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Showing 1 to 12 of 19 entries
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[Not Available].

Talanta

Popper E, Roman L, Marcu P.
PMID: 18960213
Talanta. 1967 Oct;14(10):1163-8.

Some aliphatic amines have been titrated enthalpimetrically. The heats of neutralization have been calculated from the results and correlated with the basicity of the amines and the number of hydroxyl and amine groups present. The titration curves were all...

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Popper E, Roman L, Marcu P. Sur la détermination des chaleurs de neutralisation de quelques amines aliphatiques par le titrage enthalpimétrique. [Not Available]. Talanta. 1967;14(10):1163-8
Popper, E., Roman, L., & Marcu, P. (1967). Sur la détermination des chaleurs de neutralisation de quelques amines aliphatiques par le titrage enthalpimétrique. [Not Available]. Talanta, 14(10), 1163-8.
Popper, E, et al. "Sur la détermination des chaleurs de neutralisation de quelques amines aliphatiques par le titrage enthalpimétrique." [Not Available]. Talanta vol. 14,10 (1967): 1163-8.
Popper E, Roman L, Marcu P. Sur la détermination des chaleurs de neutralisation de quelques amines aliphatiques par le titrage enthalpimétrique. [Not Available]. Talanta. 1967 Oct;14(10):1163-8. French. PMID: 18960213.
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Amine borate catabolism by bacteria isolated from contaminated metal-working fluids.

Journal of applied microbiology

Sherburn RE, Large PJ.
PMID: 10594706
J Appl Microbiol. 1999 Nov;87(5):668-75. doi: 10.1046/j.1365-2672.1999.00906.x.

Four bacterial strains (tentatively identified as strains of Aeromonas, Pseudomonas, Flavobacterium and Bacillus) isolated from contaminated metal-working fluids were assayed for the capacity to utilize the borate derivatives of monoethanolamine (MEA), diethanolamine (DEA) and triethanolamine (TEA). Two of these...

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Sherburn RE, Large PJ. Amine borate catabolism by bacteria isolated from contaminated metal-working fluids. J Appl Microbiol. 1999;87(5):668-75doi: 10.1046/j.1365-2672.1999.00906.x.
Sherburn, R. E., & Large, P. J. (1999). Amine borate catabolism by bacteria isolated from contaminated metal-working fluids. Journal of applied microbiology, 87(5), 668-75. https://doi.org/10.1046/j.1365-2672.1999.00906.x
Sherburn, and Large. "Amine borate catabolism by bacteria isolated from contaminated metal-working fluids." Journal of applied microbiology vol. 87,5 (1999): 668-75. doi: https://doi.org/10.1046/j.1365-2672.1999.00906.x
Sherburn RE, Large PJ. Amine borate catabolism by bacteria isolated from contaminated metal-working fluids. J Appl Microbiol. 1999 Nov;87(5):668-75. doi: 10.1046/j.1365-2672.1999.00906.x. PMID: 10594706.
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Syntheses, Structures, and Thermal Behavior of Cu(hfacac) Complexes Derived from Ethanolamines.

Inorganic chemistry

Pinkas J, Huffman JC, Bollinger JC, Streib WE, Baxter DV, Chisholm MH, Caulton KG.
PMID: 11669939
Inorg Chem. 1997 Jul 02;36(14):2930-2937. doi: 10.1021/ic960370h.

A series of novel precursors for MOCVD of metallic copper have been synthesized and structurally characterized. These precursors are composed of Cu(hfacac)(2), which serves as a volatile source of Cu, and amino alcohols, which act as reductants and anchor...

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Pinkas J, Huffman JC, Bollinger JC, et al. Syntheses, Structures, and Thermal Behavior of Cu(hfacac) Complexes Derived from Ethanolamines. Inorg Chem. 1997;36(14):2930-2937doi: 10.1021/ic960370h.
Pinkas, J., Huffman, J. C., Bollinger, J. C., Streib, W. E., Baxter, D. V., Chisholm, M. H., & Caulton, K. G. (1997). Syntheses, Structures, and Thermal Behavior of Cu(hfacac) Complexes Derived from Ethanolamines. Inorganic chemistry, 36(14), 2930-2937. https://doi.org/10.1021/ic960370h
Pinkas, Jirí, et al. "Syntheses, Structures, and Thermal Behavior of Cu(hfacac) Complexes Derived from Ethanolamines." Inorganic chemistry vol. 36,14 (1997): 2930-2937. doi: https://doi.org/10.1021/ic960370h
Pinkas J, Huffman JC, Bollinger JC, Streib WE, Baxter DV, Chisholm MH, Caulton KG. Syntheses, Structures, and Thermal Behavior of Cu(hfacac) Complexes Derived from Ethanolamines. Inorg Chem. 1997 Jul 02;36(14):2930-2937. doi: 10.1021/ic960370h. PMID: 11669939.
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Effect of Ethanolamines on the Electroless Deposition of Copper on Functionalized Organic Surfaces.

