Thermal expansion, elastic and thermoelastic properties including crystal structure analyses of K-, Rb- and Cs-nitrilotriacetates

Author(s):  
Eiken Haussühl ◽  
Siegfried Haussühl ◽  
Ekkehart Tillmanns

AbstractSingle crystals of the title compounds having optical quality and dimensions up to 60 mm have been grown from aqueous solutions. X-ray crystal structure analyses of K

Author(s):  
S. Haussühl ◽  
J. Schreuer

AbstractLarge single crystals of optical quality of betaine hydrogen dihydrogen iodate have been grown from aqueous solutions. An X-ray structure analysis yields space group


Author(s):  
J. Schreuer ◽  
T. Münch

AbstractLarge single crystals of optical quality of monoclinic ethylenediammonium bis(hydrogensuccinate) were grown from aqueous solutions. An X-ray structure analysis yielded space group


Author(s):  
S. Haussühl ◽  
J. Schreuer

AbstractLarge single crystals of optical quality of betaine hydrogen ammonium sulfate have been grown from aqueous solutions. An X-ray structure analysis yielded space group


Author(s):  
S. Haussühl ◽  
J. Schreuer

AbstractLarge single crystals of optical quality of (±)-tris(ethylenediamine)cobalt(III) nitrate have been grown from aequeous solutions. An X-ray structure analysis yielded space groupPyroelectric, dieletric, piezoelectric and elastic constants have been determined at room temperature. Additionally, we have studied the coefficients of thermal expansion and the thermoelastic constants in the range between 270 K and 350 K. The structure exhibits a nearly trigonal symmetry around the [unk]


Author(s):  
S. Haussühl ◽  
J. Schreuer

AbstractLarge optical quality, single crystals of triclinic ammonium hydrogen succinate have been grown from aqueous solutions. An X-ray structure analysis yields space group


Author(s):  
E. Haussühl ◽  
S. Haussühl ◽  
E. Tillmanns

AbstractSingle crystals of bis(guanidinium) tin bis(nitrilotriacetate) hydrate (GuSN) and bis(methylammonium) tin bis(nitrilotriacetate) dihydrate (MetamSN) having optical quality and dimensions up to 15 × 15 × 20 mm were grown from aqueous solutions. The isotypy with the corresponding zirconium and hafnium compounds (GuZN, GuHN, and MetamZN, respectively)) was proved by X-ray structure analyses (GuSN: space group


2017 ◽  
Vol 73 (7) ◽  
pp. 1073-1075
Author(s):  
Jascha Bandemehr ◽  
Matthias Conrad ◽  
Florian Kraus

Single crystals of K2Hg(SCN)4[dipotassium tetrathiocyanatomercurate(II)] were grown from aqueous solutions of potassium thiocyanate and mercury(II) thiocyanate and studied by single-crystal X-ray diffraction. In comparison with the previously reported structure model [Zvonkova (1952).Zh. Fiz. Khim.26, 1798–1803], all atoms in the crystal structure were located, with lattice parameters and fractional coordinates determined to a much higher precision. In the (crystal) structure, the HgIIatom is located on a twofold rotation axis and is coordinated in the form of a distorted tetrahedron by four S atoms of the thiocyanate anions. The K+cation shows a coordination number of eight.


CrystEngComm ◽  
2021 ◽  
Author(s):  
O.D. Chimitova ◽  
B.G. Bazarov ◽  
Jibzema G. Bazarova ◽  
Victor V. Atuchin ◽  
Raheleh Azmi ◽  
...  

Single crystals of RbFe5(MoO4)7 were successfully grown by the flux method, and its crystal structure was determined using the X-ray single-crystal diffraction technique. The XRD analysis showed that the compound...


Molecules ◽  
2021 ◽  
Vol 26 (13) ◽  
pp. 4067
Author(s):  
Giovanni Ricci ◽  
Giuseppe Leone ◽  
Giorgia Zanchin ◽  
Benedetta Palucci ◽  
Alessandra Forni ◽  
...  

Some novel cobalt diphenylphosphine complexes were synthesized by reacting cobalt(II) chloride with (2-methoxyethyl)diphenylphosphine, (2-methoxyphenyl)diphenylphosphine, and 2-(1,1-dimethylpropyl)-6-(diphenylphosphino)pyridine. Single crystals suitable for X-ray diffraction studies were obtained for the first two complexes, and their crystal structure was determined. The novel compounds were then used in association with methylaluminoxane (MAO) for the polymerization of 1,3-butadiene, and their behavior was compared with that exhibited in the polymerization of the same monomer by the systems CoCl2(PnPrPh2)2/MAO and CoCl2(PPh3)2/MAO. Some significant differences were observed depending on the MAO/Co ratio used, and a plausible interpretation for such a different behavior is proposed.


2008 ◽  
Vol 63 (5) ◽  
pp. 530-536 ◽  
Author(s):  
Olaf Reckeweg ◽  
Francis J. DiSalvo

Single crystals of Ca11N6[CN2]2 (dark red needles, tetragonal, P42/mnm (no. 136), a = 1456.22(5), and c = 361.86(2) pm, Z = 2), Ca4N2[CN2] (transparent yellow needles, orthorhombic, Pnma (no. 62), a = 1146.51(11), b = 358.33(4), and c = 1385.77(13) pm, Z = 4) and Ca[CN2] (transparent, colorless, triangular plates, rhombohedral, R3̅m (no. 166), a = 369.00(3), and c = 1477.5(3) pm, Z = 3) were obtained by the reaction of Na2[CN2], CaCl2 and Ca3N2 (if demanded by stoichiometry) in arc-welded Ta ampoules at temperatures between 1200 - 1400 K. Their crystal structures were re-determined by means of single crystal X-ray structure analyses. Additionally, the Raman spectra were recorded on these same single crystals, whereas the IR spectra were obtained with the KBr pellet technique. The title compounds exhibit characteristic features for carbodiimide units with D∞h symmetry (d(C-N) = 121.7 - 123.8 pm and ∡ (N-C-N) = 180°). The vibrational frequencies of these units are in the expected range (Ca11N6[CN2]2: νs = 1230, νs = 2008; δ = 673/645/624 cm−1; Ca4N2[CN2]: νs = 1230, νs = 1986; δ = 672/647 cm−1; Ca[CN2]: νs = 1274, νs = 2031, δ = 668 cm−1). The structural results are more precise than the previously reported data, and with the newly attained Raman spectrum of Ca11N6[CN2]2 we correct data reported earlier.


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