Heterotridentate organodiphosphines in Pt(η3-P1X1P2)(Y) (X1 = B, S, or Si) and Pt(η3-P1P2Si1)(Y) derivatives-structural aspects

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Milan Melník ◽  
Peter Mikuš
Keyword(s):  
Structural Data ◽  
Covalent Radius ◽  
Planar Geometry ◽  
Trans Influence ◽  
Square Planar ◽  
Structural Aspects

Abstract This review covers almost 30 Pt(II) complexes of the composition Pt(η3-P1X1P2)(Y), (X1 = BL, SL, or SiL), (Y = H, OL, NL, CL, Cl, PL, or I) and Pt(η3-P1P2Si1)(CH3). Heterotridentate ligands form six types of metallocyclic rings: P1CNB1NCP2, P1C2S1C2P2, P1C2Si1C2P2, (most common), P1CNSi1NCP2, and P1C3Si1C3P2 with common B1, S1, or Si1 atoms. In P1C2P2C3Si1 the P2 atom is common. The structural data (Pt–L, L–Pt–L) are analyzed and discussed with an attention to the distortion of a square-planar geometry about Pt(II) atoms as well as trans-influence. The sum of Pt–L(x4) bond distances growing with covalent radius of the X1 and Y atoms.

scholarly journals Variable combinations of organophosphines in PtP3X derivatives: Structural aspects

2020 ◽  
Vol 44 (1) ◽  
pp. 12-21
Author(s):  
Milan Melník ◽  
Peter Mikuš
Keyword(s):  
Structural Parameters ◽  
Covalent Radius ◽  
Planar Geometry ◽  
Trans Influence ◽  
Square Planar ◽  
Structural Aspects

Abstract This review covers over fifty Pt (II) complexes of the compositions PtP3X (X = H, OL, NL, BL, Cl, SL, Br, or I). These complexes crystallized in three crystal classes: monoclinic (23 examples) triclinic (17 examples) and orthorhombic (11 examples). The PtP3Cl is most common with 23 examples. There are variable combinations of organophosphines monodentate – P; bidentate- P,P; P,N; P,B; and tridentate – P,P,P; P,O,P; P,N,P; and P,S,P. The structural parameters (Pt–L, L–Pt–L) are analyzed and discussed with an attention to the distortion of a square-planar geometry about the Pt (II) atoms as well as of trans-influence. The sums of Pt–L (x4) bond distances growing with covalent radius of the X-atoms.

Square Planar Complexes of Cu(II) with an N2O Donor Set of a New Schiff Base Ligand: Synthesis and Structural Aspects

2004 ◽  
Vol 59 (6) ◽  
pp. 655-660 ◽  
Author(s):  
Pritha Talukder ◽  
Amitabha Datta ◽  
Samiran Mitra ◽  
Georgina Rosair
Keyword(s):  
Schiff Base ◽  
Crystal Structures ◽  
Schiff Base Ligand ◽  
Condensation Product ◽  
Planar Geometry ◽  
Square Planar ◽  
Square Planar Complexes ◽  
Tridentate Schiff Base ◽  
Copper Centre ◽  
Structural Aspects

The title compounds, [Cu(C16H23N2O)SCN] (1) and [Cu(C16H23N2O)N3] (2), containing a tridentate Schiff base ligand, which is the 1:1 condensation product of benzoylacetone and 2- diethylaminoethylamine, have been synthesised and their crystal structures determined. The structure of 1 is based on a four coordinate copper centre with square-planar geometry formed by the N2O donor set of the Schiff base and an N atom of the thiocyanate anion. A similar arrangement occurs in 2 with the N2O donor set of the Schiff base and an N atom of the azide anion. The Cu-N and Cu-O distances are 1.924(8), 2.073(8), 1.927(9) and 1.910(6)Å , for 1 and 1.960(4), 2.050(4), 1.935(4) and 1.907(3) for 2, respectively.

Heterotridentate organodiphosphines in Pt(η3–P1X1P2)(Y) derivatives-structural aspects

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Milan Melník ◽  
Peter Mikuš
Keyword(s):  
Central Atom ◽  
Donor Ligands ◽  
Planar Geometry ◽  
Cooperative Effects ◽  
Square Planar ◽  
Structural Aspects ◽  
Chelate Rings

Abstract This review covers over 30 examples of monomeric Pt(II) complexes of the types: Pt(η3–P1O1P2)(Y) (Y = PL, CL, OL), Pt(η3–P1N1P2)(Y) (Y = H, NL, CL, Cl, PL) and Pt(η3–P1P2N1)(Y) (Y = Cl). The heterotridentate donor ligands create 11 types of a couple chelate rings with common central atom O1 (η3–P1O1P2), N1 (η3–P1N1P2) and P2 (η3–P1P2N1). The most frequent is P1C2N1C2P2. Some cooperative effects between chelate rings and Y donor ligands were found and discussed. A degree of distortions of square-planar geometry about Pt(II) were also calculated.

