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Journal articles on the topic 'N-methylacetamide'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Mirkin, Noemi G., and Samuel Krimm. "Conformers of trans-N-methylacetamide." Journal of Molecular Structure 242 (January 1991): 143–60. http://dx.doi.org/10.1016/0022-2860(91)87133-3.

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2

Graziano, Giuseppe. "Hydration Thermodynamics of N-Methylacetamide." Journal of the Physical Society of Japan 69, no. 11 (November 15, 2000): 3720–25. http://dx.doi.org/10.1143/jpsj.69.3720.

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3

Luo, Zhong-Hua, Shan Liu, Shui-Ping Deng, Hong-Jun Zhu, and Hong-Sheng Jia. "2-(4-Fluorophenoxy)-N-methylacetamide." Acta Crystallographica Section E Structure Reports Online 63, no. 3 (February 7, 2007): o1099—o1100. http://dx.doi.org/10.1107/s1600536807003376.

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The asymmetric unit of the title compound, C9H10FNO2, contains two molecules. Intra- and intermolecular N—H...O and C—H...F hydrogen bonds link the molecules into a three-dimensional framework; they seem to be effective in the stabilization of the crystal structure.

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4

Gowda, B. Thimme, Sabine Foro, and Hartmut Fuess. "N-(2,6-Dimethylphenyl)-2-methylacetamide." Acta Crystallographica Section E Structure Reports Online 64, no. 2 (January 9, 2008): o380. http://dx.doi.org/10.1107/s1600536807068419.

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5

Graziano, Giuseppe. "Hydration Thermodynamics of N-Methylacetamide." Journal of the Physical Society of Japan 70, no. 7 (July 15, 2001): 2234. http://dx.doi.org/10.1143/jpsj.70.2234.

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6

Mirkin, Noemi G., and Samuel Krimm. "Conformers of cis-N-methylacetamide." Journal of Molecular Structure: THEOCHEM 236, no. 1-2 (November 1991): 97–111. http://dx.doi.org/10.1016/0166-1280(91)87010-j.

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7

Li, Cui, Peter Salén, Vasyl Yatsyna, Luca Schio, Raimund Feifel, Richard Squibb, Magdalena Kamińska, et al. "Experimental and theoretical XPS and NEXAFS studies of N-methylacetamide and N-methyltrifluoroacetamide." Physical Chemistry Chemical Physics 18, no. 3 (2016): 2210–18. http://dx.doi.org/10.1039/c5cp06441d.

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8

Lazareva, N. F., and A. Yu Nikonov. "Synthesis of N-[chloro(dimethyl)silyl]-N-methylacetamide." Russian Chemical Bulletin 64, no. 4 (April 2015): 965–66. http://dx.doi.org/10.1007/s11172-015-0965-8.

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9

Kuznetsova, L. M., V. L. Furer, and L. I. Maklakov. "Infrared intensities of N-methylacetamide associates." Journal of Molecular Structure 380, no. 1-2 (June 1996): 23–29. http://dx.doi.org/10.1016/0022-2860(95)09209-9.

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10

Kondo, Yasuhiko, Akikazu Nakano, and Shigekazu Kusabayashi. "Characterization of anion solvation in N-methylacetamide. Transfer enthalpies of anions and the reaction rates of ethyl iodide with bromide ion in N-methylacetamide–acetonitrile and N-methylacetamide–N,N-dimethylacetamide mixtures." Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases 82, no. 7 (1986): 2141. http://dx.doi.org/10.1039/f19868202141.

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11

Mayne, L. C., L. D. Ziegler, and B. Hudson. "Ultraviolet resonance Raman studies of N-methylacetamide." Journal of Physical Chemistry 89, no. 15 (July 1985): 3395–98. http://dx.doi.org/10.1021/j100261a047.

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12

Salamatova, Evgeniia, Ana V. Cunha, Robbert Bloem, Steven J. Roeters, Sander Woutersen, Thomas L. C. Jansen, and Maxim S. Pshenichnikov. "Hydrophobic Collapse in N-Methylacetamide–Water Mixtures." Journal of Physical Chemistry A 122, no. 9 (February 9, 2018): 2468–78. http://dx.doi.org/10.1021/acs.jpca.8b00276.

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13

Jensen, J. Halding, P. L. Christiansen, O. Skovgaard, O. Faurskov Nielsen, and Irving J. Bigio. "Experimental and computational study of N-methylacetamide." Physics Letters A 117, no. 3 (August 1986): 123–26. http://dx.doi.org/10.1016/0375-9601(86)90017-4.

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14

Forsting, Thomas, Hannes C. Gottschalk, Beppo Hartwig, Michel Mons, and Martin A. Suhm. "Correcting the record: the dimers and trimers of trans-N-methylacetamide." Physical Chemistry Chemical Physics 19, no. 17 (2017): 10727–37. http://dx.doi.org/10.1039/c6cp07989j.

