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Journal articles on the topic 'Phosphide telluride'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Kliche, Gerhard. "NOTIZEN: Iridiumphosphidtellurid, IrPTe / Iridium Phosphide Telluride, IrPTe." Zeitschrift für Naturforschung B 41, no. 1 (January 1, 1986): 130–31. http://dx.doi.org/10.1515/znb-1986-0126.

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IrPTe was prepared by annealing stoichiometric mixtures of IrP2 and IrTe2 in evacuated quartz tubes at 1100-1150 °C/2 davs. From the lattice constants (a = 6.030(1), b = 6.131(1), c = 12.132(1) Å) and the infrared absorption spectrum a structure similar to CoSbS (paracostibite) is concluded.

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2

Tschulik, Kristina, Michael Ruck, Michael Binnewies, Edgar Milke, Stefan Hoffmann, Walter Schnelle, Boniface P. T. Fokwa, Michael Gilleßen, and Peer Schmidt. "Chemistry and Physical Properties of the Phosphide Telluride Zr2PTe2." European Journal of Inorganic Chemistry 2009, no. 21 (July 2009): 3102–10. http://dx.doi.org/10.1002/ejic.200900346.

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3

Williams, R. H., I. M. Dharmadasa, M. H. Patterson, C. Maani, and N. M. Forsyth. "Metal contacts to semiconductors, indium phosphide and cadmium telluride." Surface Science Letters 168, no. 1-3 (March 1986): A122. http://dx.doi.org/10.1016/0167-2584(86)90452-4.

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4

Williams, R. H., I. M. Dharmadasa, M. H. Patterson, C. Maani, and N. M. Forsyth. "Metal contacts to semiconductors, indium phosphide and cadmium telluride." Surface Science 168, no. 1-3 (March 1986): 323–35. http://dx.doi.org/10.1016/0039-6028(86)90862-9.

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5

Philipp, Frauke, Peer Schmidt, Edgar Milke, Michael Binnewies, and Stefan Hoffmann. "Synthesis of the titanium phosphide telluride Ti2PTe2: A thermochemical approach." Journal of Solid State Chemistry 181, no. 4 (April 2008): 758–67. http://dx.doi.org/10.1016/j.jssc.2008.01.003.

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6

Tschulik, Kristina, Michael Ruck, Michael Binnewies, Edgar Milke, Stefan Hoffmann, Walter Schnelle, Boniface P. T. Fokwa, Michael Gilleßen, and Peer Schmidt. "Correction: Chemistry and Physical Properties of the Phosphide Telluride Zr2PTe2." European Journal of Inorganic Chemistry 2010, no. 14 (April 13, 2010): 2201. http://dx.doi.org/10.1002/ejic.201000335.

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7

Banerjee, Pushan, and B. Ghosh. "A Contacting Technology to Magnetic Semiconductors." Advances in Science and Technology 52 (October 2006): 31–35. http://dx.doi.org/10.4028/www.scientific.net/ast.52.31.

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The present paper describes the contacting technology to the diluted magnetic semiconductor Cd1-xMnxTe having potential applications in optoelectronic and spintronic devices. For efficient spin injection into a spintronic material, a matching ohmic contact is the demand of the time. Since cadmium telluride has a well-known contact problem, its manganese-doped counterpart is also facing a similar difficulty. In the present case Cd1-xMnxTe was fabricated using thermally assisted interdiffusion and compound formation between repeated stacked elemental layers of manganese, cadmium and tellurium. A wet electroless deposition technique was employed to deposit manganese doped nickel phosphide as a magnetic contact onto Cd1-xMnxTe. It appeared that the contact resistivity improved compared to the case of gold contact. The details of the contacting technology and the results have been described in the text of the paper.

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8

Sareen, Rob. "Semiconductor X-Ray Detectors." Microscopy Today 6, no. 6 (August 1998): 8–12. http://dx.doi.org/10.1017/s1551929500068152.

