Catalysis of μ-oxo-bis[porphyriniron(III)] for toluene oxidation with molecular oxygen

2006 ◽  
Vol 10 (07) ◽  
pp. 948-952 ◽  
Author(s):  
Hai-Yang Hu ◽  
Quan Jiang ◽  
Qiang Liu ◽  
Jian-Xin Song ◽  
Wei-Ying Lin ◽  
...  

Toluene oxidation with molecular oxygen as the sole oxidant, and μ-oxo-bis[tetraphenylporphinatoiron(III)] as the catalyst, are reported. Under the reaction conditions of 438 K and 0.8 MPa, the molar total yields for the products benzaldehyde and benzyl alcohol and the turnover number of the catalyst are 4.35% and 21,830 (based on the metal ion), respectively. Compared with the reaction catalyzed by the corresponding monometalloporphyrin TPPFe III Cl , the total yields of the oxidation products and the catalyst turnover number by the dimeric iron porphyrin were almost twice those by the former. A possible reaction mechanism of the toluene oxidation by μ-oxo-bis[tetraphenylporphinatoiron(III)] is proposed.

2008 ◽  
Vol 86 (3) ◽  
pp. 199-204 ◽  
Author(s):  
Guan Huang ◽  
Chun-Cai Cai ◽  
Jin Luo ◽  
Hong Zhou ◽  
Yong-An Guo ◽  
...  

The highly selective catalytic oxidation of toluene with air to benzaldehyde and benzyl alcohol in the liquid phase has been studied with the use of iron tetraphenylporphyrin (Fe TPP) supported on chitosan (CTS), (Fe TPP/CTS). The rates of toluene conversion and selectivity (aldehyde + alcohol) were subject to the reaction temperature, air pressure, and amount of iron tetraphenylporphyrin. By the use of the Fe TPP/CTS, containing 2 mg of iron tetraphenylporphyrin as catalyst, toluene oxidation with air under the optimum conditions of 190 °C and 0.6 MPa produced benzaldehyde and benzyl alcohol at 90% selectivity and 5.4% conversion of toluene, the mole turnover of the catalyst was about 6 × 106, and it could be reused efficiently for one more time. It is suggested that the amine groups (–NH2) on the chitosan chain act as a key assistor to the catalysis of Fe TPP for toluene oxidation. Compared with the conventional method of synthesizing benzaldehyde and benzyl alcohol, the new method has the advantages of reduced environmental pollution, higher selectivity for the two main products, and easy recovery of the catalyst.Key words: chitosan-supported iron porphyrin, catalysis, toluene oxidation, benzaldehyde, benzyl alcohol.


Polymers ◽  
2021 ◽  
Vol 13 (10) ◽  
pp. 1651
Author(s):  
Felipe de la Cruz-Martínez ◽  
Marc Martínez de Sarasa Buchaca ◽  
Almudena del Campo-Balguerías ◽  
Juan Fernández-Baeza ◽  
Luis F. Sánchez-Barba ◽  
...  

The catalytic activity and high selectivity reported by bimetallic heteroscorpionate acetate zinc complexes in ring-opening copolymerization (ROCOP) reactions involving CO2 as substrate encouraged us to expand their use as catalysts for ROCOP of cyclohexene oxide (CHO) and cyclic anhydrides. Among the catalysts tested for the ROCOP of CHO and phthalic anhydride at different reaction conditions, the most active catalytic system was the combination of complex 3 with bis(triphenylphosphine)iminium as cocatalyst in toluene at 80 °C. Once the optimal catalytic system was determined, the scope in terms of other cyclic anhydrides was broadened. The catalytic system was capable of copolymerizing selectively and efficiently CHO with phthalic, maleic, succinic and naphthalic anhydrides to afford the corresponding polyester materials. The polyesters obtained were characterized by spectroscopic, spectrometric, and calorimetric techniques. Finally, the reaction mechanism of the catalytic system was proposed based on stoichiometric reactions.


ChemCatChem ◽  
2014 ◽  
Vol 6 (12) ◽  
pp. 3464-3473 ◽  
Author(s):  
Aditya Savara ◽  
Carine E. Chan-Thaw ◽  
Ilenia Rossetti ◽  
Alberto Villa ◽  
Laura Prati

2020 ◽  
Vol 26 (1) ◽  
pp. 168-175
Author(s):  
Jinge Wang ◽  
Siyitemer Osman ◽  
Xinjiang Lu ◽  
Junyi Chen ◽  
Xu-Dong Xia

AbstractA convenient aerobic oxidative hydroxylation of 3-substituted oxindoles under mild reaction conditions is described herein. This process was accomplished by the activation of molecular oxygen in the air in the presence of a photocatalyst under the irradiation of visible light. The desired product was delivered in up to 89% yield without the addition of base or stoichiometric oxidant.


2021 ◽  
Vol 903 ◽  
pp. 143-148
Author(s):  
Svetlana Cornaja ◽  
Svetlana Zhizhkuna ◽  
Jevgenija Vladiko

Supported 3wt%Pd/α-Al₂O₃ catalyst was tested in selective oxidation of 1,2-propanediol by molecular oxygen. It was found that the catalyst is active in an alkaline water solution. Lactic acid was obtained as the main product of the reaction. Influence of different reaction conditions on 1,2-PDO conversion and oxidation process selectivity was studied. Partial kinetic orders of the reaction with respect to 1,2-propanediol, c0(NaOH), p(O2), n(1,2-PDO)/n(Pd)) were determined and an experimental kinetic model of the catalytic oxidation reaction was obtained. Activation energy of the process was calculated and was found to be about 53 ± 5 kJ/mol.


Sign in / Sign up

Export Citation Format

Share Document