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15

Siddaraju, B. P., Jerry P. Jasinski, James A. Golen, H. S. Yathirajan, and C. R. Raju. "2-Chloro-N-[2-(2-fluorobenzoyl)-4-nitrophenyl]-N-methylacetamide." Acta Crystallographica Section E Structure Reports Online 67, no. 9 (August 31, 2011): o2537—o2538. http://dx.doi.org/10.1107/s1600536811034969.

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16

Jelinska-Kazimierczuk, M., E. Malicka, and J. Szydłowski. "Deuterium Isotope Fractionation between N-Methylacetamide, N-Methylformamide and Water." Zeitschrift für Physikalische Chemie 175, Part_1 (January 1992): 41–49. http://dx.doi.org/10.1524/zpch.1992.175.part_1.041.

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17

Grande, María del Carmen, Carmen Raquel Barrero, Jorge Alvarez Juliá, and Carlos Miguel Marschoff. "Liquid−Liquid Equilibria for Water + Benzonitrile +N-Methylacetamide, or +N,N-Dimethylacetamide." Journal of Chemical & Engineering Data 55, no. 4 (April 8, 2010): 1645–48. http://dx.doi.org/10.1021/je9007074.

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18

Furer, V. L. "The IR spectra of N-methylacetamide chain associates." Journal of Molecular Structure 435, no. 2 (November 1997): 151–55. http://dx.doi.org/10.1016/s0022-2860(97)00171-3.

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19

Köddermann, T., and R. Ludwig. "N-Methylacetamide/water clusters in a hydrophobic solvent." Phys. Chem. Chem. Phys. 6, no. 8 (2004): 1867–73. http://dx.doi.org/10.1039/b314702a.

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20

Di Gioacchino, Michael, Fabio Bruni, and Maria Antonietta Ricci. "N-Methylacetamide Aqueous Solutions: A Neutron Diffraction Study." Journal of Physical Chemistry B 123, no. 8 (February 9, 2019): 1808–14. http://dx.doi.org/10.1021/acs.jpcb.9b00246.

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21

Mandai, Toshihiko, and Patrik Johansson. "Al conductive haloaluminate-free non-aqueous room-temperature electrolytes." Journal of Materials Chemistry A 3, no. 23 (2015): 12230–39. http://dx.doi.org/10.1039/c5ta01760b.

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22

de Haan, Andre B., Antje Heine, Kai Fischer, and Juergen Gmehling. "Vapor-Liquid Equilibria and Excess Enthalpies for Octane + N-Methylacetamide, Cyclooctane + N-Methylacetamide, and Octane + Acetic Anhydride at 125 .degree.C." Journal of Chemical & Engineering Data 40, no. 6 (November 1995): 1228–32. http://dx.doi.org/10.1021/je00022a018.

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23

Lu, Qiujian, Yuanlei Ding, Qunting Qu, Tian Gao, Xianlin Zhang, Ming Shen, and Honghe Zheng. "N-Methylacetamide as an electrolyte component for suppressing co-intercalation of propylene carbonate in lithium ion batteries." RSC Advances 6, no. 70 (2016): 65847–53. http://dx.doi.org/10.1039/c6ra06474d.

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24

Buys, H. C. W. M., F. F. Vercauteren, A. van Elven, and A. H. A. Tinnemans. "Acid hydrolysis of polymers and copolymers of N-vinyl-N-methylacetamide." Recueil des Travaux Chimiques des Pays-Bas 108, no. 4 (September 2, 2010): 123–27. http://dx.doi.org/10.1002/recl.19891080402.

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25

Zaidi, W., L. Timperman, and M. Anouti. "Deep eutectic solvent based on sodium cations as an electrolyte for supercapacitor application." RSC Adv. 4, no. 86 (2014): 45647–52. http://dx.doi.org/10.1039/c4ra08178a.

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26

Vasylyeva, Vera, Susanta K. Nayak, Giancarlo Terraneo, Gabriella Cavallo, Pierangelo Metrangolo, and Giuseppe Resnati. "Orthogonal halogen and hydrogen bonds involving a peptide bond model." CrystEngComm 16, no. 35 (2014): 8102–5. http://dx.doi.org/10.1039/c4ce01514b.

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27

Yadav, Vivek K., and Michael L. Klein. "Probing the dynamics of N-methylacetamide in methanol via ab initio molecular dynamics." Physical Chemistry Chemical Physics 19, no. 20 (2017): 12868–75. http://dx.doi.org/10.1039/c7cp00690j.

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Two-dimensional infrared (2D IR) spectroscopy of amide 1 vibrational bands provides a valuable probe of proteins as well as molecules such as N-methylacetamide (NMA), which present peptide-like H-bonding possibilities to a solvent.

