𝔖 Bobbio Scriptorium
✦   LIBER   ✦

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


📜 SIMILAR VOLUMES


15N and 13C NMR study of acylated hydraz
✍ Hans Fritz; Haukur Kristinsson; Max Mollenkopf; Tammo Winkler 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 English ⚖ 463 KB

## 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

Effects of polymorphic differences for s
✍ Alessia Portieri; Robin K. Harris; Richard A. Fletton; Robert W. Lancaster; Tere 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 172 KB

## Abstract We recorded both carbon‐13 and nitrogen‐15 NMR spectra of the three solid forms of sulfanilamide most commonly known. This study led to an interpretation of the solid‐state effects seen in cross‐polarization magic angle spinning spectra. Relaxation times for the different forms were mea

Polymorphism of N,N′′-Diacetylbiuret Stu
✍ Sven Macholl; Dieter Lentz; Frank Börner; Gerd Buntkowsky 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 280 KB 👁 2 views

## Abstract The molecular configuration and crystal structure of solid polycrystalline __N__,__N__′′‐diacetylbiuret (DAB), a potential nitrogen‐rich fertilizer, have been analyzed by a combination of solid‐ and liquid‐state NMR spectroscopy, X‐ray diffraction, and DFT calculations. Initially a pure

The reaction of furfuryl alcohol resins
✍ Xiaoqing Zhang; David H. Solomon 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 241 KB 👁 1 views

The reactions between furfuryl alcohol (FA)/poly(furfuryl alcohol) (PFA) and hexamethylenetetramine (HMTA) have been studied by 13 C and 15 N high-resolution solid-state NMR techniques. Highly crosslinked polymer networks similar to those obtained from the thermal curing of FA resins under acidic co

A 1H, 13C and 15N NMR study in solution
✍ Rosa M. Claramunt; M. Dolores Santa María; Dionisia Sanz; Ibon Alkorta; José Elg 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 177 KB

## Abstract Three __N__‐substituted pyrazoles and three __N__‐substituted indazoles [1‐(4‐nitrophenyl)‐3,5‐dimethylpyrazole (1), 1‐(2,4‐dinitrophenyl)‐3,5‐dimethylpyrazole (2), 1‐tosyl‐pyrazole (3), 1‐__p__‐chlorobenzoylindazole (4), 1‐tosylinda‐zole (5) and 2‐(2‐hydroxy‐2‐phenylethyl)‐indazole (6)