
<ns0:uwmetadata xmlns:ns0="http://phaidra.univie.ac.at/XML/metadata/V1.0" xmlns:ns1="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0" xmlns:ns10="http://phaidra.univie.ac.at/XML/metadata/provenience/V1.0" xmlns:ns11="http://phaidra.univie.ac.at/XML/metadata/provenience/V1.0/entity" xmlns:ns12="http://phaidra.univie.ac.at/XML/metadata/digitalbook/V1.0" xmlns:ns13="http://phaidra.univie.ac.at/XML/metadata/etheses/V1.0" xmlns:ns2="http://phaidra.univie.ac.at/XML/metadata/extended/V1.0" xmlns:ns3="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0/entity" xmlns:ns4="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0/requirement" xmlns:ns5="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0/educational" xmlns:ns6="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0/annotation" xmlns:ns7="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0/classification" xmlns:ns8="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0/organization" xmlns:ns9="http://phaidra.univie.ac.at/XML/metadata/histkult/V1.0">
  <ns1:general>
    <ns1:identifier>o:1241</ns1:identifier>
    <ns1:title language="sr">Sinteza, karakterizacija i biološka aktivnost kompleksa Pd(II) sa etilendiaminskim i kumarinskim derivatima aminokiselina </ns1:title>
    <ns2:alt_title language="sr">SYNTHESIS, CHARACTERIZATION AND BIOLOGICAL ACTIVITY OFPd(II) COMPLEXES WITH ETHYLENDYAMINE AND COUMARINEAMINO ACIDS DERIVATIVES  : doctoral dissertation</ns2:alt_title>
    <ns1:language>sr</ns1:language>
    <ns1:description language="sr">U ovoj Doktorskoj disertaciji opisana je sinteza i karakterizacija nekoliko novih liganada, etilendiaminskih i kumarinskih derivata nekih aminokiselina i odgovarajućih paladijum(II)-kompleksa.
Najpre je opisana sinteza i karakterizacija O,O&apos;-dialkil estara (S,S)-etilen--diamin-N,N&apos;-di-(2,2&apos;-di-(4-hidroksi-benzil))sirćetne kiseline (H2-(S,S)-eddtyr). Ova jedinjenja su dobijena direktnom reakcijom između tetradentatnog liganda (S,S)-etilendiamin-N,N&apos;-di-(2,2&apos;-di-(4-hidroksi-benzil))sirćetne kiseline i odgovara-
-jućeg apsolutnog alkohola (etanol, 1-propanol, 1-butanol i 1-pentanol) u molskom odnosu 1 : 2, uz uvođenje gasovitog hlorovodonika. Takođe, prikazana je i sinteza kumarinskih derivata nekih aminokiselina. Pomenuti ligandi dobijeni su refluktovanjem smeše
3-acetil-4-hidroksi kumarina, hidrohlorida metil estara aminokiselina S-valina, glicina, S-metionina ili S-triptofana i trimetilamina. Tok reakcije je praćen tankoslojnom hromatografijom (toluen : aceton = 8 : 2). Nakon završene reakcije, uparavanjem rastvarača do polovine svoje zapremine i dodavanjem 5 cm3 vode, dobijeni sukumarinski derivati sa pomenutim aminokiselinama. Strukture i sastav izolovanih
liganada pretpostavljene su primenom elementalne mikroanalize, infracrvene, 1H i 13C NMR spektroskopije, a potvrđene na bazi rezultata rendgenske strukturne analize u slučaju metil 2-[(1-(2,4-dioksohroman-3-iliden)etilamino-3-metil)]butanoata.
Dobijeni O,O&apos;-dialkil estri (S,S)-etilendiamin-N,N&apos;-di-(2,2&apos;-di-(4-hidroksi--benzil))sirćetne kiseline su upotrebljeni za sintezu odgovarajućih paladijum(II)--kompleksa. Sastav dobijenih kvadratno-planarnih paladijuma(II)-kompleksa potvrđen je elementalnom analizom, dok je struktura izolovanih kompleksa pretpostavljena na osnovu infracrvene, 1H i 13C NMR spektroskopije.</ns1:description>
    <ns1:description language="en">The synthesis and characterization of several new ligands, ethylenediamine and coumarin
derivatives of some amino acids and corresponding palladium(II)-complexes are described in this
PhD thesis.
Firstly, the synthesis and characterizations of O,O&apos;-dialkyl esters of (S,S)-ethylenediamine-
-N,N&apos;-di-(2,2&apos;-di-(4-hydroxy-benzyl)acetic acid, H2-(S,S)-eddtyr are described. These compounds
were obtained by direct reaction between tetradentate ligand (S,S)-ethylenediamine-N,N&apos;-di-(2,2&apos;-
-di-(4-hydroxy-benzyl)acetic acid and the corresponding absolute alcohol (ethanol, 1-propanol,
1-butanol, 1-pentanol) in a molar ratio 1:2 with the addition of gaseous hydrogen-chloride. Also,
the synthesis of coumarin derivatives of some amino acids are also shown. Mentioned ligands were
obtained refluxing a mixture of 3-acetyl-4-hydroxy coumarin, hydrochloride methyl esters of
amino acids S-valine, glycine, S-methionine or S-tryptophan and trimethylamine.
