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Journal articles on the topic 'Ytterbium(III)'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

OGINO, Tadayoshi, and Takashi ONOZAWA. "Ytterbium (III) Trifluoromethanesulfonate." Journal of Synthetic Organic Chemistry, Japan 56, no. 1 (1998): 71–73. http://dx.doi.org/10.5059/yukigoseikyokaishi.56.71.

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2

Niemeyer, Mark. "trans-Diiodopentakis(tetrahydrofuran)ytterbium(III) tetraiodo-trans-bis(tetrahydrofuran)ytterbium(III)." Acta Crystallographica Section E Structure Reports Online 57, no. 8 (2001): m363—m364. http://dx.doi.org/10.1107/s1600536801011254.

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3

Zhang, Quanquan, Guoe Cheng, Hanzhong Ke, et al. "Effects of peripheral substitutions on the singlet oxygen quantum yields of monophthalocyaninato ytterbium(iii) complexes." RSC Advances 5, no. 28 (2015): 22294–99. http://dx.doi.org/10.1039/c5ra02569a.

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A new monophthalocyaninato ytterbium(iii) complex5has been prepared and characterized. The effects of substituents on the relative singlet oxygen quantum yields of monophthalocyaninato ytterbium(iii) complexes have been investigated.

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4

Wang, Sida, Farid M. Sroor, Phil Liebing, Volker Lorenz, Liane Hilfert, and Frank T. Edelmann. "Crystal structures of two ytterbium(III) complexes comprising alkynylamidinate ligands." Acta Crystallographica Section E Crystallographic Communications 72, no. 9 (2016): 1229–33. http://dx.doi.org/10.1107/s2056989016012135.

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Two ytterbium(III) complexes comprising alkynylamidinate ligands, namely bis(η5-cyclopentadienyl)(3-cyclopropyl-N,N′-diisopropylpropynamidinato-κ2N,N′)ytterbium(III), [Yb(C5H5)2(C12H19N2)] or Cp2Yb[(iPr2N)2C—C[triple-bond]C—c-C3H5] (1) and tris(3-phenyl-N,N′-dicyclohexylpropynamidinato-κ2N,N′)ytterbium(III), [Yb(C21H27N2)3] or Yb[(CyN)2C—C[triple-bond]C—Ph]3(Cy = cyclohexyl) (2) have been synthesized and structurally characterized. Both complexes are monomers; for complex2, the contribution to the scattering from highly disordered toluene solvent molecules in these voids was removed with the S

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5

Zalkin, A., T. J. Henly, and R. A. Andersen. "Amminebis(pentamethylcyclopentadienyl)(thiophenolato)ytterbium(III)." Acta Crystallographica Section C Crystal Structure Communications 43, no. 2 (1987): 233–36. http://dx.doi.org/10.1107/s0108270187096318.

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6

Fejfarová, Karla, Rachid Essehli, Brahim El Bali, and Michal Dušek. "Ammonium ytterbium(III) diphosphate(V)." Acta Crystallographica Section E Structure Reports Online 64, no. 12 (2008): i85—i86. http://dx.doi.org/10.1107/s1600536808039664.

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7

Niemeyer, Mark. "A trigonal-bipyramidal coordinated ytterbium(III) alkyl: tris(trimethylsilylmethyl)bis(tetrahydrofuran-O)ytterbium(III)." Acta Crystallographica Section E Structure Reports Online 57, no. 12 (2001): m553—m555. http://dx.doi.org/10.1107/s1600536801018566.

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8

Nicholson, John W. "Ytterbium (III) Fluoride in Dental Materials." Inorganics 11, no. 12 (2023): 449. http://dx.doi.org/10.3390/inorganics11120449.

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(1) Background: The compound ytterbium trifluoride is used as a component of several dental materials, and this is reviewed in the current article. (2) Methods: Published articles on this substance were identified initially from PubMed, and then from Science Direct and Google Scholar. The publications identified in this way showed that ytterbium trifluoride has been included in a variety of dental restorative materials, including composite resins, glass polyalkenoate cements, and calcium trisilicate cements. (3) Results: Ytterbium trifluoride is reported to be insoluble in water. Despite this,

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9

KOROVIN, YU, Z. ZHILINA, N. RUSAKOVA, V. KUZ'MIN, S. VODZINSKY, and YU ISHKOV. "Spectral-luminescent effects in heterometallic complexes of crown-porphyrins." Journal of Porphyrins and Phthalocyanines 05, no. 05 (2001): 481–85. http://dx.doi.org/10.1002/jpp.350.

