RESUMO
The title compound, C26H23BN2O2, was obtained as by product during synthetic attempts of a complexation reaction between the tripodal ligand H2L [N,N-bis-(2-hy-droxy-benz-yl)(pyridin-2-yl)methyl-amine] and manganese(III) acetate in the presence of NaBPh4. The isolated B-phenyl dioxaza-borocine contains an NâB dative bond with a cis conformation. In the crystal, C-Hâ¯O hydrogen bonds define chains parallel to the b-axis direction. A comparative analysis with other structurally related derivatives is also included, together with a rationalization of the unexpected production of this zwitterionic heterocycle.
RESUMO
Aroylhydrazones of ortho-hydroxy aldehydes are Schiff base ligands that typically coordinate as a chelate in an O,N,O'-manner. Dinuclear complexes are normally observed, with the phenolate O atom acting as the bridging atom. The switchable protonation state of the tridentate N'-(2-hydroxybenzylidene)benzohydrazide (H2sabhz) ligand can lead to variations in the resulting supramolecular structure. The title compound, [Pb2(C14H10N2O2)2], was prepared by the reaction of [Pb(OAc)2]·3H2O (OAc is acetate) with the benzoylhydrazone derivative of salicylaldehyde, i.e. H2sabhz, in the presence of triethylamine in methanol. In the crystal structure, each Pb(II) atom of the dimer has an NO3 coordination environment, with one sabhz ligand coordinating in an O,N,O'-manner and with the second sabhz ligand coordinating via the bridging phenolate O atom, since the dimers are located on a centre of inversion. It has been found that the dimers are connected by Pb...N interactions, resulting in a two-dimensional supramolecular network which shows the [3(2).5(2),3.5(3)] net topology. The s(2) electron pair of the Pb(II) ion clearly influences the observed intermolecular interactions.
RESUMO
The title compound, [Au(C(10)H(9)N(4)O(2)S)(C(18)H(15)P)], is nearly linear at Au(I), with Au-N = 2.0707 (18) A, Au-P = 2.2310 (8) A and N-Au-P 171.93 (5) degrees. The molecules are linked by intermolecular N-H...O bonds.