Oxidation of Deactivated Cage Substrates in the System H2SO4–HNO3 View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2020-03

AUTHORS

E. A. Ivleva, I. S. Grinʼ, I. S. Uchaev, Yu. N. Klimochkin

ABSTRACT

The kinetics of oxidation of 16 carboxylic acid esters of the adamantane series in the system H2SO4–HNO3 have been studied, and the effective rate constants have been determined. The reaction is described by the pseudo-first-order kinetic equation. The primary kinetic isotope effect has been estimated at 2.9±0.3. The rate-determining step of the oxidation process is cleavage of the adamantane C–H bond. The presence of an ethyl group at the bridgehead position increases the reactivity of adamantane substrates toward oxidation, whereas methyl, ethoxycarbonyl, and ethoxycarbonylmethyl groups reduce the reactivity. More... »

PAGES

412-421

References to SciGraph publications

  • 2016-11. Synthesis of adamantane functional derivatives basing on N-[(adamantan-1-yl)alkyl]acetamides in RUSSIAN JOURNAL OF ORGANIC CHEMISTRY
  • 2017-08. Synthesis of diacetylamino and diamino derivatives of adamantane series in RUSSIAN JOURNAL OF ORGANIC CHEMISTRY
  • 2015-02. Synthesis of polycarboxylic acids of adamantane series in RUSSIAN JOURNAL OF ORGANIC CHEMISTRY
  • 2016-09. Diesters of adamantanecarboxylic acids as promising components of base stocks for industrial synthetic oils in PETROLEUM CHEMISTRY
  • 2017-12. The Synthesis, Physicochemical Properties, and Thermo-Oxidative Stability of Esters of a Tricarboxylic Acid of the Adamantane Series in PETROLEUM CHEMISTRY
  • 2011-09. Reactivity of C3-C8 alkanes with nitronium ions in sulfuric acid in THEORETICAL AND EXPERIMENTAL CHEMISTRY
  • 2016-04. Development of Synthesis Technology and Quality Control for the Immunotropic Agent Kemantane in PHARMACEUTICAL CHEMISTRY JOURNAL
  • 2018-08. Synthesis, Physicochemical Properties, and Thermo-Oxidative Stability of Diesters of 5,7-Dimethyl-3-hydroxymethyl-1-adamantanol in RUSSIAN JOURNAL OF GENERAL CHEMISTRY
  • 2018-02. Modern Trends of Organic Chemistry in Russian Universities in RUSSIAN JOURNAL OF ORGANIC CHEMISTRY
  • 2015-10. Synthesis of nitroxy- and hydroxy-substituted polycarboxylic acids of the adamantane series in RUSSIAN JOURNAL OF ORGANIC CHEMISTRY
  • 1996-02. Synthesis and psychotropic activty of diamines from the adamantane series in PHARMACEUTICAL CHEMISTRY JOURNAL
  • 2013-11-07. Adamantane-containing esters as potential components of thermostable lubricating oils in PETROLEUM CHEMISTRY
  • 2015-03-18. Diesters of mixed carboxylic acids of the adamantane series: Synthesis, physicochemical properties, and thermo-oxidative stability in PETROLEUM CHEMISTRY
  • 2014-12. Effect of the structure of adamantane-containing diesters on the thermooxidative stability in RUSSIAN JOURNAL OF GENERAL CHEMISTRY
  • 2014-01-11. A facile synthesis of saxagliptin intermediate N-Boc-3-hydroxyadamantylglycine in RESEARCH ON CHEMICAL INTERMEDIATES
  • 1976-11. Synthesis of dicarboxylic acids of adamantane series in RUSSIAN CHEMICAL BULLETIN
  • 1990-01. Synthesis and biological activity of some 1-hydroxy-3-aminoalkyladamantanes and their derivatives in PHARMACEUTICAL CHEMISTRY JOURNAL
  • 2015-07. Antiviral properties of cage compounds. New prospects in RUSSIAN CHEMICAL BULLETIN
  • 2018-07-17. Synthesis, Physicochemical Properties, and Thermo-Oxidative Stability of Diesters of 5,7-Dimethyl-1,3-Adamantanediol and 5,7-Dimethyl-1,3-bis(Hydroxymethyl)adamantane in PETROLEUM CHEMISTRY
  • 2016-10. Synthesis of amino polycarboxylic acids of the adamantane series in RUSSIAN JOURNAL OF ORGANIC CHEMISTRY
  • 2012-08. Adamantane functionalization. synthesis of polyfunctional derivatives with various substituents in bridgehead positions in RUSSIAN JOURNAL OF ORGANIC CHEMISTRY
  • Identifiers

