Relevant bibliographies by topics / Dimethyl phosphoramidate

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  1. Journal articles

Academic literature on the topic 'Dimethyl phosphoramidate'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Dimethyl phosphoramidate"

1

Shtamburg, V. G., E. A. Klots, V. V. Shtamburg, et al. "Dialkyl-N-alkoxy-N-(4-toluenesulfonyl)phosphoramidates: synthesis and structure." Voprosy Khimii i Khimicheskoi Tekhnologii, no. 2 (April 2025): 33–44. https://doi.org/10.32434/0321-4095-2025-159-2-33-44.

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This study investigates the reaction between N-alkoxy-N-chloro-4-toluenesulfonamides and N-chloro-N-(methoxy)methanesulfonamide with trialkyl phosphites, resulting in the formation of dialkyl N-alkoxy-N-(4-toluenesulfonyl)phosphoroamidates and dialkyl N-methoxy-N-methanesulfonylphosphoroamidates, respectively. The resulting dialkyl N-alkoxy-N-(4-toluenesulfonyl)phosphoramidates and N-alkoxy-N-methanesulfonylphosphoramidates are identified as products of nucleophilic substitution at the amide nitrogen atom. The structures of these compounds have been confirmed by ¹H, ³¹P, and ¹³C NMR spectrosco
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2

Seyda, Aydogdu, and Hatipoglu Arzu. "Theoretical investigation on the kinetics of dimethyl phosphoramidate with hydroxyl radicals." Journal of Indian Chemical Society Vol. 96, Sep 2019 (2019): 1117–22. https://doi.org/10.5281/zenodo.5643205.

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Department of Chemistry, Yildiz Technical University, 34220 Istanbul, Turkey <em>E-mail</em>: hatiparzu@yahoo.com <em>Manuscript received online 26 April 2019, revised and accepted 20 July 2019</em> In this paper the reaction kinetics of dimethyl phosphoramidate with hydroxyl radical was investigated with Density Functional Theory. Geometry optimization and energy calculations of the reactants, the pre-reactive complexes, the transition states and the products were performed at the B3LYP/6-31G(d) basis set. The water effect was computed by using CPCM as the solvation model. Rate constants of a
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3

Gholivand, Khodayar, Azadeh Tadjarodi, and Seik Weng Ng. "N,N-Dimethyl-N′,N′′-bis(4-methylphenyl)phosphoramidate." Acta Crystallographica Section E Structure Reports Online 58, no. 2 (2002): o200—o201. http://dx.doi.org/10.1107/s1600536802001587.

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4

Plessis, Michael P., Tomasz A. Modro, and Luigi R. Nassimbeni. "Crystal and molecular structures of two polymorphic forms of dimethyl-N-(2-ethylphenyl)-phosphoramidate (I) and dimethyl-N-(2,6-dimethylphenyl)-phosphoramidate (II)." Journal of Crystallographic and Spectroscopic Research 15, no. 6 (1985): 663–78. http://dx.doi.org/10.1007/bf01164779.

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5

Struhatska, Mariia B., Nataliia S. Kariaka, Vladimir M. Amirkhanov, Viktoriya V. Dyakonenko, and Maksym Seredyuk. "Crystal structure and Hirshfeld surface analysis of the anionic tetrakis-complex of lanthanum(III) NMe4LaL 4 with the CAPh-ligand dimethyl (2,2,2-trichloroacetyl)phosphoramidate." Acta Crystallographica Section E Crystallographic Communications 77, no. 12 (2021): 1307–10. http://dx.doi.org/10.1107/s2056989021011750.

