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Journal articles on the topic 'Ammonolysis'

Author: Grafiati

Published: 4 June 2021

Last updated: 12 June 2025

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1

Ackerhans, Carsten, Bodo Räke, Ralph Krätzner, Peter Müller, Herbert W. Roesky, and Isabel Usón. "Ammonolysis of Trichlorosilanes." European Journal of Inorganic Chemistry 2000, no. 5 (2000): 827–30. http://dx.doi.org/10.1002/(sici)1099-0682(200005)2000:5<827::aid-ejic827>3.0.co;2-j.

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2

HE, MAOXIA, DACHENG FENG, JU XIE та ZHENGTING CAI. "COMPUTATIONAL STUDIES OF THE AMMONOLYSIS FOR N-METHYL β-SULTAM". Journal of Theoretical and Computational Chemistry 04, № 02 (2005): 383–95. http://dx.doi.org/10.1142/s0219633605001544.

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As a first step toward the understanding of the aminolysis reaction of β-sultam compounds, the ammonolysis and the effect of a second ammonia on the ammonolysis reactions of N -methyl β-sultam have been studied using Density Functional Theory (DFT) method at the B3LYP/6-31G* level. The exploration of the reaction processes proposed two different mechanisms: concerted and stepwise mechanisms. There is one pathway in concerted mechanism and two pathways in stepwise mechanisms: pathways a and b. The calculations of reaction energy barriers show that the nonconcerted route is the more favored one. Solvent effects were assessed by the PCM method. The results show that the pathway a in channel II is the most favorable in both cases. The presence of solvent disfavors the reaction, and the participation of ammonia in the ammonolysis reaction plays a positive role and reduces the active energy greatly. All transition states in the assisted ammonolysis are 45–65 kJ/mol lower than those for the non-assisted reaction. The results also show that the ammonolysis reaction have a higher energy barrier than the alcoholysis reaction. This low reactivity of amines is also observed in the reactions of N -benzoyl β-sultam and p-nitrophenyl toluene-p-sulfonate where there is a distinct preference towards oxygen nucleophiles.

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3

Wang, Shaoning, Martin Karpf, and Frank Kienzle. "Ammonolysis with supercritical NH3." Journal of Supercritical Fluids 15, no. 2 (1999): 157–64. http://dx.doi.org/10.1016/s0896-8446(98)00125-9.

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4

Galkin, M. S., and S. V. Zelentsov. "Arsenic(III) chloride ammonolysis." Russian Journal of Inorganic Chemistry 60, no. 5 (2015): 589–94. http://dx.doi.org/10.1134/s003602361505006x.

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5

Forostyan, Yu N., O. V. Shirikov, and E. I. Forostyan. "Ammonolysis of technical lignins." Chemistry of Natural Compounds 23, no. 2 (1987): 231–34. http://dx.doi.org/10.1007/bf00598766.

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6

Vorob’ev, P. B., and D. Kh Sembaev. "Oxidative Ammonolysis of Dialkylpyridines." Russian Journal of General Chemistry 75, no. 1 (2005): 147–50. http://dx.doi.org/10.1007/s11176-005-0186-1.

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7

Sarkar, Saptarshi, and Biman Bandyopadhyay. "Theoretical investigation of the relative impacts of water and ammonia on the tropospheric conversion of N2O5 to HNO3." Physical Chemistry Chemical Physics 23, no. 11 (2021): 6651–64. http://dx.doi.org/10.1039/d0cp05553k.

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Catalytic effects of H<sub>2</sub>O and NH<sub>3</sub> on HNO<sub>3</sub> formation via hydrolysis and ammonolysis of N<sub>2</sub>O<sub>5</sub> have been studied. Relative rate analysis reveals that ammonolysis has negligible practical atmospheric implication compared to hydrolysis.

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8

Chen, Jian Bing, Qiang Guo, Jin Liang Sun, Xian Li Shao, and Zhi Jun Nie. "A Study on Linseed Oil Modified Waterborne Polyurethane Coatings." Materials Science Forum 686 (June 2011): 528–32. http://dx.doi.org/10.4028/www.scientific.net/msf.686.528.

