메뉴 건너뛰기




Volumn , Issue , 2003, Pages 28-1-28-42

Photochemical reaction of fullerenes and fullerene derivatives

Author keywords

[No Author keywords available]

Indexed keywords


EID: 9144238974     PISSN: None     EISSN: None     Source Type: Book    
DOI: None     Document Type: Chapter
Times cited : (3)

References (188)
  • 5
    • 0027244713 scopus 로고
    • Inhibition of the HIV-1 protease by fullerene derivatives: Model building studies and experimental verification
    • Friedmann, S., DeCamp, D.L., Sijbesma, R., Srdanov, G., Wudl, F., and Kenyon, G.L., Inhibition of the HIV-1 protease by fullerene derivatives: model building studies and experimental verification, J. Am. Chem. Soc., 115, 6506, 1993.
    • (1993) J. Am. Chem. Soc , vol.115 , pp. 6506
    • Friedmann, S.1    DeCamp, D.L.2    Sijbesma, R.3    Srdanov, G.4    Wudl, F.5    Kenyon, G.L.6
  • 7
    • 0033590932 scopus 로고    scopus 로고
    • Medicinalchemistry with fullerenes and fullerene derivatives
    • Da Ros, T. and Prato, M., Medicinalchemistry with fullerenes and fullerene derivatives, J. Chem. Soc., Chem. Commun., 663, 1999.
    • (1999) J. Chem. Soc., Chem. Commun , pp. 663
    • Da Ros, T.1    Prato, M.2
  • 9
    • 33748675706 scopus 로고    scopus 로고
    • Non-linear absorptions in pendant [60]fullerene-polystyrene polymers
    • Sun, Y.-P. and Riggs, J.E., Non-linear absorptions in pendant [60]fullerene-polystyrene polymers, J. Chem. Soc., FaradayTrans., 93, 1965-1970, 1997.
    • (1997) J. Chem. Soc., FaradayTrans , vol.93 , pp. 1965-1970
    • Sun, Y.-P.1    Riggs, J.E.2
  • 10
    • 0001484846 scopus 로고    scopus 로고
    • Opticallimiting properties of [60]fullerene derivatives
    • Sun, Y.-P., Riggs, J.E., and Bing, L., Opticallimiting properties of [60]fullerene derivatives, Chem. Mater., 9, 1268, 1997.
    • (1997) Chem. Mater , vol.9 , pp. 1268
    • Sun, Y.-P.1    Riggs, J.E.2    Bing, L.3
  • 11
    • 0027607561 scopus 로고
    • The chemistry of fullerenes
    • Taylor, R. and Walton, D.R.M., The chemistry of fullerenes, Nature, 363, 685, 1993.
    • (1993) Nature , vol.363 , pp. 685
    • Taylor, R.1    Walton, D.R.M.2
  • 13
    • 12044259832 scopus 로고
    • Synthesis, structures and properties of methanofullerenes
    • Diederich, F., Isaacs, L., and Philp, D., Synthesis, structures and properties of methanofullerenes, Chem. Soc. Rev., 23, 243, 1994.
    • (1994) Chem. Soc. Rev , vol.23 , pp. 243
    • Diederich, F.1    Isaacs, L.2    Philp, D.3
  • 15
    • 0002971459 scopus 로고    scopus 로고
    • Fullerenes and related structures
    • Hirsch, A., Ed., Fullerenes and related structures, Top. Curr. Chem., 199, 1999.
    • (1999) Top. Curr. Chem , pp. 199
    • Hirsch, A.1
  • 17
    • 0034044220 scopus 로고    scopus 로고
    • Surprises, serendipity and symmetry in fullerene chemistry
    • Taylor, R., Surprises, serendipity and symmetry in fullerene chemistry, Synlett, 776, 2000
    • (2000) Synlett , pp. 776
    • Taylor, R.1
  • 18
    • 0000415504 scopus 로고    scopus 로고
    • Discretefulleride anions and fullerenium cations
    • Reed, C.A. and Bolskar, R.D., Discretefulleride anions and fullerenium cations, Chem. Rev., 100, 1075, 2000.
    • (2000) Chem. Rev , vol.100 , pp. 1075
    • Reed, C.A.1    Bolskar, R.D.2
  • 19
    • 0001515746 scopus 로고
    • Photophysical and photochemical properties of fullerenes
    • Foote, C.S., Photophysical and photochemical properties of fullerenes, Top. Curr. Chem., 169, 347, 1994.
    • (1994) Top. Curr. Chem , vol.169 , pp. 347
    • Foote, C.S.1
  • 20
    • 84955395805 scopus 로고    scopus 로고
    • Electron transfer chemistry of fullerenes
    • Part. I, Balzani, V., Ed., Wiley-VCH, Weinheim
    • Fukuzumi, S. and Guldi, D.M., Electron transfer chemistry of fullerenes, in Electron Transfer in Chemistry, Vol. II, Part. I, Balzani, V., Ed., Wiley-VCH, Weinheim, 2001, p. 270.
    • (2001) Electron Transfer in Chemistry , vol.2 , pp. 270
    • Fukuzumi, S.1    Guldi, D.M.2
  • 21
    • 9144222905 scopus 로고    scopus 로고
    • Photophysics and photochemistry of fullerene and fullerene derivatives
    • Ramamurthy, V. and Schanze, K.S., Eds., Marcel Dekker, New York
    • Mattay, J., Ulmer, L., and Sotzmann, A., Photophysics and photochemistry of fullerene and fullerene derivatives, in Molecular and Supramolecular Photochemistry, Vol. 8, Ramamurthy, V. and Schanze, K.S., Eds., Marcel Dekker, New York, 2001, p. 637.
    • (2001) Molecular and Supramolecular Photochemistry , vol.8 , pp. 637
    • Mattay, J.1    Ulmer, L.2    Sotzmann, A.3
  • 26
    • 0001497261 scopus 로고
    • 60) in room-temperature solutions. No excitation wavelength dependence
    • 60) in room-temperature solutions. No excitation wavelength dependence, J. Am. Chem. Soc., 115, 6378, 1993.
