scholarly journals RigakuIntegrate : A New Single Crystal Integration Program

2014 ◽  
Vol 70 (a1) ◽  
pp. C1439-C1439
Author(s):  
Mark Pressprich ◽  
Joseph Ferrara

RigakuIntegrate is a new single crystal integration program designed to increase integration accuracy by optimizing the reflection domain to exclude all but relevant elastic scattering. Instead of integrating over a shoebox domain, RigakuIntegrate sums over a tailored detector region that incorporates the known diffraction physics of each reflection as it passes through the Ewald sphere, combined with the known properties of the area detector. The reciprocal space reflections are modelled by ellipsoids that account for the crystal radius, beam crossfire, mosaicity, and wavelength dispersion. In case of laboratory sources separate ellipsoids are assigned to each of the Kα1 and Kα2 components. The passage of the reflection through the diffraction condition is modeled by the intersection of the ellipsoid(s) with the Ewald sphere, resulting in a set of ellipses. This set of intersection ellipses is then projected onto the detector plane along the scattered ray direction. Interaction with the detector sensor is modeled by appropriate convolution, resulting in reflection-specific integration domains over the surface of the detector. Results from crystals ranging in quality from exquisite (a charge density analysis of oxalic acid at 100K using a RAPID IP detector) to marginal (a highly mosaic and split crystal that refines to R1(all data) = 2.6% using a Pilatus detector) will be presented.

Materials ◽  
2021 ◽  
Vol 14 (5) ◽  
pp. 1088
Author(s):  
Yuki Gunjo ◽  
Hajime Kamebuchi ◽  
Ryohei Tsuruta ◽  
Masaki Iwashita ◽  
Kana Takahashi ◽  
...  

The structural and electronic properties of interfaces composed of donor and acceptor molecules play important roles in the development of organic opto-electronic devices. Epitaxial growth of organic semiconductor molecules offers a possibility to control the interfacial structures and to explore precise properties at the intermolecular contacts. 5,6,11,12-tetraazanaphthacene (TANC) is an acceptor molecule with a molecular structure similar to that of pentacene, a representative donor material, and thus, good compatibility with pentacene is expected. In this study, the physicochemical properties of the molecular interface between TANC and pentacene single crystal (PnSC) substrates were analyzed by atomic force microscopy, grazing-incidence X-ray diffraction (GIXD), and photoelectron spectroscopy. GIXD revealed that TANC molecules assemble into epitaxial overlayers of the (010) oriented crystallites by aligning an axis where the side edges of the molecules face each other along the [1¯10] direction of the PnSC. No apparent interface dipole was found, and the energy level offset between the highest occupied molecular orbitals of TANC and the PnSC was determined to be 1.75 eV, which led to a charge transfer gap width of 0.7 eV at the interface.


2021 ◽  
Vol 4 (03) ◽  
pp. 50-71
Author(s):  
Leonardo Dos Santos ◽  
Bernardo L. Rodrigues ◽  
Camila B. Pinto

The ongoing increase in the number of experimental charge-density studies can be related to both the technological advancements and the wide applicability of the method. Regarding materials science, the understanding of bonding features and their relation to the physical properties of materials can not only provide means to optimize such properties, but also to predict and design new materials with the desired ones. In this tutorial, we describe the steps for a charge-density analysis, emphasizing the most relevant features and briefly discussing the applications of the method.


2019 ◽  
Vol 43 (23) ◽  
pp. 9039-9051 ◽  
Author(s):  
Ishaat M. Khan ◽  
Kehkashan Alam ◽  
Mohammad Jane Alam ◽  
Musheer Ahmad

The photocatalytic activity of a new CT complex was tested. Spectrophotometric studies were performed to understand its formation through N+–H⋯O− hydrogen bonding, and the structure was confirmed by single crystal XRD.


1997 ◽  
Vol 61 (406) ◽  
pp. 411-421 ◽  
Author(s):  
Giorgio Menegazzo ◽  
Susanna Carbonin ◽  
Antonio Della Giusta

AbstractDuring research on the influence of temperature on cation partitioning in natural Mg-Al-Fe2+-Fe3+ spinels, some crystals were accidentally oxidized during heat treatment. The oxidation product, studied by means of single-crystal X-ray diffraction, turned out to be a phase retaining the Fd3m parent spinel structure, but with cell edge a and oxygen coordinate u considerably smaller than the parent ones (a ∼ 8.087 as compared with ∼ 8.111 Å; u ∼ 0.2609 vs. 0.2617–0.2636) and with vacant sites due to oxidation.Assuming that the oxidation process must occur due to the addition of oxygen to the crystal boundary as cations are being preserved and rising in total valence, the site population was determined and compared with that of untreated and heated samples. It was found that, on oxidation, a charge enrichment in the tetrahedral site T had occurred, this phenomenon following that observed during heating at increasing temperatures also in other spinel series. This continuity was always in the direction of an increase in random charge distribution. Cation vacancies produced during oxidation were restricted to the octahedral site M.Examination of bulk sections by reflected light microscopy showed a few hematite lamellae as inclusions in the oxidized samples, not detectable by microprobe analysis or single-crystal structural refinement. However, hematite played a marginal part in oxidation. Vacancy-oxygen distances in oxidized spinels were determined from experimental data in the literature.


2012 ◽  
Vol 554-556 ◽  
pp. 792-795
Author(s):  
Hai Xing Liu ◽  
Jing Wang ◽  
Fang Fang Jian ◽  
Hui Juan Yue ◽  
Guang Zeng ◽  
...  

A new Eu complex [Eu (C3O9H6)] ·2(H2O) has been synthesized from a hydrothermal reaction and the crystal structure has been determined by means of single-crystal X-ray diffraction. The Eu atom is coordinated by eight O atoms. The molecular is antisymmetric structure by the C3-C3 axis. It is striking that the structure of the complex exhibits extensive O-H…O hydrogen-bonding interactions.


2020 ◽  
Vol 117 (9) ◽  
pp. 092102 ◽  
Author(s):  
Yongzhao Yao ◽  
Yoshiyuki Tsusaka ◽  
Yukari Ishikawa ◽  
Yoshihiro Sugawara ◽  
Yu Fujita ◽  
...  

1992 ◽  
Vol 255 ◽  
pp. 309-325 ◽  
Author(s):  
Pamidighantam V. Sudhakar ◽  
Koop Lammertsma ◽  
Paul von Ragué Schleyer

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