scholarly journals HYDROSOL OF C70 FULLERENE: SYNTHESIS AND STABILITY IN ELECTROLYTIC SOLUTIONS

2021 ◽  
Vol 87 (10) ◽  
pp. 63-73
Author(s):  
Nikolay Mchedlov-Petrossyan ◽  
Mykyta Marfunin ◽  
Volodymyr Klochkov ◽  
Petro Radionov

This article is devoted to the synthesis and characterization of the hydrosol of C70 of the son/nC70 type and to its coagulation by sodium chloride and cetyltrimethylammonium bromide (CTAB). At C70 concentration of 3.3×10–6 M, the electrokinetic potential is ζ= –40 ± 4 mV, the particle size expressed as Zeta-average is 97±3 nm; at higher C70 concentrations, 1.7×10–5 and 6.9×10–5 M, the size stays the same: 99 – 100 nm. The critical concentration of coagulation (CCC) values, were determined using the diameter increasing rate (DIR) on NaCl concentration. The CCCs are concentration-dependent: 250, 145, and 130 mM at C70 concentrations 3.3×10–6, 1.7×10–5, and 6.9×10–5 M, respectively. The CCC for the CTAB surfactant is much lower, about 5×10–3 mM. At 0.02 mM CTAB, however, the overcharging up to ζ = + 40 mV and stabilization of the colloidal particles take place. Interpretation of the hydrosol coagulation by NaCl using the Derjaguin–Landau–Verwey–Overbeek theory makes it possible to determine the Hamaker constant of the C70–C70 interaction in vacuum, if only electrostatic repulsion and molecular attraction are taking into account: AFF ≈ 7×10–20 J. On the other hand, if we use the value AFF = (16.0–16.6)×10–20 J, obtained earlier in the study of organosols, then the data for hydrosols can be explained only by the introduction of an additional type of interactions. Following the terms of Churaev and Derjaguin, one should take into account the structural contribution to the interaction energy, which stabilizes the hydrosol.

2012 ◽  
Vol 2012 ◽  
pp. 1-5 ◽  
Author(s):  
Esmael Salimi ◽  
Jafar Javadpour

Wormhole-like mesostructured monetite was successfully synthesized using cetyltrimethylammonium bromide (C19H42BrN, CTAB), as a porosity agent. X-ray techniques and FTIR reveal that the crystalline grains consist of highly crystalline pure monetite phase. Monetite rods with diameter around 20–40 nm and length in the range of 50–200 nm were confirmed by FESEM and TEM. Based on N2adsorption-desorption isotherms investigation, surface area increased up to 31.5 m2/g due to the removal of surfactant after calcinations at 400°C. The results indicate that CTAB can not only affect monetite crystallization but also change particles morphology from plate shape to rod-like.


Soft Matter ◽  
2018 ◽  
Vol 14 (15) ◽  
pp. 2870-2878 ◽  
Author(s):  
F. Y. de Boer ◽  
R. N. U. Kok ◽  
A. Imhof ◽  
K. P. Velikov

Driven by the growing interest in using natural ingredients in food and beverages, novel plant protein-based particles are developed as all natural, edible white colorant and clouding agent.


2021 ◽  
Vol 77 (3) ◽  
pp. 152-160
Author(s):  
Philipp Honegger ◽  
Alexander Roller ◽  
Michael Widhalm

In the course of an ongoing synthetic project on cyclic diferrocenylphosphines, we obtained a group of planar–chiral diferrocenyl compounds useful as precursors for subsequent cyclization. Here we report the crystal structures of two symmetric compounds [(FcA)2(Ph)P], one of which contains four stereogenic centres (two C chiral and two planar chiral centres), i.e. 1,1′-(phenylphosphanediyl)bis{(2S p)-2-[(1R)-1-(acetyloxy)ethyl]ferrocene}, [Fe2(C5H5)2(C24H25O4P)], and the other phosphine sulfide is a purely planar–chiral compound (two planar chiral centres), i.e. bis[(2S p)--2-ethenylferrocen-1-yl]phenylphosphane sulfide, [Fe2(C5H5)2(C20H17PS)]. Owing to the stereocentres present, reactions performed on [(FcA)2(Ph)P]-type compounds strongly favour one ferrocene unit over the other due to diastereoselectivity. Furthermore, we present four related structures where the ferrocene units are not identical [(FcA)(FcB)(Ph)P]. These are {(2S p)-2-[(1R)-1-(acetyloxy)ethyl]ferrocen-1-yl}[(2S p)-2-ethenylferrocen-1-yl]phenyl-(S)-phosphine sulfide, [Fe2(C5H5)2(C22H21O2PS)], [(2S p)-2-ethenylferrocen-1-yl]{(2S p)-2-[(1R)-1-hydroxyethyl]ferrocen-1-yl}phenyl-(S)-phosphine sulfide, [Fe2(C5H5)2(C20H19OPS)], {(2S p)-2-[(1R)-1-(acetyloxy)ethyl]ferrocen-1-yl}{(2S p)-2-[(1R)-1-hydroxyethyl]ferrocen-1-yl}phenyl-(R)-phosphine sulfide, [Fe2(C5H5)2(C22H23O3PS)], and {(2S p)-2-[(1R)-1-benzylamino)ethyl]ferrocen-1-yl}[(2S p)-2-ethenylferrocen-1-yl]phenyl-(S)-phosphine sulfide, [Fe2(C5H5)2(C27H26NPS)]. All of the structures are accessible in one step from known precursors.


