Supramolecular Objects Research Articles

Magnetic Nanocomposite Micelles and Vesicles

Novel magnetic nanocomposites (see Figure) are obtained by the self-assembly in water of polypeptide-based diblock copolymers of polybutadiene-block-poly(glutamic acid) combined with hydrophobically modified gamma-Fe2O3 nanoparticles. These hybrid supramolecular objects are either filled micelles (three dimensional) or hollow vesicles with a magnetic membrane (two dimensional), the deformation of which, under an applied magnetic field, has been evidenced.

Is the binary hard-sphere mixture a good reference system for sterically stabilized colloids?

The relevance of the hard-sphere mixture model as a starting point for the study of sterically stabilized colloids is discussed. Two physical situations are distinguished: true molecular solvent-colloid mixtures, and pseudobinary mixtures of two supramolecular objects. For the former, the limitation of the hard-sphere mixture model are recalled. Its potential use as a reference system for perturbation treatments is then analyzed. The accuracy of the latter is tested numerically. This study shows that the hard-sphere mixture is, in general, not a good reference system for sterically stabilized colloids in molecular solvents. For pseudobinary mixtures, the potential of mean force between the bigger solutes induced by the smaller ones is considered. The influence of a very short-range heteroattraction is discussed.

Exploring and expanding the three-dimensional structural diversity of supramolecular dendrimers with the aid of libraries of alkali metals of their AB(3) minidendritic carboxylates.

The synthesis of the alkali metal salts of 3,4,5-tris(n-alkan-1-yloxy)benzoic acid [(3,4,5)nG1-CO(2)M, where n is the number of methylenic units in the alkane group for n=12, 14, 16, 18 and M=Li, Na, K, Rb, Cs] is described. The structural analysis of these AB(3) molecules by a combination of methods which includes X-ray diffraction experiments was performed. These experiments have demonstrated that (3,4,5)nG1-CO(2)M self-assemble at low temperatures into supramolecular cylinders and at high temperatures into spheres which subsequently self-organize into two-dimensional c2mm rectangular columnar, p6mm hexagonal columnar, three-dimensional Pm(-)3n and Im(-)3m cubic lattices. In addition a novel unidentified liquid crystalline lattice was also discovered. The dependence between the symmetry of the lattice and the molecular structure of (3,4,5)nG1-CO(2)M was established. (3,4,5)nG1-CO(2)M represents one of the AB(3) minidendrons (i.e., first-generation monodendron attached to the periphery of larger generation dendrons) that is responsible for the control of the three-dimensional structures created from libraries of larger generations of dendrimers. Therefore, the molecular structure-lattice dependence elaborated here will aid the rational design of the three-dimensional shapes from larger generations of supramolecular dendrimers and of their lattices. In addition, the temperature responsive shape change of these supramolecular objects may generate new supramolecular concepts and technological applications.

Definitive support by transmission electron microscopy, electron diffraction, and electron density maps for the formation of a BCC lattice from poly[N-[3,4,5-tris(n-dodecan-1-yloxy)benzoyl]ethyleneimine

Transmission electron microscopy (TEM), electron diffraction (ED), and electron density maps (EDM) experiments were carried out on a poly[N-[3,4,5-tris(n-dodecan-1-yloxy)benzoyl]ethyleneimine] [poly[(3,4,5)12G1-Oxz]] with a degree of polymerization (DP) of 20. All experiments confirmed the thermotropic body-centered cubic (BCC) Im3m lattice suggested previously by X-ray diffraction (XRD) experiments. The unit cell parameter determined by ED at 23 degrees C is a = 42.4 A, in good agreement with XRD results which show a = 42.6 A after quenching from 70 degrees C. EDM of the XRD results confirm that the supramolecular minidendrimer obtained from poly[(3,4,5)12G1-Oxz] adopts a spherical "inverse micellar-like" structure, with the polyethyleneimine backbone and the aromatic groups microsegregated and concentrated in the corners and in the center of the cubic unit cell. A space-filling continuum is realized by the n-alkyl groups that radiate out of the aromatic core of the spherical dendrimer. This manuscript is only the second example of complete structural analysis of a lattice generated from supramolecular objects and complements the previous example reported from our laboratory on the Pm3n lattice.

Competing Interactions among Supramolecular Structures on Surfaces

A simple model was constructed to describe the polar ordering of non-centrosymmetric supramolecular aggregates formed by self assembling triblock rodcoil polymers. The aggregates are modeled as dipoles in a lattice with an Ising-like penalty associated with reversing the orientation of nearest neighbor dipoles. The choice of the potentials is based on experimental results and structural features of the supramolecular objects. For films of finite thickness, we find a periodic structure along an arbitrary direction perpendicular to the substrate normal, where the repeat unit is composed of two equal width domains with dipole up and dipole down configuration. When a short range interaction between the surface and the dipoles is included the balance between the up and down dipole domains is broken. Our results suggest that due to surface effects, films of finite thickness have a none zero macroscopic polarization, and that the polarization per unit volume appears to be a function of film thickness.

Heat-shrinking spherical and columnar supramolecular dendrimers: their interconversion and dependence of their shape on molecular taper angle

Synthesis and modes of self-assembly are described for the tapered monodendritic molecules 3,4,5-nGi-X of generation i = 1, 2, 3 (see structures below) that contain multiple (CH2)nH alkyl chains on their periphery (n = 12, 14, 16) and a polar group X at the apex (X = COOH, COONa, COOCs, CO(OCH2CH2)3OH). These monodendrons self-assemble into supramolecular cylindrical or spherical dendrimers, which in turn self-organise into p6mm columnar or Pm3n cubic thermotropic liquid crystals, respectively. The two principal ways of affecting the self-assembly of these compounds by means of their molecular architecture are: a) by changing the width of the wide (aliphatic) end, and b) by changing the volume at the apex. In the present work a) is controlled through temperature (conformational disorder) and b) is controlled by chaging the generation number i or the size of X, for example, through the choice of metal cation. The single most important geometric parameter of these dendritic building blocks is the molecular solid angle (taper angle) alpha; a high alpha leads to spherical and a low alpha to cylindrical supramolecular dendrimers. Furthermore, alpha also determines the equilibrium size of the supramolecular objects; a larger alpha results in a smaller diameter. The unusually strong negative thermal expansion coefficient of the cubic and columnar lattice is attributed to the excess of the increasingly highly tapered molecules being rejected from their parent aggregates and reassembling as new ones. Increasing alpha is also considered to be responsible for the observed thermotropic columnar-cubic transition.