메뉴 건너뛰기




Volumn 44, Issue 1, 2003, Pages 161-165

TTF-porphyrin dyads as novel photoinduced electron transfer systems

Author keywords

Electron transfer; Photophysics; Porphyrin; Tetrathiafulvalene

Indexed keywords

PORPHYRIN DERIVATIVE; TETRATHIAFULVALENE DERIVATIVE; ZINC COMPLEX;

EID: 0037213693     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(02)02474-7     Document Type: Article
Times cited : (43)

References (32)
  • 1
    • 0343148642 scopus 로고
    • For excellent reviews on synthetic porphyrins with a redox-active pendant, see: (a) Meyer, T. J. Acc. Chem. Res. 1989, 22, 163-170; (b) Wasielewski, M. R. Chem. Rev. 1992, 92, 435-461; (c) Gust, D.; Moore, T. A.; Moore, A. L. Acc. Chem. Res. 1993, 26, 198-205; (d) Kurreck, H.; Huber, M. Angew. Chem., Int. Ed. Engl. 1995, 34, 849-866; (e) Imahori, H.; Sakata, Y. Eur. J. Org. Chem. 1995, 2445-2457; (f) Imahori, H.; Sakata, Y. Adv. Mater. 1997, 9, 537-546; (g) Gust, D.; Moore, T. A.; Moore, A. L. Acc. Chem. Res. 2001, 34, 40-48.
    • (1989) Acc. Chem. Res. , vol.22 , pp. 163-170
    • Meyer, T.J.1
  • 2
    • 0040891425 scopus 로고
    • For excellent reviews on synthetic porphyrins with a redox-active pendant, see: (a) Meyer, T. J. Acc. Chem. Res. 1989, 22, 163-170; (b) Wasielewski, M. R. Chem. Rev. 1992, 92, 435-461; (c) Gust, D.; Moore, T. A.; Moore, A. L. Acc. Chem. Res. 1993, 26, 198-205; (d) Kurreck, H.; Huber, M. Angew. Chem., Int. Ed. Engl. 1995, 34, 849-866; (e) Imahori, H.; Sakata, Y. Eur. J. Org. Chem. 1995, 2445-2457; (f) Imahori, H.; Sakata, Y. Adv. Mater. 1997, 9, 537-546; (g) Gust, D.; Moore, T. A.; Moore, A. L. Acc. Chem. Res. 2001, 34, 40-48.
    • (1992) Chem. Rev. , vol.92 , pp. 435-461
    • Wasielewski, M.R.1
  • 3
    • 11744372773 scopus 로고
    • For excellent reviews on synthetic porphyrins with a redox-active pendant, see: (a) Meyer, T. J. Acc. Chem. Res. 1989, 22, 163-170; (b) Wasielewski, M. R. Chem. Rev. 1992, 92, 435-461; (c) Gust, D.; Moore, T. A.; Moore, A. L. Acc. Chem. Res. 1993, 26, 198-205; (d) Kurreck, H.; Huber, M. Angew. Chem., Int. Ed. Engl. 1995, 34, 849-866; (e) Imahori, H.; Sakata, Y. Eur. J. Org. Chem. 1995, 2445-2457; (f) Imahori, H.; Sakata, Y. Adv. Mater. 1997, 9, 537-546; (g) Gust, D.; Moore, T. A.; Moore, A. L. Acc. Chem. Res. 2001, 34, 40-48.
    • (1993) Acc. Chem. Res. , vol.26 , pp. 198-205
    • Gust, D.1    Moore, T.A.2    Moore, A.L.3
  • 4
    • 0029124427 scopus 로고
    • For excellent reviews on synthetic porphyrins with a redox-active pendant, see: (a) Meyer, T. J. Acc. Chem. Res. 1989, 22, 163-170; (b) Wasielewski, M. R. Chem. Rev. 1992, 92, 435-461; (c) Gust, D.; Moore, T. A.; Moore, A. L. Acc. Chem. Res. 1993, 26, 198-205; (d) Kurreck, H.; Huber, M. Angew. Chem., Int. Ed. Engl. 1995, 34, 849-866; (e) Imahori, H.; Sakata, Y. Eur. J. Org. Chem. 1995, 2445-2457; (f) Imahori, H.; Sakata, Y. Adv. Mater. 1997, 9, 537-546; (g) Gust, D.; Moore, T. A.; Moore, A. L. Acc. Chem. Res. 2001, 34, 40-48.