2010 ◽  
Vol 305-306 ◽  
pp. 89-94
Author(s):  
A. Samadi Maybodi ◽  
S.K. Hassani Nejad-Darzi

Zinc phosphate molecular sieve were synthesized using zinc chloride, phosphoric acid as a zinc and phosphor source, respectively. Different types of zinc phosphates zeolites were synthesized by conventional hydrothermal (using (2-hydroxyethyl) trimethylammonium hydroxide (2-HETMAOH) as new template. Also, ethylene glycol (EG) was utilized as co-solvent and ultrasonic tool was applied as mixer. The influence of the chemical composition of the starting sol-gel and the other parameters such as, Zn/P mole ratio, time of microwave irradiation were studied.


2019 ◽  
Vol 75 (7) ◽  
pp. 872-876
Author(s):  
Lukáš Krivosudský ◽  
Alexander Roller ◽  
Annette Rompel

The monovanadium-substituted polyoxometalate anion [VMo7O26]5−, exhibiting a β-octamolybdate archetype structure, was selectively prepared as pentapotassium [hexaikosaoxido(heptamolybdenumvanadium)]ate hexahydrate, K5[VMo7O26]·6H2O (VMo7 ), by oxidation of a reduced vanadomolybdate solution with hydrogen peroxide in a fast one-pot approach. X-ray structure analysis revealed that the V atom occupies a single position in the cluster that differs from the other positions by the presence of one doubly-bonded O atom instead of two terminal oxide ligands in all other positions. The composition and structure of VMo7 was also confirmed by elemental analyses and IR spectroscopy. The selectivity of the synthesis was inspected by a 51V NMR investigation which showed that this species bound about 95% of VV in the crystallization solution. Upon dissolution of VMo7 in aqueous solution, the [VMo7O26]5− anion is substantially decomposed, mostly into [VMo5O19]3−, α-[VMo7O26]4− and [V2Mo4O19]4−, depending on the pH.


1987 ◽  
Vol 42 (5) ◽  
pp. 599-604 ◽  
Author(s):  
Rainer Mattes ◽  
Heinz Scholand ◽  
Ulrich Mikloweit ◽  
Volker Schrenk

transThe reaction of NH2NHC(S)OR, (R = Me, Et) with MoO2(acac)2 yields the dimeric complexes MO2O3(MeC(O)CHC(Me)NNC(S)0R)2 (1) with the planar O = Mo - O - Mo = O group. The tetradentate O,N,S-donor ligand is formed through condensation of acetylacetone with the organohydrazine. The reactions of NH2NHC(S)OMe with MoO2(S2CNEt2)2 and MoO2(ONEt2)2 give the diazenido hydrazido complexes Mo(NNC(S)OMe)(NH2NC(S)OMe)(S2CNEt2)2·CH2Cl2(2) and Mo(NNC(S)OMe)(NH2NC(S)OMe)2(ONEt2) (4). The metal atoms in both compounds are seven coordinated and contain the approximately linear diazenido ligand NNC(S)OMe and one (2) or two (4) N,S-chelating hydrazido(1-) ligands NH2NC(S)OMe. 2 has crystallographically imposed mirror symmetry. Recrystallization of 2 from toluene in air gives the asymmetric dinuclear complex (Et2NCS2)(O)Mo(μ-NNC(S)OMe)2Mo(S2CNMe2) (3). The Mo-Mo distance is 267.0(2) pm. One Mo site has square pyramidal MoOS2N2 geometry, the other trigonal prismatic MoN2S4 geometry. The coordination of the bridging N atoms is slightly pyramidal. The compounds 1, 2 and 3 have been further characterized by vibrational spectroscopy.


1986 ◽  
Vol 64 (1) ◽  
pp. 208-212 ◽  
Author(s):  
Shantha David ◽  
David Dolphin ◽  
Brian R. James ◽  
John B. Paine III ◽  
Tilak P. Wijesekera ◽  
...  

Sterically hindered porphyrins having a fully hydrophobic cavity have been prepared. The cavity is capped with a 2,3,5,6-tetramethylbenzene moiety containing at the 1,4-positions methylene —(CH2)n— chains (n = 4, 5, 7) bonded at trans pyrrole rings of a porphyrin that is alkylated with methyl or ethyl groups at the other β-pyrrolic positions. The iron(III) chloride derivative of the 4,4-durene-capped base has been obtained as single crystals, and subjected to X-ray structural analysis. The typical high spin, square pyramidal geometry of five-coordinate hemin chlorides is maintained; the porphyrin core is strongly distorted and there is no interaction between the phenyl group of the strap and the iron.


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