The AlAl triple bond in Al2X5+ and Al2X62+ (X = Li, Na) clusters with multiple alkali metal coordination

2020 ◽  
Vol 44 (48) ◽  
pp. 21119-21124
Author(s):  
Yingying Liu ◽  
Changyan Zhu ◽  
Chaoxia Wen ◽  
Min Zhang ◽  
Yun Geng ◽  
...  

The AlAl triple bond does not change obviously with the increase in the number of Li+ or Na+ and [AlAl]4− is the core to stabilize these clusters and its stability is hard to be affected by the numbers and positions of the Li+ or Na+.

1997 ◽  
Vol 36 (16) ◽  
pp. 3398-3401 ◽  
Author(s):  
R. E. Dinnebier ◽  
Maren Pink ◽  
J. Sieler ◽  
P. W. Stephens

CrystEngComm ◽  
2010 ◽  
Vol 12 (4) ◽  
pp. 1311-1315 ◽  
Author(s):  
Manabu Yamada ◽  
Yoshifumi Shimakawa ◽  
Yoshihiko Kondo ◽  
Fumio Hamada

2018 ◽  
Vol 265 ◽  
pp. 92-99 ◽  
Author(s):  
Renata Łyszczek ◽  
Halina Głuchowska ◽  
Liliana Mazur ◽  
Bogdan Tarasiuk ◽  
Vasyl Kinzhybalo ◽  
...  

2013 ◽  
Vol 13 (11) ◽  
pp. 5076-5084 ◽  
Author(s):  
Kamran T. Mahmudov ◽  
M. Fátima C. Guedes da Silva ◽  
Alexander M. Kirillov ◽  
Maximilian N. Kopylovich ◽  
Archana Mizar ◽  
...  

2006 ◽  
Vol 12 (10) ◽  
pp. 2787-2797 ◽  
Author(s):  
Federico Pepi ◽  
Andreina Ricci ◽  
Marzio Rosi ◽  
Marco Di Stefano

2006 ◽  
Vol 45 (8) ◽  
pp. 3437-3443 ◽  
Author(s):  
William J. Evans ◽  
Daniel B. Rego ◽  
Joseph W. Ziller

1983 ◽  
Vol 61 (6) ◽  
pp. 1073-1076 ◽  
Author(s):  
Suzanne R. Abrams ◽  
Donato D. Nucciarone ◽  
Warren F. Steck

The lithium and sodium salts of 1,2-diaminoethane, 1,3-diaminopropane, n-butylamine, and the lithium salt of isobutylamine were studied as potential reagents for isomerization of triple bonds in alkyn-1-ols. The sodium salts of the diamines afforded high yields of the ω-alkyn-1-ol. Somewhat surprisingly, the sodium salt of n-butylamine also effects isomerization to the terminal position. The lithium salt of 1,3-diaminopropane gave the highest conversion of 2- to 3-alkyn-1-ol. A novel, selective rearrangement of one triple bond of a diynol, a 2, ω- to 3, ω-diyn-1-ol isomerization, was incorporated into a synthesis of the insect sex pheromone 3,13-octadecadienol acetate.


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