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Relevant bibliographies by topics / Boron-Nitrogen Compounds

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Journal articles

Academic literature on the topic 'Boron-Nitrogen Compounds'

Author: Grafiati

Published: 6 September 2023

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Journal articles on the topic "Boron-Nitrogen Compounds"

1

Mariategui, J. Francisco, and Kurt Niedenzu. "Boron-nitrogen compounds." Journal of Organometallic Chemistry 369, no. 2 (1989): 137–45. http://dx.doi.org/10.1016/0022-328x(89)88001-5.

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2

Köster, Roland, Günther Seidel, Susanna Kerschl, and Bernd Wrackmeyer. "Atropisomerism in Boron-Nitrogen Heterocycles/Atropisomerism in Boron-Nitrogen Heterocycles." Zeitschrift für Naturforschung B 42, no. 2 (1987): 191–94. http://dx.doi.org/10.1515/znb-1987-0212.

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Abstract Atropisomerism owing to hindered rotation about the N-aryl bond is observed in 4,5-diethyl-2,2,3-trimethyl-1-(o-trifluormethyl)phenyl-2,5-dihydro-1H-1,2,5-azasila-(2) and -azastanna-boroles (5). The compounds 2 and 5 are characterized by elemental analysis, mass spectra and 1H, 11B, 13 C, 29Si and119Sn NMR. The ortho-trifluoromethyl group serves as an additional NMR spectroscopic probe because of “through space” 19F-1H and 19F-13C spin spin coupling. Compound 5 is the first derivative of a 2,5-dihydro-1H-1,2,5-azastannaborol.

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3

Clarke, C. M., M. K. Das, E. Hanecker, et al. "Boron-nitrogen compounds. 113. Boron-halogenated pyrazaboles." Inorganic Chemistry 26, no. 14 (1987): 2310–17. http://dx.doi.org/10.1021/ic00261a029.

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4

Lötz, A., J. Voitländer, D. Stephenson, and J. A. S. Smith. "Nuclear Quadrupole Double Resonance of Compounds with Transannular Boron—Nitrogen Bonds." Zeitschrift für Naturforschung A 41, no. 1-2 (1986): 200–202. http://dx.doi.org/10.1515/zna-1986-1-233.

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The boron and nitrogen nuclear quadrupole double resonance spectra of several ring compounds with transannular boron-nitrogen bonds are reported. The electron donation from nitrogen to boron as seen by their quadrupole coupling parallels the boron-nitrogen bond lengths. One of the compounds exhibits a transannular valence topomerisation between two identical boron-nitrogen pairs in solution which is frozen in the solid state but may possibly exist in a preformed state of this equilibrium from its quadrupole coupling. The oxygen-boron π-bond in boroxines, whose extent is deduced from the quadru

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5

Bai, J., and K. Niedenzu. "Boron-nitrogen compounds. 126. N-triazolylboranes." Inorganic Chemistry 29, no. 23 (1990): 4693–96. http://dx.doi.org/10.1021/ic00348a021.

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6

Stepina, Irina, Aleksey Zhukov, and Sofia Bazhenova. "Modification of Cellulosic Materials with Boron-Nitrogen Compounds." Polymers 15, no. 13 (2023): 2788. http://dx.doi.org/10.3390/polym15132788.

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Wood fiber and its products are modified to increase fire and bio-resistance. The best results are achieved by using modifiers that enter into chemical interaction with the hydroxylated substrate, forming the organic matrix of the materials. The purpose of the research described in the article was to study the possibility of using boron-nitrogen compounds to modify cellulose and cellulose-containing materials to improve the performance, bio- and fire-protective properties of construction materials, as well as to optimize the consumption of boron-nitrogen compounds. As a result of the research,

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7

Niedenzu, Kurt, Philipp M. Niedenzu, and Kim R. Warner. "Boron-nitrogen compounds. 105. Boron derivatives of 3-methylpyrazole." Inorganic Chemistry 24, no. 10 (1985): 1604–6. http://dx.doi.org/10.1021/ic00204a041.

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8

Wang, Guodong, Jing Suming, Guoqing Liu, and Xingyong Gao. "Review on the Synthesis and Properties of the Energetic Compound Containing Boron." Current Organic Chemistry 24, no. 10 (2020): 1097–107. http://dx.doi.org/10.2174/1385272824999200516180719.

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Boron possesses the second greatest heating value of any element that can be adopted as an energetic material in the processing of propellants and explosives. It has become the first choice as a high energy fuel for solid fuel-rich propellants because of its advantages of high theoretical combustion heat. In the actual condition, the combustion efficiency of boron-containing fuel-rich propellants is low, and the potential energy of boron cannot be fully utilized. The compound containing-boron can be used as a new way to improve the combustion efficiency of fuel-rich propellants. In this paper,

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9

Paciorek, K. J. L., R. H. Kratzer, P. F. Kimble, J. H. Nakahara, K. J. Wynne, and C. S. Day. "Boron-nitrogen polymers. 3. Nitrogen- and oxygen-bridged compounds." Inorganic Chemistry 27, no. 14 (1988): 2432–36. http://dx.doi.org/10.1021/ic00287a013.

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10

Habben, C., L. Komorowski, W. Maringgele, A. Meller, and K. Niedenzu. "Boron-nitrogen compounds. 119. Reactions of boron heterocycles with pyrazole." Inorganic Chemistry 28, no. 13 (1989): 2659–63. http://dx.doi.org/10.1021/ic00312a031.

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