    • (1993) J. Am. Chem. Soc , vol.115 , pp. 6378
    • Sun, Y.P.1    Wang, P.2    Hamilton, N.B.3
  • 28
    • 54249123760 scopus 로고    scopus 로고
    • Fluorescencespectra and quantum yields of [60]fullerene and [70]fullerene under different solvent conditions. A quantitative examination using a near-infrared-sensitive emission spectrometer
    • Ma, B. and Sun, Y.-P., Fluorescencespectra and quantum yields of [60]fullerene and [70]fullerene under different solvent conditions. A quantitative examination using a near-infrared-sensitive emission spectrometer, J. Chem. Soc., Perkin Trans. 2, 2157, 1996.
    • (1996) J. Chem. Soc., Perkin Trans , vol.2 , pp. 2157
    • Ma, B.1    Sun, Y.-P.2
  • 30
    • 0001592541 scopus 로고
    • A photoluminescence study of the carbon sixtyatom and carbon seventy-atom molecules
    • Sibley, S.P., Argentine, S.M., and Francis, A.H., A photoluminescence study of the carbon sixtyatom and carbon seventy-atom molecules, Chem. Phys. Lett., 188, 187, 1992.
    • (1992) Chem. Phys. Lett , vol.188 , pp. 187
    • Sibley, S.P.1    Argentine, S.M.2    Francis, A.H.3
  • 31
    • 0042706002 scopus 로고
    • Characterization of the soluble all-carbon molecules C60 and C70
    • Wang, Y., Characterization of the soluble all-carbon molecules C60 and C70, J. Phys. Chem., 96, 764, 1992.
    • (1992) J. Phys. Chem , vol.96 , pp. 764
    • Wang, Y.1
  • 32
    • 0001737959 scopus 로고
    • 70 in room-temperature solutions -quantum yields and well-resolved spectra as a function of excitation wavelength
    • 70 in room-temperature solutions -quantum yields and well-resolved spectra as a function of excitation wavelength, J. Phys. Chem., 97, 6770, 1993.
    • (1993) J. Phys. Chem , vol.97 , pp. 6770
    • Sun, Y.P.1    Bunker, C.E.2
  • 33
    • 0001414181 scopus 로고
    • A photoluminescence study of fullerenes: Total luminescence spectroscopy of C60 and C70
    • Palewska, K., Sworakowski, J., Chojnacki, H., Meister, E.C., and Wild, U.P., A photoluminescence study of fullerenes: total luminescence spectroscopy of C60 and C70, J. Phys. Chem., 97, 12167, 1993.
    • (1993) J. Phys. Chem , vol.97 , pp. 12167
    • Palewska, K.1    Sworakowski, J.2    Chojnacki, H.3    Meister, E.C.4    Wild, U.P.5
  • 34
    • 4244141511 scopus 로고
    • 70 and its quenching by long-range intermolecular electron transfer
    • 70 and its quenching by long-range intermolecular electron transfer, Chem. Phys. Lett., 194, 446, 1992.
    • (1992) Chem. Phys. Lett , vol.194 , pp. 446
    • Williams, R.M.1    Verhoeven, J.W.2
  • 35
    • 33748483261 scopus 로고    scopus 로고
    • 70 and the intersystem crossing process studied by picosecond time-resolved spectroscopy in the visible and near-IR region
    • 70 and the intersystem crossing process studied by picosecond time-resolved spectroscopy in the visible and near-IR region, J. Phys. Chem., 100, 10518, 1996.
    • (1996) J. Phys. Chem , vol.100 , pp. 10518
    • Watanabe, A.1    Ito, O.2    Watanabe, M.3    Saito, H.4    Koishi, M.5
  • 36
    • 44949275867 scopus 로고
    • Excited-state properties of the carbon sixty-atom molecule
    • Ebbesen, T.W., Tanigaki, K., and Kuroshima, S., Excited-state properties of the carbon sixty-atom molecule, Chem. Phys. Lett., 181, 501, 1991.
    • (1991) Chem. Phys. Lett , vol.181 , pp. 501
    • Ebbesen, T.W.1    Tanigaki, K.2    Kuroshima, S.3
  • 37
    • 5344244745 scopus 로고
    • Picosecond and nanosecond studies of the excitedstate properties of the carbon seventy-atom molecule
    • Tanigaki, K., Ebbesen, T.W., and Kuroshima, S., Picosecond and nanosecond studies of the excitedstate properties of the carbon seventy-atom molecule, Chem. Phys. Lett., 185, 189, 1991.
    • (1991) Chem. Phys. Lett , vol.185 , pp. 189
    • Tanigaki, K.1    Ebbesen, T.W.2    Kuroshima, S.3
  • 41
    • 0000673771 scopus 로고
    • 70 in solution -long intrinsic lifetimes and energy pooling
    • 70 in solution -long intrinsic lifetimes and energy pooling, J. Phys. Chem., 97, 11145, 1993.
    • (1993) J. Phys. Chem , vol.97 , pp. 11145
    • Fraelich, M.R.1    Weismann, R.B.2
  • 42
    • 2842571494 scopus 로고
    • A precise determination of the triplet energy of carbon (C60) by photoacoustic calorimetry
    • Hung, R.R. and Grabowski, J.J., A precise determination of the triplet energy of carbon (C60) by photoacoustic calorimetry, J. Phys. Chem., 95, 6073, 1991.
    • (1991) J. Phys. Chem , vol.95 , pp. 6073
    • Hung, R.R.1    Grabowski, J.J.2
  • 44
    • 0002799194 scopus 로고
    • Transientabsorption, lifetime and relaxation of the carbon sixty-atom molecule in the triplet state
    • Kajii, Y., Nakagawa, T., Suzuki, S., Achiba, Y., Obi, K., and Shibuya, K., Transientabsorption, lifetime and relaxation of the carbon sixty-atom molecule in the triplet state, Chem. Phys. Lett., 181, 100, 1991.
