Boron recommendations

Boron - Recommended boron application rates range from 0.5 to 2.0 1 /ha and should be carefully followed [10]. Crop species vary considerably in their boron requirement as well as in their tolerance to overapplications. Residual effects of applied boron also vary with soil conditions, with the lowest effects found on acidic sandy soils in areas of high rainfall. Some crops with high boron requirements are alfalfa, cotton, peanuts, irrigated corn, root crops, soybean, and some fruits and vegetables. 

Ammonium Fluoroborate. Ammonium fluoroborate [13826-83-0] NH BF, is unique in that when it is exposed to a flame, it generates both a halogen and a boron flame retardant (20). Antimony oxide is usually recommended as a co-synergist. 

Inasmuch as the gas hydroly2es readily, all equipment should be purged repeatedly using inert dry gas before admitting boron trifluoride. Under anhydrous conditions, carbon steel equipment is satisfactory. Stainless steel and aluminum siUcon bron2e may also be used. Stainless steel tubing is recommended for both temporary and permanent connections. 

Two colorimetric methods are recommended for boron analysis. One is the curcumin method, where the sample is acidified and evaporated after addition of curcumin reagent. A red product called rosocyanine remains it is dissolved in 95 wt % ethanol and measured photometrically. Nitrate concentrations >20 mg/L interfere with this method. Another colorimetric method is based upon the reaction between boron and carminic acid in concentrated sulfuric acid to form a bluish-red or blue product. Boron concentrations can also be deterrnined by atomic absorption spectroscopy with a nitrous oxide—acetjiene flame or graphite furnace. Atomic emission with an argon plasma source can also be used for boron measurement. 

The nomenclature of boron hydride derivatives has been somewhat confusing and many inconsistencies exist in the Hterature. The stmctures of some reported boron hydride clusters are so compHcated that only a stmctural drawing or graph, often accompanied by explanatory text, is used to describe them. Traditional nomenclature systems often can be used to describe compounds unambiguously, but the resulting descriptions may be so long and unwieldy that they are of Htde use. The lUPAC (7) and the Chemical Abstract Service (8) have made recommendations, and nomenclature methods have now been developed that can adequately handle nearly all clusters compounds however, these methods have yet to be widely adopted. Eor the most part, nomenclature used in the original Hterature is retained herein. 

Another type of anion, confined for practical purposes to boron compounds, has no unshared electrons at the anionic site, and must be thought of as being formed by addition of hydride to a boron atom (or other atom with an incomplete valence shell). Such structures were not anticipated at the time general heterocyclic nomenclature was developed, and they are only recently being fitted into systematic nomenclature (lUPAC Provisional Recommendation 83.2). Proposals for a suffix to indicate such structures are under consideration (1982). 

Abundances of lUPAC (the International Union of Pure and Applied Chemistry). Their most recent recommendations are tabulated on the inside front fly sheet. From this it is clear that there is still a wide variation in the reliability of the data. The most accurately quoted value is that for fluorine which is known to better than I part in 38 million the least accurate is for boron (1 part in 1500, i.e. 7 parts in [O ). Apart from boron all values are reliable to better than 5 parts in [O and the majority arc reliable to better than I part in 10. For some elements (such as boron) the rather large uncertainty arises not because of experimental error, since the use of mass-spcctrometric measurements has yielded results of very high precision, but because the natural variation in the relative abundance of the 2 isotopes °B and "B results in a range of values of at least 0.003 about the quoted value of 10.811. By contrast, there is no known variation in isotopic abundances for elements such as selenium and osmium, but calibrated mass-spcctrometric data are not available, and the existence of 6 and 7 stable isotopes respectively for these elements makes high precision difficult to obtain they are thus prime candidates for improvement. 

Unsolvated organomagnesium compounds have been recommended for the synthesis of organometallic derivatives of mercury, boron, aluminum, silicon, germanium, tin, phosphorus, arsenic, and antimony6-8 and have been used in procedures for the alkylation of aromatic rings and for the production of various polymerization catalysts.4 9... 

