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1

Max, Jean-Joseph, Michel Trudel, and Camille Chapados. "Infrared Titration of Aqueous Glycine." Applied Spectroscopy 52, no. 2 (1998): 226–33. http://dx.doi.org/10.1366/0003702981943284.

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The infrared (IR) spectra of glycine in aqueous solutions were obtained in the pH range 0.2 to 14 in order to determine the ionic distribution of the molecule as a function of pH by factor analysis (FA). After subtraction of the water bands, FA was used to separate the spectra of each ionic species and determine their real abundance. The p Ka values were retrieved from the volumetric titration as a function of pH and were used to obtain the theoretical abundance of each ionic species as a function of pH. These distribution curves were compared with the distribution curves obtained from IR. The
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2

Yang, Li Min, Ni Ni Jiang, and Zhen Ying Zhao. "Synthesis of Glycine Using Two-Step Reaction Approach in Alcohol and its Purification." Advanced Materials Research 396-398 (November 2011): 1711–15. http://dx.doi.org/10.4028/www.scientific.net/amr.396-398.1711.

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A two-step reaction approach in alcohol, which comprised a step of monochoroacetic acid reacting with ammonia and a step of the resulted ammonium monochloroacetate reacting with ammonia in presence of urotropine as catalyst, was employed to synthesize glycine. Operating conditions for synthesizing glycine and for purifying glycine product were investigated through intensive experimental approach. The optimal operating conditions for the whole process including synthesis and purification of glycine were obtained and tested. Under such conditions, for methanol as reaction media and for methanol
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3

Sharma, Shashi Kant, Poonam, and Nisha Sharma. "Viscometric and Conductometric Studies of Doxycycline Hyclate in Water, Aqueous Glycine and L-Alanine Solutions at Different Temperatures." Asian Journal of Chemistry 31, no. 11 (2019): 2557–66. http://dx.doi.org/10.14233/ajchem.2019.22215.

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To investigate the behaviour of doxycycline hyclate in water, aqueous glycine and aqueous L-alanine solutions, the viscometric and conductometric studies have been conducted at different temperatures. Viscosity data has been used to derive the Jones-Dole viscosity B-coefficient, temperature derivative of B-coefficient (dB/dT), viscosity B-coefficient of transfer (ΔtrB), free energy of activation of viscous flow per mole of solvent (Δμ1 o*) and solute (Δμ2o*) respectively, activation entropy (ΔS2o*) and activation enthalpy (ΔH2o*). Conductance data has been used to compute Walden product (Λm oη
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4

Remadevi, Rechana, Stuart Gordon, Xungai Wang, and Rangam Rajkhowa. "Investigation of the swelling of cotton fibers using aqueous glycine solutions." Textile Research Journal 87, no. 18 (2016): 2204–13. http://dx.doi.org/10.1177/0040517516665267.

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The treatment of cotton fibers using different chemicals, such as alkalis, acids and salt solutions, has captured the attention of researchers because of their important effects in dyeing, cross-linking and mercerizing processes. However, these agents are difficult in terms of process application and the requirement for major effluent treatment prior to discharge. In this paper, we report on the treatment of cotton in aqueous glycine solutions that were moderated, utilizing glycine’s amphoteric nature at different pH values, to enhance the morphological and moisture regain properties of cotton
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5

Remadevi, Rechana, Stuart Gordon, Xungai Wang, and Rangam Rajkhowa. "Tensile, physical, and microstructure properties of glycine treated cotton fibers." Textile Research Journal 88, no. 12 (2017): 1356–66. http://dx.doi.org/10.1177/0040517517700196.

