Synthesis and Characterization of Niobium(IV) Porphyrins. Formation and Spectroscopic Properties of Dioxygen Adducts of Niobium(IV) Porphyrins

DOI: 10.1039/c39830001454

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 1454 - 1455 (1983)

Update date:2022-08-03

Topics:

Authors:

Richard, Philippe

Guilard, Roger

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

Article abstract of DOI:10.1039/c39830001454

The niobium(IV) porphyrins Nb^IV(X)2(por) have been prepared from Nb^V(X)3(por) ; irreversible oxygenati

Full text of DOI:10.1039/c39830001454

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

View Article Online

Products guided by the article

Product name:Nb(C₄H₂NC(C₆H₅)C₄H₂NC(C₆H₅)C₄H₂NC(C₆H₅)C₄H₂NC(C₆H₅))Br₂

Cas No:89087-23-0

R&D Labs maybe for 89087-23-0

Henan Yellow River New Material Technology Co.Ltd.

website:http://www.yellowriverchem.com

Contact:0086-373-7278760

Address:Chengguan Town, Yuanyang County
Wuxi Morality Chemical Co., Ltd(expird)

Contact:

Address:B/7F, 321th WuYun Rd, Wanda Plaza, Wuxi City, 214174, China
Beijing Stable Chemcial Co.ltd

Contact:86-10-63785052

Address:A1301 Technological Edifice. No.4 FuFeng Road,FengTai District, Beijing. China
Henan Techway Chemical Co.,Ltd.

website:http://www.techwaychem.com

Contact:+86-371-66380080

Address:No.27 Shunhe Road,
shanghai jinshan pharmaceutical Co.,Ltd

Contact:021-57363011，13681638167

Address:No. 7966 Tingfeng Road,Jinshan,Shanghai,China

Relevant to this article

Visible Light-Driven, Photocatalyst-Free Arbuzov-Like Reaction via Arylazo Sulfones

Doi:10.1002/adsc.201900953
(2019)
TRANSANNULAR CYCLISATION OF ISOGERMACRONE-EPOXIDES

Doi:10.1016/S0040-4020(01)91591-1
(1983)
Twin probes as a novel tool for the detection of single-nucleotide polymorphisms

Doi:10.1002/chem.200501526
(2006)
Solvent-free synthesis of heterocyclic thioureas using microwave technology

Doi:10.1002/jccs.200100013
(2001)
Nickel-Catalyzed Asymmetric Propargylic Amination of Propargylic Carbonates Bearing an Internal Alkyne Group

Doi:10.1021/acs.orglett.8b02325
(2018)
Stereoselective synthesis of concave spacers for long-range electron transfer models

Doi:10.1016/0040-4039(96)01299-3
(1996)

Article Doi