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The waterborne polyurethane coatings modified by linseed oil were prepared in a method of ammonolysis. The influence of reaction time and temperature of the linseed oil ammonolysis on structure and properties of the waterborne polyurethane coatings was investigated and discussed. It has been shown in this work that the preferred ammonolysis temperature would be 102~118°C, the reaction time could be about 80 min, and structure of the modified waterborne polyurethane was analysed by FTIR. The touch-dry time of the modified waterborne polyurethane with drier would be shorter than that of non-modified waterborne polyurethane, normally in a week, and the stability of the modified waterborne polyurethane coating in water could stand for 3 months under room temperature. The TGA results of the coatings showed that the weight loss started at about 294°C.

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9

Maya, L. "Ammonolysis of niobium(V) bromide." Inorganic Chemistry 26, no. 9 (1987): 1459–62. http://dx.doi.org/10.1021/ic00256a030.

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10

Orlov, V. M., V. Ya Kuznetsov, and R. N. Osaulenko. "Ammonolysis of magnesiothermic tantalum powders." Russian Journal of Inorganic Chemistry 62, no. 1 (2017): 33–38. http://dx.doi.org/10.1134/s0036023617010132.

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11

BARTKOWIAK, M., R. PELECH, and E. MILCHERT. "Ammonolysis of (3-chloropropyl)trimethoxysilane." Journal of Hazardous Materials 136, no. 3 (2006): 854–58. http://dx.doi.org/10.1016/j.jhazmat.2006.01.024.

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12

McClelland, Robert A., N. Esther Seaman, James M. Duff, and R. E. Branston. "Kinetics and equilibrium in the ammonolysis of substituted phthalimides." Canadian Journal of Chemistry 63, no. 1 (1985): 121–28. http://dx.doi.org/10.1139/v85-020.

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Kinetic studies are reported for the base hydrolysis to phthalamic acid anions (H) and ammonolysis to phthalamides (A) for seven phthalimides (P): 1, unsubstituted; 2, 4-NO2; 3, 4-Cl; 4, 4-t Bu; 5, 3-NO2; 6, 3-Me; 7, 3-Me3Si. The hydrolysis kinetics require two mechanisms, one which is first order in neutral imide and first order in hydroxide ion, and a second, which is important only in quite concentrated NaOH, which is first order in neutral phthalimide and second order in hydroxide ion. Ammonolysis kinetics for 1–5 revealed the rate law: Rate = kN [Unionized phthalimide] [NH3][OH−]. A mechanism is proposed with rate-determining breakdown of the anionic form of the tetrahedral intermediate derived by addition of NH3 to the phthalimide. The ammonolysis is reversible. The phthalamide hydrolyzes to the phthalamic acid via cyclization to an intermediate phthalimide, which is detected in concentrated base where its formation from phthalamide is more rapid than its subsequent hydrolysis. Rate constants for the cyclization follow the rate law: Rate = kcyc [Phthalamide][OH−]. This reaction is the microscopic reverse of the ammonolysis, and the ratio kN/kcyc provides the equilibrium constant Keq for the reaction P + NH3 = A. Values for 1–5 lie in the range 2 × 102 – 4 × 103. With 3-methylphthalimide, kinetics in aqueous ammonia do not obey a first-order relationship, but they could be analyzed by a scheme whereby the phthalimide is converted reversibly to the phthalamide and simultaneously undergoes an irreversible hydrolysis. The value of Keq in the system is 1.8. With 3-trimethylsilylphthalimide the value of Keq is further reduced to 0.01. The ammonolysis reaction does occur more quickly than hydrolysis but the equilibrium is so unfavorable that even in concentrated ammonia only a small amount of the phthalamide is ever formed.

