Gotowe bibliografie tematyczne / Mixed-anions compounds

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Gotowa bibliografia na temat „Mixed-anions compounds”

Autor: Grafiati
Data publikacji: 1 lutego 2025
Data aktualizacji: 31 lipca 2025

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Artykuły w czasopismach na temat "Mixed-anions compounds"

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Shmelev, M. A., T. D. Shatrov, O. V. Zvereva, et al. "Mixed-Carboxylate Cadmium–Europium Compounds with Monocarboxylic Acid Anions." Russian Journal of Coordination Chemistry 50, no. 8 (2024): 557–66. http://dx.doi.org/10.1134/s1070328424600554.

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Koksharova, T. V., A. Yu Kovalyov, T. V. Mandzii, and Ye M. Fadieiev. "COORDINATION COMPOUNDS OF 3d-METALS 5-SULFOSALICYLATES." Odesa National University Herald. Chemistry 29, no. 1(87) (2024): 5–20. http://dx.doi.org/10.18524/2304-0947.2024.1(87).307855.

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The review is devoted to the characteristic of 3d-metal coordination compounds with 5-sulfosalicylate anions and their mixed- ligand complexes. Their preparation, structure, properties and applications are considered.
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Sánchez-Lara, Eduardo, Amalia García-García, Enrique González-Vergara, Javier Cepeda, and Antonio Rodríguez-Diéguez. "Magneto-structural correlations of cyclo-tetravanadates functionalized with mixed-ligand copper(ii) complexes." New Journal of Chemistry 45, no. 11 (2021): 5081–92. http://dx.doi.org/10.1039/d0nj06004f.

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Bimetallic materials based on tetravanadate anions and mixed ligand copper(ii) complexes were readily synthesized under non-hydrothermal conditions. The compounds show interesting structural and magnetic diversity mediated by copper symmetry.
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Mazhenov, N. A., and Z. R. Syzdykova. "The formation of the mixed anions PAsO7 in solid solutions Mg2P2O7 — Mg2As2O7." Bulletin of the Karaganda University. "Physics" Series 105, no. 1 (2022): 117–22. http://dx.doi.org/10.31489/2022ph1/117-122.

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The article presents structural features at formation of solid solutions of the isostructural Mg2P2O7 and Mg2As2O7 connections. In these compounds, complex Р2О7 4- anions, As2O2 4- , as well as the formation of complex PAsO7 4 anions, is not natural. The formation of solid solutions is confirmed by the linear dependence of x-ray debaegram and optical refractive indices, depending on the concentration of P/As. In the article, phosphates are involved in energy processes in cells. For the first time, the formation of mixed anions in polyphosphates has been proven. The oscillatory spectra of pyro
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Ehlich, Hendrik, Annette Schier, and Hubert Schmidbaur. "Preparation and Crystal Structure of Bis(isocyanide)gold(I) Bis(phenylene-1,2-dithiolato)aurates(III)." Zeitschrift für Naturforschung B 57, no. 8 (2002): 890–94. http://dx.doi.org/10.1515/znb-2002-0808.

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The reaction of (isocyanide)gold(I) chlorides [(RNC)AuCl, R = tBu, cHex] with phenylene- 1,2-dithiol and sodium methoxide (molar ratio 2:1:2) in methanol / dichloromethane leads to the formation of deep green mixed-valent salts [(RNC)2Au]+[Au(S2C6H4)2]- in ca. 35% yield. As determined by single crystal X-ray diffraction methods, the two compounds have entirely different supramolecular structures. For R = tBu stacked planar anions and rod-like cations form alternating layers, while for R = cHex alternating cations and anions are arranged in chains with long S- -Au contacts [3.422 Å].
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Fábry, Jan, Michaela Fridrichová, Michal Dušek, Karla Fejfarová, and Radmila Krupková. "Mixed crystals of 2-carbamoylguanidinium with hydrogen fluorophosphonate and hydrogen phosphite in the ratios 1:0, 0.76 (2):0.24 (2) and 0.115 (7):0.885 (7)." Acta Crystallographica Section C Crystal Structure Communications 68, no. 2 (2012): o76—o83. http://dx.doi.org/10.1107/s0108270111054114.