The progress of the reactions was monitored by TLC (toluene : acetone = 8 : 2). After the finishing
of the reactions, the evaporation of solvent to the half of native volume and addition of 5 cm3 of
water, the obtained coumarin derivatives with mentioned amino acids were obtained.
The obtained O,O&apos;-dialkyl esters of (S,S)-ethylenediamine-N,N&apos;-di-(2,2&apos;-di-(4-hydroxy-
-benzyl)acetic acids are used for synthesis of the corresponding palladium(II)-complexes. The composition of obtained square-planar palladium(II)-complexes was confirmed by elemental microanalysis, and the structure of isolated complexes is assumed on basis of infrared, 1H and 13C NMR spectroscopy.</ns1:description>
    <ns1:description language="sr"></ns1:description>
    <ns1:coverage language="sr">144 lista</ns1:coverage>
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      <ns2:identifier>7323</ns2:identifier>
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    <ns1:upload_date>2020-02-28T12:20:15.053Z</ns1:upload_date>
    <ns1:status>45</ns1:status>
    <ns2:peer_reviewed>no</ns2:peer_reviewed>
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      <ns1:ext_role>mentor</ns1:ext_role>
      <ns1:entity seq="0">
        <ns3:firstname> Danijela, 1986-</ns3:firstname>
        <ns3:lastname>Stojković</ns3:lastname>
      </ns1:entity>
      <ns1:date>2018</ns1:date>
    </ns1:contribute>
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      <ns1:ext_role>mentor</ns1:ext_role>
      <ns1:entity seq="0">
        <ns3:firstname> Verica</ns3:firstname>
        <ns3:lastname>Jevtić</ns3:lastname>
      </ns1:entity>
      <ns1:date>2018</ns1:date>
    </ns1:contribute>
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      <ns1:role>63</ns1:role>
      <ns1:ext_role>član komisije</ns1:ext_role>
      <ns1:entity seq="0">
        <ns3:firstname> Srećko</ns3:firstname>
        <ns3:lastname>Trifunović</ns3:lastname>
      </ns1:entity>
      <ns1:date>2018</ns1:date>
    </ns1:contribute>
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      <ns1:role>63</ns1:role>
      <ns1:ext_role>član komisije</ns1:ext_role>
      <ns1:entity seq="0">
        <ns3:firstname> Tibor</ns3:firstname>
        <ns3:lastname>Sabo</ns3:lastname>
      </ns1:entity>
      <ns1:date>2018</ns1:date>
    </ns1:contribute>
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      <ns1:role>63</ns1:role>
      <ns1:ext_role>član komisije</ns1:ext_role>
      <ns1:entity seq="0">
        <ns3:firstname> Ratomir</ns3:firstname>
        <ns3:lastname>Jelić</ns3:lastname>
      </ns1:entity>
      <ns1:date>2018</ns1:date>
    </ns1:contribute>
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      <ns1:role>63</ns1:role>
      <ns1:ext_role>član komisije</ns1:ext_role>
      <ns1:entity seq="0">
        <ns3:firstname> Gordana</ns3:firstname>
        <ns3:lastname>Radić</ns3:lastname>
      </ns1:entity>
      <ns1:date>2018</ns1:date>
    </ns1:contribute>
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      <ns1:role>63</ns1:role>
      <ns1:ext_role>član komisije</ns1:ext_role>
      <ns1:entity seq="0">
        <ns3:firstname> Nenad</ns3:firstname>
        <ns3:lastname>Vuković</ns3:lastname>
      </ns1:entity>
      <ns1:date>2018</ns1:date>
    </ns1:contribute>
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    <ns1:size>6651545</ns1:size>
    <ns1:location>http://phaidrabg.bg.ac.rs/o:1241</ns1:location>
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  <ns1:rights>
    <ns1:cost>no</ns1:cost>
    <ns1:copyright>yes</ns1:copyright>
    <ns1:license>5</ns1:license>
  </ns1:rights>
  <ns1:annotation>
    <ns6:annotations>
      <ns6:date>2020-02-28T12:20:15.320Z</ns6:date>
    </ns6:annotations>
  </ns1:annotation>
  <ns1:classification>
    <ns1:purpose>70</ns1:purpose>
    <ns7:keyword language="sr" seq="1">R2-(S,S)-eddtyr ligandi, kumarinski derivati aminokiselina Paladijum, Kompleksna jedinjenja</ns7:keyword>
  </ns1:classification>
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    <ns8:hoschtyp>1738</ns8:hoschtyp>
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    <ns12:releaseyear>2018</ns12:releaseyear>
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