- 
2018Polyaniline Nanofiber Electrodes for Reversible Capture and Release of Mercury(II) from WaterJournal of the American Chemical Society,2018
- 
2018
- 
2018Extended π-Conjugated Structures via Dehydrative C–C CouplingJournal of the American Chemical Society,2018
- 
2017Thermally Activated Delayed Fluorescence and Aggregation Induced Emission with Through-Space Charge TransferJournal of the American Chemical Society,2017Emissive molecules comprising a donor and an acceptor bridged by 9,9-dimethylxanthene, were studied (XPT, XCT, and XtBuCT). The structures position the donor and acceptor with cofacial alignment at distances of 3.3–3.5 Å wherein efficient spatial charge transfer can occur. The quantum yields were enhanced by excluding molecular oxygen and thermally activated delayed fluorescence with lifetimes on the order of microseconds was observed. Although the molecules displayed low quantum yields in solution, higher quantum yields were observed in the solid state. Crystal structures revealed π–π intramolecular interactions between a donor and an acceptor, however, the dominant intermolecular interactions were C—H···π, which likely restrict the molecular dynamics to create aggregation-induced enhanced emission. Organic light emitting devices using XPT and XtBuCT as dopants displayed electroluminescence external quantum efficiencies as high as 10%. 
- 
2017Micro-scale optical components play a crucial role in imaging and display technology, biosensing, beam shaping, optical switching, wavefront-analysis, and device miniaturization. Herein, we demonstrate liquid compound micro-lenses with dynamically tunable focal lengths. We employ bi-phase emulsion droplets fabricated from immiscible hydrocarbon and fluorocarbon liquids to form responsive micro-lenses that can be reconfigured to focus or scatter light, form real or virtual images, and display variable focal lengths. Experimental demonstrations of dynamic refractive control are complemented by theoretical analysis and wave-optical modelling. Additionally, we provide evidence of the micro-lenses’ functionality for two potential applications—integral micro-scale imaging devices and light field display technology—thereby demonstrating both the fundamental characteristics and the promising opportunities for fluid-based dynamic refractive micro-scale compound lenses. 
- 
2017Janus emulsion assays that rely on carbohydrate–lectin binding for the detection of Escherichia coli bacteria are described. Surfactants containing mannose are self-assembled at the surface of Janus droplets to produce particles with lectin binding sites. Janus droplets orient in a vertical direction as a result of the difference in densities between the hydrocarbon and fluorocarbon solvents. Binding of lectin to mannose(s) causes agglutination and a tilted geometry. The distinct optical difference between naturally aligned and agglutinated Janus droplets produces signals that can be detected quantitatively. The Janus emulsion assay sensitively and selectively binds to E. coli at 104 cfu/mL and can be easily prepared with long-time stability. It provides the basis for the development of inexpensive portable devices for fast, on-site pathogen detection. 
- 
2017Interfacial Pressure/Area Sensing: Dual-Fluorescence of Amphiphilic Conjugated Polymers at Water InterfacesACS Macro Letters,vol.6,p.134 – 138,2017Exciton migration to emissive defects in π-conjugated polymers is a robust signal amplification strategy for optoelectronic sensors. Herein we report end-capped conjugated polymers that show two distinct emissions as a function of interpolymer distances at the air–water and hydrocarbon–water interfaces. Amphiphilic poly(phenylene ethynylene)s (PPEs) end-capped with perylene monoimides display two distinct emission colors (cyan from PPE and red from perylene), the relative intensity of which depends on the surface pressure applied on the Langmuir monolayers. This behavior produces a ratiometric interfacial pressure indicator. Relative quantum yields are maintained at the different surface pressures and hence display no sign of self-quenching of the excitons in an aggregated state. These polymers can be organized at the micelle–water interface in lytropic liquid crystals, thereby paving the way for potential applications of end-capped amphiphilic conjugated polymers in biosensors and bioimaging. 
