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On the Structures of Mo2O5(OCH3)2 and Mo2O5(OCH3)2 ·2CH3OH

Published online by Cambridge University Press:  15 February 2011

E. M. McCarron III
Affiliation:
Central Research and Development, The DuPont Company, Experimental Station, 356/341, Wilmington, DE 19880–0356, USA
R. L. Harlow I
Affiliation:
Central Research and Development, The DuPont Company, Experimental Station, 356/341, Wilmington, DE 19880–0356, USA
Z. G. Li
Affiliation:
Central Research and Development, The DuPont Company, Experimental Station, 356/341, Wilmington, DE 19880–0356, USA
C. Suto
Affiliation:
Central Research and Development, The DuPont Company, Experimental Station, 356/341, Wilmington, DE 19880–0356, USA
Y. Yuen
Affiliation:
Central Research and Development, The DuPont Company, Experimental Station, 356/341, Wilmington, DE 19880–0356, USA
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Abstract

The reaction of molybdenum trioxide dihydrate, MoO3·2H2O, with methanol produces the title compounds. That these molybdenum oxy-methoxides decompose with liberation of CH2O suggests that they represent exquisite models for selective oxidation of methanol to formaldehyde over molybdate catalysts. While a number of physical techniques have been employed to elucidate certain of their structural aspects, unfortunately, the detailed structures of these materials remain unknown. Problems, both physical and crystallographic, encountered in attempts to determine these structures are discussed. Also discussed is the recent progress made by employing the complimentary nature of electron and powder diffraction techniques.

Type
Research Article
Copyright
Copyright © Materials Research Society 1997

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References

REFERENCES

1. Cheng, W.-H., Chowdhry, U., Ferretti, A., Firment, L. E., Groff, R. P., Machiels, C. J., McCarron, E. M. III, Ohuchi, F., Staley, R. H., and Sleight, A. W., Proceedings of the 2nd Symposium of IUCCP of Dept. Chemistry, Texas A&M, 165 (1984); “Heterogeneous Catalysis”, Sharpiro, B. L., Ed., Texas A&M University Press, College Station, Texas. Google Scholar
2. McCarron, E. M. III and Sleight, A. W., Polyhedron 5, 129 (1986).Google Scholar
3. McCarron, E. M. III, Staley, R. H. and Sleight, A. W., Inorganic Chemistry 23, 1043 (1984).Google Scholar
4. McCarron, E. M. III, J. Chem. Soc, Chem. Commun., 336 (1986).Google Scholar
5. Krebs, B., Acta Cryst. B 28, 2222 (1972);Google Scholar
Günter, J. R., J.Solid State Chemistry 5, 354 (1972); and references therein.Google Scholar
6. Johnson, J. W., Jacobson, A. J., Rich, S. M., and Brody, J. F., J. Amer. Chem. Soc. 103, 5246 (1981).Google Scholar
7. Kihlborg, L., Arkiv Kemi 21, 357 (1963); and references therein.Google Scholar
8. Böschen, I. and Krebs, B., Acta Cryst. B 30, 1795 (1975).Google Scholar
9. Oswald, H. R., Günter, J. R., and Dubler, E., J.Solid State Chemistry 13, 330 (1975).Google Scholar
10. Bénard, P., Seguin, L., Louёr, D., & Figlarz, M., J.Solid State Chemistry 108, 170 (1994).Google Scholar
11. Betz, T. and Hoppe, R., J.Less-Common Metals 105, 87 (1985).Google Scholar
12. JCPDS-ICDD, card # 12–874;Google Scholar
Krishna Murti, G. R. S., Indian J.Physics 33, 458 (1959).Google Scholar