FT-TR, UV-VISIBLE AND X-RAY STUDIES OF COMPLEXES OF PYRIDINE N-OXIDES WITH PENTACHLOROPHENOL
| dc.contributor.author | Dega-Szafran, Zofia | |
| dc.contributor.author | Grunwald-Wyspianska, Monika | |
| dc.contributor.author | Kania, Anna | |
| dc.contributor.author | Kosturkiewicz, Zofia | |
| dc.contributor.author | Tykarska, Ewa | |
| dc.contributor.author | Szafran, Mirosław | |
| dc.date.accessioned | 2018-03-23T10:02:52Z | |
| dc.date.available | 2018-03-23T10:02:52Z | |
| dc.date.issued | 1995-11-01 | |
| dc.description.abstract | The crystal structure of the 4-methoxy-2,6-dimethylpyridine N-oxide pentachlorophenol complex has been determined by X-ray analysis. The O ... O distance is 2.439(6) Angstrom, the OHO angle is 152.3 degrees and the hydrogen-bonded proton is close to the phenol molecule. The FT-IR spectra of pentachlorophenol complexes with some substituted pyridine N-oxides in the solid state and seven aprotic solvents of different polarity (epsilon from 2.27 to 37.5) show a broad absorption. The broad absorption shows weak dependence upon solvent polarity and is classified as type (ii). UV spectra show that in the investigated complexes protons are not transferred from the phenol to the N-oxides. Formamide (epsilon = 111) is a much stronger proton acceptor than the pyridine N-oxides. Pentachlorophenol in formamide is converted to the phenolate ion. | pl |
| dc.identifier.citation | JOURNAL OF MOLECULAR STRUCTURE 356 (3) 169-182 | pl |
| dc.identifier.issn | 0022-2860 | |
| dc.identifier.uri | http://hdl.handle.net/10593/22341 | |
| dc.language.iso | eng | pl |
| dc.rights | info:eu-repo/semantics/openAccess | pl |
| dc.subject | Hydrogen-Bonds | pl |
| dc.subject | trifluoroacetic-acid | pl |
| dc.subject | 1:1 complex | pl |
| dc.subject | proton-transfer | pl |
| dc.subject | IR | pl |
| dc.subject | phenole | pl |
| dc.title | FT-TR, UV-VISIBLE AND X-RAY STUDIES OF COMPLEXES OF PYRIDINE N-OXIDES WITH PENTACHLOROPHENOL | pl |
| dc.type | Artykuł | pl |