    URI

    http://scigraph.springernature.com/pub.10.1134/s1070428020030082

    DOI

    http://dx.doi.org/10.1134/s1070428020030082

    DIMENSIONS

    https://app.dimensions.ai/details/publication/pub.1126896140


    Indexing Status Check whether this publication has been indexed by Scopus and Web Of Science using the SN Indexing Status Tool
    Incoming Citations Browse incoming citations for this publication using opencitations.net

    JSON-LD is the canonical representation for SciGraph data.

    TIP: You can open this SciGraph record using an external JSON-LD service: JSON-LD Playground Google SDTT

    [
      {
        "@context": "https://springernature.github.io/scigraph/jsonld/sgcontext.json", 
        "about": [
          {
            "id": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/03", 
            "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
            "name": "Chemical Sciences", 
            "type": "DefinedTerm"
          }, 
          {
            "id": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/0306", 
            "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
            "name": "Physical Chemistry (incl. Structural)", 
            "type": "DefinedTerm"
          }
        ], 
        "author": [
          {
            "affiliation": {
              "alternateName": "Samara State Technical University, 443100, Samara, Russia", 
              "id": "http://www.grid.ac/institutes/grid.445792.9", 
              "name": [
                "Samara State Technical University, 443100, Samara, Russia"
              ], 
              "type": "Organization"
            }, 
            "familyName": "Ivleva", 
            "givenName": "E. A.", 
            "id": "sg:person.01262263306.83", 
            "sameAs": [
              "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01262263306.83"
            ], 
            "type": "Person"
          }, 
          {
            "affiliation": {
              "alternateName": "Samara State Technical University, 443100, Samara, Russia", 
              "id": "http://www.grid.ac/institutes/grid.445792.9", 
              "name": [
                "Samara State Technical University, 443100, Samara, Russia"
              ], 
              "type": "Organization"
            }, 
            "familyName": "Grin\u02bc", 
            "givenName": "I. S.", 
            "id": "sg:person.011116227545.48", 
            "sameAs": [
              "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.011116227545.48"
            ], 
            "type": "Person"
          }, 
          {
            "affiliation": {
              "alternateName": "Samara State Technical University, 443100, Samara, Russia", 
              "id": "http://www.grid.ac/institutes/grid.445792.9", 
              "name": [
                "Samara State Technical University, 443100, Samara, Russia"
              ], 
              "type": "Organization"
            }, 
            "familyName": "Uchaev", 
            "givenName": "I. S.", 
            "type": "Person"
          }, 
          {
            "affiliation": {
              "alternateName": "Samara State Technical University, 443100, Samara, Russia", 
              "id": "http://www.grid.ac/institutes/grid.445792.9", 
              "name": [
                "Samara State Technical University, 443100, Samara, Russia"
              ], 
              "type": "Organization"
            }, 
            "familyName": "Klimochkin", 
            "givenName": "Yu. N.", 
            "id": "sg:person.07436126201.08", 
            "sameAs": [
              "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07436126201.08"
            ], 
            "type": "Person"
          }
        ], 
        "citation": [
          {
            "id": "sg:pub.10.1134/s1070428015020062", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1021541742", 
              "https://doi.org/10.1134/s1070428015020062"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/s11094-016-1396-z", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1010365480", 
              "https://doi.org/10.1007/s11094-016-1396-z"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1134/s1070428016110026", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1054040485", 
              "https://doi.org/10.1134/s1070428016110026"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1134/s1070428015100048", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1003822817", 
              "https://doi.org/10.1134/s1070428015100048"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/bf00769383", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1036760357", 
              "https://doi.org/10.1007/bf00769383"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/bf00973410", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1025430883", 
              "https://doi.org/10.1007/bf00973410"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1134/s1070363218080091", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1107957859", 
              "https://doi.org/10.1134/s1070363218080091"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/bf02218874", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1036570454", 
              "https://doi.org/10.1007/bf02218874"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/s11237-011-9211-0", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1044862976", 
              "https://doi.org/10.1007/s11237-011-9211-0"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1134/s096554411808008x", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1105673007", 
              "https://doi.org/10.1134/s096554411808008x"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1134/s107042801802001x", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1103949858", 