    • (1991) Chem. Phys. Lett , vol.181 , pp. 100
    • Kajii, Y.1    Nakagawa, T.2    Suzuki, S.3    Achiba, Y.4    Obi, K.5    Shibuya, K.6
  • 45
    • 0000037583 scopus 로고
    • 60 fullerene triplet and anion radical and one-electron reduction of the triplet by aromatic donors
    • 60 fullerene triplet and anion radical and one-electron reduction of the triplet by aromatic donors, Chem. Phys. Lett., 195, 339, 1992.
    • (1992) Chem. Phys. Lett , vol.195 , pp. 339
    • Biczok, L.1    Linschitz, H.2    Walter, R.I.3
  • 46
    • 0000332706 scopus 로고
    • Tripletexcited state behavior of fullerenes: Pulse radiolysis and laser flash photolysis of fullerenes (C60 and C70) in benzene
    • Dimitrijevic, N.M. and Kamat, P.V., Tripletexcited state behavior of fullerenes: pulse radiolysis and laser flash photolysis of fullerenes (C60 and C70) in benzene, J. Phys. Chem., 96, 4811, 1992.
    • (1992) J. Phys. Chem , vol.96 , pp. 4811
    • Dimitrijevic, N.M.1    Kamat, P.V.2
  • 49
    • 0000237455 scopus 로고
    • Effect of oxygenenhanced intersystem crossing on the observed efficiency of formation of singlet oxygen
    • McLean, A.J., McGarvey, D.J., Truscott, T.G., Lambert, C.R., and Land, E.J., Effect of oxygenenhanced intersystem crossing on the observed efficiency of formation of singlet oxygen, J. Chem. Soc., Faraday Trans., 86, 3075, 1990.
    • (1990) J. Chem. Soc., Faraday Trans , vol.86 , pp. 3075
    • McLean, A.J.1    McGarvey, D.J.2    Truscott, T.G.3    Lambert, C.R.4    Land, E.J.5
  • 50
    • 33751390939 scopus 로고
    • Externalheavy atom induced phosphorescence emission of fullerenes: The energy of triplet C60
    • Zeng, Y., Biczok, L., and Linschitz, H., Externalheavy atom induced phosphorescence emission of fullerenes: the energy of triplet C60, J. Phys. Chem., 96, 5237, 1992.
    • (1992) J. Phys. Chem , vol.96 , pp. 5237
    • Zeng, Y.1    Biczok, L.2    Linschitz, H.3
  • 51
    • 0001320423 scopus 로고
    • Photochemistry of fullerenes: Excited-state behavior of C60 and C70 and their reduction in poly(methyl methacrylate) films. V
    • Gevaert, M. and Kamat, P., Photochemistry of fullerenes: excited-state behavior of C60 and C70 and their reduction in poly(methyl methacrylate) films. V. J. Phys. Chem., 96, 9883, 1992.
    • (1992) J. Phys. Chem , vol.96 , pp. 9883
    • Gevaert, M.1    Kamat, P.2
  • 52
    • 0029290940 scopus 로고
    • 60 (acceptor)-aniline (donor) system. Photophysical properties of the first “active” fullerene diad
    • 60 (acceptor)-aniline (donor) system. Photophysical properties of the first “active” fullerene diad, J. Am. Chem. Soc., 117, 4093, 1995.
    • (1995) J. Am. Chem. Soc , vol.117 , pp. 4093
    • Williams, R.M.1    Zwier, J.M.2    Verhoeven, J.W.3
  • 53
    • 0000541417 scopus 로고
    • Steady-state and time-resolved direct detection EPR spectra of fullerene triplets in liquid solution and glassy matrixes: Evidence for a dynamic Jahn-Teller effect in triplet C60
    • Closs, G.L., Gautam, P., Zhang, D., Krusic, P.J., Hill, S.A., and Wassermann, E., Steady-state and time-resolved direct detection EPR spectra of fullerene triplets in liquid solution and glassy matrixes: evidence for a dynamic Jahn-Teller effect in triplet C60, J. Phys. Chem., 96, 5228, 1992.
    • (1992) J. Phys. Chem , vol.96 , pp. 5228
    • Closs, G.L.1    Gautam, P.2    Zhang, D.3    Krusic, P.J.4    Hill, S.A.5    Wassermann, E.6
  • 55
    • 0000617731 scopus 로고
    • Time-resolved EPR and Fourier transform EPR study of triplet fullerene C60: Determinations of T1 and the carbon-13 hyperfine coupling constant
    • Zhang, D., Norris, J.R., Krusic, P.J., Wassermann, E., Chen, C.C., and Lieber, C.M., Time-resolved EPR and Fourier transform EPR study of triplet fullerene C60: determinations of T1 and the carbon-13 hyperfine coupling constant, J. Phys. Chem., 97, 5886, 1993.
    • (1993) J. Phys. Chem , vol.97 , pp. 5886
    • Zhang, D.1    Norris, J.R.2    Krusic, P.J.3    Wassermann, E.4    Chen, C.C.5    Lieber, C.M.6
  • 59
    • 0040737338 scopus 로고
    • Dynamics of fullerene C70 in the lowest excited triplet state at low temperatures
    • Terazima, M., Sakurada, K., Hirota, N., Shinohara, H., and Saito, Y., Dynamics of fullerene C70 in the lowest excited triplet state at low temperatures, J. Phys. Chem., 97, 5447, 1993.
    • (1993) J. Phys. Chem , vol.97 , pp. 5447
    • Terazima, M.1    Sakurada, K.2    Hirota, N.3    Shinohara, H.4    Saito, Y.5
  • 60
    • 0002592695 scopus 로고
    • 60. Triplet-triplet annihilation, CIDEP and quenching by nitroxide radicals
    • 60. Triplet-triplet annihilation, CIDEP and quenching by nitroxide radicals, Chem. Phys. Lett., 208, 73, 1993.
    • (1993) Chem. Phys. Lett , vol.208 , pp. 73
    • Goudsmit, G.-H.1    Paul, H.2
  • 62
    • 0000836339 scopus 로고
    • A new reaction of fullerenes: [2 + 2] photocycloaddition of enones
    • Wilson, S.R., Kaprinidis, N., Wu, Y., and Schuster, D.I., A new reaction of fullerenes: [2 + 2] photocycloaddition of enones, J. Am. Chem. Soc., 115, 8495, 1993.
