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Jan Reedijk

Researcher at Leiden University

Publications -  1165
Citations -  45902

Jan Reedijk is an academic researcher from Leiden University. The author has contributed to research in topics: Ligand & Crystal structure. The author has an hindex of 80, co-authored 1163 publications receiving 43747 citations. Previous affiliations of Jan Reedijk include Nagoya City University & University of Münster.

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Spectro-electrochemical and DFT studies of a planar Cu(II)-phenolate complex active in the aerobic oxidation of primary alcohols

TL;DR: In this article, a biomimetic model of the enzyme galactose oxidase (GOase) is described as a square-planar compound, which is capable of stoichiometric aerobic oxidation of activated primary alcohols in acetonitrile/water to the corresponding aldehydes.
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Transition-metal norharmane compounds as possible cytotoxic agents: new insights based on a coordination chemistry perspective

TL;DR: The new first-row transition-metal compounds with the ligand norharmane showed clear cell growth inhibitory effects in two different cancer cell lines in vitro, with the copper and zinc complexes being the most toxic and in fact almost comparable to cisplatin.
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N-donor ligand coordination polymers of CuII, ZnII, and CdII obtained at elevated temperature and pressure

TL;DR: In this paper, the reaction of copper(II), Zinc (II), and Cadmium(II) nitrate with 2,4,6-tris(dipyridin-2-ylamino)-1,3,5-triazine (dpyatriz) at elevated temperature and pressure lead to new 1D coordination polymers which exhibit solid-state structures significantly different from those obtained at room temperature and atmospheric pressure.
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A Square-Planar Nickel(II) Monoradical Complex with a Bis(salicylidene) diamine Ligand (Eur. J. Inorg. Chem. 5/2007)

TL;DR: Reedijk et al. as discussed by the authors showed the result of the electrochemical oxidation of a square-planar nickel(II) complex, showing that the metal remains largely unchanged, and the phenoxy ligand is oxidized to the depicted radical cation.
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Formation and structure of reaction products of cis-PtCl2(NH3)2 with d(ApG) and/or d(GpA) in di-, tri- and penta-nucleotides. Preference for GpA chelation over ApG chelation.

TL;DR: The reaction products of cis-PtCl2(NH)3)2 with several deoxyribonucleotides containing d( ApG) and/or d(GpA) have been studied and the intra-molecular competition between the formation of the d(ApG) or the d-pA chelates could be studied.