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Journal articles on the topic 'Ethers. Urea'

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1

Herschede, Sarah R., Hassan Gneid, Taylor Dent, Ellen B. Jaeger, Louise B. Lawson, and Nathalie Busschaert. "Bactericidal urea crown ethers target phosphatidylethanolamine membrane lipids." Organic & Biomolecular Chemistry 19, no. 17 (2021): 3838–43. http://dx.doi.org/10.1039/d1ob00263e.

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In this manuscript we report a small molecule that can selectively bind to the bacterial lipid phosphatidylethanolamine and consequently functions as an antibacterial agent against certain Gram-positive bacteria.
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2

Gustafson, Jeffrey, Andrew Dinh, Ryan Noorbehesht, et al. "Toward a Catalytic Atroposelective Synthesis of Diaryl Ethers Through C(sp2)–H Alkylation with Nitroalkanes." Synlett 29, no. 16 (2018): 2155–60. http://dx.doi.org/10.1055/s-0037-1609581.

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We report studies toward a small-molecule-catalytic approach to access atropisomeric diaryl ethers that proceeds through a C(sp2)–H alkylation using nitroalkanes as the alkyl source. A quaternary ammonium salt derived from quinine, containing a sterically hindered urea at the C-9 position, was found to effect atroposelective C(sp2)–H alkylation with moderate to good enantioselectivities across several naphthoquinone-containing diaryl ethers. Products could then be isolated in >95:5 er after one round of trituration. For several substrates that were evaluated, we obtained nitroethylated prod
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3

Cao, Jinfeng, Jun You, Lina Zhang, and Jinping Zhou. "Homogeneous synthesis and characterization of chitosan ethers prepared in aqueous alkali/urea solutions." Carbohydrate Polymers 185 (April 2018): 138–44. http://dx.doi.org/10.1016/j.carbpol.2018.01.010.

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4

Jha, Rameshwar, and Jagdish C. Ahluwalia. "Thermodynamics of micellization of some decyl poly(oxyethylene glycol) ethers in aqueous urea solutions." Journal of the Chemical Society, Faraday Transactions 89, no. 18 (1993): 3465. http://dx.doi.org/10.1039/ft9938903465.

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5

Zabivalova, N. M., A. M. Bochek, E. N. Vlasova, and B. Z. Volchek. "Preparation of mixed ethers by reaction of carboxymethyl cellulose with urea and their physicochemical properties." Russian Journal of Applied Chemistry 81, no. 9 (2008): 1622–29. http://dx.doi.org/10.1134/s1070427208090280.

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6

Stebani, Uwe, Günter Lattermann, Michael Wittenberg, and Joachim Heinz Wendorff. "Liquid crystalline derivatives of oligoethylene-amines and -amino ethers with amide, ester, urea or urethane functions." Journal of Materials Chemistry 7, no. 4 (1997): 607–14. http://dx.doi.org/10.1039/a607819b.

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7

Galehassadi, Mohammad, and Samira Pourreza. "Base and Catalyst-Free Preparation of Silyl Ethers in the Choline Chloride/Urea Deep Eutectic Solvent (DES)." Journal of Inorganic and Organometallic Polymers and Materials 29, no. 2 (2018): 541–49. http://dx.doi.org/10.1007/s10904-018-1028-z.

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8

Töke, László, István Bitter, Béla Ágai, et al. "Benzocrown derivatives as ionophores for alkali cations, I synthesis of urethane- and urea-linked mono- and bis-crown ethers." Liebigs Annalen der Chemie 1988, no. 4 (1988): 349–53. http://dx.doi.org/10.1002/jlac.198819880408.

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9

Uiterwijk, Jos W. H. M., Gerrit J. van Hummel, Sybolt Harkema, et al. "Preparation and X-ray structures of complexes of 18-membered crown ethers with polyfunctional guests: Urea and (O-alkyliso)uronium salts." Journal of inclusion phenomena 6, no. 1 (1988): 79–100. http://dx.doi.org/10.1007/bf00659372.