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New complexes of ytterbium with porphyrins containing crown- and other oxygen-containing cyclic substituents were obtained. The absorption, excitation, ligand luminescence and 4f-luminescence spectra have been investigated. It has been shown that 4f-luminescence of ytterbium Yb ( III ) ions was a result of the intramolecular energy transfer from the triplet level of the ligands to the resonance 2F5/2 level of Yb ( III ). It has been also established that in presence of alkali metal Na , K and Cs the dimer complexes (sandwich-type) of ytterbium-crown-porphyrin were formed. Molecular luminescenc

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10

Zalkin, A., and D. J. Berg. "Bis[bis(pentamethylcyclopentadienyl)ytterbium(III)] ditelluride." Acta Crystallographica Section C Crystal Structure Communications 44, no. 8 (1988): 1488–89. http://dx.doi.org/10.1107/s0108270188004524.

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11

Kalinovskaya, I. V., and A. N. Zadorozhnaya. "Luminescence of ytterbium(III) cinnamate compounds." Russian Journal of General Chemistry 83, no. 7 (2013): 1444–47. http://dx.doi.org/10.1134/s1070363213070232.

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12

Kumar, Anil, Israr Ahmad, and M. Sudershan Rao. "Ytterbium(III) triflate catalyzed synthesis of calix[4]pyrroles in ionic liquids." Canadian Journal of Chemistry 86, no. 9 (2008): 899–902. http://dx.doi.org/10.1139/v08-121.

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Ytterbium(III) triflate has been utilized as a mild Lewis-acid catalyst for the synthesis of various calix[4]pyrroles by the condensation of pyrrole with different ketones in ionic liquids. The calix[4]pyrroles were obtained in high yield under ecofriendly, economical, and noncorrosive conditions, and the catalyst was recovered and recycled.Key words: calix[4]pyrrole, ionic liquid, ytterbium triflate.

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13

Freire, Ricardo O., Gerd B. Rocha, and Alfredo M. Simas. "Sparkle/PM3 parameters for praseodymium(III) and ytterbium(III)." Chemical Physics Letters 441, no. 4-6 (2007): 354–57. http://dx.doi.org/10.1016/j.cplett.2007.05.036.

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14

Al Sabea, Hassan, Nadège Hamon, Olivier Galangau, et al. "Efficient luminescence control in dithienylethene functionalized cyclen macrocyclic lanthanide complexes." Inorganic Chemistry Frontiers 7, no. 16 (2020): 2979–89. http://dx.doi.org/10.1039/d0qi00354a.

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We report the synthesis of an original ligand scaffold based on a dimethyl-cyclen platform Medo2pa with two dithienylethene units attached to each picolinate arm and the corresponding yttrium(iii), europium(iii) and ytterbium(iii) complexes.

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15

Kazakov, Dmitri V., та Farit E. Safarov. "A novel chemiluminescence from the reaction of singlet oxygen with β-diketonates of europium(iii), neodymium(iii) and ytterbium(iii)". Photochem. Photobiol. Sci. 13, № 12 (2014): 1646–49. http://dx.doi.org/10.1039/c4pp00234b.

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Decomposition of 1,4-dimethylnaphthalene endoperoxide, which is the source of singlet oxygen, in the presence of β-diketonates of europium(iii), neodymium(iii) and ytterbium(iii) is accompanied by bright chemiluminescence in visible and near infra-red spectral region due to characteristic emission from the lanthanides.

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16

Duncalf, David J., Peter B. Hitchcock, and Gerard A. Lawless. "Synthesis and characterisation of iodo functionalised ytterbium(II) and ytterbium(III) alkoxides." Chemical Communications, no. 2 (1996): 269. http://dx.doi.org/10.1039/cc9960000269.

