Different reactivity patterns in the reactions of the homologous trimethylelement compounds EMe3 (E = Al, Ga, In) with methylhydrazine

European Journal of Inorganic Chemistry

Volumn , Issue 4, 2008, Pages 543-551

  Uhl, Werner ^a   Abel, Thomas ^a   Hepp, Alexander ^a   Grimme, Stefan ^a   Steinmetz, Marc ^a  

^a UNIVERSITY OF MÜNSTER   (Germany)

Author keywords

Aluminum; Gallium; Heterocycles; Hydrazides; Indium

Indexed keywords

ALUMINUM; ATOMS; GALLIUM; INDIUM COMPOUNDS; METHANE; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;

2-GROUP; ALUMINUM ATOMS; GALLIUM ATOMS; HETEROCYCLES; HYDRAZIDE; METHYLHYDRAZINE; NMR-SPECTROSCOPY; REACTION COURSE; REACTIVITY PATTERN; SIMPLE++;

INDIUM;

EID: 53249156292     PISSN: 14341948     EISSN: 10990682     Source Type: Journal    
DOI: 10.1002/ejic.200700954     Document Type: Article

References (50)

1. a) B. Luo, S. Y. Lee, J. M. White, Chem. Mater. 2004, 16, 629-638;
2. b) D. K. Gaskill, N. Bottka, M. C. Lin, J. Cryst. Growth 1986, 77, 418-423;
3. c) R. T. Lee, G. B. Stringfellow, J. Electron. Mater. 1999, 28, 963-969;
4. d) V. Lakhotia, D. A. Neumayer, A. H. Cowley, R. A. Jones, J. G. Ekerdt, Chem. Mater. 1995, 7, 546-552;
5. e) Y. J. Hsu, L. S. Hong, K. F. Huang, J. E. Tsay, Thin Solid Films 2002, 419, 33-39;
6. f) E. Bourret-Courchesne, Q. Ye, D. W. Peters, J. Arnold, M. Ahmed, S. J. C. Irvine, R. Kanjolia, L. M. Smith, S. A. Rushworth, J. Cryst. Growth 2000, 217, 47-54.
7. W. Uhl, Structure and Bonding, Group 13 Chemistry III - Industrial Applications (Eds.: H. W. Roesky, D. A. Atwood), Springer Verlag, Berlin-Heidelberg-New York, 2003, pp. 41-66.
8. D. W. Peters, E. D. Bourret, M. P. Power, J. Arnold, J. Organomet. Chem. 1999, 582, 108-115.
9. W. Uhl, J. Molter, W. Saak, Z. Anorg. Allg. Chem. 1999, 625, 321-328.
10. W. Uhl, J. Molter, B. Neumüller, W. Saak, Z. Anorg. Allg. Chem. 2000, 626, 2284-2292.
11. W. Uhl, J. Molter, R. Koch, Eur. J. Inorg. Chem. 1999, 2021-2027.
12. W. Uhl, C. H. Emden, J. Organomet. Chem. 2005, 690, 1529-1539.
13. W. Uhl, C. H. Emden, G. Geiseler, K. Harms, Z. Anorg. Allg. Chem. 2003, 629, 2157-2167.
14. W. Uhl, A. Vogelpohl, J. Kösters, Z. Naturforsch. 2006, 61b, 854-861.
15. B. Luo, C. J. Cramer, W. L. Gladfelter, Inorg. Chem. 2003, 42, 3431-3437.
16. W. Uhl, J. Molter, B. Neumüller, Organometallics 2000, 19, 4422-4424.
17. H. Nöth, T. Seifert, Eur. J. Inorg. Chem. 1998, 1931-1938.
18. W. Uhl, J. Molter, B. Neumüller, Inorg. Chem. 2001, 40, 2011-2014.
19. Y. Kim, J. H. Kim, J. E. Park, H. Song, J. T. Park, J. Organomet. Chem. 1997, 545-546, 99-103.