              "https://doi.org/10.1134/s107042801802001x"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1134/s0965544115020127", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1040930796", 
              "https://doi.org/10.1134/s0965544115020127"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1134/s1070428016100043", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1038046185", 
              "https://doi.org/10.1134/s1070428016100043"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1134/s0965544113060029", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1028878313", 
              "https://doi.org/10.1134/s0965544113060029"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1134/s0965544117120040", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1101064507", 
              "https://doi.org/10.1134/s0965544117120040"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1134/s0965544116090061", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1053829775", 
              "https://doi.org/10.1134/s0965544116090061"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/s11172-015-1035-y", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1053682684", 
              "https://doi.org/10.1007/s11172-015-1035-y"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1134/s1070363214120226", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1044501341", 
              "https://doi.org/10.1134/s1070363214120226"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/s11164-013-1515-3", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1012495570", 
              "https://doi.org/10.1007/s11164-013-1515-3"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1134/s1070428012080015", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1000257212", 
              "https://doi.org/10.1134/s1070428012080015"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1134/s1070428017080024", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1091894387", 
              "https://doi.org/10.1134/s1070428017080024"
            ], 
            "type": "CreativeWork"
          }
        ], 
        "datePublished": "2020-03", 
        "datePublishedReg": "2020-03-01", 
        "description": "The kinetics of oxidation of 16 carboxylic acid esters of the adamantane\nseries in the system\nH2SO4\u2013HNO3\nhave been studied, and the effective rate constants have been determined. The\nreaction is described by the pseudo-first-order kinetic equation. The primary\nkinetic isotope effect has been estimated at 2.9\u00b10.3. The rate-determining step\nof the oxidation process is cleavage of the adamantane C\u2013H bond. The presence of\nan ethyl group at the bridgehead position increases the reactivity of adamantane\nsubstrates toward oxidation, whereas methyl, ethoxycarbonyl, and\nethoxycarbonylmethyl groups reduce the reactivity.", 
        "genre": "article", 
        "id": "sg:pub.10.1134/s1070428020030082", 
        "inLanguage": "en", 
        "isAccessibleForFree": false, 
        "isPartOf": [
          {
            "id": "sg:journal.1136317", 
            "issn": [
              "0514-7492", 
              "1070-4280"
            ], 
            "name": "Russian Journal of Organic Chemistry", 
            "publisher": "Pleiades Publishing", 
            "type": "Periodical"
          }, 
          {
            "issueNumber": "3", 
            "type": "PublicationIssue"
          }, 
          {
            "type": "PublicationVolume", 
            "volumeNumber": "56"
          }
        ], 
        "keywords": [
          "rate-determining step", 
          "order kinetic equation", 
          "kinetic isotope effects", 
          "kinetics of oxidation", 
          "carboxylic acid esters", 
          "effective rate constants", 
          "oxidation process", 
          "bridgehead position", 
          "H2SO4-HNO3", 
          "ethyl group", 
          "ethoxycarbonylmethyl group", 
          "isotope effect", 
          "rate constants", 
          "acid esters", 
          "oxidation", 
          "adamantane", 
          "reactivity", 
          "kinetic equation", 
          "bonds", 
          "ethoxycarbonyl", 
          "reaction", 
          "esters", 
          "constants", 
          "kinetics", 
          "cleavage", 
          "methyl", 
          "substrate", 
          "series", 
          "step", 
          "presence", 
          "group", 
          "process", 
          "effect", 
          "position", 
          "system", 
          "equations", 
          "reactivity of adamantane", 
          "Deactivated Cage Substrates", 
          "Cage Substrates", 
          "System H2SO4\u2013HNO3"
        ], 
        "name": "Oxidation of Deactivated Cage Substrates in the System H2SO4\u2013HNO3", 
        "pagination": "412-421", 
        "productId": [
          {
            "name": "dimensions_id", 
            "type": "PropertyValue", 
            "value": [
              "pub.1126896140"
            ]
          }, 
          {
            "name": "doi", 
            "type": "PropertyValue", 
            "value": [
              "10.1134/s1070428020030082"
            ]
          }
        ], 
        "sameAs": [
          "https://doi.org/10.1134/s1070428020030082", 
          "https://app.dimensions.ai/details/publication/pub.1126896140"
        ], 
        "sdDataset": "articles", 
        "sdDatePublished": "2022-01-01T18:55", 
        "sdLicense": "https://scigraph.springernature.com/explorer/license/", 
        "sdPublisher": {
          "name": "Springer Nature - SN SciGraph project", 
          "type": "Organization"
        }, 
        "sdSource": "s3://com-springernature-scigraph/baseset/20220101/entities/gbq_results/article/article_842.jsonl", 
        "type": "ScholarlyArticle", 
        "url": "https://doi.org/10.1134/s1070428020030082"
      }
    ]
     