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In this paper, the effect of aqueous glycine treatments at different pH on the tensile properties of cotton fibers is reported. The effects on linear density and X-ray diffraction crystallinity were also evaluated. Glycine treated fibers at alkaline pH (i.e. at pH 11) produced fibers with higher linear density than control (untreated) and glycine treatments at acidic pH. The same treatment also increased strain values in cotton fibers by as much as 36%. Interestingly, similar changes in strain were observed under acidic conditions, especially at pH4, although the changes were smaller. Specific
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6

G., Emerson Robin, Sankar U., Chithambarathanu T., and Selvarajan P. "GROWTH AND CHARACTERIZATION OF GAMMA GLYCINE CRYSTALS DOPED WITH POTASSIUM CARBONATE." International Journal of Advanced Trends in Engineering and Technology 2, no. 1 (2017): 122–30. https://doi.org/10.5281/zenodo.818044.

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Undoped and potassium carbonate doped gamma glycine crystals were grown by slow evaporation technique. Gamma glycine crystals were grown from the aqueous solution of sodium chloride. 1 mole% of potassium carbonate was added into the aqueous solution of gamma glycine to obtain the doped crystals. The harvested crystals were observed to be transparent, colourless and non-hygroscopic and these crystals crystallize in hexagonal structure. FTIR studies reveal the functional groups of the samples. NLO studies have been carried out to check the second harmonic generation (SHG). Also the grown crystal
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7

Wang, Xiaoling, Jing Li, and Yujiro Hayashi. "Oxidative peptide bond formation of glycine–amino acid using 2-(aminomethyl)malononitrile as a glycine unit." Chemical Communications 57, no. 35 (2021): 4283–86. http://dx.doi.org/10.1039/d1cc00130b.

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Amide linkage of glycine–amino acid was synthesized by coupling of substituted 2-(aminomethyl)malononitrile as a C-terminal glycine unit and N-terminal amine using CsOAc and O<sub>2</sub> in aqueous solution.
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8

Ishizuka, Shinnosuke, Oliver Reich, Grégory David, and Ruth Signorell. "Photo-induced shrinking of aqueous glycine aerosol droplets." Atmospheric Chemistry and Physics 23, no. 9 (2023): 5393–402. http://dx.doi.org/10.5194/acp-23-5393-2023.

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Abstract. Due to their small size, micrometer- and submicrometer-sized solution droplets can respond differently to physical and chemical processes compared with extended bulk material. Using optically trapped micrometer-sized aqueous glycine droplets, we demonstrate a photo-induced degradation of glycine upon irradiation with visible light, even though molecular glycine does not absorb light in the near-UV–vis range to any significant extent. This reaction is observed as photo-induced shrinking of the droplet, which we characterize by analyzing the elastic light scattering and the Raman spect
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9

Biswas, Aritri, and Bhabani S. Mallik. "Distinctive behavior and two-dimensional vibrational dynamics of water molecules inside glycine solvation shell." RSC Advances 10, no. 11 (2020): 6658–70. http://dx.doi.org/10.1039/c9ra10521b.

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We present a first principles molecular dynamics study of a deuterated aqueous solution of a single glycine moiety to explore the structure, dynamics, and two-dimensional infrared spectra of water molecules found in the solvation shell of glycine.
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10

ELSHAFEI, GAMAL M. S., and CHRISTINE A. PHILIP. "Interactions at an Alumina–Aqueous Glycine Interface: Characterization of Glycine-Modified Boehmite." Journal of Colloid and Interface Science 176, no. 1 (1995): 55–62. http://dx.doi.org/10.1006/jcis.1995.0007.

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11

Mosa, Walid F. A., Mohamed Z. M. Salem, Asma A. Al-Huqail, and Hayssam M. Ali. "Application of glycine, folic acid, and moringa extract as bio-stimulants for enhancing the production of ‘Flame Seedless’ grape cultivar." BioResources 16, no. 2 (2021): 3391–410. http://dx.doi.org/10.15376/biores.16.2.3391-3410.

