Photoinduced electron-transfer in porphyrin-quinone cyclophanes, 15. Distance dependence of photoinduced electron-transfer: Syntheses and structures of naphthalene-spacered porphyrin-quinone cyclophanes

Liebigs Annales

Volumn , Issue 11, 1997, Pages 2321-2336

  Staab, Heinz A ^a   Feurer, Achim ^a   Krieger, Claus ^a   Kumar, A Sampath ^a  

^a MAX PLANCK INSTITUTE FOR MEDICAL RESEARCH   (Germany)

Author keywords

Naphthalene spacered porphyrin quinone cyclophanes; Photoinduced electron transfer, distance dependence; Synthesis, conformations, structural analysis

Indexed keywords

EID: 33748730301     PISSN: 09473440     EISSN: None     Source Type: Journal    
DOI: 10.1002/jlac.199719971121     Document Type: Article

References (20)

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2. [2a] H. A. Staab, J. Weiser, E. Baumann, Chem.Ber. 1992, 125, 2275.
3. [2b] H. A. Staab, J. Weiser, M. Futscher, G. Voit, A. Rückemann, C. Anders, Chem.Ber. ibid. 1992, 125, 2285.
4. [2c] H. A. Staab, G. Voit, J. Weiser, M. Futscher, Chem.Ber. ibid. 1992, 125, 2303.
5. [2d] H. A. Staab, T. Carell, A. Döhling, Chem.Ber. ibid. 1994, 127, 223.
6. H. Heitele, F. Pöllinger, K. Kremer, M. E. Michel-Beyerle, M. Futscher, G. Voit, J. Weiser, H. A. Staab, Chew. Phys. Lett. 1992, 188, 270.
7. W. Frey, R. Klann, F. Laermer, T. Elsässer, E. Baumann, M. Futscher, H. A. Staab, Chew. Phys. Lett. ibid. 1992, 190, 567.
8. F. Pöllinger, H. Heitele, M. E. Michel-Beyerle, M. Tercel, H. A. Staab, Chew. Phys. Lett. ibid. 1993, 209, 251.
9. H. Heitele, F. Pöllinger, T. Häberle, M. E. Michel-Beyerle, H. A. Staab, J. Phys. Chem. (ACS) 1994, 98, 7402.
10. F. Pöllinger, C. Musewald, H. Heitele, M. E. Michel-Beyerle, C. Anders, M. Futscher, G. Voit, H. A. Staab, Ber.Bunsen-Ges. Phys.Chem. 1996, 100, 2076; further references therein.
11. Preliminary communication: H.A. Staab, A. Feurer, R. Hauck, Angew. Chem. 1994, 106, 2542;
12. Angew. Chem. Int. Ed. Engl. 1994, 33, 2428.
13. H.A. Staab, S. Quazzotti, B. Kratzer, to be published.
14. H. A. Staab, R. Hauck, B. Popp, to be published.
15. H. A. Staab, C. Krieser, C. Anders, A. Rückemann, Chem. Ber. 1994, 127, 231.
16. T. Häberle, J. Hirsch, F. Pöllinger, H. Heitele, M. E. Michel-Beyerle, C. Anders, A. Döhling, C. Krieger, A. Rückemann, H. A. Staab, J. Phys. Chem. (ACS) 1996, 100, 18269.
17. C. Krieger, M. Dernbach, G. Voit, T. Carell, H. A. Staab, Chem. Ber. 1993, 126, 811.
18. This dialdehyde was prepared from 1,4-bis(bromomethyl)-2,5-dimethoxy benzene via the corresponding 1,4-bis(cyanomethyl)-2,5-dimethoxybenzene, 1,4-bis(2-hydroxyethyl)-2,5-dimethoxybenzene and oxidation of the hydroxyethyl to formyl groups (R. E. Fischer, G. Scherr, A. Feurer, unpublished).
19. Crystallographic data (excluding structure factors) for the structures reported in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication no. CCDC-100495. Copies of the data can be obtained free of charge on application to The Director, CCDC, 12 Union Road, Cambridge CB2 1EZ, UK [fax: int. code +44(1223)336-033, e-mail: deposit@chemcrys.cam.ac.uk].
20. [2a].