1,3,2-diazaborolyl-functionalized thiophenes and dithiophenes: Synthesis, structure, electrochemistry and luminescence

Dalton Transactions

Volumn , Issue 31, 2006, Pages 3777-3784

  Weber, Lothar ^a   Werner, Vanessa ^b   Domke, Imme ^b   Stammler, Hans Georg ^b   Neumann, Beate ^b  

^a BIELEFELD UNIVERSITY   (Germany)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ELECTROCHEMISTRY; LUMINESCENCE; MOLECULAR STRUCTURE; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; SYNTHESIS (CHEMICAL); X RAY DIFFRACTION ANALYSIS;

1,3,2-DIAZABOROLYL-FUNCTIONALIZED THIOPHENES; 2-BROMO-L,3-DIETHYL-L,3,2-BENZODIAZABOROLE; SODIUM AMALGAM REDUCTION;

ORGANIC COMPOUNDS;

EID: 33746908222     PISSN: 14779226     EISSN: 14779234     Source Type: Journal    
DOI: 10.1039/b603365b     Document Type: Article

References (25)

1. (a) C. D. Entwistle and T. B. Marder, Angew. Chan., 2002, 114, 3051-3056,
2. (Angew. Chem. Int. Ed. Engl., 2002, 41, 2927-2931)
3. (b) C. D. Entwistle and T. B. Marder, Chem. Mater., 2004, 16, 4574-4585.
4. H. Doi, M. Kinoshita, K. Okumoto and Y Shirota, Chem. Mater., 2003, 15, 1080-1089.
5. M. Charlot, L. Porrès, C. D. Entwistle, A. Beeby, T. B. Marder and M. Blanchard-Desce, PhysChemPhys, 2005, 7, 600-606.
6. S. Maruyama and Y. Kawanishi, J. Mater. Chem., 2002, 12, 2245-2249.
7. L. Weber, Coord. Chem. Rev., 2001, 215, 39-77.
8. L. Weber, I. Domke, W. Greschner, K. Miqueu, A. Chrostowska and P. Baylére, Organometallies, 2005, 24, 5455-5463.
9. L. Weber, I. Domke, H.-G. Stammler and B. Neumann, Eur. J. Inorg. Chem., 2005, 4715-4722.
10. L. Weber, H. B. Wartig, H.-G. Stammler and B. Neumann, Z. Anorg. Allg. Chem., 2001, 627, 2663-2668.
11. E. N. Kuznetsova and G. V. Shishkin, Khim. Geterotsikl. Soedin., 1991, 97-100,
12. (Chem. Abslr., 1991, 115, 71537).
13. (a) K. Niedenzu and J. S. Merriam, Z. Anorg. Allg. Chem., 1976, 406, 251-259
14. (b) J. S. Merriam and K. Niedenzu, J. Organomet. Chem., 1973, 51, C1-C2.
15. L. Weber, I. Domke, A. Rausch, A. Chrostowska and A. Dargelos, Dalton Trans., 2004, 2188-2191.
16. L. Weber, I. Domke, C. Schmidt, T. Braun, H.-G. Stammler and B. Neumann, Dalton Trans., 2006, 2127.
17. M. C. Haberecht, J. B. Heilmann, A. Haghiri, M. Bolte, J. W. Bats, H. W. Leruer, M. C. Holthausen and M. Wagner, Z. Anorg. Allg. Chem., 2004, 630, 904.
18. L. Weber, E. Dobbert, R. Boese, M. T. Kirchner and D. Bläser, Eur. J. Inorg. Chem., 1998, 1145-1152.
19. L. Weber, E. Dobbert, H.-G. Stammler, B. Neumann, R. Boese and D. Bläser, Eur. J. Inorg. Chem., 1999, 491-495.
20. L. Weber, E. Dobbert, A. Rausch, H.-G. Stammler and B. Neumann, Z. Naturforsch.. B: Chem. Sci., 1999, 54, 363-371.
21. G. Schmid, M. Polk and R. Boese, Inorg. Chem., 1990, 29, 4421-4429.
22. L. Weber, E. Dobbert, H.-G. Stammler, B. Neumann, R. Boese and D. Bläser, Chem. Ber., 1997, 130, 705-710.
23. G. Schmid, J. Lehr, M. Polk and R. Boese, Angew. Chem., 1991, 103, 1029,
24. (Angew. Chem., Int. Ed. Eng!., 1991, 30, 1015-1031).
25. R. D. A. Hudson, I. Asselberghs, K. Clays, L. P. Cuffe, J. F. Gallagher, A. R. Manning, A. Persoons and K. Wostyn, J. Organomet. Chem., 2001, 637-639, 435-444.