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Synthesis and Characterization of Anionic Lanthanide(III) Complexes with a Bidentate Sulfonylamidophosphate (SAPh) Ligand

  • Iryna Olyshevets
  • , Nataliia Kariaka
  • , Kateryna Znovjyak
  • , Nikolay Gerasimchuk*
  • , Sergey Lindeman
  • , Sergii Smola
  • , Maksym Seredyuk
  • , Tetiana Yu Sliva
  • , Vladimir M. Amirkhanov
  • *Šī darba korespondējošais autors
  • Kyiv National Taras Shevchenko University
  • Missouri State University
  • Marquette University
  • National Academy of Sciences of Ukraine

Zinātniskās darbības rezultāts: Devums žurnālamZinātniskais raksts (žurnālā)koleģiāli recenzēts

17 Atsauces (Scopus)

Kopsavilkums

A series of new anionic lanthanide(III) complexes with the general formula NEt4[LnL4] (1-Ln; HL = dimethyl[(4-methylphenyl)sulfonyl]amidophosphate; Ln = La, Nd, Eu), were synthesized and characterized by IR, UV-vis, and NMR spectroscopies, the differential scanning calorimetry method, thermogravimetric and X-ray analysis, and photoluminescence measurements. Single-crystal structures of NEt4[EuL4] (1-Eu) were determined at 293 and 100 K and evidenced the single-crystal-to-single-crystal phase transition. Both phases are in the monoclinic crystal system in centrosymmetric groups of the same Laue class. The room temperature structure is in C2/c (No. 15), while low-temperature structure is in the P21/c (No. 14) space groups. The coordination environment geometry around the central europium(III) ion is a distorted square antiprism in both polymorphs, while the peripheral methoxy and tolyl groups show different orientations. This phenomenon indicates the occurrence of a thermally driven second-order phase transition during the cooling-heating process. The europium(III) complex exhibits an unusual emission spectrum, clearly dominated by the 5D0-7F4 bands, and an emission decay time equaling 3.5 ms, being among the highest values known for europium coordination compounds.

OriģinālvalodaAngļu
Lapas (no-līdz)76-85
Lapu skaits10
ŽurnālsInorganic Chemistry
Sējums59
Izdevuma numurs1
DOIs
Publikācijas statussPublicēts - 6 janv. 2020
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