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In this study, 130 uniform ‘Flame Seedless’ grape trees were selected for and subjected to the same cultural practices. The trees were sprayed three times, before flowering, during full bloom, and three weeks later with the following treatments: control (water only), 250, 500, and 750 ppm glycine; 50, 100, and 150 ppm folic acid (FA); 2%, 4%, and 6% leaf moringa aqueous extract (MLAE); and their combinations. High-performance liquid chromatography (HPLC) analysis of moringa leaf aqueous extract (MLAE) showed the presence of the phenolic compounds ellagic acid, vanillic acid, p-hydroxy benzoic
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12

Cuculić, Vlado, and Ivanka Pižeta. "Kinetics of iron(III) hydrolysis and precipitation in aqueous glycine solutions assessed by voltammetry." Collection of Czechoslovak Chemical Communications 74, no. 10 (2009): 1531–42. http://dx.doi.org/10.1135/cccc2009103.

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The kinetics of iron(III) hydrolysis and precipitation in aqueous glycine solutions were studied by cathodic voltammetry with a mercury drop electrode. The kinetics was controlled by changing ionic strength (I), pH and glycine concentration. Voltammetric measurements clearly showed formation and dissociation of a soluble Fe(III)–glycine complex, formation of iron(III) hydroxide and its precipitation. The rate constants of iron(III) hydroxide precipitation were assessed. The precipitation is first-order with respect to dissolved inorganic iron(III). The calculated rate constants of iron(III) pr
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13

Bushuev, Yuriy G., Svetlana V. Davletbaeva, and Oscar I. Koifman. "Molecular dynamics simulations of aqueous glycine solutions." CrystEngComm 19, no. 47 (2017): 7197–206. http://dx.doi.org/10.1039/c7ce01271c.

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14

Aksu, Serdar, and Fiona M. Doyle. "Electrochemistry of Copper in Aqueous Glycine Solutions." Journal of The Electrochemical Society 148, no. 1 (2001): B51. http://dx.doi.org/10.1149/1.1344532.

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15

Ghosh, Manik Kumer, Tae Hoon Choi, and Cheol Ho Choi. "Conformers of Zwitterionic Glycine in Aqueous Phase." Bulletin of the Korean Chemical Society 39, no. 2 (2018): 227–30. http://dx.doi.org/10.1002/bkcs.11372.

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16

Sabolová, Danica, Dana Mazagová, Pavol Kristian, Marián Antalík, Dušan Podhradský, and Ján Imrich. "Fluorescence Reagents for Labelling of Biomolecules. Part III. Study of the Reactions of 2- and 4-Substituted 9-Isothiocyanatoacridines with Glycine." Collection of Czechoslovak Chemical Communications 59, no. 7 (1994): 1682–90. http://dx.doi.org/10.1135/cccc19941682.

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Kinetics of nucleophilic addition reaction of 2- and 4-substituted 9-isothiocyanatoacridines I - VII with glycine in buffered aqueous dimethylformamide has been studied. The addition products, N-(9-acridinylthiocarbamoyl)glycines VIII - XIV, were characterized by IR, UV, 1H NMR, mass and fluorescence spectra. Derivatives VIII, X and XII exhibited higher fluorescence intensity than the starting isothiocyanates; the highest fluorescence was found for the unsubstituted compound X. The reaction mechanism is discussed on the basis of properties of the reaction products and kinetic characteristics.
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17

Крауклис, И. В., А. В. Тулуб, А. В. Головин та В. П. Челибанов. "Спектры комбинационного рассеяния света глицина и их моделирование в дискретно-континуальной модели сольватной оболочки воды". Журнал технической физики 128, № 10 (2020): 1488. http://dx.doi.org/10.21883/os.2020.10.50019.161-20.

