Manganese(iii)salophen supported on a silica containing triazine dendrimer: an efficient catalyst for epoxidation of alkenes with sodium periodate

RSC Advances ◽  
2016 ◽  
Vol 6 (24) ◽  
pp. 20128-20134 ◽  
Author(s):  
Mahsa Asadniaye Fardjahromi ◽  
Majid Moghadam ◽  
Shahram Tangestaninejad ◽  
Valiollah Mirkhani ◽  
Iraj Mohammadpoor-Baltork

Mn(iii) salophen supported on a nanosilica triazine dendrimer was synthesized and used for epoxidation of alkenes with sodium periodate.

2014 ◽  
Vol 4 (4) ◽  
pp. 997-1004 ◽  
Author(s):  
Yan Leng ◽  
Jian Liu ◽  
Chenjun Zhang ◽  
Pingping Jiang

A novel POSS-bridged oxo-molybdenum Schiff base complex was demonstrated to be a highly efficient catalyst for epoxidation of alkenes with aqueous tert-butyl hydroperoxide.


2010 ◽  
Vol 381 (1-2) ◽  
pp. 233-241 ◽  
Author(s):  
Shahram Tangestaninejad ◽  
Majid Moghadam ◽  
Valiollah Mirkhani ◽  
Iraj Mohammadpoor-Baltork ◽  
Mohammad Saleh Saeedi

Nanoscale ◽  
2018 ◽  
Vol 10 (4) ◽  
pp. 1591-1597 ◽  
Author(s):  
Kuo Yuan ◽  
Tianqun Song ◽  
Dawei Wang ◽  
Ye Zou ◽  
Jinfeng Li ◽  
...  

In this work, we synthesized a series of microcrystalline MnxN100−x-MOF-74 (N = Fe, Co and Ni) materials by a one-pot reaction.


2019 ◽  
Vol 23 (06) ◽  
pp. 671-678 ◽  
Author(s):  
Mojtaba Bagherzadeh ◽  
Mohammad Adineh Jonaghani ◽  
Mojtaba Amini ◽  
Anahita Mortazavi-Manesh

Condensation of pyrrole with various aldehydes in the presence of BF3•etherate as an acid catalyst in water provides good yield of some dipyrromethanes. Prolongation of the reaction time with aldehydes substituted by electron-donating (mesityl) or electron-withdrawing (2,6-dichlorophenyl) groups on the ortho positions of the phenyl did not lead to decomposition or scrambling. Manganese trans disubstituted porphyrin complexes which derive from various dipyrromethanes and manganese tetraaryl porphyrin complexes including various substituents with different steric and electronic properties show good catalytic activity in epoxidation of alkenes by NaIO4in the presence of imidazole (ImH). The study of steric and electronic effects of the catalysts on the epoxidation of olefins shows that Mn-porphyrin complexes with more bulky and electron-releasing groups on meso phenyls could increase the epoxidation yield of most alkenes.


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