scholarly journals The Influence of Silicateins on the Shape and Crystalline Habit of Silica Carbonate Biomorphs of Alkaline Earth Metals (Ca, Ba, Sr)

Crystals ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 438
Author(s):  
Nuria Sánchez-Puig ◽  
Mayra Cuéllar-Cruz ◽  
Selene R. Islas ◽  
Juana V. Tapia-Vieyra ◽  
Roberto A. Arreguín-Espinosa ◽  
...  

This contribution presents the effect of two ortholog enzymes from marine sponges called silicateins on the formation of silica carbonate biomorphs of alkaline metals (Ca, Ba, Sr). In vivo, these enzymes participate in the polymerization of silica. Silicateins from Tethya aurantia and Suberitis domuncula were produced recombinantly and presented different degrees of activity, as evidenced by their ability to cleave silyl ether-like bonds in a model compound. Biomorphs are typically inorganic structures that show characteristic shapes resembling those of biological structures such as helices, leaves, flowers, disks or spheres. Irrespective of the concentration or the enzyme used, the presence of silicateins inhibited the formation of classic morphologies of biomorphs, albeit to different extents. Thus, not only the silica condensation activity of the enzyme but also its ability to bind silica compounds is implicated in the inhibition process. The largest effect was observed for the strontium and barium biomorphs, leading to the formation of spheres similar to those observed in diatoms and Radiolaria rather than the classical non-symmetrical forms. Characterization of the samples using Raman spectroscopy showed that silicatein did not affect the crystalline structure of the alkaline earth metal carbonate but did modify the crystalline habit.

2019 ◽  
Vol 2019 ◽  
pp. 1-6 ◽  
Author(s):  
Igor Povar ◽  
Inga Zinicovscaia ◽  
Oxana Spinu ◽  
Boris Pintilie

A thermodynamic method of the global Gibbs energy variation calculation for describing heterogeneous equilibria of transformations of calcium, strontium, and barium polyvanadates, that occur in systems MeO-V2O5-H2O, where Me is the alkaline earth element, has been developed and used. Its quintessence consists in the thermodynamic analysis of the real conditions of various processes on the basis of their total thermodynamic characteristics. On the basis of the selected thermodynamic data for involved species, the thermodynamic stability areas of solid polyvanadates towards the solution pH and vanadium and alkaline earth metal ion concentrations in heterogeneous mixtures have been established, taking into account the complex formation reactions in multicomponent heterogeneous systems. The existing experimental data confirm the results on the thermodynamic stability of polyvanadates obtained in this paper.


1989 ◽  
Vol 44 (5) ◽  
pp. 519-525 ◽  
Author(s):  
Hans-Jürgen Meyer ◽  
Joachim Pickardt

By reaction of methanolic solutions of hexamethylenetetramine with aqueous solutions of hexacyanoferrates(III) of strontium and barium resp., crystals of the compounds were obtained. Sr3[Fe(CN)6]2 · 3 C6H12N4 · 18 H2O, tetragonal, space group P42/nmc, Z = 4, a = 1931.8(4), c = 1579.9(4) pm, 1358 reflections. R = 0.066. Ba3[Fe(CN)6]2 · 2 C6H12N4 · 11 Η2Ο. monoclinic. space group P21/n, Ζ = 2, a = 1148.0(4), b = 1369.7(4), c = 1584.5(4) pm, γ = 95.79(3)°, 2583 reflections, R = 0.057. The crystal structures of these adducts are compared with those of other hexamethylenetetramine adducts of alkaline and alkaline earth metal hexacyanoferrates of the general formula M,[Fe(CN)6]y · zC6H12N4 · vH2O recently investigated by us. A structural model for the adducts is presented.


1978 ◽  
Vol 9 (43) ◽  
Author(s):  
R. C. MEHROTRA ◽  
S. GOEL ◽  
A. B. GOEL ◽  
R. B. KING ◽  
K. C. NAINAN

Author(s):  
Yun Chi ◽  
Sudhir Ranjan ◽  
Tsung-Yi Chou ◽  
Chao-Shiuan Liu ◽  
Shie-Ming Peng ◽  
...  

Vestnik RFFI ◽  
2019 ◽  
pp. 58-73
Author(s):  
Ivan V. Lapshin ◽  
Alexander A. Kissel ◽  
Alexander A. Trifonov

In accordance with United Nations General Assembly resolution, the year 2019 was proclaimed the International Year of the Periodic Table of Chemical Elements. Rare-earth elements were discovered during the time of the Periodic System development. In the past few decades, their compounds have attracted great interest due to their unique reactivity. This review covers recent achievements in the field of intermolecular hydrophosphination of alkenes, dienes and alkynes, which is catalyzed by rare earth and alkaline-earth metal complexes. Catalytic hydrophosphination reaction is the addition of an P—H bond to С—С multiple bonds, and offers an efficient and elegant synthetic approach to production of the organophosphorus compounds widely used in industrial synthesis, pharmaceuticals, agrochemistry, and other areas. The high values of the ionic radii of rare earth and alkaline-earth metals in combination with the Lewis acidity provide their compounds with a pronounced tendency to complex formation and, accordingly, high coordination numbers. Due to high reactivity of M—E (E = C, H, N, P) bonds, ease of Ln—P ı-bond metathesis and multiple C—C bond insertions, these compounds offer new prospects for the catalysis of the alkenes and alkynes hydrophosphination. Therefore, complexes of non-toxic and relatively abundant in nature rare earth and alkaline earth metals can be a cheaper and more effective alternative to compounds of late transition metals in the catalysis of the C—P bond formation.


2018 ◽  
Vol 20 (19) ◽  
pp. 13331-13339 ◽  
Author(s):  
Kaushik Hatua ◽  
Avijit Mondal ◽  
Prasanta K. Nandi

In the investigated inverse sandwich complexes, charge transfer from alkali metal (M1) led to aromatically stabilized Cp ring, which prevented further charge transfer from the alkaline earth metal (M2).


Sign in / Sign up

Export Citation Format

Share Document