Nature of the Active Catalyst in the Hafnium-Pyridyl Amido-Catalyzed Alkene Polymerization

ACS Catalysis ◽  
2021 ◽  
pp. 4301-4309
Author(s):  
Eric S. Cueny ◽  
Megan R. Nieszala ◽  
Robert D. J. Froese ◽  
Clark R. Landis
Keyword(s):  
Active Catalyst ◽  
Alkene Polymerization

Co3O4-CuCoO2 hybrid nanoplates as a low-cost and highly active catalyst for producing hydrogen from ammonia borane

2021 ◽  
Author(s):  
Yufa Feng ◽  
Jinyun Liao ◽  
Xiaodong Chen ◽  
Qingyu Liao ◽  
Huize Wang ◽  
...  
Keyword(s):  
Fuel Cell ◽  
Active Catalyst ◽  
Low Cost ◽  
Ammonia Borane ◽  
Catalytic Materials ◽  
Highly Active ◽  
Promising Strategy

Developing low-cost and highly active hydrolysis catalytic materials for the dehydrogenation of hydrogen-rich chemicals is a promising strategy to store and easily release hydrogen for fuel cell applications. In this...

A copper(II) complex with rare μ1,1,1-azide ligand: Active catalyst for heterogeneous olefin epoxidation

2008 ◽  
Vol 11 (3) ◽  
pp. 265-269 ◽  
Author(s):  
Partha Roy ◽  
Koushik Dhara ◽  
Mario Manassero ◽  
Pradyot Banerjee
Keyword(s):  
Active Catalyst ◽  
Olefin Epoxidation ◽  
Azide Ligand

[RuV(NCN-Me)(bpy)(O)]3+ mediated efficient photo-driven water oxidation

RSC Advances ◽  
2016 ◽  
Vol 6 (66) ◽  
pp. 61959-61965 ◽  
Author(s):  
Jully Patel ◽  
Karunamay Majee ◽  
Sumanta Kumar Padhi
Keyword(s):  
Electron Acceptor ◽  
Water Oxidation ◽  
Phosphate Buffer ◽  
Active Catalyst

The complex [Ru(NCN-Me)(bpy)H2O](PF6)2 acts as an active catalyst for the photo-driven oxidation of water, when employed with [Ru(bpy)3]2+ as photosensitizer and Na2S2O8 as sacrificial electron acceptor at pH 6.5 phosphate buffer, with a TON of 130.

Crystal structure of meso ‐substituted pyrazolyl porphyrin complexes and their highly active catalyst for oxidation of alkylbenzenes

2017 ◽  
Vol 32 (3) ◽  
pp. e4184 ◽  
Author(s):  
Yahong Yao ◽  
Yanxia Du ◽  
Jun Li ◽  
Chen Wang ◽  
Zengqi Zhang ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Active Catalyst ◽  
Highly Active
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