Complexation boric acid

It was found in the first place that aliphatic, non-cyclic glycols without adjacent hydroxyl groups have no effect they cannot form cyclic complexes. But also most glycols with not more than two adjacent hydroxyl groups are inactive. I therefore assumed that only if two hydroxyl groups are favorably situated for the formation of a complex boric acid compound, will it be possible to observe an increase in the conductivity. 

The test for boron (page 139) in which a complex boric acid ester of -nitrobenzeneazochromotropic acid is formed, may be applied to detect boron in rocks, enamels, etc., after fusion with potassium hydroxide. The finely powdered sample is fused with potassium hydroxide in a silver crucible. The cold melt is extracted with a few drops of water the solution is filtered (using the device described on page 45) and the test for boric acid is carried out on the evaporation residue from 1 or 2 drops of the filtrate. When chromate or permanganate is formed in the fusion, the procedure described on page 139 must be used. 

The intermediate formed in this step is decomposed by water to form the formyl complex, boric acid, and hydrogen. In anhydrous tetrahydrofuran the reduction proceeds further. Scheme 10.12 ... 

Another type of demasking involves formation of new complexes or other compounds that are more stable than the masked species. For example, boric acid is used to demask fluoride complexes of tin(IV) and molybdenum(VI). Formaldehyde is often used to remove the masking action of cyanide ions by converting the masking agent to a nonreacting species through the reaction ... 

Tetraalkyl titanates react with organic borates, B(OR )2, to give complexes of the general formula Ti(OR)4 B(OR )2, which are useful as catalysts and cross-linking agents (562). Mixtures of chelated organic titanates such as TYZOR TE and TYZOR LA with alkaU metal borates, such as borax, or boric acid can be used to produce shear-stable fracturing fluids (563). 

PuUy hydroly2ed poly(vinyl alcohol) and iodine form a complex that exhibits a characteristic blue color similar to that formed by iodine and starch (171—173). The color of the complex can be enhanced by the addition of boric acid to the solution consisting of iodine and potassium iodide. This affords a good calorimetric method for the deterrnination of poly(vinyl alcohol). Color intensity of the complex is effected by molecular weight, degree of... 

The apparent acid strength of boric acid is increased both by strong electrolytes that modify the stmcture and activity of the solvent water and by reagents that form complexes with B(OH) 4 and/or polyborate anions. More than one mechanism may be operative when salts of metal ions are involved. In the presence of excess calcium chloride the strength of boric acid becomes comparable to that of carboxyUc acids, and such solutions maybe titrated using strong base to a sharp phenolphthalein end point. Normally titrations of boric acid are carried out following addition of mannitol or sorbitol, which form stable chelate complexes with B(OH) 4 in a manner typical of polyhydroxy compounds. EquiUbria of the type ... 

Alcohols react with boric acid with elimination of water to form borate esters, B(OR)3. A wide variety of borate salts and complexes have been prepared by the reaction of boric acid and inorganic bases, amines, and heavy-metal cations or oxyanions (44,45). Fusion with metal oxides yields... 

Alkylamines react with leucoquinizarin in a stepwise manner to give l-alh anaino-4-hydroxyanthraquinone, and 1,4-diaLkylamino derivatives after air oxidation. Aromatic amines react similarly in the presence of boric acid as a catalyst. The complex formed (129) causes the less nucleophilic aromatic amines to attack at the 1-, and 4-positions. 

Deposits from all-chloride solution Nickel deposits from a solution of nickel chloride and boric acid are harder, stronger and have a finer grain size than deposits from Watts solution. Lower tank voltage is required for a given current density and the deposit is more uniformly distributed over a cathode of complex shape than in Watts solution, but the deposits are dark coloured and have such high, tensile, internal stress that spontaneous cracking may occur in thick deposits. There is therefore little industrial use of all-chloride solutions. 

H[boric acid complex] + NaOH = Na[boric acid complex] + H20... 

Discussion. Minute amounts of beryllium may be readily determined spectrophotometrically by reaction under alkaline conditions with 4-nitrobenzeneazo-orcinol. The reagent is yellow in a basic medium in the presence of beryllium the colour changes to reddish-brown. The zone of optimum alkalinity is rather critical and narrow buffering with boric acid increases the reproducibility. Aluminium, up to about 240 mg per 25 mL, has little influence provided an excess of 1 mole of sodium hydroxide is added for each mole of aluminium present. Other elements which might interfere are removed by preliminary treatment with sodium hydroxide solution, but the possible co-precipitation of beryllium must be considered. Zinc interferes very slightly but can be removed by precipitation as sulphide. Copper interferes seriously, even in such small amounts as are soluble in sodium hydroxide solution. The interference of small amounts of copper, nickel, iron and calcium can be prevented by complexing with EDTA and triethanolamine. 

