Bibliografías temáticas / Hydroboranes synthesis

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Literatura académica sobre el tema "Hydroboranes synthesis"

Autor: Grafiati
Publicado: 21 de diciembre de 2024
Última modificación: 31 de julio de 2025

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Artículos de revistas sobre el tema "Hydroboranes synthesis"

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Price, Jeffrey S., Declan M. DeJordy, David J. H. Emslie, and James F. Britten. "Reactions of [(dmpe)2MnH(C2H4)]: synthesis and characterization of manganese(i) borohydride and hydride complexes." Dalton Transactions 49, no. 29 (2020): 9983–94. http://dx.doi.org/10.1039/d0dt01726d.

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Reactions of trans-[(dmpe)<sub>2</sub>MnH(C<sub>2</sub>H<sub>4</sub>)] with hydroboranes and phosphines afforded manganese(i) borohydride and hydride complexes; reaction pathways, structures and bonding are discussed.
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Kostera, Sylwia, Maurizio Peruzzini, and Luca Gonsalvi. "Recent Advances in Metal Catalyst Design for CO2 Hydroboration to C1 Derivatives." Catalysts 11, no. 1 (2021): 58. http://dx.doi.org/10.3390/catal11010058.

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The use of CO2 as a C1 building block for chemical synthesis is receiving growing attention, due to the potential of this simple molecule as an abundant and cheap renewable feedstock. Among the possible reductants used in the literature to bring about CO2 reduction to C1 derivatives, hydroboranes have found various applications, in the presence of suitable homogenous catalysts. The current minireview article summarizes the main results obtained since 2016 in the synthetic design of main group, first and second row transition metals for use as catalysts for CO2 hydroboration.
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Moroz, Antoni, and Ray L. Sweany. "Photolysis of argon matrixes containing tribromoboron and dihydrogen: synthesis of hydroboranes via dibromoboron." Inorganic Chemistry 31, no. 25 (1992): 5236–42. http://dx.doi.org/10.1021/ic00051a015.

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MOROZ, A., and R. L. SWEANY. "ChemInform Abstract: Photolysis of Argon Matrices Containing Tribromoboron and Dihydrogen: Synthesis of Hydroboranes via Dibromoboron." ChemInform 24, no. 15 (2010): no. http://dx.doi.org/10.1002/chin.199315025.

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Matsumi, Noriyoshi, Nobuaki Yoshioka, and Keigo Aoi. "Synthesis of boric ester type ion-gels by dehydrocoupling of cellulose with hydroboranes in ionic liquid." Solid State Ionics 226 (October 2012): 37–40. http://dx.doi.org/10.1016/j.ssi.2012.07.018.

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., Eishika, Himani ., and Ridhi . "Review of Synthesis and Characterization of Cu (I) Complexes." International Journal of Research and Review 11, no. 1 (2024): 195–209. http://dx.doi.org/10.52403/ijrr.20240121.

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d-block metals show great promise in inorganic catalytic research. Particularly, copper, d9 metal has contributed to catalytic properties of its complexes. A series of copper complexes was synthesized and structurally characterized. The copper (I) complexes of this series were investigated in regard to their reactivity towards dioxygen using stopped-flow techniques. For most complexes no “oxygen adduct” complexes as intermediates could be detected. In this article, some complexes of Cu (I) have been included and the ligands on which work had been done are mentioned below: 1,5-bis(benzimidazole
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Payandeh, SeyedHosein, Daniel Rentsch, Zbigniew Lodziana, et al. "Nido-Hydroborate-Based Electrolytes for All-Solid-State Lithium Batteries." Advanced Functional Materials 2021 (February 21, 2021): 2010046. https://doi.org/10.5281/zenodo.7600133.

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Hydroborate-based solid electrolytes have recently been successfully employed in high voltage, room temperature all-solid-state sodium batteries. The transfer to analogous lithium systems has failed up to now due to the lower conductivity of the corresponding lithium compounds and their high cost. Here LiB11H14 nido-hydroborate as a cost-effective building block and its high-purity synthesis is introduced. The crystal structures of anhydrous LiB11H14 as well as of LiB11H14- based mixed-anion solid electrolytes are solved and high ionic conductivities of 1.1 &times; 10&minus;4 S cm&minus;1 for
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Dunn, Simon C., Philip Mountford, and Oleg V. Shishkin. "Imidotitanium Tris(pyrazolyl)hydroborates: Synthesis, Solution Dynamics, and Solid-State Structure." Inorganic Chemistry 35, no. 4 (1996): 1006–12. http://dx.doi.org/10.1021/ic9510674.

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Bahsis, Lahoucine, Hicham Ben El Ayouchia, Hafid Anane, et al. "Clicking Azides and Alkynes with Poly(pyrazolyl)borate-Copper(I) Catalysts: An Experimental and Computational Study." Catalysts 9, no. 8 (2019): 687. http://dx.doi.org/10.3390/catal9080687.

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The synthesis of 1,4-disubstituted-1,2,3-triazoles under a copper(I)-catalyzed azide–alkyne cycloaddition (CuAAC) regime was accomplished in high yields and a regioselective manner by using two homoscorpionate poly(pyrazolyl)borate anions: tris(pyrazolyl)hydroborate (HB(pz)3−) and bis(pyrazolyl)hydroborate (H2B(pz)2−), which stabilized in situ the catalytically active copper (I) center. The [3+2] cycloaddition (32CA) reactions took place under strict click conditions, including room temperature and a mixture of environmentally benign solvents such as water/ethanol in a 1:1 (v/v) ratio. These c
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Bartholomew, Amymarie K., Louise M. Guard, Nilay Hazari, and Eddie D. Luzik. "Synthesis of Mg Complexes Supported by Tris-(1-pyrazolyl)phosphine." Australian Journal of Chemistry 66, no. 11 (2013): 1455. http://dx.doi.org/10.1071/ch13354.

