Square planar metal complexes of thiosemicarbazide

1968 ◽  
Vol 46 (20) ◽  
pp. 3241-3247 ◽  
Author(s):  
Roland A. Haines ◽  
Kenneth K. W. Sun

Square planar complexes of nickel(II), palladium(II), and platinum(II) containing the ligand thiosemicarbazide (Htsc) have been studied. Both the cis and trans geometric isomers have been obtained for the complexes with the general formula [M(tsc)2]2+ while only the trans isomer was obtained for the neutral species [M(tsc)2]. Infrared and diffuse reflectance spectra are presented and discussed with reference to the stereochemistry of the complexes.

2013 ◽  
Vol 10 (3) ◽  
pp. 650-657
Author(s):  
Baghdad Science Journal

This research involves the preparation of new ligands 1,1,2,2- tetrakis (sodium acetate thio)ethylene(L1) and 1,1,2- tris(sodiumacetatethio) ethylene(L2), through the reaction of disodium thioglycolate) with tetra chloro ethylene or tri chloro ethylene in (1:4) or (1:3) moler ratio . Homodinucliar complexes of general formlu [M2(L1)] and [M2(L2)ClH2O] , when M= Co(II), Ni(II), Cu (II) and Zn(II) also mono nuclear complexes of general formula [M(L2)] . The prepared complexes were characterized using spectral method (UV/Visible/ IR) , metal content analysis , magnetic and atomic measurements . The spectral and magnetic measurement indicats that some complexes have tetrahedral or square planar complexes environtment .


1974 ◽  
Vol 27 (12) ◽  
pp. 2557 ◽  
Author(s):  
Gowda NM Nanje ◽  
GKN Reddy

A series of square-planar complexes of platinum and palladium of the general formula MX2L2, where M is Pt or Pd, X is Cl, Br or I, and L is EtPh2As or PrPh2As, have been made. The platinum complexes (X = Cl or Br) react with the corresponding halogens to give octahedral complexes of the type PtX4L2. The dichloro complexes of platinum(II) react with carbon monoxide to give carbonyl complexes of the type trans- [PtCl(CO)L2]+. Structures have been assigned to all the compounds.


1971 ◽  
Vol 24 (10) ◽  
pp. 1993 ◽  
Author(s):  
DE Scaife

Nuclear quadrupole resonance for the 35Cl nucleus has been observed in some chloro complexes of divalent copper. Square-planar complexes each show two resonance lines, with the following frequencies (at 77�K): (CH3NH3)2CuCl4, 10.780, 12.157 MHz; (C2H5NH3)2CuCl4, 10.817, 12.074 MHz; (enH2)CuCl4, 10.271, 11.901 MHz; and (C3H7NH3)2CuCl4 at 223�K, 11.290 and 11.781 MHz. NH4CuCl3, containing dimeric Cu2Cl62- units, has resonances, at 77�K, at 11.907, 11.993, and 12.448 MHz. The trigonal pyramidal anion in Co(NH3)6CuCl5 has two resonances at 9.642 and 10.352 MHz at 77�K. ��� These results are compared with previous results for copper chloro complexes, and the implications of covalent bonding are discussed. In particular, it is suggested that the long-bond interaction between units in square-planar complexes amounts to 7-16% of the bonding interaction within the units.


1987 ◽  
Vol 65 (4) ◽  
pp. 798-803 ◽  
Author(s):  
René T. Boeré ◽  
David E. Esser ◽  
Christopher J. Willis ◽  
Douglas W. Stephan ◽  
Taras W. Obal

The compound 2-thioanisole-1,1,1,3,3,3-hexafluoro-2-propanol, CH3S—C6H4—C(CF3)2OH, HL2, has been prepared, and shown to act (in the ionized form) as a hybrid, chelating, ligand. Neutral bis-complexes M(L2)2 are formed with Pd2+ and Pt2+; the former reacts with PdCl42− to give the Cl-bridged dinuclear complex (L2)Pd(μ-Cl)2Pd(L2), which may in turn be cleaved by PPh3 or PPh2Me to give PdCl(L2)(PR3).A complete structural determination has been made for PdCl(L2)(PPh2Me); C23H20ClF6OPPdS. Crystals are monoclinic, space group P21/n, a = 15.526(5), b = 12.966(9), c = 12.900(8) Å, β = 101.84°, V = 2542(2) Å3, Z = 4. Least-squares refinement on F of 198 variables using 2801 observations converged at R1 = 0.0434, R2 = 0.0559. The complex consists of discrete square-planar molecules with phosphine and alkoxide trans-disposed. Bond lengths are Pd—O, 2.053(3); Pd—P, 2.242(1); Pd—Cl, 2.323(2); Pd—S, 2.252(2) Å. In the six-membered chelate ring, all atoms with the exception of Pd are close to coplanarity; there is a dihedral angle of 127.9° between the O—Pd—S plane and that of the aromatic ring.Multinuclear nmr measurements are used to show that both cis- and trans-forms of complexes PdCl(L2)(PR3) are present in solution, with inversion at coordinated sulfur occurring much more rapidly in the latter.


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