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Journal articles on the topic 'Mass Spectrometric Study'

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Author: Grafiati

Published: 7 September 2023

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1

Nakajima, Kunihisa, Yasuo Arai, and Toshiyuki Yamashita. "Mass-spectrometric study of PuCd2." Journal of Physics and Chemistry of Solids 66, no. 2-4 (February 2005): 639–42. http://dx.doi.org/10.1016/j.jpcs.2004.06.072.

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2

Pleshkova, A. P., Yu A. Molodtsova, Yu A. Pozdnyakova, O. I. Shchegolikhina, M. V. Nevezhin, A. B. Zachernyuk, and A. M. Muzafarov. "Mass spectrometric study of organocyclosiloxanes." Russian Chemical Bulletin 56, no. 9 (September 2007): 1809–12. http://dx.doi.org/10.1007/s11172-007-0281-z.

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3

Miranda, René, Gabriel A. Arroyo, Luis Velasco, Francisco J. Pérez, and Francisco Delgado. "Mass spectrometric study of benzylidenecyanoacetamides." Rapid Communications in Mass Spectrometry 13, no. 1 (January 15, 1999): 33–38. http://dx.doi.org/10.1002/(sici)1097-0231(19990115)13:1<33::aid-rcm444>3.0.co;2-s.

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4

Zavilopulo, A. N., M. I. Mykyta, and O. B. Shpenik. "Mass-spectrometric study of coal gases." Technical Physics Letters 37, no. 8 (August 2011): 763–66. http://dx.doi.org/10.1134/s1063785011080293.

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5

Boltalina, Olga V., Nadezhda A. Galeva, Vitaliy Yu Markov, Andrey Ya Borschevskii, Igor D. Sorokin, Lev N. Sidorov, Arkadij Popovich, and Dusan Zigon. "A mass spectrometric study of C60F48." Mendeleev Communications 7, no. 5 (January 1997): 184–86. http://dx.doi.org/10.1070/mc1997v007n05abeh000809.

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6

Lozinskii, M. O., Yu A. Fialkov, V. S. Khomenko, L. I. Krasovskaya, T. A. Rasshinina, and V. V. Berenblit. "Mass spectrometric study of fluorinated ?-diketones." Theoretical and Experimental Chemistry 21, no. 2 (1985): 174–79. http://dx.doi.org/10.1007/bf00945192.

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7

Ruscic, B., and J. Berkowitz. "Photoionization mass spectrometric study of Si2H6." Journal of Chemical Physics 95, no. 4 (August 15, 1991): 2407–15. http://dx.doi.org/10.1063/1.460946.

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8

Ruscic, B., E. H. Appelman, and J. Berkowitz. "Photoionization mass spectrometric study of CH3OF." Journal of Chemical Physics 95, no. 11 (December 1991): 7957–61. http://dx.doi.org/10.1063/1.461325.

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9

Rogowska, Agnieszka, Małgorzata Szultka-Młyńska, Basem Kanawati, Paweł Pomastowski, Adrian Arendowski, Adrian Gołębiowski, Phillipe Schmitt-Kopplin, et al. "Advanced Mass Spectrometric Techniques for the Comprehensive Study of Synthesized Silicon-Based Silyl Organic Compounds: Identifying Fragmentation Pathways and Characterization." Materials 16, no. 9 (May 6, 2023): 3563. http://dx.doi.org/10.3390/ma16093563.

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The primary objective of this study was to synthesize and characterize novel silicon-based silyl organic compounds in order to gain a deeper understanding of their potential applications and interactions with other compounds. Four new artificial silyl organic compounds were successfully synthesized: 1-O-(Trimethylsilyl)-2,3,4,6-tetra-O-acetyl-β-d-glucopyranose (compound 1), 1-[(1,1-dimethylehtyl)diphenylsilyl]-1H-indole (compound 2), O-tert-butyldiphenylsilyl-(3-hydroxypropyl)oleate (compound 3), and 1-O-tert-Butyldiphenylsilyl-myo-inositol (compound 4). To thoroughly characterize these synthesized compounds, a combination of advanced mass spectrometric techniques was employed, including nanoparticle-assisted laser desorption/ionization mass spectrometry (NALDI-MS), Fourier-transform ion cyclotron resonance mass spectrometry (FT-ICR-MS), and triple quadrupole electrospray tandem mass spectrometry (QqQ ESI-MS/MS). These analytical methods enabled the accurate identification and characterization of the synthesized silyl organic compounds, providing valuable insights into their properties and potential applications. Furthermore, the electrospray ionization–Fourier transform ion cyclotron resonance–tandem mass spectrometry (ESI-FT-ICR-MS/MS) technique facilitated the proposal of fragmentation pathways for the ionized silyl organic compounds, contributing to a more comprehensive understanding of their behavior during mass spectrometric analysis. These findings suggest that mass spectrometric techniques offer a highly effective means of investigating and characterizing naturally occurring silicon-based silyl organic compounds, with potential implications for advancing research in various fields and applications in different industries.

