This Account reports the synthesis and characterization of dendrimer-encapsulated metal nanoparticles and their applications to catalysis. These materials are prepared by sequestering metal ions within dendrimers followed by chemical reduction to yield the corresponding zerovalent metal nanoparticle. The size of such particles depends on the number of metal ions initially loaded into the dendrimer. Intradendrimer hydrogenation and carbon-carbon coupling reactions in water, organic solvents, biphasic fluorous/ organic solvents, and supercritical CO 2 are also described.

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A resistive-pulse Coulter counter based on a membrane containing a single multiwall carbon nanotube (MWNT) channel was used to simultaneously determine the size and surface charge of carboxy-terminated polystyrene nanoparticles. The membrane was prepared from an epoxy section containing a MWNT channel mounted on a poly(dimethylsiloxane) (PDMS) support structure. The PDMS support reduced the background noise level by a factor of > 20 compared to the Si/Si3N4 support structure used in our previous study. The lower noise level makes it possible to accurately measure the height and width of resistive-pulse signals resulting from transport of individual particles through the MWNT channel. Particle sizes, calculated from current pulse heights, were comparable to those determined by transmission electron microscope (TEM). The width of the current pulses is a measure of the nanoparticle transport time, and it permits calculation of the electrokinetic surface charge. Different types of polystyrene nanoparticles having nearly the same size, but different electrokinetic surface charge, could be resolved on the basis of the difference in their transport time.

This review discusses recent advances in the science and technology of Coulter counting. The Coulter counting principle has been used to determine the size, concentration, and in favorable cases the surface charge, of nanometer-scale colloidal particles, viruses, DNA and other polymers, and metal ions. A resurgence of interest in the field of COulter counting is occurring because of the advent of new technologies that permit fabrication of membranes containing single, robust, and chemically well-defined channels having smaller and more uniform sizes than could be prepared in the past. These channels are prepared from biological materials, such as self-assembling membrane proteins, and from synthetic materials such as polymers, carbon nanotubes, and silicon-based inorganic materials. In addition to particle characterization, there have been a few recent examples of using Coulter counters to study chemical processes, such as the dehybridization of DNA.

Protonation of fourth-generation poly(amidoamine) dendrimers terminated with hydroxyl and amine functional groups has been studied by potentiometric pH titration. The titration data are analyzed using a multishell structural model and a Frumkin adsorption isotherm to approximate protondendrimer binding equilibria. Site-to-site correlation is ignored, and counterions are treated according to the standard Debye-Hu ¨ckel theory. This analysis yields two binding parameters: the intrinsic proton binding constant and a constant that characterizes the strength of electrostatic interactions among occupied binding sites. For the hydroxyl-terminated dendrimers, the internal tertiary amines have an average binding constant (pK ) 6.30) 1-2 pH units lower than the value expected for a single, isolated binding site. This shift in pK is attributed to a hydrophobic microenvironment within the dendrimer interior. In contrast, no significant shift has been observed in the binding constant (pK ) 9.23) for the peripheral primary amines in the amine-terminated dendrimer because the microenvironment around the primary amines is more hydrophilic. The strength of electrostatic interactions obtained from titration data is 3 times (primary amines) and 8 times (tertiary amines) smaller than the calculated values based on the multishell model. We hypothesize that the diminished interaction strength results from ion pairing between bound protons and counterions. In addition to the Debye-Hu ¨ckel contribution from mobile ions, ion pairing provides extra Coulomb charge screening.