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Relevant bibliographies by topics / Ytterbium(III)

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Academic literature on the topic 'Ytterbium(III)'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Ytterbium(III)"

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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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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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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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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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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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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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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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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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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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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Dissertations / Theses on the topic "Ytterbium(III)"

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Wang, Jingzhou. "Spectroscopic Studies of Ytterbium Doped III-Nitride Semiconductors." Ohio University / OhioLINK, 2009. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1249551044.

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Lelli, Moreno. "Solution Structure and Solution Dynamics in Chiral Ytterbium(III) Complexes." Doctoral thesis, Scuola Normale Superiore, 2007. http://hdl.handle.net/11384/85804.

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Parreu, i. Alberich Isabel. "Crystal Growth and Characterization of ytterbium or neodymium doped type III-KGd(PO3)4. A new bifunctional nonlinear and laser crystal." Doctoral thesis, Universitat Rovira i Virgili, 2006. http://hdl.handle.net/10803/9081.

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S'anomenen cristalls bifuncionals aquells que posseeixen simultàniament propietats d'òptica no lineal i propietats làser. Aquest tipus de materials són molt interessants ja que, combinant aquestes dues propietats, poden auto-generar radiació làser en la regió electromagnètica del blau (≈ 450 nm) o del verd (≈ 550 nm). Els materials làser d'estat sòlid que generen radiació làser en el rang electromagnètic visible (≈ 400-800 nm) tenen actualment un paper molt important en el desenvolupament tecnològic de dispositius làser i òptics en general ja que són interessa

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Wang, Jingzhou. "Optical and Electrical Study of the Rare Earth Doped III-nitride Semiconductor Materials." Ohio University / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1478177382556951.

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Seghier, Djelloul. "Etude des propriétés optiques et électriques des matériaux semiconducteurs III-V dopés aux ions Terres Rares en vue de la réalisation de dispositifs électroluminescents." Lyon, INSA, 1992. http://www.theses.fr/1992ISAL0040.

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Dans ce travail, nous présentons les résultats des études de spectroscopie optique et électrique réalisées sur les semi conducteurs III-V (InP, GaAlAs) dopés aux ions Terre rares (Yb, Er, Eu…). Le but de ce travail est l’étude de la faisabilité de nouveaux composants électroluminescents réalisés à base de ces matériaux. Sur InP dopé Yb, nous avons montré pas spectroscopie d’admittance que l'ion Yb3+ se comporte comme une impureté isovalants capable de piéger à la fois les électrons et les trous. Cette caractéristique électrique est exploitée pour discuter les propriétés optiques de l'ion Yb3+.

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Jones, Amanda S. "The Reduction of Ytterbium (III) to Ytterbium (II)." 2007. http://trace.tennessee.edu/utk_gradthes/251.

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If Yb(III) could be reduced to the highly unstable Yb(II), and temporarily stabilized, the separation of Yb from the other lanthanide elements could be facilitated. This facilitation would be based upon the considerably different chemistry of Yb(II) from the trivalent forms of all other lanthanides. The reduction of Yb(III) to Yb(II) using Mg was attempted in various media. The effects of the media, precipitating agent, and environment were examined. The best experimental conditions for the reduction of Yb(III) to Yb(II) and the subsequent precipitation of YbSO4 were found to be the addition o

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Bu, Chong Yan, and 卜崇晏. "Ytterbium(III) Triflate-Catalyzed Imino Diels–Alder Reactions." Thesis, 2011. http://ndltd.ncl.edu.tw/handle/38609581210232213063.

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碩士<br>輔仁大學<br>化學系<br>100<br>This thesis uses aromatic aldehydes 3a－e to react with benzylamine to prepare arylimines 4a－e. Compounds 4a－e underwent imino Diels－Alder reactions with Danishefsky’s diene in the presence of Yb(OTf)3 catalyst to give products 1a－e. In order to increase the reaction efficiency, we tried many different conditions for compound 4a, and found that 30 mol% of Yb(OTf)3 in refluxing acetonitrile provided the best yield of 1a in 81%. With this optimized condition and slight variation of the amount of the Yb(OTf)3, the yields of 1b－e were also improved. Furthermore, we use

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Garrett, Latasha Michelle. "The Use of Lanthanide Triflates as a Method for Reducing Ytterbium(III) to Ytterbium(II)." 2008. http://etd.utk.edu/2008/December2008MastersTheses/GarrettLatashaMichelle.pdf.

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高為智. "Spectroscopic and Electrochemical Studies of Europium(III) Chloride and Ytterbium(III) Chloride in Aluminum Chloride-1-Methyl-3-ethylimidazolium Chloride Room-Temperature Molten Salts." Thesis, 1995. http://ndltd.ncl.edu.tw/handle/01356876508198645980.