- 
2017Interfacial Polymerization on Dynamic Complex Colloids: Creating Stabilized Janus DropletsACS Applied Materials & Interfaces,vol.9,p.7804 – 7811,2017Complex emulsions, including Janus droplets, are becoming increasingly important in pharmaceuticals and medical diagnostics, the fabrication of microcapsules for drug delivery, chemical sensing, E-paper display technologies, and optics. Because fluid Janus droplets are often sensitive to external perturbation, such as unexpected changes in the concentration of the surfactants or surface-active biomolecules in the environment, stabilizing their morphology is critical for many real-world applications. To endow Janus droplets with resistance to external chemical perturbations, we demonstrate a general and robust method of creating polymeric hemispherical shells via interfacial free-radical polymerization on the Janus droplets. The polymeric hemispherical shells were characterized by optical and fluorescence microscopy, scanning electron microscopy, and confocal laser scanning microscopy. By comparing phase diagrams of a regular Janus droplet and a Janus droplet with the hemispherical shell, we show that the formation of the hemispherical shell nearly doubles the range of the Janus morphology and maintains the Janus morphology upon a certain degree of external perturbation (e.g., adding hydrocarbon–water or fluorocarbon–water surfactants). We attribute the increased stability of the Janus droplets to (1) the surfactant nature of polymeric shell formed and (2) increase in interfacial tension between hydrocarbon and fluorocarbon due to polymer shell formation. This finding opens the door of utilizing these stabilized Janus droplets in a demanding environment. 
- 
2017
- 
2017Differentially Substituted Phenylene-Containing Oligoacene DerivativesSynlett,vol.28,p.323 – 326,2017We report the synthesis and characterization of seven new linearly conjugated ladder compounds of the phenylene-containing oligoacene molecule class. Each derivative incorporates a fused four-membered-ring linkage in the acene-like backbone. Crystal packing, spectroscopic and electrochemical properties of the molecules are described. 
- 
2017Chemical warfare simulant-responsive polymer nanocomposites: Synthesis and evaluationJournal of Polymer Science Part A: Polymer Chemistry,2017Nanomaterials that undergo a physical change upon chemical warfare agent (CWA) exposure can potentially be used in detectors to warn soldiers of their presence or in fabrics to provide on-demand protection. In this study, hybrid nanoparticles (NPs) were prepared by grafting a CWA-responsive polymer from a silicon dioxide (SiO2) surface using ring opening metathesis polymerization; the covalent functionalization of the polymers on the NP surface was confirmed by gel permeation chromatography, dynamic light scattering, and transmission electron microscopy analysis. The polymer-grafted SiO2 NPs were found to undergo a pronounced decrease (approximately 200 nm) in their hydrodynamic radius upon exposure to CWA simulants trifluoroacetic acid and diethyl chlorophosphate in toluene. This decrease in hydrodynamic radius is attributed to the electrophile-mediated ionization of the triarylmethanol responsive unit and represents a rare example of polycation formation leading to polymer chain collapse. We have ascribed this ionization-induced collapse to the formation of a favorable stacking interaction between the planar triarylcations. These studies have important implications for the development of breathable fabrics that can provide on-demand protection for soldiers in combat situations. 
- 
2017
- 
2017
- 
2017
- 
2017
- 
2017Domino Direct Arylation and Cross-Aldol for Rapid Construction of Extended Polycyclic π-ScaffoldsJournal of the American Chemical Society,2017
- 
2017Naphthazarin-Polycyclic Conjugated Hydrocarbons and IptycenesThe Journal of Organic Chemistry,2017
- 
2017
- 
201750th Anniversary Perspective : Conducting/Semiconducting Conjugated Polymers. A Personal Perspective on the Past and the FutureMacromolecules,vol.50,p.4867 – 4886,2017
- 
2017Donor-Acceptor Iptycenes with Thermally Activated Delayed FluorescenceEuropean Journal of Organic Chemistry,2017
