Traditionally small-molecule crystallographers have not usually observed or recognized significant radiation damage to their samples during diffraction experiments. However, the increased flux densities provided by third-generation synchrotrons have resulted in increasing numbers of observations of this phenomenon. The diversity of types of small-molecule systems means it is not yet possible to propose a general mechanism for their radiation-induced sample decay, however characterization of the effects will permit attempts to understand and mitigate it. Here, systematic experiments are reported on the effects that sample temperature and beam attenuation have on radiation damage progression, allowing qualitative and quantitative assessment of their impact on crystals of a small-molecule test sample. To allow inter-comparison of different measurements, radiation-damage metrics (diffraction-intensity decline, resolution fall-off, scaling B-factor increase) are plotted against the absorbed dose. For ease-of-dose calculations, the software developed for protein crystallography, RADDOSE-3D, has been modified for use in small-molecule crystallography. It is intended that these initial experiments will assist in establishing protocols for small-molecule crystallographers to optimize the diffraction signal from their samples prior to the onset of the deleterious effects of radiation damage.

The rules underpinning the dynamic low-symmetry conformation of a symmetric organic cage are decoded, and rationally reapplied to access new cages with constrained symmetry. This allows tuning of conformation, height and shape for guest binding.

A series of mixed ligand, photoluminescent organometallic Ir(III) complexes have been synthesized to incorporate substituted 2-phenyl-1H-naphtho[2,3-d]imidazole cyclometalating ligands. The structures of three example complexes were categorically confirmed using X-ray crystallography each sharing very similar structural traits including evidence of interligand hydrogen bond contacts that account for the shielding effects observed in the ¹H NMR spectra. The structural iterations of the cyclometalated ligand provide tuning of the principal electronic transitions that determine the visible absorption and emission properties of the complexes: emission can be tuned in the visible region between 550 and 610 nm and with triplet lifetimes up to 10 μs. The nature of the emitting state varies across the series of complexes, with different admixtures of ligand-centered and metal-to-ligand charge transfer triplet levels evident. Finally, the use of the complexes as photosensitizers in triplet-triplet annihilation energy upconversion (TTA-UC) was investigated in the solution state. The study showed that the complexes possessing the longest triplet lifetimes showed good viability as photosensitizers in TTA-UC. Therefore, the use of an electron-withdrawing group on the 2-phenyl-1H-naphtho[2,3-d]imidazole ligand framework can be used to rationally promote TTA-UC using this class of complex.

A new dual-chain oligothiophene-based organic semiconductor, EH-5T-TTC, is presented. The molecule contains two conjugated chains linked by a fused tetrathiocin core. X-ray crystallography reveals a boat conformation within the 8-membered sulfur heterocycle core and extensive π–π and intermolecular sulfur–sulfur interactions in the bulk, leading to a 2-dimensional structure. This unusual molecule has been studied as a ternary component in organic solar cell blends containing the electron donor PTB7-Th and both fullerene (PC₇₁BM) and non-fullerene acceptors ITIC and EH-IDTBR. By incorporating EH-5T-TTC as a ternary component, the power conversion efficiency of the binary blends containing non-fullerene acceptor increases by 17% (from 7.8% to 9.2%) and by 85% for the binary blend with fullerene acceptor (from 3.3% to 6.3%). Detailed characterisation of the ternary blend systems implies that the ternary small molecule EH-5T-TTC functions differently in polymer:fullerene and polymer:non-fullerene blends and has dual functions of morphology modification and complementary spectral absorption.

The synthesis and characterization of a triborate salt, [H₂N(CH₂CH₂)₂NH₂][B₃O₃(OH)₄]₂ (1), and four pentaborate salts, [H₂N(CH₂CH₂)₂NH][B₅O₆(OH)₄] (2a), [MeHN(CH₂CH₂)₂NH][B₅O₆(OH)₄] (2b), [MeHN(CH₂CH₂)₂NMe][B₅O₆(OH)₄] (2c) and [Me₂N(CH₂CH₂)₂NMe₂][B₅O₆(OH)₄]₂ (2d) are described. TGA and DSC analysis (in air, 25–1000 °C) indicate that triborate 1 decomposes to B₂O₃via a multistage process, with the first stage (<250 °C) being dehydration to condensed polymeric hexaborate of approximate composition: [H₂N(CH₂CH₂)₂NH₂][B₆O₁₀]. The pentaborates (2a–2d) are thermally decomposed to B₂O₃via a 2 stage process involving polymeric [NMC][B₅O₈]. The anhydrous polyborates were amorphous. BET analysis of materials derived from the thermolysis of 1 at 250, 400, 600, and 1000 °C, were all non-porous (surface area <1.8 m² g⁻¹). A single-crystal X-ray diffraction study of 1 showed that it contains isolated triborate(1−) anions in a structure comprised of alternating cationic and anionic layers held together via extensive H-bonds. Single-crystal XRD structural studies on pentaborate salts 2c and 2d are also reported.