    Download the RDF metadata as:  json-ld nt turtle xml License info

    HOW TO GET THIS DATA PROGRAMMATICALLY:

    JSON-LD is a popular format for linked data which is fully compatible with JSON.

    curl -H 'Accept: application/ld+json' 'https://scigraph.springernature.com/pub.10.1134/s1070428020030082'

    N-Triples is a line-based linked data format ideal for batch operations.

    curl -H 'Accept: application/n-triples' 'https://scigraph.springernature.com/pub.10.1134/s1070428020030082'

    Turtle is a human-readable linked data format.

    curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1134/s1070428020030082'

    RDF/XML is a standard XML format for linked data.

    curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1134/s1070428020030082'


     

    This table displays all metadata directly associated to this object as RDF triples.

    202 TRIPLES      22 PREDICATES      87 URIs      58 LITERALS      6 BLANK NODES

    Subject Predicate Object
    1 sg:pub.10.1134/s1070428020030082 schema:about anzsrc-for:03
    2 anzsrc-for:0306
    3 schema:author N0923f5acb6c3494f9bc6fec0b2b6bfa5
    4 schema:citation sg:pub.10.1007/bf00769383
    5 sg:pub.10.1007/bf00973410
    6 sg:pub.10.1007/bf02218874
    7 sg:pub.10.1007/s11094-016-1396-z
    8 sg:pub.10.1007/s11164-013-1515-3
    9 sg:pub.10.1007/s11172-015-1035-y
    10 sg:pub.10.1007/s11237-011-9211-0
    11 sg:pub.10.1134/s0965544113060029
    12 sg:pub.10.1134/s0965544115020127
    13 sg:pub.10.1134/s0965544116090061
    14 sg:pub.10.1134/s0965544117120040
    15 sg:pub.10.1134/s096554411808008x
    16 sg:pub.10.1134/s1070363214120226
    17 sg:pub.10.1134/s1070363218080091
    18 sg:pub.10.1134/s1070428012080015
    19 sg:pub.10.1134/s1070428015020062
    20 sg:pub.10.1134/s1070428015100048
    21 sg:pub.10.1134/s1070428016100043
    22 sg:pub.10.1134/s1070428016110026
    23 sg:pub.10.1134/s1070428017080024
    24 sg:pub.10.1134/s107042801802001x
    25 schema:datePublished 2020-03
    26 schema:datePublishedReg 2020-03-01
    27 schema:description The kinetics of oxidation of 16 carboxylic acid esters of the adamantane series in the system H2SO4–HNO3 have been studied, and the effective rate constants have been determined. The reaction is described by the pseudo-first-order kinetic equation. The primary kinetic isotope effect has been estimated at 2.9±0.3. The rate-determining step of the oxidation process is cleavage of the adamantane C–H bond. The presence of an ethyl group at the bridgehead position increases the reactivity of adamantane substrates toward oxidation, whereas methyl, ethoxycarbonyl, and ethoxycarbonylmethyl groups reduce the reactivity.
    28 schema:genre article
    29 schema:inLanguage en
    30 schema:isAccessibleForFree false
    31 schema:isPartOf N5058e5cb70a24d4c903a90a4f94cc1d0
    32 Ne1b71b483b9a40d4b2407714b2114934
