The long wavelength (far-red to NIR) analyte-responsive fluorescent probes are advantageous for in vivo bioimaging because of minimum photo-damage to biological samples, deep tissue penetration, and minimum interference from background auto-fluorescence by biomolecules in the living systems. Thus, great interest in the development of new long wavelength analyte-responsive fluorescent probes has emerged in recent years. This review highlights the advances in the development of far-red to NIR fluorescent probes since 2000, and the probes are classified according to their organic dye platforms into various categories, including cyanines, rhodamine analogues, BODIPYs, squaraines, and other types (240 references).

We demonstrate the new features of a polyurethane shape memory polymer: water-driven actuation and recovery in sequence (i.e., programmable). Hydrogen bonding is identified as the reason behind these features. In addition, the absorbed water is quantitatively separated into two parts, namely, the free water and bound water. Their individual contribution on the glass transition temperature is identified.

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Shape-memory polymers (SMPs) offer a number of potential technical advantages that surpass other shape-memory materials such as shape-memory metallic alloys and shape-memory ceramics. The advantages include high recoverable strain (up to 400%), low density, ease of processing and the ability to tailor the recovery temperature, programmable and controllable recovery behavior, and more importantly, low cost. This article presents the state-of-the-art regarding SMPs. First, the architecture, type, and main properties of the traditional and recently developed SMPs are introduced. Second, structural and multifunctional SMP composites are summarized and discussed. These composites greatly enhance the performance of the SMPs and widen their potential applications. Finally, current applications of SMP materials in aerospace engineering, textiles, automobiles, and medicine are presented.

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The electrical resistivity of a thermoresponsive polyurethane shape-memory polymer ͑SMP͒ filled with micron sized Ni powders is investigated in this letter. We show that, by forming conductive Ni chains under a weak static magnetic field ͑0.03 T͒, the electrical conductivity of the SMP composite in the chain direction can be improved significantly, which makes it more suitable for Joule heat induced shape recovery. In addition, Ni chains reinforce the SMP significantly but their influence on the glass transition temperature is about the same as that of the randomly distributed Ni powders.

We demonstrate an approach to significantly reduce the electrical resistivity in a polyurethane shape-memory polymer (SMP) filled with randomly distributed carbon black (CB). With an additional small amount of randomly distributed Ni microparticles (0.5vol%) in the SMP/CB composite, its electrical resistivity is only reduced slightly. However, if these Ni particles are aligned into chains (by applying a low magnetic field on the SMP/CB/Ni solution before curing), the drop of the electrical resistivity is significant. This approach, although demonstrated in a SMP, is applicable to other conductive polymers.

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