pages 25634-25650

Long-Lived Photoinduced Charge Separation in Inclusion Complexes Composed of a Phenothiazine-Bridged Cyclic Porphyrin Dimer and Fullerenes

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC COMPOUNDS; CHROMOPHORES; ELECTRON SPIN RESONANCE SPECTROSCOPY; ELECTRON TRANSITIONS; ESTERS; FULLERENES; INSECTICIDES; LITHIUM; PORPHYRINS; POSITIVE IONS;

EID: 84946882269     PISSN: 19327447     EISSN: 19327455     Source Type: Journal    
DOI: 10.1021/acs.jpcc.5b09147     Document Type: Article
Times cited : (26)

References (111)
  • 1
    • 67849128456 scopus 로고    scopus 로고
    • Powering the Planet with Solar Fuel
    • Gray, H. B. Powering the Planet with Solar Fuel Nat. Chem. 2009, 1, 7 10.1038/nchem.141
    • (2009) Nat. Chem. , vol.1 , pp. 7
    • Gray, H.B.1
  • 3
    • 33750458683 scopus 로고    scopus 로고
    • Powering the Planet: Chemical Challenges in Solar Energy Utilization
    • Lewis, N. S.; Nocera, D. G. Powering the Planet: Chemical Challenges in Solar Energy Utilization Proc. Natl. Acad. Sci. U. S. A. 2006, 103, 15729-15735 10.1073/pnas.0603395103
    • (2006) Proc. Natl. Acad. Sci. U. S. A. , vol.103 , pp. 15729-15735
    • Lewis, N.S.1    Nocera, D.G.2
  • 4
    • 49649085195 scopus 로고    scopus 로고
    • Bioinspired Energy Conversion Systems for Hydrogen Production and Storage
    • Fukuzumi, S. Bioinspired Energy Conversion Systems for Hydrogen Production and Storage Eur. J. Inorg. Chem. 2008, 2008 (9) 1351-1362 10.1002/ejic.200701369
    • (2008) Eur. J. Inorg. Chem. , vol.2008 , Issue.9 , pp. 1351-1362
    • Fukuzumi, S.1
  • 5
    • 80052701478 scopus 로고    scopus 로고
    • Molecular Devices Featuring Sequential Photoinduced Charge Separations for the Storage of Multiple Redox Equivalents
    • Pellegrin, Y.; Odobel, F. Molecular Devices Featuring Sequential Photoinduced Charge Separations for the Storage of Multiple Redox Equivalents Coord. Chem. Rev. 2011, 255, 2578-2593 10.1016/j.ccr.2010.12.017
    • (2011) Coord. Chem. Rev. , vol.255 , pp. 2578-2593
    • Pellegrin, Y.1    Odobel, F.2
  • 6
    • 0031208887 scopus 로고    scopus 로고
    • Photophysics of Photosynthesis. Structure and Spectroscopy of Reaction Centers of Purple Bacteria
    • Hoff, A. J.; Deisenhofer, J. Photophysics of Photosynthesis. Structure and Spectroscopy of Reaction Centers of Purple Bacteria Phys. Rep. 1997, 287, 1-247 10.1016/S0370-1573(97)00004-5
    • (1997) Phys. Rep. , vol.287 , pp. 1-247
    • Hoff, A.J.1    Deisenhofer, J.2
  • 7
    • 79959818384 scopus 로고    scopus 로고
    • Energy Conversion in Photosynthesis: a Paradigm for Solar Fuel Production
    • Moore, G. F.; Brudvig, G. W. Energy Conversion in Photosynthesis: a Paradigm for Solar Fuel Production Annu. Rev. Condens. Matter Phys. 2011, 2, 303-327 10.1146/annurev-conmatphys-062910-140503
    • (2011) Annu. Rev. Condens. Matter Phys. , vol.2 , pp. 303-327
    • Moore, G.F.1    Brudvig, G.W.2
  • 8
    • 0035148647 scopus 로고    scopus 로고
    • Mimicking Photosynthetic Solar Energy Transduction
    • Gust, D.; Moore, T. A.; Moore, A. L. Mimicking Photosynthetic Solar Energy Transduction Acc. Chem. Res. 2001, 34, 40-48 10.1021/ar9801301
    • (2001) Acc. Chem. Res. , vol.34 , pp. 40-48
    • Gust, D.1    Moore, T.A.2    Moore, A.L.3
  • 9
    • 77953893584 scopus 로고    scopus 로고
    • Covalent and Noncovalent Phthalocyanine-Carbon Nanostructure Systems: Synthesis, Photoinduced Electron Transfer, and Application to Molecular Photovoltaics
    • Bottari, G.; de la Torre, G.; Guldi, D. M.; Torres, T. Covalent and Noncovalent Phthalocyanine-Carbon Nanostructure Systems: Synthesis, Photoinduced Electron Transfer, and Application to Molecular Photovoltaics Chem. Rev. 2010, 110, 6768-6816 10.1021/cr900254z
    • (2010) Chem. Rev. , vol.110 , pp. 6768-6816
    • Bottari, G.1    De La Torre, G.2    Guldi, D.M.3    Torres, T.4
  • 10
    • 0034804017 scopus 로고    scopus 로고
    • Charge Separation in a Novel Artificial Photosynthetic Reaction Center Lives 380 ms
    • Imahori, H.; Guldi, D. M.; Tamaki, K.; Yoshida, Y.; Luo, C.; Sakata, Y.; Fukuzumi, S. Charge Separation in a Novel Artificial Photosynthetic Reaction Center Lives 380 ms J. Am. Chem. Soc. 2001, 123, 6617-6628 10.1021/ja004123v
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 6617-6628
    • Imahori, H.1    Guldi, D.M.2    Tamaki, K.3    Yoshida, Y.4    Luo, C.5    Sakata, Y.6    Fukuzumi, S.7