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Annotation. The Raman spectra of glycine in crystalline form and in aqueous solution were obtained. The model of stabilization of the zwitterion state of glycine with a single water molecule connected by hydrogen bonds with the –COO- and –NH3+ groups is proposed. It is shown that quantum chemical calculations at the level of B3LYP/6-311++G(3df,2p) using the discrete-continuum model of water environment of glycine complexes Gly + n H2O (n = 1–3) provide a good description of the Raman spectra of glycine.
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18

Azhagan, S. Anbu Chudar, V. S. Kathiravan, and N. Sathiya Priya. "Crystallization, habit modification and control of nucleation of glycine polymorphs from aqueous solutions doped with magnesium sulfate impurity." Materials Science-Poland 36, no. 3 (2018): 483–93. http://dx.doi.org/10.2478/msp-2018-0075.

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AbstractThe influence of magnesium sulfate as an additive in the nucleation of α and γ-polymorphs of glycine crystallized from aqueous solutions has been explored for the first time. Based on crystallization experiments, it was concluded that lower concentration of magnesium sulfate, say less than 2 g/mL, favors α-nucleation sites, whereas the optimized concentration of magnesium sulfate impurity to yield -nucleation sites is 2 g/mL and above. The nucleation time span (in days), solubility and pH were measured for α- and γ-nucleation sites in the aqueous solutions doped with magnesium sulfate.
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19

Lu, Fei. "Selective Glycine Polymorph Crystallization by Using Silver Nanoparticles." Applied Mechanics and Materials 300-301 (February 2013): 1344–47. http://dx.doi.org/10.4028/www.scientific.net/amm.300-301.1344.

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In the present study, we demonstrate that silver colloid can serve as additive and induced the γ-form polymorph of glycine crystals in the netural solution. The silver colloid could quickly affect the packing arrangements of glycine molecules in aqueous solution leading to the competitive nucleation of the two polymorphs.
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20

Chen, Jie, Sheng Fang, Yu-Gang Shi, Yue-Cheng Meng, and Da-Hai Ren. "Effect of Hydroxylamine Sulfate on Volumetric Behavior of Glycine,L-Alanine, andL-Arginine in Aqueous Solution." Journal of Chemistry 2013 (2013): 1–5. http://dx.doi.org/10.1155/2013/481341.

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The apparent molar volumes of glycine,L-alanine, andL-arginine in aqueous hydroxylamine sulfate solutions have been determined atT=298.15 K and atmospheric pressure. The standard partial molar volumes,V20, corresponding partial molar volumes of transfer,ΔtrV20, and hydration numbers,NH, have been calculated for theseα-amino acids from the experimental data. TheΔtrV20values are positive for glycine,L-alanine, andL-arginine and are all increased with the increase in the concentration of hydroxylamine ions. These parameters obtained from the volumetric data are interpreted in terms of various mix
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21

Godahewa, Sahan M., and Aashani Tillekaratne. "An Insightful Approach to Understanding the Mechanism of Amino Acid Adsorption on Inorganic Surfaces: Glycine on Silica." Chemistry & Chemical Technology 17, no. 2 (2023): 253–61. http://dx.doi.org/10.23939/chcht17.02.253.

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The adsorption of glycine on amorphous silica surface has been studied to demonstrate the catalytic activity of silica surfaces towards the formation of peptide bonds on prebiotic earth. Silica nanoparticles were synthesized using a microwave assisted method and the nanoparticles were characterized using SEM. Glycine was adsorbed from aqueous solution on the nanoparticles and the adsorption behavior was characterized using FTIR and TGA analyses. At a glycine concentration of 0.5M and at pH=7, favorable adsorption was observed which obeyed the Langmuir isotherm model. From the FTIR characteriza
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22

Faraji, Mohammad, Karim Zare, Hossien Aghaei, Ali Farajtabar, Zouhair Asfari, and Farrokh Gharib. "Complexation of p-Sulphonato-calix[6]arene by Glycine, Glycyl-glycine, and Glycyl-glycyl-glycine in Aqueous Solution." Journal of Solution Chemistry 41, no. 11 (2012): 2074–81. http://dx.doi.org/10.1007/s10953-012-9924-2.