    33 sg:journal.1136317
    34 schema:keywords Cage Substrates
    35 Deactivated Cage Substrates
    36 H2SO4-HNO3
    37 System H2SO4–HNO3
    38 acid esters
    39 adamantane
    40 bonds
    41 bridgehead position
    42 carboxylic acid esters
    43 cleavage
    44 constants
    45 effect
    46 effective rate constants
    47 equations
    48 esters
    49 ethoxycarbonyl
    50 ethoxycarbonylmethyl group
    51 ethyl group
    52 group
    53 isotope effect
    54 kinetic equation
    55 kinetic isotope effects
    56 kinetics
    57 kinetics of oxidation
    58 methyl
    59 order kinetic equation
    60 oxidation
    61 oxidation process
    62 position
    63 presence
    64 process
    65 rate constants
    66 rate-determining step
    67 reaction
    68 reactivity
    69 reactivity of adamantane
    70 series
    71 step
    72 substrate
    73 system
    74 schema:name Oxidation of Deactivated Cage Substrates in the System H2SO4–HNO3
    75 schema:pagination 412-421
    76 schema:productId N946953344cca420b80a837aa3933ed4d
    77 Nad207b5ea2704a2ca1c0d320d4c65be3
    78 schema:sameAs https://app.dimensions.ai/details/publication/pub.1126896140
    79 https://doi.org/10.1134/s1070428020030082
    80 schema:sdDatePublished 2022-01-01T18:55
    81 schema:sdLicense https://scigraph.springernature.com/explorer/license/
    82 schema:sdPublisher N0bd88ac418d8432393edae349877cfa4
    83 schema:url https://doi.org/10.1134/s1070428020030082
    84 sgo:license sg:explorer/license/
    85 sgo:sdDataset articles
    86 rdf:type schema:ScholarlyArticle
    87 N0923f5acb6c3494f9bc6fec0b2b6bfa5 rdf:first sg:person.01262263306.83
    88 rdf:rest N122fbdb6ca3c45cbb32d2f96742562fa
    89 N0bd88ac418d8432393edae349877cfa4 schema:name Springer Nature - SN SciGraph project
    90 rdf:type schema:Organization
    91 N122fbdb6ca3c45cbb32d2f96742562fa rdf:first sg:person.011116227545.48
    92 rdf:rest N2913a06fc6f544b1a4fc8125c59c067b
    93 N2913a06fc6f544b1a4fc8125c59c067b rdf:first Nb5ec95e1ad6f46f0a481c37e77017e0c
    94 rdf:rest N8ecc85836ca445bbad381d0b7b62ba5e
    95 N5058e5cb70a24d4c903a90a4f94cc1d0 schema:issueNumber 3
    96 rdf:type schema:PublicationIssue
    97 N8ecc85836ca445bbad381d0b7b62ba5e rdf:first sg:person.07436126201.08
    98 rdf:rest rdf:nil
    99 N946953344cca420b80a837aa3933ed4d schema:name doi
    100 schema:value 10.1134/s1070428020030082
    101 rdf:type schema:PropertyValue
    102 Nad207b5ea2704a2ca1c0d320d4c65be3 schema:name dimensions_id
    103 schema:value pub.1126896140
    104 rdf:type schema:PropertyValue
    105 Nb5ec95e1ad6f46f0a481c37e77017e0c schema:affiliation grid-institutes:grid.445792.9
    106 schema:familyName Uchaev
    107 schema:givenName I. S.
    108 rdf:type schema:Person
    109 Ne1b71b483b9a40d4b2407714b2114934 schema:volumeNumber 56
    110 rdf:type schema:PublicationVolume