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The title compounds, 2-carbamoylguanidinium hydrogen fluorophosphonate, C2H7N4O+·HFO3P−, (I), 2-carbamoylguanidinium–hydrogen fluorophosphonate–hydrogen phosphite (1/0.76/0.24), C2H7N4O+·0.76HFO3P−·0.24H2O3P−, (II), and 2-carbamoylguanidinium–hydrogen fluorophosphonate–hydrogen phosphite (1/0.115/0.885), C2H7N4O+·0.115HFO3P−·0.885H2O3P−, (III), are isostructural with guanylurea hydrogen phosphite, C2H7N4O+·H2O3P−[Fridrichová, Němec, Císařová & Němec (2010).CrystEngComm,12, 2054–2056]. They constitute structures where the hydrogen phosphite anion has been fully or partially replaced by hydr
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Herberhold, Max, Guo-Xin Jin, Achim Müller та Michael Penk. "The Reactions of Dioxobis(acetylacetonato)moIybdenum, MoO2(acac)2, with Tetrathiomolybdate and Tetrathiotungstate. High Formation Tendency of the {Mvi(μ-S)2Miv} (μ-S )2MVI} Group and the [MVI,S3(S2)]2- Type Ligand (M = Mo, W)". Zeitschrift für Naturforschung B 46, № 1 (1991): 25–34. http://dx.doi.org/10.1515/znb-1991-0107.

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1Tetraphenylphosphonium tetrathiometalates, (PPh4)2MS4 (M = Mo, W), react with MoO2 (acac)2 (2:1) in boiling acetonitrile in redox processes to give mixed-crystal compounds (as expected) of the approximate composition (PPh4)2[Mo3O1.9S8.1] (1) and (PPh4)2[Mo1.4W1.6O1.3S8.3] (2), respectively. and 2 were characterized by single crystal X-ray structure analyses. The various anions o f 1 and 2 contain {MVI(μ-S)2MoIVO (μ-S )2MVI} cores (M = Mo (1); Mo, W (2); bond angle M ··· Mo ··· M = 151.3° (1) 152.2 - 154.3° (2)), which have high formation tendencies. The terminal positions are occupied by S an
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Černý, Radovan, Matteo Brighi, and Fabrizio Murgia. "The Crystal Chemistry of Inorganic Hydroborates." Chemistry 2, no. 4 (2020): 805–26. http://dx.doi.org/10.3390/chemistry2040053.

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The crystal structures of inorganic hydroborates (salts and coordination compounds with anions containing hydrogen bonded to boron) except for the simplest anion, borohydride BH4−, are analyzed regarding their structural prototypes found in the inorganic databases such as Pearson’s Crystal Data [Villars and Cenzual (2015), Pearson’s Crystal Data. Crystal Structure Database for Inorganic Compounds, Release 2019/2020, ASM International, Materials Park, Ohio, USA]. Only the compounds with hydroborate as the only type of anion are reviewed, although including compounds gathering more than one diff
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Schneider, Daniel, та Annette Schier. "Random Interstitial Halide Accommodation in an α,ω-Alkylidene-diammonium Template". Zeitschrift für Naturforschung B 59, № 11-12 (2004): 1395–99. http://dx.doi.org/10.1515/znb-2004-11-1205.

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N,N,N′,N′-Tetramethylethylenediammonium diiodide [Me2HNCH2]2I2 (1) as well as a set of I/Br- (2) and Br/Cl-mixed-halide salts (4 and 5) have been prepared, and their structures determined by single crystal X-ray diffraction. The results show the [Me2HNCH2]2 2+ dication to be a highly flexible template for halide inclusion, thereby tolerating the assembly of anions of different size, with phase widths of 0 ≤ x ≤ 2 for a monoclinic form with [Me2HNCH2]2I2−xBrx and 0 ≤ x ≤ 1 for a triclinic form with [Me2HNCH2]2Br2−xClx. The isotypic mixed halide compounds [Me2HNCH2]2IBr (2) and [Me2HNCH2]2BrCl (
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Matveev, Evgenii Yu, Varvara V. Avdeeva, Konstantin Yu Zhizhin, Elena A. Malinina, and Nikolay T. Kuznetsov. "Effect of Nature of Substituents on Coordination Properties of Mono- and Disubstituted Derivatives of Boron Cluster Anions [BnHn]2– (n = 10, 12) and Carboranes with exo-Polyhedral B–X Bonds (X = N, O, S, Hal)." Inorganics 10, no. 12 (2022): 238. http://dx.doi.org/10.3390/inorganics10120238.

