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Journal articles on the topic 'Organoarsenic compounds. Mass spectrometry'

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Published: 4 June 2021
Last updated: 14 February 2022

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1

Ojo, Abiodun A., and Amos Onasanya. "Closed Anaerobic Biotransformation Products of Organoarsenic Compounds in Fucus distichus." ISRN Environmental Chemistry 2013 (July 14, 2013): 1–7. http://dx.doi.org/10.1155/2013/684297.

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The closed anaerobic decomposition extracts of Fucus distichus incubated with seawater and sediment, and without sediment as control, were subjected to extractions and isolation on Sephadex LH 20 and Cellulose Thin Layer Chromatography. The decomposition extracts and isolates were analyzed by using both the Hydride Generation Gas Chromatography Atomic Absorption Spectrometry (HG-GC-AAS) and High Performance Liquid Chromatography Inductively Coupled Plasma Mass Spectrometry (HPLC-ICPMS) to identify the arsenic species in the equilibrium mixtures of the seaweed and filtrates separately. In the m
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2

García-Salgado, Sara, Georg Raber, Reingard Raml, Christoph Magnes, and Kevin A. Francesconi. "Arsenosugar phospholipids and arsenic hydrocarbons in two species of brown macroalgae." Environmental Chemistry 9, no. 1 (2012): 63. http://dx.doi.org/10.1071/en11164.

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Environmental contextAlthough organoarsenic compounds occur in marine organisms at high concentrations, the origin and role of these compounds is unknown. Arsenic-containing lipids (arsenolipids) are newly discovered compounds in fish. We identify a range of arsenolipids in algae and propose that algae are the origin of these unusual arsenic compounds in marine ecosystems. AbstractFourteen arsenolipids, including 11 new compounds, were identified and quantified in two species of brown algae, Wakame (Undaria pinnatifida) and Hijiki (Hizikia fusiformis), by high resolution mass spectrometry, hig
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3

PERGANTIS, SPIROS A., WITOLD WINNIK, and DON BETOWSKI. "Determination of Ten Organoarsenic Compounds Using Microbore High-performance Liquid Chromatography Coupled With Electrospray Mass Spectrometry–Mass Spectrometry." J. Anal. At. Spectrom. 12, no. 5 (1997): 531–36. http://dx.doi.org/10.1039/a606416g.

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4

SERPE, F. P., R. RUSSO, P. GALLO, and L. SEVERINO. "Method for Speciation of Organoarsenic in Mussels by Liquid Chromatography Coupled to Electrospray Ionization and QTRAP Tandem Mass Spectrometry." Journal of Food Protection 76, no. 7 (2013): 1293–99. http://dx.doi.org/10.4315/0362-028x.jfp-12-525.

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Arsenic toxicity to humans critically depends on the chemical form of the arsenic. The Expert Committee of the Food and Agriculture Organization and the World Health Organization defined a tolerable intake only for inorganic arsenic, although the toxicity of some organoarsenic compounds is known. Arsenobetaine (AsB), arsenocholine (AsC), dimethylarsinic acid (DMA), and monomethylarsonic acid (MMA) are abundant in shellfish. We present a fast and reliable method for identification of the type of organic arsenic in mussels by using liquid chromatography coupled to electrospray ionization tandem
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5

Kuramata, Masato, Futa Sakakibara, Ryota Kataoka, et al. "Arsinothricin, a novel organoarsenic species produced by a rice rhizosphere bacterium." Environmental Chemistry 13, no. 4 (2016): 723. http://dx.doi.org/10.1071/en14247.

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Environmental contextRice is a major human dietary source of arsenic. We identified a novel organoarsenic species, arsinothricin, produced by a bacterium in the rice rhizosphere. This result suggests diverse biochemical dynamics and microbial biodiversity of arsenic metabolism in the rice rhizosphere. AbstractMethylated arsenic compounds in rice grains originate from the action of soil bacteria in the rice rhizosphere. Here, we investigated the chemical structures of arsenic compounds produced by a bacterium, Burkholderia gladioli strain GSRB05, in the rice rhizosphere. When cultured in liquid
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6

Chen, Lei, Yaeko Suzuki, and Takashi Korenaga. "Lithium Ion Attachment Mass Spectrometry for the Direct Detection of Organoarsenic Compounds in the Metallomics Studies." Chemistry Letters 36, no. 2 (2007): 336–37. http://dx.doi.org/10.1246/cl.2007.336.

