scholarly journals Tethered Pincer Complexes as Recyclable Homogeneous Catalysts

Author(s):  
Aidan R. McDonald ◽  
Harm P. Dijkstra
ChemInform ◽  
2006 ◽  
Vol 37 (34) ◽  
Author(s):  
Fatima Churruca ◽  
Raul SanMartin ◽  
Imanol Tellitu ◽  
Esther Dominguez

Author(s):  
Zufar N. Gafurov ◽  
Ekaterina M. Zueva ◽  
Giyjaz E. Bekmukhamedov ◽  
Alexey A. Kagilev ◽  
Artyom O. Kantyukov ◽  
...  

2006 ◽  
Vol 47 (19) ◽  
pp. 3233-3237 ◽  
Author(s):  
Fátima Churruca ◽  
Raul SanMartin ◽  
Imanol Tellitu ◽  
Esther Domínguez

2018 ◽  
Author(s):  
Tasneem Siddiquee ◽  
Abdul Goni

Chemical treatment of CoX<sub>2</sub><b><sup>. </sup></b>6H<sub>2</sub>O (X = Cl, Br, I) with the potentially tridentate PNP pincer ligand 2,6-bis(di-<i>tert</i>-butylphosphinomethyl)pyridine in 1:1 molar ratio results in cobalt(II) halide-PNP pincer complexes. The effect of the hydrated metal source on molecular structure and geometry of the complexes was studied by single crystal X-ray diffraction analysis. The complexes are neutral and the cobalt center adopts a penta-coordinate system with potential atropisomerization. Within the unit cell there are two distinct molecules per asymmetric unit. One of the two phosphorus atoms in the PNP ligand was observed to be partially oxidized to phosphinoxide. Disorder in the structure reflects a mixture of square pyramidal and distorted tetrahedral geometry.


2012 ◽  
Vol 1 (2) ◽  
pp. 100-106 ◽  
Author(s):  
I. Such-Basanez ◽  
C. Salinas-Martinez de Lecea ◽  
M. C. Roman-Martinez

2021 ◽  
Author(s):  
Antonio Aldair Castillo-García ◽  
González-Sebastián Lucero ◽  
Leticia Lomas-Romero ◽  
Simon Hernandez-Ortega ◽  
Ruben Alfredo Toscano ◽  
...  
Keyword(s):  

The synthesis of four novel non-symmetric Ni(II)-POCOP pincer complexes meta-functionalized with either benzothiazole or benzimidazole at the central aryl ring is described. All complexes were fully characterised in solution by...


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Wenjun Yang ◽  
Ivan Yu. Chernyshov ◽  
Robin K. A. van Schendel ◽  
Manuela Weber ◽  
Christian Müller ◽  
...  

AbstractAny catalyst should be efficient and stable to be implemented in practice. This requirement is particularly valid for manganese hydrogenation catalysts. While representing a more sustainable alternative to conventional noble metal-based systems, manganese hydrogenation catalysts are prone to degrade under catalytic conditions once operation temperatures are high. Herein, we report a highly efficient Mn(I)-CNP pre-catalyst which gives rise to the excellent productivity (TOF° up to 41 000 h−1) and stability (TON up to 200 000) in hydrogenation catalysis. This system enables near-quantitative hydrogenation of ketones, imines, aldehydes and formate esters at the catalyst loadings as low as 5–200 p.p.m. Our analysis points to the crucial role of the catalyst activation step for the catalytic performance and stability of the system. While conventional activation employing alkoxide bases can ultimately provide catalytically competent species under hydrogen atmosphere, activation of Mn(I) pre-catalyst with hydride donor promoters, e.g. KHBEt3, dramatically improves catalytic performance of the system and eliminates induction times associated with slow catalyst activation.


2021 ◽  
Vol 507 ◽  
pp. 111553
Author(s):  
Animesh Chowdhury ◽  
Santu Biswas ◽  
Sourav Ghoshal ◽  
Anup Pramanik ◽  
Pranab Sarkar

2021 ◽  
Author(s):  
Ruixiang Guo ◽  
Gang Wang ◽  
Wei Liu ◽  
Zibei Yao ◽  
Wei-Sheng Liu

Traditionally, the immobilized catalyst sacrifices a part of catalytic activity for its recyclability. To reproduce the catalytic activity of active specie, we construct a novel strategy called "adsorption-desorption-adsorption". Since the...


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