Zeolite- and MgO-Supported Molecular Iridium Complexes: Support and Ligand Effects in Catalysis of Ethene Hydrogenation and H–D Exchange in the Conversion of H2+ D2

ACS Catalysis ◽  
2011 ◽  
Vol 1 (11) ◽  
pp. 1549-1561 ◽  
Author(s):  
Jing Lu ◽  
Pedro Serna ◽  
Bruce C. Gates

2011 ◽  
Vol 17 (52) ◽  
pp. 15027-15031 ◽  
Author(s):  
Jacques Lalevée ◽  
Mathieu Peter ◽  
Frédéric Dumur ◽  
Didier Gigmes ◽  
Nicolas Blanchard ◽  
...  


2005 ◽  
Vol 24 (25) ◽  
pp. 6250-6259 ◽  
Author(s):  
Wesley H. Bernskoetter ◽  
Emil Lobkovsky ◽  
Paul J. Chirik


2019 ◽  
Vol 25 (23) ◽  
pp. 6026-6037 ◽  
Author(s):  
Po‐Ni Lai ◽  
Thomas S. Teets


2015 ◽  
Vol 436 ◽  
pp. 146-151 ◽  
Author(s):  
Saheed A. Popoola ◽  
E.A. Jaseer ◽  
Abdulaziz A. Al-Saadi ◽  
Victor Polo ◽  
Miguel A. Casado ◽  
...  


2022 ◽  
Vol 517 ◽  
pp. 112050
Author(s):  
Jingyi Wang ◽  
Chengyu Liu ◽  
Liming Cao ◽  
Yan Xiong ◽  
Jinxing Ye ◽  
...  


2020 ◽  
Author(s):  
Boris Sheludko ◽  
Cristina Castro ◽  
Chaitanya Khalap ◽  
Thomas Emge ◽  
Alan Goldman ◽  
...  

<b>Abstract:</b> The production of olefins via on-purpose dehydrogenation of alkanes allows for a more efficient, selective and lower cost alternative to processes such as steam cracking. Silica-supported pincer-iridium complexes of the form [(≡SiO-<sup>R4</sup>POCOP)Ir(CO)] (<sup>R4</sup>POCOP = κ<sup>3</sup>-C<sub>6</sub>H<sub>3</sub>-2,6-(OPR<sub>2</sub>)<sub>2</sub>) are effective for acceptorless alkane dehydrogenation, and have been shown stable up to 300 °C. However, while solution-phase analogues of such species have demonstrated high regioselectivity for terminal olefin production under transfer dehydrogenation conditions at or below 240 °C, in open systems at 300 °C, regioselectivity under acceptorless dehydrogenation conditions is consistently low. In this work, complexes <a>[(≡SiO-<i><sup>t</sup></i><sup>Bu4</sup>POCOP)Ir(CO)] </a>(<b>1</b>) and [(≡SiO-<i><sup>i</sup></i><sup>Pr4</sup>PCP)Ir(CO)] (<b>2</b>) were synthesized via immobilization of molecular precursors. These complexes were used for gas-phase butane transfer dehydrogenation using increasingly sterically demanding olefins, resulting in observed selectivities of up to 77%. The results indicate that the active site is conserved upon immobilization.



1982 ◽  
Vol 42 (4) ◽  
pp. 339-345
Author(s):  
W. G. Zijlstra ◽  
B. Oeseburg ◽  
G. Kwant ◽  
A. Zwart


1985 ◽  
Author(s):  
Gregory James Sevenich
Keyword(s):  


2006 ◽  
Vol 71 (2) ◽  
pp. 197-206 ◽  
Author(s):  
Martin Pošta ◽  
Jan Čermák ◽  
Pavel Vojtíšek ◽  
Ivana Císařová

The first rhodium complexes of diphosphinoazines [{RhCl(1,2-η:5,6-η-CH=CHCH2CH2CH=CHCH2CH2)}2 {μ-R2PCH2C(But)=NN=C(But)CH2PR2] (R = Ph, Cy, Pri) were prepared by cleavage of the bridge in chloro(cycloocta-1,5-diene)rhodium(I) dimer, the analogous iridium(I) complexes were also prepared for the first time. The X-ray structures of isostructural rhodium and iridium complexes with bis(dicyclohexylphosphino)pinacoloneazine were determined. Diphosphinoazine ligands in the complexes remained in (Z,Z) configuration bridging two RhCl(C8H12) units.



RSC Advances ◽  
2021 ◽  
Vol 11 (18) ◽  
pp. 11004-11010
Author(s):  
Zequn Ma ◽  
Chaojun Jing ◽  
Deyu Hang ◽  
Hongtao Fan ◽  
Lumeng Duan ◽  
...  

Three high-efficient green light iridium complexes were designed and prepared. Thermal stabilities, electrochemical properties, electroluminescence performances and substituents effects are presented and discussed in this study.



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