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17

Korolev, V. V., T. N. Lomova, A. G. Ramazanova, O. V. Balmasova, and E. G. Mozhzhukhina. "Magnetocaloric behavior of REE porphyrin-based paramagnets at room temperature." Journal of Porphyrins and Phthalocyanines 23, no. 10 (2019): 1110–17. http://dx.doi.org/10.1142/s1088424619501220.

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REE complexes with cyclic aromatic ligands are ranked as the molecular materials with both electronic functionality and a single-molecule magnet behavior at temperatures lower 80 K. At the temperature close to room, they display a positive magnetocaloric effect (MCE) often comparable with one in ferromagnetics. We were determined MCE during the magnetization of both (5,10,15,20-tetra(4-tert-butylphenylporphinato))ytterbium(III)chloride, (Cl)YbT[Formula: see text]BuPP and (5,10,15,20-tetraphenylporphinato)ytterbium(III)chloride, (Cl)YbTPP in their aqueous suspensions over the temperature range

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18

Ying, Huacheng, Mingzhu Gong, and Chengfu Pi. "Generation and reactivity of neutral 1,3-benzazaphosphole and anionic 1,3-benzazaphospholide ytterbium(iii) complexes." Dalton Transactions 48, no. 8 (2019): 2722–29. http://dx.doi.org/10.1039/c8dt04768e.

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19

Deacon, Glen B., Craig M. Forsyth, and Dallas L. Wilkinson. "Diverse Heteroleptic Ytterbium(III) Thiocyanate Complexes by Oxidation from Bis(thiocyanato)ytterbium(II)." Chemistry 7, no. 8 (2001): 1784–95. http://dx.doi.org/10.1002/1521-3765(20010417)7:8<1784::aid-chem17840>3.0.co;2-7.

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20

Kawamura, Yuichiro, Yuji Wada, Mitsunori Iwamuro, Takayuki Kitamura, and Shozo Yanagida. "Near-infrared Electroluminescence from Ytterbium(III) Complex." Chemistry Letters 29, no. 3 (2000): 280–81. http://dx.doi.org/10.1246/cl.2000.280.

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21

Eggers, S. H., J. Kopf та R. D. Fischer. "Structure of tris(η5-cyclopentadienyl)ytterbium(III)". Acta Crystallographica Section C Crystal Structure Communications 43, № 12 (1987): 2288–90. http://dx.doi.org/10.1107/s0108270187088036.

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22

Lisowski, Jerzy, та Przemysław Starynowicz. "Di-μ-hydroxy macrocyclic ytterbium(III) complex". Inorganic Chemistry Communications 6, № 5 (2003): 593–97. http://dx.doi.org/10.1016/s1387-7003(03)00051-0.

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23

Wegh, R. T., and A. Meijerink. "Cooperative luminescence of ytterbium(III) in La2O3." Chemical Physics Letters 246, no. 4-5 (1995): 495–98. http://dx.doi.org/10.1016/0009-2614(95)01145-6.

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24

Balasooriya, Dinesh, Beibei Liu, Hongshan He, Andew Sykes, and P. Stanley May. "A conjugated porphyrin as a red-light sensitizer for near-infrared emission of ytterbium(iii) ion." New Journal of Chemistry 44, no. 43 (2020): 18756–62. http://dx.doi.org/10.1039/d0nj04910g.

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25

He, Hongshan, James D. Bosonetta, Kraig A. Wheeler, and Stanley P. May. "Sisters together: co-sensitization of near-infrared emission of ytterbium(iii) by BODIPY and porphyrin dyes." Chemical Communications 53, no. 73 (2017): 10120–23. http://dx.doi.org/10.1039/c7cc05437h.

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26

He, Hongshan, James D. Bosonetta, Kraig A. Wheeler, and Stanley P. May. "Correction: Sisters together: co-sensitization of near-infrared emission of ytterbium(iii) by BODIPY and porphyrin dyes." Chem. Commun. 53, no. 86 (2017): 11842. http://dx.doi.org/10.1039/c7cc90394d.

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27

Kukoyi, Adedayo, Eric A. Micheli, Beibei Liu, Hongshan He, and P. Stanley May. "BODIPY-functionalized 1,10-phenanthroline as a long wavelength sensitizer for near-infrared emission of the ytterbium(iii) ion." Dalton Transactions 48, no. 36 (2019): 13880–87. http://dx.doi.org/10.1039/c9dt02850a.