    111 anzsrc-for:03 schema:inDefinedTermSet anzsrc-for:
    112 schema:name Chemical Sciences
    113 rdf:type schema:DefinedTerm
    114 anzsrc-for:0306 schema:inDefinedTermSet anzsrc-for:
    115 schema:name Physical Chemistry (incl. Structural)
    116 rdf:type schema:DefinedTerm
    117 sg:journal.1136317 schema:issn 0514-7492
    118 1070-4280
    119 schema:name Russian Journal of Organic Chemistry
    120 schema:publisher Pleiades Publishing
    121 rdf:type schema:Periodical
    122 sg:person.011116227545.48 schema:affiliation grid-institutes:grid.445792.9
    123 schema:familyName Grinʼ
    124 schema:givenName I. S.
    125 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.011116227545.48
    126 rdf:type schema:Person
    127 sg:person.01262263306.83 schema:affiliation grid-institutes:grid.445792.9
    128 schema:familyName Ivleva
    129 schema:givenName E. A.
    130 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01262263306.83
    131 rdf:type schema:Person
    132 sg:person.07436126201.08 schema:affiliation grid-institutes:grid.445792.9
    133 schema:familyName Klimochkin
    134 schema:givenName Yu. N.
    135 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07436126201.08
    136 rdf:type schema:Person
    137 sg:pub.10.1007/bf00769383 schema:sameAs https://app.dimensions.ai/details/publication/pub.1036760357
    138 https://doi.org/10.1007/bf00769383
    139 rdf:type schema:CreativeWork
    140 sg:pub.10.1007/bf00973410 schema:sameAs https://app.dimensions.ai/details/publication/pub.1025430883
    141 https://doi.org/10.1007/bf00973410
    142 rdf:type schema:CreativeWork
    143 sg:pub.10.1007/bf02218874 schema:sameAs https://app.dimensions.ai/details/publication/pub.1036570454
    144 https://doi.org/10.1007/bf02218874
    145 rdf:type schema:CreativeWork
    146 sg:pub.10.1007/s11094-016-1396-z schema:sameAs https://app.dimensions.ai/details/publication/pub.1010365480
    147 https://doi.org/10.1007/s11094-016-1396-z
    148 rdf:type schema:CreativeWork
    149 sg:pub.10.1007/s11164-013-1515-3 schema:sameAs https://app.dimensions.ai/details/publication/pub.1012495570
    150 https://doi.org/10.1007/s11164-013-1515-3
    151 rdf:type schema:CreativeWork
    152 sg:pub.10.1007/s11172-015-1035-y schema:sameAs https://app.dimensions.ai/details/publication/pub.1053682684
    153 https://doi.org/10.1007/s11172-015-1035-y
    154 rdf:type schema:CreativeWork
    155 sg:pub.10.1007/s11237-011-9211-0 schema:sameAs https://app.dimensions.ai/details/publication/pub.1044862976
    156 https://doi.org/10.1007/s11237-011-9211-0
    157 rdf:type schema:CreativeWork
    158 sg:pub.10.1134/s0965544113060029 schema:sameAs https://app.dimensions.ai/details/publication/pub.1028878313
    159 https://doi.org/10.1134/s0965544113060029
    160 rdf:type schema:CreativeWork
    161 sg:pub.10.1134/s0965544115020127 schema:sameAs https://app.dimensions.ai/details/publication/pub.1040930796
