<?xml version="1.0" encoding="UTF-8"?>
<collection xmlns="http://www.loc.gov/MARC21/slim">
 <record>
  <leader>     caa a22        4500</leader>
  <controlfield tag="001">463219554</controlfield>
  <controlfield tag="003">CHVBK</controlfield>
  <controlfield tag="005">20180405153208.0</controlfield>
  <controlfield tag="007">cr unu---uuuuu</controlfield>
  <controlfield tag="008">170326e20070301xx      s     000 0 eng  </controlfield>
  <datafield tag="024" ind1="7" ind2="0">
   <subfield code="a">10.1134/S1061934807030057</subfield>
   <subfield code="2">doi</subfield>
  </datafield>
  <datafield tag="035" ind1=" " ind2=" ">
   <subfield code="a">(NATIONALLICENCE)springer-10.1134/S1061934807030057</subfield>
  </datafield>
  <datafield tag="245" ind1="0" ind2="0">
   <subfield code="a">Study of the chemical mechanism of color reactions of selenium(IV) with o -arylenediamines</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Yu. Dedkov, A. Musatov]</subfield>
  </datafield>
  <datafield tag="520" ind1="3" ind2=" ">
   <subfield code="a">o-Arylenediamines are promising for the photometric determination of selenium. The search for new reagents of this group is desirable. To obtain information necessary for this purpose, the chemical mechanism of color reactions of selenium(IV) with o-arylenediamines was studied. The optimum conditions of these reactions and the spectrophotometric characteristics of reagents and complexes were found. The ratio of components in the reaction products (piazoselenols) of 1: 1 was determined by elemental analysis, NMR spectroscopy, and the isomolar series method. The formation of the selenium-nitrogen bond was confirmed and the quasiaromatic character of piazoselenols was revealed by IR and NMR spectroscopy. Binding energies of valence orbitals, electron density distribution, and charges of nitrogen and selenium atoms were estimated by x-ray photoelectron spectroscopy. In the case of piazoselenol from 1,2-phenylenediamine, the existence of two tautomeric forms with the oxidation numbers of selenium close to +2 and +4 were found. Piazoselenol based on N-phenyl-1,2-phenylenediamine predominantly occurs as a single compound with the oxidation number of selenium close to +2. The most probable structures of the resulting piazoselenols were proposed, and the probable schemes of the reactions of selenium(IV) with 1,2-phenylenediamine and N-phenyl-1,2-phenylenediamine were justified.</subfield>
  </datafield>
  <datafield tag="540" ind1=" " ind2=" ">
   <subfield code="a">Pleiades Publishing, Ltd., 2007</subfield>
  </datafield>
  <datafield tag="700" ind1="1" ind2=" ">
   <subfield code="a">Dedkov</subfield>
   <subfield code="D">Yu</subfield>
   <subfield code="u">Moscow State Regional University, ul. Radio 10a, 105005, Moscow, Russia</subfield>
   <subfield code="4">aut</subfield>
  </datafield>
  <datafield tag="700" ind1="1" ind2=" ">
   <subfield code="a">Musatov</subfield>
   <subfield code="D">A.</subfield>
   <subfield code="u">Moscow State Regional University, ul. Radio 10a, 105005, Moscow, Russia</subfield>
   <subfield code="4">aut</subfield>
  </datafield>
  <datafield tag="773" ind1="0" ind2=" ">
   <subfield code="t">Journal of Analytical Chemistry</subfield>
   <subfield code="d">Nauka/Interperiodica</subfield>
   <subfield code="g">62/3(2007-03-01), 225-232</subfield>
   <subfield code="x">1061-9348</subfield>
   <subfield code="q">62:3&lt;225</subfield>
   <subfield code="1">2007</subfield>
   <subfield code="2">62</subfield>
   <subfield code="o">10809</subfield>
  </datafield>
  <datafield tag="856" ind1="4" ind2="0">
   <subfield code="u">https://doi.org/10.1134/S1061934807030057</subfield>
   <subfield code="q">text/html</subfield>
   <subfield code="z">Onlinezugriff via DOI</subfield>
  </datafield>
  <datafield tag="908" ind1=" " ind2=" ">
   <subfield code="D">1</subfield>
   <subfield code="a">research-article</subfield>
   <subfield code="2">jats</subfield>
  </datafield>
  <datafield tag="950" ind1=" " ind2=" ">
   <subfield code="B">NATIONALLICENCE</subfield>
   <subfield code="P">856</subfield>
   <subfield code="E">40</subfield>
   <subfield code="u">https://doi.org/10.1134/S1061934807030057</subfield>
   <subfield code="q">text/html</subfield>
   <subfield code="z">Onlinezugriff via DOI</subfield>
  </datafield>
  <datafield tag="950" ind1=" " ind2=" ">
   <subfield code="B">NATIONALLICENCE</subfield>
   <subfield code="P">700</subfield>
   <subfield code="E">1-</subfield>
   <subfield code="a">Dedkov</subfield>
   <subfield code="D">Yu</subfield>
   <subfield code="u">Moscow State Regional University, ul. Radio 10a, 105005, Moscow, Russia</subfield>
   <subfield code="4">aut</subfield>
  </datafield>
  <datafield tag="950" ind1=" " ind2=" ">
   <subfield code="B">NATIONALLICENCE</subfield>
   <subfield code="P">700</subfield>
   <subfield code="E">1-</subfield>
   <subfield code="a">Musatov</subfield>
   <subfield code="D">A.</subfield>
   <subfield code="u">Moscow State Regional University, ul. Radio 10a, 105005, Moscow, Russia</subfield>
   <subfield code="4">aut</subfield>
  </datafield>
  <datafield tag="950" ind1=" " ind2=" ">
   <subfield code="B">NATIONALLICENCE</subfield>
   <subfield code="P">773</subfield>
   <subfield code="E">0-</subfield>
   <subfield code="t">Journal of Analytical Chemistry</subfield>
   <subfield code="d">Nauka/Interperiodica</subfield>
   <subfield code="g">62/3(2007-03-01), 225-232</subfield>
   <subfield code="x">1061-9348</subfield>
   <subfield code="q">62:3&lt;225</subfield>
   <subfield code="1">2007</subfield>
   <subfield code="2">62</subfield>
   <subfield code="o">10809</subfield>
  </datafield>
  <datafield tag="900" ind1=" " ind2="7">
   <subfield code="a">Metadata rights reserved</subfield>
   <subfield code="b">Springer special CC-BY-NC licence</subfield>
   <subfield code="2">nationallicence</subfield>
  </datafield>
  <datafield tag="898" ind1=" " ind2=" ">
   <subfield code="a">BK010053</subfield>
   <subfield code="b">XK010053</subfield>
   <subfield code="c">XK010000</subfield>
  </datafield>
  <datafield tag="949" ind1=" " ind2=" ">
   <subfield code="B">NATIONALLICENCE</subfield>
   <subfield code="F">NATIONALLICENCE</subfield>
   <subfield code="b">NL-springer</subfield>
  </datafield>
 </record>
</collection>
