Диссертация (Имидазолиевые ионные жидкости в качестве экстрагентов, модификаторов кварцевого капилляра и хиральных селекторов в капиллярном электрофорезе), страница 19

2009 V. 100 P. 6385.153.Li M., Pham P.J., Wang T., Pittman Jr. C.U., Li T. Selective extraction andenrichment of polyunsaturated fatty acid methyl esters from fish oil by novel πcomplexing sorbents // Sep. Purif. Technol. 2009 V. 66 P. 1.154.Tian M., Yan H., Row K.H. Solid-Phase Extraction of Caffeine andTheophylline from Green Tea by a New Ionic Liquid-Modified Functional PolymerSorbent // Anal.

Lett. 2010 V. 43 P. 110.155. Ruiz-Palomero C., Soriano M.L., Valcarce M. Ternary composites ofnanocellulose, carbonanotubes and ionic liquids as new extractants for directimmersion single drop microextraction // Talanta 2014 V. 125 P. 72.156. Yang J., Wei H., Teng X., Zhang H., Shi Y. Dynamic Ultrasonic NebulisationExtraction Coupled with Headspace Ionic Liquid-based Single-drop Microextractionfor the Analysis of the Essential Oil in Forsythia suspensa// Phytochem. Anal. 2014148V.

25 P. 178.157. Mokhtar S.U., Chin S., Vijayaraghavan R., Macfarlane D.R., Drummer O.H.,Marriott P.J. Direct ionic liquid extractant injection for volatile chemical analysis – agas chromatography sampling technique// Green Chem. 2015 V. 17 P. 573.158.Li Z., Chen F., Wang X., Wang C. Ionic liquids dispersive liquid –liquidmicroextraction and high-performance liquid chromatographic determination ofirbesartanand valsartan in human urine // Biomed. Chromatogr. 2013 V. 27 P. 254.159.Xu X., Liu Z., Zhao X., Su R., Zhang Y., Shi J., Zhao Y., Wu L., Ma Q., Zhou X.,Zhang H., Wang Z. Ionic liquid-based microwave-assisted surfactant-improveddispersive liquid-liquid microextraction and derivatization of aminoglycosides in milksamples // J.

Sep. Sci. 2013 V. 36 P. 585.160. Chen S., Sun Y., Chao J., Cheng L., Chen Y., Liu J. Dispersive liquid–liquidmicroextraction of silver nanoparticles in water using ionic liquid 1-octyl-3methylimidazolium hexafluorophosphate //J. Environ. Sci. 2016 V. 41 P. 211.161. Li G., Wang L., Fei T., Liu H., Wu D., Zheng S. Ionic Liquid-BasedUltrasonic-Assisted Extraction Combined with HPLC–MS/MS for the Determinationof Seven Mercapturic Acids in Human Urine // Chromatographia 2015 V.

78 P. 641.162. Wang L., Zhang D., Xu X., Zhang L. Application of ionic liquid-baseddispersiveliquidphasemicroextractionforhighlysensitivesimultaneousdetermination of three endocrine disrupting compounds in food packaging // FoodChemistry 2016 V. 197 P. 754.163. De Boeck, et al. Development and validation of a fast ionic liquid-baseddispersive liquid–liquid microextraction procedure combined with LC–MS/MSanalysis for the quantification of benzodiazepines and benzodiazepine-like hypnoticsinwholeblood//ForensicSci.Int.2017http://dx.doi.org/10.1016/j.forsciint.2016.12.026149164. Zhang R., Cheng X., Guo J., Zhang H., Hao X. Comparison of Two IonicLiquid-BasedPretreatmentMethodsforThreeSteroids’SeparationandDetermination in Water Samples by HPLC // Chromatographia 2017 V.80 P. 237.165.

Magiera S., Sobik A. Ionic liquid-based ultrasound-assisted extraction coupledwith liquid chromatography to determine isoflavones in soy foods // Journal of FoodComposition and Analysis 2017 V. 57 P. 94.166.Ebrahimpour B., Yamini Y., Esrafili A. Acid-induced homogenous liquid-phase microextraction: Application of medium-chain carboxylic acid as extractionphase //J. Sep. Sci. 2013 V. 36 P. 1493.167.