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This review systematizes data on the coordination ability of mono- and disubstituted derivatives of boron cluster anions and carboranes in complexation with transition metals. Boron clusters anions [BnHn]2–, monocarborane anions [CBnHn–1]–, and dicarboranes [C2BnHn–2] (with non-functionalized carbon atoms) (n = 10, 12) containing the B–X exo-polyhedral bonds (X = N, O, S, Hal) are discussed. Synthesis and structural features of complexes known to date are described. The effect of complexing metal and substituent attached to the boron cage on the composition and structures of the final complexe
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Rozprawy doktorskie na temat "Mixed-anions compounds"

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Hyrondelle, Helies. "Ordre/désordre anionique dans les hydroxyfluorures à base de Mg, Ni, Cu & Zn : corrélation composition/structure & propriétés physico-chimiques." Electronic Thesis or Diss., Bordeaux, 2024. http://www.theses.fr/2024BORD0496.

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Les hydroxyfluorures (HyFs) de métaux et de métaux de transition divalents sont des composés dans lesquels les ligands hydroxyles (OH-) et fluorures (F-) sont présents simultanément dans la sphère de coordination du métal. Les similarités entre ces anions (taille, valence, préférences cristallographiques) facilitent leur substitution tandis que leur importante différence d'électronégativité/de polarisabilité permet de contrôler finement la nature des liaisons chimiques au sein du matériau. Ces variations influencent de nombreuses propriétés physiques comme l'acido-basicité, la stabilité thermi
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Stolze, Karoline. "Synthese und Charakterisierung niedervalenter Actinoidphosphidtelluride und ternärer Selen-Halogenid-Komplexe des Iridiums." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2016. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-202233.

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Metallpniktide und -chalkogenide erfahren zunehmend mehr Aufmerksamkeit in Chemie und Festkörperphysik. Dieses Interesse liegt unter anderem in der ungewöhnlichen Strukturchemie der Verbindungen begründet. In den Pniktogen(Pn)- bzw. Chalkogen(Q)-reichen Verbindungen dieser Systeme ist besonders häufig die Bildung der jeweiligen Oligo- oder Polyanionen bzw. Moleküle zu beobachten. Einerseits können die homoatomaren Pn–Pn- bzw. Q–Q-Bindungen zur Ausbildung niederdimensionaler Strukturmotive mit anisotropen Eigenschaften, wie bspw. Supraleitung und Metall-Halbleiter-Übergänge, führen; andererseit
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Menu, Marie-Joëlle. "Nouveaux reactifs dans la chimie des complexes du rhodium, du chrome et du tungstene : les anions diazo rc(n::(2))**(-)." Toulouse 3, 1988. http://www.theses.fr/1988TOU30068.

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Synthese des complexes de rh, cr et w contenant le coordinat diazo en faisant reagir les sels de li des anions rc(n::(2))**(-) sur les complexes metalliques. On a isole: (pme::(3))::(4) rhc(n::(2))sime::(3) (pet::(3))::(3) rhc(n::(2))sime::(3), (pme::(3))::(2) rhc(n::(2))(s)p(n-ipr::(2))::(2). On a mis en evidence un complexe carbenique dimere possedant un groupe ylure, lors de la photolyse de (pet::(3))::(3) rhc(n::(2))sime::(3)
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Stolze, Karoline. "Synthese und Charakterisierung niedervalenter Actinoidphosphidtelluride und ternärer Selen-Halogenid-Komplexe des Iridiums." Doctoral thesis, 2015. https://tud.qucosa.de/id/qucosa%3A29471.

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Metallpniktide und -chalkogenide erfahren zunehmend mehr Aufmerksamkeit in Chemie und Festkörperphysik. Dieses Interesse liegt unter anderem in der ungewöhnlichen Strukturchemie der Verbindungen begründet. In den Pniktogen(Pn)- bzw. Chalkogen(Q)-reichen Verbindungen dieser Systeme ist besonders häufig die Bildung der jeweiligen Oligo- oder Polyanionen bzw. Moleküle zu beobachten. Einerseits können die homoatomaren Pn–Pn- bzw. Q–Q-Bindungen zur Ausbildung niederdimensionaler Strukturmotive mit anisotropen Eigenschaften, wie bspw. Supraleitung und Metall-Halbleiter-Übergänge, führen; andererseit
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Części książek na temat "Mixed-anions compounds"

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"Synthesis Methods of Mixed-anion Compounds." In Mixed-anion Compounds. Royal Society of Chemistry, 2024. http://dx.doi.org/10.1039/bk9781839166372-00021.