  • 19
    • 0037747461 scopus 로고    scopus 로고
    • New Perspective of Electron Transfer Chemistry
    • Fukuzumi, S. New Perspective of Electron Transfer Chemistry Org. Biomol. Chem. 2003, 1, 609-620 10.1039/b300053b
    • (2003) Org. Biomol. Chem. , vol.1 , pp. 609-620
    • Fukuzumi, S.1
  • 20
    • 2442453629 scopus 로고    scopus 로고
    • Intermolecular and Supramolecular Photoinduced Electron Transfer Processes of Fullerene-Porphyrin/Phthalocyanine System
    • El-Khouly, M. E.; Ito, O.; Smith, P. M.; D'Souza, F. Intermolecular and Supramolecular Photoinduced Electron Transfer Processes of Fullerene-Porphyrin/Phthalocyanine System J. Photochem. Photobiol., C 2004, 5, 79-104 10.1016/j.jphotochemrev.2004.01.003
    • (2004) J. Photochem. Photobiol., C , vol.5 , pp. 79-104
    • El-Khouly, M.E.1    Ito, O.2    Smith, P.M.3    D'Souza, F.4
  • 21
    • 28844454263 scopus 로고    scopus 로고
    • Carbon Nanotubes in Electron Donor-Acceptor Nanocomposites
    • Guldi, D. M.; Rahman, G. M. A.; Zerbetto, F.; Prato, M. Carbon Nanotubes in Electron Donor-Acceptor Nanocomposites Acc. Chem. Res. 2005, 38, 871-878 10.1021/ar040238i
    • (2005) Acc. Chem. Res. , vol.38 , pp. 871-878
    • Guldi, D.M.1    Rahman, G.M.A.2    Zerbetto, F.3    Prato, M.4
  • 22
    • 42149130269 scopus 로고    scopus 로고
    • Development of Bioinspired Artificial Photosynthetic Systems
    • Fukuzumi, S. Development of Bioinspired Artificial Photosynthetic Systems Phys. Chem. Chem. Phys. 2008, 10, 2283-2297 10.1039/b801198m
    • (2008) Phys. Chem. Chem. Phys. , vol.10 , pp. 2283-2297
    • Fukuzumi, S.1
  • 24
    • 68749089831 scopus 로고    scopus 로고
    • Supramolecular Donor-Acceptor Hybrids of Porphyrins/Phthalocyanines with Fullerenes/Carbon Nanotubes: Electron Transfer, Sensing, Switching, and Catalytic Applications
    • D'Souza, F.; Ito, O. Supramolecular Donor-Acceptor Hybrids of Porphyrins/Phthalocyanines with Fullerenes/Carbon Nanotubes: Electron Transfer, Sensing, Switching, and Catalytic Applications Chem. Commun. 2009, 4913-4928 10.1039/b905753f
    • (2009) Chem. Commun. , pp. 4913-4928
    • D'Souza, F.1    Ito, O.2
  • 25
    • 84880539666 scopus 로고    scopus 로고
    • Reflections on a Fifty-Year Career in Organic Photochemistry: A Personal Perspective
    • Schuster, D. I. Reflections on a Fifty-Year Career in Organic Photochemistry: A Personal Perspective J. Org. Chem. 2013, 78, 6811-6841 10.1021/jo4007078
    • (2013) J. Org. Chem. , vol.78 , pp. 6811-6841
    • Schuster, D.I.1
  • 26
    • 84886814390 scopus 로고    scopus 로고
    • Long-Lived Photoinduced Charge Separation for Solar Cell Applications in Supramolecular Complexes of Multi-Metalloporphyrins and Fullerenes
    • Fukuzumi, S.; Ohkubo, K. Long-Lived Photoinduced Charge Separation for Solar Cell Applications in Supramolecular Complexes of Multi-Metalloporphyrins and Fullerenes Dalton Trans. 2013, 42, 15846-15858 10.1039/c3dt51883c
    • (2013) Dalton Trans. , vol.42 , pp. 15846-15858
    • Fukuzumi, S.1    Ohkubo, K.2
  • 27
    • 84901283253 scopus 로고    scopus 로고
    • Long-Lived Charge Separation and Applications in Artificial Photosynthesis
    • Fukuzumi, S.; Ohkubo, K.; Suenobu, S. Long-Lived Charge Separation and Applications in Artificial Photosynthesis Acc. Chem. Res. 2014, 47, 1455-1464 10.1021/ar400200u
    • (2014) Acc. Chem. Res. , vol.47 , pp. 1455-1464
    • Fukuzumi, S.1    Ohkubo, K.2    Suenobu, S.3
  • 28
    • 3142728629 scopus 로고    scopus 로고
    • Long-Lived Charge-Separated State Generated in a Ferrocene-meso, meso-Linked Porphyrin Trimer-Fullerene Pentad with a High Quantum Yield
    • Imahori, H.; Sekiguchi, Y.; Kashiwagi, Y.; Sato, T.; Araki, Y.; Ito, O.; Yamada, H.; Fukuzumi, S. Long-Lived Charge-Separated State Generated in a Ferrocene-meso, meso-Linked Porphyrin Trimer-Fullerene Pentad with a High Quantum Yield Chem.-Eur. J. 2004, 10, 3184-3196 10.1002/chem.200305308
    • (2004) Chem. - Eur. J. , vol.10 , pp. 3184-3196
    • Imahori, H.1    Sekiguchi, Y.2    Kashiwagi, Y.3    Sato, T.4    Araki, Y.5    Ito, O.6    Yamada, H.7    Fukuzumi, S.8
  • 29
    • 77952381569 scopus 로고    scopus 로고
    • Chiroselective Assembly of a Chiral Porphyrin-Fullerene Dyad: Photoconductive Nanofiber with a Top-Class Ambipolar Charge-Carrier Mobility