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The preparation and characterisation of two Mg coordination compounds supported by the tris(1-pyrazolyl)phosphine (P(pz)3) ligand, [{P(pz)3}Mg(MeCN)3](I)2 and [Mg{P(pz)3}2](I)2, is described. This is the first time this ligand has been coordinated to Mg or any other s-block metal and the complexes are the first examples of crystallographically characterised P(pz)3 complexes on any metal. The structures of the new Mg complexes are compared with related species with the more common tridentate facial ligands, tris(pyrazolyl)hydroborate (Tp), tris(pyrazolyl)methane (Tpm), and tris(pyrazolyl)methan
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Tesis sobre el tema "Hydroboranes synthesis"

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Zwart, Guilhem. "Hydrogénolyse de (pseudo-)haloboranes et de chlorophosphines." Electronic Thesis or Diss., université Paris-Saclay, 2024. http://www.theses.fr/2024UPASF049.

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Cette thèse examine les défis posés par l’accès incertain aux éléments chimiques, exacerbée par un paradigme économique linéaire de leur exploitation. L’étude se concentre sur le bore et le phosphore, dont l’utilisation et le recyclage restent sous-étudiés. Le bore, crucial dans diverses industries, nécessite des processus énergivores pour être transformé en hydroboranes actifs, utilisés en chimie fine. Deux voies existent pour leur synthèse : la méthode industrielle à partir de borate, et la réaction de BCl₃ avec un donneur d’hydrure. Utiliser H₂ comme agent réducteur pourrait améliorer ces p
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Chen, Heng-Guang, and 陳恒光. "Syntheses and Structures of Hydroborate Zirconium and Titanium Complexes." Thesis, 2013. http://ndltd.ncl.edu.tw/handle/10140107312553336807.

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Panda, Monalisa [Verfasser]. "Synthesis and characterization of alkali metal borides and closo Hydroborates / vorgelegt von Monalisa Panda." 2007. http://d-nb.info/983937869/34.

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Li, Kun-Yu, and 李坤育. "Synthesis and Reactivity Study of the Tris[3-2-pyridyl)pyrazolyl]hydroborate Iron Complexes." Thesis, 2015. http://ndltd.ncl.edu.tw/handle/4ywxbq.

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碩士<br>高雄醫學大學<br>醫藥暨應用化學系碩士班<br>103<br>Trispyrazolylborate (Tp&;#8722;) type compound is a very important ligand set for small molecules activation the metalloenzyme mimicking system. Tris[3-(2-pyridyl)pyrazolyl]-hydroborate (Tp(py)&;#8722;) is a new type of Tp- ligand set which provides additional pyridine coordination site in 3-postion to explore some new coordination behavior for metal complexes. It is worth mentioning that there are no example of iron complexes containing Tp(py)&;#8722; ligand. Therefore, we focus on the synthesis and reactivity study of Tp(py)FeCl compound for the outer py
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Kim, Do Young. "Synthesis of metal hydroborates as potential chemical vapor deposition precursors : chemical vapor deposition of titanium-doped magnesium diboride thin films /." 2007. http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqdiss&rft_dat=xri:pqdiss:3269943.

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Thesis (Ph. D.)--University of Illinois at Urbana-Champaign, 2007.<br>Source: Dissertation Abstracts International, Volume: 68-06, Section: B, page: 3782. Adviser: Gregory S. Girolami. Includes bibliographical references. Available on microfilm from Pro Quest Information and Learning.
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Capítulos de libros sobre el tema "Hydroboranes synthesis"

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Klanberg, F., E. L. Muetterties, Alfred L. Moye, and James C. Carter. "Polyhedral Hydroborates, Undecahydro-Undecaborate, Nonahydrononaborate, and Octahydrooctaborate." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132425.ch6.

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Brown, Charles Allan, Sheldon C. Shore, and George Medford. "Potassium Tri(sec -Butyl)Hydroborate(1-)." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132487.ch7.

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"Comprehensive Survey of Combustion Agents." In High-energy Combustion Agents of Organic Borohydrides. Royal Society of Chemistry, 2023. http://dx.doi.org/10.1039/bk9781837670017-00001.

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This chapter presents a comprehensive survey of the most recent achievements on advanced combustion agents, including ionic hydroborate, carborane and its derivatives, metal carborane, and borane energetic ionic liquids (salts), and summarizes the synthesis progress of carborane derivatives, and the progress of application of carborane derivatives and hydroborate salts in propellants and explosives.
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Taber, Douglass F. "The Trauner Synthesis of (−)-Nitidasin." In Organic Synthesis. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190646165.003.0101.

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The sesterterpene (−)–nitidasin 4 is a component of the Peruvian infusion “hercam­puri,” prepared from the shrubs Gentianella nitida and Gentianella alborosea, that was used traditionally to treat hepatitis, diabetes, and hypertension. Dirk Trauner of Ludwig–Maximilians–Universität München envisioned (Angew. Chem. Int. Ed. 2014, 53, 8513) the assembly of 4 by the convergent coupling of 1 with 2 to give 3. For this strategy to be effective, both 1 and 2 had to be prepared in enantio­merically–enriched form. The skeleton of 1 was found in the enone 5, prepared by asymmetric Robinson annulation,
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