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13

Szczęsny, Robert, Tuan K. A. Hoang, Liliana Dobrzańska, and Duncan H. Gregory. "Solution/Ammonolysis Syntheses of Unsupported and Silica-Supported Copper(I) Nitride Nanostructures from Oxidic Precursors." Molecules 26, no. 16 (2021): 4926. http://dx.doi.org/10.3390/molecules26164926.

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Herein we describe an alternative strategy to achieve the preparation of nanoscale Cu3N. Copper(II) oxide/hydroxide nanopowder precursors were successfully fabricated by solution methods. Ammonolysis of the oxidic precursors can be achieved essentially pseudomorphically to produce either unsupported or supported nanoparticles of the nitride. Hence, Cu3N particles with diverse morphologies were synthesized from oxygen-containing precursors in two-step processes combining solvothermal and solid−gas ammonolysis stages. The single-phase hydroxochloride precursor, Cu2(OH)3Cl was prepared by solution-state synthesis from CuCl2·2H2O and urea, crystallising with the atacamite structure. Alternative precursors, CuO and Cu(OH)2, were obtained after subsequent treatment of Cu2(OH)3Cl with NaOH solution. Cu3N, in the form of micro- and nanorods, was the sole product formed from ammonolysis using either CuO or Cu(OH)2. Conversely, the ammonolysis of dicopper trihydroxide chloride resulted in two-phase mixtures of Cu3N and the monoamine, Cu(NH3)Cl under similar experimental conditions. Importantly, this pathway is applicable to afford composite materials by incorporating substrates or matrices that are resistant to ammoniation at relatively low temperatures (ca. 300 °C). We present preliminary evidence that Cu3N/SiO2 nanocomposites (up to ca. 5 wt.% Cu3N supported on SiO2) could be prepared from CuCl2·2H2O and urea starting materials following similar reaction steps. Evidence suggests that in this case Cu3N nanoparticles are confined within the porous SiO2 matrix.

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14

Müller, Thomas, та Natascha Breuer. "Consecutive Alkynylation–Michael Addition–Cyclocondensation (AMAC) Multicomponent Syntheses of α-Pyrones and α-Pyridones". Synthesis 50, № 14 (2018): 2741–52. http://dx.doi.org/10.1055/s-0037-1610129.

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A novel consecutive three-component synthesis of α-pyrones is based upon an alkynylation–Michael addition–cyclocondensation (AMAC) sequence, starting from (hetero)aroyl chloride and terminal alkyne to furnish the alkynone which reacts with malonates to give the α-pyrones in moderate to very good yields. By concatenating ammonolysis of the α-pyrones, an alkynylation–Michael addition–cyclocondensation–ammonolysis (AMACA) synthesis of α-pyridones can be conceived. α-Pyridone products with and without ester functionality are obtained in moderate yields.

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15

Lei, Xianchi, Guoding Gu, Yafei Hu, Haoshang Wang, Zhaoxia Zhang, and Shuai Wang. "Structural Requirements for Chemoselective Ammonolysis of Ethylene Glycol to Ethanolamine over Supported Cobalt Catalysts." Catalysts 11, no. 6 (2021): 736. http://dx.doi.org/10.3390/catal11060736.

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Ethylene glycol is regarded as a promising C2 platform molecule due to the fast development of its production from sustainable biomass. This study inquired the structural requirements of Co-based catalysts for the liquid-phase ammonolysis of ethylene glycol to value-added ethanolamine. We showed that the rate and selectivity of ethylene glycol ammonolysis on γ-Al2O3-supported Co catalysts were strongly affected by the metal particle size within the range of 2–10 nm, among which Co nanoparticles of ~4 nm exhibited both the highest ethanolamine selectivity and the highest ammonolysis rate based on the total Co content. Doping of a moderate amount of Ag further promoted the catalytic activity without affecting the selectivity. Combined kinetic and infrared spectroscopic assessments unveiled that the addition of Ag significantly destabilized the adsorbed NH3 on the Co surface, which would otherwise be strongly bound to the active sites and inhibit the rate-determining dehydrogenation step of ethylene glycol.