    • (1993) J. Am. Chem. Soc , vol.115 , pp. 8495
    • Wilson, S.R.1    Kaprinidis, N.2    Wu, Y.3    Schuster, D.I.4
  • 66
    • 0642303804 scopus 로고    scopus 로고
    • Nomenclature and terminology of fullerenes: A preliminary survey
    • Taylor, R., Nomenclature and terminology of fullerenes: a preliminary survey, Pure Appl. Chem., 69, 1411, 1997.
    • (1997) Pure Appl. Chem , vol.69 , pp. 1411
    • Taylor, R.1
  • 67
    • 37049074602 scopus 로고
    • 84: Numbering, π-bond order calculations and addition pattern considerations
    • 84: numbering, π-bond order calculations and addition pattern considerations, J. Chem. Soc., Perkin Trans. 2, 813, 1993.
    • (1993) J. Chem. Soc., Perkin Trans , vol.2 , pp. 813
    • Taylor, R.1
  • 69
    • 0031562456 scopus 로고    scopus 로고
    • Functionalization of [60]fullerene by photoinduced electron transfer (PET): Synthesis of 1-substituted 1,2-dihydro[60]fullerenes
    • Siedschlag, C., Luftmann, H., Wolff, C., and Mattay, J., Functionalization of [60]fullerene by photoinduced electron transfer (PET): synthesis of 1-substituted 1,2-dihydro[60]fullerenes, Tetrahedron, 53, 3587, 1997.
    • (1997) Tetrahedron , vol.53 , pp. 3587
    • Siedschlag, C.1    Luftmann, H.2    Wolff, C.3    Mattay, J.4
  • 70
    • 0033580803 scopus 로고    scopus 로고
    • [60]Fullerene radical cation: Reactions and mechanism
    • Siedschlag, C., Luftmann, H., Wolff, C., and Mattay, J., [60]Fullerene radical cation: reactions and mechanism, Tetrahedron, 55, 7805, 1999.
    • (1999) Tetrahedron , vol.55 , pp. 7805
    • Siedschlag, C.1    Luftmann, H.2    Wolff, C.3    Mattay, J.4
  • 77
    • 0029203548 scopus 로고
    • Addition of alcohols and hydrocarbons to fullerenes by photosensitized electron transfer
    • Lem, G., Schuster, D.I., Courtney, S.H., Lu, Q., and Wilson, S.R., Addition of alcohols and hydrocarbons to fullerenes by photosensitized electron transfer, J. Am. Chem. Soc., 117, 554, 1995.
    • (1995) J. Am. Chem. Soc , vol.117 , pp. 554
    • Lem, G.1    Schuster, D.I.2    Courtney, S.H.3    Lu, Q.4    Wilson, S.R.5
  • 78
    • 37049078935 scopus 로고
    • Photoaddition of silyl ketene acetal to [60]fullerene. Synthesis of α-fullerene-substituted carboxylic esters
    • Tokuyama, H., Isobe, H., and Nakamura, E., Photoaddition of silyl ketene acetal to [60]fullerene. Synthesis of α-fullerene-substituted carboxylic esters, J. Chem. Soc., Chem. Commun., 2753, 1994.
    • (1994) J. Chem. Soc., Chem. Commun , pp. 2753
    • Tokuyama, H.1    Isobe, H.2    Nakamura, E.3
  • 80
    • 85034500442 scopus 로고
    • 60 with ketene silyl acetals: Fullerene functionalization chemistry
    • 60 with ketene silyl acetals: fullerene functionalization chemistry, Synlett, 229, 1995
    • (1995) Synlett , pp. 229
    • Mikami, K.1    Matsumoto, S.2
  • 82
    • 0001765236 scopus 로고
    • Electron-transfer oxidation of ketene silyl acetals and other organosilanes. The mechanistic insight into Lewis acid mediated electron transfer
    • Fukuzumi, S., Fujita, M., Otera, J., and Fujita, Y., Electron-transfer oxidation of ketene silyl acetals and other organosilanes. The mechanistic insight into Lewis acid mediated electron transfer, J. Am. Chem. Soc., 114, 10271, 1992.
    • (1992) J. Am. Chem. Soc , vol.114 , pp. 10271
    • Fukuzumi, S.1    Fujita, M.2    Otera, J.3    Fujita, Y.4
  • 85
    • 37049082418 scopus 로고
    • Regio-reversal in the thermal and photochemical reduction of 10-methylacridinium ion by allylic silanes and stannanes
    • Fukuzumi, S., Fujita, M., and Otera, J., Regio-reversal in the thermal and photochemical reduction of 10-methylacridinium ion by allylic silanes and stannanes, J. Chem. Soc., Chem. Commun., 1536, 1993.
    • (1993) J. Chem. Soc., Chem. Commun , pp. 1536
    • Fukuzumi, S.1    Fujita, M.2    Otera, J.3
  • 90
    • 0001310751 scopus 로고
    • 70 with aromatic amines in the ground and excited states. Evidence for fullerene-benzene interaction in the ground state
    • 70 with aromatic amines in the ground and excited states. Evidence for fullerene-benzene interaction in the ground state, Chem. Phys. Lett., 205, 395, 1993.
    • (1993) Chem. Phys. Lett , vol.205 , pp. 395
    • Seshadri, R.1    Rao, C.N.R.2    Pal, H.3    Mukherjee, T.4    Mittal, J.P.5
  • 91
    • 33750527713 scopus 로고
    • Electrondonor-acceptor interactions of fullerenes C60 and C70 with triethylamine
    • Sun, Y.-P., Ma, B., and Lawson, G.E., Electrondonor-acceptor interactions of fullerenes C60 and C70 with triethylamine, Chem. Phys. Lett., 95, 57, 1995.
    • (1995) Chem. Phys. Lett , vol.95 , pp. 57
    • Sun, Y.-P.1    Ma, B.2    Lawson, G.E.3
  • 93
    • 44949273917 scopus 로고
    • Ultrafastphoto induced electron transfer to carbon sixty-atom molecule
    • Sension, R.J., Szarka, A.Z., Smith, G.R., and Hochstrasser, R.M., Ultrafastphoto induced electron transfer to carbon sixty-atom molecule, Chem. Phys. Lett., 185, 179, 1991.
