Rare-earth metal hydrides supported by silicon-bridged boratabenzene fluorenyl ligands: synthesis, structure and reactivity

2017 ◽  
Vol 46 (4) ◽  
pp. 1218-1227 ◽  
Author(s):  
Chunhong Wang ◽  
Li Xiang ◽  
Xuebing Leng ◽  
Yaofeng Chen

The first boratabenzene derivatives of rare-earth metal hydrides were synthesized, and their reactivity was studied.

2015 ◽  
Vol 11 ◽  
pp. 1-8 ◽  
Author(s):  
Gert Kollenz ◽  
Ralf Smounig ◽  
Ferdinand Belaj ◽  
David Kvaskoff ◽  
Curt Wentrup

The structures of two derivatives of the bisdioxine diisocyanate 1, the bisurea 4 and the biscarbamate 5, are established by X-ray crystallography and DFT calculations. These compounds possess endo,endo structures, in the case of the bisurea 4 with two nearly parallel pendant chains. The X-ray structures are reproduced very well by DFT calculations. Similar endo,endo conformations are calculated for the bisamide crown ether derivatives 7, where two proximate and nearly parallel crown ether units endow the molecules with a claw-like molecular cleft or tweezer structure as evidenced by an enhanced ability to extract some alkali, alkaline earth and rare earth metal ions.


1995 ◽  
Vol 11 (6) ◽  
pp. 893-902 ◽  
Author(s):  
Keisuke OHTO ◽  
Masayuki YANO ◽  
Katsutoshi INOUE ◽  
Takehisa YAMAMOTO ◽  
Masahiro GOTO ◽  
...  

Author(s):  
Thomas Schleid ◽  
Ingo Hartenbach

AbstractHalide derivatives of rare-earth metal(III) oxidomolybdates(VI) have been investigated comprehensively over the last decade comprising the halogens fluorine, chlorine, and bromine. Iodide-containing compounds are so far unknown. The simple composition


2021 ◽  
Vol 129 (15) ◽  
pp. 153101
Author(s):  
Dmitrii Moldarev ◽  
Levin Stolz ◽  
Marcos V. Moro ◽  
Sigurbjörn M. Aðalsteinsson ◽  
Ioan-Augustin Chioar ◽  
...  

2008 ◽  
Vol 64 (a1) ◽  
pp. C610-C610
Author(s):  
A. Machida ◽  
T. Watanuki ◽  
A. Ohmura ◽  
K. Aoki ◽  
K. Takemura

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Hyunsoo Jeon ◽  
Chongze Wang ◽  
Seho Yi ◽  
Jun-Hyung Cho

Abstract The rare-earth metal hydrides with clathrate structures have been highly attractive because of their promising high-$$T_{\rm{c}}$$ T c superconductivity at high pressure. Recently, cerium hydride $$\hbox {CeH}_9$$ CeH 9 composed of Ce-encapsulated clathrate H cages was synthesized at much lower pressures of 80–100 GPa, compared to other experimentally synthesized rare-earth hydrides such as $$\hbox {LaH}_{{10}}$$ LaH 10 and $$\hbox {YH}_6$$ YH 6 . Based on density-functional theory calculations, we find that the Ce 5p semicore and 4f/5d valence states strongly hybridize with the H 1s state, while a transfer of electrons occurs from Ce to H atoms. Further, we reveal that the delocalized nature of Ce 4f electrons plays an important role in the chemical precompression of clathrate H cages. Our findings not only suggest that the bonding nature between the Ce atoms and H cages is characterized as a mixture of ionic and covalent, but also have important implications for understanding the origin of enhanced chemical precompression that results in the lower pressures required for the synthesis of $$\hbox {CeH}_9$$ CeH 9 .


2014 ◽  
Vol 54 (6) ◽  
pp. 1724-1736 ◽  
Author(s):  
Waldemar Fegler ◽  
Ajay Venugopal ◽  
Mathias Kramer ◽  
Jun Okuda

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