PbCN2 – an elucidation of its modifications and morphologies

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Cordula Braun ◽  
Liuda Mereacre ◽  
Helmut Ehrenberg

Abstract Concerning the crystal structure of PbCN2 there exist two different descriptions in the literature, one based on the non-centrosymmetric structure, space group Pna21, another one on the centrosymmetric one in space group Pnma. To elucidate the conditions for their appearance, comprehensive preparative and structural investigations have been conducted which proved the existence of two distinct modifications of PbCN2. A detailed comparison of the two phases is provided. The growth conditions and crystallization processes of the two PbCN2 structures are reported with focus on the influence of the pH value on the products. Depending on the growth conditions several different morphologies arise, namely PbCN2 in needle-shaped and platelet-shaped crystals, as well as pompon-shaped and lance-shaped crystals.

2020 ◽  
Vol 75 (4) ◽  
pp. 393-402 ◽  
Author(s):  
Eva M. Heppke ◽  
Stefan Berendts ◽  
Martin Lerch

AbstractAg2CdSnS4 was synthesized by a two step mechanochemical synthesis route. From a detailed analysis of the observed reflections in the X-ray powder diffraction pattern, the crystal structure proposed in the literature (space group Cmc21 [E. Parthé, K. Yvon, R. H. Deitch, Acta Crystallogr.1969, B25, 1164–1174; O. V. Parasyuk, I. D. Olekseyuk, L. V. Piskach, S. V. Volkov, V. I. Pekhnyo, J. Alloys Compd.2005, 399, 173–177]) is questionable. Our structural investigations presented in this contribution point to the fact that Ag2CdSnS4 crystallizes in the monoclinic wurtzkesterite-type structure (space group Pn). At around T = 200°C, a phase transition to the orthorhombic wurtzstannite-type structure (space group Pmn21) is observed.


Crystals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 172
Author(s):  
Kirill Shubin ◽  
Agris Bērziņš ◽  
Sergey Belyakov

New pseudopolymorphs of ivermectin (IVM), a potential anti-COVID-19 drug, were prepared. The crystal structure for three pseudopolymorphic crystalline forms of IVM has been determined using single-crystal X-ray crystallographic analysis. The molecular conformation of IVM in crystals has been compared with the conformation of isolated molecules modeled by DFT calculations. In a solvent with relatively small molecules (ethanol), IVM forms monoclinic crystal structure (space group I2), which contains two types of voids. When crystallized from solvents with larger molecules, like γ-valerolactone (GVL) and methyl tert-butyl ether (MTBE), IVM forms orthorhombic crystal structure (space group P212121). Calculations of the lattice energy indicate that interactions between IVM and solvents play a minor role; the main contribution to energy is made by the interactions between the molecules of IVM itself, which form a framework in the crystal structure. Interactions between IVM and molecules of solvents were evaluated using Hirshfeld surface analysis. Thermal analysis of the new pseudopolymorphs of IVM was performed by differential scanning calorimetry and thermogravimetric analysis.


Author(s):  
Feodor Belov ◽  
Alexander Villinger ◽  
Jan von Langermann

This article provides the first single-crystal XRD-based structure of enantiopure (R)-baclofen (form C), C10H12ClNO2, without any co-crystallized substances. In the enantiopure title compound, the molecules arrange themselves in an orthorhombic crystal structure (space group P212121). In the crystal, strong hydrogen bonds and C—H ... Cl bonds interconnect the zwitterionic molecules.


