scholarly journals Tuning the Gate‐Opening Pressure in a Switching pcu Coordination Network, X‐pcu‐5‐Zn, by Pillar‐Ligand Substitution

2019 ◽  
Vol 131 (50) ◽  
pp. 18380-18385 ◽  
Author(s):  
Ai‐Xin Zhu ◽  
Qing‐Yuan Yang ◽  
Soumya Mukherjee ◽  
Amrit Kumar ◽  
Cheng‐Hua Deng ◽  
...  
2019 ◽  
Vol 58 (50) ◽  
pp. 18212-18217 ◽  
Author(s):  
Ai‐Xin Zhu ◽  
Qing‐Yuan Yang ◽  
Soumya Mukherjee ◽  
Amrit Kumar ◽  
Cheng‐Hua Deng ◽  
...  

2018 ◽  
Vol 130 (20) ◽  
pp. 5786-5791 ◽  
Author(s):  
Qing-Yuan Yang ◽  
Prem Lama ◽  
Susan Sen ◽  
Matteo Lusi ◽  
Kai-Jie Chen ◽  
...  

2019 ◽  
Vol 48 (14) ◽  
pp. 4685-4695 ◽  
Author(s):  
Ahmed Awadallah-F ◽  
Febrian Hillman ◽  
Shaheen A. Al-Muhtaseb ◽  
Hae-Kwon Jeong

In this article, zeolitic-imidazolate framework-8 (ZIF-8) and its mixed metal CoZn-ZIF-8 were synthesized via a rapid microwave method. They exhibited a nanogate opening pressure threshold for the adsorption of C3 and C4 compounds.


2017 ◽  
Vol 46 (40) ◽  
pp. 14002-14011 ◽  
Author(s):  
Hiroki Miura ◽  
Volodymyr Bon ◽  
Irena Senkovska ◽  
Sebastian Ehrling ◽  
Satoshi Watanabe ◽  
...  

Controlled nucleation in a micromixer was used to synthesize DUT-8(Ni) with narrow particle size distribution in a range from few nm to several μm.


2012 ◽  
Vol 134 (37) ◽  
pp. 15201-15204 ◽  
Author(s):  
Nour Nijem ◽  
Haohan Wu ◽  
Pieremanuele Canepa ◽  
Anne Marti ◽  
Kenneth J. Balkus ◽  
...  

2018 ◽  
Vol 47 (37) ◽  
pp. 13158-13163 ◽  
Author(s):  
Xiaodong Sun ◽  
Yali Ma ◽  
Jun Zhao ◽  
Dong-Sheng Li ◽  
Guanghua Li ◽  
...  

JLU-Liu33F has been solvothermally synthesized by utilizing the ligand functionalization strategy. Compared with JLU-Liu33, JLU-Liu33F exhibits a completely different breathing behavior.


2011 ◽  
Vol 42 (S 01) ◽  
Author(s):  
D Tibussek ◽  
F Distelmaier ◽  
S Kummer ◽  
E Mayatepek

2020 ◽  
Author(s):  
Matthew Stout ◽  
Brian Skelton ◽  
Alexandre N. Sobolev ◽  
Paolo Raiteri ◽  
Massimiliano Massi ◽  
...  

<p>Three Re(I) tricarbonyl complexes, with general formulation Re(N^L)(CO)<sub>3</sub>X (where N^L is a bidentate ligand containing a pyridine functionalized in the position 2 with a thione or a thiazol-2-ylidene group and X is either chloro or bromo) were synthesized and their reactivity explored in terms of solvent-dependent ligand substitution, both in the ground and excited states. When dissolved in acetonitrile, the complexes bound to the thione ligand underwent ligand exchange with the solvent resulting in the formation of Re(NCMe)<sub>2</sub>(CO)<sub>3</sub>X. The exchange was found to be reversible, and the starting complex was reformed upon removal of the solvent. On the other hand, the complexes appeared inert in dichloromethane or acetone. Conversely, the complex bound to the thiazole-2-ylidene ligand did not display any ligand exchange reaction in the dark, but underwent photoactivated ligand substitution when excited to its lowest metal-to-ligand charge transfer manifold. Photolysis of this complex in acetonitrile generated multiple products, including Re(I) tricarbonyl and dicarbonyl solvato-complexes as well as free thiazole-2-ylidene ligand.</p>


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