    • (1991) Chem. Phys. Lett , vol.185 , pp. 179
    • Sension, R.J.1    Szarka, A.Z.2    Smith, G.R.3    Hochstrasser, R.M.4
  • 94
    • 0001250335 scopus 로고
    • 70 and N, N-diethylaniline -fluorescence quenching due to solvent polarity and polarizibality
    • 70 and N, N-diethylaniline -fluorescence quenching due to solvent polarity and polarizibality, Chem Phys. Lett., 236, 285, 1995
    • (1995) Chem Phys. Lett , vol.236 , pp. 285
    • Sun, Y.P.1    Ma, B.2
  • 95
    • 33751392543 scopus 로고
    • Nonlinear optical properties of fullerenes and charge-transfer complexes of fullerenes
    • Wang, Y. and Cheng, L.-T., Nonlinear optical properties of fullerenes and charge-transfer complexes of fullerenes, J. Phys. Chem., 96, 1530, 1992.
    • (1992) J. Phys. Chem , vol.96 , pp. 1530
    • Wang, Y.1    Cheng, L.-T.2
  • 98
    • 0003108445 scopus 로고    scopus 로고
    • Photoinduced reactions of tertiary amines with [60]fullerene. Addition of an α-C-H bond of amines to [60]fullerene
    • Liou, K.-F. and Cheng, C.-H., Photoinduced reactions of tertiary amines with [60]fullerene. Addition of an α-C-H bond of amines to [60]fullerene, J. Chem. Soc., Chem. Commun., 1423, 1996.
    • (1996) J. Chem. Soc., Chem. Commun , pp. 1423
    • Liou, K.-F.1    Cheng, C.-H.2
  • 99
    • 0042722348 scopus 로고    scopus 로고
    • 60 with cyclic amino acids: Reparation of dihydrofullerenes by decarboxylation
    • 60 with cyclic amino acids: reparation of dihydrofullerenes by decarboxylation, Chem. Lett., 1007, 1997.
    • (1997) Chem. Lett , pp. 1007
    • Zhang, W.1    Su, Y.2    Gan, L.3    Jiang, J.4    Huang, C.5
  • 100
    • 0000955564 scopus 로고    scopus 로고
    • Synthesis of pyrrolidine ring-fused fullerene multicarboxylates by photoreaction
    • Gan, L., Jiang, J., Zhang, W., Su, Y., Shi, Y., Huang, C., Pan, J., Lü, M., and Wu, Y., Synthesis of pyrrolidine ring-fused fullerene multicarboxylates by photoreaction, J. Org. Chem., 63, 4240, 1998.
    • (1998) J. Org. Chem , vol.63 , pp. 4240
    • Gan, L.1    Jiang, J.2    Zhang, W.3    Su, Y.4    Shi, Y.5    Huang, C.6    Pan, J.7    Lü, M.8    Wu, Y.9
  • 101
    • 0000333701 scopus 로고
    • A simple and convenient photo-decarboxylation method of intact carboxylic acids in the presence of aza aromatic compounds
    • Okada, K., Okubo, K., and Oda, M., A simple and convenient photo-decarboxylation method of intact carboxylic acids in the presence of aza aromatic compounds, J. Photochem. Photobiol. A: hem., 57, 265, 1991.
    • (1991) J. Photochem. Photobiol. A: Hem , vol.57 , pp. 265
    • Okada, K.1    Okubo, K.2    Oda, M.3
  • 102
    • 0037128529 scopus 로고    scopus 로고
    • Photochemicaladdition reactions of [60]fullerene with 1,2-ethylenediamine and piperazine
    • Wang, N.-X., Photochemicaladdition reactions of [60]fullerene with 1,2-ethylenediamine and piperazine, Tetrahedron, 58, 1017, 2002.
    • (2002) Tetrahedron , vol.58 , pp. 1017
    • Wang, N.-X.1
  • 106
    • 0001578049 scopus 로고
    • Regiospecific coordination of tert-butylfulleride ion and 1,4-dicyclopropyltropylium ion. Synthesis of a dialkyldihydrofullerene having a heterolytically dissociative carbon-carbon σ-bond
    • Kitagawa, T., Tanaka, T., Takata, Y., and Takeuchi, K., Regiospecific coordination of tert-butylfulleride ion and 1,4-dicyclopropyltropylium ion. Synthesis of a dialkyldihydrofullerene having a heterolytically dissociative carbon-carbon σ-bond, J. Org. Chem., 60, 1490, 1995
    • (1995) J. Org. Chem , vol.60 , pp. 1490
    • Kitagawa, T.1    Tanaka, T.2    Takata, Y.3    Takeuchi, K.4
  • 107
    • 0030870079 scopus 로고    scopus 로고
    • Synthesis of a hydrocarbon salt having a fullerene framework
    • Tanaka, T., Kitagawa, T., Komatsu, K., and Takeuchi, K., Synthesis of a hydrocarbon salt having a fullerene framework, J. Am. Chem. Soc., 119, 9313, 1997.
    • (1997) J. Am. Chem. Soc , vol.119 , pp. 9313
    • Tanaka, T.1    Kitagawa, T.2    Komatsu, K.3    Takeuchi, K.4
  • 108
    • 0002194268 scopus 로고    scopus 로고
    • Protonmigration on the [60]fullerene cage of 1-tert-butyl-1,4-dihydro[60]fullerene to yield the 1,2-isomer
    • Banim, F., Cardin, D.J., and Heath, P., Protonmigration on the [60]fullerene cage of 1-tert-butyl-1,4-dihydro[60]fullerene to yield the 1,2-isomer, J. Chem. Soc., Chem. Commun., 60, 1997.