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28

Ivakha, N. B., O. S. Berezhnytska, O. O. Rohovtsov, I. O. Savchenko, N. V. Rusakova, and O. K. Trunova. "Spectral-luminescent characteristics of coordination compounds and metal polymers of Yb(III)." Voprosy Khimii i Khimicheskoi Tekhnologii, no. 3 (June 2023): 77–85. http://dx.doi.org/10.32434/0321-4095-2023-148-3-77-85.

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New mono- and heteroligand (with phenanthroline or dipyridyl) metal complexes of ytterbium (III) with 2-methyl-5-biphenylpentene-1-3,5-dione were synthesized in this work. Homo- and copolymers of ytterbium complex with methyl methacrylate or styrene were obtained by the method of radical polymerization. Coordination compounds were investigated by IR spectroscopy, diffuse reflectance spectroscopy, thermal and luminescence analyses. It was determined that the -diketone molecules are bidentate-cyclically coordinated to the central atom, and the coordination sphere of the monoligand complex is su

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29

Ivakha, Nadiia, Oleksandra Berezhnytska, Oleksandr Rohovtsov, Nataliia Rusakova та Olena Trunova. "MONO- AND MIXED- LIGAND COMPLEXES OF Yb(III) WITH NEW β-DIKETONES". Ukrainian Chemistry Journal 87, № 2 (2021): 65–76. http://dx.doi.org/10.33609/2708-129x.87.02.2021.65-76.

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New ytterbium (III) compounds with β-diketones (2,7-dimethyl-octene-1-dione-3,5 and 2,6-dimethylheptene-1-dione-3,5) and their derivatives with phenanthroline have been synthesized. The composition and chemical structure of the obtained complexes have been determined by several Physico-chemical investigations. It has been shown, that the Yb (III) ion coordinates three ligand molecules and the coordination sphere of the complexes is supplemented by two molecules of water or a molecule of phenanthroline. It has been shown that the СN of the ytterbium ion is 8, the coordination polyhedron is a

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30

Gendron, Frédéric, Maxime Grasser, and Boris Le Guennic. "Near-infrared circular dichroism of the ytterbium DOTMA complex: an ab initio investigation." Physical Chemistry Chemical Physics 24, no. 9 (2022): 5404–10. http://dx.doi.org/10.1039/d1cp01675j.

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The electronic structure and circular dichroism spectra of the ytterbium(iii) complex [Yb(DOTMA)]− are calculated using multi-configurational wavefunction methods with the spin–orbit coupling treated by the state interaction approach.

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31

Gray, A. K., B. R. Martin, and P. K. Dorhout. "Crystal structure of sodium ytterbium(III) selenide, NaYbSe2." Zeitschrift für Kristallographie - New Crystal Structures 218, no. 1 (2003): 19. http://dx.doi.org/10.1524/ncrs.2003.218.1.19.

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32

Gray, A. K., B. R. Martin, and P. K. Dorhout. "Crystal structure of potassium ytterbium(III) selenide, KYbSe2." Zeitschrift für Kristallographie - New Crystal Structures 218, no. 1 (2003): 20. http://dx.doi.org/10.1524/ncrs.2003.218.1.20.

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33

Gray, A. K., B. R. Martin, and P. K. Dorhout. "Crystal structure of sodium ytterbium(III) selenide, NaYbSe2." Zeitschrift für Kristallographie - New Crystal Structures 218, JG (2003): 19. http://dx.doi.org/10.1524/ncrs.2003.218.jg.19.

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34

Gray, A. K., B. R. Martin, and P. K. Dorhout. "Crystal structure of potassium ytterbium(III) selenide, KYbSe2." Zeitschrift für Kristallographie - New Crystal Structures 218, JG (2003): 20. http://dx.doi.org/10.1524/ncrs.2003.218.jg.20.

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35

Gray, A. K., J. M. Knaust, B. C. Chan, L. A. Polyakova, and P. K. Dorhout. "Crystal structure of potassium ytterbium(III) tetrathiosilicate, KYbSiS4." Zeitschrift für Kristallographie - New Crystal Structures 220, no. 1-4 (2005): 313. http://dx.doi.org/10.1524/ncrs.2005.220.14.313.

