Elizabeth Amir

Stimuli-Responsive Azulene-Based Conjugated Oligomers with Polyaniline-like Properties

Novel azulene building blocks, prepared via the cycloaddition of thiophene-S,S-dioxides and fulvenes, allow for incorporation of the seven-membered ring of the azulene nucleus directly into the backbone of conjugated materials. This unique mode of incorporation gives remarkably stable, stimuli-responsive materials upon exposure to acid. This simple doping/dedoping strategy provides for effective optical band gap control and on/off fluorescence switching, reminiscent of polyaniline.

Breakdown of interference rules in azulene, a nonalternant hydrocarbon.

We have designed and synthesized five azulene derivatives containing gold-binding groups at different points of connectivity within the azulene core to probe the effects of quantum interference through single-molecule conductance measurements. We compare conducting paths through the 5-membered ring, 7-membered ring, and across the long axis of azulene. We find that changing the points of connectivity in the azulene impacts the optical properties (as determined from UV-vis absorption spectra) and the conductivity. Importantly, we show here that simple models cannot be used to predict quantum interference characteristics of nonalternant hydrocarbons. As an exemplary case, we show that azulene derivatives that are predicted to exhibit destructive interference based on widely accepted atom-counting models show a significant conductance at low biases. Although simple models to predict the low-bias conductance do not hold with all azulene derivatives, we demonstrate that the measured conductance trend for all molecules studied actually agrees with predictions based on the more complete GW calculations for model systems.

Enhanced bioactivity of internally functionalized cationic dendrimers with PEG cores.

Hybrid dendritic-linear block copolymers based on a 4-arm poly(ethylene glycol) (PEG) core were synthesized using an accelerated AB2/CD2 dendritic growth approach through orthogonal amine/epoxy and thiol-yne chemistries. The biological activity of these 4-arm and the corresponding 2-arm hybrid dendrimers revealed an enhanced, dendritic effect with an exponential increase in cell internalization concomitant with increasing amine end groups and low cytotoxicity. Furthermore, the ability of these hybrid dendrimers to induce endosomal escape combined with their facile and efficient synthesis makes them attractive platforms for gene transfection. The 4-arm-based dendrimer showed significantly improved DNA binding and gene transfection capabilities in comparison with the 2-arm derivative. These results combined with the MD simulation indicate a significant effect of both the topology of the PEG core and the multivalency of these hybrid macromolecules on their DNA binding and delivery capablities.

Azulene-based conjugated polymers: unique seven-membered ring connectivity leading to stimuli-responsiveness

A novel family of stimuli-responsible polyazulenes connected through the seven-membered ring, in contrast to traditional five-membered connectivity, have been prepared by Yamamoto-, Sonogashira-, and Stille-coupling of 4,7-dibromoazulenes. Polymer absorption can be tuned by structural modification of the conjugated backbones with UV-vis and EPR studies indicating that the seven-membered ring connection of the azulene unit is effective for the generation and stabilization of azulenium cations. The degree of conjugation and the reversibility of optical properties upon protonation and deprotonation is sensitive to the steric environment of the seven-membered ring and can be tuned by both substitution and incorporation of linkers between the azulene units.

Conjugated oligomers incorporating azulene building blocks-seven- vs. Five-membered ring connectivity

The properties of isomeric azulene derivatives based on 7- versus 5-membered ring substitution were examined by the synthesis and characterization of well-defined electroactive oligomers. The substitution pattern was shown to dramatically influence solid-state, electronic and optical properties of the oligomers with acid-responsive materials only being observed when the azulenium cation could be directly stabilized by substituents in the 7-membered ring. Protonation was accompanied by a reversible color change and a strong red-shift of the absorption maximum as indicated by UV-vis studies. In addition, we show that the absorption maxima and optical band-gaps of azulenium cations can be tuned by the nature of the chromophore connected to the seven-membered ring of the azulene nucleus.

Biodegradable, multi-layered coatings for controlled release of small molecules

Incorporation of orthogonal functional groups into biodegradable polymers permits the fabrication of multi-layered thin films with improved adhesion and tunable degradation profiles. The bi-layer structure also allows for accurate control over small molecule release.