    162 https://doi.org/10.1134/s0965544115020127
    163 rdf:type schema:CreativeWork
    164 sg:pub.10.1134/s0965544116090061 schema:sameAs https://app.dimensions.ai/details/publication/pub.1053829775
    165 https://doi.org/10.1134/s0965544116090061
    166 rdf:type schema:CreativeWork
    167 sg:pub.10.1134/s0965544117120040 schema:sameAs https://app.dimensions.ai/details/publication/pub.1101064507
    168 https://doi.org/10.1134/s0965544117120040
    169 rdf:type schema:CreativeWork
    170 sg:pub.10.1134/s096554411808008x schema:sameAs https://app.dimensions.ai/details/publication/pub.1105673007
    171 https://doi.org/10.1134/s096554411808008x
    172 rdf:type schema:CreativeWork
    173 sg:pub.10.1134/s1070363214120226 schema:sameAs https://app.dimensions.ai/details/publication/pub.1044501341
    174 https://doi.org/10.1134/s1070363214120226
    175 rdf:type schema:CreativeWork
    176 sg:pub.10.1134/s1070363218080091 schema:sameAs https://app.dimensions.ai/details/publication/pub.1107957859
    177 https://doi.org/10.1134/s1070363218080091
    178 rdf:type schema:CreativeWork
    179 sg:pub.10.1134/s1070428012080015 schema:sameAs https://app.dimensions.ai/details/publication/pub.1000257212
    180 https://doi.org/10.1134/s1070428012080015
    181 rdf:type schema:CreativeWork
    182 sg:pub.10.1134/s1070428015020062 schema:sameAs https://app.dimensions.ai/details/publication/pub.1021541742
    183 https://doi.org/10.1134/s1070428015020062
    184 rdf:type schema:CreativeWork
    185 sg:pub.10.1134/s1070428015100048 schema:sameAs https://app.dimensions.ai/details/publication/pub.1003822817
    186 https://doi.org/10.1134/s1070428015100048
    187 rdf:type schema:CreativeWork
    188 sg:pub.10.1134/s1070428016100043 schema:sameAs https://app.dimensions.ai/details/publication/pub.1038046185
    189 https://doi.org/10.1134/s1070428016100043
    190 rdf:type schema:CreativeWork
    191 sg:pub.10.1134/s1070428016110026 schema:sameAs https://app.dimensions.ai/details/publication/pub.1054040485
    192 https://doi.org/10.1134/s1070428016110026
    193 rdf:type schema:CreativeWork
    194 sg:pub.10.1134/s1070428017080024 schema:sameAs https://app.dimensions.ai/details/publication/pub.1091894387
    195 https://doi.org/10.1134/s1070428017080024
    196 rdf:type schema:CreativeWork
    197 sg:pub.10.1134/s107042801802001x schema:sameAs https://app.dimensions.ai/details/publication/pub.1103949858
    198 https://doi.org/10.1134/s107042801802001x
    199 rdf:type schema:CreativeWork
    200 grid-institutes:grid.445792.9 schema:alternateName Samara State Technical University, 443100, Samara, Russia
    201 schema:name Samara State Technical University, 443100, Samara, Russia
    202 rdf:type schema:Organization
     




    Preview window. Press ESC to close (or click here)


    ...