Langmuir : the ACS journal of surfaces and colloids

Ellsworth AA, Walker AV.
PMID: 29526106
Langmuir. 2018 Apr 10;34(14):4142-4149. doi: 10.1021/acs.langmuir.7b03725. Epub 2018 Mar 27.

Electroless deposition (ELD) is widely used in industry to deposit metals because it is inexpensive and compatible with organic materials. The deposition rate and deposited film properties critically depend on the reducing agent, complexing agent, and bath pH and...

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Ellsworth AA, Walker AV. Effect of Ethanolamines on the Electroless Deposition of Copper on Functionalized Organic Surfaces. Langmuir. 2018;34(14):4142-4149doi: 10.1021/acs.langmuir.7b03725.
Ellsworth, A. A., & Walker, A. V. (2018). Effect of Ethanolamines on the Electroless Deposition of Copper on Functionalized Organic Surfaces. Langmuir : the ACS journal of surfaces and colloids, 34(14), 4142-4149. https://doi.org/10.1021/acs.langmuir.7b03725
Ellsworth, Ashley A, and Walker, Amy V. "Effect of Ethanolamines on the Electroless Deposition of Copper on Functionalized Organic Surfaces." Langmuir : the ACS journal of surfaces and colloids vol. 34,14 (2018): 4142-4149. doi: https://doi.org/10.1021/acs.langmuir.7b03725
Ellsworth AA, Walker AV. Effect of Ethanolamines on the Electroless Deposition of Copper on Functionalized Organic Surfaces. Langmuir. 2018 Apr 10;34(14):4142-4149. doi: 10.1021/acs.langmuir.7b03725. Epub 2018 Mar 27. PMID: 29526106.
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Ceria nanoparticles as heterogeneous catalyst for CO2 fixation by omega-aminoalcohols.

Chemical communications (Cambridge, England)

Juárez R, Concepción P, Corma A, García H.
PMID: 20411187
Chem Commun (Camb). 2010 Jun 21;46(23):4181-3. doi: 10.1039/c001955k. Epub 2010 Apr 21.

In contrast to gamma-Al(2)O(3), TiO(2), ZrO(2), MgO and Y(2)O(3), CeO(2) is a reusable catalyst for the reaction of CO(2) with omega-aminoalcohols to form cyclic carbamates; the highest yield (68%) was obtained for the preparation of N-alkyl 1,3-oxazolidin-2-ones from N-alkyl...

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Juárez R, Concepción P, Corma A, et al. Ceria nanoparticles as heterogeneous catalyst for CO2 fixation by omega-aminoalcohols. Chem Commun (Camb). 2010;46(23):4181-3doi: 10.1039/c001955k.
Juárez, R., Concepción, P., Corma, A., & García, H. (2010). Ceria nanoparticles as heterogeneous catalyst for CO2 fixation by omega-aminoalcohols. Chemical communications (Cambridge, England), 46(23), 4181-3. https://doi.org/10.1039/c001955k
Juárez, Raquel, et al. "Ceria nanoparticles as heterogeneous catalyst for CO2 fixation by omega-aminoalcohols." Chemical communications (Cambridge, England) vol. 46,23 (2010): 4181-3. doi: https://doi.org/10.1039/c001955k
Juárez R, Concepción P, Corma A, García H. Ceria nanoparticles as heterogeneous catalyst for CO2 fixation by omega-aminoalcohols. Chem Commun (Camb). 2010 Jun 21;46(23):4181-3. doi: 10.1039/c001955k. Epub 2010 Apr 21. PMID: 20411187.
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Low-Temperature Reductive Aminolysis of Carbohydrates to Diamines and Aminoalcohols by Heterogeneous Catalysis.