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Detection of characteristic x-rays is a fascinating and challenging subject. From its early beginnings with gas proportional counters it has evolved, like many branches of technology, into the use of a variety of semiconductors.The lithium compensated silicon detector [Si(Li)] has been the predominant measuring tool over the last two decades, in the last five years, increasing numbers of high purity germanium detectors (HPG) have appeared and more recently a plethora of new materials and concepts are seeing a successful introduction. Among these newer materials are compound semiconductors like mercuric iodide, cadmium telluride, cadmium zinc telluride, gallium arsenide, lead iodide, indium phosphide and diamond. Among the new concepts are Bolometers, Transition Edge Detectors, Drift Detectors, PIN Diodes, CCD arrays and PN CCD arrays.

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9

Beaunier, L., H. Cachet, R. Cortes, and M. Froment. "Epitaxial electrodeposition of lead telluride films on indium phosphide single crystals." Journal of Electroanalytical Chemistry 532, no. 1-2 (September 2002): 215–18. http://dx.doi.org/10.1016/s0022-0728(02)00758-1.

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10

Tschulik, Kristina, Stefan Hoffmann, Boniface P. T. Fokwa, Michael Gilleßen, and Peer Schmidt. "Studies regarding the homogeneity range of the zirconium phosphide telluride Zr2+δPTe2." Solid State Sciences 12, no. 12 (December 2010): 2030–35. http://dx.doi.org/10.1016/j.solidstatesciences.2010.08.022.

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11

Schmidt, Peer, Hannelore Dallmann, Gudrun Kadner, Jutta Krug, Frauke Philipp, and Klaus Teske. "The Thermochemical Behaviour of Te8O10(PO4)4and its Use for Phosphide Telluride Synthesis." Zeitschrift für anorganische und allgemeine Chemie 635, no. 13-14 (November 2009): 2153–61. http://dx.doi.org/10.1002/zaac.200900350.

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12

Tschulik, Kristina, Stefan Hoffmann, Boniface P. T. Fokwa, Michael Gillessen, and Peer Schmidt. "ChemInform Abstract: Studies Regarding the Homogeneity Range of the Zirconium Phosphide Telluride Zr2+δPTe2." ChemInform 42, no. 9 (February 3, 2011): no. http://dx.doi.org/10.1002/chin.201109016.

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13

Scholz, Tanja, and Peer Schmidt. "Homogeneity Range of the Zirconium Phosphide Telluride Zr2+xPTe2and the High-Temperature Phase Transformation to Zr2PTe." European Journal of Inorganic Chemistry 2015, no. 8 (February 9, 2015): 1457–62. http://dx.doi.org/10.1002/ejic.201403043.

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14

Scholz, Tanja, and Peer Schmidt. "ChemInform Abstract: Homogeneity Range of the Zirconium Phosphide Telluride Zr2+xPTe2and the High-Temperature Phase Transformation to Zr2PTe." ChemInform 46, no. 21 (May 2015): no. http://dx.doi.org/10.1002/chin.201521011.

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15

Kuhn, Norbert, Gerald Henkel, Hans Schumann, and Roland Fröhlich. "Die Bindungsverhältnisse in Phosphantelluriden. Eine empirische NMR-Studie und die Kristallstruktur von (iso-C3H7)3PTe [1] / The Nature of the Bonding in Phosphane Tellurides. An Empirical NMR Study and the Crystal Structure of (iso-C3H7)3PTe [1]." Zeitschrift für Naturforschung B 45, no. 7 (July 1, 1990): 1010–18. http://dx.doi.org/10.1515/znb-1990-0717.

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31P and 125Te NMR data of trialkylphosphane tellurides are compared. The deviation of the shifts for Me3PTe and 'Bu3PTe from those of other phosphane tellurides is interpreted in terms of high s-character of the P–Te bond originating from the phosphorus (R = Me) and the tellurium (R = 'Bu) atom, respectively. The molecular structure of 'Pr3PTe has been determined by X-ray crystallography (P–Te 2.365 A). A reduction of the bond order is suggested based also on a comparison of the R3PSe and R3PTe NMR data.

