Peroxynitric Acid: A Convenient Oxygen Source for Oxidation of Organic Compounds Catalyzed by Polyimide-Supported Manganese (III) Tetrakis(4-methoxylphenyl)porphyrin Acetate

Authors

  • Gholamreza Karimipour Department of Chemistry, Faculty of Sciences, Yasouj University, P.O. box 75918-74831Yasouj, IRAN
  • Massomeh Bahramian Department of Chemistry, Yasouj University, P.O. Box 75918-74831, I.R. IRAN
  • Zahra Rafiee Department of Chemistry, Yasouj University, P.O. Box 75918-74831, I.R. IRAN
Abstract:

In this work, a polyimide (PI) containing triazole units was synthesized using 3,5-diamino-1,2,4-triazole and pyromellitic dianhydride in N-methyl-2-pyrrolidinone. This polymer was used as the support of manganese (III) tetrakis(4-methoxylphenyl)porphyrin acetate to attain a heterogeneous catalyst; namely Mn(T4-OMePP)OAc@PI. The synthesized PI and Mn(T4-OMePP)OAc@PI were characterized by different spectroscopic and analytical techniques. The resulted catalyst was applied for epoxidation of alkenes and dehydrogenation of Hantzsch 1,4-dihydropyridines (1,4-DHP) by peroxynitric acid (PNA; HOONO2) as a convenient new oxygen source. In association with HOONO2, Mn(T4-OMePP)OAc@PI was stable and proved to be an efficient, reusable and selective catalyst for epoxidation of alkenes (36-96% yield) and dehydrogenation of Hantzsch 1,4-DHP’s ( 94-100% yield).

Upgrade to premium to download articles

Sign up to access the full text

Already have an account?login

similar resources

Microbial manganese(III) reduction fuelled by anaerobic acetate oxidation.

Soluble manganese in the intermediate +III oxidation state (Mn3+ ) is a newly identified oxidant in anoxic environments, whereas acetate is a naturally abundant substrate that fuels microbial activity. Microbial populations coupling anaerobic acetate oxidation to Mn3+ reduction, however, have yet to be identified. We isolated a Shewanella strain capable of oxidizing acetate anaerobically with M...

full text

Microbial Manganese ( Iii ) Reduction Fueled by Anaerobic Acetate Oxidation

Background: Microbial manganese (Mn) cycling in marine and freshwater environments is generally assumed to consist of Mn oxidation in oxic water columns and Mn(IV) oxide reduction in anoxic sediments [1] as the only two bioavailable Mn redox species. This dogma was recently overturned with the discovery that soluble Mn dominates the soluble Mn pool at μM concentrations in suboxic environments [...

full text

Biomimetic oxidation of piperine and piplartine catalyzed by iron(III) and manganese(III) porphyrins.

Synthetic metalloporphyrins, in the presence of monooxygen donors, are known to mimetize various reactions of cytochrome P450 enzymes systems in the oxidation of drugs and natural products. The oxidation of piperine and piplartine by iodosylbenzene using iron(III) and manganese(III) porphyrins yielded mono- and dihydroxylated products, respectively. Piplartine showed to be a more reactive subst...

full text

Mild and Efficient Oxidation of Alcohols with NaIO4 Catalyzed by a Manganese Porphyrin-polyoxometalate Hybrid Material

Efficient and selective oxidation of alcohols with NaIO4 catalyzed by an organic-inorganic hybrid material in which manganese(III)5,10,15,20-tetrakis(4-aminophenyl)porphyrin chloride, MnIII(TAPP)Cl, is covalently linked to a Lindqvist structure of polyoxometalate, Mo6O192-, at room temperature is reported. The effect of various parameters such as catalyst amount, solvent and oxidant were studie...

full text

Unsaturated lipide oxidation catalyzed by hematin compounds.

Hematin catalysis of unsaturated lipide oxidation is probably a primary reaction in many types of pathological unsaturated fat oxidation in viva (l-3) and in the spoilage of frozen meat products by oxidative fat rancidity (4). Some of the properties of hematin catalysis have been described (4-8), but knowledge of the reaction mechanism and the reaction products is relatively meager. The catalyt...

full text

My Resources

Save resource for easier access later

Save to my library Already added to my library

{@ msg_add @}


Journal title

volume 36  issue 2

pages  17- 28

publication date 2017-05-01

By following a journal you will be notified via email when a new issue of this journal is published.

Hosted on Doprax cloud platform doprax.com

copyright © 2015-2023