By Narayan S. Hosmane

ISBN-10: 1283350114

ISBN-13: 9781283350112

Boron has made an important effect in our lives via its quiet use in fertilizers, fungicides, soaps, detergents, and heat-resistant glassware. Boron technological know-how: New applied sciences and Applications addresses the functions of boron in chemistry, undefined, drugs, and pharmacology via explaining its position in difficulties comparable to catalysis and hydroboration in addition to its use in superconductors, fabrics, magnetic/nonmagnetic nanoparticles, and clinical functions together with melanoma therapy.

Illustrating the sensible versatility of boron, the 29 chapters are divided into seven significant sections:

  • Boron for residing: Medicine
  • Boron for dwelling: overall healthiness and Nutrition
  • Boron for dwelling: Radioisotope
  • Boron for dwelling: Boron Neutron seize Therapy
  • Boron for Electronics: Optoelectronics
  • Boron for strength: power garage, area, and different Applications
  • Boron for Chemistry and Catalysis: Catalysis and natural Transformations

More than simply an up-to-date compilation of growth within the utilized technology of boron, this e-book is a tribute to the legions of employees who've spent years undertaking groundbreaking reviews. The ebook celebrates those scientists and their protégés, who jointly reworked boron technology into the fascinating and growing to be sector it's at the present time.

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Additional info for Boron Science: New Technologies and Applications

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A. Devirian, S. L. Volpe, The physiological effects of dietary boron, Crit. Rev. Food Sci. , 2003, 43, 219–231. 7. R. F. Barth, J. A. Coderre, M. G. H. Vicente, T. E. Blue, Boron neutron capture therapy of cancer: Current status and future prospects, Clin. , 2005, 11, 3987–4002. 8. M. F. Hawthorne, New horizons for therapy based on the boron neutron capture reaction, Mol. Med. Today, 1998, 4, 174–181. 9. J. ). , New York, 1998. 10. A. F. Armstrong, J. F. , 2007, 4240–4251. 11. V. I. Bregadze, I.

J. Org. Chem. ) Carbaboranyl bisglycophosphonates were synthesized according to the phosphoramidite method from meta- or para-carbaboranyl bisphosphonite and isopropylidene-protected galactose (59) with benzimidazolium triflate (BIT) as the promoter. Due to strong P⋅⋅⋅P interactions in ortho-carborane derivatives, the synthesis of the respective carbaboranyl bisglycophosphonates was unsuccessful. Synthesis of disodium salts 62 and 63 starts from meta-carbaboranyl bisphosphonite 58, which acts as a phosphoramidite analog.

However, no data concerning the biological activity of these compounds were given. Besides carboranes, dodecaborates are attractive for modification with phosphate and ­phosphonate entities. In 2002, Kultyshev et al. 3 ortho-Carbaboranylalkyl- and -vinylphosphonates. (Adapted from Semioshkin, A. A. et al. 1997. Advances in Boron Chemistry, W. ), 311. The Royal Society of Chemistry: Cambridge; Semioshkin, A. A. et al. 1998. Russ. Chem. Bull. 4 Examples of bisphosphonic acid derivatives of ortho-carborane reported in the patent literature.

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