Dendrimers are presently one of the most intensely studied classes of compounds because of their unusual structure. They can be described as a jungle of entangled branches traversed by winding trails which lead to sweet fruits and bright blossoms. On these trails one can reach the thicket's interior as well as find a way out. Expressed less lyrically, this thicket stands for regularly branched, densely packed structures, and the trails represent voids and channels not filled by bent back branches but by solvent. The fruit and blossoms are photochemically, electrochemically, or synthetically addressable units, catalytically active sites, etc., and the back and forth on the trails stands for transport processes. In a mathematical sense dendrimers are enveloped by an interface, which defines what is either in or out. This interface is shaped like a sphere if the trails are filled to bursting. Otherwise dendrimers are more flattened like amoeba, especially if in contact with a surface. The high density of the functional groups, the expansion of these compounds to a range of several nanometers, the existence of usable "surface" and transport possibilities in and with them have made dendrimers interesting candidates for many applications. This review describes how dendrimer construction and polymer synthesis were combined and used to move from fully or flattened spherical shapes to cylindrical ones. The shape-inducing influence of dendritic substituents can be driven to create nanoobjects with a cylindrical shape, which not only considerably widens the range of applications for the dendrimer class but also opens up new perspectives for supramolecular and polymer chemistry. Because of the sheer size of the described objects and complexity of shape-related properties, research in this area must necessarily be interdisciplinary. This article tries to mirror this by giving special attention not only to synthesis but also the characterization and behavior of these compounds in bulk and at interfaces. Furthermore, potential application fields are described.

Dedicated to Dr. Wiihelm A . Schhuler on the occasion of his 70th birthday a-Methylene-y-butyrolactones [dihydro-3-methylene-2(3H)furanones] constitute an important group of natural products and possess wide-ranging biological activities. Progress in the synthesis of the heterocycle and the classification of the synthetic methods are not only of practical interest, but also fundamentally important as a current example for the construction of an unusual 1,4-functionality distance and an a-substituted acrylic ester moiety which is susceptible to nucleophilic attack.

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The surface morphology of a symmetric poly(styrene-block-butadiene-block-methyl methacrylate) triblock copolymer (PS-b-PB-b-PMMA) with 6 wt % PB has been investigated by tapping mode scanning force microscopy (SFM). The results are compared to the bulk morphology as determined by transmission electron microscopy (TEM). In solvent-cast films PS/PMMA lamellae are formed, which are oriented nearly perpendicular to the free surface. Like in the bulk, also at the free film surface polybutadiene spheres are located at the lamellar PS/PMMA interface. However, contrary to the bulk, the surface morphology includes a large number of defects such as curved lamellar and disclinations, and the lamellar long period is doubled, from 42.7 ± 0.5 nm in the bulk to 85 ± 5 nm at the free surface, indicating a surface reconstruction. The double spacing can be explained by a surface buckling in registry with the underlying PS/PMMA lamellae. The composition of the outermost surface layer is discussed.