Hosseini M.H., Rezaee M., Akbarian S., Mizani F., Pourjavid M.R., Arabieh M.Homogeneous liquid–liquid microextraction via flotation assistance for rapid andefficient determination of polycyclic aromatic hydrocarbons in water samples // Anal.Chim. Acta 2013 V. 762 P. 54.168. Xiao Y., Zhang H. Homogeneous ionic liquid microextraction of the activeconstituents from fruits of Schisandra chinensis and Schisandra sphenanthera// Anal.Chim. Acta 2012 V.

712 P. 78.169. Wang Z., He M., Jiang C., Zhang F., Du S., Feng W., Zhang H. Matrix solidphase dispersion coupled with homogeneous ionic liquid microextraction for thedetermination of sulfonamides inanimal tissues using high-performance liquidchromatography // J. Sep. Sci. 2015 V. 38 P. 4127.170.Liu Zh., Yu W., Zhan H., Gu F., Jin X. Salting-out homogenous extractionfollowed by ionic liquid/ionic liquid liquid–liquid micro-extraction for determinationof sulfonamides in blood by high performance liquid chromatography // Talanta 2016V.

161 P. 748.171. Han D., Row K H. Recent Applications of Ionic Liquids in SeparationTechnology// Molecules 2010 V. 15 P. 2405.150172. Vičkačkaitė V., Padarauskas A. Ionic liquids in microextraction techniques //Cent. Eur. J. Chem. 2012 V. 10 (3) P. 652.173. Vidal L., Riekkola M.-L., Canals A. Ionic liquid-modified materials for solidphase extraction and separation: A review// Anal. Chim. Acta 2012 V.

715 P. 19.174. Trujillo-Rodriguez M.J., Rocio-Bautista Pr., Pino V., Afonso A.M. Ionic liquidsin dispersive liquid-liquid microextraction// Trends in Analytical Chemistry 2013 V.51 P. 87.175. Marcinkowski Ł., Pena-Pereira Fr., Kloskowski A., Namiesnik J. Opportunitiesand shortcomings of ionic liquids in single-drop microextraction // Trends inAnalytical Chemistry 2015 V.

72 P. 153.176. Alopina E.V., Dobryakov Yu. G., Safonova E.A., Smirnova N.A. L-Proline basedalkylmethylimidazoliumphysicochemicalionicliquidspropertiesof[Cnmim][L-Pro]:theirsynthesisaqueousandsomesolutions//Актуальные вопросы биологической физики и химии 2016 Номер 1-2 С. 173.177. Dobryakov, Y; Tuma, D.; Maurer, G. Activity Coefficients at Infinite Dilutionof Alkanols in the Ionic Liquids 1-Butyl-3-methylimidazolium Hexafluorophosphate,1-Butyl-3-methylimidazolium Methyl Sulfate, and 1-Hexyl-3-methylimidazoliumBis(trifluoromethylsulfonyl) Amide Using the Dilutor Technique. // J. Chem.

Eng.Data 2008 V. 53 P. 2154.178. Alopina E.V., E.A. Safonova, I.B. Pukinsky, N.A. Smirnova. Liquid−LiquidEquilibria in Aqueous Mixtures of Alkylmethylimidazolium Glutamate withPotassiumCarbonateandSomePhysicochemicalPropertiesofAqueous[Cnmim][Glu] (n = 4, 6, 8) Solutions // J. Chem. Eng. Data 2016 V. 61 P. 2013.179. Карцова Л.А., Бессонова Е.А., Сидорова А.А., Тверьянович И.А., КазаковВ.А., Великанова Л.И. Определение адреналина, норадреналина, дофамина151методом капиллярного электрофореза // Журнал прикл. химии 2004 т. 77.с.1164.180.

Колобова Е.А., Карцова Л.А., Бессонова Е.А. Применение ионныхжидкостей на основе имидазолия при электрофоретическом определенииаминокислот в моче // Журнал аналитической химии 2015 Т.70 № 11 С.1179.181. Колобова Е.А., Карцова Л.А., Бессонова Е.А. «Ионные жидкости на основеимидазолия в качестве модификаторов электрофоретических систем приопределении биогенных аминов и стероидных гормонов» // Вестник СПбГУ.Сер. 4. Т. 2. (60).