    • (1995) Angew. Chem., Int. Ed. Engl. , vol.34 , pp. 849-866
    • Kurreck, H.1    Huber, M.2
  • 5
    • 0012084141 scopus 로고
    • For excellent reviews on synthetic porphyrins with a redox-active pendant, see: (a) Meyer, T. J. Acc. Chem. Res. 1989, 22, 163-170; (b) Wasielewski, M. R. Chem. Rev. 1992, 92, 435-461; (c) Gust, D.; Moore, T. A.; Moore, A. L. Acc. Chem. Res. 1993, 26, 198-205; (d) Kurreck, H.; Huber, M. Angew. Chem., Int. Ed. Engl. 1995, 34, 849-866; (e) Imahori, H.; Sakata, Y. Eur. J. Org. Chem. 1995, 2445-2457; (f) Imahori, H.; Sakata, Y. Adv. Mater. 1997, 9, 537-546; (g) Gust, D.; Moore, T. A.; Moore, A. L. Acc. Chem. Res. 2001, 34, 40-48.
    • (1995) Eur. J. Org. Chem. , pp. 2445-2457
    • Imahori, H.1    Sakata, Y.2
  • 6
    • 0031161872 scopus 로고    scopus 로고
    • For excellent reviews on synthetic porphyrins with a redox-active pendant, see: (a) Meyer, T. J. Acc. Chem. Res. 1989, 22, 163-170; (b) Wasielewski, M. R. Chem. Rev. 1992, 92, 435-461; (c) Gust, D.; Moore, T. A.; Moore, A. L. Acc. Chem. Res. 1993, 26, 198-205; (d) Kurreck, H.; Huber, M. Angew. Chem., Int. Ed. Engl. 1995, 34, 849-866; (e) Imahori, H.; Sakata, Y. Eur. J. Org. Chem. 1995, 2445-2457; (f) Imahori, H.; Sakata, Y. Adv. Mater. 1997, 9, 537-546; (g) Gust, D.; Moore, T. A.; Moore, A. L. Acc. Chem. Res. 2001, 34, 40-48.
    • (1997) Adv. Mater. , vol.9 , pp. 537-546
    • Imahori, H.1    Sakata, Y.2
  • 7
    • 0035148647 scopus 로고    scopus 로고
    • For excellent reviews on synthetic porphyrins with a redox-active pendant, see: (a) Meyer, T. J. Acc. Chem. Res. 1989, 22, 163-170; (b) Wasielewski, M. R. Chem. Rev. 1992, 92, 435-461; (c) Gust, D.; Moore, T. A.; Moore, A. L. Acc. Chem. Res. 1993, 26, 198-205; (d) Kurreck, H.; Huber, M. Angew. Chem., Int. Ed. Engl. 1995, 34, 849-866; (e) Imahori, H.; Sakata, Y. Eur. J. Org. Chem. 1995, 2445-2457; (f) Imahori, H.; Sakata, Y. Adv. Mater. 1997, 9, 537-546; (g) Gust, D.; Moore, T. A.; Moore, A. L. Acc. Chem. Res. 2001, 34, 40-48.
    • (2001) Acc. Chem. Res. , vol.34 , pp. 40-48
    • Gust, D.1    Moore, T.A.2    Moore, A.L.3
  • 20
    • 0012049467 scopus 로고    scopus 로고
    • In a preliminary experiment, the direct synthesis of the TTF-porphyrin dyad by the Lindsey-type hybrid condensation of 1 equiv. of 3-formyltetrathiafulvalene, 3 equiv. of benzaldehyde, and 4 equiv. of pyrrole was unsuccessful
    • In a preliminary experiment, the direct synthesis of the TTF-porphyrin dyad by the Lindsey-type hybrid condensation of 1 equiv. of 3-formyltetrathiafulvalene, 3 equiv. of benzaldehyde, and 4 equiv. of pyrrole was unsuccessful.
  • 23
    • 0012054026 scopus 로고    scopus 로고
    • note
    • 6S: C, 77.15; H, 4.21; N, 13.50%. Found: C, 77.22; H, 4.16; N, 13.54%.
  • 31
    • 0012049813 scopus 로고    scopus 로고
    • -=5.0 Å
    • -=5.0 Å.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.