Distortion isomers of cis-PtP2X2 and cis-PtP2XY derivatives – structural aspects

2020 ◽  
Vol 0 (0) ◽  
Author(s):  
Milan Melník ◽  
Peter Mikuš
Keyword(s):  
Crystal Packing ◽  
Structural Parameters ◽  
Coordination Complexes ◽  
Mean Value ◽  
Covalent Radius ◽  
Mean Values ◽  
Trans Influence ◽  
Coordination Spheres ◽  
The Mean ◽  
Structural Aspects

AbstractIn this review, the structural parameters of distortion isomers of cis-monomeric Pt(II) coordination complexes with inner coordination spheres: Pt(PL)2X2 (X = OL, NL, SL, Br, I); Pt(PL)2(η2-X2L) (X = O2L, N2L, S2L, OSL, NSL, NSeL); Pt(η2-P2L)X2 (X = Br, I); Pt(η2-P2L)(η2-X2L) (X = O2L, OSL, NSL); Pt(η2-P2L)(NL)(Cl) and Pt(PL)(η2-P,SiL)(H) are analyzed. None of the distortion isomers with cis-configuration has a trans-partner. The distortion isomers differ mostly by the degree of distortion in the Pt-L and L-Pt-L angles. Some of the isomers also differ by crystal packing. The total mean values of Pt-P (monodentate) and Pt-P (bidentate) bond distances are 2.279 Å and 2.244 Å, respectively. The mean value of Pt-P (monodentate) (trans to H¯) of 2.320 Å is the highest one because of higher trans-influence of H¯ over PP3. The total mean values of Pt-X (trans to P) elongate quite well with the covalent radius of the X in the sequence: 1.57 Å (X = H) < 2.062 Å (O2L) < 2.095 Å (OL) < 2.108 Å (NL) < 2.154 Å (N2L) < 2.329 Å (Cl) < 2.342 Å (S2L) < 2.347 Å (SL) < 2.480 Å (Br) < 2.616 Å (I).

scholarly journals Tetradentate organophosphines in Pt(η4–A4L) (A = P4, P3Si, P2X2 (X2 = N2, S2, C2), PX3 (X3 = N3, N2O)): Structural aspects

2021 ◽  
Vol 44 (1) ◽  
pp. 270-280
Author(s):  
Milan Melník ◽  
Peter Mikuš
Keyword(s):  
Structural Characterization ◽  
Platinum Complexes ◽  
Planar Geometry ◽  
Bond Angles ◽  
Pyramidal Geometry ◽  
Tetradentate Ligands ◽  
Square Planar ◽  
Structural Aspects

Abstract We report herein structural characterization of monomeric platinum complexes of the composition: Pt(η4–P4L), Pt(η4–P3SiL), Pt(η4–P2N2L), Pt(η4–P2S2L), Pt(η4–P2C2L), Pt(η4–PN3L), and Pt(η4–PN2OL). The tetradentate ligands with 10-, 11-, 12-, 14-, and 16-membered macrocycles create a variety of chelate bond angles. A distorted square-planar geometry about Pt(II) atoms with cis–configuration by far prevail. There is an example Pt(η4–P3SiL) in which the respective donor atoms build up a trigonal-pyramidal geometry about Pt(II) atom.

New Platinum (II) Ternary Complexes of Formamidine and Pyrophosphate: Synthesis, Characterization and DFT Calculations and In vitro Cytotoxicity

2020 ◽  
Vol 23 (7) ◽  
pp. 611-623
Author(s):  
Ahmed A. Soliman ◽  
Fawzy A. Attaby ◽  
Othman I. Alajrawy ◽  
Azza A.A. Abou-hussein ◽  
Wolfgang Linert
Keyword(s):  
Cell Line ◽  
Cancer Cell ◽  
Theoretical Calculations ◽  
Thermal Analyses ◽  
Cancer Cell Line ◽  
Cellular Growth ◽  
Planar Geometry ◽  
Square Planar ◽  
Vis Spectroscopy

Aim and Objective: Platinum (II) and platinum (IV) of pyrophosphate complexes have been prepared and characterized to discover their potential as antitumor drugs. This study was conducted to prepare and characterize new ternary platinum (II) complexes with formamidine and pyrophosphate as an antitumor candidate. Materials and Methods: The complexes have been characterized by mass, infrared, UV-Vis. spectroscopy, elemental analysis, magnetic susceptibility, thermal analyses, and theoretical calculations. They have been tested for their cytotoxicity, which was carried out using the fastcolorimetric assay for cellular growth and survival against MCF-7 (breast cancer cell line), HCT- 116 (colon carcinoma cell line), and HepG-2 (hepatocellular cancer cell line). Results: All complexes are diamagnetic, and the electronic spectral data displayed the bands due to square planar Pt(II) complexes. The optimized complexes structures (1-4) indicated a distorted square planar geometry where O-Pt-O and N-Pt-N bond angles were 82.04°-96.44°, respectively. Conclusion: The complexes showed noticeable cytotoxicity and are considered as promising antitumor candidates for further applications.