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10

Masur, Monika, Hans-Fr Grützmacher, Helmut Münster, and Herbert Budzikiewicz. "Mass spectrometric fragmentation of the tautomers of 1,3-diketones. A gas chromatographic/mass spectrometric study." Organic Mass Spectrometry 22, no. 8 (August 1987): 493–500. http://dx.doi.org/10.1002/oms.1210220804.

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11

Shornikov, S. I. "Mass-Spectrometric Study of Evaporation of Perovskite." Russian Journal of Physical Chemistry A 93, no. 6 (June 2019): 1024–31. http://dx.doi.org/10.1134/s0036024419060293.

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12

Enami, Shinichi. "Mass Spectrometric Study on Heterogeneous Radical Reactions." Molecular Science 11, no. 1 (2017): A0090. http://dx.doi.org/10.3175/molsci.11.a0090.

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13

Isaev, Sergei D., Nataliya F. Karpenko, Aleksandr G. Yurchenko, Luděk Vodička, Valentin I. Kadentsev, and Pavel Zachař. "Compounds of aziadamantane type: Mass spectrometric study." Collection of Czechoslovak Chemical Communications 54, no. 3 (1989): 691–98. http://dx.doi.org/10.1135/cccc19890691.

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Azi and hydrazi derivatives of adamantane,adamantanone and diamantane were studied by mass spectrometry. The EI spectra of azi derivatives lack completely molecular ions; the presence of abundant dehydroadamantane or dehydrodiamantane ions corresponds to elimination of nitrogen molecule from the molecular ion. Comparison of the EI ionization with photolysis or pyrolysis allowed to deduce some analogies and to suggest the mechanism of decomposition of the molecular ion.

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14

Blagin, A. V., D. P. Valyukhov, L. S. Lunin, R. V. Pigulev, and I. M. Khabibulin. "Mass spectrometric study of GaInPAsSb/GaSb heterostructures." Inorganic Materials 44, no. 8 (August 2008): 793–95. http://dx.doi.org/10.1134/s0020168508080013.

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15

Shevtsov, V. K., A. V. Varlamov, Nazrul Islam, and N. S. Prostakov. "Mass-spectrometric study of nitro-substituted dihydrosilaazaanthrones." Chemistry of Heterocyclic Compounds 21, no. 4 (April 1985): 445–49. http://dx.doi.org/10.1007/bf00504409.

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16

Gładyszewski, L. "Mass spectrometric study of ion thermoemission noise." International Journal of Mass Spectrometry and Ion Processes 69, no. 2 (March 1986): 185–90. http://dx.doi.org/10.1016/0168-1176(86)87032-x.

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17

Shevtsov, V. K., A. V. Varlamov, S. G. Poshivalov, L. A. Simonova, and N. S. Prostakov. "Mass-spectrometric study of benzopyridosilaazepines and -azepinones." Chemistry of Heterocyclic Compounds 22, no. 5 (May 1986): 577–80. http://dx.doi.org/10.1007/bf00519544.

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18

Deng, R., A. Clegg, and O. Echt. "Mass spectrometric study of K+ + C60 collisions." International Journal of Mass Spectrometry 223-224 (January 2003): 695–701. http://dx.doi.org/10.1016/s1387-3806(02)00941-7.

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19

Golovenko, N. Ya, V. G. Zin'kovskii, G. B. Vasilinin, E. A. Stankevich, S. A. Andronati, and O. S. Timofeev. "Mass spectrometric study of metabolites of bromonordiazepam." Pharmaceutical Chemistry Journal 22, no. 7 (July 1988): 503–7. http://dx.doi.org/10.1007/bf00763515.