    • Hizume, Y.; Tashiro, K.; Charvet, R.; Yamamoto, Y.; Saeki, A.; Seki, S.; Aida, T. Chiroselective Assembly of a Chiral Porphyrin-Fullerene Dyad: Photoconductive Nanofiber with a Top-Class Ambipolar Charge-Carrier Mobility J. Am. Chem. Soc. 2010, 132, 6628-6629 10.1021/ja1014713
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 6628-6629
    • Hizume, Y.1    Tashiro, K.2    Charvet, R.3    Yamamoto, Y.4    Saeki, A.5    Seki, S.6    Aida, T.7
  • 30
    • 84890814098 scopus 로고    scopus 로고
    • Conformational Gating of Charge Separation in Porphyrin Oligomer-Fullerene Systems
    • Gilbert, M.; Esdaile, L. J.; Hutin, M.; Sawada, K.; Anderson, H. L.; Albinsson, B. Conformational Gating of Charge Separation in Porphyrin Oligomer-Fullerene Systems J. Phys. Chem. C 2013, 117, 26482-26492 10.1021/jp4098342
    • (2013) J. Phys. Chem. C , vol.117 , pp. 26482-26492
    • Gilbert, M.1    Esdaile, L.J.2    Hutin, M.3    Sawada, K.4    Anderson, H.L.5    Albinsson, B.6
  • 31
    • 84908450369 scopus 로고    scopus 로고
    • Electron Transfer through Rigid Organic Molecular Wires Enhanced by Electronic and Electron-Vibration Coupling
    • Sukegawa, J.; Schubert, C.; Zhu, X.; Tsuji, H.; Guldi, D. M.; Nakamura, E. Electron Transfer through Rigid Organic Molecular Wires Enhanced by Electronic and Electron-Vibration Coupling Nat. Chem. 2014, 6, 899-905 10.1038/nchem.2026
    • (2014) Nat. Chem. , vol.6 , pp. 899-905
    • Sukegawa, J.1    Schubert, C.2    Zhu, X.3    Tsuji, H.4    Guldi, D.M.5    Nakamura, E.6
  • 33
    • 37549049407 scopus 로고    scopus 로고
    • Implementation of a Hamiliton-Receptor-Based Hydrogen-Bonding Motif toward a New Electron Donor-Acceptor Prototype: Electron versus Energy transfer
    • Wessendorf, F.; Gnichwitz, J.; Sarova, G. H.; Hager, K.; Hartnagel, U.; Guldi, D. M.; Hirsch, A. Implementation of a Hamiliton-Receptor-Based Hydrogen-Bonding Motif toward a New Electron Donor-Acceptor Prototype: Electron versus Energy transfer J. Am. Chem. Soc. 2007, 129, 16057-16071 10.1021/ja075751g
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 16057-16071
    • Wessendorf, F.1    Gnichwitz, J.2    Sarova, G.H.3    Hager, K.4    Hartnagel, U.5    Guldi, D.M.6    Hirsch, A.7
  • 36
    • 1642346153 scopus 로고    scopus 로고
    • Convergent Synthesis and Photophysics of [60]Fullerene/Porphyrin-Based Rotaxanes
    • Li, K.; Schuster, D. I.; Guldi, D. M.; Herranz, M. A.; Echegoyen, L. Convergent Synthesis and Photophysics of [60]Fullerene/Porphyrin-Based Rotaxanes J. Am. Chem. Soc. 2004, 126, 3388-3389 10.1021/ja039698h
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 3388-3389
    • Li, K.1    Schuster, D.I.2    Guldi, D.M.3    Herranz, M.A.4    Echegoyen, L.5
  • 37
    • 67749106303 scopus 로고    scopus 로고
    • Supramolecular Donor-Acceptor Heterojunctions by Vectorial Stepwise Assembly of Porphyrins and Coordination-Bonded Fullerene Arrays for Photocurrent Generation
    • Kira, A.; Umeyama, T.; Matano, Y.; Yoshida, K.; Isoda, S.; Park, J. K.; Kim, D.; Imahori, H. Supramolecular Donor-Acceptor Heterojunctions by Vectorial Stepwise Assembly of Porphyrins and Coordination-Bonded Fullerene Arrays for Photocurrent Generation J. Am. Chem. Soc. 2009, 131, 3198-3200 10.1021/ja8096465
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 3198-3200
    • Kira, A.1    Umeyama, T.2    Matano, Y.3    Yoshida, K.4    Isoda, S.5    Park, J.K.6    Kim, D.7    Imahori, H.8
  • 39
    • 84855645742 scopus 로고    scopus 로고
    • Control over Photoinduced Energy and Electron Transfer in Supramolecular Polyads of Covalently linked azaBODIPY-Bisporphyrin 'Molecular Clip' Hosting Fullerene
    • D'Souza, F.; Amin, A. N.; El-Khouly, M. E.; Subbaiyan, N. K.; Zandler, M. E.; Fukuzumi, S. Control over Photoinduced Energy and Electron Transfer in Supramolecular Polyads of Covalently linked azaBODIPY-Bisporphyrin 'Molecular Clip' Hosting Fullerene J. Am. Chem. Soc. 2012, 134, 654-664 10.1021/ja209718g
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 654-664
    • D'Souza, F.1    Amin, A.N.2    El-Khouly, M.E.3    Subbaiyan, N.K.4    Zandler, M.E.5    Fukuzumi, S.6
  • 40
    • 0242666861 scopus 로고    scopus 로고
    • Supramolecular Peapods Composed of a Metalloporphyrin Nanotube and Fullerenes
    • Yamaguchi, T.; Ishii, N.; Tashiro, K.; Aida, T. Supramolecular Peapods Composed of a Metalloporphyrin Nanotube and Fullerenes J. Am. Chem. Soc. 2003, 125, 13934-13935 10.1021/ja038178j
