In Situ Generated Palladium on Aluminum Phosphate as Catalytic System for the Preparation of β,β-Diarylated Olefins by Matsuda–Heck Reaction

2017 ◽  
Vol 21 (11) ◽  
pp. 1835-1842 ◽  
Author(s):  
Sandra Lucks ◽  
Heiko Brunner
Molecules ◽  
2018 ◽  
Vol 23 (9) ◽  
pp. 2358 ◽  
Author(s):  
David Lopez-Tejedor ◽  
Blanca de las Rivas ◽  
Jose M. Palomo

A novel heterogeneous enzyme-palladium (Pd) (0) nanoparticles (PdNPs) bionanohybrid has been synthesized by an efficient, green, and straightforward methodology. A designed Geobacillus thermocatenulatus lipase (GTL) variant genetically and then chemically modified by the introduction of a tailor-made cysteine-containing complementary peptide- was used as the stabilizing and reducing agent for the in situ formation of ultra-small PdNPs nanoparticles embedded on the protein structure. This bionanohybrid was an excellent catalyst in the synthesis of trans-ethyl cinnamate by Heck reaction at 65 °C. It showed the best catalytic performance in dimethylformamide (DMF) containing 10–25% of water as a solvent but was also able to catalyze the reaction in pure DMF or with a higher amount of water as co-solvent. The recyclability and stability were excellent, maintaining more than 90% of catalytic activity after five cycles of use.


Molecules ◽  
2018 ◽  
Vol 23 (10) ◽  
pp. 2413 ◽  
Author(s):  
Cheng Chen ◽  
Yang Miao ◽  
Kimmy De Winter ◽  
Hua-Jing Wang ◽  
Patrick Demeyere ◽  
...  

Transition-metal-catalyzed amide-bond formation from alcohols and amines is an atom-economic and eco-friendly route. Herein, we identified a highly active in situ N-heterocyclic carbene (NHC)/ruthenium (Ru) catalytic system for this amide synthesis. Various substrates, including sterically hindered ones, could be directly transformed into the corresponding amides with the catalyst loading as low as 0.25 mol.%. In this system, we replaced the p-cymene ligand of the Ru source with a relatively labile cyclooctadiene (cod) ligand so as to more efficiently obtain the corresponding poly-carbene Ru species. Expectedly, the weaker cod ligand could be more easily substituted with multiple mono-NHC ligands. Further high-resolution mass spectrometry (HRMS) analyses revealed that two tetra-carbene complexes were probably generated from the in situ catalytic system.


2017 ◽  
Vol 19 (9) ◽  
pp. 2101-2106 ◽  
Author(s):  
Hu Li ◽  
Wenfeng Zhao ◽  
Anders Riisager ◽  
Shunmugavel Saravanamurugan ◽  
Zhongwei Wang ◽  
...  

A sustainable catalytic system is developed to be efficient for producing the biofuel 2,5-dimethylfuran directly from carbohydrate biomass via an in situ domino process under mild conditions.


2019 ◽  
Vol 25 (72) ◽  
pp. 16439-16439
Author(s):  
Dmitry B. Eremin ◽  
Ekaterina A. Denisova ◽  
Alexander Yu. Kostyukovich ◽  
Jonathan Martens ◽  
Giel Berden ◽  
...  

2012 ◽  
Vol 2012 ◽  
pp. 1-6 ◽  
Author(s):  
Paula Zapata ◽  
Raúl Quijada

Polypropylene nanocomposites containing silica nanospheres based on the sol-gel methods were produced viain situpolymerization using a rac-Et(Ind)2ZrCl2/methylaluminoxane (MAO) system. Two different routes were used depending on the interaction between the silica nanoparticles with the catalytic system. In route 1 the nanoparticles were added together with the catalytic system (rac-Et(Ind)2ZrCl2)/(MAO) directly into the reactor, and in route 2 the metallocene rac-Et(Ind)2ZrCl2was supported on silica nanospheres pretreated with (MAO). SEM images show that when the nanospheres were added by both routes, they were replicated in the final polymer particle morphology; this phenomenon was more pronounced for PP obtained by route 2. The polypropylene (PP) nanocomposites obtained by both routes had a slightly higher percent crystallinities and crystallinity temperatures than pure PP. Transmission electron microscopy (TEM) images show that the nanospheres were well dispersed into the polypropylene matrix, particularly in the nanocomposites obtained by the support system (route 2).


2020 ◽  
Vol 34 (4) ◽  
Author(s):  
Hao Zhang ◽  
Ji‐Hua Zhu ◽  
Fei Hou ◽  
Zheng‐Jun Quan ◽  
Xi‐Cun Wang

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