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10

Tsai, Chia-Wei, Anthony Midey, Ching Wu, and Richard A. Yost. "Analysis of Ammonium Nitrate/Urea Nitrate with Crown Ethers and Sugars as Modifiers by Electrospray Ionization-Mass Spectrometry and Ion Mobility Spectrometry." Analytical Chemistry 88, no. 19 (2016): 9435–42. http://dx.doi.org/10.1021/acs.analchem.6b01322.

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11

de Perre, Chloé, Adelheid Prado, and Bruce R. McCord. "Rapid and specific detection of urea nitrate and ammonium nitrate by electrospray ionization time-of-flight mass spectrometry using infusion with crown ethers." Rapid Communications in Mass Spectrometry 26, no. 2 (2011): 154–62. http://dx.doi.org/10.1002/rcm.5300.

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12

Bhattacharya, R. N., Pradip Kundu, and Gourhari Maiti. "Antimony trichloride catalyzed three-component reaction of urea, aldehydes and cyclic enol ethers: a novel route to 4-arylhexahydrofuro[2,3-d]pyrimidin-2(3H)-ones." Tetrahedron Letters 52, no. 1 (2011): 26–28. http://dx.doi.org/10.1016/j.tetlet.2010.10.064.

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13

Li, Qian, Yuehu Li, Zehua Jin, Yujie Li, Yifan Chen, and Jinping Zhou. "Viscoelasticity and Solution Stability of Cyanoethylcellulose with Different Molecular Weights in Aqueous Solution." Molecules 26, no. 11 (2021): 3201. http://dx.doi.org/10.3390/molecules26113201.

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Water-soluble cellulose ethers are widely used as stabilizers, thickeners, and viscosity modifiers in many industries. Understanding rheological behavior of the polymers is of great significance to the effective control of their applications. In this work, a series of cyanoethylcellulose (CEC) samples with different molecular weights were prepared with cellulose and acrylonitrile in NaOH/urea aqueous solution under the homogeneous reaction. The rheological properties of water-soluble CECs as a function of concentration and molecular weight were investigated using shear viscosity and dynamic rh
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14

Bhattacharya, R. N., Pradip Kundu, and Gourhari Maiti. "ChemInform Abstract: Antimony Trichloride Catalyzed Three-Component Reaction of Urea, Aldehydes and Cyclic Enol Ethers: A Novel Route to 4-Arylhexahydrofuro[2,3-d]pyrimidin-2(3H)-ones." ChemInform 42, no. 14 (2011): no. http://dx.doi.org/10.1002/chin.201114184.

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15

Hiltz, John A. "Analytical pyrolysis gas chromatography/mass spectrometry (py-GC/MS) of poly(ether urethane)s, poly(ether urea)s and poly(ether urethane-urea)s." Journal of Analytical and Applied Pyrolysis 113 (May 2015): 248–58. http://dx.doi.org/10.1016/j.jaap.2015.01.013.

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16

El-Eswed, B. I., M. B. Zughul, and G. A. W. Derwish. "Crown ether molecular complexes with urea and thiourea." Journal of Inclusion Phenomena and Molecular Recognition in Chemistry 24, no. 4 (1996): 325–40. http://dx.doi.org/10.1007/bf01041117.

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17

Chen, Chang’an, Kai Huang, Jingjing Zhu, et al. "A novel elastic and controlled-release poly(ether-ester-urethane)urea scaffold for cartilage regeneration." Journal of Materials Chemistry B 8, no. 18 (2020): 4106–21. http://dx.doi.org/10.1039/c9tb02754h.

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18

Chatterjee, G., A. A. Houde, and S. A. Stern. "Poly(ether urethane) and poly(ether urethane urea) membranes with high H2S/CH4 selectivity." Journal of Membrane Science 135, no. 1 (1997): 99–106. http://dx.doi.org/10.1016/s0376-7388(97)00134-8.

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19

Labow, Rosalind S., Douglas J. Erfle, and J. Paul Santerre. "Elastase-induced hydrolysis of synthetic solid substrates: poly(ester-urea-urethane) and poly(ether-urea-urethane)." Biomaterials 17, no. 24 (1996): 2381–88. http://dx.doi.org/10.1016/s0142-9612(96)00088-9.

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20

Akhuli, Bidyut, and Pradyut Ghosh. "Selective recognition and extraction of KBr via cooperative interactions with a urea functionalized crown ether dual-host." Chemical Communications 51, no. 92 (2015): 16514–17. http://dx.doi.org/10.1039/c5cc07291c.