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 13934-13935
    • Yamaguchi, T.1    Ishii, N.2    Tashiro, K.3    Aida, T.4
  • 41
    • 20344391651 scopus 로고    scopus 로고
    • Fullerene-Porphyrin Constructs
    • Boyd, P. D. W.; Reed, C. A. Fullerene-Porphyrin Constructs Acc. Chem. Res. 2005, 38, 235-242 10.1021/ar040168f
    • (2005) Acc. Chem. Res. , vol.38 , pp. 235-242
    • Boyd, P.D.W.1    Reed, C.A.2
  • 42
    • 33846660022 scopus 로고    scopus 로고
    • Metalloporphyrin Hosts for Supramolecular Chemistry of Fullerenes
    • Tashiro, K.; Aida, T. Metalloporphyrin Hosts for Supramolecular Chemistry of Fullerenes Chem. Soc. Rev. 2007, 36, 189-197 10.1039/B614883M
    • (2007) Chem. Soc. Rev. , vol.36 , pp. 189-197
    • Tashiro, K.1    Aida, T.2
  • 43
    • 71549117270 scopus 로고    scopus 로고
    • Configurational Isomers of a Stilbene-Linked Bis(porphyrin) Tweezer: Synthesis and Fullerene-Binding Studies
    • Fathalla, M.; Jayawickramarajah, J. Configurational Isomers of a Stilbene-Linked Bis(porphyrin) Tweezer: Synthesis and Fullerene-Binding Studies Eur. J. Org. Chem. 2009, 2009, 6095-6099 10.1002/ejoc.200901002
    • (2009) Eur. J. Org. Chem. , vol.2009 , pp. 6095-6099
    • Fathalla, M.1    Jayawickramarajah, J.2
  • 45
    • 80053140113 scopus 로고    scopus 로고
    • Wraparound Hosts for Fullerenes: Tailored Macrocycles and Cages
    • Canevet, D.; Pérez, E. M.; Martín, N. Wraparound Hosts for Fullerenes: Tailored Macrocycles and Cages Angew. Chem., Int. Ed. 2011, 50, 9248-9259 10.1002/anie.201101297
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 9248-9259
    • Canevet, D.1    Pérez, E.M.2    Martín, N.3
  • 46
    • 80053992820 scopus 로고    scopus 로고
    • Enhanced Binding Strengths of Acyclic Porphyrin Hosts with Endohedral Metallofullerenes
    • Grimm, B.; Schornbaum, J.; Cardona, C. M.; Van Paauwe, J. D.; Boyd, P. D. W.; Guldi, D. M. Enhanced Binding Strengths of Acyclic Porphyrin Hosts with Endohedral Metallofullerenes Chem. Sci. 2011, 2, 1530-1537 10.1039/c0sc00569j
    • (2011) Chem. Sci. , vol.2 , pp. 1530-1537
    • Grimm, B.1    Schornbaum, J.2    Cardona, C.M.3    Van Paauwe, J.D.4    Boyd, P.D.W.5    Guldi, D.M.6
  • 55
    • 34250618283 scopus 로고    scopus 로고
    • New Development of Photoinduced Electron-Transfer Catalytic Systems
    • Fukuzumi, S. New Development of Photoinduced Electron-Transfer Catalytic Systems Pure Appl. Chem. 2007, 79, 981-991 10.1351/pac200779060981
    • (2007) Pure Appl. Chem. , vol.79 , pp. 981-991
    • Fukuzumi, S.1
  • 56
    • 33750563834 scopus 로고    scopus 로고
    • Bioinspired Electron-Transfer Systems and Applications
    • Fukuzumi, S. Bioinspired Electron-Transfer Systems and Applications Bull. Chem. Soc. Jpn. 2006, 79, 177-195 10.1246/bcsj.79.177
    • (2006) Bull. Chem. Soc. Jpn. , vol.79 , pp. 177-195
    • Fukuzumi, S.1
  • 57
    • 84866241647 scopus 로고    scopus 로고
    • Supramolecular Electron Transfer by Anion Binding
    • Fukuzumi, S.; Ohkubo, K.; D'Souza, F.; Sessler, J. L. Supramolecular Electron Transfer by Anion Binding Chem. Commun. 2012, 48, 9801-9815 10.1039/c2cc32848h
    • (2012) Chem. Commun. , vol.48 , pp. 9801-9815
    • Fukuzumi, S.1    Ohkubo, K.2    D'Souza, F.3    Sessler, J.L.4
  • 64
    • 33947689595 scopus 로고    scopus 로고
    • Continuum of Outer- and Inner-Sphere Mechanisms for Organic Electron Transfer. Steric Modulation of the Precursor Complex in Paramagnetic (Ion-Radical) Self-Exchanges
    • Rosokha, S. V.; Kochi, J. K. Continuum of Outer- and Inner-Sphere Mechanisms for Organic Electron Transfer. Steric Modulation of the Precursor Complex in Paramagnetic (Ion-Radical) Self-Exchanges J. Am. Chem. Soc. 2007, 129, 3683-3697 10.1021/ja069149m
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 3683-3697
    • Rosokha, S.V.1    Kochi, J.K.2
  • 65
    • 0034676586 scopus 로고    scopus 로고
    • Synthesis of Functionalized Ethynylphenothiazine Fluorophores
    • Krämer, C. S.; Zeitler, K.; Müller, T. J. J. Synthesis of Functionalized Ethynylphenothiazine Fluorophores Org. Lett. 2000, 2, 3723-3726 10.1021/ol0066328
    • (2000) Org. Lett. , vol.2 , pp. 3723-3726
    • Krämer, C.S.1    Zeitler, K.2    Müller, T.J.J.3
  • 66
    • 0141839149 scopus 로고    scopus 로고
    • Synthesis and Electronic Properties of Alkynylated Phenothiazines