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16

Chung, Younglim, Jayoung Kim, and Hongkee Sah. "Reactivity of ethyl acetate and its derivatives toward ammonolysis: ramifications for ammonolysis-based microencapsulation process." Polymers for Advanced Technologies 20, no. 10 (2009): 785–94. http://dx.doi.org/10.1002/pat.1329.

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17

Lu, Qiyi, Juanjuan Zhang, Yuanya Wu, and Shihong Chen. "Conjugated polymer dots/oxalate anodic electrochemiluminescence system and its application for detecting melamine." RSC Advances 5, no. 78 (2015): 63650–54. http://dx.doi.org/10.1039/c5ra10809h.

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18

Drygas, Mariusz, Maciej Sitarz, and Jerzy F. Janik. "Ammonolysis of gallium phosphide GaP to the nanocrystalline wide bandgap semiconductor gallium nitride GaN." RSC Advances 5, no. 128 (2015): 106128–40. http://dx.doi.org/10.1039/c5ra23144b.

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19

Stephenson, Nickeisha A., Samuel H. Gellman, and Shannon S. Stahl. "Ammonolysis of anilides promoted by ethylene glycol and phosphoric acid." RSC Adv. 4, no. 87 (2014): 46840–43. http://dx.doi.org/10.1039/c4ra09065a.

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20

Nascimento, Evandro A., Sérgio A. L. Morais, Dorila Piló Veloso, and Sônia M. C. Menezes. "Oxidative Ammonolysis of theEucalyptus GrandisKraft Lignin." Journal Of The Brazilian Chemical Society 5, no. 1 (1994): 5–14. http://dx.doi.org/10.5935/0103-5053.19940002.

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21

DURHAM, BERNARD G., MARLYN J. MURTHA, and GEORGE BURNET. "Si3N4by the Carbothermal Ammonolysis of Silica." Advanced Ceramic Materials 3, no. 1 (1988): 45–48. http://dx.doi.org/10.1111/j.1551-2916.1988.tb00167.x.

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22

Zuazo, Beatriz N., and Inge M. E. Thiel. "Ammonolysis reaction of octa-O-benzoylmelibiononitrile." Carbohydrate Research 172, no. 1 (1988): 156–59. http://dx.doi.org/10.1016/s0008-6215(00)90849-8.

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23

Efanov, M. V., D. V. Dudkin, and M. V. Popova. "Oxidative Ammonolysis of Vegetable Raw Materials." Russian Journal of Applied Chemistry 77, no. 4 (2004): 645–48. http://dx.doi.org/10.1023/b:rjac.0000038685.87109.cc.

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24

Lu, Qiyi, Juanjuan Zhang, Yuanya Wu, Ruo Yuan, and Shihong Chen. "Cathodic electrochemiluminescence behavior of an ammonolysis product of 3,4,9,10-perylenetetracarboxylic dianhydride in aqueous solution and its application for detecting dopamine." RSC Advances 5, no. 28 (2015): 22289–93. http://dx.doi.org/10.1039/c4ra16387g.

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25

Lv, Honggui, Jingjing Shi, Junjun Huang, Chao Zhang, and Wei Yi. "Rhodium(iii)-catalyzed and MeOH-involved regioselective mono-alkenylation of N-arylureas with acrylates." Organic & Biomolecular Chemistry 15, no. 34 (2017): 7088–92. http://dx.doi.org/10.1039/c7ob01627a.

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26

Przychodzeń, Witold, Jarosław Chojnacki, and Łukasz Nierzwicki. "Medium-sized cyclic bis(anisylphosphonothioyl)disulfanes and their corresponding cyclic sulfane-structures and most characteristic reactions." New Journal of Chemistry 43, no. 38 (2019): 15413–34. http://dx.doi.org/10.1039/c9nj03682b.

