Electronic spectra of mono- and dinuclear complexes of fully π-conjugated salphen ligands synthesized by using 2,6-dihydroxynaphthalene carbaldehydes

European Journal of Inorganic Chemistry

Volumn , Issue 4, 2009, Pages 533-538

  Houjou, Hirohiko ^a   Motoyama, Takatoshi ^a   Araki, Koji ^a  

^a INSTITUTE OF INDUSTRIAL SCIENCE   (Japan)

Author keywords

Conjugation; Molecular electronics; N,O ligands; Through bond interactions; Transition metals

Indexed keywords

ABSORPTION SPECTROSCOPY; CONDENSATION REACTIONS; COPPER COMPOUNDS; IRON COMPOUNDS; NICKEL COMPOUNDS; SYNTHESIS (CHEMICAL); TRANSITION METALS; ZINC COMPOUNDS;

CARBALDEHYDES; CONJUGATION; DIHYDROXYNAPHTHALENES; DINUCLEAR; DINUCLEAR COMPLEX; N,O LIGAND; O LIGANDS; SPECTRA'S; SYNTHESISED; THROUGH-BOND INTERACTIONS;

LIGANDS;

EID: 60149101541     PISSN: 14341948     EISSN: 10990682     Source Type: Journal    
DOI: 10.1002/ejic.200801030     Document Type: Article

References (45)