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21

Mehdipour-Ataei, Shahram, Yaghoub Sarrafi, and Mehdi Amiri Pirjel. "Synthesis, characterization, and properties of novel poly(ether urea)s." Journal of Applied Polymer Science 93, no. 2 (2004): 961–65. http://dx.doi.org/10.1002/app.20499.

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22

Vlad, Stelian. "Hydrolytic Stability of Some Thermoplastic Poly(Ether-Urethane-Urea)s." High Performance Polymers 16, no. 1 (2004): 81–88. http://dx.doi.org/10.1177/0954008304038963.

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23

Gou, M. M., W. J. Koros, and G. Goldman. "Dimethylacetamide sorption kinetics in a urethane/urea/ether block copolymer." Journal of Applied Polymer Science 51, no. 10 (1994): 1685–99. http://dx.doi.org/10.1002/app.1994.070511001.

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24

GOMES, D., K. PEINEMANN, S. NUNES, W. KUJAWSKI, and J. KOZAKIEWICZ. "Gas transport properties of segmented poly(ether siloxane urethane urea) membranes." Journal of Membrane Science 281, no. 1-2 (2006): 747–53. http://dx.doi.org/10.1016/j.memsci.2006.05.002.

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25

Koevoets, Rolf A., S. Karthikeyan, Pieter C. M. M. Magusin, E. W. Meijer, and Rint P. Sijbesma. "Cross-Polymerization of Hard Blocks in Segmented Copoly(ether urea)s." Macromolecules 42, no. 7 (2009): 2609–17. http://dx.doi.org/10.1021/ma801220q.

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26

Gou, M. M., W. J. Koros, and G. W. Goldman. "Dimethyl acetamide sorption equilibria in a urethane/urea/ether block copolymer." Journal of Applied Polymer Science 43, no. 11 (1991): 1991–98. http://dx.doi.org/10.1002/app.1991.070431105.

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27

Monteiro, E. E. C., and J. L. C. Fonseca. "Phase segregation and viscoelastic behavior of poly(ether urethane urea)s." Journal of Applied Polymer Science 65, no. 11 (1997): 2227–36. http://dx.doi.org/10.1002/(sici)1097-4628(19970912)65:11<2227::aid-app20>3.0.co;2-z.

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28

Sousa-Alves, Wagner, João-Paulo S. Rigueira, Marielly M. Almeida-Moura, et al. "Fermentative characteristics and nutritional value of sugarcane silage added with two types of urea." Revista Colombiana de Ciencias Pecuarias 33, no. 3 (2019): 182–94. http://dx.doi.org/10.17533/udea.rccp.v33n3a02.

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Background: Dry matter (DM) loss is high in sugarcane silage due to its high content of soluble carbohydrates which favors yeast growth and ethanol production, thus reducing the nutritional value of the preserved forage. Objective: To determine the effect of adding two types of urea at two concentration levels to sugarcane silage on the nutritional value and fermentative characteristics of the silage. Methods: A completely randomized 2×2+1 factorial design was used, based on two types of urea (conventional and protected), two urea concentration (0.5 and 1.0% of the natural matter), and a contr
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29

Fuensanta, Mónica, Abbas Khoshnood, Francisco Rodríguez-Llansola, and José Miguel Martín-Martínez. "New Waterborne Polyurethane-Urea Synthesized with Ether-Carbonate Copolymer and Amino-Alcohol Chain Extenders with Tailored Pressure-Sensitive Adhesion Properties." Materials 13, no. 3 (2020): 627. http://dx.doi.org/10.3390/ma13030627.

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New waterborne polyurethane-urea dispersions with adequate adhesion and cohesion properties have been synthesized by reacting isophorone diisocyanate, copolymer of ether and carbonate diol polyol and three amino-alcohols with different number of OH groups chain extenders using the prepolymer method. The waterborne polyurethane-urea dispersions were characterized by pH, particle-size distribution, and viscosity, and the polyurethane-urea films were characterized by attenuated total reflectance infrared (ATR-IR) spectroscopy, differential scanning calorimetry (DSC), thermal gravimetric analysis
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30

Magalhães, K. A., S. C. Valadares Filho, P. V. R. Paulino, M. F. Paulino, and R. F. D. Valadares. "Performance, digestibility and carcass characteristics of feedlot dairy steers fed diets with different urea levels." Arquivo Brasileiro de Medicina Veterinária e Zootecnia 58, no. 5 (2006): 860–67. http://dx.doi.org/10.1590/s0102-09352006000500023.