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23

Amalendu, Pal, and Kumar Suresh. "Apparent molar volumes of L-glycine in aqueous glucose solutions at different temperatures." Journal of Indian Chemical Society Vol. 79, Nov 2002 (2002): 866–70. https://doi.org/10.5281/zenodo.5847701.

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Department of Chemistry, Kurukshetra University, Kurukshetra-136 119, India E-mail : search@vidya.kuk.ernet.in&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; Fax : 91-1744-38277 <em>Manuscript received 22 April 2002, accepted 16 July 2002</em> Densities of L-glycine have measured at 288.15, 298.15 and 308.15 Kin aqueous glucose solutions ranging from pure water to 25% glucose by mass. From these densities, apparent molar volumes and limiting apparent molar volumes of L-glycine in various aqueous glucose solutions ban been evaluated. Transfer volumes and the infinite dilution par
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24

Amalendu, Pal, and Kumar Suresh. "Apparent molar volumes and adiabatic compressibilities of L-glycine in aqueous solutions of (CH3)4NI, NaBr and NaI at 298.15 K." Journal of Indian Chemical Society Vol. 81, Dec 2004 (2004): 1019–24. https://doi.org/10.5281/zenodo.5833155.

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Department of Chemistry, Kurukshetra University, Kurukshctra-136 119. India <em>E-mail</em> : palchem@sify.com <em>Manuscript received 27 July 2004</em> The densities and sound speeds of L-glycine in aqueous (CH<sub>3</sub>)<sub>4</sub>Nl, NaBr and NaI are reported at 298.15 K. These data are used to derive apparent molar volumes \(V_\phi\), and compressibilities \(K_{\phi,S}\)&middot; Partial molar volumes \(V^0_\phi\) and partial molar adiabatic compressibilities \(K^0_{\phi,S}\) of L-glycine at infinite dilution were evaluated. These v:Jlucs are required for calculating hydration number n<s
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25

T., Gladys Vimala, Bena Jothy E., and Selvarajan P. "CHARACTERIZATION OF GAMMA GLYCINE CRYSTALS GROWN USING RUBIDIUM CHLORIDE AS AN ADDITIVE (GGRC)." International Journal of Advanced Trends in Engineering and Technology 2, no. 1 (2017): 142–48. https://doi.org/10.5281/zenodo.823275.

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Gamma glycine crystals using rubidium chloride as an additive (GGRC) were grown at room temperature (31 <sup>o</sup>C). The saturated aqueous solution was prepared by dissolving glycine and rubidium chloride in 3:1 molar ratio and single crystals of gamma glycine were grown in a period of four weeks by slow evaporation method. The grown crystals of GGRC were characterized by single crystal XRD analysis, UV-visible transmittance studies, dielectric studies, mechanical studies, LDT studies, The Second Harmonic Generation (SHG) efficiency of the sample was measured using a Nd:YAG laser. The resul
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26

Surovtsev, N. V., S. V. Adichtchev, V. K. Malinovsky, et al. "Glycine phases formed from frozen aqueous solutions: Revisited." Journal of Chemical Physics 137, no. 6 (2012): 065103. http://dx.doi.org/10.1063/1.4739532.

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27

Hamad, Said, and C. Richard A. Catlow. "Are glycine cyclic dimers stable in aqueous solution?" CrystEngComm 13, no. 13 (2011): 4391. http://dx.doi.org/10.1039/c0ce00877j.

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28

Ramos, M. Elena, and F. Javier Huertas. "Adsorption of glycine on montmorillonite in aqueous solutions." Applied Clay Science 80-81 (August 2013): 10–17. http://dx.doi.org/10.1016/j.clay.2013.05.007.

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29

Shaikh, Muhammad Shuaib, Mohd Shariff Azmi, Mohammad Azmi Bustam, and Ghulam Murshid. "Study of CO2 Solubility in Aqueous Blend of Potassium Carbonate Promoted with Glycine." Applied Mechanics and Materials 625 (September 2014): 19–23. http://dx.doi.org/10.4028/www.scientific.net/amm.625.19.

