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Volumn 14, Issue 9, 2008, Pages 2827-2841

Light-harvesting supramolecular porphyrin macrocycle accommodating a fullerene-tripodal ligand

Author keywords

Fullerenes; Photochemistry; Photosynthesis; Porphyrinoids; Self assembly

Indexed keywords

ELECTROMAGNETIC WAVES; FULLERENES; HARVESTING; ZINC;

EID: 47949112592     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200701720     Document Type: Article
Times cited : (57)

References (101)
  • 9
    • 0001046005 scopus 로고    scopus 로고
    • For recent reviews, see: a, Eds, J. L. Atwood, J. E. D. Davies, D. D. MacNicol, F. Vögtle, Pergamon. Oxford
    • For recent reviews, see: a) J. K. M. Sanders in Comprehensive Supramolecular Chemistry, Vol.9 (Eds.: J. L. Atwood, J. E. D. Davies, D. D. MacNicol, F. Vögtle), Pergamon. Oxford. 1996, pp. 131;
    • (1996) Comprehensive Supramolecular Chemistry , vol.9 , pp. 131
    • Sanders, J.K.M.1
  • 10
    • 0001110345 scopus 로고    scopus 로고
    • Eds, K.M. Kadish, K.M. Smith, R. Guilard, Academic Press, New York
    • b) J. Chambron, V. Heitz, J. P. Sauvage in The Porphyrin Handbook, Vol.6 (Eds.: K.M. Kadish, K.M. Smith, R. Guilard), Academic Press, New York, 2000, pp. 1;
    • (2000) The Porphyrin Handbook , vol.6 , pp. 1
    • Chambron, J.1    Heitz, V.2    Sauvage, J.P.3
  • 12
    • 84940906688 scopus 로고    scopus 로고
    • R D. Harvey in The Porphyrin Handbook, 18 (Eds.: K.M. Kadish, K.M. Smith, R. Guilard), Academic Press, New York, 2003, pp. 63;
    • d) R D. Harvey in The Porphyrin Handbook, Vol. 18 (Eds.: K.M. Kadish, K.M. Smith, R. Guilard), Academic Press, New York, 2003, pp. 63;
  • 30
    • 0001919604 scopus 로고    scopus 로고
    • For recent reports of noncovalently linked cyclic array, see: a
    • For recent reports of noncovalently linked cyclic array, see: a) C. M. Drain, K. C. Russell, J.-M. Lehn, Chem. Commun. 1996, 337;
    • (1996) Chem. Commun , pp. 337
    • Drain, C.M.1    Russell, K.C.2    Lehn, J.-M.3
  • 41
    • 0000085682 scopus 로고    scopus 로고
    • For reviews of covalently linked porphyrin and fullerene conjugates, see: a, Eds, K.M. Kadish, K.M. Smith, R. Guilard, Academic Press, New York
    • For reviews of covalently linked porphyrin and fullerene conjugates, see: a) D. Gust, T. A. Moore in The Porphyrin Handbook, Vol.8, (Eds.: K.M. Kadish, K.M. Smith, R. Guilard), Academic Press, New York, 2000. pp. 153;
    • (2000) The Porphyrin Handbook , vol.8 , pp. 153
    • Gust, D.1    Moore, T.A.2
  • 71
    • 53849123200 scopus 로고    scopus 로고
    • When the evaporation speed of the solvent became slow during the concentration process, the solvent tended to increase in methanol concentration, which resulted in slight dissociation of the cyclic trimer. Therefore, it is better for the evaporation process to be conducted at high speed so that the solvent composition does not change significantly
    • When the evaporation speed of the solvent became slow during the concentration process, the solvent tended to increase in methanol concentration, which resulted in slight dissociation of the cyclic trimer. Therefore, it is better for the evaporation process to be conducted at high speed so that the solvent composition does not change significantly.
  • 77
    • 53849127385 scopus 로고    scopus 로고
    • In ref, 15] we reported that the compound was D3h-symmetric and this has since been corrected to C3h-symmetric
    • 3h-symmetric.
  • 82
    • 53849147510 scopus 로고    scopus 로고
    • MATERIAL STUDIO Version 4.1/Forcite/Force Field UNIVERSAL, Accelrys, Inc, San Diego, CA, USA, 2001
    • MATERIAL STUDIO (Version 4.1/Forcite/Force Field UNIVERSAL), Accelrys, Inc. (San Diego, CA, USA, 2001).
  • 84
    • 53849134088 scopus 로고    scopus 로고
    • 3 reflects three-point binding from pyridyl to the zinc(II) ion.
    • 3 reflects three-point binding from pyridyl to the zinc(II) ion.
  • 85
    • 53849135084 scopus 로고    scopus 로고
    • -6M.
    • -6M.
  • 86
    • 53849124569 scopus 로고    scopus 로고
    • -1 in toluene from the UV/Vis titration.
    • -1 in toluene from the UV/Vis titration.
  • 87
    • 53849123613 scopus 로고    scopus 로고
    • 60-Tripod, accurate binding constants could not be obtained in toluene and o-dichlorobenzene.
    • 60-Tripod, accurate binding constants could not be obtained in toluene and o-dichlorobenzene.
  • 88
    • 53849098344 scopus 로고    scopus 로고
    • 3 showed no change in the UV/Vis absorption and fluorescence measurements under the same titration conditions.
    • 3 showed no change in the UV/Vis absorption and fluorescence measurements under the same titration conditions.
  • 89
    • 53849106445 scopus 로고    scopus 로고
    • 12: 7752.9). Furthermore, the plot of retention time (12.3 min) against molecular weight was added to a calibration curve for the series of cyclic compounds (Figure 6).
    • 12: 7752.9). Furthermore, the plot of retention time (12.3 min) against molecular weight was added to a calibration curve for the series of cyclic compounds (Figure 6).
  • 91
    • 19944415264 scopus 로고    scopus 로고
    • The first oxidation potentials of the coordinated monomeric and the slipped-cofacial dimeric porphyrin in dichloromethane were estimated to be 0.60 and 0.63 V, respectively, see: a H. Ozeki, A. Nomoto, K. Ogawa, Y. Kobuke, M. Murakami, K. Hosoda, M. Ohtani, S. Nakashima, H. Miyasaka, T. Okada, Chem. Eur. J. 2004, 10, 6393;
    • The first oxidation potentials of the coordinated monomeric and the slipped-cofacial dimeric porphyrin in dichloromethane were estimated to be 0.60 and 0.63 V, respectively, see: a) H. Ozeki, A. Nomoto, K. Ogawa, Y. Kobuke, M. Murakami, K. Hosoda, M. Ohtani, S. Nakashima, H. Miyasaka, T. Okada, Chem. Eur. J. 2004, 10, 6393;
  • 92
    • 33645530779 scopus 로고    scopus 로고
    • 3 would have similar oxidation potentials,
    • 3 would have similar oxidation potentials,
  • 94
    • 53849085447 scopus 로고    scopus 로고
    • Both absorption and fluorescence spectra of the monomeric porphyrins were shifted towards longer wavelengths by complexation of ligands, and approached those of the slipped-cofacial dimeric porphyrin. Thus, the energy gaps between the lowest excited state and the ground state of the coordinated monomeric and the complementary coordinated dimeric porphyrins became almost the same (2.02 eV for 6-Zn/Im and 2.00 eV for N-(5-Zn)3, Table l
    • 3, Table l).
  • 99
    • 53849128131 scopus 로고    scopus 로고
    • 3 hid them.
    • 3 hid them.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.