Angewandte Chemie (International ed. in English)

Pelckmans M, Vermandel W, Van Waes F, Moonen K, Sels BF.
PMID: 28892238
Angew Chem Int Ed Engl. 2017 Nov 13;56(46):14540-14544. doi: 10.1002/anie.201708216. Epub 2017 Oct 13.

Short amines, such as ethanolamines and ethylenediamines, are important compounds in today's bulk and fine chemicals industry. Unfortunately, current industrial manufacture of these chemicals relies on fossil resources and requires rigorous safety measures when handling explosive or toxic intermediates....

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Pelckmans M, Vermandel W, Van Waes F, et al. Low-Temperature Reductive Aminolysis of Carbohydrates to Diamines and Aminoalcohols by Heterogeneous Catalysis. Angew Chem Int Ed Engl. 2017;56(46):14540-14544doi: 10.1002/anie.201708216.
Pelckmans, M., Vermandel, W., Van Waes, F., Moonen, K., & Sels, B. F. (2017). Low-Temperature Reductive Aminolysis of Carbohydrates to Diamines and Aminoalcohols by Heterogeneous Catalysis. Angewandte Chemie (International ed. in English), 56(46), 14540-14544. https://doi.org/10.1002/anie.201708216
Pelckmans, Michiel, et al. "Low-Temperature Reductive Aminolysis of Carbohydrates to Diamines and Aminoalcohols by Heterogeneous Catalysis." Angewandte Chemie (International ed. in English) vol. 56,46 (2017): 14540-14544. doi: https://doi.org/10.1002/anie.201708216
Pelckmans M, Vermandel W, Van Waes F, Moonen K, Sels BF. Low-Temperature Reductive Aminolysis of Carbohydrates to Diamines and Aminoalcohols by Heterogeneous Catalysis. Angew Chem Int Ed Engl. 2017 Nov 13;56(46):14540-14544. doi: 10.1002/anie.201708216. Epub 2017 Oct 13. PMID: 28892238.
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Carbamate stabilities of sterically hindered amines from quantum chemical methods: relevance for CO2 capture.

Chemphyschem : a European journal of chemical physics and physical chemistry

Gangarapu S, Marcelis AT, Zuilhof H.
PMID: 24203852
Chemphyschem. 2013 Dec 02;14(17):3936-43. doi: 10.1002/cphc.201300820. Epub 2013 Nov 06.

The influence of electronic and steric effects on the stabilities of carbamates formed from the reaction of CO2 with a wide range of alkanolamines was investigated by quantum chemical methods. For the calculations, B3LYP, M11-L, MP2, and spin-component-scaled MP2...

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Gangarapu S, Marcelis AT, Zuilhof H. Carbamate stabilities of sterically hindered amines from quantum chemical methods: relevance for CO2 capture. Chemphyschem. 2013;14(17):3936-43doi: 10.1002/cphc.201300820.
Gangarapu, S., Marcelis, A. T., & Zuilhof, H. (2013). Carbamate stabilities of sterically hindered amines from quantum chemical methods: relevance for CO2 capture. Chemphyschem : a European journal of chemical physics and physical chemistry, 14(17), 3936-43. https://doi.org/10.1002/cphc.201300820
Gangarapu, Satesh, et al. "Carbamate stabilities of sterically hindered amines from quantum chemical methods: relevance for CO2 capture." Chemphyschem : a European journal of chemical physics and physical chemistry vol. 14,17 (2013): 3936-43. doi: https://doi.org/10.1002/cphc.201300820
Gangarapu S, Marcelis AT, Zuilhof H. Carbamate stabilities of sterically hindered amines from quantum chemical methods: relevance for CO2 capture. Chemphyschem. 2013 Dec 02;14(17):3936-43. doi: 10.1002/cphc.201300820. Epub 2013 Nov 06. PMID: 24203852.
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The Ability of Metabolomics to Discriminate Non-Small-Cell Lung Cancer Subtypes Depends on the Stage of the Disease and the Type of Material Studied.

Cancers

Kowalczyk T, Kisluk J, Pietrowska K, Godzien J, Kozlowski M, Reszeć J, Sierko E, Naumnik W, Mróz R, Moniuszko M, Kretowski A, Niklinski J, Ciborowski M.
PMID: 34282765
Cancers (Basel). 2021 Jul 01;13(13). doi: 10.3390/cancers13133314.

Identification of the NSCLC subtype at an early stage is still quite sophisticated. Metabolomics analysis of tissue and plasma of NSCLC patients may indicate new, and yet unknown, metabolic pathways active in the NSCLC. Our research characterized the metabolomics...