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16

Sun, Haochen, Fudong Wang, and William E. Buhro. "Tellurium Precursor for Nanocrystal Synthesis: Tris(dimethylamino)phosphine Telluride." ACS Nano 12, no. 12 (November 19, 2018): 12393–400. http://dx.doi.org/10.1021/acsnano.8b06468.

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17

Yoneyama, Hiroshi, Kenji Sugimura, and Susumu Kuwabata. "Effects of electrolytes on the photoelectrochemical reduction of carbon dioxide at illuminated p-type cadmium telluride and p-type indium phosphide electrodes in aqueous solutions." Journal of Electroanalytical Chemistry and Interfacial Electrochemistry 249, no. 1-2 (July 1988): 143–53. http://dx.doi.org/10.1016/0022-0728(88)80355-3.

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18

Sandblom, Nicole, Tom Ziegler, and Tristram Chivers. "A density functional study of the bonding in tertiary phosphine chalcogenides and related molecules." Canadian Journal of Chemistry 74, no. 11 (November 1, 1996): 2363–71. http://dx.doi.org/10.1139/v96-263.

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The nature of the phosphorus–tellurium bond in tertiary phosphine tellurides is not well understood. There is also controversy over the nature of multiple bonding in the lighter chalcogenides and the related ylides and imides. Density functional theory (DFT) was used to investigate the interactions in the molecule, Me3PE (E = O, S, Se, Te, BH3, CH2, NH). The calculated PE bond energies and orbital populations reveal contributions from both σ donation from the phosphine and π back-donation to the phosphine in all of the above cases. Down the group from oxygen to tellurium, the PE bond weakens from 544 kJ mol−1 to 184 kJ mol−1, but multiple bonding becomes more significant with respect to the single bond. For E = BH3, the PB bond energy is 166 kJ mol−1. Trimethylphosphine ylide was found to have a π-bond order of 0.5, while that of trimethylphosphine imine is 0.6. For comparison, the oxides of trimethylamine and trimethylarsine were also calculated to examine the pnictogen–oxygen bond; Me3N does not participate in multiple bonding with oxygen, while the π-bond orders for Me3PO and Me3AsO were calculated as 0.7 and 0.6, respectively. Key words: phosphine chalcogenides, phosphine ylides, phosphine imides, DFT calculations

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19

Wang, Mei Ping, Jin Hui Lin, and Xiao Li Hao. "Preparation and Characterization of CdTe/SiO₂ Composite." Advanced Materials Research 233-235 (May 2011): 1946–49. http://dx.doi.org/10.4028/www.scientific.net/amr.233-235.1946.

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TGA- stabilized CdTe nanocrystals (NCs) were prepared using sodium tellurite as tellurium source, which avoids the cumbersome processes associated with H2Te or NaHTe sources. Fluorescent CdTe/SiO2composites were prepared by a sol–gel method without the exchange of surface ligands. The composites were characterized with TEM and fluorescence spectrophotometer and investigated their stability in phosphate-buffered saline (PBS) buffer. CdTe NCs were loaded into the core of silica spheres during the formation of composite spheres. In contrast to CdTe NCs in aqueous solutions, CdTe NCs in the composite revealed better stability and the luminescence peak show red-shift.

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20

Hou, Mingyue, Zhaohua Zhou, Ao Xu, Kening Xiao, Jiakun Li, Donghuan Qin, Wei Xu, and Lintao Hou. "Synthesis of Group II-VI Semiconductor Nanocrystals via Phosphine Free Method and Their Application in Solution Processed Photovoltaic Devices." Nanomaterials 11, no. 8 (August 15, 2021): 2071. http://dx.doi.org/10.3390/nano11082071.

