메뉴 건너뛰기




Volumn 101, Issue 12, 1997, Pages 2218-2220

Mediated energy transfer in covalently linked porphyrin dimers

Author keywords

[No Author keywords available]

Indexed keywords


EID: 0000475590     PISSN: 10895639     EISSN: None     Source Type: Journal    
DOI: 10.1021/jp970246z     Document Type: Article
Times cited : (87)

References (42)
  • 1
    • 3943082506 scopus 로고    scopus 로고
    • For recent reviews, see: (a) Speiser, S. Chem. Rev. 1996, 96, 1953-1976. (b) Sauvage, J.-P.; Collin, J.-P.; Chambron, J.-C.; Guillerez, S.; Coudret, C. Balzani, V.; Barigelletti, F.; De Cola, L.; Flamigni, L. Chem. Rev. 1994, 94, 993-1019.
    • (1996) Chem. Rev. , vol.96 , pp. 1953-1976
    • Speiser, S.1
  • 25
    • 0000051912 scopus 로고
    • Donor-acceptor systems linked with aromatic spacers have been reported. See, for example: (a) Osuka, A.; Yamada, H.; Maruyama, K.; Mataga, N.; Asahi, T.; Ohkouchi, M.; Okada, T.; Yamazaki, I.; Nishimura, Y. J. Am. Chem. Soc. 1993, 115, 9439-9452. (b) Seth, J.; Palaniappan, V.; Johnson, T. E.; Prathapan, S.; Lindsey, J. S.; Bocian, D. F. J. Am. Chem. Soc. 1994, 116, 10578-10592. (c) Hsiao, J.-S.; Krueger, B. P.; Wagner, R. W.; Johnson, T. E.; Delaney, J. K.; Mauzerall, D. C.; Fleming, G. R.; Lindsey, J. S.; Bochian, D. F.; Donohoe, R. J. J. Am. Chem. Soc. 1996, 118, 11181-11193. (d) Seth, J.; Palaniappan, V.; Wagner, R. W.; Johnson, T. E.; Lindsey, J. S.; Bocian, D. F. J. Am. Chem. Soc. 1996, 118, 11194-11207.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 9439-9452
    • Osuka, A.1    Yamada, H.2    Maruyama, K.3    Mataga, N.4    Asahi, T.5    Ohkouchi, M.6    Okada, T.7    Yamazaki, I.8    Nishimura, Y.9
  • 26
    • 0028549485 scopus 로고
    • Donor-acceptor systems linked with aromatic spacers have been reported. See, for example: (a) Osuka, A.; Yamada, H.; Maruyama, K.; Mataga, N.; Asahi, T.; Ohkouchi, M.; Okada, T.; Yamazaki, I.; Nishimura, Y. J. Am. Chem. Soc. 1993, 115, 9439-9452. (b) Seth, J.; Palaniappan, V.; Johnson, T. E.; Prathapan, S.; Lindsey, J. S.; Bocian, D. F. J. Am. Chem. Soc. 1994, 116, 10578-10592. (c) Hsiao, J.-S.; Krueger, B. P.; Wagner, R. W.; Johnson, T. E.; Delaney, J. K.; Mauzerall, D. C.; Fleming, G. R.; Lindsey, J. S.; Bochian, D. F.; Donohoe, R. J. J. Am. Chem. Soc. 1996, 118, 11181-11193. (d) Seth, J.; Palaniappan, V.; Wagner, R. W.; Johnson, T. E.; Lindsey, J. S.; Bocian, D. F. J. Am. Chem. Soc. 1996, 118, 11194-11207.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 10578-10592
    • Seth, J.1    Palaniappan, V.2    Johnson, T.E.3    Prathapan, S.4    Lindsey, J.S.5    Bocian, D.F.6
  • 27
    • 0029680988 scopus 로고    scopus 로고
    • Donor-acceptor systems linked with aromatic spacers have been reported. See, for example: (a) Osuka, A.; Yamada, H.; Maruyama, K.; Mataga, N.; Asahi, T.; Ohkouchi, M.; Okada, T.; Yamazaki, I.; Nishimura, Y. J. Am. Chem. Soc. 1993, 115, 9439-9452. (b) Seth, J.; Palaniappan, V.; Johnson, T. E.; Prathapan, S.; Lindsey, J. S.; Bocian, D. F. J. Am. Chem. Soc. 1994, 116, 10578-10592. (c) Hsiao, J.-S.; Krueger, B. P.; Wagner, R. W.; Johnson, T. E.; Delaney, J. K.; Mauzerall, D. C.; Fleming, G. R.; Lindsey, J. S.; Bochian, D. F.; Donohoe, R. J. J. Am. Chem. Soc. 1996, 118, 11181-11193. (d) Seth, J.; Palaniappan, V.; Wagner, R. W.; Johnson, T. E.; Lindsey, J. S.; Bocian, D. F. J. Am. Chem. Soc. 1996, 118, 11194-11207.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 11181-11193