    • (1997) J. Chem. Soc., Chem. Commun , pp. 60
    • Banim, F.1    Cardin, D.J.2    Heath, P.3
  • 110
    • 4143117505 scopus 로고
    • Photochemicalfulleroid to methanofullerene conversion via the di-π-methane (Zimmermann) rearrangement
    • Jansen, R.A.J., Hummelen, J.C., and Wudl, F., Photochemicalfulleroid to methanofullerene conversion via the di-π-methane (Zimmermann) rearrangement, J. Am. Chem. Soc., 117, 544, 1995
    • (1995) J. Am. Chem. Soc , vol.117 , pp. 544
    • Jansen, R.A.J.1    Hummelen, J.C.2    Wudl, F.3
  • 111
    • 0001088562 scopus 로고
    • The specific acid-catalyzed and photochemical isomerization of a robust fulleroid to a methanofullerene
    • Gonzalez, R., Hummelen, J.C., and Wudl, F., The specific acid-catalyzed and photochemical isomerization of a robust fulleroid to a methanofullerene, J. Org. Chem., 60, 2618, 1995.
    • (1995) J. Org. Chem , vol.60 , pp. 2618
    • Gonzalez, R.1    Hummelen, J.C.2    Wudl, F.3
  • 123
    • 0028900556 scopus 로고
    • 60 -synthesis of fulleroaziridines and thermal rearrangement to fullerooxazoles
    • 60 -synthesis of fulleroaziridines and thermal rearrangement to fullerooxazoles, Tetrahedron, 51, 2543, 1995.
    • (1995) Tetrahedron , vol.51 , pp. 2543
    • Averdung, J.1    Mattay, J.2    Jacobi, D.3    Abraham, W.4
  • 124
    • 0028070793 scopus 로고
    • 60 by in situ generated 6b,10adihydrofluoranthene
    • 60 by in situ generated 6b,10adihydrofluoranthene, Tetrahedron Lett., 35, 6661, 1994.
    • (1994) Tetrahedron Lett , vol.35 , pp. 6661
    • Averdung, J.1    Mattay, J.2
  • 126
    • 0000020654 scopus 로고    scopus 로고
    • [2 + 2] Cycloaddition of fullerenes with electron-rich alkenes and alkynes
    • Zhang, X., Fan, A., and Foote, C S., [2 + 2] Cycloaddition of fullerenes with electron-rich alkenes and alkynes, J, Org. Chem., 61, 5456, 1996.
    • (1996) J, Org. Chem , vol.61 , pp. 5456
    • Zhang, X.1    Fan, A.2    Foote, C.S.3
  • 129
    • 0032582096 scopus 로고    scopus 로고
    • 60 with alkyl-substituted 1,3-butadienes: A mechanistic approach. Stereochemistry and isotope effects
    • 60 with alkyl-substituted 1,3-butadienes: a mechanistic approach. Stereochemistry and isotope effects, J. Am. Chem. Soc., 120, 9911, 1998.
    • (1998) J. Am. Chem. Soc , vol.120 , pp. 9911
    • Vassilikogiannakis, G.1    Chronakis, N.2    Orfanopoulos, M.3
  • 131
    • 0032927123 scopus 로고    scopus 로고
    • Regio-and stereoselectivity of the [2 + 2] photocycloaddition of acyclic enones to C60
    • Vassilikogiannakis, G. and Orfanopoulos, M., Regio-and stereoselectivity of the [2 + 2] photocycloaddition of acyclic enones to C60, J. Org. Chem., 64, 3392, 1999.
    • (1999) J. Org. Chem , vol.64 , pp. 3392
    • Vassilikogiannakis, G.1    Orfanopoulos, M.2
  • 134
    • 0002497872 scopus 로고
    • New insights into an old mechanism: [2 + 2] photocycloaddition of enones to alkenes
    • For a recent review, see
    • For a recent review, see: Schuster, D.I., Lem, G., and Kaprinidis, N., New insights into an old mechanism: [2 + 2] photocycloaddition of enones to alkenes, Chem. Rev., 93, 3, 1993.
    • (1993) Chem. Rev , vol.93 , pp. 3
    • Schuster, D.I.1    Lem, G.2    Kaprinidis, N.3
  • 136
    • 0342677835 scopus 로고
    • 60: Synthesis, characterization and functionalization of fullerene pyrrolidines
    • 60: synthesis, characterization and functionalization of fullerene pyrrolidines, J. Am. Chem. Soc., 115, 9798, 1993
    • (1993) J. Am. Chem. Soc , vol.115 , pp. 9798
    • Maggini, M.1    Scorrano, G.2    Prato, M.3
  • 138
  • 141
    • 0000977750 scopus 로고    scopus 로고
    • Singletoxygen involvement in the photochemical reaction of C60 and amines. Synthesis of an alkyne-containing fullerene
    • Bernstein, R. and Foote, C.S., Singletoxygen involvement in the photochemical reaction of C60 and amines. Synthesis of an alkyne-containing fullerene, J. Phys. Chem. A, 103, 7244, 1999.
    • (1999) J. Phys. Chem. A , vol.103 , pp. 7244
    • Bernstein, R.1    Foote, C.S.2
  • 142
    • 0033529840 scopus 로고    scopus 로고
    • Photoinducedelectron-transfer reactions of [60]fullerene with triethylamine
    • Lawson, G.E., Kitaygorodskiy, A., and Sun, Y.-P., Photoinducedelectron-transfer reactions of [60]fullerene with triethylamine, J. Org. Chem., 64, 5913, 1999.
    • (1999) J. Org. Chem , vol.64 , pp. 5913
    • Lawson, G.E.1    Kitaygorodskiy, A.2    Sun, Y.-P.3
  • 144
    • 0029881482 scopus 로고    scopus 로고
    • Exohedralfunctionalization of [60]fullerene by [3 + 2] cycloadditions: Ynthesis and chemical properties of triazolino[60]fullerenes and 1,2-(3,4-dihydro-2H-pyrrolo)[60]fullerenes
    • Averdung, J. and Mattay, J., Exohedralfunctionalization of [60]fullerene by [3 + 2] cycloadditions: ynthesis and chemical properties of triazolino[60]fullerenes and 1,2-(3,4-dihydro-2H-pyrrolo)[60]fullerenes, Tetrahedron, 52, 5407, 1996.