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Solution-processed CdTe semiconductor nanocrystals (NCs) have exhibited astonishing potential in fabricating low-cost, low materials consumption and highly efficient photovoltaic devices. However, most of the conventional CdTe NCs reported are synthesized through high temperature microemulsion method with high toxic trioctylphosphine tellurite (TOP-Te) or tributylphosphine tellurite (TBP-Te) as tellurium precursor. These hazardous substances used in the fabrication process of CdTe NCs are drawing them back from further application. Herein, we report a phosphine-free method for synthesizing group II-VI semiconductor NCs with alkyl amine and alkyl acid as ligands. Based on various characterizations like UV-vis absorption (UV), transmission electron microscope (TEM), and X-ray diffraction (XRD), among others, the properties of the as-synthesized CdS, CdSe, and CdTe NCs are determined. High-quality semiconductor NCs with easily controlled size and morphology could be fabricated through this phosphine-free method. To further investigate its potential to industrial application, NCs solar cells with device configuration of ITO/ZnO/CdSe/CdTe/Au and ITO/ZnO/CdS/CdTe/Au are fabricated based on NCs synthesized by this method. By optimizing the device fabrication conditions, the champion device exhibited power conversion efficiency (PCE) of 2.28%. This research paves the way for industrial production of low-cost and environmentally friendly NCs photovoltaic devices.

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21

Darkowski, Andrzej, and Michael Cocivera. "Electrodeposition of Cadmium Telluride Using Phosphine Telluride." Journal of The Electrochemical Society 132, no. 11 (November 1, 1985): 2768–71. http://dx.doi.org/10.1149/1.2113661.

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22

Wu, Min, Yixuan Wang, Hongyu Wang, Hao Wang, Yongming Sui, Fei Du, Xinyi Yang, and Bo Zou. "Phosphine-free engineering toward the synthesis of metal telluride nanocrystals: the role of a Te precursor coordinated at room temperature." Nanoscale 10, no. 46 (2018): 21928–35. http://dx.doi.org/10.1039/c8nr07595f.

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We developed a new phosphine-free strategy for fabricating high-quality metal telluride nanocrystals (NCs) by using a highly reactive Te precursor coordinated at room temperature. These metal telluride NCs with good optical properties possess excellent application prospects.

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23

Lao, Zhiqi, and Patrick H. Toy. "Catalytic Wittig and aza-Wittig reactions." Beilstein Journal of Organic Chemistry 12 (November 30, 2016): 2577–87. http://dx.doi.org/10.3762/bjoc.12.253.

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This review surveys the literature regarding the development of catalytic versions of the Wittig and aza-Wittig reactions. The first section summarizes how arsenic and tellurium-based catalytic Wittig-type reaction systems were developed first due to the relatively easy reduction of the oxides involved. This is followed by a presentation of the current state of the art regarding phosphine-catalyzed Wittig reactions. The second section covers the field of related catalytic aza-Wittig reactions that are catalyzed by both phosphine oxides and phosphines.

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24

Tantaleán, Juan C., Manuel A. Araya, Claudia P. Saavedra, Derie E. Fuentes, José M. Pérez, Iván L. Calderón, Philip Youderian, and Claudio C. Vásquez. "The Geobacillus stearothermophilus V iscS Gene, Encoding Cysteine Desulfurase, Confers Resistance to Potassium Tellurite in Escherichia coli K-12." Journal of Bacteriology 185, no. 19 (October 1, 2003): 5831–37. http://dx.doi.org/10.1128/jb.185.19.5831-5837.2003.

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ABSTRACT Many eubacteria are resistant to the toxic oxidizing agent potassium tellurite, and tellurite resistance involves diverse biochemical mechanisms. Expression of the iscS gene from Geobacillus stearothermophilus V, which is naturally resistant to tellurite, confers tellurite resistance in Escherichia coli K-12, which is naturally sensitive to tellurite. The G. stearothermophilus iscS gene encodes a cysteine desulfurase. A site-directed mutation in iscS that prevents binding of its pyridoxal phosphate cofactor abolishes both enzyme activity and its ability to confer tellurite resistance in E. coli. Expression of the G. stearothermophilus iscS gene confers tellurite resistance in tellurite-hypersensitive E. coli iscS and sodA sodB mutants (deficient in superoxide dismutase) and complements the auxotrophic requirement of an E. coli iscS mutant for thiamine but not for nicotinic acid. These and other results support the hypothesis that the reduction of tellurite generates superoxide anions and that the primary targets of superoxide damage in E. coli are enzymes with iron-sulfur clusters.

