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Showing papers by "Milan Melnik published in 2017"


Journal ArticleDOI
TL;DR: More than 100 monomeric derivatives in which the Pt(II) atom is in a distorted square planar environment with inner coordination spheres of PtP2X2 (X=Br, I, Se, Si, I or Te) are reviewed in this article.
Abstract: Abstract This review includes more than 100 monomeric derivatives in which the Pt(II) atom is in a distorted square planar environment with inner coordination spheres of PtP2X2 (X=Br, I, Se, Si or Te). The P-donor ligands are organomonophosphanes. These complexes crystallize in three crystal systems: orthorhombic (5.7%), triclinic (37.5%) and monoclinic (56.8%). The X-donor ligands are mono- Br, Se, Si, I or Te or bi- Se, Si, Te, dentate. The chelating ligands form a wide variety of three-, four-, five-, six-, and even seven-membered metallocycles. There are at least two types of isomerism: cis-trans and distortion. Several relationships were found and are discussed.

3 citations


Journal ArticleDOI
TL;DR: In this paper, the structural parameters of 20 mononuclear Pt(II) coordination complexes with an inner coordination sphere of PtPX3 (X=O, N, Cl, S, I or Te) are summarized and analyzed.
Abstract: Abstract In this review the structural parameters of 20 mononuclear Pt(II) coordination complexes with an inner coordination sphere of PtPX3 (X=O, N, Cl, S, I or Te) are summarized and analyzed. The P-donor ligands are organomonophosphines. These complexes are crystallized in two crystal systems: monoclinic and triclinic (each ×10). The X-donor ligands are mono-: O, N, C, S, or I; bi-: O/O; N/N; S/S and ter-: N/N/N; S/S/S, or Te/Te/Te-dentate. The mean Pt-X (homo-trans) bond distances elongate in the order: 2.00 Å (O)<2.02 Å (N)<2.302 Å (Cl)<2.325 Å (S)<2.590 Å (Te)<2.638 Å (I). The mean Pt-P (trans to X) bond distances are in the order: 2.218 Å (X=N)<2.230 Å (Cl)<2.233 Å (O)<2.258 Å (I)<2.287 Å (S)<2.308 Å (Te). The chelating ligands form four-, five-, and six-membered metallocyclic rings.

1 citations