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20

Pei, Weiwei, Peng Wang, and Meiyu He. "Mass spectrometric study of ?-aryl-?,�?-diethoxy-?, ?-butenolides." Rapid Communications in Mass Spectrometry 14, no. 1 (January 15, 2000): 1–5. http://dx.doi.org/10.1002/(sici)1097-0231(20000115)14:1<1::aid-rcm821>3.0.co;2-d.

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21

He, Jiangtao, Aihua Nie, Meiyu He, Xiaoran He, Zhenpei Yu, Xiulin Ye, and Qiyi Xing. "Mass spectrometric study of six cyclic esters." Rapid Communications in Mass Spectrometry 14, no. 9 (May 15, 2000): 765–71. http://dx.doi.org/10.1002/(sici)1097-0231(20000515)14:9<765::aid-rcm941>3.0.co;2-f.

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22

Duarte, M. Filomena, Filipa Martins, M. Tereza Fernandez, G. John Langley, Paula Rodrigues, M. Teresa Barros, and M. Lourdes Costa. "Mass spectrometric study of aliphatic?-carbonyl azides." Rapid Communications in Mass Spectrometry 17, no. 9 (2003): 957–62. http://dx.doi.org/10.1002/rcm.1005.

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23

Saad, Esmat F., Nagwa M. Hamada, Saber M. Sharaf, Samir K. El Sadany, Adel M. Moussa, and Mohamed Elba. "Mass spectrometric study of some pyrazoline derivatives." Rapid Communications in Mass Spectrometry 12, no. 13 (July 15, 1998): 833–36. http://dx.doi.org/10.1002/(sici)1097-0231(19980715)12:13<833::aid-rcm235>3.0.co;2-k.

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24

Drowart, Jean, and Richard E. Honig. "Mass Spectrometric Study of Gallium and Indium." Bulletin des Sociétés Chimiques Belges 66, no. 1 (September 1, 2010): 411–12. http://dx.doi.org/10.1002/bscb.19570660134.

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25

HIRAYAMA, KAZUO. "Mass spectrometric analysis of refractory body composition. 7. Structure study of protein using mass spectrometric analysis." Kagaku To Seibutsu 34, no. 8 (1996): 547–52. http://dx.doi.org/10.1271/kagakutoseibutsu1962.34.547.

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26

Saraví Cisneros, Hebe, Sergio Laurella, Danila L. Ruiz, Agustín Ponzinibbio, Patricia E. Allegretti, and Jorge J. P. Furlong. "Spectrometric Study of the Nitrile-Ketenimine Tautomerism." International Journal of Spectroscopy 2009 (September 9, 2009): 1–18. http://dx.doi.org/10.1155/2009/408345.

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Mass spectrometry is used to evaluate the occurrence of the nitrile-ketenimine tautomerism. Mass spectra of two differently substituted nitriles, ethyl-4,4-dicyano-3-methyl-3-butenoate and diethyl-2-cyano-3-methyl-2-pentenodiate are examined looking for common mass spectral behaviors. Ion fragmentation assignments for specific tautomers allow to predict the presence of the corresponding structures. Additionally, the mass spectrum and nuclear magnetic resonance spectra of ethyl-4,4-dicyano-2,2-diethyl-3-methyl-3-butenoate and that of the corresponding amination product support the occurrence of the ketenimine tautomer in the equilibrium.

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27

Ivanova, Bojidarka, and Michael Spiteller. "Physical Properties and Molecular Conformations of Indole Alkaloids and Model Protein Interactions – Theoretical vs. Experimental Study." Natural Product Communications 7, no. 2 (February 2012): 1934578X1200700. http://dx.doi.org/10.1177/1934578x1200700206.

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The physical properties and molecular structure of five natural indole alkaloids (IAs) and their interaction with protein targets have been studied, experimentally and theoretically. Electronic absorption (EAs) and CD spectroscopy, electrospray ionization (ESI) and matrix-assisted laser desorption/ionization (MALDI) mass spectrometry (MS), as well as imaging mass spectrometric techniques (IMS) were used, analyzing the isolated alkaloids and corresponding IAs/protein molecular complexes. Theoretical quantum chemical DFT calculations were also applied. The mechanism of their biological activity and structure-activity relationship as potential neurologically active compounds were studied, using the model interactions with 5HT2A receptors. The gas-phase stable molecular fragments of the IAs are discussed comparing the experimental mass spectrometric data and theoretical quantum chemical DFT calculations of the different molecular fragments of the IAs.

