Nuclear magnetic resonance boronates

Boron s electron deficiency does not permit conventional two-electron bonds. Boron can form multicenter bonds. Thus the boron hydrides have stmctures quite unlike hydrocarbons. The B nucleus, which has a spin of 3/2, which has been employed in boron nuclear magnetic resonance spectroscopy. 

The section on Spectroscopy has been retained but with some revisions and expansion. The section includes ultraviolet-visible spectroscopy, fluorescence, infrared and Raman spectroscopy, and X-ray spectrometry. Detection limits are listed for the elements when using flame emission, flame atomic absorption, electrothermal atomic absorption, argon induction coupled plasma, and flame atomic fluorescence. Nuclear magnetic resonance embraces tables for the nuclear properties of the elements, proton chemical shifts and coupling constants, and similar material for carbon-13, boron-11, nitrogen-15, fluorine-19, silicon-19, and phosphoms-31. 

Noth, H., and Wrackmeyer, B. (1978) Nuclear Magnetic Resonance Spectroscopy of Boron Compounds, Springer-Verlag, New York. 

H. Noth, B. Wrackmeyer, Nuclear Magnetic Resonance Spectroscopy of Boron Compounds, in NMR - Basic Principles and Progress, P. Diehl, E. Fluck, R. Kosfeld, eds., Vol. 14, Springer Verlag, Berlin-Heidelberg-New York, 1978. 

Normalization, 6 Normal modes, 240-244 of benzene, 438-439 of boron trifluoride, 281, 290 of carbon dioxide, 242, 248, 262, 265 of ethylene, 291 and group frequencies, 266-268 IR active, 457 Raman active, 457 and symmetry, 246-249,430-439 of water, 431-437 Normal operator, 108 Nuclear g factor, 3 24 Nuclear magnetic moments, 323-325 Nuclear magnetic resonance, 129-130, 323-366... 

So far, only one detailed discussion of boron-11 nuclear magnetic resonance spectra of aminoborane systems has been reported 31>. It was found that the 1 lB chemical shifts of aminoborane systems can be described fairly well in terms of a set of additive substituent contributions. In consonance with earlier work on trisubstituted boron compounds 35> these contributions depend on the mesomeric effects of substituents rather than their electronegativity. 1,3,2-diazaboracycloalkanes can be considered as aminoborane derivatives and in the case of the known heterocycles the exocyclic boron substituent will govern primarily the boron chemical shifts and will do so by mesomeric effects. However, the available data are rather limited and it may be possible that additional factors must be considered. Steric effects appear to be negligible, however, since the heterocycles with either six or seven annular atoms have almost identical shifts (Table 5). 

Nuclear Magnetic Resonance Spectroscopy of Boron Compounds... 

Oppolzer et al. used (2M)-bornanc-10, 2-sultam as an effective chiral auxiliary to achieve a highly enantioselective syn-aldol reaction17 (Scheme 2.1p). Treatment of A-propionylsultam (46) with dibutylboron triflate and Hunig s base at -5°C in CH2CI2 followed by addition of aldehydes at -78° C provided, after a simple crystallization, the pure vyn-aldols 47a. It is noteworthy that no anti-aldol product was observed in the aldol reactions with any of the aldehydes. From the1 nuclear magnetic resonance (NMR) study, it was confirmed that the boron... 

Turner, G. L., K. A. Smith, R. J. Kirkpatrick, and E. Oldfield (1986). Boron-11 nuclear magnetic resonance spectroscopic study of borate and borosilicate minerals and a borosilicate glass. J. Mag. Res. 67, 544-50. 

Most of the publications dealing with heterocycles contain nuclear magnetic resonance (NMR) data. While H and NMR data are the most important, NMR data are particularly relevant to boron-containing heterocyles. The H, B, and NMR data of unsaturated, anionic, and transition metal 7t-coordinated rings are useful probes of their electronic structures. 

B-1978MI417-01 H. Noth and B. Wrackmeyer Nuclear magnetic resonance spectroscopy of boron compounds, in NMR- Basic Principles... 

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