N-Triazolyboranes

Abstract

1,3-Dimethyl-2-(N-triazolyl)-1,3,2-diazaboracycloalkanes, (tz) BNCH3(CH2)(n)NCH3 (where Htz = 1,2,3-triazole (1), 1,2,4-triazole (2), benzotriazole (4); n = 2,3) have been synthesized by condensation procedures. The resultant species are monomeric and contain three-coordinate boron; they do not dimerize at temperatures as low as -50 C. Compounds of type 1, however, exist as a mixture of the 1- and 2-isomers, whereas 2 and 4 are the 1-isomers exclusively. Only species of type 2 are fluxional at elevated temperatures, those of type 1 and 4 are static up to 80 C. However, the monomeric N- triazolylboranes have remaining Lewis acidity and can complex with additional Htz. Based on this feature, representative bis(1-triazolyl)diorganylborates, Na((tz)2BR2) (Htz = 1,2,4-triazole; R = C2H5 or 1/2 (C8H14) where (C8H14)BH = 9- borabicyclo(3.3.1)nonane), were readily obtained by the reaction of (dimethylamino)diorganylboranes with 1 molar equiv of Htz and subsequent treatment with 1 molar equiv of M(tz) (M = alkali metal). The salts were converted to some representative complexes, e.g., R2B(mu-tz)2Pd(pi-CH2CHCH2).

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Document Details

Document Type
Technical Report
Publication Date
Aug 01, 1990
Accession Number
ADA224893

Entities

People

  • Junwu Bai
  • Kurt S. Niedenzu

Organizations

  • University of Kentucky

Tags

Communities of Interest

  • Advanced Electronics
  • C4I
  • Ground and Sea Platforms
  • Weapons Technologies

DTIC Thesaurus Topics

  • Alkali Metals
  • Chemical Shifts
  • Chemical Synthesis
  • Chemistry
  • Chlorides
  • Inorganic Chemistry
  • Isomers
  • Magnetic Resonance
  • Mass Spectra
  • Materials
  • Metals
  • Military Research
  • Mixtures
  • New York
  • Nuclear Magnetic Resonance
  • Spectra
  • United States

Fields of Study

  • Chemistry

Readers

  • Analytical Mechanics
  • Organic Chemistry