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- Title
The <sup>1</sup>H, <sup>13</sup>C, <sup>15</sup>N, and <sup>19</sup>F NMR chemical shifts assignments in 5,10,15-tris (pentafluorophenyl)tetra-<sup>15</sup>N corrole at 191 K.
- Authors
Bocian, Wojciech; Paluch, Piotr; Nowak‐Król, Agnieszka; Gryko, Daniel T.; Potrzebowski, Marek; Śniechowska, Justyna; Sitkowski, Jerzy; Bednarek, Elżbieta; Kozerski, Lech
- Abstract
The article focuses on a study which examined the nuclear magnetic resonance (NMR) analysis of chemical shift assignments in 5,10,15-tris (pentafluorophenyl) corrole compounds. Topics discussed include an overview of corroles, which are aromatic tetrapyrrolic macrocycles closely related toporphyrins, the three interior N-pyrrolic protons of corroles, the mechanism of tautomerization, and the structure of corrole tautomer.
- Subjects
NUCLEAR magnetic resonance; CHEMICAL shift (Nuclear magnetic resonance); TAUTOMERISM; AROMATIC compounds spectra; PYRROLES
- Publication
Magnetic Resonance in Chemistry, 2015, Vol 53, Issue 2, p167
- ISSN
0749-1581
- Publication type
Other
- DOI
10.1002/mrc.4145