STRUCTURE OF OCTAETHYLPORPHYRIN N-OXIDE AND THE CHARACTERIZATION OF ITS NICKEL(II) AND COPPER(II) COMPLEXES

DOI: 10.1021/ja00294a033

Source and publish data:

Journal of the American Chemical Society p. 2393 - 2398 (1985)

Update date:2022-08-05

Topics:

Authors:

Balch, Alan L.

Chan, Yee Wai

Olmstead, Marilyn

Renner, Mark W.

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

Article abstract of DOI:10.1021/ja00294a033

The structure of octaethylporphyrin N-oxide has been determined by X-ray crystallography.It crystallizes in the triclic space group P1 (No. 2) with one molecule per unit cell of dimensions a= 7.612 (3) Angstroem, b= 9.740 (4) Angstroem, c=10.566 (4) Angst

Full text of DOI:10.1021/ja00294a033

Products guided by the article

Product name:nickel(II) octaethylporphyrin N-oxide

Cas No:95156-28-8

R&D Labs maybe for 95156-28-8

Laizhou City Laiyu Chemical CO.,Ltd

Contact:+86-535-2719337/2719339

Address:Chenggang road zhuyou laizhou City Shangdong China
Engineering Research Center of Pesticide, Heilongjiang Province

Contact:+86-451-86609001

Address:No.74 of Xuefu Road, Nangang District,
Nanjing Ruizhi Industry & Technologh Co.，Ltd.

Contact:+86-25-86808110

Address:441-4-A5,NO.12 Longzang Avenue,Yuhuatai District,210039,Nanjing
XZL BIO-TECHNOLOGY CO., LTD.

Contact:0086 533 2282832

Address:Zibo，Shandong
Weifang Arylchem Chemical Co., LTD

Contact:86-536-5217866

Address:Development Zone, Shouguang, Shandong Province

Relevant to this article

Aziridinium from N,N-dibenzyl serine methyl ester: Synthesis of enantiomerically pure β-amino and α,β-diamino esters

Doi:10.1021/ol060700u
(2006)
Facile and efficient synthesis of substituted 1,4-dithiafulvalenes from β-dicarbonyl compounds

Doi:10.1080/00397910701544646
(2007)
Molecularly imprinted cavities template the macrocyclization of tetrapeptides

Doi:10.1039/b813439a
(2008)
AN EFFICIENT SYNTHESIS OF ISOCARBACYCLIN STARTING FROM FURFURAL

Doi:10.1016/S0040-4039(01)91126-8
(1984)
A Convenient and Simple Method for the α'-Chlorination of α,β and Conjugated Ketones

Doi:10.1021/jo00181a033
(1984)
Application of the goldilocks effect to the design of potent and selective inhibitors of phenylethanolamine N-methyltransferase: Balancing pK_a and steric effects in the optimization of 3-methyl-1,2,3,4- tetrahydroisoquinoline inhibitors by β-fluorination

Doi:10.1021/jm051262k
(2006)

Article Doi