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25

Wynands, H., and M. Cocivera. "Photoelectrodeposition of In2Te3 using nonaqueous phosphine telluride." Solar Energy Materials 17, no. 3 (April 1988): 185–99. http://dx.doi.org/10.1016/0165-1633(88)90025-1.

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26

Gusarova, N. K., N. A. Chernysheva, S. V. Yas’ko, L. V. Klyba, and B. A. Trofimov. "Reaction of divinyl telluride with secondary phosphine chalcogenides." Russian Journal of General Chemistry 81, no. 12 (December 2011): 2506–9. http://dx.doi.org/10.1134/s1070363211120152.

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27

Turner, Mark S., Yu Pei Tan, and Philip M. Giffard. "Inactivation of an Iron Transporter in Lactococcus lactis Results in Resistance to Tellurite and Oxidative Stress." Applied and Environmental Microbiology 73, no. 19 (August 3, 2007): 6144–49. http://dx.doi.org/10.1128/aem.00413-07.

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ABSTRACT In Lactococcus lactis, the interactions between oxidative defense, metal metabolism, and respiratory metabolism are not fully understood. To provide an insight into these processes, we isolated and characterized mutants of L. lactis resistant to the oxidizing agent tellurite (TeO3 2−), which generates superoxide radicals intracellularly. A collection of tellurite-resistant mutants was obtained using random transposon mutagenesis of L. lactis. These contained insertions in genes encoding a proton-coupled Mn2+/Fe2+ transport homolog (mntH), the high-affinity phosphate transport system (pstABCDEF), a putative osmoprotectant uptake system (choQ), and a homolog of the oxidative defense regulator spx (trmA). The tellurite-resistant mutants all had better survival than the wild type following aerated growth. The mntH mutant was found to be impaired in Fe2+ uptake, suggesting that MntH is a Fe2+ transporter in L. lactis. This mutant is capable of carrying out respiration but does not generate as high a final pH and does not exhibit the long lag phase in the presence of hemin and oxygen that is characteristic of wild-type L. lactis. This study suggests that tellurite-resistant mutants also have increased resistance to oxidative stress and that intracellular Fe2+ can heighten tellurite and oxygen toxicity.

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28

Yao, Dong, Yi Liu, Wujun Zhao, Haotong Wei, Xintao Luo, Zhennan Wu, Chunwei Dong, Hao Zhang, and Bai Yang. "A totally phosphine-free synthesis of metal telluride nanocrystals by employing alkylamides to replace alkylphosphines for preparing highly reactive tellurium precursors." Nanoscale 5, no. 20 (2013): 9593. http://dx.doi.org/10.1039/c3nr03553k.

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29

Ukon, Sakiko, Yasuhito Tsujiie, Shunsuke Murai, Koji Fujita, and Katsuhisa Tanaka. "Second-Harmonic Generation in Thermally Poled Na₂O-Al₂O₃-TeO₂ Glasses." Advanced Materials Research 39-40 (April 2008): 247–52. http://dx.doi.org/10.4028/www.scientific.net/amr.39-40.247.

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Tellurite glasses exhibit attractive optical properties such as high refractive index, high transmittance in the infrared-to-visible region, and large third-order nonlinear susceptibility. Poled tellurite glasses also show second-harmonic generation (SHG) as revealed by the present authors. However, there exist many unresolved problems in second-harmonic generation of oxide glasses; SH intensity is low and it decays at room temperature. In this work, the effect of Al2O3 addition on SH intensity and its decay has been explored for thermally poled sodium tellurite glasses. The decay rate of SH intensity is reduced by the addition of Al2O3. The result is similar to those reported for phosphate and silicate glasses containing Al2O3. Also, the glasses poled at a voltage of 4 kV manifest optimum poling temperature lower than that for the same glasses poled at 3 kV.

