a series of new heteroleptic chelated copper(ii) complexes that encompass n,n-dibezyl substituted derivative of ethylenediamine (x-diamine) and acetylacetonate (acac) were prepared.  the ir and electronic absorption spectra and the molar conductivity of the complexes are presented and discussed.  the molar conductivity values of the complexes in different solvents reveals a predominance of elec...

A series of new heteroleptic chelated copper(II) complexes that encompass N,N-dibezyl substituted derivative of ethylenediamine (X-diamine) and acetylacetonate (acac) were prepared.  The IR and electronic absorption spectra and the molar conductivity of the complexes are presented and discussed.  The molar conductivity values of the complexes in different solvents reveals a predominance of elec...

The infrared and electronic absorption spectra of a series of new heteroleptic chelated copper (II) complexes [Cu(diamine)(acac)]X that encompass N,N'-1,6-bis(2-bromophenyl)-2,5-diazahexane (diamine), acetylacetonate (acac) and ClO , BPh , PF and BF (X) were studied. The IR, electronic absorption spectra and 4 4 6 4 the molar conductivity of the newly prepared complexes were presented and discu...

Three new heteroleptic copper(II) complexes, [(tmen)Cu(dike)H2O]X where tmen = N,N,N',N'-tetramethylethylenediamine, dike = 2-acetylcyclopentanone anion and X= ClO4- (1), Cl- (2) and Br- (3) are prepared and characterized by elemental analyses, molar conductance measurements and IR and UV-Vis spectroscopy techniques. The complex 1 is fairly soluble in various organic solvents and demonstrates d...

Although less famous than low-spin trivalent cobalt found in [CoIII(NH3)6?xClx]Cl3?x (x ? 3), which was exploited by Alfred Werner during the early part of 20th century for establishing basic rules coordination chemistry, related chromium complexes exhibit comparable kinetic inertness, a rare property along 3d-transition series. The associated slow isomerisation processes are compatible with is...

the kinetics of the de complexation by hydroxyl ions of some pervanadyl, molybdate and tungstate amionocarboxylate complexes have been studied spectrophotometrically by means of a stopped flow technique. the chelate groups used were the iminodiacetic acid (ida), ethylenediarnine-n,n' -diacetic acid (edda), nitrilotriacetic acid (nta) and ethylene diamine-n,n,n' ,n'-tetraacetic ac...

The new class of homo- and heteroleptic n-butyl-N,N'-disubstituted amidinato group 14 metal(II) complexes were prepared by salt elimination from starting lithium amidinates and metal(II) chlorides both in stoichiometric ratio 2:1 and 1:1, respectively. The target amidinates contain less bulky isopropyl or cyclohexyl as well as a sterically demanding aromatic substituent. Desired 1:1 Pb(II) comp...

The preparation of a series of homoleptic, four-coordinate lanthanide(ii) complexes, [Ln(Priso)(2)] (Ln = Sm, Eu or Yb) incorporating the bulky guanidinate ligand Priso(-) ([(ArN)(2)CNPr(i)(2)](-), Ar = 2,6-diisopropylphenyl) is described. X-ray crystallography shows the complexes to be isostructural and to exhibit coordination geometries midway between tetrahedral and planar. Comparisons betwe...

A series of heteroleptic platinum(II) complexes (1a-3a and 1b-3b) bearing a dicarbene ligand and a cyclometalated bidentate ligand have been prepared. Two of the complexes (1a and 3a) were characterized by X-ray diffraction analyses, confirming the square-planar structures. Detailed spectroscopic properties of the complexes have been studied, and two complexes, 3a and 3b bearing a carbene chela...

The reaction between the binuclear cobalt complex, [Co2(Et2dtc)5]+, and Me2pipdt Ph2pipdt ligands has provided almost quantitatively tris-chelate heteroleptic complexes [Co(Et2dtc)2(R2pipdt)]BF4 (1 2). molecular structure of 2 shows metal in a distorted octahedral geometry. nature bonding these been elucidated with support DFT TD-DFT calculations. Both chelating S,S donors work as weak-field li...