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28

Perticaroli, Stefania, Barmak Mostofian, Georg Ehlers, Joerg C. Neuefeind, Souleymane O. Diallo, Christopher B. Stanley, Luke Daemen, et al. "Structural relaxation, viscosity, and network connectivity in a hydrogen bonding liquid." Physical Chemistry Chemical Physics 19, no. 38 (2017): 25859–69. http://dx.doi.org/10.1039/c7cp04013j.

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29

Sijpkes, A. H., and G. Somsen. "Enthalpies of dilution of N,N-dialkylformamides dissolved in formamide, N-methylformamide, and N-methylacetamide." Journal of Solution Chemistry 19, no. 8 (August 1990): 755–65. http://dx.doi.org/10.1007/bf00647102.

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30

Akiyama, Minoru. "Study on hydration enthalpy of N-methylacetamide in water." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 58, no. 9 (July 2002): 1943–50. http://dx.doi.org/10.1016/s1386-1425(01)00654-0.

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31

Hamzaoui, F., and F. Baert. "X-ray study of static disorder in N-methylacetamide." Acta Crystallographica Section C Crystal Structure Communications 50, no. 5 (May 15, 1994): 757–59. http://dx.doi.org/10.1107/s0108270193010832.

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32

Barthes, Mariette, and Michèle Ribet. "Compared 13C NMR spectra of acetanilide and N-methylacetamide." Berichte der Bunsengesellschaft für physikalische Chemie 102, no. 3 (March 1998): 419–21. http://dx.doi.org/10.1002/bbpc.19981020321.

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33

Sousa, Alvaro S. de, Helder M. Marques, and Manuel A. Fernandes. "2-Chloro-N-methylacetamide revisited: a low-temperature study." Acta Crystallographica Section E Structure Reports Online 63, no. 4 (March 9, 2007): o1642—o1644. http://dx.doi.org/10.1107/s1600536807009956.

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34

Wei, Bin. "(1-Hydroxyethylidene)(methyl)azanium bromide–N-methylacetamide (1/1)." Acta Crystallographica Section E Structure Reports Online 68, no. 5 (April 21, 2012): o1491. http://dx.doi.org/10.1107/s1600536812016984.

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35

Cheam, T. C. "Ab initio vibrational spectra of hydrogen-bonded N-methylacetamide." Journal of Molecular Structure: THEOCHEM 257, no. 1-2 (May 1992): 57–73. http://dx.doi.org/10.1016/0166-1280(92)87180-8.

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36

Mannfors, B., N. G. Mirkin, K. Palmo, and S. Krimm. "A polarizable electrostatic model of the N-methylacetamide dimer." Journal of Computational Chemistry 22, no. 16 (2001): 1933–43. http://dx.doi.org/10.1002/jcc.1143.

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37

Świergiel, Jolanta, and Jan Jadżyn. "Static Dielectric Permittivity and Electric Conductivity ofN-Methylacetamide +N,N-Dimethylacetamide Mixtures." Journal of Chemical & Engineering Data 54, no. 8 (August 13, 2009): 2296–300. http://dx.doi.org/10.1021/je9002515.

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38

Terbojevich, Maria, Claudio Carraro, Alessandro Cosani, and Enrico Marsano. "Solution studies of the chitin-lithium chloride-N,N-di-methylacetamide system." Carbohydrate Research 180, no. 1 (September 1988): 73–86. http://dx.doi.org/10.1016/0008-6215(88)80065-x.

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39

Osuga, T., T. Hasegawa, T. Nakane, M. Aoki, N. Shimizu, M. Takanashi, M. Fujie, Y. Tamura, S. Makino, and T. Asai. "N-Methylacetamide and N-Methylformamide: Low cytotoxic cryopreservatives—alternatives to dimethyl sulfoxide." Cytotherapy 20, no. 5 (May 2018): S121—S122. http://dx.doi.org/10.1016/j.jcyt.2018.02.361.

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40

Pikkarainen, Liisa. "Excess enthalpies of (2,2,2-trifluoroethanol + 2-butanone or N-methylacetamide or N,N-dimethylacetamide)." Journal of Chemical Thermodynamics 20, no. 4 (April 1988): 481–84. http://dx.doi.org/10.1016/0021-9614(88)90187-5.

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41

Choi, Jin Seok, Sung Woo Kim, Dan-Bi Shin, Yeoung-Gyu Ko, Yoon-Jung Do, Dong-Hun Kim, Il-Keun Kong, and Soo-Bong Park. "Effects of N-Methylacetamide on the Viability, Fertility and Hatchability of Cryopreserved Ogye (Korean Native Black Fowl) Semen." Korean Journal of Poultry Science 39, no. 4 (December 31, 2012): 291–95. http://dx.doi.org/10.5536/kjps.2012.39.4.295.

