Synthesis and vibrational spectra of lead(II) thiocyanate complexes

1976 ◽  
Vol 54 (8) ◽  
pp. 1189-1196 ◽  
Author(s):  
Anthony D. Baranyi ◽  
Ramesh Makhija ◽  
Mario Onyszchuk
Keyword(s):  
Raman Spectra ◽  
Vibrational Spectra ◽  
Infrared And Raman Spectra ◽  
Bidentate Ligands ◽  
Thiocyanate Complexes ◽  
Vibrational Bands ◽  
Thiocyanate Group

The preparation, properties, and vibrational spectra are reported for the following complexes of lead(II) thiocyanate with mono- and bidentate ligands: Pb(NCS)2•2py, Pb(NCS)2•phen, Pb(NCS)2•2phen, Pb(NCS)2•tmen, Pb(NCS)2•en, Pb(NCS)2•2en, Pb(NCS)2•2dmso, and Pb(NCS)2•2dma. Assignments are made for the ν(CN), ν(CS), and δ(NCS) vibrational bands of the thiocyanate group and the results are discussed in terms of the type of coordination of NCS with lead(II). Values are consistent with bridge-bonded and/or N-bonded thiocyanate. Infrared and Raman spectra of the complexes Pb(NCS)2•bipy and Pb(NCS)2•4tu are reexamined and new assignments are made which support bridge-bonded and/or N-bonded NCS contrary to previous reports of S-bonded NCS.

Low frequency infrared and Raman spectra of the N,N,N′,N′-tetramethyl-ethylenediamine adducts of the Group IIb dihalides

1970 ◽  
Vol 48 (1) ◽  
pp. 181-184 ◽  
Author(s):  
M. H. Abraham ◽  
F. W. Parrett
Keyword(s):  
Solid State ◽  
Raman Spectra ◽  
Vibrational Spectra ◽  
Low Frequency ◽  
Infrared And Raman Spectra ◽  
Cadmium Complexes ◽  
Mercury Complexes ◽  
Vibrational Bands

A study of the low frequency vibrational spectra of the complexes MX2.TMED (where M = Zn, Cd, Hg; X = Cl, Br, I; TMED = N,N,N′,N′-tetramethylethylenediamine suggests that in the solid state the zinc and mercury complexes are 4-coordinated but the cadmium complexes are all based on octahedral halogen bridged structures. Assignments of the vibrational bands are discussed.

Synthesis and vibrational spectra of some lead(II) halide adducts with O-, S-, and N-donor atom ligands

1976 ◽  
Vol 54 (21) ◽  
pp. 3430-3438 ◽  
Author(s):  
Ivor Wharf ◽  
Thor Gramstad ◽  
Ramesh Makhija ◽  
Mario Onyszchuk
Keyword(s):  
Raman Spectra ◽  
Vibrational Spectra ◽  
Vibrational Frequencies ◽  
Infrared And Raman Spectra ◽  
Donor Atom ◽  
Bidentate Ligands ◽  
Experimental Conditions ◽  
Monodentate Ligands

Lead(II) halides (PbX2 where X = Cl, Br, and I) formed five types of adducts with monodentate (L) and bidentate (LL) ligands: PbX2•L, PbX2•2L, 2PbX2•L, PbX2•LL, and PbX2•2LL, but not all halides and ligands produced each type. Monodentate ligands were dimethylsulphoxide, N,N-dimethylacetamide, N,N-dimethylthioacetamide, thioacetamide, 2,6-dimethyl-γ-pyrone, N-methyl-2-pyridone, N-methyl-2-pyrollidinone, thiourea, pyridine, piperidine, and aniline, while bidentate ligands were ethylenediamine, tetramethylethylenediamine, 1,10-phenanthroline, and 2,2′-bipyridine. Infrared and Raman spectra are reported together with ligand vibrational frequencies shifted by coordination. Under similar experimental conditions qualitative trends in acceptor and donor abilities appeared to be PbI2 > PbBr2 > PbCl2 and S-donors > O-donors, respectively.