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7

Kaise, Toshikazu, Shigenobu Watanabe, Kazutoshi Ito, et al. "The study of organoarsenic compounds in fish and alga by exact mass measurement using fast atom bombardment mass spectrometry." Chemosphere 16, no. 1 (1987): 91–97. http://dx.doi.org/10.1016/0045-6535(87)90112-3.

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8

Ojo, Abiodun A., and Amos Onasanya. "Characterization of Arsenic Biotransformation Products from an Open Anaerobic Degradation of Fucus distichus by Hydride Generation Gas Chromatography Atomic Absorption Spectrometry and High Performance Liquid Chromatography Inductively Coupled Plasma Mass Spectrometry." ISRN Spectroscopy 2013 (November 2, 2013): 1–6. http://dx.doi.org/10.1155/2013/431801.

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This work reports on the isolation and determination of biotransformation products obtained from the organoarsenic compounds that are present in Fucus distichus when it was subjected to an open anaerobic decomposition by using the Hydride Generation Gas Chromatography Atomic Absorption Spectrometry (HG-GC-AAS) and High Performance Liquid Chromatography Inductively Coupled Plasma Mass Spectrometry (HPLC-ICP-MS). The seaweed and filtrate residues obtained from the open anaerobic degradation procedure were extracted in methanol and partitioned in phenol-ether-water mixtures to obtain water solubl
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9

Caumette, G., I. Koch, K. House, and K. J. Reimer. "Arsenic cycling in freshwater phytoplankton and zooplankton cultures." Environmental Chemistry 11, no. 5 (2014): 496. http://dx.doi.org/10.1071/en14039.

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Environmental context Understanding how arsenic is changed from toxic to non-toxic chemical forms in lakes and rivers is important in understanding the overall risk from arsenic. Freshwater plankton exposed in laboratory cultures to different sources of toxic inorganic arsenate formed arsenosugars, but at higher exposure levels, in water and through contaminated sediment, inorganic arsenate remained unchanged. In arsenic-contaminated freshwater bodies, plankton may provide a source of toxic inorganic arsenic to consumers. Abstract Freshwater phytoplankton (Chlamydomonas) and zooplankton (Daphn
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10

Glabonjat, Ronald A., Georg Raber, Kenneth B. Jensen, Florence Schubotz, Eric S. Boyd, and Kevin A. Francesconi. "Origin of arsenolipids in sediments from Great Salt Lake." Environmental Chemistry 16, no. 5 (2019): 303. http://dx.doi.org/10.1071/en19135.

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Environmental contextArsenic is a globally distributed element, occurring in various chemical forms with toxicities ranging from harmless to highly toxic. We examined sediment samples from Great Salt Lake, an extreme salt environment, and found a variety of organoarsenic species not previously recorded in nature. These new compounds are valuable pieces in the puzzle of how organisms detoxify arsenic, and in our understanding of the global arsenic cycle. AbstractArsenic-containing lipids are natural products found predominantly in marine organisms. Here, we report the detection of known and new
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11

Wu, Jingcun, Zoltán Mester, and Janusz Pawliszyn. "Speciation of organoarsenic compounds by polypyrrole-coated capillary in-tube solid phase microextraction coupled with liquid chromatography/electrospray ionization mass spectrometry." Analytica Chimica Acta 424, no. 2 (2000): 211–22. http://dx.doi.org/10.1016/s0003-2670(00)01153-3.

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12

Pergantis, Spiros A., William R. Cullen, and Guenter K. Eigendorf. "Evaluation of matrix-assisted laser desorption/ionization time-of-flight mass spectrometry for the analysis of organoarsenic compounds of environmental interest." Biological Mass Spectrometry 23, no. 12 (1994): 749–55. http://dx.doi.org/10.1002/bms.1200231206.

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13

Larsen, B. R., C. Astorga-Llorens, M. H. Florêncio, and A. M. Bettencourt. "Fragmentation pathways of organoarsenical compounds by electrospray ion trap multiple mass spectrometry (MS6)." Journal of Chromatography A 926, no. 1 (2001): 167–74. http://dx.doi.org/10.1016/s0021-9673(01)00905-0.

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14

Nischwitz, Volker, and Spiros A. Pergantis. "Mapping of arsenic species and identification of a novel arsenosugar in giant clams Tridacna maxima and Tridacna derasa using advanced mass spectrometric techniques." Environmental Chemistry 4, no. 3 (2007): 187. http://dx.doi.org/10.1071/en07009.

