Relevant bibliographies by topics / Polyhedral Borane

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Polyhedral Borane'

Author: Grafiati
Published: 4 June 2021
Last updated: 6 September 2023

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Journal articles on the topic "Polyhedral Borane"

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Hawthorne, M. Frederick, and Alexei Pushechnikov. "Polyhedral borane derivatives: Unique and versatile structural motifs." Pure and Applied Chemistry 84, no. 11 (2012): 2279–88. http://dx.doi.org/10.1351/pac-con-12-02-11.

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Compounds with polyhedral borane moieties have demonstrated numerous unique properties for a variety of applications, including nanoelectronics, drug delivery vehicles, and live cell imaging. Polyhedral boranes are good pharmacophore analogs of carbocycles because polyhedral boranes are inherently insensitive to many undesirable enzymatic metabolic transformations typical for a majority of aromatic compounds. The defined shape, low molecular volume, and high 3D symmetry of the surface are useful for the application of the polyhedral borane scaffolds as universal and convenient spacers for the
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Golub, Igor E., Oleg A. Filippov, Vasilisa A. Kulikova, Natalia V. Belkova, Lina M. Epstein, and Elena S. Shubina. "Thermodynamic Hydricity of Small Borane Clusters and Polyhedral closo-Boranes." Molecules 25, no. 12 (2020): 2920. http://dx.doi.org/10.3390/molecules25122920.

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Thermodynamic hydricity (HDAMeCN) determined as Gibbs free energy (ΔG°[H]−) of the H− detachment reaction in acetonitrile (MeCN) was assessed for 144 small borane clusters (up to 5 boron atoms), polyhedral closo-boranes dianions [BnHn]2−, and their lithium salts Li2[BnHn] (n = 5–17) by DFT method [M06/6-311++G(d,p)] taking into account non-specific solvent effect (SMD model). Thermodynamic hydricity values of diborane B2H6 (HDAMeCN = 82.1 kcal/mol) and its dianion [B2H6]2− (HDAMeCN = 40.9 kcal/mol for Li2[B2H6]) can be selected as border points for the range of borane clusters’ reactivity. Bor
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Greenwood, N. N., and J. D. Kennedy. "Some thought-provoking polyhedral borane chemistry." Pure and Applied Chemistry 63, no. 3 (1991): 317–26. http://dx.doi.org/10.1351/pac199163030317.

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Kiremire, Enos Masheija Rwantale, and Ivan Lule. "Categorization of Boranes Into Clan Series." International Journal of Chemistry 12, no. 1 (2020): 107. http://dx.doi.org/10.5539/ijc.v12n1p107.

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Boranes, despite their instability in nature, can be regarded as hydrocarbon relatives since a [BH] fragment corresponds to a carbon [C] skeletal element in terms of the number of valence electrons. The borane formula which can be expressed as BnHm usually appears in such a way that when (n) is even, then (m) is even and when (n) is odd, (m) is odd as well. Through the study of cluster series, it appears that the cluster number K which represents skeletal linkages is usually a whole number. This inherent characteristic confers unique order within borane clusters with nodal connectivity of 5 an
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Cao, Ke, Cai-Yan Zhang, Tao-Tao Xu, et al. "Synthesis of Polyhedral Borane Cluster Fused Heterocycles via Transition Metal Catalyzed B-H Activation." Molecules 25, no. 2 (2020): 391. http://dx.doi.org/10.3390/molecules25020391.

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Aromatic heterocycles are ubiquitous building blocks in bioactive natural products, pharmaceutical and agrochemical industries. Accordingly, the carborane-fused heterocycles would be potential candidates in drug discovery, nanomaterials, metallacarboranes, as well as photoluminescent materials. In recent years, the transition metal catalyzed B-H activation has been proved to be an effective protocol for selective functionalization of B-H bond of o-carboranes, which has been further extended for the synthesis of polyhedral borane cluster-fused heterocycles via cascade B-H functionalization/annu
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Dziedzic, Rafal M., and Alexander M. Spokoyny. "Metal-catalyzed cross-coupling chemistry with polyhedral boranes." Chemical Communications 55, no. 4 (2019): 430–42. http://dx.doi.org/10.1039/c8cc08693a.