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27

Podila, Seetharamulu, Sharif F. Zaman, Hafedh Driss, Yahia A. Alhamed, Abdulrahim A. Al-Zahrani, and Lachezar A. Petrov. "Hydrogen production by ammonia decomposition using high surface area Mo2N and Co3Mo3N catalysts." Catalysis Science & Technology 6, no. 5 (2016): 1496–506. http://dx.doi.org/10.1039/c5cy00871a.

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28

Kumar, Rudra, Thiruvelu Bhuvana, and Ashutosh Sharma. "Ammonolysis synthesis of nickel molybdenum nitride nanostructures for high-performance asymmetric supercapacitors." New Journal of Chemistry 44, no. 33 (2020): 14067–74. http://dx.doi.org/10.1039/d0nj01693d.

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29

AlShibane, Ihfaf, Justin S. J. Hargreaves, Andrew L. Hector, William Levason, and Andrew McFarlane. "Synthesis and methane cracking activity of a silicon nitride supported vanadium nitride nanoparticle composite." Dalton Transactions 46, no. 27 (2017): 8782–87. http://dx.doi.org/10.1039/c7dt00285h.

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30

Moriga, Toshihiro, Katsuya Shiozaki, Hironori Fujito, et al. "Tuning of Optical Properties in La_1-xBa_xTaON₂ Oxynitride through Composition and Particle Size Controls." Journal of Nano Research 24 (September 2013): 213–19. http://dx.doi.org/10.4028/www.scientific.net/jnanor.24.213.

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La1-xBaxTa (O,N)3 oxynitrides were synthesized by ammonolysis of oxide precursors, prepared by a complex polymerization method. The absorption edge of the solid-solutions did not show a blueshift with an increase of x, in spite of the increase of O/N ratio, but rather the edge was redshifted. The substitution of La3+ by Ba2+ was thought to cause the bandgap to be redshifted due to the improved symmetry in (O,N)-Ta-(O,N) linkages in the perovskite structure. Addition of a NaCl flux during the ammonolysis of oxide precursors suppressed agglomeration of primary particles to inhibit the deterioration in the reflectivity after the longer wavelength region of the absorption edge.

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31

Yoon, Songhak, Alexandra E. Maegli, Santhosh Kumar Matam та ін. "The Influence of the Ammonolysis Temperature on the Photocatalytic Activity ofβ-TaON". International Journal of Photoenergy 2013 (2013): 1–8. http://dx.doi.org/10.1155/2013/507194.

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Phase-pure tantalum oxynitride (β-TaON) powders were synthesized by thermal ammonolysis of Ta2O5powders. X-ray diffraction revealed an enlargement of the unit cell and an increase of the crystallite size with increasing ammonolysis temperature. Scanning electron microscopy showed reduced particle sizes forβ-TaON synthesized at 800 and compared to the precursor oxide. With increasing nitridation temperature the Brunauer-Emmett-Teller surface area was reduced and the nitrogen content increased. UV-Vis spectroscopy showed a bandgap energy of 2.6–2.4 eV. The highest oxygen evolution rate of 220 μmol·g−1·h−1was achieved forβ-TaON synthesized at . The factors determining the photocatalytic activity ofβ-TaON powders were found to be the specific surface area and defects in theβ-TaON.

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32

Shang, Mengmeng, Jing Wang, Jian Fan, Hongzhou Lian, Yang Zhang, and Jun Lin. "ZnGeN2 and ZnGeN2:Mn2+ phosphors: hydrothermal-ammonolysis synthesis, structure and luminescence properties." Journal of Materials Chemistry C 3, no. 36 (2015): 9306–17. http://dx.doi.org/10.1039/c5tc01864a.

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33

Wang, Yuqiao, Chuanyong Jian, Wenting Hong, and Wei Liu. "Nonlayered 2D ultrathin molybdenum nitride synthesized through the ammonolysis of 2D molybdenum dioxide." Chemical Communications 57, no. 2 (2021): 223–26. http://dx.doi.org/10.1039/d0cc07065c.

