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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-


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[2+4] and [2+2] Cycloaddition Reactions
✍ David J. Brauer; Hans Bürger; Gottfried Pawelke; Jürgen Rothe 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 German ⚖ 86 KB

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