Hybrid organic-inorganic, hexa-arm dendrimers based on an Mo6Cl8 core

Chemical Communications

Volumn , Issue 10, 1999, Pages 877-878

  Gorman, Christopher B ^a   Wendy, Y Su ^a   Jiang, Hongwei ^a   Watson, Christopher M ^a   Boyle, Paul ^a  

^a NORTH CAROLINA STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHLORIDE; DENDRIMER; INORGANIC COMPOUND; MOLYBDENUM; ORGANIC COMPOUND;

ARTICLE; CHEMICAL STRUCTURE; MOLECULAR WEIGHT; PROTON NUCLEAR MAGNETIC RESONANCE;

EID: 0344299138     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/a901590f     Document Type: Article

References (25)

1. C. B. Gorman, Adv. Mater., 1998, 10, 295.
2. C. B. Gorman, B. L. Parkhurst, K.-Y. Chen and W. Y. Su, J. Am. Chem. Soc., 1997, 119, 1141.
3. C. B. Gorman, Adv. Mater., 1997, 9, 1117.
4. P. Bhyrappa, J. K. Young, J. S. Moore and K. S. Suslick, J. Am. Chem. Soc., 1996, 118, 5708.
5. J. P. Collman, L. Fu, A. Zingg and F. Diederich, Chem. Commun., 1997, 193.
6. P. J. Dandliker, F. Diederich, M. Gross, C. B. Knobler, A. Louati and E. M. Sanford, Angew. Chem., Int. Ed. Engl., 1994, 33, 1739.
7. P. J. Dandliker, F. Diederich, J.-P. Gisselbrecht, A. Louati and M. Gross, Angew. Chem. Int., Ed. Engl., 1995, 34, 2725.
8. D.-L. Jiang and T. Aida, Chem. Commun., 1996, 1523..
9. J. Issberner, F. Vögtle, L. De Cola and V. Balzani, Chem. Eur. J., 1997, 3, 706.
10. B. Hong, T. P. S. Thoms, H. J. Murfee and M. J. Lebrun, Inorg. Chem., 1997, 36, 6146.
11. F. J. Feher and K. D. Wyndham, Chem. Commun., 1998, 323.
12. 8 core has also recently been reported: Z. Zheng and R. Wang, 217th American Chemical Society Meeting, Anaheim, CA, March 1999, Paper INOR563.
13. N. Prokopuk and D. F. Shriver, Inorg. Chem., 1997, 36, 5609.
14. P. Nannelli and B. P. Block, Inorg. Chem., 1969, 8, 1767.
15. P. Nannelli and B. P. Block, Inorg. Chem., 1968, 7, 2423-2426
16. N. Perchenek and A. Simon, Z. Anorg. Allg. Chem., 1993, 619, 103.
17. D. H. Johnston, D. C. Gaswick, M. C. Lonergan, C. L. Stern and D. F. Shriver, Inorg. Chem., 1992, 31, 1869.
18. J. H. Golden, H. Deng, F. J. DiSalvo, J. M. J. Fréchet and P. M. Thompson, Science, 1995, 268, 1463.
19. K.-Y. Chen and C. B. Gorman, J. Org. Chem., 1996, 61, 9229.
20. P. Nannelli and B. P. Block, Inorg. Synth., 1971, 13, 99.
21. For experimental details see http://www.rsc.org/suppdata/cc/1999/877/
22. 2O several times (yield: 92% for G1). Molecule GO was prepared similarly except that DMF was substituted for 1.2-dichlorobenzene.
23. w were 0.036 and 0.041 respectively. CCDC 182/1218. See: http: //www.rsc.org/suppdata/cc/1999/877/ for crystallographic files in .cif format.
24. M. H. Chisholm, J. A. Heppert and J. C. Huffman, Polyhedron, 1984, 3, 475.
25. C. G. Enke, Anal. Chem., 1997, 69, 4885.