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Jasper, Steve A., Richard B. Jones, John Mattern, John C. Huffman, and Lee J. Todd. "Palladium-Mediated Substitution Reactions of Polyhedral Borane Anions." Inorganic Chemistry 33, no. 25 (1994): 5620–24. http://dx.doi.org/10.1021/ic00103a005.

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GREENWOOD, N. N., and J. D. KENNEDY. "ChemInform Abstract: Some Thought-Provoking Polyhedral Borane Chemistry." ChemInform 22, no. 21 (2010): no. http://dx.doi.org/10.1002/chin.199121298.

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Nagasawa, Koichiro, and Masayuki Narisada. "Synthesis of polyhedral borane derivatives having a carboxy group." Tetrahedron Letters 31, no. 28 (1990): 4029–32. http://dx.doi.org/10.1016/s0040-4039(00)94491-5.

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Rej, Sourav, Mahesh Madasu, Chih-Shan Tan, Chi-Fu Hsia, and Michael H. Huang. "Polyhedral Cu2O to Cu pseudomorphic conversion for stereoselective alkyne semihydrogenation." Chemical Science 9, no. 9 (2018): 2517–24. http://dx.doi.org/10.1039/c7sc05232d.

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Dissertations / Theses on the topic "Polyhedral Borane"

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Romero, Jennifer V. "A study on the formation of solid state nanoscale materials using polyhedral borane compounds." Related electronic resource: Current Research at SU : database of SU dissertations, recent titles available full text, 2008. http://wwwlib.umi.com/cr/syr/main.

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Farha, Omar K. "Synthesis of novel polyhedral borane and carborane derivatives with applications in materials science and medicine." Diss., Restricted to subscribing institutions, 2006. http://proquest.umi.com/pqdweb?did=1260800321&sid=1&Fmt=2&clientId=1564&RQT=309&VName=PQD.

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Palmer, Alycia M. "Iodinated Polyhedral Boranes for Cancer Detection." The Ohio State University, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=osu1315339711.

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Chan, Karen K. "Vertex differentiation of polyhedral boranes synthesis of multifunctional nanomolecular drug delivery platforms /." Diss., Restricted to subscribing institutions, 2009. http://proquest.umi.com/pqdweb?did=1723138291&sid=1&Fmt=2&clientId=1564&RQT=309&VName=PQD.

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Tang, Betty. "Synthesis of closomer derivatives of polyhedral boranes for use as drug delivery vehicles." Diss., Restricted to subscribing institutions, 2008. http://proquest.umi.com/pqdweb?did=1779690201&sid=5&Fmt=2&clientId=48051&RQT=309&VName=PQD.

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Michel, Sheila. "Polyhedral Boranes and Carboranes as Versatile Species Employed in the Pursuit of Imaging Methods and of Nanostructured Materials." Thèse, Université d'Ottawa / University of Ottawa, 2012. http://hdl.handle.net/10393/23283.

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Polyhedral boranes and carboranes have acquired their popularity for constructing meso and nano-size structures for an array of applications from pharmaceuticals to material science. These three-dimensional boranes range from 4 to 22 boron atom per molecules with delocalized bonding analogous to aromatic compounds. The unique vibrational spectroscopy of the BH function allows for possible application of these species to bioimaging. Silver nanoparticles functionalized with ortho-carboranes have been reported for bioimaging using Surface-enhanced Raman scattering (SERS). The silver nanoparticles
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Neamatian, Monemi Rahimeh. "Fixed cardinality linear ordering problem, polyhedral studies and solution methods." Thesis, Clermont-Ferrand 2, 2014. http://www.theses.fr/2014CLF22516/document.

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Le problème d’ordre linéaire (LOP) a reçu beaucoup d’attention dans différents domaines d’application, allant de l’archéologie à l’ordonnancement en passant par l’économie et même de la psychologie mathématique. Ce problème est aussi connu pour être parmi les problèmes NP-difficiles. Nous considérons dans cette thèse une variante de (LOP) sous contrainte de cardinalité. Nous cherchons donc un ordre linéaire d’un sous-ensemble de sommets du graphe de préférences de cardinalité fixée et de poids maximum. Ce problème, appelé (FCLOP) pour ’fixed-cardinality linear ordering problem’, n’a pas été ét
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Shameema, O. "Computational Studies On Macropolyhedral Boranes And Metallaboranes." Thesis, 2009. http://hdl.handle.net/2005/995.