20. D. Cho, J. E. Park, B. J. Bae, K. Lee, B. Kim, J. T. Park, J. Organomet. Chem. 1999, 592, 162-167.
21. D. W. Peters, M. P. Power, E. D. Bourret, J. Arnold, Chem. Commun. 1998, 753-756.
22. a) B. Luo, W. L. Gladfelter, Chem. Commun. 2000, 825-826;
23. b) B. Luo, W. L. Gladfelter, J. Organomet. Chem. 2004, 689, 666-671.
24. D. A. Neumayer, A. H. Cowley, A. Decken, R. A. Jones, V. Lakhotia, J. G. Ekerdt, Inorg. Chem. 1995, 34, 4698-4700.
25. R. J. Wehmschulte, P. P. Power, Inorg. Chem. 1996, 35, 2717-2718.
26. W. Uhl, J. Molter, R. Koch, Eur. J. Inorg. Chem. 2000, 2255-2262.
27. W. Uhl, C. H. Emden, W. Massa, J. Organomet. Chem. 2006, 691, 1382-1388.
28. H. Nöth, T. Seifert, Eur. J. Inorg. Chem. 2002, 602-612.
29. S. S. Kumar, S. Singh, F. Hongjun, H. W. Roesky, D. Vidovic, J. Magull, Organometallics 2004, 23, 6327-6329.
30. V. C. Gibson, C. Redshaw, A. J. P. White, D. J. Williams, Angew. Chem. 1999, 111, 1014-1016;
31. Angew. Chem. Int. Ed. 1999, 38, 961-964.
32. J. S. Silverman, C. D. Abernethy, R. A. Jones, A. H. Cowley, Chem. Commun. 1999, 1645-1646.
33. W. Uhl, J. Molter, B. Neumüller, Chemistry Eur. J. 2001, 7, 1510-1515.
34. a) W. Uhl, J. Molter, B. Neumüller, F. Schmock, Z. Anorg. Allg. Chem. 2001, 627, 909-917;
35. b) W. Uhl, J. Molter, B. Neumüller, J. Organomet. Chem. 2001, 634, 193-197.
36. B. Neumüller, Chem. Soc. Rev. 2003, 32, 50-55.
37. J. March, Advanced Organic Chemistry, 3rd ed., Wiley, New York, 1985.
38. H. C. Clark, A. L. Pickard, J. Organomet. Chem. 1967, 8, 427-434.
39. T. Hahn (Ed.), International Tables for Crystallography, Space-Group Symmetry, Vol. A, Kluwer Academic Publishers, Dordrecht-Boston-London, 1989.
40. SHELXTL-Plus, REL. 4.1, Siemens Analytical X-RAY Instruments Inc., Madison, WI, 1990;
41. G. M. Sheldrick, SHELXL-97, Program for the Refinement of Structures, University of Göttingen, 1997.
42. CCDC-648118 (for 1), -648119 (for 3), -648120 (for 4), and -648121 (for 5) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.
43. S. Grimme, J. Chem. Phys. 2003, 118, 9095-9102.
44. R. Ahlrichs et al., TURBOMOLE, version 5.7, University of Karlsruhe, 2003; see http://www.turbomole.com.
45. a) F. Weigend, M. Häser, Theor. Chem. Acc. 1997, 97, 331-340;
46. b) F. Weigend, M. Häser, Theor. Chem. Acc. 1997, 97, 331-340.
47. J. P. Perdew, K. Burke, M. Ernzerhof, Phys. Rev. Lett. 1996, 77, 3865-3868.
48. a) S. Grimme, J. Comput. Chem. 2004, 25, 1463-1476;
49. b) S. Grimme, J. Comput. Chem. 2006, 27, 1787-1799.
50. A. Schäfer, C. Huber, R. Ahlrichs, J. Chem. Phys. 1994, 100, 5829-5835.