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Kowalczyk T, Kisluk J, Pietrowska K, et al. The Ability of Metabolomics to Discriminate Non-Small-Cell Lung Cancer Subtypes Depends on the Stage of the Disease and the Type of Material Studied. Cancers (Basel). 2021;13(13)doi: 10.3390/cancers13133314.
Kowalczyk, T., Kisluk, J., Pietrowska, K., Godzien, J., Kozlowski, M., Reszeć, J., Sierko, E., Naumnik, W., Mróz, R., Moniuszko, M., Kretowski, A., Niklinski, J., & Ciborowski, M. (2021). The Ability of Metabolomics to Discriminate Non-Small-Cell Lung Cancer Subtypes Depends on the Stage of the Disease and the Type of Material Studied. Cancers, 13(13), . https://doi.org/10.3390/cancers13133314
Kowalczyk, Tomasz, et al. "The Ability of Metabolomics to Discriminate Non-Small-Cell Lung Cancer Subtypes Depends on the Stage of the Disease and the Type of Material Studied." Cancers vol. 13,13 (2021). doi: https://doi.org/10.3390/cancers13133314
Kowalczyk T, Kisluk J, Pietrowska K, Godzien J, Kozlowski M, Reszeć J, Sierko E, Naumnik W, Mróz R, Moniuszko M, Kretowski A, Niklinski J, Ciborowski M. The Ability of Metabolomics to Discriminate Non-Small-Cell Lung Cancer Subtypes Depends on the Stage of the Disease and the Type of Material Studied. Cancers (Basel). 2021 Jul 01;13(13). doi: 10.3390/cancers13133314. PMID: 34282765; PMCID: PMC8268630.
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Fatty acid composition of milk phospholipids. II. Sheep, Indian buffalo and human milks.

Lipids

Morrison WR, Smith LM.
PMID: 17805746
Lipids. 1967 Mar;2(2):178-82. doi: 10.1007/BF02530919.

Phospholipids were isolated from sheep, Indian buffalo, and human milks, and their fatty acid compositions determined by gas chromatography. The specific distributions of fatty acids in phosphatidyl cholines (PC) and phosphatidyl ethanolamines (PE) were determined after phospholipase A hydrolysis.Fatty...

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Morrison WR, Smith LM. Fatty acid composition of milk phospholipids. II. Sheep, Indian buffalo and human milks. Lipids. 1967;2(2):178-82doi: 10.1007/BF02530919.
Morrison, W. R., & Smith, L. M. (1967). Fatty acid composition of milk phospholipids. II. Sheep, Indian buffalo and human milks. Lipids, 2(2), 178-82. https://doi.org/10.1007/BF02530919
Morrison, W R, and Smith, L M. "Fatty acid composition of milk phospholipids. II. Sheep, Indian buffalo and human milks." Lipids vol. 2,2 (1967): 178-82. doi: https://doi.org/10.1007/BF02530919
Morrison WR, Smith LM. Fatty acid composition of milk phospholipids. II. Sheep, Indian buffalo and human milks. Lipids. 1967 Mar;2(2):178-82. doi: 10.1007/BF02530919. PMID: 17805746.
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Stereoselective addition of alpha-sulfinyl carbanions to N-p-tolylsulfinylketimines: synthesis of optically pure 1,2,2'-trialkyl-2-aminoethanols.

The Journal of organic chemistry

García Ruano JL, Alemán J, del Prado M, Fernández I.
PMID: 15202901
J Org Chem. 2004 Jun 25;69(13):4454-63. doi: 10.1021/jo049666s.

The reactions of lithium carbanions derived from both enantiomers of methyl (1) and ethyl p-tolyl sulfoxide (2) with (S)-N-arylsulfinylketimines 3 and 4 took place in a highly stereoselective manner and good isolated yields. The configuration of the carbon bonded...