The trans influence of F, Cl, Br and I ligands in a series of square-planar Pd(II) complexes. Relative affinities of halide anions for the metal centre in trans-[(Ph3P)2Pd(Ph)X]

1998 ◽  
Vol 280 (1-2) ◽  
pp. 87-98 ◽  
Author(s):  
Jeffrey P. Flemming ◽  
Mark C. Pilon ◽  
Oleg Ya. Borbulevitch ◽  
Mikhail Yu. Antipin ◽  
Vladimir V. Grushin
Keyword(s):  
Metal Centre ◽  
Trans Influence ◽  
Halide Anions ◽  
Square Planar ◽  
In Trans

{1-[2-(Methylamino)ethyliminomethyl]naphthalen-2-olato}thiocyanatocopper(II)

2006 ◽  
Vol 62 (7) ◽  
pp. m1533-m1534 ◽  
Author(s):  
Han-Na Hou
Keyword(s):  
Schiff Base ◽  
Schiff Base Ligand ◽  
Title Compound ◽  
Planar Geometry ◽  
Asymmetric Unit ◽  
Thiocyanate Anion ◽  
Square Planar

The title compound, [Cu(C14H15N2O)(NCS)], is a mononuclear copper(II) complex, with two molecules in the asymmetric unit. The CuII ion is coordinated by one O and two N atoms of a Schiff base ligand, and by one N atom of a thiocyanate anion, forming a square-planar geometry.

scholarly journals Crystal structures of [Mn(bdc)(Hspar)2(H2O)0.25]·2H2O containing MnO6+1capped trigonal prisms and [Cu(Hspar)2](bdc)·2H2O containing CuO4squares (Hspar = sparfloxacin and bdc = benzene-1,4-dicarboxylate)

2016 ◽  
Vol 72 (1) ◽  
pp. 96-101
Author(s):  
Zhe An ◽  
Jing Gao ◽  
William T. A. Harrison
Keyword(s):  
Hydrogen Bonds ◽  
Water Molecule ◽  
Crystal Structures ◽  
Metal Ion ◽  
Three Dimensional ◽  
Trigonal Prism ◽  
Planar Geometry ◽  
Cationic Complex ◽  
Counter Ion ◽  
Square Planar

The syntheses and crystal structures of 0.25-aqua(benzene-1,4-dicarboxylato-κ2O,O′)bis(sparfloxacin-κ2O,O′)manganese(II) dihydrate, [Mn(C8H4O4)(C19H22F2N4O3)2(H2O)0.25]·2H2O or [Mn(bdc)(Hspar)2(H2O)0.25]·2H2O, (I), and bis(sparfloxacin-κ2O,O′)copper(II) benzene-1,4-dicarboxylate dihydrate, [Cu(C19H22F2N4O3)2](C8H4O4)·2H2O or [Cu(Hspar)2](bdc)·2H2O, (II), are reported (Hspar = sparfloxacin and bdc = benzene-1,4-dicarboxylate). The Mn2+ion in (I) is coordinated by twoO,O′-bidentate Hspar neutral molecules (which exist as zwitterions) and anO,O′-bidentate bdc dianion to generate a distorted MnO6trigonal prism. A very long bond [2.580 (12) Å] from the Mn2+ion to a 0.25-occupied water molecule projects through a square face of the prism. In (II), the Cu2+ion lies on a crystallographic inversion centre and a CuO4square-planar geometry arises from its coordination by twoO,O′-bidentate Hspar molecules. The bdc dianion acts as a counter-ion to the cationic complex and does not bond to the metal ion. The Hspar ligands in both (I) and (II) feature intramolecular N—H...O hydrogen bonds, which closeS(6) rings. In the crystals of both (I) and (II), the components are linked by N—H...O, O—H...O and C—H...O hydrogen bonds, generating three-dimensional networks.

scholarly journals Unsymmetrical Schiff Base Functionalized as Monobasic Tridentate Ligand on Complexation with Some Transition Metal Ions

2012 ◽  
Vol 9 (2) ◽  
pp. 532-544
Author(s):  
Bibhesh K. Singh ◽  
Narendar Bhojak ◽  
Anant Prakash
Keyword(s):  
Schiff Base ◽  
Transition Metal Ions ◽  
Tridentate Ligand ◽  
Planar Geometry ◽  
Physico Chemical ◽  
Square Planar ◽  
Unsymmetrical Schiff Base ◽  
Mm2 Calculations ◽  
Microbial Potential

Cu(II), Co(II), Ni(II) and Mn(II) complexes of Schiff base derived from 2-aminophenol and pyrrole-2- carbaldehyde have been prepared. The complexes are formed by coordination of N and O atoms of the ligand. Their structures were characterized by physico-chemical and spectroscopic methods. Molecular structure of the complexes has been optimized by MM2 calculations and suggests a tetrahedral/ square planar geometry. The bio-efficacy of the ligand and their complexes has been examined against the growth of bacteriain vitroto evaluate their anti-microbial potential.

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