B Boric acid acts as a Lewis acid. The boron atom in B(OH)3 has an incomplete octet and forms a bond by accepting a lone pair of electrons from a water molecule, which is acting as a Lewis base. The complex formed is a weak Bronsted acid in which an acidic proton can be lost from the H20 molecule in the complex. 

Another related host-guest complex has been constructed from citric acid, boric acid, and a strontium salt in a 2 1 1 stoichiometry. In this complex the strontium cation is surrounded by four water molecules, two monodentate carboxyl groups and one oxygen atom of the BO4 unit [161]. 

Barker and Kahn have made a detailed study of the exchange in carbon tetrachloride media using the isotope " Sb to label the Sb(III) species. The reaction was carried out in sealed ampoules covered with A1 foil in the presence of an atmosphere of He or Ar gas. The separation method used involved complexing the Sb(V) with fluoride (brought about by addition of ethanol, HCl and HF) followed by precipitation of the Sb(III) with H2S and finally addition of boric acid and HCl, removal of the CCI4, and treatment with H2S to remove the Sb(V). Zero-time exchange was 5 %. 

The system has been used as an analytical tool (4), because the complex formed shows greater conductivity than the sum of the conductivities of the boric acid and the diol compound. Favorably situated diols have a pronounced effect in increasing the conductivity. cis-l,2-Diols fixed in position by molecular structure—e.g., o-dihydroxyphenols and cis-dicyclic polyols—are favorable structures. The reaction is depicted in Figure 2. 

Boric acid can form complexes with hydroxyl compounds. The control of the delay time requires control of the pH, the availability of borate ions, or both. Control of pH can be effective in freshwater systems [17]. However,... 

Figure 17-14. Formation of complexes of boric acid with glycerol. Three hydroxyl units form an ester and one unit forms a complex bond. Here a proton will be released that lowers the pH. The scheme is valid also for polyhydroxy compounds. In this case, two polymer chains are connected via such a link.

H20, or colomanite Ca[B30(0H)3] H2O 1 are added under identical reaction conditions, the reaction mixture remains colourless even after two months, and ribose can be detected, apparently stabilized by boric acid. The corresponding ribose-diborate complex (with a molecular weight of 307) has been clearly identified (Ricardo et al., 2004). 

Capillary zone electrophoresis coupled with fast cyclic voltammetric detection was developed by Zhou et al. [27] for the separation and determination of OTC, TC, and CTC antibiotics. All compounds were well separated by optimization of pH and complexation with a boric acid sodium tetraborate buffer. The detection limit using fast on-line cyclic voltammetric detection with Hg-film-microm electrode was 1.5 x 10-6 mol/L for OTC (signal to noise ratio > 2). A continuous flow manifold coupled on-line to a capillary electrophoresis system was developed by Nozal et al. [28] for determining the trace levels of OTC, TC, and DC in surface water samples. 

Boron complex azo dyes have also been reported. These include solvent soluble boron complexes, such as the red dye (32) used for dyeing polyester and coloring plastics25,26 and water-soluble dyes for the detection of boron (as boric acid) by a color change27 (Scheme 5). 

The reaction of phenylphosphine with boric acid and 2 mol of salicylic aldehyde was carried out in the presence of pyridine with azeotropic removal of water and gave rise to the complex of pyridine with B(III) (116), bonded to three oxygen atoms (87IZV2118 89IZV946) [Eq. (75)]. 

On the basis of its structure, explain why boric acid is a weak acid that functions by complexing with Oil. Draw the structure for the product. 

Marcantoncetos et al. [112] have described a phosphorimetric method for the determination of traces of boron in seawater. This method is based on the observation that in the glass formed by ethyl ether containing 8% of sulfuric acid at 77 K, boric acid gives luminescent complexes with dibenzoylmethane. A 0.5 ml sample is diluted with 10 ml 96% sulfuric acid, and to 0.05-0.3 ml of this solution 0.1ml 0.04 M dibenzoylmethane in 96% sulfuric acid is added. The solution is diluted to 0.4 ml with 96% sulfuric acid, heated at 70 °C for 1 h, cooled, ethyl ether added in small portions to give a total volume of 5 ml, and the emission measured at 77 K at 508 nm, with excitation at 402 nm. At the level of 22 ng boron per ml, hundredfold excesses of 33 ionic species give errors of less than 10%. However, tungsten and molybdenum both interfere. 

This conclusion is based on a high char yield and similar rates of mass loss at 300°C for untreated and boric acid treated samples. Boric acid samples also had much higher AH+ s and, consequently, higher Ea s. Our results suggest that certain thermally-stable, weak polybasic acids which can complex with polysaccharides may provide fire-resistant properties to lignocellulosics. The results and conclusions were strongly influenced by the technique used to analyze the TGA data. 

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