Complex formation between UO22+ and α-isosaccharinic acid: insights on a molecular level. Issue 35 (23rd August 2019)
- Record Type:
- Journal Article
- Title:
- Complex formation between UO22+ and α-isosaccharinic acid: insights on a molecular level. Issue 35 (23rd August 2019)
- Main Title:
- Complex formation between UO22+ and α-isosaccharinic acid: insights on a molecular level
- Authors:
- Brinkmann, Hannes
Patzschke, Michael
Kaden, Peter
Raiwa, Manuel
Rossberg, André
Kloditz, Roger
Heim, Karsten
Moll, Henry
Stumpf, Thorsten - Abstract:
- Abstract : This study elucidates the mutual influence of the interaction of ISA with UO2 2+ on their speciation, based on spectroscopic techniques. Abstract : Cellulosic materials present as tissue, paper, wood, or filter materials in low and intermediate level waste will degrade under alkaline conditions if water ingresses in a cementitious backfilled repository. The main degradation product is isosaccharinic acid. Complex formation with isosaccharinic acid may adversely affect the retention of radionuclides by the sorption or formation of solid phases. Hence, this compound is of particular concern in the context of nuclear waste disposal. Structural information of complexes is limited to spherical metal centers and little is known about the interaction of uranyl (U VI O2 2+ ) with isosaccharinic acid. Therefore, the interaction of UO2 2+ with α-isosaccharinate (ISA) was studied under acidic conditions focusing particularly on the structural characterization of the formed complexes. Attenuated total reflection Fourier-transform infrared (ATR-FTIR), nuclear magnetic resonance (NMR), UV-Vis, extended X-ray absorption fine structure (EXAFS) spectroscopy and electrospray-ionization mass spectrometry (ESI-MS) were combined with theoretical calculations to obtain a process understanding on the molecular level. The dominant binding motifs in the formed complexes are 5- and 6-membered rings involving the carboxylic group as well as the α- or β-hydroxy group of ISA. TwoAbstract : This study elucidates the mutual influence of the interaction of ISA with UO2 2+ on their speciation, based on spectroscopic techniques. Abstract : Cellulosic materials present as tissue, paper, wood, or filter materials in low and intermediate level waste will degrade under alkaline conditions if water ingresses in a cementitious backfilled repository. The main degradation product is isosaccharinic acid. Complex formation with isosaccharinic acid may adversely affect the retention of radionuclides by the sorption or formation of solid phases. Hence, this compound is of particular concern in the context of nuclear waste disposal. Structural information of complexes is limited to spherical metal centers and little is known about the interaction of uranyl (U VI O2 2+ ) with isosaccharinic acid. Therefore, the interaction of UO2 2+ with α-isosaccharinate (ISA) was studied under acidic conditions focusing particularly on the structural characterization of the formed complexes. Attenuated total reflection Fourier-transform infrared (ATR-FTIR), nuclear magnetic resonance (NMR), UV-Vis, extended X-ray absorption fine structure (EXAFS) spectroscopy and electrospray-ionization mass spectrometry (ESI-MS) were combined with theoretical calculations to obtain a process understanding on the molecular level. The dominant binding motifs in the formed complexes are 5- and 6-membered rings involving the carboxylic group as well as the α- or β-hydroxy group of ISA. Two concentration dependent complex formation mechanisms were identified involving either mono- ([UO2 (ISA)(H2 O)3 ] + ) or binuclear ([(UO2 )2 (ISA)(H2 O)6 ] 3+ ) species. Furthermore, this study unveils the interaction of UO2 2+ with the protonated α-isosaccharinic acid (HISA) promoting its transformation to the corresponding α-isosaccharinate-1, 4-lactone (ISL) and inhibiting the formation of polynuclear UO2 2+ –ISA species. Future studies on related systems will benefit from the comprehensive knowledge concerning the behavior of ISA as a complexing agent gained in the present study. … (more)
- Is Part Of:
- Dalton transactions. Volume 48:Issue 35(2019)
- Journal:
- Dalton transactions
- Issue:
- Volume 48:Issue 35(2019)
- Issue Display:
- Volume 48, Issue 35 (2019)
- Year:
- 2019
- Volume:
- 48
- Issue:
- 35
- Issue Sort Value:
- 2019-0048-0035-0000
- Page Start:
- 13440
- Page End:
- 13457
- Publication Date:
- 2019-08-23
- Subjects:
- Chemistry, Inorganic -- Periodicals
Chemistry, Physical and theoretical -- Periodicals
Chemistry, Inorganic -- Periodicals
546.05 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/dt#!issueid=dt043040&type=current&issnprint=1477-9226 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c9dt01080g ↗
- Languages:
- English
- ISSNs:
- 1477-9226
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3517.830000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 11644.xml