Spin‐wave based technologies that use collective oscillation of electrons termed magnons have been proposed for future computing landscapes due to their low energy consumption and high data transfer speeds. Magnonic crystals, materials with magnetic properties periodically varied in space, are central to such technologies. However, they are currently limited by the lithography techniques used for the magnetic patterning. To address this issue, bottom‐up self‐assembly using polymer templates to order magnetic cargo is presented. In this work, block copolymer micelles are used as templates to direct the organization of polyoxometalate (POM) molecules into organized assemblies. The structural organization of these assemblies is evaluated using microscopy and scattering techniques. The organized POM assemblies are demonstrated to modulate spin‐waves excited in permalloy thin films. This work demonstrates the first use of a bottom‐up approach to realize the fabrication of a magnonic assembly at the nanoscale. It further paves the way to achieve magnon‐mediated self‐assembled computing architectures.

As a step toward the bottom-up construction of magnonic systems, this paper demonstrates the use of a largeamplitude surface-pressure annealing technique to generate 2-D order in a Langmuir−Blodgett monolayer of magnetic soft spheres comprising a surfactant-encapsulated polyoxometalate. The films show a distorted square lattice interpreted as due to geometric frustration caused by 2-D confinement between soft walls, one being the air interface and the other the aqueous subphase. Hysteresis and relaxation phenomena in the 2-D layers are suggested to be due to folding and time-dependent interpenetration of surfactant chains.

Campestarene is a planar, shape-persistent macrocycle with 5-fold symmetry. A range of derivatives bearing peripheral functional groups suitable for generating supramolecular interactions has been designed and synthesised for potential applications in creating 2D quasicrystal molecular assemblies. The new campestarene derivatives bear ester, carboxylic acid, methoxy, bromo, 4-pyridyl, 4-cyanophenyl and 4-phenyl carboxylic acid groups, including further derivatives of the latter two bearing alkyl chains on the phenyl groups to improve solubility. The campestarene derivatives were prepared by reductive condensation of phenol precursors bearing nitro and formyl groups using Na2S2O4. The target functional groups were installed either by pre-cyclisation derivatisation or by synthesis of methoxy-substituted campestarene and subsequent derivatisation. The cyclisation reaction is tolerant of the functional groups introduced. The ten new campestarene derivatives were characterised by NMR spectroscopy and MALDI-TOF MS, although the poor solubility of some examples precluded their detailed characterisation.