Two Organic Phase Suspension Polymerization for Novel Hypercrosslinked Resin Bead by Polycondensation of CMB

Here we describe the synthesis and electrochemical testing of a heteroleptic bis(tridentate) ruthenium(II) complex [RuII(LR)(L)]0 (LR =2,6-bis(1-(2-octyldodecan)benzimidazol-2-yl)pyridine, L = 2,6-bis(benzimidazolate)pyridine). It is a neutral complex which undergoes a quasireversible oxidation and reduction at relatively low potential. The newly synthetized compound was used for studies of ion-transfer at the three-phase junction because of the sensitivity of this method to cation expulsion. The [RuII(LR)(L)]0 shows exceptional stability during cycling and is sufficiently lipophilic even after oxidation to persist in the organic phase also using very hydrophilic anions such as Cl−. Given its low redox potential and strong lipophilicity this compound will be of interest as an electron donor in liquid-liquid electrochemistry.

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Three-Phase Electrochemistry of a Highly Lipophilic Neutral Ru-Complex Having a Tridentate Bis(benzimidazolate)pyridine Ligand

10.26434/chemrxiv.12170136.v1 ◽

2020 ◽

Author(s):

Vishwanath R.S ◽

Masa-aki Haga ◽

Takumi Watanabe ◽

Emilia Witkowska Nery ◽

Martin Jönsson-Niedziolka

Keyword(s):

Redox Potential ◽

Organic Phase ◽

Electron Donor ◽

Ion Transfer ◽

Neutral Complex ◽

Pyridine Ligand ◽

Electrochemical Testing ◽

Ru Complex ◽

Three Phase ◽

Exceptional Stability

Here we describe the synthesis and electrochemical testing of a heteroleptic bis(tridentate) ruthenium(II) complex [RuII(LR)(L)]0 (LR =2,6-bis(1-(2-octyldodecan)benzimidazol-2-yl)pyridine, L = 2,6-bis(benzimidazolate)pyridine). It is a neutral complex which undergoes a quasireversible oxidation and reduction at relatively low potential. The newly synthetized compound was used for studies of ion-transfer at the three-phase junction because of the sensitivity of this method to cation expulsion. The [RuII(LR)(L)]0 shows exceptional stability during cycling and is sufficiently lipophilic even after oxidation to persist in the organic phase also using very hydrophilic anions such as Cl−. Given its low redox potential and strong lipophilicity this compound will be of interest as an electron donor in liquid-liquid electrochemistry.

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Three-Phase Electrochemistry of a Highly Lipophilic Neutral Ru-Complex Having a Tridentate Bis(benzimidazolate)pyridine Ligand

10.26434/chemrxiv.12170136 ◽

2020 ◽

Author(s):

Vishwanath R.S ◽

Masa-aki Haga ◽

Takumi Watanabe ◽

Emilia Witkowska Nery ◽

Martin Jönsson-Niedziolka

Keyword(s):

Redox Potential ◽

Organic Phase ◽

Electron Donor ◽

Ion Transfer ◽

Neutral Complex ◽

Pyridine Ligand ◽

Electrochemical Testing ◽

Ru Complex ◽

Three Phase ◽

Exceptional Stability

Here we describe the synthesis and electrochemical testing of a heteroleptic bis(tridentate) ruthenium(II) complex [RuII(LR)(L)]0 (LR =2,6-bis(1-(2-octyldodecan)benzimidazol-2-yl)pyridine, L = 2,6-bis(benzimidazolate)pyridine). It is a neutral complex which undergoes a quasireversible oxidation and reduction at relatively low potential. The newly synthetized compound was used for studies of ion-transfer at the three-phase junction because of the sensitivity of this method to cation expulsion. The [RuII(LR)(L)]0 shows exceptional stability during cycling and is sufficiently lipophilic even after oxidation to persist in the organic phase also using very hydrophilic anions such as Cl−. Given its low redox potential and strong lipophilicity this compound will be of interest as an electron donor in liquid-liquid electrochemistry.