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42

Kim, Sung Woo, Jin Seok Choi, Yeoung-Gyu Ko, Yoon-Jung Do, Mijeong Byun, Soo-Bong Park, Hwan-Hoo Seong, and Chong-Dae Kim. "Effect of N-Methylacetamide Concentration on the Fertility and Hatchability of Cryopreserved Ogye Rooster Semen." Korean Journal of Poultry Science 41, no. 1 (March 31, 2014): 21–27. http://dx.doi.org/10.5536/kjps.2014.41.1.21.

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43

Cheam, T. C., and S. Krimm. "Infrared intensities of amide modes in N‐methylacetamide and poly(glycine I) from ab initio calculations of dipole moment derivatives of N‐methylacetamide." Journal of Chemical Physics 82, no. 4 (February 15, 1985): 1631–41. http://dx.doi.org/10.1063/1.448395.

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44

Shokouhi, Mohammad, Hadi Farahani, Masih Hosseini-Jenab, and Amir Hossein Jalili. "Solubility of Hydrogen Sulfide in N-Methylacetamide and N,N-Dimethylacetamide: Experimental Measurement and Modeling." Journal of Chemical & Engineering Data 60, no. 3 (January 16, 2015): 499–508. http://dx.doi.org/10.1021/je500478t.

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45

Seipelt, C. G., and M. D. Zeidler. "Correlation Times and Quadrupole Coupling Constants in Liquid N-Methylformamide and N-Methylacetamide." Berichte der Bunsengesellschaft für physikalische Chemie 101, no. 10 (October 1997): 1501–8. http://dx.doi.org/10.1002/bbpc.199700013.

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46

Kondo, Yasuhiko, and Shigekazu Kusabayashi. "Theoretical analysis of activation parameters in mixed solvents involving various chemical equilibria. Reaction of ethyl iodide with bromide ion in N-methylacetamide-acetonitrile and N-methylacetamide–N,N-dimethylacetamide mixtures." Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases 83, no. 4 (1987): 1089. http://dx.doi.org/10.1039/f19878301089.

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47

Pranay Kumar, K., B. Swathi, and M. Shanmugam. "Cryopreservation of Rooster Semen Using N-Methylacetamide as Cryoprotective Agent." International Journal of Agriculture Sciences(IJAS) 10, no. 3 (February 15, 2018): 5123. http://dx.doi.org/10.9735/0975-3710.10.3.5123-5126.

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48

Lee, Mi-Young. "Validation of urinary N-methylacetamide reference material for proficiency test." Analytical Science and Technology 27, no. 6 (December 25, 2014): 339–46. http://dx.doi.org/10.5806/ast.2014.27.6.339.

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49

Ben Haj Amara, A., J. Ben Brahim, G. Besson, and C. H. Pons. "Etude d'une nacrite intercalée par du dimethylsulfoxide et n-methylacetamide." Clay Minerals 30, no. 4 (December 1995): 295–306. http://dx.doi.org/10.1180/claymin.1995.030.4.03.

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ResumeUne nacrite est intercalée par deux composés organiques polaires: le diméthylsulfoxide (DMSO) et le n-méthylacétamide (NMA). Les deux solvants ont des moments dipolaires très voisins (4 debyes) mais des constantes diélectriques différentes (49 pour le DMSO et 179 pour le NMA). L'intercalation du NMA est plus rapide que celle du DMSO. Les deux complexes homogènes obtenus sont étudiés par diffraction des rayons X, spectroscopie infrarouge et ATD. L'étude par spectroscopie IR a montré que la nacrite expansée par du DMSO se comporte comme la kaolinite expansée par le même solvant. Dans le cas de la nacrite intercalée par du NMA, trois nouvelles bandes d'absorption dues aux vibrations de valence des OH liés par pont hydrogène avec le groupement C=O et situées respectivement à 3500, 3543 et 3589 cm−1 apparaissent. La fréquence v(N-H) du NMA est intermédiaire entre celles du liquide et d'une solution diluée, indiquant une liaison par pont hydrogène probablement avec les oxygènes de la couche tétraédrique du silicate. La diffraction des rayons X sur des échantillons orientés nous a permis d'obtenir 13 réflexions 00l pour chaque complexe. Une étude quantitative, par transformée de Fourier monodimensionnelle dans la direction perpendiculaire au plan du feuillet, a permis de déterminer le nombre de molécules organiques intercalées (une molécule par Si2Al2O5(OH)4) et leur orientation dans l'espace interlamellaire. L'ATD a montré par ailleurs que le complexe Nac.DMSO est plus stable que le complexe Nac.NMA.

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50

Paul, Subrata, and Sandip Paul. "Trehalose Induced Modifications in the Solvation Pattern of N-Methylacetamide." Journal of Physical Chemistry B 118, no. 4 (January 21, 2014): 1052–63. http://dx.doi.org/10.1021/jp407782x.

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