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30

Rada, S., M. Culea, M. Rada, T. Rusu, and E. Culea. "Competitive role of the tellurium and gadolinium cations in structural aspects of the gadolinium–phosphate–tellurate glasses." Journal of Alloys and Compounds 490, no. 1-2 (February 2010): 270–76. http://dx.doi.org/10.1016/j.jallcom.2009.09.174.

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31

Darkowski, Andrzej, and Michael Cocivera. "Performance and Properties of CdTe Electrodeposited from Phosphine Telluride Solution." Journal of The Electrochemical Society 134, no. 1 (January 1, 1987): 226–29. http://dx.doi.org/10.1149/1.2100412.

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32

Abdel‐Kader, A., R. El‐Mallawany, and M. M. ElKholy. "dc electrical conductivity of tellurite phosphate glasses." Journal of Applied Physics 73, no. 1 (January 1993): 75–77. http://dx.doi.org/10.1063/1.353831.

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33

Li, Dongchan, Yafei Guo, Tianlong Deng, Yu-Wei Chen, and Nelson Belzile. "Solvent Extraction of Tellurium from Chloride Solutions Using Tri-n-butyl Phosphate: Conditions and Thermodynamic Data." Scientific World Journal 2014 (2014): 1–6. http://dx.doi.org/10.1155/2014/458705.

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The extractive separation of tellurium (IV) from hydrochloric acid media with tri-n-butyl phosphate (TBP) in kerosene was investigated. The dependence on the extraction of tellurium species, concentrations of tellurium and TBP, extraction time and stage, organic/aqueous ratio, and interferences from coexist metallic ions were examined and are discussed. Besides, the stripping agent and stripping time were also studied. It was found that the extraction reaction corresponds to the neutral complex formation mechanism and the extracted species is TeCl4·3TBP and that the extraction process is exothermic. The thermodynamic parameters of enthalpyΔH, entropyΔS, and free energyΔGof the extraction process were evaluated at −26.2 kJ·mol−1, −65.6 J·mol−1·K−1, and −7.0 kJ·mol−1, respectively at 293 K.

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34

Viswanathan, K., V. U. Nayar, and G. Aruldhas. "Vibrational spectra of cesium tellurate phosphate." Infrared Physics 26, no. 6 (November 1986): 353–56. http://dx.doi.org/10.1016/0020-0891(86)90057-6.

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35

Elisa, Mihail, Raluca Constantina Stefan, Ileana Cristina Vasiliu, Stefan Marian Iordache, Ana-Maria Iordache, Bogdan Alexandru Sava, Lucica Boroica, et al. "A New Zinc Phosphate-Tellurite Glass for Magneto-Optical Applications." Nanomaterials 10, no. 9 (September 18, 2020): 1875. http://dx.doi.org/10.3390/nano10091875.

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This work investigates the structural, magnetic and magneto-optical properties of a new zinc phosphate-tellurite glass belonging to the 45ZnO-10Al2O3-40P2O5-5TeO2 system. The glass was prepared by a wet method of processing the starting reagents followed by suitable melting–stirring–quenching–annealing steps. Specific parameters such as density, average molecular mass, molar volume, oxygen packaging density, refractive index, molar refractivity, electronic polarizability, reflection loss, optical transmission, band gap and optical basicity have been reported together with thermal, magnetic and magneto-optical characteristics. Absorption bands appear in the blue and red visible region, while over 600 nm the glass becomes more transparent. FTIR and Raman spectra evidenced phosphate-tellurite vibration modes proving the P2O5 and TeO2 network forming role. Magnetic measurements reveal the diamagnetic character of the Te-doped glass with an additional weak ferromagnetic signal, specific to diluted ferromagnetic oxides. Positive Faraday rotation angle with monotonous decreasing value at increasing wavelength was evidenced from magneto-optical measurements. The final product is a composite material comprising of a non-crystalline vitreous phase and Te-based nanoclusters accompanied by oxygen vacancies. The metallic-like Te colloids are responsible for the dark reddish color of the glass whereas the accompanying oxygen vacancies might be responsible for the weak ferromagnetic signal persisting up to room temperature.

