Research output: Contribution to journal › Article › peer-review
Effect of solution acidity on the structure of amino acid-bearing uranyl compounds. / Nazarchuk, Evgeny V.; Ikhalaynen, Yuri A.; Charkin, Dmitri O.; Siidra, Oleg I.; Petrov, Vladimir G.; Kalmykov, Stepan N.; Borisov, Artem S.
In: Radiochimica Acta, Vol. 107, No. 4, 26.03.2019, p. 311-325.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Effect of solution acidity on the structure of amino acid-bearing uranyl compounds
AU - Nazarchuk, Evgeny V.
AU - Ikhalaynen, Yuri A.
AU - Charkin, Dmitri O.
AU - Siidra, Oleg I.
AU - Petrov, Vladimir G.
AU - Kalmykov, Stepan N.
AU - Borisov, Artem S.
PY - 2019/3/26
Y1 - 2019/3/26
N2 - A series of uranyl sulfates and selenates templated by protonated forms of amino acids (glycine, α- and β-alanine, threonine, nicotinic, and isonicotinic acid) has been prepared via isothermal evaporation of strongly acidic solutions. Their structures have been refined by the direct methods and can be classified as inorganic [(UO 2 ) m (TO 4 ) n (H 2 O) k ] (T=S 6+ , Se 6+ ) moieties combined with the protonated amino acid cations, water molecules and hydronium ions. Their overall motifs demonstrate common features with related structures templated by organic amines. The role of carboxylic acid groups depends on the nature of the corresponding amino acid. They can either link two protonated organic moieties into dimers, or contribute to hydrogen bonding between organic and inorganic parts of the structure. The ammonium ends of the amino acid cations form strong directional bonds to the oxygens of the uranyl and TO 4 anions.
AB - A series of uranyl sulfates and selenates templated by protonated forms of amino acids (glycine, α- and β-alanine, threonine, nicotinic, and isonicotinic acid) has been prepared via isothermal evaporation of strongly acidic solutions. Their structures have been refined by the direct methods and can be classified as inorganic [(UO 2 ) m (TO 4 ) n (H 2 O) k ] (T=S 6+ , Se 6+ ) moieties combined with the protonated amino acid cations, water molecules and hydronium ions. Their overall motifs demonstrate common features with related structures templated by organic amines. The role of carboxylic acid groups depends on the nature of the corresponding amino acid. They can either link two protonated organic moieties into dimers, or contribute to hydrogen bonding between organic and inorganic parts of the structure. The ammonium ends of the amino acid cations form strong directional bonds to the oxygens of the uranyl and TO 4 anions.
KW - Amino acids
KW - crystal structures
KW - templated uranyl compounds
KW - X-ray diffraction
UR - http://www.scopus.com/inward/record.url?scp=85060014971&partnerID=8YFLogxK
U2 - 10.1515/ract-2018-3050
DO - 10.1515/ract-2018-3050
M3 - Article
AN - SCOPUS:85060014971
VL - 107
SP - 311
EP - 325
JO - Radiochimica Acta
JF - Radiochimica Acta
SN - 0033-8230
IS - 4
ER -
ID: 45305276