    • (1996) Tetrahedron , vol.52 , pp. 5407
    • Averdung, J.1    Mattay, J.2
  • 145
    • 37049135440 scopus 로고
    • Photochemical reactions. II. Cycloaddition reactions of photoenols from 2-methylbenzaldehyde and realted systems
    • Arnold, B.J., Mellows, S.M., Sammes, P.G., and Wallace, T.W., Photochemical reactions. II. Cycloaddition reactions of photoenols from 2-methylbenzaldehyde and realted systems, J. Chem. Soc., Perkin Trans. 1, 401, 1974
    • (1974) J. Chem. Soc., Perkin Trans , vol.1 , pp. 401
    • Arnold, B.J.1    Mellows, S.M.2    Sammes, P.G.3    Wallace, T.W.4
  • 146
    • 0001331615 scopus 로고
    • Photoenolization
    • Sammes, P.G., Photoenolization, Tetrahedron, 32, 405, 1976.
    • (1976) Tetrahedron , vol.32 , pp. 405
    • Sammes, P.G.1
  • 148
    • 0034701582 scopus 로고    scopus 로고
    • Facilemodification of [60]fullerene by photochemically generated hydroxy-o-quinodimethane derivatives
    • O-kawa, K., Nakamura, Y., and Nishimura, J., Facilemodification of [60]fullerene by photochemically generated hydroxy-o-quinodimethane derivatives, Tetrahedron Lett., 41, 3103, 2000
    • (2000) Tetrahedron Lett , vol.41 , pp. 3103
    • O-Kawa, K.1    Nakamura, Y.2    Nishimura, J.3
  • 149
    • 0037154740 scopus 로고    scopus 로고
    • Photochemicalsynthesis, conformational analysis and transformation of [60]fullerene-o-quinodimethane adducts bearing a hydroxy group
    • Nakamura, Y., O-kawa, K., Minami, S., Ogawa, T., Tobita, S., and Nishimura, J., Photochemicalsynthesis, conformational analysis and transformation of [60]fullerene-o-quinodimethane adducts bearing a hydroxy group, J. Org. Chem., 67, 1247, 2002.
    • (2002) J. Org. Chem , vol.67 , pp. 1247
    • Nakamura, Y.1    O-Kawa, K.2    Minami, S.3    Ogawa, T.4    Tobita, S.5    Nishimura, J.6
  • 150
    • 0032575192 scopus 로고    scopus 로고
    • Solidstate photochemistry for fullerene functionalization: Solid state photoinduced electron transfer in the Diels-Alder reaction with anthracenes
    • Mikami, K., Matsumoto, S., Tonoi, T., and Okubo, Y., Solidstate photochemistry for fullerene functionalization: solid state photoinduced electron transfer in the Diels-Alder reaction with anthracenes, Tetrahedron Lett., 39, 3733, 1998.
    • (1998) Tetrahedron Lett , vol.39 , pp. 3733
    • Mikami, K.1    Matsumoto, S.2    Tonoi, T.3    Okubo, Y.4
  • 152
    • 31444439577 scopus 로고
    • Syntheticchemistry with fullerenes. Photooxygenation of olefins
    • Tokuyama, H. and Nakamura, E., Syntheticchemistry with fullerenes. Photooxygenation of olefins, J. Org. Chem., 59, 1135, 1994
    • (1994) J. Org. Chem , vol.59 , pp. 1135
    • Tokuyama, H.1    Nakamura, E.2
  • 156
    • 0029961154 scopus 로고    scopus 로고
    • Sequence-specific modification of guanosine in DNA by a C-60-linked deoxyoligonucleotide: Evidence for a non-singlet oxygen mechanism
    • An, Y.-Z., Anderson, J.L., Sigman, D.S., Foote, C.S., and Rubin, Y., Sequence-specific modification of guanosine in DNA by a C-60-linked deoxyoligonucleotide: evidence for a non-singlet oxygen mechanism, Tetrahedron, 89, 5179, 1996.
    • (1996) Tetrahedron , vol.89 , pp. 5179
    • An, Y.-Z.1    Anderson, J.L.2    Sigman, D.S.3    Foote, C.S.4    Rubin, Y.5
  • 157
    • 33751156558 scopus 로고
    • Unusualregioselectivity in the singlet oxygen ene reaction of cyclohexenobuckminsterfullerene, Y
    • An, Y.-Z., Viado, A.L., Arce, M.-J., and Rubin, Y., Unusualregioselectivity in the singlet oxygen ene reaction of cyclohexenobuckminsterfullerene, Y. J. Org. Chem., 60, 8330, 1995.
    • (1995) J. Org. Chem , vol.60 , pp. 8330
    • An, Y.-Z.1    Viado, A.L.2    Arce, M.-J.3    Rubin, Y.4
  • 158
    • 0000913128 scopus 로고
    • Photosensitizedoxygenations and the role of singlet oxygen
    • Foote, C.S., Photosensitizedoxygenations and the role of singlet oxygen, Acc. Chem. Res., 1, 104, 1968
    • (1968) Acc. Chem. Res , vol.1 , pp. 104
    • Foote, C.S.1
  • 159
    • 33847086362 scopus 로고
    • 2 to 1-methylcycloalkenes. Correlation with ground-state geometry
    • 2 to 1-methylcycloalkenes. Correlation with ground-state geometry, J. Am. Chem. Soc., 102, 1738, 1980.
    • (1980) J. Am. Chem. Soc , vol.102 , pp. 1738
    • Schulte-Elte, K.H.1    Rautenstrauch, V.2
  • 160
    • 0041808822 scopus 로고    scopus 로고
    • Synthesis and self-photooxygenation of alkenyl-linked [60]fullerene derivatives. A regioselective ene reaction
    • Chronakis, N., Vougioukalakis, G.C., and Orfanopoulos, M., Synthesis and self-photooxygenation of alkenyl-linked [60]fullerene derivatives. A regioselective ene reaction, Org. Lett., 4, 945, 2002.
