Steric effects: the problem of their quantitative assessment and manifestation in the reactivity of hetero-organic compounds

1991 ◽  
Vol 60 (8) ◽  
pp. 815-829 ◽  
Author(s):  
Vladimir I Galkin ◽  
R D Sayakhov ◽  
Rafael A Cherkasov
Nature ◽  
1954 ◽  
Vol 173 (4394) ◽  
pp. 117-119 ◽  
Author(s):  
E. A. BRAUDE ◽  
F. SONDHEIMER ◽  
W. F. FORBES

1979 ◽  
Vol 44 (6) ◽  
pp. 950-953 ◽  
Author(s):  
Fereidoon Shahidi ◽  
Patrick G. Farrell ◽  
John T. Edward ◽  
Persephone Canonne

Soil Systems ◽  
2021 ◽  
Vol 5 (2) ◽  
pp. 33
Author(s):  
Stella Gypser ◽  
Elisabeth Schütze ◽  
Dirk Freese

Phosphorus (P) fixation is a global problem for soil fertility and negatively impacts agricultural productivity. This study characterizes P desorption of already fixed P by using KCl, KNO3, histidine, and malic acid as inorganic and organic compounds, which are quite common in soil. Goethite, gibbsite, and ferrihydrite, as well as hydroxide mixtures with varying Fe- and Al-ratio were selected as model substances of crystalline and amorphous Fe- and Al-hydroxides. Especially two- and multi-component hydroxide systems are common in soils, but they have barely been included in desorption studies. Goethite showed the highest desorption in the range from 70.4 to 81.0%, followed by gibbsite with values in the range from 50.7 to 42.6%. Ferrihydrite had distinctive lower desorption in the range from 11.8 to 1.9%. Within the group of the amorphous Fe-Al-hydroxide mixtures, P desorption was lowest at the balanced mixture ratio for 1 Fe: 1 Al, increased either with increasing Fe or Al amount. Precipitation and steric effects were concluded to be important influencing factors. More P was released by crystalline Fe-hydroxides, and Al-hydroxides of varying crystallinity, but desorption using histidine and malic acid did not substantially influence P desorption compared to inorganic constituents.


1962 ◽  
Vol 40 (3) ◽  
pp. 449-454 ◽  
Author(s):  
D. C. Bradley ◽  
I. M. Thomas

Reactions involving niobium pentachloride and lithium dialkylamides (LiNR2, where R = Me, Et, Prn, Bun) led to considerable reduction of niobium to Nb(IV) as the length of the alkyl chains increased. Nb(NMe2)5 was isolated by sublimation but distillation of the other products gave tetrakis-(dialkylamino)-niobium(IV) compounds. Steric factors are apparently responsible for the low stability of pentakis-(dialkylamino)-niobium(V) compounds. The smaller steric effects of —NMeBun and piperidino groups allowed the isolation of pentakis derivatives. The thermal decomposition of Nb(NMeBun)5 gave mainly Nb(NMeBun)4 with some BunN=Nb(NMeBun)3. Steric effects were also revealed in the replacement of —NMe2 groups in Nb(NMe2)5 by —NEt2 groups and in replacement of —NEt2 groups in Nb(NEt2)4 by piperidino groups.


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