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CO2solubility in aqueous potassium carbonate promoted with amino acid (glycine) was measured at temperatures (303.15, 313.15, and 333.15) K over the partial pressure range from 200 to 1000 kPa. The solubility of CO2is reported as the loading capacity of the CO2in the solvent, defined as (moles of CO2per mole of solvent). It was found that the loading capacity of the CO2increases by increasing the partial pressure of the CO2, whereas, it reduces with increase in temperature. CO2loading capacity in aqueous potassium carbonate (PC) promoted with glycine (GLY) was also compared with different solv
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30

Wu, Xiuxiu, Liang Gao, Jinxiang Liu, Hongfang Yang, Shoushan Wang, and Yuxiang Bu. "Excess electron reactivity in amino acid aqueous solution revealed by ab initio molecular dynamics simulation: anion-centered localization and anion-relayed electron transfer dissociation." Physical Chemistry Chemical Physics 17, no. 40 (2015): 26854–63. http://dx.doi.org/10.1039/c5cp03720d.

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31

Kitayama, Akira, Kazunori Kadota, Yuichi Tozuka, Atsuko Shimosaka, Mikio Yoshida, and Yoshiyuki Shirakawa. "Molecular aspects of glycine clustering and phase separation in an aqueous solution during anti-solvent crystallization." CrystEngComm 22, no. 31 (2020): 5182–90. http://dx.doi.org/10.1039/d0ce00542h.

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32

Khandelwal, Mahima, and Anil Kumar. "Electrochemical behavior of glycine-mediated N-doped reduced graphene oxide." New Journal of Chemistry 41, no. 16 (2017): 8333–40. http://dx.doi.org/10.1039/c7nj01662j.

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33

Hawtrey, Arthur O., Mario Ariatti, and Johann M. Van ZYL. "Polymerization of Glycine and L-Phenylalanine to Short Homooligopeptides by Nitrobiuret Under Aqueous Conditions." International Journal of Scientific Research 2, no. 6 (2012): 20–21. http://dx.doi.org/10.15373/22778179/june2013/7.

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34

Bujaroska, Biljana, Kiro Stojanoski, and Ljupco Pejov. "On the differential hydration of various forms of glycine in diluted aqueous solutions: a Monte Carlo study." Macedonian Journal of Chemistry and Chemical Engineering 31, no. 2 (2012): 295. http://dx.doi.org/10.20450/mjcce.2012.11.

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Rigid-body Monte Carlo simulations were carried out to study the differential hydration of zwitterionic and neutral forms of glycine in water. To account for the solute polarization by the rather polar liquid environment, initial geometries were chosen as minima on the MP2/aug-cc-pVTZ potential energy surfaces of neutral and zwitterionic glycine continuously solvated by water, implementing the polarizable continuum model (PCM) within the integral equation formalism (IEFPCM). The dynamically changing hydrogen bonding network between the solute and solvent molecules was analyzed imposing distanc
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35

Muneer, Mohammad, and Colin Boxall. "Photocatalyzed Degradation of a Pesticide Derivative Glyphosate in Aqueous Suspensions of Titanium Dioxide." International Journal of Photoenergy 2008 (2008): 1–7. http://dx.doi.org/10.1155/2008/197346.

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The photocatalytic degradation of a herbicide derivative, glyphosate [(N-phosphonomethyl) glycine] has been investigated in aqueous suspensions of titanium dioxide at different pH values. This compound was found to degrade more efficiently under alkaline pH, where no adsorption takes place on the surface of the catalyst in the dark. The main degradation route involves the cleavage of the P–C bond giving rise to sarcosine and glycine as the intermediate products formed during the photooxidation process.
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36

Zyablov, A. N., A. V. Kalach, and V. F. Selemenev. "Determination of glycine and glycyl-glycine in aqueous and alcoholic solutions using a piezoresonance sensor." Journal of Analytical Chemistry 61, no. 12 (2006): 1209–11. http://dx.doi.org/10.1134/s106193480612015x.