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34

Paździoch, Waldemar, and Eugeniusz Milchert. "Ammonolysis of Allyl Chloride by Ammonia Solution." Industrial & Engineering Chemistry Research 41, no. 11 (2002): 2602–10. http://dx.doi.org/10.1021/ie010564r.

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35

Abarca, Angel, Pilar Gómez-Sal, Avelino Martín, Miguel Mena, Josep María Poblet, and Carlos Yélamos. "Ammonolysis of Mono(pentamethylcyclopentadienyl) Titanium(IV) Derivatives§." Inorganic Chemistry 39, no. 4 (2000): 642–51. http://dx.doi.org/10.1021/ic9907718.

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36

García, María Jesús, Francisca Rebolledo та Vicente Gotor. "Chemoenzymatic aminolysis and ammonolysis of β-ketoesters". Tetrahedron Letters 34, № 38 (1993): 6141–42. http://dx.doi.org/10.1016/s0040-4039(00)61751-3.

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37

Jinqiang, Liu, and Chen Xinzhi. "Preparation of Nitroanilines by Ammonolysis of Multinitrobenzenes." Synthetic Communications 38, no. 16 (2008): 2782–86. http://dx.doi.org/10.1080/00397910701837412.

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38

Griffin, Joseph, John Atherton, and Michael I. Page. "The ammonolysis of esters in liquid ammonia." Journal of Physical Organic Chemistry 26, no. 12 (2013): 1032–37. http://dx.doi.org/10.1002/poc.3148.

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39

ZOETE, M. C. DE, A. C. KOCK-VAN DALEN, F. VAN RANTWIJK, and R. A. SHELDON. "Ammonolysis of Carboxylic Esters Catalyzed by Lipases." Annals of the New York Academy of Sciences 799, no. 1 Enzyme Engine (1996): 346–50. http://dx.doi.org/10.1111/j.1749-6632.1996.tb33224.x.

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40

Masubuchi, Yuji, Chihiro Yamakami, Teruki Motohashi, and Shinichi Kikkawa. "Ammonolysis of HTiNbO5–n-Propylamine Intercalation Compound." Chemistry Letters 40, no. 11 (2011): 1238–39. http://dx.doi.org/10.1246/cl.2011.1238.

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41

Friberg, Stig E., Ching Chang Yang, Remon Goubran, and Richard E. Partch. "Ammonia microemulsions and ammonolysis of silicon tetrachloride." Langmuir 7, no. 6 (1991): 1103–6. http://dx.doi.org/10.1021/la00054a014.

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42

Matsumoto, Kiyoshi, Shiro Hashimoto, Tadashi Okamoto, Shinichi Otani, and Jun’ichi Hayami. "High-pressure Ammonolysis of Lactones to Hydroxyamides." Chemistry Letters 16, no. 5 (1987): 803–4. http://dx.doi.org/10.1246/cl.1987.803.

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43

Unuma, Hidero, Mitsuyoshi Yamamoto, Yoshikazu Suzuki, and Sumio Sakka. "Ammonolysis of silica gels containing methyl groups." Journal of Non-Crystalline Solids 128, no. 3 (1991): 223–30. http://dx.doi.org/10.1016/0022-3093(91)90460-n.

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44

Wang, Hairong, Jinlin He, Dongling Cao, et al. "Synthesis of an acid-labile polymeric prodrug DOX-acetal-PEG-acetal-DOX with high drug loading content for pH-triggered intracellular drug release." Polymer Chemistry 6, no. 26 (2015): 4809–18. http://dx.doi.org/10.1039/c5py00569h.

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PEGylated doxorubicin (DOX) prodrugs with high drug loading content have been prepared via a combination of CuAAC “click” reaction and ammonolysis reaction, which can be used for pH-triggered delivery of doxorubicin.

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45

Li, Xianji, Andrew L. Hector, John R. Owen, and S. Imran U. Shah. "Evaluation of nanocrystalline Sn3N4derived from ammonolysis of Sn(NEt2)4as a negative electrode material for Li-ion and Na-ion batteries." Journal of Materials Chemistry A 4, no. 14 (2016): 5081–87. http://dx.doi.org/10.1039/c5ta08287k.

