RESUMO
The PdII complex bis-{(S)-(-)-N-[(biphenyl-2-yl)methyl-idene]1-(4-meth-oxy-phen-yl)ethanamine-κN}di-chlorido-palladium(II), [PdCl2(C22H21NO)2], crystallizes in the monoclinic Sohncke space group P21 with a single mol-ecule in the asymmetric unit. The coordination environment around the palladium is slightly distorted square planar. The N-Pd-Cl bond angles are 91.85â (19), 88.10â (17), 89.96â (18), and 90.0â (2)°, while the Pd-Cl and Pd-N bond lengths are 2.310â (2) and 2.315â (2)â Å and 2.015â (2) and 2.022â (6)â Å, respectively. The crystal structure features inter-molecular N-Hâ¯Cl and intramolecular C-Hâ¯Pd inter-actions, which lead to the formation of a supramolecular framework structure.
RESUMO
The title complex, [PdCl2(C9H13N)2], comprises a single mol-ecule in the asymmetric unit. The PdII atom is tetra-coordinated by two N atoms from two trans-aligned organic ligands and two Cl ligands, forming a square-planar metal coordination environment. The distances from the ortho-H atoms on the phenyl ring to the central PdII atom fall within the range 4.70-5.30â Å, precluding any significant intra-molecular Pdâ¯H inter-actions.
RESUMO
The (S)-(+)-1-(4-bromo-phen-yl)-N-[(4-methoxyphen-yl)methyl-idene]ethyl-amine ligand, C16H16BrNO, (I), was synthesized through the reaction of 4-meth-oxy-anisaldehyde with (S)-(-)-1-(4-bromo-phen-yl)ethyl-amine. It crystallizes in the ortho-rhom-bic space group P212121 belonging to the Sohncke group, featuring a single mol-ecule in the asymmetric unit. The refinement converged successfully, achieving an R factor of 0.0508. The PdII com-plex bis-{(S)-(+)-1-(4-bromo-phen-yl)-N-[(4-methoxyphen-yl)methyl-idene]ethyl-amine-κN}di-chlorido-pal-ladium(II), [PdCl2(C16H16BrNO)2], (II), crystallizes in the monoclinic space group P21 belonging to the Sohncke group, with two mol-ecules in the asymmetric unit. The central atom is tetra-coordinated by two N atoms and two Cl atoms, resulting in a square-planar configuration. The imine moieties exhibit a trans configuration around the PdII centre, with average Cl-Pd-N angles of approximately 89.95 and 90°. The average distances within the palladium com-plex for the two mol-ecules are â¼2.031â Å for Pd-N and â¼2.309â Å for Pd-Cl.
RESUMO
The title compound, [Fe(C5H5)(C8H7N2S)], was synthesized by the direct reaction of acetyl-ferrocene, thio-urea and resublimed iodine. The structure shows one mol-ecule in the asymmetric unit. The amino-thia-zole ring makes an angle of 14.53â (13)° with the ferrocenyl ring to which it is attached. In the crystal, pairs of complex mol-ecules inter-act via inter-molecular N-Hâ¯N hydrogen bonds, forming a cyclic dimer which then inter-acts with other dimers through C-Hâ¯π inter-actions.
RESUMO
1,1'-Di-formyl-ruthenocene, [Ru(C6H5O)2], crystallizes in the ortho-rhom-bic system in the P212121 space group at room temperature. There are two crystallographically independent mol-ecules in the asymmetric unit. The cyclo-penta-dienyl rings have eclipsed configuration. The mol-ecules self-assemble in a two-dimensional structure by C-Hâ¯O and C-Hâ¯π inter-actions with cisoid relative orientations of the two formyl groups. The crystal studied was refined as an inversion twin.