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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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Poly beta-diketones : Prime ligands to generate supramolecular metalloclusters

TL;DR: In this article, the authors present a compendium of all the relevant ligands made that have been employed in this context, summarizing the synthetic routes to their preparation and discuss the synthesis, structure and some aspects of the coordination compounds that have resulted from their reactions with various metals.
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High-spin α low-spin transition in [Fe(NCS)2(4,4′-bis-1,2,4-triazole)2](H2O). X-ray crystal structure and magnetic, mössbauer and EPR properties

TL;DR: In this paper, the Mossbauer ligand-field spectra and magnetic behaviour of both the hydrated and non-hydrated compounds are discussed, and the spin transition has been followed by EPR measurements with the aid of traces of Cu2+ ions which could be substituted for Fe2+ in the tetragonal structure.
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Chemical Modification of a Bridging Ligand Inside a Metal–Organic Framework while Maintaining the 3D Structure

TL;DR: In this paper, a new metal-organic framework with amino groups situated inside the pores has been synthesized, which has been modified by post-synthesis with two different functionalities, showing that it is possible to transform the cavities of a MOF without modifying its original 3D structure.
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Formation and Repair of Cisplatin-induced Adducts to DNA in Cultured Normal and Repair-deficient Human Fibroblasts

TL;DR: The formation and repair of cisplatin [cis-PtCl2(NH3)2] adducts in the DNA of cultured normal and repair-deficient human fibroblasts are presented in relation to cell survival after cis platin treatment.
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The hydrolysis of the anti-cancer ruthenium complex NAMI-A affects its DNA binding and antimetastatic activity: an NMR evaluation.

TL;DR: It is proposed that the selective antimetastatic activity of NAMI-A during in vivo experiments can be attributed to its hydrolysed species, which apparently are easier taken up by the metGM cells, showing intracellular ruthenium concentrations one order of magnitude greater than those of intact NAMI