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Stabilization of pH in Solid-matrix Hydroponic Systems

HortScience ◽

10.21273/hortsci.28.10.981 ◽

1993 ◽

Vol 28 (10) ◽

pp. 981-984 ◽

Cited By ~ 3

Author(s):

Jay Frick ◽

Cary A. Mitchell

Keyword(s):

Seed Yield ◽

Seed Oil ◽

Exchange Resin ◽

Cation Exchange Resin ◽

Solid Matrix ◽

Resin Bead ◽

Resin Beads ◽

Hydroponic Systems ◽

Ethanesulfonic Acid ◽

Substrate Ph

2-[N-morpholino] ethanesulfonic acid (MES) buffer or Amberlite DP-1 (cation-exchange resin beads) were used to stabilize substrate pH of passive-wicking, solid-matrix hydroponic systems in which small canopies of Brassica napus L. (CrGC 5-2, genome: ACaacc) were grown to maturity. Two concentrations of MES (5 or 10 m m) were included in Hoagland 1 nutrient solution. Alternatively, resin beads were incorporated into the 2 vermiculite: 1 perlite (v/v) growth medium at 6% or 12% of total substrate volume. Both strategies stabilized pH without toxic side effects on plants. Average seed yield rates for all four pH stabilization treatments (13.3 to 16.9 g·m-2·day-1) were about double that of the control (8.2 g·m-2·day-1), for which there was no attempt to buffer substrate pH. Both the highest canopy seed yield rate (16.9 g·m-2·day-1) and the highest shoot harvest index (19.5%) occurred with the 6% resin bead treatment, even though the 10 mm MES and 12% bead treatments maintained pH within the narrowest limits. The pH stabilization methods tested did not significantly affect seed oil and protein contents.

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Extraction of hafnium(IV) with organophosphorus reagents from solutions of mineral acids mixtures

Collection of Czechoslovak Chemical Communications ◽

10.1135/cccc19793656 ◽

1979 ◽

Vol 44 (12) ◽

pp. 3656-3664

Author(s):

Oldřich Navrátil ◽

Jiří Smola ◽

Rostislav Kolouch

Keyword(s):

Ionic Strength ◽

Aqueous Phase ◽

Organic Phase ◽

Perchloric Acid ◽

Synergic Effect ◽

Salting Out ◽

Initial Concentration ◽

Mixed Complexes ◽

Synergic Extraction ◽

Mineral Acids

Extraction of hafnium(IV) was studied from solutions of mixtures of perchloric and nitric acids and of perchloric and hydrochloric acids for constant ionic strength, I = 2, 4, 6, or 8, and for cHf 4 . 10-4 mol l-1. The organic phase was constituted by solutions of some acidic or neutral organophosphorus reagents or of 2-thenoyltrifluoroacetone, 1-phenyl-3-methyl-4-benzoyl-5-pyrazolone, or N-benzoyl-N-phenylhydroxylamine in benzene, chloroform, or n-octane. A pronounced synergic extraction of hafnium proceeds only on applying organophosphorus reagents from an aqueous phase whose acidity is not lower than 3M-(HClO4 + HNO3) or 5M-(HClO4 + HCl). The synergic effect was not affected markedly by a variation of the initial concentration of hafnium in the range 1 . 10-8 -4 .10-4 mol l-1, it lowered with increasing initial concentration of the organophosphorus reagent and decreasing concentration of the H+ ions. It is suggested that the hafnium passes into the organic phase in the form of mixed complexes, the salting-out effect of perchloric acid playing an appreciable part.

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Extraction of strontium and barium salts by the nitrobenzene solution of dicarbolide in the presence of glymes

Collection of Czechoslovak Chemical Communications ◽

10.1135/cccc19850581 ◽

1985 ◽

Vol 50 (3) ◽

pp. 581-599 ◽

Cited By ~ 41

Author(s):

Petr Vaňura ◽

Emanuel Makrlík

Keyword(s):

