scholarly journals The synthesis of ternary acetylides with tellurium: Li2TeC2 and Na2TeC2

RSC Advances ◽  
2015 ◽  
Vol 5 (69) ◽  
pp. 55986-55993 ◽  
Author(s):  
Károly Németh ◽  
Aditya K. Unni ◽  
Christopher Kalnmals ◽  
Carlo U. Segre ◽  
James Kaduk ◽  
...  

Novel ternary acetylides Li2TeC2 and Na2TeC2 were synthesized via the robust direct reaction of tellurium powder and mono- or bialkali acetylides in liquid ammonia.

Science ◽  
2011 ◽  
Vol 331 (6023) ◽  
pp. 1426-1429 ◽  
Author(s):  
A. D. Sutton ◽  
A. K. Burrell ◽  
D. A. Dixon ◽  
E. B. Garner ◽  
J. C. Gordon ◽  
...  

ChemInform ◽  
2011 ◽  
Vol 42 (26) ◽  
pp. no-no
Author(s):  
Andrew D. Sutton ◽  
Anthony K. Burrell ◽  
David A. Dixon ◽  
Edward B. III Garner ◽  
John C. Gordon ◽  
...  

1976 ◽  
Vol 73 ◽  
pp. 849-851 ◽  
Author(s):  
Thomas Kottarathil ◽  
Gérard Lepoutre

1999 ◽  
Vol 40 (4-5) ◽  
pp. 107-114 ◽  
Author(s):  
A. Kornmüller ◽  
U. Wiesmann

The continuous ozonation of polycyclic aromatic hydrocarbons (PAH) was studied in a two stage ozonation system followed by serobic biological degradation. The highly condensed PAH benzo(e)pyrene and benzo(k)fluoranthene were oxidized selectiely in synthetic oil/water-emulsions. The influence of the ozone mass transfer gas-liquid on the reaction rate of benzo(k)fluoranthene was studied for process optimization. The dissolved ozone concentration is influenced by temperature to a higher degree than the reaction rate of PAH. In dependence on pH, PAH oxidation occurs by a direct reaction with ozone inside the oil droplets. Two main ozonation products of benzo(e)pyrene were quantified at different retention times during ozonation and their transformation could be shown in the biological treatment step.


1970 ◽  
Vol 35 (12) ◽  
pp. 3757-3761 ◽  
Author(s):  
J. Matouš ◽  
J. Šobr ◽  
J. P. Novák

1981 ◽  
Vol 46 (10) ◽  
pp. 2345-2353 ◽  
Author(s):  
Karel Baše ◽  
Bohumil Štíbr ◽  
Jiří Dolanský ◽  
Josef Duben

The 6-N(CH3)3-6-CB9H11 carbaborane reacts with sodium in liquid ammonia with the formation of 6-CB9H12- which was used as a starting compound for preparing the 4-CB8H14, 9-L-6-CB9H13 (L = (CH3)2S, CH3CN and P(C6H5)3), 1-(η5-C5H5)-1,2-FeCB9H10-, and 2,3-(η5-C5H5)2-2,31-Co2CB9H10- carboranes. The 4-CB8H14 compound was dehydrogenated at 623 K to give 4-(7)-CB8H12 carborane. Base degradation of 6-N(CH3)3-6-CB9H11 in methanol resulted in the formation of 3,4-μ-N(CH3)3CH-B5H10. The structure of all compounds was proposed on the basis of their 11B and 1H NMR spectra and X-ray diffraction was used in the case of the transition metal complexes.


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