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36

Kuhn, Norbert, and Hans Schumann. "Phosphorus–tellurium compounds. Part 3. Cyclopentadienyliron tellurophosphorane complexes: tellurium-bridged iron phosphine compounds?" J. Chem. Soc., Dalton Trans., no. 3 (1987): 541–44. http://dx.doi.org/10.1039/dt9870000541.

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37

Jones, C. H. W., and R. D. Sharma. "Tellurium-125 NMR and Moessbauer spectroscopy of tellurium-phosphine complexes and the tellurocyanates." Organometallics 6, no. 7 (July 1987): 1419–23. http://dx.doi.org/10.1021/om00150a009.

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38

du Mont, Wolf-W. "Die Reaktion von Tri-t-butylphosphan und Tri-t-butylarsan mit Selen und Tellur: Bildung inerter und labiler Chalkogenophosphorane und -arsorane / The Reaction of Tri-t-butylphosphane and Tri-t-butylarsane with Selenium and Tellurium: Formation of Inert and Labile Chalcogenophosphoranes and -arsoranes." Zeitschrift für Naturforschung B 40, no. 11 (November 1, 1985): 1453–56. http://dx.doi.org/10.1515/znb-1985-1106.

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The reactions of tri-t-butylphosphane 1 with selenium and tellurium proceed quantitatively with formation of seleno- and the telluro-tri-t-butylphosphorane. respectively (3, 4). Tri-t-butylarsane 2 reacts with selenium to give seleno-tri-t-butylarsorane (5), but no significant interaction is observed between 2 and elemental tellurium. 1H and 31P NMR spectra provide evidence for rapid tellurium transfer between telluro-tri-t-butylphosphorane (4) and tri-t-butylphosphane (1), tri-t-butylarsane (2) or tris(dimethylamino)phosphane. Selenium transfer between seleno-tri-t-butylarsorane (5) and tri-t-butylarsane (2) leads to 1H and 13C NMR line broadening. Vibrational spectra of t-Bu3E−Y (3: E = P, Y = Se; 4: E = P, Y = Te; 5: E = As, X = Se) indicate coupling of E−C and E−Y stretching vibrations in 3 and 4.

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39

Polosan, S., A. Nitescu, and M. Secu. "Optical spectroscopy and dielectric properties of phosphate-tellurite glasses." Physica Scripta 95, no. 3 (February 6, 2020): 034005. http://dx.doi.org/10.1088/1402-4896/ab5263.

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40

Abdel-Kader, A., R. El-Mallawany, M. Elkholy, and H. Farag. "Thermoluminescence dosimetry of rare-earth doped tellurite phosphate glasses." Materials Chemistry and Physics 36, no. 3-4 (January 1994): 365–70. http://dx.doi.org/10.1016/0254-0584(94)90056-6.

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41

Lithgow, James K., Emma J. Hayhurst, Gerald Cohen, Yair Aharonowitz, and Simon J. Foster. "Role of a Cysteine Synthase in Staphylococcus aureus." Journal of Bacteriology 186, no. 6 (March 15, 2004): 1579–90. http://dx.doi.org/10.1128/jb.186.6.1579-1590.2004.