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The effects of urea levels on feed intake, digestibility and carcass traits of 27 confined cross bred steers weighing 303.25 ± 60.8kg, were evaluated. After weighing, castrating, vaccinating and a period of seven days, three steers were slaughtered at the beginning of the experiment and the remaining 24 were allotted in a completely randomized design to four isonitogenous experimental diets (12% of crude protein) and increasing level of urea on the dry matter-basis (0.0; 0.65; 1.30 and 1.65%) to replace soybean meal, so that the final content of the experimental diets were approximately 22, 37
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31

Liu, He, Aiting Wang, Xu Xu, et al. "Porous aerogels prepared by crosslinking of cellulose with 1,4-butanediol diglycidyl ether in NaOH/urea solution." RSC Advances 6, no. 49 (2016): 42854–62. http://dx.doi.org/10.1039/c6ra07464b.

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32

Kovač, S., and V. Rapić. "Ferrocene compounds XVII. Synthesis of some ferrocenyl carbinols, ethers, and ureas." Journal of Organometallic Chemistry 384, no. 1-2 (1990): 147–53. http://dx.doi.org/10.1016/0022-328x(90)87062-i.

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33

Medimagh, Raouf, Maissa Meddeb Smaidia, Haythem Bennour, and Saber Chatti. "Synthesis and evaluation of the thermal properties of biosourced poly(ether)ureas and copoly(ether)ureas from 1,4:3,6-dianhydrohexitols." Polymer International 64, no. 4 (2014): 513–20. http://dx.doi.org/10.1002/pi.4819.

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34

Pegoretti, A., L. Fambri, A. Penati, and J. Kolarik. "Hydrolytic resistance of model poly(ether urethane ureas) and poly(ester urethane ureas)." Journal of Applied Polymer Science 70, no. 3 (1998): 577–86. http://dx.doi.org/10.1002/(sici)1097-4628(19981017)70:3<577::aid-app20>3.0.co;2-x.

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35

Collazos Silva, Roicer, Nuri Carito Vilca Valqui, and Jesús Rascón. "Utilización de fitohormonas para la inducción floral del cultivo de piña (Ananas comosus (L.) Merr.) en el distrito de Santa Rosa, Rodríguez de Mendoza, región Amazonas (Perú)." Revista de Investigación de Agroproducción Sustentable 1, no. 1 (2017): 55. http://dx.doi.org/10.25127/aps.20171.351.

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&lt;p&gt;Uno de los problemas más comunes en la producción de piña es la floración natural, que genera pérdidas económicas cuantiosas en todas las escalas de la producción, siendo una alternativa para controlar dicho problema, la inducción floral mediante la utilización de fito hormona. En tal sentido, el presente estudio se realizó con el objetivo de evaluar el efecto de diferentes tipos y dosis de fito hormonas sobre la inducción floral de los cultivares de piña MD2 – Goldeny “EcotipovSanta Rosa”. Los tratamientos evaluados fueron soluciones líquidas compuestas por: TI (Ethrel + Urea + Calag
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36

Alves, Francisco Gleyson da Silveira, Maria Socorro de Souza Carneiro, Ricardo Loiola Edvan, et al. "Agronomic and nutritional responses of Carajas elephant grass fertilized with protected and non-protected urea." Semina: Ciências Agrárias 39, no. 5 (2018): 2181. http://dx.doi.org/10.5433/1679-0359.2018v39n5p2181.

