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Journal ArticleDOI

The formation of dinucsear μ-hydroxo-cobalt(III) complexes

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TLDR
The acidity constants of the deprotonated triaminocyclohexane have been determined with a rapid flow apparatus as mentioned in this paper, but it proved to be impossible to study the slow condensation to polynuclears quantitatively because of decomposition with production of ammonia.
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This article is published in Journal of Inorganic and Nuclear Chemistry.The article was published on 1971-07-01. It has received 27 citations till now. The article focuses on the topics: Triol & Stability constants of complexes.

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Journal ArticleDOI

Neue μ-Hydroxo-Übergangsmetallkomplexe, I. Darstellung und Struktur des trans-Diaqua-di-μ-hydroxo-bis[(1,4,7-triazacyclononan)cobalt(III)]-Kations; Kinetik und Mechanismus seiner Bildung

TL;DR: In this paper, a mechanism for the first hydroxo-bridge cleavage of the triply-bridged complex was proposed, involving cis-trans isomerization of 2 as the rate determining step.
Book ChapterDOI

Hydroxo-Bridged Complexes of Chromium (III), Cobalt (III), Rhodium (III), and Iridium (III)

TL;DR: In this paper, a review of the chemistry of hydroxo-bridged chromium(III), cobalt(III) and rhodium-III complexes is presented.
Journal ArticleDOI

Hydrolysis of the Organometallic Aqua Ion fac-Triaquatricarbonylrhenium(I). Mechanism, pKa, and Formation Constants of the Polynuclear Hydrolysis Products

TL;DR: In this paper, the hydrolytic pathways of the organometallic aqua ion [Re(CO)3(H2O)3]+ in aqueous media were investigated by means of potentiometric titration experiments.
Journal ArticleDOI

Structure and Reactivity of a Dinuclear Cobalt(III) Complex with a Bridging Phosphate Monoester

TL;DR: In this article, the bidentate monoester (2-H) was converted to tridentate inorganic phosphate (3) using the crystal structure of an analog of 2-H.
Journal ArticleDOI

Synthesis, Structure, and DNA Cleavage Properties of Copper(II) Complexes of 1,4,7-Triazacyclononane Ligands Featuring Pairs of Guanidine Pendants

TL;DR: Two new ligands, L(1) and L(2), have been prepared via N-functionalization of 1,4,7-triazacyclononane with pairs of ethyl- or propyl-guanidine pendants, suggesting some degree of cooperativity between the copper center and guanidinium pendants in the hydrolysis of the phosphate ester linkages of DNA.
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