Stability Constants ◽

Organic Phase ◽

Equilibrium Constants ◽

Minor Role ◽

Nitrobenzene Solution ◽

Ligand Structure ◽

Stability Constants Of Complexes ◽

Separation Factors ◽

The Stability ◽

A Minor

Extraction of microamounts of Sr2+ and Ba2+ (henceforth M2+) from the aqueous solutions of perchloric acid (0.0125-1.02 mol/l) by means of the nitrobenzene solutions of dicarbolide (0.004-0.05 mol/l of H+{Co(C2B9H11)2}-) was studied in the presence of monoglyme (only Ba2+), diglyme, triglyme, and tetraglyme (CH3O-(CH2-CH2O)nCH3, where n = 1, 2, 3, 4). The distribution of glyme betweeen the aqueous and organic phases, the extraction of the protonized glyme molecule HL+ together with the extraction of M2+ ion and of the glyme complex with the M2+ ion, i.e., ML2+ (where L is the molecule of glyme), were found to be the dominating reactions in the systems under study. In the systems with tri- and tetraglymes the extraction of H+ and M2+ ions solvated with two glyme molecules, i.e., the formation of HL2+ and ML22+ species, can probably play a minor role. The values of the respective equilibrium constants, of the stability constants of complexes formed in the organic phase, and the theoretical separation factors αBa/Sr were determined. The effect of the ligand structure on the values of extraction and stability constants in the organic phase is discussed.

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Europium and cerium extraction by the nitrobenzene solution of dicarbolide in the presence of polyethylene glycols

Collection of Czechoslovak Chemical Communications ◽

10.1135/cccc19860498 ◽

1986 ◽

Vol 51 (3) ◽

pp. 498-515 ◽

Cited By ~ 13

Author(s):

Emanuel Makrlík ◽

Petr Vaňura

Keyword(s):

Molecular Weight ◽

Polyethylene Glycol ◽

Organic Phase ◽

Perchloric Acid ◽

Equilibrium Constants ◽

Polyethylene Glycols ◽

Individual Species ◽

Nitrobenzene Solution ◽

Separation Factors ◽

Equilibrium Data

Extraction of Eu3+ and Ce3+ microamounts from 0.1-0.4M perchloric acid by the nitrobenzene solution of dicarbolide H+[Co(C2B9H11)2]- in the presence of polyethylene glycols (Mr = 200, 300, 400) has been studied. The equilibrium data and the typical maxima on the dependence of the metal distribution ratio on the total analytical concentration of polyethylene glycol in the system can be explained assuming that the species ML3+org, ML3+2org, ML3+3org, MLH2+-1org, and HL+org (where M3+ = Eu3+, Ce3+; L = polyethylene glycol) are extracted into the organic phase. The values of extraction and equilibrium constants in the organic phase were determined and the effect of the polyethylene glycol molecular weight on the equilibrium constants and on the abundances of individual species in the organic phase is discussed. It has been found that the addition of polyethylene glycol to the acid - nitrobezene - dicarbolide system increases the values of the separation factors αCe/Eu.

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Extraction of Am(III) by benzyldibutylamine from nitrate solutions of lanthanides

Collection of Czechoslovak Chemical Communications ◽

10.1135/cccc19810194 ◽

1981 ◽

Vol 46 (1) ◽

pp. 194-200 ◽

Cited By ~ 2

Author(s):

Marta Vojtíšková ◽

Věra Jedináková ◽

Libor Kuča

Keyword(s):

Nitric Acid ◽

Nuclear Fuel ◽

Organic Phase ◽

Spent Nuclear Fuel ◽

Optimum Conditions ◽

Separation Factors ◽

Nitrate Solutions

Benzyldibutylamine is a suitable extractant for the separation of Am(III) and Ln(III) from the acidic nitrate solutions. The effect of lanthanides and yttrium on the extraction of Am(III) has been followed under the conditions modelling the content of these components in the spent nuclear fuel. The separation factors αAm/Ln were evaluated for the optimum conditions found for the separation of Am(III) from the lanthanides. The coextraction of nitric acid and water into the organic phase is discussed.

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Determination of trace amounts of cobalt by homogeneous isotope exchange in an organic phase

Collection of Czechoslovak Chemical Communications ◽

10.1135/cccc19803332 ◽

1980 ◽

Vol 45 (12) ◽

pp. 3332-3337

Author(s):

Václav Jiránek

Keyword(s):

Organic Phase ◽

Isotope Exchange ◽

Radiochemical Method

A new radiochemical method for determining trace amounts of cobalt has been worked out. It is based on a homogeneous isotope exchange between cobalt(III) diethyldithiocarbamate and cobalt(III) caprate in an organic phase. The method, tested in the range 0.005-8 μg Co, has proved to be selective.

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