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Environmental context. Arsenic is known to accumulate in various marine organisms. The high acute toxicity of inorganic arsenic species and the potential chronic toxicity of some organoarsenic species require detailed knowledge about the occurrence and metabolism of arsenic compounds in marine organisms. The application of advanced analytical techniques still allows, even after decades of arsenic speciation, the identification of novel species. In addition, comprehensive mapping of all arsenic species present in marine organisms may allow for a more detailed understanding of arsenic metabolism
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15

Wang, Wei-Xun, Tzung-Jie Yang, Zu-Guang Li, Ting-Ting Jong, and Maw-Rong Lee. "A novel method of ultrasound-assisted dispersive liquid–liquid microextraction coupled to liquid chromatography–mass spectrometry for the determination of trace organoarsenic compounds in edible oil." Analytica Chimica Acta 690, no. 2 (2011): 221–27. http://dx.doi.org/10.1016/j.aca.2011.02.033.

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16

Cubadda, Francesco, Federica Aureli, Marilena D’Amato, Andrea Raggi, Anna Chiara Turco, and Alberto Mantovani. "Speciated urinary arsenic as a biomarker of dietary exposure to inorganic arsenic in residents living in high-arsenic areas in Latium, Italy." Pure and Applied Chemistry 84, no. 2 (2012): 203–14. http://dx.doi.org/10.1351/pac-con-11-09-29.

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Current knowledge indicates that total urinary arsenic is not a suitable biomarker of exposure to toxic, i.e., inorganic, arsenic (iAs), whereas measurement of iAs and its methylated metabolites in urine using speciation analysis provides much more reliable estimates of exposure. The relative proportions of urinary iAs, monomethylarsonate (MA), and dimethylarsinate (DMA) can be used as a measure of methylation capacity, provided that there are no confounding factors such as consumption of food rich in DMA or containing As compounds metabolized to DMA.We analyzed by gradient elution anion-excha
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17

Michael Siu, K. W., Graeme J. Gardner, and Shier S. Berman. "Atmospheric pressure chemical ionization and electrospray mass spectrometry of some organoarsenic species." Rapid Communications in Mass Spectrometry 2, no. 4 (1988): 69–71. http://dx.doi.org/10.1002/rcm.1290020405.

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18

Kiremire, Bernard, Robert Seraglia, and Pietro Traldi. "Mass spectrometry of macrocyclic compounds." Rapid Communications in Mass Spectrometry 5, no. 11 (1991): 543–56. http://dx.doi.org/10.1002/rcm.1290051112.

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19

Lebedev, Albert T. "Mass spectrometry of diazo compounds." Mass Spectrometry Reviews 10, no. 2 (1991): 91–132. http://dx.doi.org/10.1002/mas.1280100202.

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20

TORNES, J., A. OPSTAD, and B. JOHNSEN. "Determination of organoarsenic warfare agents in sediment samples from Skagerrak by gas chromatography-mass spectrometry." Science of The Total Environment 356, no. 1-3 (2006): 235–46. http://dx.doi.org/10.1016/j.scitotenv.2005.03.031.

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21

Traeger, John C. "Electrospray mass spectrometry of organometallic compounds." International Journal of Mass Spectrometry 200, no. 1-3 (2000): 387–401. http://dx.doi.org/10.1016/s1387-3806(00)00346-8.

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22

Ostah, N., and G. Lawson. "Mass spectrometry studies of organolead compounds." Applied Organometallic Chemistry 15, no. 9 (2001): 749–56. http://dx.doi.org/10.1002/aoc.226.

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23

Gavalas-Olea, Antonio, Jose Luis Garrido, Pilar Riobo, Susana Alvarez, and Belen Vaz. "Mass Spectrometry of Algal Chlorophyll c Compounds." Current Organic Chemistry 22, no. 9 (2018): 836–41. http://dx.doi.org/10.2174/1385272821666170919155604.

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24

LEBEDEV, A. T. "ChemInform Abstract: Mass Spectrometry of Diazo Compounds." ChemInform 22, no. 45 (2010): no. http://dx.doi.org/10.1002/chin.199145364.

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25

Takhistov, Vyacheslav V., A. A. Rodin, and B. N. Maksimova. "Mass spectrometry of halogen-containing organic compounds." Russian Chemical Reviews 60, no. 10 (1991): 1101–14. http://dx.doi.org/10.1070/rc1991v060n10abeh001132.

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26

KIREMIRE, B., R. SERAGLIA, and P. TRALDI. "ChemInform Abstract: Mass Spectrometry of Macrocyclic Compounds." ChemInform 23, no. 13 (2010): no. http://dx.doi.org/10.1002/chin.199213349.

