Preparation of dinuclear zirconium hydride complexes containing the fulvalene ligand and their reactions with carbon monoxide

1991 ◽  
Vol 10 (9) ◽  
pp. 3220-3226 ◽  
Author(s):  
Calvin J. Curtis ◽  
R. Curtis. Haltiwanger
2018 ◽  
Vol 54 (45) ◽  
pp. 5724-5727 ◽  
Author(s):  
Zhongbao Jian ◽  
Constantin G. Daniliuc ◽  
Gerald Kehr ◽  
Gerhard Erker

Carbon monoxide reacts with zirconium hydride and methyl–B(6F5)2 to give a Zr-bound acetyl(hydrido)borate as the major product. This reacts further with CO to form a Zr-coordinated borata-β-lactone.


1983 ◽  
Vol 105 (9) ◽  
pp. 2643-2650 ◽  
Author(s):  
Patricia A. Belmonte ◽  
F. Geoffrey N. Cloke ◽  
Richard R. Schrock

Author(s):  
A. P. Pivovarov ◽  
Yu. V. Gak ◽  
L. M. Ioffe ◽  
A. P. Borisov ◽  
V. D. Makhaev

1983 ◽  
Vol 14 (32) ◽  
Author(s):  
P. A. BELMONTE ◽  
F. G. N. CLOKE ◽  
R. R. SCHROCK

Author(s):  
G.J.C. Carpenter

In zirconium-hydrogen alloys, rapid cooling from an elevated temperature causes precipitation of the face-centred tetragonal (fct) phase, γZrH, in the form of needles, parallel to the close-packed <1120>zr directions (1). With low hydrogen concentrations, the hydride solvus is sufficiently low that zirconium atom diffusion cannot occur. For example, with 6 μg/g hydrogen, the solvus temperature is approximately 370 K (2), at which only the hydrogen diffuses readily. Shears are therefore necessary to produce the crystallographic transformation from hexagonal close-packed (hep) zirconium to fct hydride.The simplest mechanism for the transformation is the passage of Shockley partial dislocations having Burgers vectors (b) of the type 1/3<0110> on every second (0001)Zr plane. If the partial dislocations are in the form of loops with the same b, the crosssection of a hydride precipitate will be as shown in fig.1. A consequence of this type of transformation is that a cumulative shear, S, is produced that leads to a strain field in the surrounding zirconium matrix, as illustrated in fig.2a.


2000 ◽  
Vol 12 (4) ◽  
pp. 354-357
Author(s):  
David R Smart ◽  
Paul D Mark

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