Solid-state and Solution-state NMR Studies of the Chlorophosphane (2,6-(CF3)2C6H3)(2,4-(CF3)2C6H3)PCl, (Ar′Ar′′PCl), and its Crystal Structure at 150 K
✍ Scribed by Andrei S. Batsanov; Stephanie M. Cornet; Lindsey A. Crowe; Keith B. Dillon; Robin K. Harris; Paul Hazendonk; Mark D. Roden
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 319 KB
- Volume
- 2001
- Category
- Article
- ISSN
- 1434-1948
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✦ Synopsis
The title compound has been synthesised, and characterised by multinuclear magnetic resonance spectroscopy, both in solution and in the solid state. The bandshapes of variabletemperature solution-state 19 F NMR spectra have been iteratively fitted to obtain information on the kinetics of rotation about the PC bond for one of the aryl groups, and values for the enthalpy and entropy of activation of the process have been derived. Magic-angle spinning NMR techniques have been extensively applied to the solid, using 19 F, 31 P and 13 C nuclei. Triple-channel methods and different magnetic field strengths have been employed to yield a range of complementary information. Heteronuclear interactions and intram-
📜 SIMILAR VOLUMES
N-sulfinylacylamides R-C(ϭO)-NϭSϭO react with (CF 3 ) 2 BNMe 2 (1) to form, by [2ϩ4] cycloaddition, six-membered rings cyclo-(CF 3 ) 2 B-NMe 2 -S(ϭO)-NϭC(R)-O for R ϭ Me (2), t-Bu (3), C 6 H 5 (4), and p-CH 3 C 6 H 4 (5) while N-sulfinylcarbamic acid esters R-O-C(ϭO)-NϭSϭO react with 1 to yield mixt