Liquid crystal dimers and the twist-bend nematic phase: on the role of spacers and terminal alkyl chains.

The synthesis and characterisation of four series of liquid crystal dimers based on benzylideneaniline mesogenic units, and in which the lengths of terminal alkyloxy chains are varied are reported. The series differ in terms of their flexible spacers, namely, heptamethylene, nonamethylene, hexyloxy, and oxypentyloxy chains. The heptamethylene- and nonamethylene-linked dimers both show conventional nematic, N, and twist-bend nematic, NTB, phases with short terminal chains, and smectic behaviour emerges on increasing terminal chain length. This is attributed to increased molecular inhomogeneity driving microphase separation. The dimers containing the shorter heptamethylene spacer show a smectic A phase whereas those with the longer nonamethylene spacer exhibit an anticlinic smectic C phase. Smectic behaviour is not observed for the dimers containing either a hexyloxy spacer which exhibit nematic and twist-bend nematic phases, or with an oxypentyloxy spacer which show only a conventional nematic phase. A general observation is that TNTBN and TNI alternate in the same sense in a homologous series on varying the length of the terminal alkyl chains suggesting that the spatial uniformity of the molecular curvature is an important factor in stabilising the NTB phase. The transitional properties of the four corresponding dimers possessing nitrile terminal substituents are also described. These show enantiotropic nematic phases, and in addition, for those containing either polymethylene or hexyloxy spacers, a twist-bend nematic phase is observed. Differences in the thermal behaviour of the dimers may be attributed largely to changes in molecular shape arising from the nature of the link between the spacer and mesogenic units

Flexoelectric Polarization in a Nematic Liquid Crystal Enhanced by Dopants with Different Molecular Shape Polarities

Funding Information: We would like to acknowledge the great support which we received from Prof. I. Muševič, JSI, Ljubljana, Slovenia, Dr M. Klasen-Memmer, Merck, Germany, Dr Santanu Kumar Pal and Dr Golam Mohiuddin, Indian Institute of Science Education and Research (IISER) Mohali, India, and Prof. P. Kula and K. Garbat, MUT, Warsaw, Poland. This work has been partially supported by SeeReal Technologies and MUT Research Grants 13-843/WAT/2022.Peer reviewedPublisher PD

Development of hydrogel-based standards and phantoms for non-linear imaging at depth

Significance: Rapid advances in medical imaging technology, particularly the development of optical systems with non-linear imaging modalities, are boosting deep tissue imaging. The development of reliable standards and phantoms is critical for validation and optimization of these cutting-edge imaging techniques. Aim: We aim to design and fabricate flexible, multi-layered hydrogel-based optical standards and evaluate advanced optical imaging techniques at depth. Approach: Standards were made using a robust double-network hydrogel matrix consisting of agarose and polyacrylamide. The materials generated ranged from single layers to more complex constructs consisting of up to seven layers, with modality-specific markers embedded between the layers. Results: These standards proved useful in the determination of the axial scaling factor for light microscopy and allowed for depth evaluation for different imaging modalities (conventional one-photon excitation fluorescence imaging, two-photon excitation fluorescence imaging, second harmonic generation imaging, and coherent anti-Stokes Raman scattering) achieving actual depths of 1550, 1550, 1240, and 1240 μm, respectively. Once fabricated, the phantoms were found to be stable for many months. Conclusions: The ability to image at depth, the phantom's robustness and flexible layered structure, and the ready incorporation of "optical markers" make these ideal depth standards for the validation of a variety of imaging modalities

Distinct differences in the nanoscale behaviors of the twist-bend liquid crystal phase of a flexible linear trimer and homologous dimer

This work was supported by National Science Foundation Materials Research Science and Engineering Center Grant DMR-1420736 and Grant DMR-1307674. M.R.T. acknowledges support from the Advanced Light Source Doctoral Fellowship in Residence offered by Lawrence Berkeley National Laboratory. M.S. acknowledges the support of the US National Science Foundation I2CAM International Materials Institute Award, Grant DMR-1411344. We acknowledge use of beamlines 11.0.1.2 and 7.3.3. of the Advanced Light Source supported by the Director of the Office of Science, Office of Basic Energy Sciences, of the US Department of Energy under Contract DE-AC02-05CH11231.Peer reviewedPublisher PD

Iona in the Viking Age: laying a ‘zombie narrative’ to rest

The traditional story of Iona’s early medieval monastery ends in tragedy and bloodshed, with the religious community wiped out by vicious Viking raiders. Increasingly, though, the archaeological and historical evidence does not support this persistent narrative, as Adrián Maldonado, Ewan Campbell, Thomas Owen Clancy, and Katherine Forsyth report

Early medieval sculpture of the Forteviot area

No abstract available

Early medieval sculpture of the Forteviot area

No abstract available

Two-Photon Absorption: An Open Door to the NIR-II Biological Window?

The way in which photons travel through biological tissues and subsequently become scattered or absorbed is a key limitation for traditional optical medical imaging techniques using visible light. In contrast, near-infrared wavelengths, in particular those above 1000 nm, penetrate deeper in tissues and undergo less scattering and cause less photo-damage, which describes the so-called “second biological transparency window”. Unfortunately, current dyes and imaging probes have severely limited absorption profiles at such long wavelengths, and molecular engineering of novel NIR-II dyes can be a tedious and unpredictable process, which limits access to this optical window and impedes further developments. Two-photon (2P) absorption not only provides convenient access to this window by doubling the absorption wavelength of dyes, but also increases the possible resolution. This review aims to provide an update on the available 2P instrumentation and 2P luminescent materials available for optical imaging in the NIR-II window

Hydrogel-based standards for single and multiphoton imaging at depth

Medical imaging is advancing rapidly through the development of novel laser sources and non-linear imaging methodologies. These developments are boosting deep tissue imaging allowing researchers to study diseases deep in the body enabling early diagnosis and better treatment. To help with the testing and optimization of these imaging systems and to aid in this process of deep tissue imaging, it's important to have robust, stable and reproducible standards and phantoms. Herein we present the design and fabrication of robust, multi-layered, hydrogel-based standards. The hydrogel used is a double network hydrogel consisting of two interpenetrating networks agarose and polyacrylamide. Thin layers of tough double network hydrogels are stacked to form multilayered depth standards having modality specific signaling markers embedded in between. Standard design and assembly ensured long term stability and easy transport. These proved useful in-depth imaging studies, utilizing multiple imaging modalities, including one photon fluorescence (1PEF), two photon fluorescence (2PEF), coherent anti-Stokes Raman imaging (CARS) and second harmonic generation imaging (SHG)