A critical evaluation of the location and refinement of a bridging hydrogen atom in a transition-metal hydride, .mu.-hydrido-.mu.-dimethylphosphido-bis(.eta.5-cyclopentadienyldicarbonylmolybdenum), by x-ray diffraction

1978 ◽  
Vol 17 (5) ◽  
pp. 1308-1312 ◽  
Author(s):  
Jeffrey L. Petersen ◽  
Jack M. Williams
1984 ◽  
Vol 23 (18) ◽  
pp. 2823-2829 ◽  
Author(s):  
Robert Bau ◽  
Michael Y. Chiang ◽  
Douglas M. Ho ◽  
Sidney G. Gibbins ◽  
Thomas J. Emge ◽  
...  

2021 ◽  
Author(s):  
Magdalena Woińska ◽  
Michał L. Chodkiewicz ◽  
Krzysztof Woźniak

Positions and anisotropic thermal motion of H-Atoms bound to heavy atoms in transition-metal hydride complexes were successfully refined using Hirshfeld Atom Refinement (HAR) against low resolution X-ray diffraction data.


1981 ◽  
Vol 46 (10) ◽  
pp. 2345-2353 ◽  
Author(s):  
Karel Baše ◽  
Bohumil Štíbr ◽  
Jiří Dolanský ◽  
Josef Duben

The 6-N(CH3)3-6-CB9H11 carbaborane reacts with sodium in liquid ammonia with the formation of 6-CB9H12- which was used as a starting compound for preparing the 4-CB8H14, 9-L-6-CB9H13 (L = (CH3)2S, CH3CN and P(C6H5)3), 1-(η5-C5H5)-1,2-FeCB9H10-, and 2,3-(η5-C5H5)2-2,31-Co2CB9H10- carboranes. The 4-CB8H14 compound was dehydrogenated at 623 K to give 4-(7)-CB8H12 carborane. Base degradation of 6-N(CH3)3-6-CB9H11 in methanol resulted in the formation of 3,4-μ-N(CH3)3CH-B5H10. The structure of all compounds was proposed on the basis of their 11B and 1H NMR spectra and X-ray diffraction was used in the case of the transition metal complexes.


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