    • Krämer, C. S.; Müller, T. J. J. Synthesis and Electronic Properties of Alkynylated Phenothiazines Eur. J. Org. Chem. 2003, 2003, 3534-3548 10.1002/ejoc.200300250
    • (2003) Eur. J. Org. Chem. , vol.2003 , pp. 3534-3548
    • Krämer, C.S.1    Müller, T.J.J.2
  • 67
    • 84864838313 scopus 로고    scopus 로고
    • Synthesis and Crystal Structure of N-Hexyl-3,7-diformylphenothiazine
    • Wang, H.; Xu, W.; Zhang, B. Synthesis and Crystal Structure of N-Hexyl-3,7-diformylphenothiazine J. Chem. Crystallogr. 2012, 42, 846-850 10.1007/s10870-012-0323-8
    • (2012) J. Chem. Crystallogr. , vol.42 , pp. 846-850
    • Wang, H.1    Xu, W.2    Zhang, B.3
  • 68
    • 80052186923 scopus 로고    scopus 로고
    • Synthesis, Crystal Structures, Photophysical Properties, and Bioimaging of Living Cells of Bis-β-Diketonate Phenothiazine Ligands and Its Cyclic Dinuclear Complexes
    • Li, D.; Tian, X.; Hu, G.; Zhang, Q.; Wang, P.; Sun, P.; Zhou, H.; Meng, X.; Yang, J.; Wu, J. et al. Synthesis, Crystal Structures, Photophysical Properties, and Bioimaging of Living Cells of Bis-β-Diketonate Phenothiazine Ligands and Its Cyclic Dinuclear Complexes Inorg. Chem. 2011, 50, 7997-8006 10.1021/ic200150h
    • (2011) Inorg. Chem. , vol.50 , pp. 7997-8006
    • Li, D.1    Tian, X.2    Hu, G.3    Zhang, Q.4    Wang, P.5    Sun, P.6    Zhou, H.7    Meng, X.8    Yang, J.9    Wu, J.10
  • 69
    • 65449135971 scopus 로고    scopus 로고
    • Long-Lived Photoinduced Charge Separation in Flexible 9,10-Bis(phenylethynyl)anthracene-Phenothiazine Dyads
    • Suneesh, C. V.; Gopidas, K. R. Long-Lived Photoinduced Charge Separation in Flexible 9,10-Bis(phenylethynyl)anthracene-Phenothiazine Dyads J. Phys. Chem. C 2009, 113, 1606-1614 10.1021/jp8091072
    • (2009) J. Phys. Chem. C , vol.113 , pp. 1606-1614
    • Suneesh, C.V.1    Gopidas, K.R.2
  • 70
    • 78650347083 scopus 로고    scopus 로고
    • Long-Lived Photoinduced Charge Separation Due to the Inverted Region Effect in 1,6-Bis(phenylethynyl)pyrene-Phenothiazine Dyad
    • Suneesh, C. V.; Gopidas, K. R. Long-Lived Photoinduced Charge Separation Due to the Inverted Region Effect in 1,6-Bis(phenylethynyl)pyrene-Phenothiazine Dyad J. Phys. Chem. C 2010, 114, 18725-18734 10.1021/jp107606t
    • (2010) J. Phys. Chem. C , vol.114 , pp. 18725-18734
    • Suneesh, C.V.1    Gopidas, K.R.2
  • 72
    • 0347362671 scopus 로고    scopus 로고
    • Dynamics of Photoinduced Electron-Transfer Processes in Fullerene-Based Dyads: Effects of Varying the Donor Strength
    • Thomas, K. G.; Biju, V.; Kamat, P. V.; George, M. V.; Guldi, D. M. Dynamics of Photoinduced Electron-Transfer Processes in Fullerene-Based Dyads: Effects of Varying the Donor Strength ChemPhysChem 2003, 4, 1299-1307 10.1002/cphc.200200561
    • (2003) ChemPhysChem , vol.4 , pp. 1299-1307
    • Thomas, K.G.1    Biju, V.2    Kamat, P.V.3    George, M.V.4    Guldi, D.M.5
  • 73
    • 53349141814 scopus 로고    scopus 로고
    • Photoinduced Charge-Separation and Charge-Recombination Processes of Fullerene[60] Dyads Covalently Connected with Phenothiazine and Its Trimer
    • Kawauchi, H.; Suzuki, S.; Kozaki, M.; Okada, K.; Islam, D. M. S.; Araki, Y.; Ito, O.; Yamanaka, K. I. Photoinduced Charge-Separation and Charge-Recombination Processes of Fullerene[60] Dyads Covalently Connected with Phenothiazine and Its Trimer J. Phys. Chem. A 2008, 112, 5878-5884 10.1021/jp800716e
    • (2008) J. Phys. Chem. A , vol.112 , pp. 5878-5884
    • Kawauchi, H.1    Suzuki, S.2    Kozaki, M.3    Okada, K.4    Islam, D.M.S.5    Araki, Y.6    Ito, O.7    Yamanaka, K.I.8
  • 74
    • 79851483544 scopus 로고    scopus 로고
    • Sequential Charge Separation in Two Axially Linked Phenothiazine-Aluminum(III) Porphyrin-Fullerene Triads
    • Poddutoori, P. K.; Sandanayaka, A. S. D.; Zarrabi, N.; Hasobe, T.; Ito, O.; Van Der Est, A. Sequential Charge Separation in Two Axially Linked Phenothiazine-Aluminum(III) Porphyrin-Fullerene Triads J. Phys. Chem. A 2011, 115, 709-717 10.1021/jp110156w
    • (2011) J. Phys. Chem. A , vol.115 , pp. 709-717
    • Poddutoori, P.K.1    Sandanayaka, A.S.D.2    Zarrabi, N.3    Hasobe, T.4    Ito, O.5    Van Der Est, A.6
  • 75
    • 84904409274 scopus 로고    scopus 로고
    • Design and Synthesis of Bipyridine Platinum(II) Bisalkynyl Fullerene Donor-Chromophore-Acceptor Triads with Ultrafast Charge Separation
