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Oligomer nanoparticles (OL NPs) have been considered unsuitable for solid-state lighting due to their low quantum yields and low temperature stability of their emission. Here, we address these problems by forming highly emissive and stable OL NPs solids to make them applicable in lighting. For this purpose, we incorporated OL NPs into sucrose matrix and then prepared their all-organic monoliths. We show that wrapping the OL NPs in sucrose significantly increases their quantum yield up to 44%, while the efficiency of their dispersion and direct solid-film remain only at ∼6%. We further showed ∼3-fold improved temperature stability of OL NP emission within these monoliths. Our experiments revealed that a physical passivation mechanism is responsible from these improvements. As a proof-of-concept demonstration, we successfully employed these high-stability, high-efficiency monoliths as color converters on a blue LED chip. Considering the improved optical features, low cost, and simplicity of the presented methodology, we believe that this study holds great promise for a ubiquitous use of organic OL NPs in lighting and possibly in other photonic applications. NRF (Natl Research Foundation, S’pore) Accepted version

A series of blue, green and red emitting polymers that are appropriately functionalized with alkyne and azide functional groups have been prepared and clicked together to construct bi-layered and tri-layered white emitting core-shell type nanoparticles. Here the use of these organic hetero-nanoparticles as colour converters to realize a white light-emitting diode platform acquiring a colour quality comparable to the existing phosphor-based ones was also demonstrated. © The Royal Society of Chemistry.

Here, we describe the optical and thermal isomerization kinetics, and photoinduced realignment properties of 2-nitro-4-methoxy-azobenzene tethered to an azacrown-type multi-cation (HNA) or a linear cationic poly(methacrylamide) (PNA) in solution and in a multilayered film. The thermal back-isomerization of HNA in solution followed ‘zeroth-order’ kinetics, whereas that of PNA confirmed to a first-order exponential function. UV/vis spectrometry tilt angle analysis of the azobenzenes in a multilayer film (composed of HNA/ι-carrageenan (CAG) bilayers) is lying relatively flat (θ = 23.2 ± 1.3°, with respect to the substrate surface). It was found that the orientation of the azobenzenes in the multilayer films significantly influenced the realignment of the transition moment of the photochromic moieties (with regard to the polarization of the irradiation light). The order parameter S (which gives an indication of the dichroic level), induced on the (HNA/CAG) multilayer film was found to be 20 times larger than that observed for the (PNA/CAG) film, in which the chromophores were isotropically distributed.

In the present article, we present a new and convenient optical method for the preparation of self-standing polyelectrolyte multilayer films. This method employs the disassembly of a sacrificial layer stratum composed of five poly(acrylate, merocyanine) PMC/poly(diallyldimethylammonium chloride) PDADMAC bilayers, which is triggered by the irradiation with visible light. This leads to the conversion of the zwitterionic PMC to its neutral isomer poly(acrylate, spiropyran) PSP, whereby the attractive ionic interactions between the neighboring bilayers vanish. The disassembly of the sacrificial layers in deionized water was completed within 47 s, when in-situ monitored at the maximum absorbance of PSP (λ = 360 nm), employing UV/visible spectrometry. Surprisingly, the disassembly duration of the sacrificial layers increased very little with an upper target film composed of 75 PDADMAC/PSS bilayers. The quick release of a thick target film (d ∼ 232 nm) composed of 100 (PDADMAC)/(PSS) bilayers in a large scale (7 × 18 mm(2)) could be ascribed not only to the vanished electrostatic attractive interaction between the layer pairs but also to increased hydrophobicity of the sacrificial layer element due to the photoisomerization of zwitterionic ionic PMC to neutral PSP. The unique advantages of this method as compared to the conventional approaches are demonstrated with the fast release (~2 min) of self-standing film combined with a well-defined, thin sacrificial layer (d ~ 30 nm). Moreover, harsh release conditions are also avoided, which significantly broadens the choice of materials that can be incorporated into the free-standing film.

