دورية أكاديمية

Thorium nanochemistry: The solution structure of the Th(iv)-hydroxo pentamer

التفاصيل البيبلوغرافية
العنوان: Thorium nanochemistry: The solution structure of the Th(iv)-hydroxo pentamer
المؤلفون: Walther, C., Rothe, J., Schimmelpfennig, B., Fuss, M.
المصدر: Dalton Transactions 41 (2012), Nr. 36
بيانات النشر: Royal Society of Chemistry
سنة النشر: 2012
المجموعة: Institutional Repository of Leibniz Universität Hannover
مصطلحات موضوعية: Dominant species, Electrospray mass spectrometry, High energy x-rays, Nano chemistry, Orders of magnitude, Pentamers, Polymeric species, Quantum chemical calculations, Solubility limits, Solution chemistry, Solution structures, Thermodynamic data, X ray absorption fine structures, Polymers, Quantum chemistry, Solubility, Thorium, Dimers, ddc:540
الوصف: Tetravalent thorium exhibits a strong tendency towards hydrolysis and subsequent polymerization. Polymeric species play a crucial role in understanding thorium solution chemistry, since their presence causes apparent solubility several orders of magnitude higher than predicted by thermodynamic data bases. Although electrospray mass spectrometry (ESI MS) identifies Th(iv) dimers and pentamers unequivocally as dominant species close to the solubility limit, the molecular structure of Th 5(OH) y polymers was hitherto unknown. In the present study, X-ray absorption fine structure (XAFS) spectroscopy, high energy X-ray scattering (HEXS) measurements, and quantum chemical calculations are combined to solve the pentamer structure. The most favourable structure is represented by two Th(iv) dimers linked by a central Th(iv) cation through hydroxide bridges. © 2012 The Royal Society of Chemistry.
نوع الوثيقة: article in journal/newspaper
اللغة: English
تدمد: 1477-9226
العلاقة: http://dx.doi.org/10.15488/2212Test; http://www.repo.uni-hannover.de/handle/123456789/2237Test
DOI: 10.15488/2212
الإتاحة: https://doi.org/10.15488/2212Test
https://doi.org/10.1039/c2dt30243hTest
http://www.repo.uni-hannover.de/handle/123456789/2237Test
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رقم الانضمام: edsbas.11EA01B4
قاعدة البيانات: BASE