Expanding the limits of synthetic macromolecular chemistry through Polyphenylene Dendrimers.

Polyphenylene dendrimers (PPDs) are a unique class of macromolecules because their backbone is made from twisted benzene repeat units that result in a rigid, shape-persistent architecture as reported by Hammer et al. (Chem Soc Rev 44:4072-4090, 2015) and Hammer and Müllen (Chem Rev 116:2103-210, 2016) These dendrimers can be synthetically tailored at their core, scaffold, and surface to introduce a wide range of chemical functionalities that influence their applications. It is the balance between the macromolecular properties of polyphenylene dendrimers with grandiose synthetic ingenuity that presents a template for the next generation of synthetic dendrimers to achieve complex structures other chemistry fields cannot.

Controlling Cellular Uptake and Toxicity of Polyphenylene Dendrimers by Chemical Functionalization.

Polyphenylene dendrimers (PPDs) represent a unique class of macromolecules based on their monodisperse and shape-persistent nature. These characteristics have enabled the synthesis of a new genre of "patched" surface dendrimers, where their exterior can be functionalized with a variety of polar and nonpolar substituents to yield lipophilic binding sites in a site-specific way. Although such materials are capable of complexing biologically relevant molecules, show high cellular uptake in various cell lines, and low to no toxicity, there is minimal understanding of the driving forces to these characteristics.

Dimensional Evolution of Polyphenylenes: Expanding in All Directions.

Polyphenylenes (PPs) represent a class of conjugated polymers that have been used in applications ranging from organic electronic devices, sensors, polymer film additives to manipulate their mechanical properties, and even fluorescent tags or nanocarriers in biological media.1-3 The versatility of PPs stem from innovative synthetic strategies that have evolved throughout the years to provide avenues that precisely tune their architecture and function for specific purposes. This Review will cover the state of the art research on various PPs related to the relationship between their structure and resulting properties.

The polar side of polyphenylene dendrimers.

Polyphenylene dendrimers (PPDs) represent a unique class of dendrimers based on their rigid, shape persistent chemical structure. These macromolecules are typically looked at as nonpolar precursors for conjugated systems. Yet over the years there have been synthetic achievements that have produced PPDs with a range of polarities that break the hydrophobic stereotype, and provide dendrimers that can be synthetically tuned to be used in applications such as stable transition metal catalysts, nanocarriers for biological drug delivery, and sensors for volatile organic compounds (VOCs), among many others.

Morphology-dependent electronic properties in cross-linked (P3HT-b-P3MT) block copolymer nanostructures.

Combined Kelvin probe force microscopy and wavelength-resolved photoluminescence measurements on individual pre- and post-cross-linked poly(3-hexylthiophene)-b-poly(3-methyl alcohol thiophene) (P3HT-b-P3MT) nanofibers have revealed striking differences in their optical and electronic properties driven by structural perturbation of the crystalline aggregate nanofiber structures after cross-linking. Chemical cross-linking from diblock copolymer P3HT-b-P3MT using a hexamethylene diisocyanate cross-linker produces a variety of morphologies including very small nanowires, nanofiber bundles, nanoribbons, and sheets, whose relative abundance can be controlled by reaction time and cross-linker concentration. While the different cross-linked morphologies have almost identical photophysical characteristics, KPFM measurements show that the surface potential contrast, related to the work function of the sample, depends sensitively on nanostructure morphology related to chain-packing disorder.

Reversible, self cross-linking nanowires from thiol-functionalized polythiophene diblock copolymers.

Poly(3-hexylthiophene)-block-poly(3-(3-thioacetylpropyl) oxymethylthiophene) (P3HT)-b-(P3TT) diblock copolymers were synthesized and manipulated by solvent-induced crystallization to afford reversibly cross-linked semiconductor nanowires. To cross-link the nanowires, we deprotected the thioacetate groups to thiols and they subsequently oxidized to disulfides. Cross-linked nanowires maintained their structural integrity in solvents that normally dissolve the polymers.

Covalent attachment and release of small molecules from functional polyphenylene dendrimers.

Herein, we report the synthesis of 2nd generation PPDs functionalized with free thiol moieties within the scaffold, which were used as anchor points for the covalent attachment of guest species (p-nitrophenol derivatives) through the oxidative formation of disulfide linkages. The disulfide bonds were then cleaved under reductive conditions using dithiothreitol to discharge the molecules.