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The objective of this study was to assess the agronomic and nutritional responses of the elephant grass cultivar Carajas when subjected to fertilization with protected and conventional urea. A randomized block design with 4×2+1 factorial arrangement was adopted. The treatments consisted of four doses (100, 200, 400, and 800 kg N ha-1), two nitrogen sources (conventional and protected urea), and one additional treatment without fertilization. The experiment was carried out from October 2015 to March 2016, in a semi-arid region with a dystrophic yellow latosol type soil. The application of conve
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37

Wölper, Christoph, Alejandra Rodríguez-Gimeno, Katherine Chulvi Iborra, Peter G. Jones, and Armand Blaschette. "Polysulfonylamine, CLXXXIX [1]. Weitere Beispiele für die O-Protonierung von Harnstoffen mit Di(organosulfonyl)aminen: Bildung und Kristallstrukturen von 1,1-Dimethyluroniumdi( 4-fluorbenzolsulfonyl)amid und Di(1-methylharnstoff)- hydrogen(I)-di(4-fluorbenzolsulfonyl)amid/ Polysulfonylamines, CLXXXIX. Additional Examples of the O-Protonation of Ureas by Di(organosulfonyl)amines: Formation and Crystal Structures of 1,1-Dimethyluronium Di(4-fluorobenzenesulfonyl)amide and Di(1-methylurea)hydrogen(I)Di(4-fluorobenzenesulfonyl) amide." Zeitschrift für Naturforschung B 65, no. 11 (2010): 1363–71. http://dx.doi.org/10.1515/znb-2010-1112.

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Co-crystallization of N-methyl-substituted ureas with di(organosulfonyl)amines, (RSO2)2NH, leads unpredictably to either molecular co-crystals or, via proton transfer, to uronium salts. As a sequel to former reports, this communication describes the formation and the crystal structures of the new ionic compounds 1,1-dimethyluronium di(4-fluorobenzenesulfonyl)amide (1, monoclinic, space group P21/c, Z´ = 1) and di(1-methylurea)hydrogen(I) di(4-fluorobenzenesulfonyl)amide (2, triclinic, P1̄, Z´ = 1); both salts were obtained from dichloromethane/petroleum ether. In the structure of 2, the urea m
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38

Tongraung, Pan, Nuanphun Chantarasiri, and Thawatchai Tuntulani. "Calix[4]arenes containing urea and crown/urea moieties: effects of the crown ether unit and Na+ towards anion binding ability." Tetrahedron Letters 44, no. 1 (2003): 29–32. http://dx.doi.org/10.1016/s0040-4039(02)02530-3.

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39

Zhang, Tian, Xin Chen, Qiyan Zhang, and Q. M. Zhang. "Dielectric enhancement over a broad temperature by nanofiller at ultra-low volume content in poly(ether methyl ether urea)." Applied Physics Letters 117, no. 7 (2020): 072905. http://dx.doi.org/10.1063/5.0020280.

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40

Versteegen, Ron M., Rint P. Sijbesma, and E. W. Meijer. "Synthesis and Characterization of Segmented Copoly(ether urea)s with Uniform Hard Segments." Macromolecules 38, no. 8 (2005): 3176–84. http://dx.doi.org/10.1021/ma0478207.

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41

Toiserkani, Hojjat. "Synthesis and Characterization of Soluble and Thermally Stable Poly(ether–imide–urea)s." Bulletin of the Chemical Society of Japan 87, no. 5 (2014): 631–38. http://dx.doi.org/10.1246/bcsj.20130330.

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42

Versteegen, Ron M., Ralf Kleppinger, Rint P. Sijbesma, and E. W. Meijer. "Properties and Morphology of Segmented Copoly(ether urea)s with Uniform Hard Segments." Macromolecules 39, no. 2 (2006): 772–83. http://dx.doi.org/10.1021/ma051874e.

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43

Marchant, R. E., Q. Zhao, J. M. Anderson, and A. Hiltner. "Degradation of a poly(ether urethane urea) elastomer: infra-red and XPS studies." Polymer 28, no. 12 (1987): 2032–39. http://dx.doi.org/10.1016/0032-3861(87)90037-1.

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44

Zhao, Xu, Yu Hong Qi, Ke Jiao Li, and Zhan Ping Zhang. "Hydrogen Bonds and FTIR Peaks of Polyether Polyurethane-Urea." Key Engineering Materials 815 (August 2019): 151–56. http://dx.doi.org/10.4028/www.scientific.net/kem.815.151.