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碩士<br>國立成功大學<br>化學學系<br>83<br>UV-visible absorption spectroscopy and amperometric titration experiments indicate that the EuCl3 and YbCl3 are complexed as the [EuCl6]3- and [YbCl6]3-, in basic aluminum chloride-1-methyl-3-ethylimidazolium chloride molten salt, respectively, and they can be reduced to Eu(II) and Yb(II) species via quasi reversible one-electron charge-transfer process. The standard heterogeneous rate constant and the cathodic transfer coefficient were calculated for the reduction of these two complexes. The formal redox potential, E0', obtained from Nernst plots is dependent up

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Yen, Shih-Yao, and 顏士堯. "2-(Acetylsulfanyl)methyl Benzoate and 4-Acetoxybenzyl Carbonate: Two New Orthogonal Protecting Groups, and Selective Deprotection by Ytterbium(III) Triflate." Thesis, 2019. http://ndltd.ncl.edu.tw/handle/exan3u.

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碩士<br>國立中興大學<br>化學系所<br>107<br>The concept of orthogonality has become a mainstream for development of building blocks to carbohydrate synthesis. In this work, we developed two new orthogonal protecting groups for carbohydrates, namely 4-Acetoxybenzyl Carbonate (ABC) and 2-(Acetylsulfanyl)methyl Benzoate (ASMB). Both of them can be efficiently installed into different carbohydrate glycosides. Moreover, the two protecting groups can be selectively removed using Ytterbium(III) trifluoromethanesulfonate [Yb(OTf)3] under mild reaction conditions. The ABC group was selectively removed by deprotecti

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Book chapters on the topic "Ytterbium(III)"

1

Pardasani, R. T., and P. Pardasani. "Magnetic properties of ytterbium(III) bis(indenyl)-diazabutadiene complex." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 5. Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-662-65098-1_500.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of ytterbium(III) bis(indenyl)-diazabutadiene complex." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 5. Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-662-65098-1_501.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of ytterbium(III) complex with p-chlorophenyl-glyoxalthiosemicarbazone." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_746.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed ligand complex of ytterbium(III) with bis(phenylsulphinyl)propane ands bipyridyl." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49202-4_284.

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Lorbeer, Chantal, and Anja-Verena Mudring. "Nanomaterials for Energy Conversion-The Synthesis of Highly Crystalline Ytterbium(III) Fluoride Nanoparticles From Ionic Liquids." In Ceramic Materials for Energy Applications V. John Wiley & Sons, Inc., 2015. http://dx.doi.org/10.1002/9781119211709.ch12.

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Nakai, Takeshi, and Katsuhiko Tomooka. "Lanthanide(III) Reagents." In Lewis Acid Reagents. Oxford University PressOxford, 1999. http://dx.doi.org/10.1093/oso/9780198500995.003.0012.

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Abstract The lanthanide group consists of the 15 elements from lanthanum to lutetium in the periodic table. In the past two decades the synthetic uses of a variety of lanthanide complexes, in terms of the kind of central lanthanides, the oxidation state ( +2-+4), and the kind of ligands, have been developed.1 This chapter focuses primarily on the four classes of the most popular trivalent lanthanides, namely, cerium(III) complexes (CeL3), europium(III) complexes (EuL3), ytterbium complexes (YbL3), and lanthanum(III) complexes (LaL3). Note that many synthetic applications have been found not on

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Schweitzer, George K., and Lester L. Pesterfield. "The Scandium Group." In The Aqueous Chemistry of the Elements. Oxford University Press, 2010. http://dx.doi.org/10.1093/oso/9780195393354.003.0014.

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The members of the Sc Group are Sc scandium, Y yttrium, La lanthanum, Ce cerium, Pr praseodymium, Nd neodymium, Pm promethium, Sm samarium, Eu europium, Gd gadolinium, Tb terbium, Dy dysprosium, Ho holmium, Er erbium, Tm thulium, Yb ytterbium, Lu lutetium, and Ac actinium. All these elements resemble each other greatly, especially in the series La–Lu (called the lanthanoids). Their slight differences may be assigned largely to size similarities, but a few oxidation state changes give rise to marked differences. The predominant oxidation state is III, but the IV state for Ce, and the II state f

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Conference papers on the topic "Ytterbium(III)"

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Tropin, O. A., and V. A. Volkovich. "Reduction of ytterbium(III) species in alkali chloride based melts." In 3RD ELECTRONIC AND GREEN MATERIALS INTERNATIONAL CONFERENCE 2017 (EGM 2017). Author(s), 2017. http://dx.doi.org/10.1063/1.5002942.

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Wang, Chun-can, Fan Zhang, Yu-chun Lu, et al. "Novel method to optimize the distributed pump powers in kilowatt ytterbium-doped double-clad fiber laser." In Passive Components and Fiber-based Devices III. SPIE, 2006. http://dx.doi.org/10.1117/12.687507.

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Boivinet, Simon, Jean-Bernard Lecourt, and Yves Hernandez. "Study of periodic amplitude fluctuations in a mode-lock Ytterbium fiber laser delivering 1 MHz pulse train." In Fiber Lasers and Glass Photonics: Materials through Applications III, edited by Stefano Taccheo, Maurizio Ferrari, and Angela B. Seddon. SPIE, 2022. http://dx.doi.org/10.1117/12.2621645.

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