The 'H and "C NMR spectra of anhydroerythromycin A in methanol-d, and buffered D,O have been fully assigned using a range of one-and two-dimensional N M R techniques.
1H- and 13C-NMR analyses of aqueous polyamideamine–epichlorohydrin resin solutions
✍ Scribed by Takao Obokata; Akira Isogai
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 148 KB
- Volume
- 92
- Category
- Article
- ISSN
- 0021-8995
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
More accurate signal assignment for ^1^H‐ and ^13^C‐NMR spectra of aqueous solutions of polyamideamine‐epichlorohydrin (PAE) resin and its related compounds was achieved by using distortionless enhancement of polarization transfer (DEPT) and C‐H correlation spectroscopy (COSY) methods. On the basis of the assignment, we developed new methods to determine the content of four‐membered azetidinium ring (AZR) and number‐average degree of polymerization (DP~n~) of the repeating unit of PAE by using NMR. Degree of introduction of epichlorohydrin into polyamideamine chains at the initial stage was 75–80%, and the resultant AZR content per one repeating unit in the PAE sample prepared in this study was about 72%. DP~n~ of the initial polyamideamine was 32, and this value decreased to about 18 during the PAE preparation process. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 1847–1854, 2004
📜 SIMILAR VOLUMES
The 'H and 13C N M R spectra of anhydroerythromycin A in methanol-d, and buffered D,O have been fully assigned using a range of one-and two-dimensional NM R techniques.
Careful analysis of the 1H and 13C NMR spectra of a series of isochromanylacetylarylhydrazone derivatives indicated the diastereomeric selective character in the synthetic step used to obtain the derivatives employing acidic conditions during the condensation of the corresponding acylhydrazides with
1 H and 13 C NMR spectral data for phytochelatin, NH 3 C --Glu-Cys 2 -Gly-COO , were assigned by a combination of one-( 1 H, 13 C) and two-dimensional (DQF-COSY, CH-COSY, HMBC) NMR experiments.
The indole alkaloid strychnobrasiline was studied using one-and two-dimensional NMR techniques. The interpretation of these spectra led to the complete assignments of all carbon and proton chemical shifts.