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36

Lu, Weimin, Bin Wu, Lina Wang, and Yueqing Lu. "Aquatris(1,10-phenanthroline)(trans-2,3-dimethylacrylato)ytterbium(III)." Acta Crystallographica Section C Crystal Structure Communications 56, no. 3 (2000): 316–18. http://dx.doi.org/10.1107/s0108270199016169.

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37

Barrett, Anthony G. M., Nathalie Bouloc, D. Christopher Braddock, et al. "Synthesis of some ytterbium(III) tris-(perfluoroalkylsulfonyl)methides." Tetrahedron 58, no. 20 (2002): 3835–40. http://dx.doi.org/10.1016/s0040-4020(02)00210-7.

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38

Kasuga, Kuninobu, Kumi Nishikori, Takuya Mihara, Makoto Handa, Kunihisa Sogabe, and Kimio Isa. "Preparation of bis(tetra-2,3-pyradinoporphyrazinato)ytterbium(III)." Inorganica Chimica Acta 174, no. 2 (1990): 153–54. http://dx.doi.org/10.1016/s0020-1693(00)80292-3.

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39

Ganjali, Mohammad Reza, Leila Naji, Tahereh Poursaberi, Mojtaba Shamsipur, and Soheila Haghgoo. "Ytterbium(III)-selective membrane electrode based on cefixime." Analytica Chimica Acta 475, no. 1-2 (2003): 59–66. http://dx.doi.org/10.1016/s0003-2670(02)01226-6.

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40

Shuvaev, Sergey, and David Parker. "A near-IR luminescent ratiometric ytterbium pH probe." Dalton Transactions 48, no. 14 (2019): 4471–73. http://dx.doi.org/10.1039/c9dt00411d.

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41

Xiao, Xiao, Hongjiang Mei, Quangang Chen, et al. "Direct asymmetric vinylogous Michael addition of 3-alkylidene oxindoles to chalcones catalyzed by a chiral N,N′-dioxide ytterbium(iii) complex." Chemical Communications 51, no. 3 (2015): 580–83. http://dx.doi.org/10.1039/c4cc07204a.

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A chiral ytterbium(iii)–N,N′-dioxide complex was applied in the catalytic direct asymmetric vinylogous Michael addition of 3-alkylidene oxindoles to chalcones, giving the corresponding γ-addition products with high yields, enantioselectivities andZ/Eselectivities.

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42

Kawamura, Yuichiro, Yuji Wada, and Shozo Yanagida. "Near-Infrared Photoluminescence and Electroluminescence of Neodymium(III), Erbium(III), and Ytterbium(III) Complexes." Japanese Journal of Applied Physics 40, Part 1, No. 1 (2001): 350–56. http://dx.doi.org/10.1143/jjap.40.350.

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43

Aerts, Robin, Bart Geboes, Karen Van Hecke, Koen Binnemans, and Thomas Cardinaels. "Electrochemical Reduction of Ytterbium in Non-Aqueous Solvents - Towards Production of Pure Medical Lutetium-177." ECS Meeting Abstracts MA2023-02, no. 25 (2023): 1384. http://dx.doi.org/10.1149/ma2023-02251384mtgabs.

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In recent years targeted radionuclide therapy has become a topic of great interest as a growing number of cancers can potentially be treated with radionuclides like lutetium-177 and samarium-153. To facilitate this growth and meet the demand, preparation and purification of lutetium-177 is increasing in importance. In the most common production route, enriched ytterbium-176 targets are irradiated and the produced lutetium-177 is separated from the ytterbium target material. This challenging separation is commonly performed using ion exchange resins, a method limited in scalability as the chemi

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44

Prajzler, Vaclav, Ivan Huttel, Oleksiy Lyutakov, Jiri Oswald, Vladimir Machovic, and Vitezslav Jerabek. "Optical properties of PMMA doped with erbium(III) and ytterbium(III) complexes." Polymer Engineering & Science 49, no. 9 (2009): 1814–17. http://dx.doi.org/10.1002/pen.21418.

