Crystal Structure of 2-[2-hydroxy-3-methoxyphenyl]-3-[2-hydroxy-3-methoxybenzylamino]-1,2-dihydroquinazolin-4(3H)-one and the Synthesis, Spectral and Thermal Investigation of its Transition Metal Complexes

A new 1,2-dihydroquinazolin-4(3H)-one ligand, 2-[2-hydroxy-3-methoxyphenyl]-3-[2-hydroxy-3-methoxybenzylamino]-1,2-dihydroquinazolin-4(3H)-one (Hmpbaq), formed by the condensation of 2-aminobenzoylhydrazide with 2-hydroxy-3-methoxybenzaldehyde and its copper(II), nickel(II), cobalt(II), manganese(II), zinc(II) and cadmium(II) complexes, have been synthesized. Their structures have been elucidated on the basis of elemental analyses, conductance measurements, magnetic moments, spectral (i.r., ¹H-n.m.r., u.v.–vis., e.p.r. and FAB-mass) and thermal studies. The formation of 1,2-dihydroquinazolin-4(3H)-one rather than hydrazone in the reaction of 2-aminobenzoylhydrazide with 2-hydroxy-3-methoxybenzaldehyde is confirmed by the ¹H-n.m.r. spectra and single crystal X-ray diffraction studies. The tridentate behavior of the ligand was proposed on the basis of spectral studies. X-band e.p.r. spectra of the copper(II) and manganese(II) complexes in the polycrystalline state at room temperature and liquid nitrogen temperature were recorded and their salient features are reported. Thermal stabilities of the manganese(II) and zinc(II) complexes have been studied.     

Crystal Structure of 2-pyridine-2-yl-3(pyridine-2-carboxylideneamino)quinazolin-4(3H)-one and its Ligating Diversity Towards Transition Metal(II) Ions

The synthesis of a new ligand 2-pyridine-2-yl-3(pyridine-2-carboxylideneamino)-quinazolin-4(3H)-one (PPCAQ) is described together with its manganese(II), cobalt(II), nickel(II), copper(II), zinc(II) and cadmium(II) complexes. The single crystal X-ray diffraction studies of the ligand reveal the presence of two crystallographically independent molecules in asymmetric unit cell, which exhibit N…N attractive interaction. The PPCAQ and its metal complexes were characterized by analytical, spectroscopic (i.r., n.m.r and u.v.–vis), magnetic moment, conductance and thermal studies. The i.r. spectral studies reveal the ligational diversity of the PPCAQ towards different metal ions as NNN donor in cobalt(II), copper(II), zinc(II) and cadmium(II) complexes and as ONN donor in manganese(II) and nickel(II) complexes. The antimicrobial activity of all the compounds was tested; copper(II), zinc(II) and cadmium(II) complexes show enhanced antibacterial activity compared to the free ligand.     

Transition metal complexes of a potential anticancer quinazoline ligand

A new heterocycle, namely 2-(furyl)-3-(furfuralimino)-1,2-dihydroquinazolin-4(3H)-one (ffdq) was formed by the condensation of 2-aminobenzoylhydrazide with furfural and characterized by physico-chemical, spectroscopic, and single crystal X-ray diffraction studies. A series of complexes of ffdq have been synthesized and characterized by physico-chemical, spectroscopic, and thermal studies. According to the i.r. and ¹H-n.m.r. spectra ffdq behaves as a bidentate ligand coordinating through quinazoline oxygen and azomethine nitrogen. The FAB-mass spectrum of the Cd(II) complex indicates the monomeric nature of this complex. The X-band e.p.r. spectrum of the Cu(II) complex and thermal stabilities of the Co(II) and Ni(II) complexes are discussed.     

Transition metal complexes of a hydrazone derived from hydralazine hydrochloride and 3,5-di-tert-butylsalicylaldehyde

Mononuclear Co(III), Ni(II) and Cu(II) coordination compounds of (E)-1-(3,5-di-tert-butyl-2-hydroxybenzylidene)-2-(phthalazin-1-yl)hydrazine (LH) were prepared and characterized by physicochemical and spectroscopic methods. The metal-to-ligand ratio was found to be 1:2 in [Co(L)₂]Cl·2H₂O (1) and [Ni(L)₂]·2H₂O (2), while it is 1:1 in [Cu(L)Cl]·2CH₃OH (3). The X-ray crystal structures of LH and complex 1 is are reported. LH shows monobasic behavior, coordinating through NNO donor atoms. The complexes were investigated for their antimicrobial properties. Complexes 1 and 3 show excellent antibacterial and antifungal activities, respectively.