2015. Вып. 3. С.175.182. Albers E., Müller B.W. Complexation of steroid hormones with cyclodextrinderivatives: substituent effects of the guest molecule on solubility and stability inaqueous solution // J. Pharm. Sci. 1992 V.81 P. 756.183. Kolobova Е.А., Kartsova L.A., Bessonova E.A., Alopina E.V., Safonova E.A.The possibilities of amino acid ionic liquids as a chiral selectors at separation ofenantiomers of amino acids and β-blockers // Journal of Chromatography &Separation Techniques, 2016, 7:5(Suppl).184.

Fitts J.P., Persson P., Brown G.E.Jr., Parks G.A. Structure and Bonding of Cu(II)–Glutamate Complexes at the g-Al2O3–Water Interface // Journal of Colloid andInterface Science 1999 V. 220 P. 133.185. Schmid M.G., Lecnic O., Sitte U., Gübitz G. Application of ligand-exchangecapillary electrophoresis to the chiral separation of α-hydroxy acids and β-blockers.//J. Chromatogr. A.

2000. V. 875. P. 307.186. КарцоваЛ.А.,БессоноваЕ.А.,ОбъедковаЕ.В.,ДаванковВ.А.Использование сверхсшитого полистирола как сорбента для твердофазнойэкстракции при анализе лекарств в биологических объектах методом152высокоэффективной тонкослойной хроматографии (ВЭТСХ)// Сорбционные ихроматографические процессы 2010 Т.10. Вып. 1 С. 5.187. Zhang Q., Qi X., Chunlai Feng, Tong Sh., Rui M. Three chiral ionic liquids asadditives for enantioseparation incapillary electrophoresis and their comparison withconventionalmodifiers // J. Chromatogr. A 2016 V.

1462 P. 146.153ПРИЛОЖЕНИЕ 1. ЯМР-спектры [C2MIm][L-Pro] на ядрах 1Н и 13С.1H ЯМР-спектр [C2MIm][L-Pro] (400 МГц, D2O): δ = 1.38~1.41 (t, 3H), 1.69~1.71 (m, 4H), 2.06~2.08 (m, 1H) 2.79~2.81 (m, 1H), 3.033.04 (m, 1H), 3.52~3.54 (m, 1H), 3.80 (s，3H), 4.10~ 4.16 (t, 2H), 7.33 (d, 1H)，7.40 (d, 1H) ppm.15413C ЯМР-спектр [C2MIm][L-Pro] (D2O): δ = 180.06, 135.64, 123.39, 121.80, 61.44, 46.0, 44.71, 35.54, 30.28, 24.77, 14.44 ppm.1553.001.2231.2040.8370.8180.8002.021.7451.7261.7011.6961.6851.300.115.911.243.0423.0333.0142.8002.7741.244.7064.1114.0934.0753.7903.5443.5293.5243.5092.032.931.191.837.3827.3777.3347.329ПРИЛОЖЕНИЕ 2. ЯМР-спектры [C4MIm][L-Pro] на ядрах 1Н и 13С.1H ЯМР-спектр [C4MIm][Pro] (400 МГц, D2O): δ = 0.80~0.84 (t, 3H), 1.20~1.22 (m, 2H), 1.69~1.75 (m, 6H), 2.00~2.12 (m, 1H),2.77~2.80 (m, 1H), 3.01~4.09 (m, 1H), 3.51~3.54 (m, 1H), 3.79 (s, 3H), 4.08~ 4.11 (t, 2H), 7.33 (d, 1H)，7.38 (d, 1H) ppm.15613C ЯМР-спектр [C4MIm][L-Pro]: δ = 180.25, 135.59, 123.43, 122.16, 61.5, 49.22, 46.00, 35.57, 31.22, 30.31, 24.79, 18.72, 12.61 ppm.157ПРИЛОЖЕНИЕ 3.