    • Lee, S.-H.; Chan, C. T.-L.; Wong, K. M.-C.; Lam, W. H.; Kwok, W.-M.; Yam, V. W.-W. Design and Synthesis of Bipyridine Platinum(II) Bisalkynyl Fullerene Donor-Chromophore-Acceptor Triads with Ultrafast Charge Separation J. Am. Chem. Soc. 2014, 136, 10041-10052 10.1021/ja5040073
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 10041-10052
    • Lee, S.-H.1    Chan, C.T.-L.2    Wong, K.M.-C.3    Lam, W.H.4    Kwok, W.-M.5    Yam, V.W.-W.6
  • 76
    • 84913528600 scopus 로고    scopus 로고
    • Internal Energy Dependence of the H + Allene/H + Propyne Product Branching from the Unimolecular Dissociation of 2-Propenyl Radicals
    • Karimata, A.; Suzuki, S.; Kozaki, M.; Kimoto, K.; Nozaki, K.; Matsushita, H.; Ikeda, N.; Akiyama, K.; Kosumi, D.; Hashimoto, H. et al. Internal Energy Dependence of the H + Allene/H + Propyne Product Branching from the Unimolecular Dissociation of 2-Propenyl Radicals J. Phys. Chem. A 2014, 118, 11261-11271 10.1021/jp509643q
    • (2014) J. Phys. Chem. A , vol.118 , pp. 11261-11271
    • Karimata, A.1    Suzuki, S.2    Kozaki, M.3    Kimoto, K.4    Nozaki, K.5    Matsushita, H.6    Ikeda, N.7    Akiyama, K.8    Kosumi, D.9    Hashimoto, H.10
  • 77
    • 37549043530 scopus 로고    scopus 로고
    • Polymer-Fullerene Composite Solar Cells
    • Thompson, B. C.; Fréchet, J. M. J. Polymer-Fullerene Composite Solar Cells Angew. Chem., Int. Ed. 2008, 47, 58-77 10.1002/anie.200702506
    • (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 58-77
    • Thompson, B.C.1    Fréchet, J.M.J.2
  • 78
    • 66149086912 scopus 로고    scopus 로고
    • Polymer-Fullerene Bulk-Heterojunction Solar Cells
    • Dennler, G.; Scharber, M. C.; Brabec, C. J. Polymer-Fullerene Bulk-Heterojunction Solar Cells Adv. Mater. 2009, 21, 1323-1338 10.1002/adma.200801283
    • (2009) Adv. Mater. , vol.21 , pp. 1323-1338
    • Dennler, G.1    Scharber, M.C.2    Brabec, C.J.3
  • 79
    • 79251577124 scopus 로고    scopus 로고
    • Fullerene Derivative Acceptors for High Performance Polymer Solar Cells
    • He, Y.; Li, Y. Fullerene Derivative Acceptors for High Performance Polymer Solar Cells Phys. Chem. Chem. Phys. 2011, 13, 1970-1983 10.1039/C0CP01178A
    • (2011) Phys. Chem. Chem. Phys. , vol.13 , pp. 1970-1983
    • He, Y.1    Li, Y.2
  • 80
    • 33644630570 scopus 로고    scopus 로고
    • A Strong Regioregularity Effect in Self-Organizing Conjugated Polymer Films and High-Efficiency Polythiophene:Fullerene Solar Cells
    • Kim, Y.; Cook, S.; Tuladhar, S. M.; Choulis, S. A.; Nelson, J.; Durrant, J. R.; Bradley, D. D. C.; Giles, M.; McCulloch, I.; Ha, C.-S. et al. A Strong Regioregularity Effect in Self-Organizing Conjugated Polymer Films and High-Efficiency Polythiophene:Fullerene Solar Cells Nat. Mater. 2006, 5, 197-203 10.1038/nmat1574
    • (2006) Nat. Mater. , vol.5 , pp. 197-203
    • Kim, Y.1    Cook, S.2    Tuladhar, S.M.3    Choulis, S.A.4    Nelson, J.5    Durrant, J.R.6    Bradley, D.D.C.7    Giles, M.8    McCulloch, I.9    Ha, C.-S.10
  • 81
    • 70350484189 scopus 로고    scopus 로고
    • "Plastic" Solar Cells: Self-Assembly of Bulk Heterojunction Nanomaterials by Spontaneous Phase Separation
    • Peet, J.; Heeger, A. J.; Bazan, G. C. "Plastic" Solar Cells: Self-Assembly of Bulk Heterojunction Nanomaterials by Spontaneous Phase Separation Acc. Chem. Res. 2009, 42, 1700-1708 10.1021/ar900065j
    • (2009) Acc. Chem. Res. , vol.42 , pp. 1700-1708
    • Peet, J.1    Heeger, A.J.2    Bazan, G.C.3
  • 83
    • 84859575070 scopus 로고    scopus 로고
    • Photoinduced Charge Carrier Generation and Decay in Sequentially Deposited Polymer/Fullerene Layers: Bulk Heterojunction vs. Planar Interface
    • Nardes, A. M.; Ayzner, A. L.; Hammond, S. R.; Ferguson, A. J.; Schwartz, B. J.; Kopidakis, N. Photoinduced Charge Carrier Generation and Decay in Sequentially Deposited Polymer/Fullerene Layers: Bulk Heterojunction vs. Planar Interface J. Phys. Chem. C 2012, 116, 7293-7305 10.1021/jp212390p
    • (2012) J. Phys. Chem. C , vol.116 , pp. 7293-7305
    • Nardes, A.M.1    Ayzner, A.L.2    Hammond, S.R.3    Ferguson, A.J.4    Schwartz, B.J.5    Kopidakis, N.6
  • 85
    • 49449098895 scopus 로고    scopus 로고
    • Fullerene Bisadducts for Enhanced Open-Circuit Voltages and Efficiencies in Polymer Solar Cells
    • Lenes, M.; Wetzelaer, G.-J. A. H.; Kooistra, F. B.; Veenstra, S. C.; Hummelen, J. C.; Blom, P. W. M. Fullerene Bisadducts for Enhanced Open-Circuit Voltages and Efficiencies in Polymer Solar Cells Adv. Mater. 2008, 20, 2116-2119 10.1002/adma.200702438