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27

KIREMIRE, B., R. SERAGLIA, and P. TRALDI. "ChemInform Abstract: Mass Spectrometry of Macrocyclic Compounds." ChemInform 25, no. 32 (2010): no. http://dx.doi.org/10.1002/chin.199432308.

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28

Anisimova, O. S., Yu N. Sheinker, S. Ordzhonikidze, and A. P. Pleshkova. "Secondary ion mass spectrometry of dispirotripiperazinium compounds." Organic Mass Spectrometry 25, no. 8 (1990): 432–34. http://dx.doi.org/10.1002/oms.1210250810.

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29

Wei, Junhua, Ji Chen, and Jack Martin Miller. "Electrospray ionization mass spectrometry of organogermanium compounds." Rapid Communications in Mass Spectrometry 15, no. 3 (2001): 169–81. http://dx.doi.org/10.1002/1097-0231(20010215)15:3<169::aid-rcm207>3.0.co;2-8.

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30

POLYAKOVA, A. A. "ChemInform Abstract: Mass Spectrometry of Organosulfur Compounds." ChemInform 22, no. 28 (2010): no. http://dx.doi.org/10.1002/chin.199128308.

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31

Flammang, Robert, and Curt Wentrup. "Neutralization-Reionization Mass Spectrometry of Sulfurcontaining Compounds." Sulfur reports 20, no. 2 (1997): 255–78. http://dx.doi.org/10.1080/01961779708047921.

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32

Dunn, W. J., and Dorothy Swain. "Computer-assisted interpretation of mass spectrometry—mass spectrometry data of potentially hazardous environmental compounds." Chemometrics and Intelligent Laboratory Systems 19, no. 2 (1993): 175–79. http://dx.doi.org/10.1016/0169-7439(93)80101-m.

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33

Atallah, Raja H., and David A. Kalman. "On-line photo-oxidation for the determination of organoarsenic compounds by atomic-absorption spectrometry with continuous arsine generation." Talanta 38, no. 2 (1991): 167–73. http://dx.doi.org/10.1016/0039-9140(91)80125-j.

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34

Perreault, Hélène, and Catherine E. Costello. "Differentiation of cerebroside isomers and study of fragmentation by liquid secondary ion mass spectrometry and mass spectrometry/mass spectrometry of selected derivatives." Canadian Journal of Chemistry 74, no. 9 (1996): 1682–95. http://dx.doi.org/10.1139/v96-185.

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The possibility of distinguishing two cerebroside isomers, whose structural variation is in the sugar rings, was investigated by liquid secondary ion mass spectrometry (LSIMS) and tandem mass spectrometry (MS/MS). In addition to the native materials, four types of derivatives of these cerebroside isomers were prepared and studied using these techniques. A first level of comparison between isomers consisted of seeking differences in the conventional LSIMS spectra. Native compounds, galactosyl and glucosyl ceramides, did not yield consistent and meaningful elements of comparison and a few nanomo
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35

Miclea, Manuela, Kerstin Kunze, Joachim Franzke, and Kay Niemax. "Microplasma jet mass spectrometry of halogenated organic compounds." Journal of Analytical Atomic Spectrometry 19, no. 8 (2004): 990. http://dx.doi.org/10.1039/b401319k.

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36

Fisher, Dixie L., M. Arthur Moseley, James O. Mullis, Daniel L. Norwood, and Thomas A. Baillie. "Recognition of quaternary ammonium compounds using mass spectrometry." Rapid Communications in Mass Spectrometry 8, no. 1 (1994): 65–70. http://dx.doi.org/10.1002/rcm.1290080113.

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37

Bojesen, Gustav. "Fast atom bombardment mass spectrometry of coordination compounds." Organic Mass Spectrometry 20, no. 6 (1985): 413–15. http://dx.doi.org/10.1002/oms.1210200606.

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38

Gower, John Leveson. "Matrix compounds for fast atom bombardment mass spectrometry." Biological Mass Spectrometry 12, no. 5 (1985): 191–96. http://dx.doi.org/10.1002/bms.1200120502.

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39

Lawson, G., and N. Ostah. "Speciation of organotin compounds by tandem mass spectrometry." Applied Organometallic Chemistry 7, no. 3 (1993): 183–91. http://dx.doi.org/10.1002/aoc.590070305.

