Transition-metal Complexes of Pyrrole Pigments. XIX. Electrochemical and Coordination Behaviors of (5,10,15,20-Tetraphenylporphinato)niobium(V) Complexes

DOI: 10.1246/bcsj.54.452

Source and publish data:

Bulletin of the Chemical Society of Japan p. 452 - 457 (1981)

Update date:2022-09-26

Topics:

Authors:

Matsuda, Yoshihisa

Yamada, Sunao

Goto, Takashi

Murakami, Yukito

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

Article abstract of DOI:10.1246/bcsj.54.452

The redox chemistry of acetato(5,10,15,20-tetraphenylporphinato)oxoniobium(V) (1) was investigated in dichloromethane by means of cyclic voltammetry and controlled potential electrolysis.One-electron reduction potentials were observed at -0.89, -1.05, and

Full text of DOI:10.1246/bcsj.54.452

Products guided by the article

Product name:acetato(5,10,15,20-tetraphenylporphinato)oxoniobium(V)

Cas No:57665-75-5

R&D Labs maybe for 57665-75-5

Wuhan Hanye Chemical New Material Co.,Ltd

Contact:+86-27-85308141

Address:LiuDian, Panlongcheng Economic Development Zone, HuangPi district, Wuhan, Hubei 430311 P.R.China
SuZhou Yacoo Science Co., Ltd

Contact:86-512-87182055

Address:No.128 Fangzhou Rd, Suzhou Industrial Park, China, 215125, China
zhangjiagang bonded areas banggao co;ltd

website:http://www.shunchangchem.com

Contact:0086-13921972933

Address:Dongsha Chemical Zone.Zhangjiagang, Jiangsu Province
Anhui Asahikasei Chemical Co., Ltd

Contact:86-551-4259770

Address:No. 88 Linquan Road Hefei Anhui China
ZHEJIANG JIANYE CHEMICAL CO.,LTD.

Contact:86-571-64149273,64149234

Address:No. 48, Fuxi Road, Meicheng Town

Relevant to this article

Doi:10.1021/ja00421a028
(1976)
Stereoselective total synthesis of copa and ylango sesquiterpenoids: (-) Copacamphene, (-) Cyclocopacamphene, (+) Sativene, (+) Cyclosativene

Doi:10.1139/v75-404
(1975)
Discovery of selective phosphonamide-based inhibitors of tumor necrosis factor-α converting enzyme (TACE)

Doi:10.1016/S0960-894X(03)00292-0
(2003)
Synthesis of Oligosaccharide Fragments of Mannosylated Lipoarabinomannan Appropriately Functionalized for Neoglycoconjugate Preparation

Doi:10.1081/CAR-120025322
(2003)
Stereochemical studies. XXXIX. A novel method for the preparation of optically active aldehydes. Syntheses of optically active (R)(+)-α-cyclocitral, (S) (+)-dehydrovomifoliol, and (S) (+)-abscisic acid

Doi:10.1248/cpb.24.315
(1976)
Allylic and Homoallylic Exciton Coupled CD: A Sensitive Method for Determining the Absoute Stereochemistry of Natural Products

Doi:10.1021/jo00116a048
(1995)

Article Doi