    • (2008) Adv. Mater. , vol.20 , pp. 2116-2119
    • Lenes, M.1    Wetzelaer, G.-J.A.H.2    Kooistra, F.B.3    Veenstra, S.C.4    Hummelen, J.C.5    Blom, P.W.M.6
  • 86
    • 84858239953 scopus 로고    scopus 로고
    • Charge Transport and Recombination in Low-Bandgap Bulk Heterojunction Solar Cell Using Bis-adduct Fullerene
    • Azimi, H.; Senes, A.; Scharber, M. C.; Hingerl, K.; Brabec, C. J. Charge Transport and Recombination in Low-Bandgap Bulk Heterojunction Solar Cell Using Bis-adduct Fullerene Adv. Energy Mater. 2011, 1, 1162-1168 10.1002/aenm.201100331
    • (2011) Adv. Energy Mater. , vol.1 , pp. 1162-1168
    • Azimi, H.1    Senes, A.2    Scharber, M.C.3    Hingerl, K.4    Brabec, C.J.5
  • 87
    • 84890379846 scopus 로고    scopus 로고
    • Application of Bis-PCBM in Polymer Solar Cells with Improved Voltage
    • Ye, L.; Zhang, S.; Qian, D.; Wang, Q.; Hou, J. Application of Bis-PCBM in Polymer Solar Cells with Improved Voltage J. Phys. Chem. C 2013, 117, 25360-25366 10.1021/jp409216e
    • (2013) J. Phys. Chem. C , vol.117 , pp. 25360-25366
    • Ye, L.1    Zhang, S.2    Qian, D.3    Wang, Q.4    Hou, J.5
  • 88
    • 84890517838 scopus 로고    scopus 로고
    • Quantifying the Relationship between the Maximum Achievable Voltage and Current Levels in Low-Bandgap Polymer Photovoltaics
    • Rodovsky, D. B.; Peet, J.; Shao, N.; Azoulay, J. D.; Bazan, G. C.; Drolet, N.; Wu, Q.; Sfeir, M. Y. Quantifying the Relationship between the Maximum Achievable Voltage and Current Levels in Low-Bandgap Polymer Photovoltaics J. Phys. Chem. C 2013, 117, 25955-25960 10.1021/jp410234u
    • (2013) J. Phys. Chem. C , vol.117 , pp. 25955-25960
    • Rodovsky, D.B.1    Peet, J.2    Shao, N.3    Azoulay, J.D.4    Bazan, G.C.5    Drolet, N.6    Wu, Q.7    Sfeir, M.Y.8
  • 89
    • 84884671346 scopus 로고    scopus 로고
    • Fullerene-Bisadduct Acceptors for Polymer Solar Cells
    • Li, Y. Fullerene-Bisadduct Acceptors for Polymer Solar Cells Chem.-Asian J. 2013, 8, 2316-2328 10.1002/asia.201300600
    • (2013) Chem. - Asian J. , vol.8 , pp. 2316-2328
    • Li, Y.1
  • 90
    • 84921287420 scopus 로고    scopus 로고
    • 60 Complex Confined in Vertical Nanocylinders of Amphiphilic Block Copolymer Films
    • 60 Complex Confined in Vertical Nanocylinders of Amphiphilic Block Copolymer Films Chem. Commun. 2015, 51, 1685-1688 10.1039/C4CC09262G
    • (2015) Chem. Commun. , vol.51 , pp. 1685-1688
    • Kamimura, T.1    Komura, M.2    Komiyama, H.3    Iyoda, T.4    Tani, F.5
  • 92
    • 0029290940 scopus 로고
    • 60 (Acceptor)-Aniline (Donor) System; Photophysical Properties of the First "Active" Fullerene Dyad
    • 60 (Acceptor)-Aniline (Donor) System; Photophysical Properties of the First "Active" Fullerene Dyad J. Am. Chem. Soc. 1995, 117, 4093-4099 10.1021/ja00119a025
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 4093-4099
    • Williams, R.M.1    Zwier, J.M.2    Verhoeven, J.W.3
  • 95
    • 0001005923 scopus 로고
    • Electron Transfer with Organometals. Steric Effects as Probes for Outer-Sphere and Inner-Sphere Oxidations of Homoleptic Alkylmetals with Iron(III) and Iridate(IV) Complexes
    • Wong, C. L.; Kochi, J. K. Electron Transfer with Organometals. Steric Effects as Probes for Outer-Sphere and Inner-Sphere Oxidations of Homoleptic Alkylmetals with Iron(III) and Iridate(IV) Complexes J. Am. Chem. Soc. 1979, 101, 5593-5603 10.1021/ja00513a024
    • (1979) J. Am. Chem. Soc. , vol.101 , pp. 5593-5603
    • Wong, C.L.1    Kochi, J.K.2
  • 96
    • 14544283254 scopus 로고    scopus 로고
    • 12 Model Compounds and Facile Cleavage of the Cobalt(IV)-Carbon Bond via Charge-Transfer Complexes with Bases. A Negative Temperature Dependence of the Rates
    • 12Model Compounds and Facile Cleavage of the Cobalt(IV)-Carbon Bond via Charge-Transfer Complexes with Bases. A Negative Temperature Dependence of the Rates J. Phys. Chem. A 2005, 109, 1105-1113 10.1021/jp0453008
    • (2005) J. Phys. Chem. A , vol.109 , pp. 1105-1113
    • Ohkubo, K.1    Fukuzumi, S.2
  • 99
    • 84904656829 scopus 로고    scopus 로고
    • Nanosecond Intersystem Crossing Times in Fullerene Acceptors: Implications for Organic Photovoltaic diodes
    • Chow, P. C. Y.; Albert-Seifried, S.; Gélinas, S.; Friend, R. H. Nanosecond Intersystem Crossing Times in Fullerene Acceptors: Implications for Organic Photovoltaic diodes Adv. Mater. 2014, 26, 4851-4854 10.1002/adma.201400846