1995 ◽  
Vol 50 (3) ◽  
pp. 439-447 ◽  
Author(s):  
Roland Köster ◽  
Günter Seidel ◽  
Roland Boese ◽  
Bernd Wrackmeyer

The exhaustive hydroboration of the (C ≡ C )-groups in Me2Si(C ≡ CMe)2 (A ) by adding ethyldiboranes(6) at room temperature is presumed to lead initially to the formation of a mixture of the threo- and erythro-3,3,5,6-tetrakis(diethylboryl)-4,4-dimethyl-4-silaheptanes (1a , b). The threo-1a reacts further by borane catalysed intermolecular condensation to the substituted disilatetraboratricyclo[6.2.1.16.9]dodecane 2 with the formula , whose crystal structure [space group C2/c, a = 19.696(2), b = 10.371(1), c = 16.580(2) Å; β = 125.90(1)°; at 122 K] has been established by X -ray diffraction. In contrast, the erythro-1b undergoes intramolecular, thermal elimination of Et3B to give the 1,2-diethyl-2,4-bis(diethylboryl)- 3,3,5-trim ethyl-3-silaborolane (4). If A is added to an excess of undiluted B (“hydridebath”), then the two substituted diastereomers of the 1-carba-arachno-pentaboranes(10) (endo/exo-Et,SiH Me2) (3a, b), are formed preferentially as the result of an initial Si-C ≡-c le a v e d hydroboration.


1979 ◽  
Vol 34 (10) ◽  
pp. 1373-1376 ◽  
Author(s):  
Albrecht Mewis

Abstract The ABX-compounds MgCuP, BaCuP(As) and BaAgP(As) have been prepared and their structures determined. MgCuP crystallizes orthorhombically in an anti-PbCl2-structure (space group Pnma-D162h, a = 653.2(1) pm, b - 383.5(1) pm, c = 717.0(1) pm). The compounds BaCuP(As) and BaAgP(As) are isotypic and crystallize in a modified Ni2ln-structure (space group P63/mmc-D46h) with the lattice constants:BaCuP a = 423.9(1) pm, c = 900.6(2) pm,BaCuAs a = 437.2(1) pm, c = 907.3(2) pm,BaAgP a = 449.6(1) pm, c = 882.8(2) pm,BaAgAs a = 461.3(1 )pm, c = 889.6(1) pm.


Remarkable aspects of the crystallization of 3,4-dihydroxybenzoic acid (protocatechuic acid, PCA) from water as described by R. W. Wood ( Proc. R. Soc. Lond . A 197,283-294 (1949)) are confirmed. This compound crystallizes as the monohydrate in four different polymorphic phases: three are triclinic (oblique needles, needles and rhombs) and belong to one subgroup, while the fourth, monoclinic, phase constitutes a separate subgroup. It is probable that the triclinic rhombs are the stable phase at 25° C, with the other phases monotropically related to it. Crystal data for the triclinic needles are a = 9.926(9), b = 9.532(9), c = 8.131(8)Å, α = 100.8(1), β = 90.7(1), γ = 102.4(1)°, Z = 4, space group P1 - ; and for th e triclinic rhombs a = 12.693(9), b = 8.011(6), c = 8.121(6) Å, α = 72.2(1), β = 108.5(1), γ = 103.2(1)°, Z = 4, space group P1 - . Both crystals can be described in terms of a unit cell containing eight formula units, with dimensions a ≈ 12.7, b ≈ 9.5, c ≈ 13.0 Å, α ≈ 88, β ≈ 101, γ ≈ 107°; the space group for the triclinic needles is B1 - and for the triclinic rhombs A1 - . Crystal structure analyses (four-circle diffractometer, MoKα) of these two phases (triclinic needles, 1287 reflexions used in the final refinement cycle, R F = 11.1%; triclinic rhombs, 1761 reflexions, R F = 6.9%) show that both contain essentially similar layer pairs of PCA and H 2 O molecules, with hydrogen bonding both within each layer and, apparently, between them; however, the stacking of the layer pairs in the two phases differs. The crystals of the oblique needles are so small and unstable to stress that crystal structure analysis was not possible. The crystal structure of the monoclinic needles ( a = 12.32(1), b = 3.64(1), c = 17.60(2) Å, β = 107.7(2)°, Z = 4, space group P2 1 / n was determined (CuK α , 787 reflexions, R F = 6.8%); the overall molecular arrangement differs from that in the triclinic phases in an absence of PCA•H 2 O layers although there are distinct resemblances between the hydrogen bonding schemes. The phase transition ‘oblique needles → triclinic needles’ is ‘single crystal to single crystal’ and is a topotaxic transition. The phase transition ‘triclinic needles → triclinic rhombs’ is ‘single crystal to oriented polycrystal’ and is described as partially topotaxic, there being preservation of layer arrangement but not of complete three-dimensional orientation.


