Thermal decomposition of hydrotalcites. An infrared and nuclear magnetic resonance spectroscopic study

1992 ◽  
Vol 88 (15) ◽  
pp. 2233-2238 ◽  
Author(s):  
Fernando Rey ◽  
Vicente Fornés ◽  
José M. Rojo
1988 ◽  
Vol 6 (2) ◽  
pp. 183-191 ◽  
Author(s):  
Stephen F. Lincoln ◽  
Andrea M. Hounslow ◽  
John H. Coates ◽  
Rosa P. Villani ◽  
Robert L. Schiller

1984 ◽  
Vol 62 (3) ◽  
pp. 621-627 ◽  
Author(s):  
Tim Allman ◽  
Ram G. Goel

Cationic complexes of the type [Hg(phosphine)n](ClO4)2 (n = 2, 3, 4) (phosphine = P(t-Bu)3, PCy3, P(4-Me2NC6H4)3, P(4-MeOC6H4)3, P(4-MeC6H4)3, P(3-MeC6H4)3, P(2-MeC6H4)3, P(4-FC6H4)3, P(4-ClC6H4)3) have been prepared and studied by vibrational spectroscopy in the perchlorate and low frequency regions, as well as by 31P and 199Hg nmr. The skeletal Hg—P frequencies have been assigned in both solution and the solid state. It was found that 1J(Hg—P) decreases with increasing phosphine basicity and that it is also dependent upon sample concentration and temperature.


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