Iron(III) Porphyrin promoted Aerobic Oxidation of Sulphur Dioxide

DOI: 10.1039/c39900000461

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 461 - 462 (1990)

Update date:2022-08-17

Topics:

Authors:

Shin, Koo

Goff, Harold M.

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1039/c39900000461

In the presence of sulphur dioxide and oxygen gas, the oxo-bridged tetraphenylporphyrinatoiron(III) dinuclear complex has been converted to the corresponding sulphato-bridged iron(III) complex

Full text of DOI:10.1039/c39900000461

View Article Online / Journal Homepage / Table of Contents for this issue

View Article Online

Products guided by the article

Product name:(tetraphenylporphinato)Fe-SO₄-Fe(tetraphenylporphinato)

Cas No:72895-19-3

R&D Labs maybe for 72895-19-3

TIANJIN NORTH JINHENG CHEMICAL PLANT.

Contact:0086-22-59952083

Address:DongShigu Country In JiXian TianJin China
Phantom-pharma

Contact:

Address:
Xiamen Hisunny Chemical Co.,Ltd

website:http://www.hisunnychem.com

Contact:+86-592-3327115

Address:Unit 603,No.879,Xiahe Road,Meixin Building,Xiamen,China
Beijing Mediking Biopharm Co., Ltd.

Contact:+86-10-89753524/81760121/81769521

Address:Hongxianghong Incubator, Beiqijia Town, Changping district, Beijing, China
NINGBO YINZHOU PRECISE COLOR CO.,LTD.

Contact:86-574-88139809 86-574-83033159

Address:Qiming Road,Yinzhou,Ningbo,China

Relevant to this article

Non-precious Mn_1.5Co_1.5O₄-FeN_:X/C nanocomposite as a synergistic catalyst for oxygen reduction in alkaline media

Doi:10.1039/c6ra15040c
(2016)
Photo-oxidation of some flavonoids with photochemically generated t-BuO^? radicals in a t-BuOH water system using a kinetic approach

Doi:10.1002/jccs.201700342
(2018)
Syntheses, thermal analyses, crystal structures and antimicrobial properties of silver(I)-saccharinate complexes with diverse diamine ligands

Doi:10.1016/j.ica.2010.02.013
(2010)
Nickel complexes as efficient catalysts in multicomponent synthesis of tetrahydropyridine derivatives

Doi:10.1080/00397911.2020.1803357
(2020)
Doi:10.1021/ja01139a501
(1952)
Elimination reactions of aryl phenylacetates promoted by R₂NH/R₂NH₂⁺ in 70 mol % MeCn(aq). Effect of the β-phenyl group on the ketene-forming transition state

Doi:10.1021/jo991473v
(2000)

Article Doi