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García Ruano JL, Alemán J, del Prado M, et al. Stereoselective addition of alpha-sulfinyl carbanions to N-p-tolylsulfinylketimines: synthesis of optically pure 1,2,2'-trialkyl-2-aminoethanols. J Org Chem. 2004;69(13):4454-63doi: 10.1021/jo049666s.
García Ruano, J. L., Alemán, J., del Prado, M., & Fernández, I. (2004). Stereoselective addition of alpha-sulfinyl carbanions to N-p-tolylsulfinylketimines: synthesis of optically pure 1,2,2'-trialkyl-2-aminoethanols. The Journal of organic chemistry, 69(13), 4454-63. https://doi.org/10.1021/jo049666s
García Ruano, José L, et al. "Stereoselective addition of alpha-sulfinyl carbanions to N-p-tolylsulfinylketimines: synthesis of optically pure 1,2,2'-trialkyl-2-aminoethanols." The Journal of organic chemistry vol. 69,13 (2004): 4454-63. doi: https://doi.org/10.1021/jo049666s
García Ruano JL, Alemán J, del Prado M, Fernández I. Stereoselective addition of alpha-sulfinyl carbanions to N-p-tolylsulfinylketimines: synthesis of optically pure 1,2,2'-trialkyl-2-aminoethanols. J Org Chem. 2004 Jun 25;69(13):4454-63. doi: 10.1021/jo049666s. PMID: 15202901.
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Vaporization and Conversion of Ethanolamines used in Metalworking Operations.

Safety and health at work

Kim SB, Yoon CS, Park D.
PMID: 22953178
Saf Health Work. 2010 Dec;1(2):175-82. doi: 10.5491/SHAW.2010.1.2.175. Epub 2010 Dec 30.

OBJECTIVES: This study examined how ethanolamines (EAs) with the same functional alcohol group (HOCH(2)CH(2)), such as mono-EA (MEA), di-EA (DEA), and tri-EA (TEA), in water-based metalworking fluids (wbMWFs) are vaporized, condensed, and transformed by heat generated during metalworking.METHODS: Two...

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Kim SB, Yoon CS, Park D. Vaporization and Conversion of Ethanolamines used in Metalworking Operations. Saf Health Work. 2010;1(2):175-82doi: 10.5491/SHAW.2010.1.2.175.
Kim, S. B., Yoon, C. S., & Park, D. (2010). Vaporization and Conversion of Ethanolamines used in Metalworking Operations. Safety and health at work, 1(2), 175-82. https://doi.org/10.5491/SHAW.2010.1.2.175
Kim, Shin-Bum, et al. "Vaporization and Conversion of Ethanolamines used in Metalworking Operations." Safety and health at work vol. 1,2 (2010): 175-82. doi: https://doi.org/10.5491/SHAW.2010.1.2.175
Kim SB, Yoon CS, Park D. Vaporization and Conversion of Ethanolamines used in Metalworking Operations. Saf Health Work. 2010 Dec;1(2):175-82. doi: 10.5491/SHAW.2010.1.2.175. Epub 2010 Dec 30. PMID: 22953178; PMCID: PMC3430889.
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The Transition States for CO2 Capture by Substituted Ethanolamines.

Chemphyschem : a European journal of chemical physics and physical chemistry

Gangarapu S, Marcelis AT, Alhamed YA, Zuilhof H.
PMID: 26285916
Chemphyschem. 2015 Oct 05;16(14):3000-6. doi: 10.1002/cphc.201500511. Epub 2015 Aug 18.

Quantum chemical studies are used to understand the electronic and steric effects on the mechanisms of the reaction of substituted ethanolamines with CO2. SCS-MP2/6-311+G(2d,2p) calculations are used to obtain the activation energy barriers and reaction energies for both the...

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Gangarapu S, Marcelis AT, Alhamed YA, et al. The Transition States for CO2 Capture by Substituted Ethanolamines. Chemphyschem. 2015;16(14):3000-6doi: 10.1002/cphc.201500511.
Gangarapu, S., Marcelis, A. T., Alhamed, Y. A., & Zuilhof, H. (2015). The Transition States for CO2 Capture by Substituted Ethanolamines. Chemphyschem : a European journal of chemical physics and physical chemistry, 16(14), 3000-6. https://doi.org/10.1002/cphc.201500511
Gangarapu, Satesh, et al. "The Transition States for CO2 Capture by Substituted Ethanolamines." Chemphyschem : a European journal of chemical physics and physical chemistry vol. 16,14 (2015): 3000-6. doi: https://doi.org/10.1002/cphc.201500511
Gangarapu S, Marcelis AT, Alhamed YA, Zuilhof H. The Transition States for CO2 Capture by Substituted Ethanolamines. Chemphyschem. 2015 Oct 05;16(14):3000-6. doi: 10.1002/cphc.201500511. Epub 2015 Aug 18. PMID: 26285916.
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