1978 ◽  
Vol 33 (6) ◽  
pp. 606-609 ◽  
Author(s):  
Albrecht Mewis

Abstract Four ternary compounds with the formulas CaMn2P2, CaMn2As2, SrMn2P2, and SrMn2As2 have been prepared and investigated by X-ray methods. They are isotypic and crystallize trigonally in a CaAl2Si2-type structure (space group P3̅m 1-D33d) with the lattice constants: CaMn2P2 a = 4,096 ± 0,001 Å, c = 6,848 ± 0,002 Å, CaMn2As2 a = 4,239 ± 0,001 Å, c = 7,027 ± 0,003 Å, SrMn2P2 a = 4,168 ± 0,001 Å, c = 7,132 ± 0,001 Å, SrMn2As2 a = 4,306 ± 0,001 Å, c = 7,315 ± 0,001 Å. The lattice constants of BaMn2P2 and BaMn2As2 are given


1985 ◽  
Vol 40 (7) ◽  
pp. 878-882 ◽  
Author(s):  
Kurt O. Klepp

Abstract Na4GeSe4 was obtained from a stoichiometric melt of Na2Se, Ge and Se at 750 °C. It crystallizes with a new orthorhombic structure, space group Pnma, with a = 28.518(8), b - 9.447(5), c = 7.128(2) Å , Z = 8. The crystal structure was refined to a conventional R of 0.074 for 1236 reflections with I > 3 σ (I) (diffractometer data). It is characterized by discrete GeSe44--anions with almost regular tetrahedral geometry. Two independent anions appear in the structure, the mean Ge - Se-bond lengths are 2.345 and 2.353 Å, resp. The Na+-ions are coordinated to 4 -6 chalcogen atoms in the range 2.88-3.28 Å. The structure is composed of mixed cation-anion-slabs, 2∞ [Na2(GeSe4)2-], which run parallel to the bc-plane and are separated from each other by corrugated 36-layers of Na+-ions.


2020 ◽  
Vol 34 (11) ◽  
pp. 2050101
Author(s):  
R. F. Hashimov ◽  
F. A. Mikailzade ◽  
S. V. Trukhanov ◽  
A. V. Trukhanov ◽  
D. M. Mirzayeva

In this work, powder [Formula: see text] samples (purity of 99.99 % and density of [Formula: see text] were used. The crystal structure of [Formula: see text] compound was studied by X-ray diffraction method. It was determined that the crystal structure of this compound consists of two phases at room-temperature and under normal condition. These structure phases correspond to the cubic symmetry with Pm-3m space group and rhombohedral symmetry with the R-3c space group. Thermo Gravimetric (TG), Differential Scanning Calorimetry (DSC), Differential Thermo Gravimetric (DTG) and Differential Thermal Analysis (DTA) of [Formula: see text] compound were carried out in a high-temperature range of [Formula: see text]. It has been found that at high-temperatures, two-phase transition occurs in this compound. The value of thermodynamic parameters was found out for each phase transit.


1998 ◽  
Vol 53 (8) ◽  
pp. 900-902 ◽  
Author(s):  
Werner Urland ◽  
Helmut Person

Abstract Starting from HoSe2-x powder and holmium metal bright brownish-yellow, plate-like single crystals of Ho2Se3 could be prepared by chemical transport with AlCl3. Holmium sesquiselenide crystallizes in the Sc2S3-type structure, space group Fddd, with lattice constants a = 1140,7(2), b -812,6(1) and c = 2423,9(3) pm.


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