1. A. S. Abd-El-Aziz, C. E. Carraher Jr, C. U. Pittman Jr, M. Zeldin (Eds.), Macromolecules Containing Metal and Metal-Like Elements Vol. 5: Metal-Coordination Polymers, John Wiley & Sons, Hoboken, NJ, 2005.
2. G. R. Whittell, I. Manners, Adv. Mater. 2007, 19, 3439-3468.
3. A. C. W. Leung, M. J. Maclachlan, J. Inorg. Organomet. Polym. Mater. 2007, 17, 57-89.
4. H. Hofmeier, U. S. Schubert, Chem. Commun. 2005, 2423-2432.
5. T. Hirao, Coord. Chem. Rev. 2002, 226, 81-91.
6. B. J. Holiday, T. M. Swager, Chem. Commun. 2005, 23-36.
7. P. G. Pickup, J. Mater. Chem. 1999, 9, 1641-1653.
8. A. C. W. Leung, J. H. Chong, B. O. Patrick, M. J. MacLachlan, Macromolecules 2003, 36, 5051-5054.
9. H.-C. Zhang, W.-S. Huang, L. Pu, J. Org. Chem. 2001, 66, 481-487.
10. Y. Dai, T. J. Katz, D. A. Nichols, Angew. Chem. Int. Ed. Engl. 1996, 35, 2109-2111.
11. F. Galbrecht, X. H. Yang, B. S. Nehls, D. Neher, T. Farrell, U. Scherf, Chem. Commun. 2005, 2378-2380.
12. V. G. Manecke, W. E. Wille, Makromol. Chem. 1970, 133, 61-82;
13. G. Maneke, W. E. Wille, G. Kossmehl, Makromol. Chem. 1972, 160, 111-126.
14. S. J. Wezenberg, A. W. Kleij, Angew. Chem. Int. Ed. 2008, 47, 2354-2364.
15. P. Audebert, P. Capdevielle, M. Maumy, New J. Chem. 1991, 15, 235-237.
16. C. E. Dahm, D. G. Peters, Anal. Chem. 1994, 66, 3117-3123.
17. E. A. Dmitrieva, S. A. Logviv, V. V. Kurdakova, V. V. Kondrat'ev, V. V. Malev, A. M. Timonov, Russ. J. Electrochem. 2005, 41, 381-387.
18. For a recent example, see: S. J. Wezenberg, A. W. Kleij, Org. Lett. 2008, 10, 3311-3314.
19. H. Houjou, S.-K. Lee, Y. Hishikawa, Y. Nagawa, K. Hiratani, Chem. Commun. 2000, 2197-2198;
20. H. Houjou, S. Tsuzuki, Y. Nagawa, K. Hiratani, Bull. Chem. Soc. Jpn. 2002, 75, 831-839;
21. H. Houjou, T. Sasaki, Y. Shimizu, N. Koshizaki, M. Kanesato, Adv. Mater. 2005, 17, 606-610;
22. H. Houjou, Y. Shimizu, N. Koshizaki, M. Kanesato, Adv. Mater. 2003, 15, 1458-1461.
23. H. Masui, Coord. Chem. Rev. 2001, 219-221, 957-992.
24. E. Evangelio, D. Ruiz-Molina, Eur. J. Inorg. Chem. 2005, 2957-2971;
25. O. Sato, J. Tao, Y.-Z. Zhang, Angew. Chem. Int. Ed. 2007, 46, 2152-2187.
26. Y. Shimazaki, F. Tani, K. Fukui, Y. Naruta, O. Yamauchi, J. Am. Chem. Soc. 2003, 125, 10512-10513;
27. Y. Shimazaki, R. Kabe, S. Huth, F. Tani, Y. Naruta, O. Yamauchi, Inorg. Chem. 2007, 46, 6083-6090.
28. O. Rotthaus, F. Thomas, O. Jarjayes, C. Philouze, E. Saint-Aman, J.-L. Pierre, Chem. Eur. J. 2006, 12, 6953-6962.
29. M. J. S. Dewer, A. M. Talati, J. Am. Chem. Soc. 1963, 85, 1874;
30. M. J. S. Dewer, A. M. Talati, J. Am. Chem. Soc. 1964, 86, 1592-1595.
31. C. Schiele, G. Arnold, H. O. Kalinowski, D. Hendriks, Tetrahedron 1968, 24, 2293-2296;
32. C. Dax, F. Duffieux, N. Chabot, M. Coincon, J. Sygusch, P. A. M. Michels, C. Blonski, J. Med. Chem. 2006, 49, 1499-1502.
33. A. P. Kuriakose, S. Sethna, J. Ind. Chem. Soc. 1966, 43, 437-439;
34. A. P. Kuriakose, Ind. J. Chem. 1975, 13, 1149-1151.
35. D. T. Rosa, R. A. Reynolds III, S. M. Malinak, D. Coucouvanis, Inorg. Synth. 2002, 33, 112-119.
36. S. M. Crawford, Spectrochim. Acta 1963, 19, 255-270.
37. D. H. Brown, J. H. Morris, G. Oates, W. E. Smith, Spectrochim. Acta 1982, 38, 333-338.
38. M. S. El-Shahawi, Anal. Sci. 1991, 7, 443-446.
39. M. M. Abd-Elzaher, Synth. React. Inorg. Met.-Org. Chem. 2000, 30, 1805-1816.
40. D. Wohrle, H. Bohlen, Makromol. Chem. 1983, 184, 763-778.
41. A. W. Kleij, D. M. Tooke, A. L. Spek, J. N. H. Reek, Eur. J. Inorg. Chem. 2005, 4626-4634;
42. S. Crreli, E. C. Escudero-Adan, J. Benet-Buchholz, A. W. Kleij, Eur. J. Inorg. Chem. 2008, 2863-2873.
43. T. Glaser, M. Heidemeier, R. Fröhlich, P. Hildebrandt, E. Bothe, E. Bill, Inorg. Chem. 2005, 44, 5467-5482;
44. H. Theil, C.-G. F. von Richthofen, A. Stammler, H. Bögge, T. Glaser, Inorg. Chim. Acta 2008, 361, 916-924.
45. [25] To a solution of Mannich base 4 (6.60 g, 24 mmol) dissolved in aqueous acetic acid (81 vol.-%, 148 mL) was added hexamethylenetetramine (9.45 g, 67.5 mmol). The mixture was stirred at 130 °C for 4 h. After the mixture cooled to room temperature, the precipitate was collected by filtration and washed with methanol. For details, see: H. Houjou, T. Motoyama, S. Banno, I. Yoshikawa, K. Araki, J. Org. Chem., in press.