    • (2002) Org. Lett , vol.4 , pp. 945
    • Chronakis, N.1    Vougioukalakis, G.C.2    Orfanopoulos, M.3
  • 162
    • 0035966569 scopus 로고    scopus 로고
    • Photooxygenativepartial ring cleavage of bis(fulleroid): Synthesis of a novel fullerene derivative with a 12-membered ring
    • Inoue, H., Yamaguchi, H., Iwamatsu, S.-I., Uozaki, T., Suzuki, T., Akasaka, T., Nagase, S., and Mutata, S., Photooxygenativepartial ring cleavage of bis(fulleroid): synthesis of a novel fullerene derivative with a 12-membered ring, Tetrahedron Lett., 42, 895, 2001.
    • (2001) Tetrahedron Lett , vol.42 , pp. 895
    • Inoue, H.1    Yamaguchi, H.2    Iwamatsu, S.-I.3    Uozaki, T.4    Suzuki, T.5    Akasaka, T.6    Nagase, S.7    Mutata, S.8
  • 166
    • 0001578392 scopus 로고
    • A methodology for the reversible solubilization of fullerenes
    • An, Y.-Z., Ellis, G.A., Viado, A.L., and Rubin, Y., A methodology for the reversible solubilization of fullerenes, J. Org. Chem., 60, 6353, 1995.
    • (1995) J. Org. Chem , vol.60 , pp. 6353
    • An, Y.-Z.1    Ellis, G.A.2    Viado, A.L.3    Rubin, Y.4
  • 170
    • 0001456992 scopus 로고
    • The chemical properties of buckminsterfullerene (C60) and the birth and infancy of fulleroids
    • Wudl, F., The chemical properties of buckminsterfullerene (C60) and the birth and infancy of fulleroids, Acc. Chem. Res., 25, 157, 1992
    • (1992) Acc. Chem. Res , vol.25 , pp. 157
    • Wudl, F.1
  • 171
    • 12044259832 scopus 로고
    • Syntheses, structures and properties of methanofullerenes
    • references therein
    • Diederich, F., Isaacs, L., and Philp, D., Syntheses, structures and properties of methanofullerenes, Chem. Soc. Rev., 243, 1994 and references therein
    • (1994) Chem. Soc. Rev , pp. 243
    • Diederich, F.1    Isaacs, L.2    Philp, D.3
  • 173
    • 37049080793 scopus 로고
    • Valenceisomerism and rearrangement to methanofullerenes
    • Diederich, F., Isaacs, L., and Philp, D., Valenceisomerism and rearrangement to methanofullerenes, J. Chem. Soc. Perkin Trans., 2, 391, 1994.
    • (1994) J. Chem. Soc. Perkin Trans , vol.2 , pp. 391
    • Diederich, F.1    Isaacs, L.2    Philp, D.3
  • 174
    • 0030197414 scopus 로고    scopus 로고
    • Progress in fullerene chemistry: From exohedral functionalization to heterofullerenes
    • Averdung, J., Torres-Garcia, G., Luftmann, H., Schlachter, I., and Mattay, J., Progress in fullerene chemistry: from exohedral functionalization to heterofullerenes, Full. Sci. Techn., 4, 633, 1996.
    • (1996) Full. Sci. Techn , vol.4 , pp. 633
    • Averdung, J.1    Torres-Garcia, G.2    Luftmann, H.3    Schlachter, I.4    Mattay, J.5
  • 175
    • 0002496765 scopus 로고    scopus 로고
    • Opening and closure of the fullerene cage in cis-1-bisimino adducts of C-60: The influence of the addition pattern and the addend
    • Schick, G., Hirsch, A., Mauser, H., and Clark, T., Opening and closure of the fullerene cage in cis-1-bisimino adducts of C-60: the influence of the addition pattern and the addend, Chem.-Eur. J., 2, 935, 1996.
    • (1996) Chem.-Eur. J , vol.2 , pp. 935
    • Schick, G.1    Hirsch, A.2    Mauser, H.3    Clark, T.4
  • 176
    • 0031021142 scopus 로고    scopus 로고
    • Synthesis of 1,2,3,4-bisiminofullerene and 1,2,3,4-bis(triazolino) fullerene -on the mechanism of the addition reactions of organic azides to [60]fullerene
    • Shen, C.K.-F., Yu, H.-H., Juo, C.-G., Chien, K.-M., Her, G.-R., and Luh, T.-Y., Synthesis of 1,2,3,4-bisiminofullerene and 1,2,3,4-bis(triazolino) fullerene -on the mechanism of the addition reactions of organic azides to [60]fullerene, Chem.-Eur. J., 4, 744, 1997
    • (1997) Chem.-Eur. J , vol.4 , pp. 744
    • Shen, C.K.-F.1    Yu, H.-H.2    Juo, C.-G.3    Chien, K.-M.4    Her, G.-R.5    Luh, T.-Y.6
  • 178
    • 37049090786 scopus 로고
    • Shiu, L.-L., Chien, K.-M., Liu, T.-Y., Lin, T.-I., Her, G.-R., and Luh, T.-Y., Bisazafulleroids, J. Chem. Soc., Chem. Commun., 1159, 1995
    • (1995) J. Chem. Soc., Chem. Commun , pp. 1159
  • 180
    • 0031733268 scopus 로고    scopus 로고
    • Aza-aziridinofullerene: Nterconversion between aza-aziridinofullerene and bis-azafulleroid
    • Kanakamma, P.P., Huang, S.-H., Juo, C.-G., Her, G.-R., and Luh, T.-Y., Aza-aziridinofullerene: nterconversion between aza-aziridinofullerene and bis-azafulleroid, Chem.-Eur. J., 4, 2037, 1998.
    • (1998) Chem.-Eur. J , vol.4 , pp. 2037
    • Kanakamma, P.P.1    Huang, S.-H.2    Juo, C.-G.3    Her, G.-R.4    Luh, T.-Y.5
  • 181
    • 0031036682 scopus 로고    scopus 로고
    • Whyis the rearrangement of [6,5] open fulleroids to [6,6] closed fullerenes zero order?
    • Li, Z. and Shevlin, P.B., Whyis the rearrangement of [6,5] open fulleroids to [6,6] closed fullerenes zero order? J. Am. Chem. Soc., 119, 1149, 1997.
    • (1997) J. Am. Chem. Soc , vol.119 , pp. 1149
    • Li, Z.1    Shevlin, P.B.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.