This review highlights recent advances towards non-invasive and continuous glucose monitoring devices, with a particular focus placed on monitoring glucose concentrations in alternative physiological fluids to blood.
With
the advent of direct laser writing using two-photon polymerization,
the generation of high-resolution three-dimensional microstructures
has increased dramatically. However, the development of stimuli-responsive
photoresists to create four-dimensional (4D) microstructures remains
a challenge. Herein, we present a supramolecular cholesteric liquid
crystalline photonic photoresist for the fabrication of 4D photonic
microactuators, such as pillars, flowers, and butterflies, with submicron
resolution. These micron-sized features display structural color and
shape changes triggered by a variation of humidity or temperature.
These findings serve as a roadmap for the design and creation of high-resolution
4D photonic microactuators.
Over the past decade, progress in direct laser writing by two‐photon polymerization (DLW‐TPP) of stimuli‐responsive materials has made considerable inroads into the realization of microactuators. With the focus on performing complex tasks such as walking, grasping, or delivering drugs, these actuators require a controlled preprogrammed actuation. Liquid crystalline microactuators enable such programmed movement when the mesogenic alignment can be successfully controlled. To date, this has necessitated low crosslink density networks, which are not readily conducive to the fabrication of 3D geometries. Herein, a liquid crystalline photoresist is reported, which results in a highly crosslinked network, that permits fabrication of 4D microactuators having a highly crosslinked network in which the molecular alignment is determined by the alignment layers in the cell construct. In addition to controllable deformation of the microactuators, they also display a characteristic and unique polarization color that can be used for both identification and reporting in real time, enabling their integration into sensing and anti‐anticounterfeiting microdevices.
A series of Ir(III) complexes, based on 1,10-phenanthroline featuring aryl acetylene chromophores, were prepared and investigated as triplet photosensitizers. The complexes were synthesized by Sonogashira cross-coupling reactions using a "chemistry-on-the-complex" method. The absorption properties and luminescence lifetimes were successfully tuned by controlling the number and type of light-harvesting group. Intense UV/Vis absorption was observed for the Ir(III) complexes with two light-harvesting groups at the 3- and 8-positions of the phenanthroline. The asymmetric Ir(III) complex (with a triphenylamine (TPA) and a pyrene moiety attached) exhibited the longest lifetime. Red emission was observed for all the complexes in deaerated solutions at room temperature. Their emission at low temperature (77 K) and nanosecond time-resolved transient difference absorption spectra revealed the origin of their triplet excited states. The singlet-oxygen ((1) O2 ) sensitization and triplet-triplet annihilation (TTA)-based upconversion were explored. Highly efficient TTA upconversion (ΦUC =28.1 %) and (1) O2 sensitization (ΦΔ =97.0 %) were achieved for the asymmetric Ir(III) complex, which showed intense absorption in the visible region (λabs =482 nm, ϵ=50900 m(-1) cm(-1) ) and had a long-lived triplet excited state (53.3 μs at RT).
Molecular architectures (Kagome networks, coordinated/covalent dimers and branched coordination chains) via self-assembly, Ullmann reaction and pyridine coordination of 4-[(4-bromophenyl)ethynyl]pyridine are found to be sensitive to the underlying metallic surfaces. The molecular species were characterised on the surface by low-temperature scanning tunnelling microscopy (LT-STM) at sub-molecular level.
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