G. I. Zharkova

Structure and properties of terbium(III) dipivaloylmethanate and its adducts with Bipy and Phen

The complex of terbium(III) with dipivaloylmethane (2,2,6,6-tetramethylheptane-3,5-dione = Htmhd) [Tb(tmhd)3]2 (1) and two its adducts with bipyridyl (Bipy) and phenanthroline (Tb(tmhd)3·Bipy (2) and Tb(tmhd)3·Phen (3)) are synthesized and analyzed by single crystal X-ray diffraction. The crystals of [Tb(tmhd)3]2 (1) belong to the monoclinic crystal system: P21/n space group, a = 12.2238(2) Å, b = 27.6369(5) Å, c = 21.8740(4) Å, β = 105.146(1)°, V = 7133.0(2)Å3, Z = 4; the crystals of Tb(tmhd)3·Bipy (2) and Tb(tmhd)3·Phen (3) belong to the triclinic crystal system with unit cell parameters: (2)

Packing of complexes and intermolecular interactions in the crystals of volatile palladium(II) β-diketonates. crystal structure of palladium(II) benzoyltrifluoroacetonate

P\bar 1

Crystal structure of adducts of copper(II) acetylacetonate and hexafluoroacetylacetonate with 4-aminopyridine

space group, a = 11.0554(6) Å, b = 12.2761(7) Å, c = 17.7096(8) Å, α = 77.457(2)°, β = 85.557(2)°, γ = 69.659(2)°, V = 2199.8(2) Å3, Z = 2; (3)

Vapour Pressure and Thermoanalytical Study of Diethyldithiocarbamates of Platinum Metals

P\bar 1

Crystal structure of volatile pyridine adducts of trimethylplatinum(IV) β-diketonates

space group, a = 10.8814(3) Å, b = 12.2852(4) Å, c = 18.3590(6) Å, α = 80.463(1)°, β = 87.587(1)°, γ = 68.640(1)°, V = 2253.6(1) Å3, Z = 2. The structures of the complexes are molecular and involve isolated [Tb2(tmhd)6] (1), Tb(tmhd)3·Bipy (2), and Tb(tmhd)3·Phen (3) molecules. The thermal properties of the obtained terbium complexes are studied by TG-DTA.

Low-Temperature VUV-Stimulated MO CVD Process of Palladium Layer Deposition

This paper reports on the synthesis and crystal structure analysis of palladium(II) bis-(trans-benzoyltrifluoroacetonate). Crystal data for PdO4C20F6H12:a= 4.748, b = 22.237, c = 9.410 Å, P = 105.44° Z = 2, space group P21/c, dcalc. = 1.86 g/cm . CAD-4 diffmctometer(MoKa), heavy atom method, R = 0.041 for 986 reflections. The structure is molecular; the planar molecules are stacked. The Pd atom is surrounded by a square of four O atoms (Pd−O = 1.97 Å, chelate angle 94.4°); Pd is involved in additional intemctions with the Cγatoms of two neighboring molecules (Pd...Cγ= 3.44 Å). The molecular structure of palladium β-diketonate complexes, molecular packing in crystal, and intermolecular intemctions are considered. The van der Waals energies of the crystal lattice are calculated. The results are compared with the experimental values. In the structures of palladium( 11) β-diketonates, three groups of crystals are isolated: one group with 2 nearest-neighbor interactions (stacks), the second with 4 nearest-neighbor interactions (two-dimensional nets), and the third with 1 nearest-neighbor interaction (dimers). The latter are characteristic of the cis-complexes. The intemctions with 10–12 nearest neighbor molecules determine the energetics of the whole crystal. The high volatility of Pd(hfa)2 is explained by the weaker intermolecular contacts between stacks in crystal.