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This chapter provides an overview of the synthetic methods of mixed-anion compounds, highlighting their distinctive characteristics compared to the synthesis of single-anion compounds, with the commonly employed solid-state reaction provided as an illustrative example. We then explore reactions advantageous in the synthesis of mixed-anion compounds, such as anion confinement and the utilization of active secondary anions. We specifically discuss high-temperature reaction methods such as solid–gas phase reaction and high-pressure synthesis, which facilitate anion confinement and activation. Add
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Ogino, H., Y. Masubuchi, Y. Inaguma, et al. "Synthesis Methods of Mixed-anion Compounds." In Mixed Anion Compounds. Royal Society of Chemistry, 2024. https://doi.org/10.1039/9781839166372-00021.

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This chapter provides an overview of the synthetic methods of mixed-anion compounds, highlighting their distinctive characteristics compared to the synthesis of single-anion compounds, with the commonly employed solid-state reaction provided as an illustrative example. We then explore reactions advantageous in the synthesis of mixed-anion compounds, such as anion confinement and the utilization of active secondary anions. We specifically discuss high-temperature reaction methods such as solid–gas phase reaction and high-pressure synthesis, which facilitate anion confinement and activation. Add
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"Chemistry of Mixed-anion Compounds." In Mixed-anion Compounds. Royal Society of Chemistry, 2024. http://dx.doi.org/10.1039/bk9781839166372-00001.

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This chapter provides an overview of chemical bonding in solids, with a specific focus on the differences in properties among single-anion compounds, such as oxides, chlorides, nitrides and sulfides, from the perspective of anions. We will explore the distinct properties due to anion mixing, such as the impact on chemical bonds, coordination geometry and energy levels. Understanding these characteristics is essential for comprehending the fundamental principles of mixed-anion chemistry, which are crucial in their synthesis, analysis and applications.
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Kageyama, H., and F. Takeiri. "Chemistry of Mixed-anion Compounds." In Mixed Anion Compounds. Royal Society of Chemistry, 2024. https://doi.org/10.1039/9781839166372-00001.

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This chapter provides an overview of chemical bonding in solids, with a specific focus on the differences in properties among single-anion compounds, such as oxides, chlorides, nitrides and sulfides, from the perspective of anions. We will explore the distinct properties due to anion mixing, such as the impact on chemical bonds, coordination geometry and energy levels. Understanding these characteristics is essential for comprehending the fundamental principles of mixed-anion chemistry, which are crucial in their synthesis, analysis and applications.
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Hyett, Geoffrey. "Heteroanionic Materials: The Structures and Applications of Mixed Anion Materials." In Non-oxide and Heteroanionic Materials. Royal Society of Chemistry, 2025. https://doi.org/10.1039/9781839165924-00242.

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In this chapter we discuss the structures, properties and applications of mixed anion materials—solid state compounds that contain at least two different anions directly co-ordinated to metal ions, which are also known as heteroanionic materials. We focus on the most common types found in the literature, materials containing two different anions of which one is oxide, and divide these into two classes dependant on the nature of the second anion. In the first type the oxide anion is paired with an isoelectronic ‘light’ anion such as oxide or fluoride. We use the widely investigated oxynitrides
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Suzuki, M., and R. Noyori. "Conjugate addition–enolate-trapping reactions." In Organocopper Reagents: A Practical Approach. Oxford University PressOxford, 1995. http://dx.doi.org/10.1093/oso/9780198557579.003.0009.

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Abstract Enolate anions are one of the most widely used nucleophilic species in organic synthesis. Organocopper conjugate addition to α,β-unsaturated carbonyl compounds generates in situ metal enolates under mild conditions with the incorporation of an organic group to the β-position. Therefore, the organocopper-mediated reaction followed by the regioselective enolate trapping provides an extremely powerful tool for controlled construction of organic frameworks (see Scheme 9.1). The organocopper reagents commonly used for this tandem reaction can be divided into four general classes: (1) Grign
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