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Bulk nanocrystalline Sn<sub>3</sub>N<sub>4</sub>powders were synthesised by a two step ammonolysis route. These provided good capacities in sodium and lithium cells, and good stability in sodium cells.

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46

Capanema, Ewellyn A., Mikhail Yu Balakshin, Chen-Loung Chen, Josef S. Gratzl, and Adrianna G. Kirkman. "Oxidative Ammonolysis of Technical Lignins. Part 1. Kinetics of the Reaction under Isothermal Condition at 130°C." Holzforschung 55, no. 4 (2001): 397–404. http://dx.doi.org/10.1515/hf.2001.066.

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Summary Investigations were conducted on the oxidative ammonolysis of REPAP organosolv lignin at 130 °C in 0.8M NH4OH solution under oxygen pressure of 12 bar. The lignin was completely solubilized at the reaction time of 165 min. The kinetics of the nitrogen incorporation consists of two phases. The first phase is up to the reaction time of approximately 35 min including 15 min heating up period. The rate of nitrogen incorporation in the first phase is 2.3 times higher than that in the second phase: κ1 = 4.58 × 10−4 s−1 versus κ2 = 1.90 × 10−4 s−1. The oxygen uptake and CO2 formation in the reaction is rather high. When the nitrogen incorporation was ceased after reaction for 255 minutes, more than 4 moles of oxygen/C9-unit of lignin were consumed and approximately 1.5 moles of carbon dioxide/C9-unit of lignin were released. In addition, extensive O-demethylation of methoxyl groups occurred. The molar ratio of the nitrogen incorporation to the methoxyl group eliminated is approximately 1.4 and 0.7 for the soluble and insoluble N-modified lignins, respectively. Structural analyses of the soluble N-modified lignins by FTIR and 1H NMR spectroscopic techniques showed only quantitative differences in the spectra obtained at different reaction times. This indicates that the reaction pathways do not change in the course of the oxidative ammonolysis. Possible reaction mechanisms of the oxidative ammonolysis are discussed on the basis of the experimental data.

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47

Sarkar, Saptarshi, Subhasish Mallick, Pradeep Kumar, and Biman Bandyopadhyay. "Ammonolysis of ketene as a potential source of acetamide in the troposphere: a quantum chemical investigation." Physical Chemistry Chemical Physics 20, no. 19 (2018): 13437–47. http://dx.doi.org/10.1039/c8cp01650j.

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Quantum chemical calculations at the CCSD(T)/CBS//MP2/aug-cc-pVTZ levels of theory have been carried out to investigate a potential new source of acetamide in Earth's atmosphere through the ammonolysis of the simplest ketene.

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48

Wu, Chun Jiang, Chen Chen, Cheng Yu Sun, et al. "Synthesis of Substituted Ethyl Argiosulfonylcarbamates." Advanced Materials Research 1015 (August 2014): 574–76. http://dx.doi.org/10.4028/www.scientific.net/amr.1015.574.

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A series of substituted ethyl argiosulfonylcarbamates were synthesized from substituted aromatics through three steps including chlorosulfonation, ammonolysis, nucleophilic addition and their structures were confirmed by1H NMR and MS spectrum. The results showed that the yields of compounds were higher than 80%.

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49

Bem, D. S., J. D. Houmes, and H. C. zur Loye. "Ternary Nitride Synthesis: Ammonolysis of Ternary Oxide Precursors." Materials Science Forum 152-153 (March 1994): 183–86. http://dx.doi.org/10.4028/www.scientific.net/msf.152-153.183.

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Maslova, N. V., and Z. G. Osipova. "Propylene effect on propane dehydrogenation in oxidative ammonolysis." Reaction Kinetics & Catalysis Letters 43, no. 1 (1991): 201–7. http://dx.doi.org/10.1007/bf02075434.

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