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Various types of hydrogen bonds exist in polyether polyurethane, polyurethane-urea and polyurea (PUA) and can cause microphase separation. The morphology, properties and applications of polyether PUA are determined by the microphase separation. All kinds of hydrogen bonds make it difficult to assignments of Fourier transform infrared spectroscopy (FTIR) peaks of ether linkage, amine and carbonyl group. This affects the calculation of the hydrogen bonding degree of the hard segments for estimating the degree of microphase separation. This paper summarized hydrogen bonding structures between pro
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45

Labadie, J. W., K. R. Carter, J. L. Hedrick, H. Jonsson, S. Y. Kim, and R. J. Twieg. "Cyclic ureas as solvents for poly(aryl ether) synthesis." Polymer Bulletin 30, no. 1 (1993): 25–31. http://dx.doi.org/10.1007/bf00296230.

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46

Guan, Jianjun, Michael S. Sacks, Eric J. Beckman, and William R. Wagner. "Biodegradable poly(ether ester urethane)urea elastomers based on poly(ether ester) triblock copolymers and putrescine: synthesis, characterization and cytocompatibility." Biomaterials 25, no. 1 (2004): 85–96. http://dx.doi.org/10.1016/s0142-9612(03)00476-9.

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47

Simonovsky, Felix I., Stephen C. Porter, and Buddy D. Ratner. "Synthesis of segmented poly(ether urethane)s and poly(ether urethane urea)s incorporating various side-chain or backbone functionalities." Journal of Biomaterials Science, Polymer Edition 16, no. 2 (2005): 267–84. http://dx.doi.org/10.1163/1568562053115462.

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48

Mayer, Matthias, Markus A. Keller, Katrin Watschinger, Gabriele Werner-Felmayer, Ernst R. Werner, and Georg Golderer. "Expression of full-length human alkylglycerol monooxygenase and fragments in Escherichia coli." Pteridines 24, no. 1 (2013): 111–15. http://dx.doi.org/10.1515/pterid-2013-0014.

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AbstractAlkylglycerol monooxygenase (AGMO; EC 1.14.16.5) is the only enzyme known to cleave the O-alkyl ether bond of alkylglycerols in humans. It is an integral membrane protein with nine predicted transmembrane domains. We attempted to express and purify full-length and truncated forms of AGMO in Escherichia coli. Full-length AGMO could not be expressed in three different E. coli expression strains, three different expression vectors and several induction systems. We succeeded, however, in expression of three N-terminally strep-tagged truncated forms, named active sites 1, 2 and 3, with 205,
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49

Liang, Huan, Erlong Zhao, Chunyan Feng, et al. "Effects of slow-release urea on in vitro rumen fermentation parameters, growth performance, nutrient digestibility and serum metabolites of beef cattle." Semina: Ciências Agrárias 41, no. 4 (2020): 1399. http://dx.doi.org/10.5433/1679-0359.2020v41n4p1349.

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Two experiments were conducted to investigate the effects of slow-release urea (SRU) on in vitro rumen fermentation parameters, growth performances, nutrient digestibility, and serum metabolites of beef cattle. The single factor design was applied in both experiments. Three diets with different nitrogen sources including soybean meal (Control group), slow-release urea (SRU group), and common urea (Urea group) was designed (concentrate to forage ratio was 4:6). The diets were formulated to be isoenergetic and isonitrogenous, 75% of the soybean meal in the control diet was replaced by 1.41% SRU
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50

Sultana, R., D. K. Jamee, S. Islam, S. M. A. Islam, M. R. Amin, and M. R. I. Khan. "Preservation of wet rice straw using urea and molasses in monsoon of Bangladesh." Journal of Fisheries, Livestock and Veterinary Science 01, no. 02 (2020): 36–44. http://dx.doi.org/10.18801/jflvs.010220.05.

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An experiment of treated and ensiled wet rice straw with urea and molasses was performed to explore the chemical composition, physical quality, in vitro digestibility and its potentiality as a quality feed for ruminants. In this experiment, plastic containers were used to preserve chopped wet rice straw under airtight condition based on the treatment as T1 (wet rice straw only), T2 (straw with 5% molasses), T3 (straw with 5% urea), T4 (straw with 5% urea and 5% molasses) and T5 (straw with 10% urea and 5% molasses) to analyze chemical composition, physical quality, metabolizable energy (ME) co
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