Non-symmetric Schiff base Co(II) complexes. Synthesis and catalytic activity in the oxidation of 2,6-Di-tert-butylphenol by molecular oxygen

1987 ◽  
Vol 134 (1) ◽  
pp. 53-57 ◽  
Author(s):  
I. Sasaki ◽  
D. Pujol ◽  
A. Gaudemer
Keyword(s):  
Schiff Base ◽  
Catalytic Activity ◽  
Molecular Oxygen

Catalytic Oxidation of a Trialkyl-Substituted Phenol and Aniline with Biomimetic Schiff Base Complexes

2000 ◽  
Vol 55 (1) ◽  
pp. 86-93 ◽  
Author(s):  
Jutta Knaudt ◽  
Stefan Förster ◽  
Ulrich Bartsch ◽  
Anton Rieker ◽  
Ernst-G Jäger
Keyword(s):  
Schiff Base ◽  
Catalytic Activity ◽  
Catalytic Oxidation ◽  
Molecular Oxygen ◽  
Product Distribution ◽  
Schiff Base Complexes ◽  
Salen Complex ◽  
Tert Butylhydroperoxide

The catalytic oxidation of 2,4.6-tri-tert-butylphenol and 2,4,6-tri-tert-butylaniline with molecular oxygen and tert-butylhydroperoxide was investigated using biomimetic Mn-, Fe- and Co-complexes as catalysts. The catalytic activity and product distribution were determined and compared with those observed in the reactions of the well-known Co(salen) complex

Synthesis, structural characterization and catalytic activity of chlororuthenium(II) complexes with substituted Schiff base/phosphine ancillary ligands

2020 ◽  
Vol 75 (9-10) ◽  
pp. 851-857
Author(s):  
Chong Chen ◽  
Fule Wu ◽  
Jiao Ji ◽  
Ai-Quan Jia ◽  
Qian-Feng Zhang
Keyword(s):  
Schiff Base ◽  
Catalytic Activity ◽  
Structural Characterization ◽  
Room Temperature ◽  
Molecular Structures ◽  
Cationic Complex ◽  
Neutral Complex ◽  
Ancillary Ligands ◽  
X Ray ◽  
X Ray Crystallography

AbstractTreatment of [(η6-p-cymene)RuCl2]2 with one equivalent of chlorodiphenylphosphine in tetrahydrofuran at reflux afforded a neutral complex [(η6-p-cymene)RuCl2(κ1-P-PPh2OH)] (1). Similarly, the reaction of [Ru(bpy)2Cl2·2H2O] (bpy = 2,2′-bipyridine) and chlorodiphenylphosphine in methanol gave a cationic complex [Ru(bpy)2Cl(κ1-P-PPh2OCH3)](PF6) (2), while treatment of [RuCl2(PPh3)3] with [2-(C5H4N)CH=N(CH2)2N(CH3)2] (L1) in tetrahydrofuran at room temperature afforded a ruthenium(II) complex [Ru(PPh3)Cl2(κ3-N,N,N-L1)] (3). Interaction of the chloro-bridged complex [Ru(CO)2Cl2]n with one equivalent of [Ph2P(o-C6H4)CH=N(CH2)2N(CH3)2] (L2) led to the isolation of [Ru(CO)Cl2(κ3-P,N,N-L2)] (4). The molecular structures of the ruthenium(II) complexes 1–4 have been determined by single-crystal X-ray crystallography. The properties of the ruthenium(II) complex 4 as a hydrogenation catalyst for acetophenone were also tested.

Ferrocene-based porous organic polymer derived high-performance electrocatalysts for oxygen reduction

2017 ◽  
Vol 5 (42) ◽  
pp. 22163-22169 ◽  
Author(s):  
Baolong Zhou ◽  
Liangzhen Liu ◽  
Pingwei Cai ◽  
Guang Zeng ◽  
Xiaoqiang Li ◽  
...  
Keyword(s):  
Schiff Base ◽  
Catalytic Activity ◽  
Oxygen Reduction Reaction ◽  
Oxygen Reduction ◽  
Porous Carbon ◽  
High Performance ◽  
Reduction Reaction ◽  
Organic Polymer ◽  
Porous Organic Polymers ◽  
Porous Organic Polymer

Two nitrogen-rich porous organic polymers (POPs) were prepared via Schiff base chemistry. Carbonization of these POPs results in porous carbon nanohybrids which exhibit excellent catalytic activity toward the oxygen reduction reaction (ORR).

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