Note It is reported that the use of chlorobenzene as solvent is essential when the reagent is to be used to detect aromatic amines [1]. In the case of steroids, penicillins, diuretics and alkaloids the reaction should be accelerated and intensified by spraying afterwards with dimethylsulfoxide (DMSO) or dimethylformamide (DMF), indeed this step makes it possible to detect some substances when this would not otherwise be possible [5,9-11] this latter treatment can, like heating, cause color changes [5,9]. Penicillins and diuretics only exhibit weak reactions if not treated afterwards with DMF [10, 11]. Steroids alone also yield colored derivatives with DMSO [9]. Tlreatment afterwards with diluted sulfuric acid (c = 2 mol/L) also leads to an improvement in detection sensitivity in the case of a range of alkaloids. In the case of pyrrolizidine alkaloids it is possible to use o-chloranil as an alternative detection reagent however, in this case it is recommended that the plate be treated afterwards with a solution of 2 g 4-(dimethyl-amino)-benzaldehyde and 2 ml boron trifluoride etherate in 100 ml anhydrous ethanol because otherwise the colors initially produced with o-chloranil rapidly fade [12]. 

Safety considerations are paramount in any boron hydride synthesis. The energy yield from the oxidations of boron hydrides is too high for any cavalier treatment of boron hydrides. Exclusion of air is the critical consideration in diborane reactions. Decaborane(14) is less reactive, generally, in a kinetic sense, but the thermodynamic potential is comparable. In addition, all volatile boron hydrides are toxic. The procedures described in the latter two preparations are within our experience non-hazardous. These procedures should be followed in every detail improvisation is not recommended. 

Reactions of boron hydrides must be carried out with special care. If properly conducted, the reactions reported here proceed without difficulty, but fires which do occur as the result of equipment failures or similar incidents are usually vigorous. It is recommended that all carborane preparations be carried out in areas designated for the use of hazardous materials. 

The original method1 reported for the preparation of trichloroborazine involves the use of borazine. However, this procedure is not recommended because of the difficulty of preparing this heterocycle and its hydrolytic instability. More recently, this trichloroborazine has been prepared directly from ammonium chloride and boron trichloride at elevated temperatures with or without a solvent.2-8 Ammonium chloride may be replaced by a primary aliphatic or aromatic amine or its hydrochloride, and organodihaloboranes can be used in place of the boron trichloride to give the respective N- and B-substituted borazines.6 Boron tribromide has been used in analogous reactions to yield -B,/ , .B"-tribromoborazines.6... 

These are classified as those with a requirement below one pg (microgram) per day. Elements in this class include boron, chromium, fluoride, iodine, molybdenum, nickel, selenium, cobalt and manganese. Cobalt is part of vitamin (see above). However, there appear to be no recommended dietary intakes for any of these except molybdenum. 

National Institute for Occupational Safety and Health, US Department of Health, Education and Welfare Criteria for a Recommended Standard... Occupational Exposure to Boron Trifluoride. DHEW (NIOSH) Pub No 77-22, Washington, DC, US Government Printing Office, 1976... 

Several catalysts have been recommended for the N-acetylation of carbazole with acetic anhydride boron trifluoride, phosphorus pentoxide, concentrated sulfuric acid, zinc chloride, and phosphoric acid all gave 9-acetylcarbazole in moderate to good yield. 9-Acetylcarbazole can also be prepared using the Vilsmeier complex of N,N-dimethylacetamide and phosgene. ... 

More research is needed on the accurate measurement of boron in biological materials when the concentrations are <1.0 mg B/kg (Sullivan and Culver 1998). Standard biological reference materials with low boron levels need to be produced for use in interlaboratory comparisons. This becomes especially important in studies on boron-deficiency states and the ability of the organism to conserve boron at very low intakes (Sullivan and Culver 1998). More research is needed on homeostatic regulation of boron and functional markers of boron metabolism (Sutherland et al. 1998). Sullivan and Culver (1998) recommend additional studies to establish ... 

New advances in boron nntrition research shonld include better characterization of the mechanisms through which boron modulates immune function and insulin release (Hunt 1998). Epidemiological studies should be initiated to identify health conditions associated with inadequate dietary boron (Sutherland et al. 1998). Finally, Dourson et al. (1998) recommend more research on uncertainty factors used in establishing tolerable daily intake values for the protection of human health, with emphasis on variations in interspecies and intraspecies differences in resistance to boron. 

Boron criteria recommended for the protection of sensitive species include ... 

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