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A phosphorus-31 NMR study of solid carbonylhydridotris(triphenylphosphine)rhodium(I). Unusual MAS sideband intensities in second-order NMR spin systems
Author(s) -
Gang Wu,
Roderick E. Wasylishen,
Ronald D. Curtis
Publication year - 1992
Publication title -
canadian journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.323
H-Index - 68
eISSN - 1480-3291
pISSN - 0008-4042
DOI - 10.1139/v92-114
Subject(s) - chemistry , rhodium , triphenylphosphine , chemical shift , phosphorus 31 nmr spectroscopy , crystallography , nmr spectra database , nuclear magnetic resonance spectroscopy , magic angle , solid state nuclear magnetic resonance , carbon 13 nmr satellite , spin (aerodynamics) , carbon 13 nmr , spectral line , stereochemistry , fluorine 19 nmr , nuclear magnetic resonance , catalysis , organic chemistry , physics , astronomy , thermodynamics
The CP/MAS 31P NMR spectrum of carbonylhydridotris(triphenylphosphine)rhodium(I), RhH(CO)(PPh3)3 (1), can be described as a tightly coupled ABMX spin system (X = 103Rh). In contrast to the solution 31P NMR spectrum, the three equatorial phosphorus nuclei are nonequivalent in the solid state and this structural feature allows us to measure the two-bond spin–spin couplings, 2J(31P,31P). A new method is proposed for extracting the principal components of the chemical shift tensor from slow MAS NMR spectra in a tightly J-coupled two-spin system. For compound 1, the principal components of the 31P chemical shift tensors calculated using this method are in good agreement with those obtained from NMR spectra of a static sample. The principal components of the 31P chemical shift tensors determined for 1 are compared with those reported previously for Wilkinson's catalyst, RhCl(PPh3)3. The δ22 component of the 31P chemical shift tensors in 1 shows the largest variation with structure. This is ascribed to differenc...

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