Liquid-crystalline derivatives of poly(propylene imine)dendrimers of the 0th, 1st and 2nd generations, complexed with copper(II) ions, were studied by EPR spectroscopy. The structures of copper (II) complexes with different Cu(II) loadings x per dendrimer ligand L (x = Cu/L) were determined. At the lowest concentration, the Cu(II) ions form monomeric complexes with approximately square-planar N2O2 coordination of both carbonyl oxygen and amido nitrogen atoms. At higher copper content, two kinds of Cu(II) complex sites with different geometries exist. The orienting effect of a high magnetic field was used to investigate the structure and magnetic properties of the copper(II) complexes. This effect, for the first time in dendrimers, allowed the resolution of five nitrogen super-hyperfine lines on g(z) components with the unusual coupling constant of a(Nz)= 35.9 x 10(-4) cm(-1). The combination of the magnetic parameters and the orienting effect indicates the presence of a monomeric complex with pseudotetrahedral N2O2 coordination of the Cu(II) ion, as well as a "dimer" structure with fivefold coordination, presumably due to an N3O2 environment. Higher copper loadings lead to increased exchange coupling between the complex sites.

The unusual magnetic behavior of the first dendritic Fe(3+) complex with general formula [Fe(L)2](+)Cl(-)·H2O based on a branched Schiff base has been investigated by electron paramagnetic resonance (EPR) and Mössbauer spectroscopy. EPR displays that complex consists of the three types of magnetically active iron centers: one S = 1/2 low-spin (LS) and two S = 5/2 high-spin (HS) centers with strong low-symmetry and weak distorted octahedral crystal fields. Analysis of the magnetic behavior reflected by I versus T (where I is the EPR lines integrated intensity of the spectrum) demonstrates that the dendritic Fe(3+) complex has sufficiently different behavior in three temperature intervals. The first (4.2-50 K) interval corresponds to the antiferromagnetic exchange interactions between LS-LS, LS-HS, and HS-HS centers. The appearance of a presumable magnetoelectric effect is registered in the second (50-200 K) temperature interval, whereas a spin transition process between LS and HS centers occurs in the third (200-330 K) one. The coexistence of the magnetic ordering, presumable magnetoelectric effect, and spin crossover in one and the same material has been detected for the first time. The Mössbauer spectroscopy data completely confirm the EPR results.

Here, we report the first results of investigation the local structure and photoactive properties of iron‐containing dendromesogens based on decyloxybenzoate substituted poly(propylene imine) dendrimers of the first to fifth generations. Iron ions existing in a high‐spin state are coordinated in dendrimer ligands by two kinds of iron‐complexing sites with an octahedral and a tetrahedral symmetry. Octahedral (high‐symmetry) centers are located at the border of the dendrimeric core, while the tetrahedral centers with strong rhombic distortion of iron environment are distributed throughout all branching of the dendrimeric core. It has been found that all iron‐containing dendromesogens exhibit light‐harvesting and fluorescence properties.

The iron(III) complexes that were formed by coordination of the Fe III ion with the asymmetric tridentate liquid crystalline Schiff base ligand (L), the water molecules and the different counterions [PF 6 -(1), NO 3 -(2), and Cl -(3)] were studied by electron paramagnetic resonance (EPR) spectroscopy. EPR spectroscopy demonstrated that each of the complexes investigated consists of two types of iron centers: S = 1/2 low-spin (LS) and S = 5/2 high-spin (HS). LS iron complexes 2, 3 and LS complex 1 in the temperature range 4. + X -, with X = PF 6 -as the counterion. The LS and HS iron centers of 1 are coupled together antiferromagnetically and form a dimer structure by means of the water molecules and the PF 6 -counterion. The second-type of LS and HS cen-