    • Hsiao, J.-S.1    Krueger, B.P.2    Wagner, R.W.3    Johnson, T.E.4    Delaney, J.K.5    Mauzerall, D.C.6    Fleming, G.R.7    Lindsey, J.S.8    Bochian, D.F.9    Donohoe, R.J.10
  • 28
    • 0029982120 scopus 로고    scopus 로고
    • Donor-acceptor systems linked with aromatic spacers have been reported. See, for example: (a) Osuka, A.; Yamada, H.; Maruyama, K.; Mataga, N.; Asahi, T.; Ohkouchi, M.; Okada, T.; Yamazaki, I.; Nishimura, Y. J. Am. Chem. Soc. 1993, 115, 9439-9452. (b) Seth, J.; Palaniappan, V.; Johnson, T. E.; Prathapan, S.; Lindsey, J. S.; Bocian, D. F. J. Am. Chem. Soc. 1994, 116, 10578-10592. (c) Hsiao, J.-S.; Krueger, B. P.; Wagner, R. W.; Johnson, T. E.; Delaney, J. K.; Mauzerall, D. C.; Fleming, G. R.; Lindsey, J. S.; Bochian, D. F.; Donohoe, R. J. J. Am. Chem. Soc. 1996, 118, 11181-11193. (d) Seth, J.; Palaniappan, V.; Wagner, R. W.; Johnson, T. E.; Lindsey, J. S.; Bocian, D. F. J. Am. Chem. Soc. 1996, 118, 11194-11207.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 11194-11207
    • Seth, J.1    Palaniappan, V.2    Wagner, R.W.3    Johnson, T.E.4    Lindsey, J.S.5    Bocian, D.F.6
  • 36
    • 85033183369 scopus 로고    scopus 로고
    • note
    • The MM+ force field as implemented in the program package HyperChem, Hypercube Inc.
  • 37
    • 85033160231 scopus 로고    scopus 로고
    • note
    • AM1 model Hamiltonian as implemented in the program package MOPAC 6.0. The angular deviation at room temperature was estimated from the Boltzmann distribution by varying the dihedral angle between the porphyrin and phenyl planes, optimizing the structure, and calculating the potential energy at these fixed dihedral angles.
  • 38
    • 0000375824 scopus 로고
    • Wagner, R. W.; Johnson, T. E.; Li, F.; Lindsey, J. S. J. Org. Chem. 1995, 60, 5266-5273. All compounds exhibited satisfactory spectral (NMR, UV/vis, and mass spectroscopy) characteristics. Synthesis will be presented elsewhere.
    • (1995) J. Org. Chem. , vol.60 , pp. 5266-5273
    • Wagner, R.W.1    Johnson, T.E.2    Li, F.3    Lindsey, J.S.4
  • 39
    • 85033161474 scopus 로고    scopus 로고
    • note
    • The fluorescence lifetimes were measured with the phase and modulation technique using a SPEX Fluorolog τ2 spectrofluorimeter. Fifteen modulation frequencies were selected on a logarithmic scale in the range 10-300 MHz. The samples were excited at 530 nm, and the emission was collected through a 540 nm cutoff filter. A diluted silica sol scattering solution was used as reference.
  • 41
    • 85033165613 scopus 로고    scopus 로고
    • note
    • 2P to be polarized at 45° relative to the vector connecting the porphyrin centers.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.