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ABSTRACT The gram-positive human pathogen Staphylococcus aureus is often isolated with media containing potassium tellurite, to which it has a higher level of resistance than Escherichia coli. The S. aureus cysM gene was isolated in a screen for genes that would increase the level of tellurite resistance of E. coli DH5α. The protein encoded by S. aureus cysM is sequentially and functionally homologous to the O-acetylserine (thiol)-lyase B family of cysteine synthase proteins. An S. aureus cysM knockout mutant grows poorly in cysteine-limiting conditions, and analysis of the thiol content in cell extracts showed that the cysM mutant produced significantly less cysteine than wild-type S. aureus SH1000. S. aureus SH1000 cannot use sulfate, sulfite, or sulfonates as the source of sulfur in cysteine biosynthesis, which is explained by the absence of genes required for the uptake and reduction of these compounds in the S. aureus genome. S. aureus SH1000, however, can utilize thiosulfate, sulfide, or glutathione as the sole source of sulfur. Mutation of cysM caused increased sensitivity of S. aureus to tellurite, hydrogen peroxide, acid, and diamide and also significantly reduced the ability of S. aureus to recover from starvation in amino acid- or phosphate-limiting conditions, indicating a role for cysteine in the S. aureus stress response and survival mechanisms.

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42

Kikuta, Toshio, Yoshikazu Kawagishi, El-maghraby Mohamed El-Maghraby, Toshinari Yamazaki, and Noriyuki Nakatani. "Polarization reversal of telluric acid ammonium phosphate." Materials Science and Engineering: B 120, no. 1-3 (July 2005): 134–36. http://dx.doi.org/10.1016/j.mseb.2005.02.023.

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43

Chernysheva, Nataliya A., Svetlana V. Yas’ko, Nina K. Gusarova, Anna A. Tatarinova, Ludmila V. Klyba, and Boris A. Trofimov. "Radical addition of secondary phosphine sulfides and selenides to vinyl tellurides." Mendeleev Communications 20, no. 6 (November 2010): 346–47. http://dx.doi.org/10.1016/j.mencom.2010.11.015.

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Levason, William, Gillian Reid, Majella Victor, and Wenjian Zhang. "Tellurium(II) and tellurium(IV) complexes of phosphine chalcogenide ligands, synthesis and X-ray structures." Polyhedron 28, no. 18 (December 2009): 4010–16. http://dx.doi.org/10.1016/j.poly.2009.08.025.

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Polosan, Silviu. "Structure and low field magnetic properties in phosphate-tellurite glasses." Journal of Non-Crystalline Solids 524 (November 2019): 119651. http://dx.doi.org/10.1016/j.jnoncrysol.2019.119651.

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Yousef, El Sayed. "Deduction of kinetics parameters in composition: Tellurite–phosphate–sodium oxide." Solid State Sciences 19 (May 2013): 136–43. http://dx.doi.org/10.1016/j.solidstatesciences.2013.02.009.

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47

El-Mallawany, R., and A. Abd El-Moneim. "Comparison between the Elastic Moduli of Tellurite and Phosphate Glasses." physica status solidi (a) 166, no. 2 (April 1998): 829–34. http://dx.doi.org/10.1002/(sici)1521-396x(199804)166:2<829::aid-pssa829>3.0.co;2-y.

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48

Polosan, Silviu, Paul Ganea, and Andrei Nitescu. "Structural, magneto-optical and dielectric properties of phosphate tellurite glasses." Materials Research Bulletin 143 (November 2021): 111455. http://dx.doi.org/10.1016/j.materresbull.2021.111455.

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Tang, Guowu, Qi Qian, Xin Wen, Guanxiang Zhou, Xiaodong Chen, Min Sun, Dongdan Chen, and Zhongmin Yang. "Phosphate glass-clad tellurium semiconductor core optical fibers." Journal of Alloys and Compounds 633 (June 2015): 1–4. http://dx.doi.org/10.1016/j.jallcom.2015.02.007.

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Leiderman, A. Yu, A. S. Saidov, M. M. Khashaev, and U. Kh Rakhmonov. "Study of properties of tellurium-doped indium phosphide as photoconversion material." Applied Solar Energy 50, no. 3 (July 2014): 143–45. http://dx.doi.org/10.3103/s0003701x14030098.

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