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Reaction between 1,10-phenanthroline and platinum(II) compounds. I. Reaction in aqueous solution

Frank A. Palocsay, +1 more
- 01 Mar 1969 - 
- Vol. 8, Iss: 3, pp 524-528
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This article is published in Inorganic Chemistry.The article was published on 1969-03-01. It has received 82 citations till now. The article focuses on the topics: Phenanthroline & Platinum.

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2,2′-Bipyridinebutyldithiocarbamatoplatinum(II) and palladium(II) complexes: Synthesis, characterization, cytotoxicity, and rich DNA-binding studies

TL;DR: In the interaction studies between the Pt( II) and Pd(II) complexes with DNA, several binding and thermodynamic parameters have been determined, which may provide deeper insights into the mechanism of action of these types of complexes with nucleic acids.
Journal ArticleDOI

A Photochromic Platinum(II) Bis(alkynyl) Complex Containing a Versatile 5,6-Dithienyl-1,10-phenanthroline

TL;DR: A luminescent diarylethene-functionalized platinum(II) diimine bis(alkynyl) complex displays interesting photochromic behavior with successful photosensitization by excitation into the 3MLCT/LLCT excited state of this complex to trigger photocyclization.
Journal ArticleDOI

Complexes of platinum(II) or palladium(II) with 1,10-phenanthroline and amino acids

TL;DR: The amino acids complexes of [Pt(phen)(AA)]NO3·xH2O and [Pd(phen)Cl2] have been prepared by the interaction of palladium and platinum complexes with salts of amino acids in methanol and characterized by 1H NMR and IR spectroscopy as mentioned in this paper.
Journal ArticleDOI

Peptide targeting of platinum anti-cancer drugs.

TL;DR: Cell toxicity assay and competition assay revealed selective delivery and destruction of PC-3 cells using targeted Pt-peptide conjugates 7 and 8 significantly more than untargeted carboplatin, indicating selective activation of the CD13 receptors and delivery of the conjugate to CD13 positive cells.
Journal ArticleDOI

Chiral Platinum(II) Metallointercalators with Potent in vitro Cytotoxic Activity

TL;DR: Chiral discrimination for [Pt(S,S‐dach)(phen)](ClO4)2 over its R,R‐enantiomer was observed in all 13 cancer cell lines investigated and was more active than cisplatin in all cell lines tested.
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