Insights from theoretical calculations on structure, dynamics, phase behavior and hydrogen sorption in nanoporous metal organic frameworks

2012 ◽  
Vol 987 ◽  
pp. 42-56 ◽  
Author(s):  
Mousumi Mani-Biswas ◽  
Tahir Cagin
Author(s):  
Francisco Colmenero

Cobalt squarate hydroxide (Co3(C4O4)2(OH)2), zinc squarate tetrahydrate (ZnC4O4·4 H2O) and titanium oxalate trioxide dihydrate (Ti2(C2O4)O3·2 H2O) are nanoporous metal-organic frameworks possessing empty channels in their crystal structures. The crystal structures...


2014 ◽  
Vol 43 (16) ◽  
pp. 5994-6010 ◽  
Author(s):  
V. Stavila ◽  
A. A. Talin ◽  
M. D. Allendorf

Emergent properties resulting from the ordered structure and synthetic versatility of nanoporous metal–organic frameworks offer exciting possibilities for electronic devices.


ChemInform ◽  
2012 ◽  
Vol 43 (23) ◽  
pp. no-no
Author(s):  
Martin P. Attfield ◽  
Pablo Cubillas

2009 ◽  
Vol 21 (19) ◽  
pp. 1931-1935 ◽  
Author(s):  
Patricia Horcajada ◽  
Christian Serre ◽  
David Grosso ◽  
Cedric Boissière ◽  
Sandrine Perruchas ◽  
...  

ChemPhysChem ◽  
2017 ◽  
Vol 18 (24) ◽  
pp. 3504-3504
Author(s):  
Mahnaz Saghanejhadtehrani ◽  
Erik K. Schneider ◽  
Lars Heinke

2012 ◽  
Vol 427 ◽  
pp. 123-127
Author(s):  
Yuan Hui Ma ◽  
Lei Zhang ◽  
Cheng Chun Tang

The nanoporous metal-organic frameworks were synthesized under solvothermal conditions using organic solvent dimethylformamide. The samples were characterized by XRD, SEM, TGA, FT-IR and specific surface area for their properties difference. When the reaction temperature rises, the particle size becomes larger. All TGA curves are the basically same, the framework structure begins to be destroyed from 500°C up to around 600°C. The metal-organic frameworks accepted at reaction temperature 190°C have larger specific surface area and better structure stability.


2011 ◽  
Vol 23 (47) ◽  
pp. 5629-5632 ◽  
Author(s):  
Chun-Yi Sun ◽  
Chao Qin ◽  
Chun-Gang Wang ◽  
Zhong-Min Su ◽  
Shuang Wang ◽  
...  

ChemPhysChem ◽  
2017 ◽  
Vol 18 (24) ◽  
pp. 3548-3552 ◽  
Author(s):  
Mahnaz Saghanejhadtehrani ◽  
Erik K. Schneider ◽  
Lars Heinke

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