This paper describes a pH-responsive multilayer film composed of two layered components, namely poly(allylamine hydrochloride) (PAH) and a copolymer of acrylic acid and [1,3]oxazine-modified acrylate (POA). The oxazine ring is an acidochromic chromophore and opens to form either cationic 3H-indolium or anionic hemiaminal in a pH-dependent manner. This structural transition was used to generate a net positive or negative charge on the membrane for selective ion permeation. Interestingly, the reversible oxazine ring opening and closing proceeded smoothly without significant steric hindrance in the multilayer film comprising 10 PAH/POA bilayers. The pH-responsive permselectivity for cationic and anionic probe molecules was demonstrated using a POA monolayer film adsorbed electrostatically onto an amino-functionalized ITO electrode. The origin of the excellent ion-transport selectivity in the 1 nm ultrathin POA membrane is discussed in terms of alternating charges of the aromatic amphoteric group, oxazine, in the polyeletrolyte membrane.

Toward the realization of nanoscale device control, we report a novel method for photoregulation of ion flux through a polyelectrolyte multilayer membrane by chromophore orientation that is adjusted either by illumination at normal incidence or by slantwise irradiation at an angle of 10 degrees with respect to the surface. Our results indicate that the chromophore reorientation caused by the slantwise irradiation controls the effective pore size and, consequently, the transport behavior on the nanoscale. The slantwise illumination, which includes six EZE photoisomerization cycles generated by alternately irradiating with ultraviolet (lambda = 360 nm) and visible (lambda = 450 nm) light, reversibly switches the orientation of E-azobenzene in the membrane between 53 +/- 2 degrees (high tilt) and 17 +/- 5 degrees (low tilt) with respect to the surface. The novel feature of this light-gated valve system is its extremely long-lived open-switch state; this behavior stands in contrast to that of other systems based on labile photoisomers, which tend to instantly return to the thermodynamically stable state.

Cataloged from PDF version of article. Here we report the synthesis of nanoparticles based on a conjugated oligomer which is synthesized through Heck-coupling of divinylfluorene and dibromobenzothiodiazole monomers. These water dispersible nanoparticles emit in the region of red tailing to the near-infrared region of the spectrum with high fluorescent quantum yield and brightness. The nanoparticles were found to be stable in water for a prolonged time without forming any aggregates and could carry camptothecin, an anticancer drug with high loading efficiency. MTT cell viability studies performed with breast cancer cell lines showed that half-maximal inhibitory concentration (IC50) values of nanoparticles for MCF7 and MDA-MB-231 were 44.7 μM and 24.8 μM, respectively. In order to further decrease the cytotoxicity and increase the stability of nanoparticles, amine groups were disguised by capping with cucurbit[7]uril (CB7). Drug release studies showed that drugs were released at low pH (at 5.0) faster than physiological pH (7.4) confirming the pH-responsive nature of the nanoparticles. On the other hand, CB7-capped drug-loaded nanoparticles regulated the release rate by providing slower release at pH 7.4 than the nanoparticles in the absence of CB7s. IC50 values for camptothecin in the presence of nanoparticles with or without CB7 were significantly reduced in MCF7 and MDA-MB-231 cells. © 2014 American Chemical Society.

Cataloged from PDF version of article. In this article, pH-responsive near-infrared emitting conjugated polymer nanoparticles (CPNs) are prepared, characterized, and their stabilities are investigated under various conditions. These nanoparticles have capacity to be loaded with water insoluble, anticancer drug, camptothecin (CPT), with around 10% drug loading efficiency. The in vitro release studies demonstrate that the release of CPTs from CPNs is pH-dependent such that significantly faster drug release at mildly acidic pH of 5.0 compared with physiological pH 7.4 is observed. Time and dose-dependent in vitro cytotoxicity tests of blank and CPT-loaded nanoparticles are performed by real-time cell electronic sensing (RT-CES) assay with hepatocellular carcinoma cells (Huh7). The results indicate that CPNs can be effectively utilized as vehicles for pH-triggered release of anticancer drugs. (c) 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2015, 53, 114-122