Reductions with sulfurated borohydrides. I. Preparation of sulfurated borohydrides

1968 ◽  
Vol 46 (16) ◽  
pp. 2754-2757 ◽  
Author(s):  
J. M. Lalancette ◽  
A. Frêche ◽  
R. Monteux

Sodium borohydride reacts with sulfur at room temperature in the presence of appropriate organic solvents to give a sulfurated borohydride: NaBH2S3. The formulation of this hydride has been established by infrared, nuclear magnetic resonance, and elementary analysis. Thermal decomposition and hydrolysis are reported. The reaction observed with NaBH4 appears to be general between borohydrides and the lower elements of Group VIA: Se and Te. A facile preparative method of NaBH2S3 is presented.

ChemInform ◽  
2013 ◽  
Vol 44 (9) ◽  
pp. no-no
Author(s):  
J. Maziero ◽  
R. Auccaise ◽  
L. C. Celeri ◽  
D. O. Soares-Pinto ◽  
E. R. deAzevedo ◽  
...  

1985 ◽  
Vol 40 (2) ◽  
pp. 126-130 ◽  
Author(s):  
N. Weiden ◽  
H. Rager

The angular dependence of the chemical shift of the 29Si nuclear magnetic resonance has been measured in a synthetic single crystal of Mg2SiO4 (space group Pbnm, Z = 4). The measurements were performed at room temperature at a frequency of 39.758 MHz using the FT-NMR technique. The eigenvalues of the shift tensor with respect to 29Si in TMS are δx = - 38.8 ppm, δv = -55.3 ppm and δz = - 95.4 ppm, with the eigenvector y parallel to c and the eigenvector z forming an angle of 7.5° with a. The results show clearly the influence of the individual S i - O bonds on the chemical shift tensor. The chemical shift along the S i -O bond depends in good approximation exponentially on the S i - O bond distance.


2015 ◽  
Vol 44 (36) ◽  
pp. 16156-16163 ◽  
Author(s):  
Alejandro G. Lichtscheidl ◽  
Michael T. Janicke ◽  
Brian L. Scott ◽  
Andrew T. Nelson ◽  
Jaqueline L. Kiplinger

The synthesis and full characterization by Nuclear Magnetic Resonance (1H,13C{1H} and119Sn{1H}) of eleven Me3SnX complexes in six common organic solvents is presented.


1971 ◽  
Vol 49 (8) ◽  
pp. 1151-1160 ◽  
Author(s):  
P. R. Heckley ◽  
D. G. Holah ◽  
D. Brown

Reactions between niobium(V), tantalum(V), and protactinium(V) chlorides and bromides and sodium N,N-diethyldithiocarbamate (Nadtc) have been examined in non-aqueous, non-oxygenated organic solvents. Complexes obtained are of the types Mdtc4X, Mdtc3X2, Mdtc3S, Mdtc2X3, and Mdtc2X3.nC6H6 (n = 0.7–1.0); not all complexes have been isolated for each metal. Within each group the niobium(V) and tantalum(V) complexes are isostructural; possible structures are discussed in the light of results from infrared (i.r.) and nuclear magnetic resonance (n.m.r.) spectra, molecular weight, and electrical conductivity measurements.


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