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28

March, Raymond E., and Christopher J. Stadey. "A tandem mass spectrometric study of saccharides at high mass resolution." Rapid Communications in Mass Spectrometry 19, no. 6 (2005): 805–12. http://dx.doi.org/10.1002/rcm.1860.

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29

Suganyadevi, P., M. Saravanakumar, and S. Mohandas. "Characterization of anthocyanin from red sorghum (Sorghum bicolor) bran by liquid chromatography-electron spray ionization mass spectrometry analysis." European Journal of Mass Spectrometry 27, no. 2-4 (July 29, 2021): 107–14. http://dx.doi.org/10.1177/14690667211035720.

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In the present study, anthocyanin pigments from red sorghum ( Sorghum bicolor) bran were identified and characterized by Liquid Chromatography-Electron Spray Ionization Mass Spectrometry. The individual anthocyanins were identified by comparing their mass spectrometric data and retention times, published data. 3-deoxyanthocyanidins and methyl 3-deoxyanthocyanidins were identified in red sorghum bran. This paper presents complete LCMS profile and MS spectrometric data of red sorghum bran.

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30

Kuleshov, D. O., T. E. Kuleshova, D. E. Bobkov, A. A. Diachenko, N. R. Gall, and L. N. Gall. "MASS-SPECTROMETRIC STUDY OF UNITHIOL WATER-ACETONITRIL SOLUTIONS." NAUCHNOE PRIBOROSTROENIE 28, no. 3 (August 29, 2018): 72–83. http://dx.doi.org/10.18358/np-28-3-i7283.

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31

Stolyarova, V. L., S. I. Lopatin, and V. V. Bondar’. "Mass spectrometric study of the Al2O3-SiO2 System." Doklady Physical Chemistry 399, no. 4 (December 2004): 302–4. http://dx.doi.org/10.1007/pl00021844.

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32

Wei, Lixia, Bin Yang, Jing Wang, Chaoqun Huang, Liusi Sheng, Yunwu Zhang, Fei Qi, Chow-Shing Lam, and Wai-Kee Li. "Vacuum Ultraviolet Photoionization Mass Spectrometric Study of Ethylenediamine." Journal of Physical Chemistry A 110, no. 29 (July 2006): 9089–98. http://dx.doi.org/10.1021/jp061876g.

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33

Park, J., and M. C. Lin. "A Mass Spectrometric Study of the NH2+ NO2Reaction." Journal of Physical Chemistry A 101, no. 14 (April 1997): 2643–47. http://dx.doi.org/10.1021/jp963720u.

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34

Chandran, Jisha, Usha K. Aravind, and C. T. Aravindakumar. "Sonochemical transformation of thymidine: A mass spectrometric study." Ultrasonics Sonochemistry 27 (November 2015): 178–86. http://dx.doi.org/10.1016/j.ultsonch.2015.05.016.

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35

Alikhanian, A. S., V. N. Guskov, J. H. Greenberg, M. Fiederle, and K. W. Benz. "Mass spectrometric study of the CdTe–ZnTe system." Journal of Alloys and Compounds 371, no. 1-2 (May 2004): 82–85. http://dx.doi.org/10.1016/j.jallcom.2003.06.008.

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36

Didonato, Gerald C., and Kenneth L. Busch. "A mass spectrometric study of copper(II) acetate." International Journal of Mass Spectrometry and Ion Processes 69, no. 1 (February 1986): 67–83. http://dx.doi.org/10.1016/0168-1176(86)87042-2.

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37

Chizhov, O. S., V. I. Kadentsev, S. A. Shevelev, V. N. Solkan, and G. G. Pal'mbakh. "Chemical ionization mass spectrometric study of aliphatic nitramines." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 34, no. 10 (October 1985): 2217–20. http://dx.doi.org/10.1007/bf00963267.

