Conformational Selection in Anion Recognition: cGMP-Selective Binding by a Naphthalimide-Functionalized Amido-Amine Macrocycle.

Amido-amine macrocycles with two and four naphthalimide dyes were designed to bind nucleoside monophosphates and oligonucleotides in an aqueous buffered solution. Anion-templated synthesis was used to direct the macrocyclization reaction to the [2+2] product, while high dilution conditions favored the formation of the [4+4] macrocycle with an unprecedented geometry, as revealed from the X-ray analysis. The [2+2] product was found to exhibit a remarkable binding strength and fluorescence response for cyclic guanosine monophosphate (cGMP) in an aqueous solution. To our knowledge, this is the first synthetic receptor for cGMP, which also demonstrates a high preference to bind guanine-rich sequences accomplished by a strong fluorescence quenching. The receptor conformation is very sensitive to the guest structure in an aqueous solution, thus modeling the adaptive behavior of proteins. The study of synthetic systems with a detectable conformational equilibrium represents a great potential for understanding highly specific and tightly regulated interactions in biological systems.

Liquid-Crystalline Order and Film Thickness Determine the Semicrystalline Morphology in Diketopyrrolopyrrole-Based Copolymers.

Lyotropic liquid crystalline (LC) phases offer a means of controlling molecular order and orientation in thin films of conjugated polymers. Surface energy, surface-induced ordering, and film thickness are additional factors determining the molecular order in thin films. Through solvent vapor annealing and in situ atomic force microscopy in the swollen state, we show that in ultrathin films of a poly(dithiazolyldiketopyrrolopyrrole-tetrafluorobenzene) (PTzDPPTzF4) alternating copolymer stacks of monomolecular-thick layers with a 2.1 nm step height form, which resemble a lyotropic smectic LC phase. Within the smectic layers, the polymer backbones are aligned parallel to the film plane, with edge-on oriented diketopyrrolopyrrole (DPP) cores. Thicker films resemble a semicrystalline morphology with lamellae consisting of blocks. Such lamellae are typical for polymers crystallizing via Strobl's block-forming model. Our findings indicate that molecular order, molecular orientation, and the morphology of PTzDPPTzF4 copolymer films are tunable by LC order and by varying the film thickness according to the desired application of the particular organic electronic devices.

Nanoscale Swelling Heterogeneities in Type I Collagen Fibrils.

The distribution of water within the supramolecular structure of collagen fibrils is important for understanding their mechanical properties as well as the biomineralization processes in collagen-based tissues. We study the influence of water on the shape and the mechanical properties of reconstituted fibrils of type I collagen on the nanometer scale. Fibrils adsorbed on a silicon substrate were imaged with multiset point intermittent contact (MUSIC)-mode atomic force microscopy (AFM) in air at 28% relative humidity (RH) and in a hydrated state at 78% RH. Our data reveal the differences in the water uptake between the gap and overlap regions during swelling. This provides direct evidence for different amounts of bound and free water within the gap and overlap regions. In the dry state, the characteristic D-band pattern visible in AFM images is due to height corrugations along a fibril's axis. In the hydrated state, the fibril's surface is smooth and the D-band pattern reflects the different mechanical properties of the gap and overlap regions.

The effect of diiodooctane on the charge carrier generation in organic solar cells based on the copolymer PBDTTT-C.

Microstructural changes and the understanding of their effect on photocurrent generation are key aspects for improving the efficiency of organic photovoltaic devices. We analyze the impact of a systematically increased amount of the solvent additive diiodooctane (DIO) on the morphology of PBDTTT-C:PC71BM blends and related changes in free carrier formation and recombination by combining surface imaging, photophysical and charge extraction techniques. We identify agglomerates visible in AFM images of the 0% DIO blend as PC71BM domains embedded in an intermixed matrix phase. With the addition of DIO, a decrease in the size of fullerene domains along with a demixing of the matrix phase appears for 0.6% and 1% DIO. Surprisingly, transient absorption spectroscopy reveals an efficient photogeneration already for the smallest amount of DIO, although the largest efficiency is found for 3% DIO. It is ascribed to a fine-tuning of the blend morphology in terms of the formation of interpenetrating donor and acceptor phases minimizing geminate and nongeminate recombination as indicated by charge extraction experiments. An increase in the DIO content to 10% adversely affects the photovoltaic performance, most probably due to an inefficient free carrier formation and trapping in a less interconnected donor-acceptor network.