Please use this identifier to cite or link to this item:
https://olympias.lib.uoi.gr/jspui/handle/123456789/9542Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Antoniadis, C. D. | en |
| dc.contributor.author | Hadjikakou, S. K. | en |
| dc.contributor.author | Hadjiliadis, N. | en |
| dc.contributor.author | Kubicki, M. | en |
| dc.contributor.author | Butler, I. S. | en |
| dc.date.accessioned | 2015-11-24T16:49:54Z | - |
| dc.date.available | 2015-11-24T16:49:54Z | - |
| dc.identifier.issn | 1144-0546 | - |
| dc.identifier.uri | https://olympias.lib.uoi.gr/jspui/handle/123456789/9542 | - |
| dc.rights | Default Licence | - |
| dc.subject | charge-transfer complexes | en |
| dc.subject | crystal-structures | en |
| dc.subject | molecular-complexes | en |
| dc.subject | polyiodide salts | en |
| dc.subject | pressure superconductivity | en |
| dc.subject | electrical-properties | en |
| dc.subject | chemical oxidation | en |
| dc.subject | antithyroid drugs | en |
| dc.subject | diiodine adducts | en |
| dc.subject | ft-raman | en |
| dc.title | Synthesis, X-ray characterization and study of new ionic complexes of 2-pyridone, obtained by oxidation with I-2 | en |
| heal.type | journalArticle | - |
| heal.type.en | Journal article | en |
| heal.type.el | Άρθρο Περιοδικού | el |
| heal.identifier.primary | Doi 10.1039/B417828a | - |
| heal.identifier.secondary | <Go to ISI>://000228744800011 | - |
| heal.identifier.secondary | http://pubs.rsc.org/en/content/articlepdf/2005/nj/b417828a | - |
| heal.language | en | - |
| heal.access | campus | - |
| heal.recordProvider | Πανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείας | el |
| heal.publicationDate | 2005 | - |
| heal.abstract | The reaction of 2-pyridone (C5H5NO or PYOH) with diiodine in molar ratios of 2 : 1 and 1 : 2 resulted in the formation of complexes {[(PYOH)(3)(PYOH)(+)]center dot I-3(-)} (1) and {{(PYOH)(6)center dot[(PYOH)(2)](2+)}center dot 0.5I(-)center dot 1.5I(7)(-)center dot I-2} (2), respectively. The reactions were carried out in dichloromethane solutions in air. The compounds were characterized by elemental analysis, DTA-TGA chromatography, FT-Raman, FT-IR, UV-vis and EPR spectroscopies. Crystal structures of the named complexes have been determined by X-ray diffraction at 120(1) K (1) and 293(2) K (2). Compound 1, [(C20H20N4O4)I-3], monoclinic, space group C2/c, consists of a cationic PYOH+ radical species and an I-3(-) counter anion; three neutral PYOH molecules are also bound to the complex. The crystal structure of [(C40H40N8O8)I-13] (2) reveals a centrosymmetric P-1 triclinic space group containing two cationic PYOH+ species, with the anionic counterparts being one half I- and three halves I-7(-). Also, a neutral diiodine molecule I-2 is retained by weak halogen-halogen interactions to I-, as well as six neutral PYOH ligands. The structures of 1 and 2 consist of hydrogen-bonded pyridine layers; polyiodide fragments fill the spaces between the layers, additionally kept together by a number of weak C-H center dot center dot center dot I interactions. | en |
| heal.publisher | Royal Society of Chemistry | en |
| heal.journalName | New Journal of Chemistry | en |
| heal.journalType | peer reviewed | - |
| heal.fullTextAvailability | TRUE | - |
| Appears in Collections: | Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| Antoniadis-2005-Synthesis, X-ray cha.pdf | 684.86 kB | Adobe PDF | View/Open Request a copy |
This item is licensed under a Creative Commons License