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37

Isaeva, V. A., G. A. Gamov, and K. V. Grazhdan. "Protolytic Equilibrium of Glycine and Glycylglycine: Structure of Ionic Forms and Solvent Effect on the Thermodynamic Parameters of Processes." Журнал физической химии 97, no. 12 (2023): 1718–28. http://dx.doi.org/10.31857/s0044453723120142.

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Quantum-chemical calculations of the structure of the molecular forms of glycine and glycylglycine and conjugate ionic forms have been performed. Our own and published data on the thermodynamic characteristics of the reactions of acid–base interactions of glycine and glycylglycine in aqueous organic solutions are summarized, and the influence of the composition of mixed solvents on the acid dissociation constant of the amide group in the copper(II) peptide complex is considered.
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38

Jabbari, Morteza, and Farrokh Gharib. "Equilibrium studies of triphenyltin(IV) complexes with glycine, glycyl-glycine, and glycyl-glycyl-glycine in different aqueous solutions of ethanol." Canadian Journal of Chemistry 88, no. 9 (2010): 877–85. http://dx.doi.org/10.1139/v10-067.

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The protonation equilibria of glycine (gly), glycyl-glycine (gly-gly), and glycyl-glycyl-glycine (gly-gly-gly) and their formation constants with triphenyltin(IV) chloride were studied over a wide pH range (pH 1–11), using a combination of spectrophotometric and potentiometric methods at constant temperature (25 °C), different ethanol–water mixtures (50%–80%, v/v), and constant ionic strength (0.1 mol dm–3 NaClO4). Least-squares regression calculations are consistent with the formation of ph3SnHL+, ph3SnL, and ph3SnH–1L– complex species, where L– represents the fully dissociated form of each l
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39

Ranu, Banerjee, M. Nandi M., and Ranjana. "Inhibition effect of glycine derivatives on corrosion of brass in 0.6 M aqueous sodium chloride solution." Journal of Indian Chemical Society Vol. 88, Sep 2011 (2011): 1389–98. https://doi.org/10.5281/zenodo.5787925.

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Department of Chemistry, National Institute of Technology, Durgapur-713 209, West Bengal. India <em>E-mail </em>: murarimohan_nandi@yahoo.co. in <em>Manuscript received 02 June 2010, accepted 31 December 2010</em> The inhibition effect of glycine (1), N-benzenesulphonyl glycine (2), N-henzoyl glycine (3), N-benzenesulphonamidomethylbenzimidazole (4) and <em>N</em>-ben10ylmethylbenzimidazole (5) towards the corrosion of brass in 0.6 <em>M</em> aqueous sodium chloride solution has been studied using potentiodynamic polarization and electrochemical impedance spectroscopy. The inhibition efficienc
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40

Md, Imad Uddin, Kalyani D, Tejasri N, et al. "Green Synthesis and Characterization of Silver Nanoparticles using Glycine Max L. Seed Extract and their Antiepileptic Activity in Rats." International Journal of Pharmaceutical Sciences and Nanotechnology 10, no. 6 (2017): 3909–14. http://dx.doi.org/10.37285/ijpsn.2017.10.6.6.

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Glycine max is an edible oil seed and commonly known as Soybean. In this study, we report green, inexpensive method for synthesis of silver nanoparticles (SNPs) using of Glycine max seeds aqueous extract. Synthesized SNPs were characterized by UV-Visible spectroscopy (UV), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), X-ray diffraction (XRD) and Zeta Potential. Formation of Silver Nanoparticles from Glycine max Aqueous Extract (SNGMAE), indicated by appearance of dark brown color. UV depicted peak at 440nm, FTIR showed various functional groups present in
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41

Herrero, Roberto, Isabel Brandariz, Sarah Fiol, and Manuel Sastre de Vicente. "Pitzer and Thermodynamic Parameters of Triethanolamine and Glycine in Aqueous Saline Solutions." Collection of Czechoslovak Chemical Communications 58, no. 6 (1993): 1269–78. http://dx.doi.org/10.1135/cccc19931269.