    • (2014) Adv. Mater. , vol.26 , pp. 4851-4854
    • Chow, P.C.Y.1    Albert-Seifried, S.2    Gélinas, S.3    Friend, R.H.4
  • 100
    • 84949116506 scopus 로고    scopus 로고
    • Synthesis and Photodynamics of Diphenylethynyl-Bridged Porphyrin-Quinoidal Porphyrin Hybrids
    • Sakatani, S.; Kamimura, T.; Ohkubo, K.; Fukuzumi, S.; Tani, F. Synthesis and Photodynamics of Diphenylethynyl-Bridged Porphyrin-Quinoidal Porphyrin Hybrids J. Porphyrins Phthalocyanines 2015, 19, 219-232 10.1142/S1088424614501144
    • (2015) J. Porphyrins Phthalocyanines , vol.19 , pp. 219-232
    • Sakatani, S.1    Kamimura, T.2    Ohkubo, K.3    Fukuzumi, S.4    Tani, F.5
  • 101
    • 0011929925 scopus 로고    scopus 로고
    • Magnetic Field Effects on the Decay Rate of Photogenerated Biradical from Intramolecular Electron Transfer of Triplet Excited Fullerene in a Fullerene-Phenothiazine Linked Compound
    • Yonemura, H.; Tokudome, H.; Yamada, S. Magnetic Field Effects on the Decay Rate of Photogenerated Biradical from Intramolecular Electron Transfer of Triplet Excited Fullerene in a Fullerene-Phenothiazine Linked Compound Chem. Phys. Lett. 2001, 346, 361-367 10.1016/S0009-2614(01)00986-1
    • (2001) Chem. Phys. Lett. , vol.346 , pp. 361-367
    • Yonemura, H.1    Tokudome, H.2    Yamada, S.3
  • 102
    • 0347362671 scopus 로고    scopus 로고
    • Dynamics of Photoinduced Electron-Transfer Processes in Fullerene-Based Dyads: Effects of Varying the Donor Strength
    • Thomas, K. G.; Biju, V.; Kamat, P. V.; George, M. V.; Guldi, D. M. Dynamics of Photoinduced Electron-Transfer Processes in Fullerene-Based Dyads: Effects of Varying the Donor Strength ChemPhysChem 2003, 4, 1299-1307 10.1002/cphc.200200561
    • (2003) ChemPhysChem , vol.4 , pp. 1299-1307
    • Thomas, K.G.1    Biju, V.2    Kamat, P.V.3    George, M.V.4    Guldi, D.M.5
  • 103
    • 34249337375 scopus 로고    scopus 로고
    • 60) and Amine-Substituted Fluorenes Studied by Laser Flash Photolysis
    • 60) and Amine-Substituted Fluorenes Studied by Laser Flash Photolysis Spectrochim. Acta, Part A 2007, 67, 636-642 10.1016/j.saa.2006.08.022
    • (2007) Spectrochim. Acta, Part A , vol.67 , pp. 636-642
    • El-Khouly, M.E.1
  • 106
    • 20744441858 scopus 로고    scopus 로고
    • Drastic Difference in Lifetimes of the Charge-Separated State of the Formanilide-Anthraquinone Dyad versus the Ferrocene-Formanilide-Anthraquinone Triad and Their Photoelectrochemical Properties of the Composite Films with Fullerene Clusters
    • Okamoto, K.; Hasobe, T.; Tkachenko, N. V.; Lemmetyinen, H.; Kamat, P. V.; Fukuzumi, S. Drastic Difference in Lifetimes of the Charge-Separated State of the Formanilide-Anthraquinone Dyad versus the Ferrocene-Formanilide-Anthraquinone Triad and Their Photoelectrochemical Properties of the Composite Films with Fullerene Clusters J. Phys. Chem. A 2005, 109, 4662-4670 10.1021/jp045042e
    • (2005) J. Phys. Chem. A , vol.109 , pp. 4662-4670
    • Okamoto, K.1    Hasobe, T.2    Tkachenko, N.V.3    Lemmetyinen, H.4    Kamat, P.V.5    Fukuzumi, S.6
  • 107
    • 0001672288 scopus 로고
    • Chemical and Electrochemical Electron-Transfer Theory
    • Marcus, R. A. Chemical and Electrochemical Electron-Transfer Theory Annu. Rev. Phys. Chem. 1964, 15, 155-196 10.1146/annurev.pc.15.100164.001103
    • (1964) Annu. Rev. Phys. Chem. , vol.15 , pp. 155-196
    • Marcus, R.A.1
  • 108
    • 0022004980 scopus 로고
    • Electron Transfers in Chemistry and Biology
    • Marcus, R. A.; Sutin, N. Electron Transfers in Chemistry and Biology Biochim. Biophys. Acta, Rev. Bioenerg. 1985, 811, 265-322 10.1016/0304-4173(85)90014-X
    • (1985) Biochim. Biophys. Acta, Rev. Bioenerg. , vol.811 , pp. 265-322
    • Marcus, R.A.1    Sutin, N.2
  • 109
    • 0000419295 scopus 로고
    • Electron-Transfer Reactions in Chemistry: Theory and Experiment (Nobel Lecture)
    • Marcus, R. A. Electron-Transfer Reactions in Chemistry: Theory and Experiment (Nobel Lecture) Angew. Chem. 1993, 105, 1161-1172 10.1002/ange.19931050804
    • (1993) Angew. Chem. , vol.105 , pp. 1161-1172
    • Marcus, R.A.1
  • 110
    • 33748216903 scopus 로고
    • Angew. Chem., Int. Ed. Engl. 1993, 32, 1111-1121.10.1002/anie.199311113
    • (1993) Angew. Chem., Int. Ed. Engl. , vol.32 , pp. 1111-1121


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