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45

Schmidt, L., A. Dimitrov, and E. Kemnitz. "A new approach to prepare nanoscopic rare earth metal fluorides: the fluorolytic sol–gel synthesis of ytterbium fluoride." Chem. Commun. 50, no. 50 (2014): 6613–16. http://dx.doi.org/10.1039/c4cc02626h.

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The sol–gel synthesis of nanoscopic ytterbium fluoride is reported. The transparent and stable sols have been characterized by DLS, TEM and XRD. A new Yb<sup>III</sup> complex has been structurally characterized by single crystal X-ray analysis.

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46

Deacon, GB, and DL Wilkinson. "Organolanthanoids. XV. The Preparation of Carboxylatobis(cyclopentadienyl)ytterbium(III) Complexes by Oxidation of Bis(cyclopentadienyl)ytterbium(II)." Australian Journal of Chemistry 42, no. 6 (1989): 845. http://dx.doi.org/10.1071/ch9890845.

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The complexes, Cp2Yb(O2CR) [Cp = cyclopentadienyl; R = Me, CF3, Ph, C6F5, C6Br5, o- MeO2CC6F4 (tmcp), 2,4,6-Me3C6H2 (tmp), pyridin-2-yl (pyr), or quinolin-2-yl (quin)] have been prepared in good yield by oxidation of bis(cyclopentadienyl)(1,2-dimethoxyethane)ytterbium(II) with the appropriate mercury(ll) or thallium(I) carboxylate, generally in tetrahydrofuran. Structural data suggest that four complexes (R=Me, CF3, Ph or C6F5) are dimeric with bridging bidentate carboxylate groups, three (R = tmp, pyr or quin) are monomeric with chelating carboxylates, but the structure is less clear for R =

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47

WU, HUI, SHANG-XIANG GU, GANG-QIANG YIN, RU-WEN DENG, and FU-LI ZENG. "Crystal Structure of Dimeric Tetraquadipyridinioacetateytterbium(III) Perchlorate [Yb(C5H5NCH2CO2)2.4(H2O) ]2.(Cl04 )6." Journal of Indian Chemical Society Vol. 75, May 1998 (1998): 276–78. https://doi.org/10.5281/zenodo.5925270.

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Department of Chemistry, Lanzhou University, Lanzhou 730000, China Department of Biology, Lanzhou University, Lanzhou 730000, China <em>Manuscript received 16 April 1997, accepted 19 September 1997</em> The title complex ilimeric tetraquadipyridinioacatateytterbium perchlorate ([Yb{C<sub>5</sub>H<sub>5</sub>NCH2COO)<sub>2</sub>.4(H<sub>2</sub>O)]<sub>2</sub>.(ClO<sub>4</sub>)<sub>6</sub>) has been prepared by reacting ytterbium perchlorate with pyridine betaine (pyridinioacetate) in warm water and its X-ray crystal structure has been determined. The ytterbium(III) ion is surrounded by four car

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48

Karaçoban, Betül, and Leyla Özdemir. "Transition Energies of Ytterbium (Z=70)." Zeitschrift für Naturforschung A 66, no. 8-9 (2011): 543–51. http://dx.doi.org/10.5560/zna.2011-0003.

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Abstract Transition energies of neutral ytterbium (Yb I, Z = 70, belonging to the lanthanide series), including ionization potential, excitation energies, and electron affinity are calculated by the multiconfiguration Hartree-Fock (MCHF) method within the framework of the Breit-Pauli Hamiltonian and the relativistic Hartree-Fock (HFR) method. Ionization potential and excitation energies of Yb II and Yb III are also reported. The obtained results have been compared with other works.

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Zalkin, A., and D. J. Berg. "A pentamethylcyclopentadienyl, chloro, oxo, ether complex of ytterbium(III)." Acta Crystallographica Section C Crystal Structure Communications 45, no. 10 (1989): 1630–31. http://dx.doi.org/10.1107/s0108270189001812.

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Kim, Byung-So. "Efficient Synthesis of Xanthene Derivatives Utilizing Ytterbium(III) Triflate." Journal of the Korean Chemical Society 51, no. 3 (2007): 298–300. http://dx.doi.org/10.5012/jkcs.2007.51.3.298.

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