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40

SUGIMOTO, Shigeko, Masaaki ARIME, Shozo KAWABATA, and Yukio ONO. "Characterization of organic tin compounds by mass spectrometry." NIPPON KAGAKU KAISHI, no. 11 (1986): 1700–1702. http://dx.doi.org/10.1246/nikkashi.1986.1700.

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41

Bawa, F., D. G. Cameron, C. S. Creaser, et al. "Fast Atom Bombardment Mass Spectrometry of Organophosphorus Compounds." Phosphorus and Sulfur and the Related Elements 30, no. 3-4 (1987): 743. http://dx.doi.org/10.1080/03086648708079237.

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42

Van Bramer, S. E., and M. V. Johnston. "10.5-eV photoionization mass spectrometry of aliphatic compounds." Journal of the American Society for Mass Spectrometry 1, no. 6 (1990): 419–26. http://dx.doi.org/10.1016/1044-0305(90)85024-g.

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43

Mason, Rod, and Dafydd Milton. "Glow discharge mass spectrometry of some organic compounds." International Journal of Mass Spectrometry and Ion Processes 91, no. 2 (1989): 209–25. http://dx.doi.org/10.1016/0168-1176(89)83010-1.

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44

Traeger, John C. "ChemInform Abstract: Electrospray Mass Spectrometry of Organometallic Compounds." ChemInform 32, no. 21 (2010): no. http://dx.doi.org/10.1002/chin.200121299.

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45

Morozik, Yu I., V. Dudkin, I. V. Rybal’chenko, and K. N. Smirnov. "Alkene subspectra of monofunction compounds mass spectra: Tandem mass spectrometry investigation." Russian Journal of General Chemistry 86, no. 10 (2016): 2295–300. http://dx.doi.org/10.1134/s107036321610008x.

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46

Halket, John M., and Vladimir G. Zaikin. "Derivatization in Mass Spectrometry—1. Silylation." European Journal of Mass Spectrometry 9, no. 1 (2003): 1–21. http://dx.doi.org/10.1255/ejms.527.

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This is the first of a series of reviews on the application of derivatization in mass spectrometry. A description is given of advances in silylation as a powerful tool used for increasing the volatility, thermal and thermo-catalytic stability, and chromatographic mobility of polar and unstable organic compounds. In addition to chemical aspects of silylation, mass spectral properties of silyl derivatives useful for structure determination and quantitation of various organic and biologically-active compounds, mainly by GC/MS, are described. Practically all tested and widely used silylating agent
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47

Huikko, Katri, Tapio Kotiaho, Jari Yli-Kauhaluoma, and Risto Kostiainen. "Electrospray ionization mass spectrometry and tandem mass spectrometry of clodronate and related bisphosphonate and phosphonate compounds." Journal of Mass Spectrometry 37, no. 2 (2002): 197–208. http://dx.doi.org/10.1002/jms.273.

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48

Annesley, Thomas M. "Ion Suppression in Mass Spectrometry." Clinical Chemistry 49, no. 7 (2003): 1041–44. http://dx.doi.org/10.1373/49.7.1041.

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Abstract Background: Mass spectrometry (MS) is being introduced into a large number of clinical laboratories. It provides specificity because of its ability to monitor selected mass ions, sensitivity because of the enhanced signal-to-noise ratio, and speed because it can help avoid the need for intensive sample cleanup and long analysis times. However, MS is not without problems related to interference, especially through ion suppression effects. Ion suppression results from the presence of less volatile compounds that can change the efficiency of droplet formation or droplet evaporation, whic
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49

Wheat, Thomas E., Kim A. Lilley, and J. Fred Banks. "Capillary electrophoresis with electrospray mass spectrometry detection for low-molecular-mass compounds." Journal of Chromatography A 781, no. 1-2 (1997): 99–105. http://dx.doi.org/10.1016/s0021-9673(97)00372-5.

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50

Martínez-Alvarez, Roberto, Nazario Martín, Carlos Seoane, et al. "Mass Spectrometry Study of Acylthioureas and Acylthiocarbamates." European Journal of Mass Spectrometry 8, no. 5 (2002): 367–74. http://dx.doi.org/10.1255/ejms.511.

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A variety of acylthiocarbamates and acylthioureas have been investigated under electron impact ionization (EI), chemical ionization (CI) and electrospray ionization (ESI) conditions. Sequential product-ion fragmentation (MSn) was performed to elucidate the degradation pathways for these compounds. Comparisons are made between positive and negative even-electron ions from ESI and CI and the odd-electron ions obtained under EI conditions. The data collected in this paper provide information on the strong differences found in the fragmentation process of these compounds.
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