iron compound
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2021 ◽  
Vol 70 (5) ◽  
pp. 170-176
Author(s):  
Yoshifumi Konari ◽  
Kenji Kono ◽  
Koki Ikeda ◽  
Li-Bin Niu

2020 ◽  
Vol 220 ◽  
pp. 157-167 ◽  
Author(s):  
Wei-Qiang Pang ◽  
Luigi T. DeLuca ◽  
Xue-Zhong Fan ◽  
Oleg G. Glotov ◽  
Ke Wang ◽  
...  

2020 ◽  
Vol 268 ◽  
pp. 122362 ◽  
Author(s):  
J.G. Tirado González ◽  
B.T. Reyes Segura ◽  
J. Esguerra-Arce ◽  
A. Bermúdez Castañeda ◽  
Y. Aguilar ◽  
...  

2020 ◽  
Author(s):  
Rory Waterman ◽  
Matthew B. Reuter

Si–O and Si–N heterodehydrocoupling catalyzed by the commercially available iron dimer (<b>1</b>) under photochemical conditions is reported. Mechanistic study reveals that the most immediate hurdle in the catalysis is the poor activation of <b>1</b>, demonstrating the necessity to fully activate the catalyst to realize the potential of iron in this reactivity.


2020 ◽  
Author(s):  
Rory Waterman ◽  
Matthew B. Reuter

Si–O and Si–N heterodehydrocoupling catalyzed by the commercially available iron dimer (<b>1</b>) under photochemical conditions is reported. Mechanistic study reveals that the most immediate hurdle in the catalysis is the poor activation of <b>1</b>, demonstrating the necessity to fully activate the catalyst to realize the potential of iron in this reactivity.


2020 ◽  
Vol 44 (4) ◽  
pp. 506-515
Author(s):  
Zhenghong Guo ◽  
Yanqun Pan ◽  
Ruifeng Guo ◽  
Zhengping Fang

2020 ◽  
Vol 49 (9) ◽  
pp. 2972-2978 ◽  
Author(s):  
Matthew B. Reuter ◽  
Michael P. Cibuzar ◽  
James Hammerton ◽  
Rory Waterman

A commercially available iron readily engages in catalytic Si–O and Si–N bond formation under visible light irradiation.


2019 ◽  
Author(s):  
Rory Waterman ◽  
Matthew B. Reuter

Si–O and Si–N heterodehydrocoupling catalyzed by the commercially available iron dimer (<b>1</b>) under photochemical conditions is reported. Mechanistic study reveals that the most immediate hurdle in the catalysis is the poor activation of <b>1</b>, demonstrating the necessity to fully activate the catalyst to realize the potential of iron in this reactivity.


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