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The analysis of nature of bonding in non-classical structures is always an intriguing area of research. Typical examples of such systems are polyhedral boranes that exhibit fascinating cluster bonding where the traditional 2-center-2-electron (2c-2e) bond model fails. This thesis involves the investigation of such polyhedral borane structures and their reactivity by employing both qualitative and quantitative tools of electronic structure theory. There is an intense current interest in the macropolyhedral boranes for their applications pharmaceuticals and materials chemistry. The mno rule had
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Books on the topic "Polyhedral Borane"

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Sivaev, Igor B. Polyhedral boron hydrides in use: Current status and perspectives. Nova Science Publishers, 2009.

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Book chapters on the topic "Polyhedral Borane"

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Hawthorne, M. Frederick. "Discovery of the Polyhedral Borane Anions [closo-B10H10]2− and [closo-B12H12]2−." In Boranes and Beyond. Springer New York, 2023. http://dx.doi.org/10.1007/978-1-0716-2908-6_2.

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Waller, R. Corey, Jennifer Spinler, and Debra A. Feakes. "Evaluation of the Binding of Polyhedral Borane Compounds to Intracellular Protein Moieties and Monomeric Amino Acids." In Frontiers in Neutron Capture Therapy. Springer US, 2001. http://dx.doi.org/10.1007/978-1-4615-1285-1_160.

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Hawthorne, M. Frederick, Omar K. Farha, Richard Julius, et al. "Polyhedral Boranes in the Nanoworld." In ACS Symposium Series. American Chemical Society, 2005. http://dx.doi.org/10.1021/bk-2005-0917.ch022.

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Oliva, Josep M., Antonio Francés-Monerris, and Daniel Roca-Sanjuán. "Quantum Chemistry of Excited States in Polyhedral Boranes." In Challenges and Advances in Computational Chemistry and Physics. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-22282-0_4.

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Hawthorne, M. Frederick. "Highly Alkylated Carborane Icosahedral [closo-B12H12]2− Derivatives (“Camouflaged Carboranes and Polyhedral Boranes”)." In Boranes and Beyond. Springer New York, 2023. http://dx.doi.org/10.1007/978-1-0716-2908-6_11.

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Balakrishnarajan, Musiri M., and Pattath D. Pancharatna. "Electronic Requirements and Structural Preferences for Large Polyhedral Boranes." In Challenges and Advances in Computational Chemistry and Physics. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-22282-0_7.

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Grimes, Russell N. "Thomas Jefferson, Alice in Wonderland, Polyhedral Boranes, and the Lipscomb Legacy." In ACS Symposium Series. American Chemical Society, 2002. http://dx.doi.org/10.1021/bk-2002-0827.ch002.

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Priyakumari, Chakkingal P., and Eluvathingal D. Jemmis. "Electron-Counting Rules in Cluster Bonding - Polyhedral Boranes, Elemental Boron, and Boron-Rich Solids." In The Chemical Bond. Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527664658.ch5.

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Feakes, Debra. "Design and Development of Polyhedral Borane Anions for Liposomal Delivery." In Boron Science. CRC Press, 2011. http://dx.doi.org/10.1201/b11199-17.

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Kar, Sourav, and Sundargopal Ghosh. "Borane Polyhedra Beyond Icosahedron." In Structure and Bonding. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/430_2021_85.

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Conference papers on the topic "Polyhedral Borane"

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Cox, Barry J., and James M. Hill. "Polyhedral model for boron nitride nanotubes." In ADVANCED MATERIALS AND NANOTECHNOLOGY: Proceedings of the International Conference (AMN‐4). American Institute of Physics, 2009. http://dx.doi.org/10.1063/1.3203251.

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Reports on the topic "Polyhedral Borane"

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Hawthorne, M. Frederick, Satish S. Jalisatgi, Alexander V. Safronov, Han Beak Lee, and Jianguo Wu. Chemical Hydrogen Storage Using Polyhedral Borane Anions and Aluminum-Ammonia-Borane Complexes. Office of Scientific and Technical Information (OSTI), 2010. http://dx.doi.org/10.2172/990217.

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