Single crystal X-ray study of a volatile trans -bis-(2-methoxy-2,6-dimethyl-3-iminoheptane-5-onato)Pd(II) complex

Single crystal X-ray diffraction is used to investigate two synthesized β-diketonate complexes of copper(II) with aminopyridine: Cu(4-NH2Py)(aa)2 (I) and Cu(4-NH2Py)(hfa)2 (II). The crystals of I and II have a monoclinic system; the unit cell parameters of I are: P21/n space group, a = 8.2921(3) Å, b = 14.7243(5) Å, c = 13.4970(4) Å, β = 102.426(1)°, V = 1609.32(9) Å3, Z = 4; for II: C2/c space group, a = 23.5704(5) Å, b = 11.4977(2) Å, c = 16.0285(3) Å, β = 109.265(1)°, V = 4100.6(1) Å3, Z = 8. The structures of I and II are molecular; they are composed of isolated molecules. The coordination polyhedron of the copper atom is formed by the O atoms of two acetylacetonate ligands (Cu-O 1.940(2)–2.171(2) I and the O atoms of two hexafluoroacetylacetonate ligands (Cu-O 1.940(2)–2.215(3) Å) in II. The molecules of 4-NH2Py are bonded to the copper atom via the nitrogen atom of the aromatic ring (Cu-N 2.008(2) Å in I and Cu-N 1.978(3) Å in II). Noncoordinated amino groups join the molecules of the complexes together by means of N-H…O hydrogen bonds.

Volatile fluorinated trimethylplatinum(IV) β-diketonates with pyridine: Synthesis, properties, and structure

A thermoanalytical study of the diethyldithiocarbamates of the platinum metals Pt(II), Pd(II), Rh(III), Ir(III) and Ru(III) was carried out by means of DTA techniques in an inert atmosphere and in vacuum. Decomposition temperatures were determined and the mass loss curves were obtained for these compounds in helium and in vacuum. The X-ray diffraction patterns of the solid products of M(dtk)n thermolysis were studied. The temperature dependences of the saturated vapour pressures of the listed chelates were measured by flow and Knudsen methods, and the vaporization parameters were determined.

Crystal and Molecular Structure of Nickel(II) trans-Bis-(1,1,1-trifluoro-4-iminopentan-2-onate)

The structures of volatile pyridine adducts of trimethylplatinum(IV) β-diketonates derived from acetylacetone (Hacac) and dipivaloylmethane (Hdpm) are studied for the first time. Their preparation is reported and the data of thermal studies obtained by the DTA technique are presented. The structures of the compounds in question comprise monomeric complexes. The platinum atom is coordinated to three carbon atoms of methyl groups, two oxygen atoms of β-diketone, and the nitrogen atom of the pyridine molecule. The (PtC3O2N) coordination core has the shape of a slightly distorted octahedron. The geometrical characteristics of the coordination cores are the following: in all complexes, the values of Pt-O, Pt-CMe, Pt-N bond lengths and O-Pt-O chelate angles fall within 2.122–2.146 Å, 1.986–2.079 Å, 2.131–2.186 Å and 89.3–90.6° respectively.

Structure and thermal properties of a novel volatile bis(1,1,1-trifluoro-5,5-dimethyl-3-hexene-4-imino-2-onate) platinum(II) compound

Attention to low-temperature processes of metal film deposition is due to the necessity to obtain electrically conducting layers on different surfaces including those containing polymeric regions. The use of a highly volatile precursor, for example Pd(hfa)2, with simultaneous stimulation of its decomposition in the atmosphere of hydrogen using the VUV radiation of excimer lamps with the wavelength 116 to 126 nm allows one to decrease the temperature for the deposition of mirror metal films. In the present work, the composition and morphology of palladium films are examined by means of scanning electron microscopy, ESCA, spectral ellipsometry, depending on the temperature of substrate and precursor, deposition time, flow rates of hydrogen and argon. The nature of the substrate, its activation by VUV radiation allow selective deposition of palladium films on combined substrates (metal - polymer) with a complicated spatial relief.