The rippled β-sheet is a peptidic structural motif related to but distinct from the pleated β-sheet. Both the pleated and the rippled β-sheet motifs were predicted in the early 1950s...

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Considering that biological and synthetic reactivity of small molecule compounds differs between enantiomers, the confident determination of a chiral molecule's absolute configuration is of much importance to pharmaceutical and synthetic chemistry. By virtue of resonant scattering phenomena, which break Friedel symmetry in a diffraction pattern, X-ray crystallography remains the most well-established method for determining the absolute structure of a chiral, enantiopure molecular crystal. As 3D electron diffraction (3D ED) now enables atomic structure determination from crystals on the order of nanometers in size, circumventing the traditional X-ray crystallography bottleneck of growing macroscopic crystals, it is pertinent to study the extent to which information about molecular handedness might be extracted from electron diffraction. In this work, we quantify features in X-ray and electron diffraction intensities that might predict the confident resolution of a chiral crystal's absolute structure. Considering X-ray diffraction as a well-understood model to identify such qualities, we focus both on the magnitudes of intensity differences between Bijvoet pairs for diffraction data collected on a single crystal, and how these measured differences for commonly observed pairs of reflections correlate between diffraction collected on different crystals of either like or opposite hand. Our substrate scope includes crystals with a range of expected anomalous scattering. We assess the degree to which dynamical scattering might impact intensity differences between Bijvoet pairs in measured data at 200 and 300 keV. We also investigate the influence of parameters that may influence the degree of multiple elastic scattering, such as the thickness of the crystal, the scattering mean free path, and the incident wavelength of irradiation, on measured Bijvoet differences. To do so, we collect 3D electron diffraction data on large populations of nanocrystals of chiral, enantiopure substrates and separate data by enantiomer. For each crystal sampled, following diffraction data collection, we also obtain tilt series images to yield intermediate resolution tomograms from which crystal thickness can be estimated, in terms of the number of its elastic mean free path. We are sampling crystalline molecular substrates that vary in atomic composition and scattering cross-section, and collect data at a series of accelerating voltages across different TEMs. Ultimately, we aim to understand the relationship between experimental conditions or substrates and diffraction metrics that might predict accurate absolute structure prediction. If successful, we might understand when scattering differences observed for chiral crystals are meaningful and predictive of crystal chirality.

Every electron diffraction experiment is fundamentally limited by radiation damage. Immediately as the crystal of interest is illuminated by the incident beam, a complex set of inelastic scattering events initiates a cascade of radiolytic reactions within the sample, breaking chemical bonds and ultimately destroying the structural integrity of the crystal lattice. In 3D electron crystallography, an irradiated specimen is unidirectionally rotated within a transmission electron microscope while reciprocal space is periodically sampled in regular intervals, generating a tomographic series of diffraction patterns. Here we analyze a series of diffraction datasets acquired from repeated, consecutive sampling of single nanocrystals formed by organic and organometallic compounds. These species represent groups of small-molecule structures featuring site-specific modifications to an otherwise conserved scaffold. Our results indicate that chemically inspired substitutions can exert a significant effect on either accelerating or arresting the onset and progression of radiolytic damage, thus diminishing or enhancing the dose tolerance of specific crystalline specimens. Motifs explored include loss of aromaticity and removal of heavier atoms with relatively favorable elastic-to-inelastic cross-section ratios.