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38

Iwanek, Waldemar, Alicja Wzorek, Zdzisława Nowakowska, and Grzegorz Schroeder. "Mass spectrometric study of amino acid–triethylborane chelates." Monatshefte für Chemie - Chemical Monthly 140, no. 3 (November 28, 2008): 359–64. http://dx.doi.org/10.1007/s00706-008-0095-1.

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39

Yoo, R. K., B. Ruscic, and J. Berkowitz. "Vacuum ultraviolet photoionization mass spectrometric study of C60." Journal of Chemical Physics 96, no. 2 (January 15, 1992): 911–18. http://dx.doi.org/10.1063/1.462112.

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40

Musin, R. R., Yu Ya Efremov, V. I. Gavrilov, and F. R. Garieva. "Mass-spectrometric study of As-substituted 10H-phenoxarsines." Russian Chemical Bulletin 47, no. 7 (July 1998): 1401–2. http://dx.doi.org/10.1007/bf02495576.

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41

Stolyarova, V. L., S. I. Lopatin, and V. V. Bondar? "Mass spectrometric study of the Al2O3-SiO2 System." Doklady Physical Chemistry 399, no. 4 (December 2004): 302–4. http://dx.doi.org/10.1007/s10634-005-0003-x.

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42

Stolyarova, V. L., S. I. Lopatin, and V. V. Bondar’. "Mass spectrometric study of the Al2O3-SiO2 System." Doklady Physical Chemistry 399, no. 4-6 (December 2004): 302–4. http://dx.doi.org/10.1007/s10634-005-0015-6.

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43

Stølen, Svein, Tsuneo Matsui, and Keiji Naito. "Mass spectrometric vaporization study on palladium-zirconium alloys." Journal of Nuclear Materials 173, no. 1 (September 1990): 48–58. http://dx.doi.org/10.1016/0022-3115(90)90311-a.

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44

Alikhanian, A. S., V. N. Guskov, A. M. Natarovsky, J. H. Greenberg, M. Fiederle, and K. W. Benz. "Mass spectrometric study of the CdTe–ZnTe system." Journal of Crystal Growth 240, no. 1-2 (April 2002): 73–79. http://dx.doi.org/10.1016/s0022-0248(02)00871-0.

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45

Kagramanov, N. D., P. S. Zuev, A. A. Kutin, I. O. Bragilevskii, A. K. Mal'tsev, and O. M. Nefedov. "Mass spectrometric study of vacuum pyrolysis of perfluoroolefins." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 38, no. 1 (January 1989): 37–42. http://dx.doi.org/10.1007/bf00953695.

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46

RUSCIC, B., and J. BERKOWITZ. "ChemInform Abstract: Photoionization Mass Spectrometric Study of Si2H6." ChemInform 22, no. 46 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199146006.

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47

Fernandez-Arciniega, M. A., L. Hernandez, A. H. R. Habeeb, R. M. Alonso, and R. M. Jimenez. "Proton NMR and Mass Spectrometric Study of Triazolobenzodiazepines." Bulletin des Sociétés Chimiques Belges 94, no. 8 (September 1, 2010): 585–89. http://dx.doi.org/10.1002/bscb.19850940806.

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48

Schornikov, S. I., V. L. Stolyarova, and M. M. Shultz. "High temperature mass spectrometric study of 3Al2O3 · 2SiO2." Rapid Communications in Mass Spectrometry 8, no. 6 (June 1994): 478–80. http://dx.doi.org/10.1002/rcm.1290080610.

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49

Grafova, Irina A., Ludmila I. Koval, Pietro Traldi, Silvia Catinella, Giovanni A. Battiston, Eugene A. Mazurenko, and Andrei V. Grafov. "Mass Spectrometric Study of Some Dimethylindium Cyclic Imides." Rapid Communications in Mass Spectrometry 10, no. 14 (November 1996): 1761–65. http://dx.doi.org/10.1002/(sici)1097-0231(199611)10:14<1761::aid-rcm677>3.0.co;2-i.

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50

Day, Elizabeth F., Tiffany A. Payne, and Crystal A. Holt. "Mass spectrometric study of dirhenium biscarboxylate:purine dinucleotide complexes." Rapid Communications in Mass Spectrometry 21, no. 6 (March 30, 2007): 903–10. http://dx.doi.org/10.1002/rcm.2910.

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