Organopalladium(IV) and platinum(IV) complexes containing the bis(pyrazol-1-yl)borate ligand. Structures of PtMe3{(pz)2BH2}(py) (py=pyridine) and Pt(mq)Me2{(pz)2BH2} (mq=8-methylquinolinyl) and detection of a neutral organopalladium(IV) phosphine complex

Neutral palladium(IV) complexes containing the bis(pyrazol-1-yl)borate ligand, PdMe₃{(pz)₂BH₂}(L) [L=py-d₅ (4), PMe₂Ph (6)], are generated in solution by oxidative addition of iodomethane to [PdMe₂{(pz)₂BH₂}]⁻ at −70 °C followed by addition of L; the Pd(IV) complexes reductively eliminate ethane above 0 °C. Stable Pt(IV) analogues of 4 and 6 have been isolated, and comparison of NMR spectra for Pd(IV) and Pt(IV) species support structural assignments for the unstable Pd(IV) complexes. The complex PtMe₃{(pz)₂BH₂}(py) (1a) has been characterised by X-ray diffraction, together with Pt(mq)Me₂{(pz)₂BH₂} (2) (mq=8-methylquinolinyl); both complexes show a fac-PtC₃ configuration for Pt(IV), and for 2 the PtN distances are ∼0.03 Å shorter than in the isostructural Pd(IV) complex.     

Synthesis and characterization of two novel isostructural polymeric 1D mono-halo-bridged octahedral copper (II) chains with a diaza-diamine ligand

Two novel isostructural (Π = 0.0045, I_v = 93.292) one-dimensional mono-halo-bridged octahedral copper (II) polymeric complexes [Cu(L)Cl]_n(ClO₄)_n (1) and [Cu(L)Br]_n(ClO₄)_n (2) (L = 1,9-diamino-5-methyl-5-nitro-3,7-diazanonane) were prepared and characterized by CHN, IR, EPR and magnetic moment studies under a tetra coordinating (diaza-diamine type) ligand environment. The X-ray structure analysis indicates that in both 1 and 2, independent consecutive [Cu(L)X]⁺ (X = Cl or Br) cations with crystallographic C_s symmetry propagate through the a glide plane of the orthorhombic space group Pnma to give the polymeric chain structure along the a axis. In 1, the Cu-Cl bond length is 2.740 which under bridging condition elongates to 3.024 and the bridging angle, Cu-Cl-Cu, is 164.9 while parameters for 2 are 2.961(2), 3.074(2) and 157.4(5), respectively. Each monomeric unit in both the complexes is under extensive intra and inter-molecular hydrogen bonding, leading to three dimensional structures.     

Four three-dimensional lanthanide coordination polymer constructed from benzene-1,4-dioxydiacetic acid

Four crystalline lanthanide(III) three-dimensional (3D) coordination polymers {[La(BDOA)_1.5(H₂O)] · H₂O}_n (1), {[Nd(BDOA)_1.5(H₂O)] · H₂O}_n (2), [Tm(BDOA)_1.5(H₂O)]_n (3), [Yb(BDOA)_1.5(H₂O)]_n (4) were obtained under hydrothermal conditions and characterized by elemental analysis, IR, as well as single-crystal X-ray diffraction. Compounds 1 and 2 crystallize in the monoclinic system, space group P2₁/c, they are isostructural and exhibit the same 3²¹.4⁵⁷.5¹³ topological network constructed from different coordination modes of two BDOA ligands, whereas isostructural 3 and 4 crystallizes in the triclinic system, space group , it holds 3⁹.4²⁰.5⁷ topological architecture based on another two different coordination modes BDOA ligands. Moreover, a computational method is applied to evaluate the potential porosity of complex 1.