Thiol exchange reactions of iron–molybdenum–sulphur clusters; preparation and X-ray crystal structure of [Et4N]3[Fe6Mo2S8(SCH2CH2OH)9], a water soluble iron–molybdenum–sulphur cluster

Author(s):  
George Christou ◽  
C. David Garner ◽  
Frank E. Mabbs ◽  
Michael G. B. Drew
2018 ◽  
Vol 82 (5) ◽  
pp. 1057-1077 ◽  
Author(s):  
Elena S. Zhitova ◽  
Oleg I. Siidra ◽  
Dmitry I. Belakovsky ◽  
Vladimir V. Shilovskikh ◽  
Anton A. Nuzhdaev ◽  
...  

AbstractAmmoniovoltaite, (NH4)2Fe2+5Fe3+3Al(SO4)12(H2O)18, is a new voltaite-group mineral. The mineral was discovered at the Severo-Kambalny (North-Kambalny) geothermal field, Kambalny volcanic ridge, Southern Kamchatka, Russia. Ammoniovoltaite forms at ~100°C around geothermal gas/steam vents in association with alunogen, tschermigite and pyrite. Crystals of ammoniovoltaite have euhedral habit, are up to 50 µm in size and grow on alunogen plates. Ammoniovoltaite is black with vitreous lustre, opaque, brittle and water-soluble. Neither cleavage nor parting is found, the fracture is conchoidal. The mineral is isotropic, with the refractive index n = 1.602(2) (589 nm). Infrared spectra contain an absorption band at 1433 cm–1 distinctive for the ammonium ion. The chemical composition is (iron content is given in accordance with Mössbauer data, H2O calculated from a crystal-structure refinement, wt.%): FeO 13.26, Fe2O3 11.58, MgO 2.33, ZnO 0.04, Al2O3 2.74, SO3 47.46, K2O 0.19, CaO 0.11, (NH4)2O 2.96, H2O 16.03, total 96.70. The empirical formula based on S = 12 atoms per formula unit is [(NH4)1.88K0.08Ca0.04]Σ2.00(Fe2+3.74Mg1.17Fe3+0.05Zn0.01)Σ4.97(Fe3+2.89Al0.09)Σ2.98Al1.00(SO4)12.00(H2O)18.00. The crystal structure has been refined to R1 = 0.031 and 0.030 on the basis of 1217 and 1462 unique reflections with I >2σ(I) collected at 100 K and room temperature, respectively. Ammoniovoltaite is the ammonium analogue of voltaite. The mineral is cubic, Fd$\bar{3}$c, a = 27.250(1) Å and V = 20234(3) Å3 (at 100 K); and a = 27.322(1) Å and V = 20396(3) Å3 (at RT), with Z = 16. The strongest lines of the powder X-ray diffraction pattern [d, Å (I, %) (hkl)] are: 9.67 (74) (022), 7.90 (56) (222), 5.58 (84) (422), 3.560 (100) (731), 3.418 (100) (008) and 2.8660 (37) (931). A brief review of ammonium minerals from various volcanically active geological environments is given.


2014 ◽  
Vol 1033-1034 ◽  
pp. 1172-1175
Author(s):  
Li Ping Lin ◽  
Feng Hua Huang ◽  
Pei Feng Chen

The water-soluble ZnSe:Ag quantum dots were synthesized in aqueous medium by chemical co-precipitation method with L-cysteine as surface modifier. The crystal structure and optical properties of the obtained ZnSe:Ag quantum dots have been characterized by X-ray power diffraction, infrared spectrum, UV-Vis absorption spectrum and photoluminescence spectrum. Results indicate that ZnSe:Ag quantum dots belong to the cubic blende structure and have good fluorescent characteristics. The L-cysteine modified on the surface of ZnSe:Ag quantum dots renders the quantum dots water-soluble, biocompatible.


2002 ◽  
Vol 80 (11) ◽  
pp. 1410-1414 ◽  
Author(s):  
Mark RJ Elsegood ◽  
Liam M Gilby ◽  
Kathryn E Holmes ◽  
Paul F Kelly

Treatment of the thio-ether crown [9-ane]S3 (1) with 1 equiv of O-mesitylsulfonylhydroxylamine (MSH) yields the water-soluble protonated sulfimide {[9-ane]S2S(NH2)}+ (2). Two equiv of MSH leads to the formation of {[9-ane]SS(NH2)S(NH2)}2+ (3), while excess MSH generates the {[9-ane]S(NH2)S2(μ-N)}2+ cation (4) (2–4 form as salts of the [Me3C6H2SO3]– anion); the X-ray crystal structure of 2 and 3 confirms that one and two of the ring sulfurs, respectively, have been converted to terminal protonated sulfimides, while that of 4 reveals the presence of both terminal and bridging nitrogens.Key words: sulfur-nitrides, macrocycles, sulfimides, amination.


1993 ◽  
Vol 32 (2) ◽  
pp. 218-222 ◽  
Author(s):  
Matthew E. Riehl ◽  
Scott R. Wilson ◽  
Gregory S. Girolami

Sign in / Sign up

Export Citation Format

Share Document