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On the basis of the ionic strength dependence of the equilibrium constant (pK*) of thriethanolamine (TEA) and glycine, the ionic interaction parameters of the species involved in the equilibria TEAH+ ↔ TEA + H+ (for TEA), AH2+ ↔ AH + H+ and AH ↔ A- + H+ (for glycine) in aqueous solutions of KCl and KNO3, respectively, were determined using the Pitzer equations. Values of pK* were expressed on both the molarity and the molality scale at various temperatures and values of thermodynamic quantities ∆G0, ∆H0 and ∆S0 ascertained, for TEA.
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42

Ershov, O. V., M. Yu Ievlev, V. A. Tafeenko, and O. E. Nasakin. "Glycine catalyzed diastereoselective domino-synthesis of 6-imino-2,7-dioxabicyclo[3.2.1]octane-4,4,5-tricarbonitriles in water." Green Chemistry 17, no. 8 (2015): 4234–38. http://dx.doi.org/10.1039/c5gc00909j.

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The first example of glycine catalyzed directly synthesis of 6-imino-2,7-dioxabicyclo[3.2.1]octane-4,4,5-tricarbonitriles in aqueous medium was described, giving products in excellent yields and up to excellent diastereoselectivities.
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43

Civera, Monica, Arianna Fornili, Maurizio Sironi, and Sandro L. Fornili. "Molecular dynamics simulation of aqueous solutions of glycine betaine." Chemical Physics Letters 367, no. 1-2 (2003): 238–44. http://dx.doi.org/10.1016/s0009-2614(02)01707-4.

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44

Shikata, Toshiyuki. "Dielectric Relaxation Behavior of Glycine Betaine in Aqueous Solution." Journal of Physical Chemistry A 106, no. 34 (2002): 7664–70. http://dx.doi.org/10.1021/jp020957j.

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45

Nummela, Mikko, Hannes Raebiger, Daisuke Yoshida, and Masanori Tachikawa. "Positron Binding Properties of Glycine and Its Aqueous Complexes." Journal of Physical Chemistry A 120, no. 23 (2016): 4037–42. http://dx.doi.org/10.1021/acs.jpca.6b01780.

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46

Yu, Li, Xingen Hu, Ruisen Lin, Shuang Shao, and Honglin Zhang. "Enthalpic interactions of glycine in aqueous sodium halide solutions." Thermochimica Acta 378, no. 1-2 (2001): 1–8. http://dx.doi.org/10.1016/s0040-6031(01)00592-5.

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47

Hua, Tianyi, Celymar Valentín-Valentín, Omar Gowayed, Seongha Lee, Bruce A. Garetz, and Ryan L. Hartman. "Microfluidic Laser-Induced Nucleation of Supersaturated Aqueous Glycine Solutions." Crystal Growth & Design 20, no. 10 (2020): 6502–9. http://dx.doi.org/10.1021/acs.cgd.0c00669.

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48

Lu, Jie, Xiu-Juan Wang, Xia Yang, and Chi-Bun Ching. "Solubilities of Glycine and Its Oligopeptides in Aqueous Solutions." Journal of Chemical & Engineering Data 51, no. 5 (2006): 1593–96. http://dx.doi.org/10.1021/je0600754.

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49

Campo, Mario G. "Molecular dynamics simulation of glycine zwitterion in aqueous solution." Journal of Chemical Physics 125, no. 11 (2006): 114511. http://dx.doi.org/10.1063/1.2352756.

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50

Tuñón, Iñaki, Estanislao Silla, and Manuel F. Ruiz-López. "On the tautomerization process of glycine in aqueous solution." Chemical Physics Letters 321, no. 5-6 (2000): 433–37. http://dx.doi.org/10.1016/s0009-2614(00)00365-1.

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