Vibrational spectra of aquadioxotetra; peroxodivanadates(V) M2[V2O2(O2)4(H2O)]·xH2O (M = N(CH3)4, Cs)

1990 ◽  
Vol 55 (6) ◽  
pp. 1485-1490 ◽  
Author(s):  
Peter Schwendt ◽  
Milan Sýkora
Keyword(s):  
Raman Spectra ◽  
Vibrational Spectra ◽  
Normal Coordinate Analysis ◽  
Force Constants ◽  
Infrared And Raman Spectra ◽  
Empirical Correlations ◽  
Normal Coordinate ◽  
Bond Lengths ◽  
Stretching Vibrations

The infrared and Raman spectra of M2[V2O2(O2)4(H2O)]·xH2O and M2[V2O2(O2)4(D2O)]·xD2O (M = N(CH3)4, Cs) were measured. In the region of the vanadium-oxygen stretching vibrations, the spectra were interpreted based on normal coordinate analysis, employing empirical correlations between the bond lengths and force constants.

Synthesis, crystal and molecular structure, and vibrational spectra of the complex (COOH)2•2H2O•18-crown-6

1986 ◽  
Vol 64 (1) ◽  
pp. 142-147 ◽  
Author(s):  
Suzanne Deguire ◽  
François Brisse ◽  
Jacques Ouellet ◽  
Rodrigue Savoie
Keyword(s):  
Molecular Structure ◽  
Hydrogen Bonds ◽  
Oxalic Acid ◽  
Raman Spectra ◽  
Vibrational Spectra ◽  
Crystal And Molecular Structure ◽  
Unit Cell ◽  
Infrared And Raman Spectra ◽  
O 18 ◽  
Stoichiometric Complex

A stoichiometric complex of formula (COOH)2•2H2O•18-crown-6 has been obtained from oxalic acid and the macrocyclic polyether 18-crown-6. The crystals of the complex have a monoclinic unit cell and belong to the P21/c space group. The components in the adduct are linked through hydrogen bonds in a polymer-like fashion: -crown–H2O–HOOCCOOH–OH2–crown–, where the oxalic acid molecules are present in two distinct disordered orientations. The infrared and Raman spectra of the complex are also reported and interpreted.

Schwingungsspektren und Kraftkonstanten der Hexacyano-Komplexe des Mangan(I), Technetium(I) und Rhenium(I) / Vibrational Spectra and Force Constants of the Hexacyano Complexes of Mangan(l), Technicium(I) and Rhenium(l)

1972 ◽  
Vol 27 (8-9) ◽  
pp. 1193-1196 ◽  
Author(s):  
W. Krasser ◽  
K. Schwochau
Keyword(s):  
Force Field ◽  
Raman Spectra ◽  
Vibrational Spectra ◽  
Point Group ◽  
Force Constants ◽  
Irreducible Representations ◽  
Infrared And Raman Spectra ◽  
Valence Force ◽  
Valence Force Field ◽  
Complex Salts

The infrared and Raman spectra of the complex salts K5[Mn(CN)6], K5[Tc(CN)6] and K5[Re(CN)s] have been recorded in the range from 4000 to 40 cm-1. All expected fundamental vibrations have been observed and could be assigned to the irreducible representations of the sym­metry point group Oh . The calculation of the force constants is based on the concept of the generalized valence force field. The low CN-valence force constants indicate the relatively strong Π-bonding character of the metal carbon bond, which is especially pronounced for K5[Tc(CN)6).

Kristallstruktur und Schwingungsspektren des Di-Blei-Hexaselenohypodiphosphates Pb2P2Se6 / Crystal Structure and Vibrational Spectra of Pb2P2Se6

1984 ◽  
Vol 39 (4) ◽  
pp. 357-361 ◽  
Author(s):  
Robert Becker ◽  
Wolfgang Brockner ◽  
Herbert Schäfer
Keyword(s):  
Crystal Structure ◽  
Raman Spectra ◽  
Vibrational Spectra ◽  
Title Compound ◽  
Far Infrared ◽  
Infrared And Raman Spectra ◽  
Monoclinic System ◽  
Space Group ◽  
Lattice Constants

Pb2P2Se6 crystallizes in the monoclinic system, space group Pn (No. 13) with the lattice constantsa = 974.2 (4) pm. b = 766.2 (3) pm. c = 689.8 (3) pm, β=91.44(5)°.The title compound is isotypic to the homologous Pb2P2S6. In the structure there are discrete P2Se4-6 anions.Far infrared, infrared and Raman spectra of this compound have been recorded. The observed frequencies are assigned on the basis of P2Se4-6 units with C2h symmetry in the crystal. DTA-data have been determined and interpreted.

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