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The anionic tetrakis-complex of lanthanum(III) NMe4LaL 4 with the CAPh-ligand dimethyl (2,2,2-trichloroacetyl)phosphoramidate (HL), namely, tetramethylammonium tetrakis{2,2,2-trichloro-1-[(dimethoxyphosphoryl)imino]ethanolato}lanthanum(III), (C4H12N)[La(C4H6Cl3NO4P)4], has been synthesized, crystallized and structurally characterized by X-ray diffraction. The lanthanide ion is surrounded by four anionic, bis-chelating CAPh ligands forming the complex anion with a coordination number of eight for La3+ and NMe4 + as the counter-ion. The coordination polyhedron of the La3+ ion was interpreted as
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6

Kahn, Brian A., John P. Damicone, Kenneth E. Jackson, James E. Motes, and Mark E. Payton. "Comparing Chitin-urea to Other Materials for Control of Northern Root-knot Nematode on Paprika Pepper." HortScience 37, no. 6 (2002): 948–49. http://dx.doi.org/10.21273/hortsci.37.6.948.

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Nine nematicide treatments were evaluated from 1993 through 1995 in field experiments on paprika pepper (Capsicum annuum L.). Materials tested included a chitinurea soil amendment and six chemicals: fosthiazate, carbofuran, aldicarb, oxamyl, fenamiphos, and 1,3-dichloropropene (1,3-D). Stands at harvest were increased relative to the control by chitin-urea, fosthiazate, and 1,3-D, but only fosthiazate increased marketable fruit yield relative to the control. Aldicarb reduced preharvest nematode populations relative to the control, but aldicarb did not result in a significant fruit yield increa
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7

Wang, Huaifang, Yingli Cai, Zhiming Jiang, Shengnan Guo, and Ping Zhu. "Synthesis of a phosphoramidate flame retardant and its flame retardancy on cotton fabrics." e-Polymers 20, no. 1 (2020): 550–60. http://dx.doi.org/10.1515/epoly-2020-0059.

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AbstractA phosphoramidate flame retardant (dimethyl N,N-bis(2-hydroxyletheyl)phosphoramidate, DMBHP) was synthesized and applied to cotton fabrics for enhancing the flame retardancy. The structure of DMBHP was characterized by FT-IR and NMR. The flame retardancy and combustion behavior of the treated cotton fabrics were evaluated using the vertical flammability test (VFT), limiting oxygen index (LOI), and the cone calorimetric test. Moreover, to further analyze the flame retardant action of DMBHP in cotton fabrics, thermal degradability of the treated fabrics, as well as the chemical structure
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8

Ko, Seongjae, Ayaka Matsuoka, Wenting Chen, et al. "Multifunctional Cyclic Phosphoramidate Solvent for Safe Lithium-Ion Batteries." ECS Meeting Abstracts MA2024-02, no. 10 (2024): 4911. https://doi.org/10.1149/ma2024-02104911mtgabs.

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To enhance the overall safety of electronic devices and energy storage systems, the development of functional electrolytes that improve the thermal stability of rechargeable batteries is of utmost importance. Here, we report a novel cyclic phosphoramidate, 2-(N,N-dimethylamino)-1,3,2-dioxaphospholane-2-oxide (DMAP), which has been newly designed and synthesized as a multifunctional solvent for safe Li-ion batteries.1 Its unique molecular structure, incorporating an amine moiety into a five-membered cyclic phosphate, provides both high electrochemical and thermal benefits: (i) a stable DMAP-der
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9

Liang, Shuyu, Patrick Hemberger, Joëlle Levalois‐Grützmacher, Hansjörg Grützmacher, and Sabyasachi Gaan. "Probing Phosphorus Nitride (P≡N) and Other Elusive Species Formed upon Pyrolysis of Dimethyl Phosphoramidate." Chemistry – A European Journal 23, no. 23 (2017): 5595–601. http://dx.doi.org/10.1002/chem.201700402.

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10

Vilanova, E., M. K. Johnson, and J. L. Vicedo. "Interaction of some unsubstituted phosphoramidate analogs of methamidophos (O,S-dimethyl phosphorothioamidate) with acetylcholinesterase and neuropathy target esterase of hen brain." Pesticide Biochemistry and Physiology 28, no. 2 (1987): 224–38. http://dx.doi.org/10.1016/0048-3575(87)90021-6.

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