## Abstract Trifluoroacethydrazide is unstable even in the solid state with respect to hydrazonium __N,N__′‐ditrifluoroacetyl hydrazinate, as shown by ^15^N and ^13^C NMR spectroscopy. The ^1^H, ^13^C and ^15^N NMR data and rotamer distributions of formyl‐, acet‐ and trifluoroacet‐hydrazide and of
Solid-State NMR Characterization of13C- and15N-Labeled Phthalimides as Model Compounds for Studying Polyimides
✍ Scribed by WILLIAM L. JARRETT; GREG C. JOHNSON; LON J. MATHIAS
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 116 KB
- Volume
- 116
- Category
- Article
- ISSN
- 1064-1858
No coin nor oath required. For personal study only.
✦ Synopsis
Tensor evaluations of biological polymers are usually bisphthalimide compounds. The 15 N CSA tensor elements (d 11 , based on labeled-model-compound studies; thus, a series of d 22 , and d 33 ) for the labeled derivatives were determined from CSA labeled model imide compounds based on the phthalimide lineshape analysis. In addition, the CSA spectrum for the 15 N, 13 Cmoiety (C 6 H 4 (CO) 2 N*-R with R Å 0H, 0CH 3 , 0C 16 H 33 , labeled N-methylphthalimide was obtained. From CSA lineshape 0CH 2 C 6 H 5 ) have been synthesized and analyzed by solidanalysis, it was determined that d 33 lies approximately along the state 15 N NMR spectroscopy. In addition, N-[ 13 C]methyl-N-C bond axis, with d 22 assumed to be approximately perpendicu-[ 15 N]phthalimide was synthesized and its solid-state 15 N lar to the imide plane. The angles a and b were found to be 90Њ NMR spectrum acquired in order to obtain information on and 7Њ, respectively. The dipolar coupling constant for the 13 Cthe orientation of the d tensor with respect to the local molec-15 N bond was 883 Hz, corresponding to a bond length of 1.51 A ˚. ular geometry, with the eventual purpose of this study to
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