Synthesis of phthalide-containing dihalogeno derivatives and polyarylene ether ketones based on them View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2000-06

AUTHORS

S. N. Salazkin, V. V. Shaposhnikova, K. I. Donetskii, G. V. Gorshkov, P. V. Petrovskii, L. I. Komarova, M. M. Genina, A. S. Tkachenko

ABSTRACT

New activated phthalide-containing dihalogeno derivatives were synthesized, and cardo polyarylene ether ketones based on them were prepared. The effect of the type of the halogen atom (fluorine, chlorine, or bromine) on the efficiency of polycondensation was estimated. It was demonstrated that high-molecular-weight cardo polyarylene ether ketones can be obtained only from the difluoro derivative. The synthesized polymers are amorphous compounds characterized by high glass transition temperatures (210–250°C). These polymers are soluble in many organic solvents and form strong transparent films. More... »

PAGES

1093-1096

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf02494901

DOI

http://dx.doi.org/10.1007/bf02494901

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1001687749


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/2008/0303", 
        "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
        "name": "Macromolecular and Materials Chemistry", 
        "type": "DefinedTerm"
      }, 
      {
        "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"
      }
    ], 
    "author": [
      {
        "affiliation": {
          "alternateName": "Russian Academy of Sciences", 
          "id": "https://www.grid.ac/institutes/grid.4886.2", 
          "name": [
            "A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 117813, Moscow, Russian Federation"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Salazkin", 
        "givenName": "S. N.", 
        "id": "sg:person.013234277712.17", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.013234277712.17"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Russian Academy of Sciences", 
          "id": "https://www.grid.ac/institutes/grid.4886.2", 
          "name": [
            "A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 117813, Moscow, Russian Federation"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Shaposhnikova", 
        "givenName": "V. V.", 
        "id": "sg:person.01171546735.26", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01171546735.26"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Russian Academy of Sciences", 
          "id": "https://www.grid.ac/institutes/grid.4886.2", 
          "name": [
            "A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 117813, Moscow, Russian Federation"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Donetskii", 
        "givenName": "K. I.", 
        "id": "sg:person.011643514167.72", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.011643514167.72"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Russian Academy of Sciences", 
          "id": "https://www.grid.ac/institutes/grid.4886.2", 
          "name": [
            "A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 117813, Moscow, Russian Federation"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Gorshkov", 
        "givenName": "G. V.", 
        "id": "sg:person.016143234253.92", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016143234253.92"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Russian Academy of Sciences", 
          "id": "https://www.grid.ac/institutes/grid.4886.2", 
          "name": [
            "A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 117813, Moscow, Russian Federation"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Petrovskii", 
        "givenName": "P. V.", 
        "id": "sg:person.014725472203.42", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014725472203.42"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Russian Academy of Sciences", 
          "id": "https://www.grid.ac/institutes/grid.4886.2", 
          "name": [
            "A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 117813, Moscow, Russian Federation"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Komarova", 
        "givenName": "L. I.", 
        "id": "sg:person.016132576163.09", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016132576163.09"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Russian Academy of Sciences", 
          "id": "https://www.grid.ac/institutes/grid.4886.2", 
          "name": [
            "A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 117813, Moscow, Russian Federation"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Genina", 
        "givenName": "M. M.", 
        "id": "sg:person.013223445453.84", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.013223445453.84"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Russian Academy of Sciences", 
          "id": "https://www.grid.ac/institutes/grid.4886.2", 
          "name": [
            "A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 117813, Moscow, Russian Federation"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Tkachenko", 
        "givenName": "A. S.", 
        "id": "sg:person.012751450542.75", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.012751450542.75"
        ], 
        "type": "Person"
      }
    ], 
    "citation": [
      {
        "id": "https://doi.org/10.1070/mc1997v007n05abeh000850", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1035885433"
        ], 
        "type": "CreativeWork"
      }
    ], 
    "datePublished": "2000-06", 
    "datePublishedReg": "2000-06-01", 
    "description": "New activated phthalide-containing dihalogeno derivatives were synthesized, and cardo polyarylene ether ketones based on them were prepared. The effect of the type of the halogen atom (fluorine, chlorine, or bromine) on the efficiency of polycondensation was estimated. It was demonstrated that high-molecular-weight cardo polyarylene ether ketones can be obtained only from the difluoro derivative. The synthesized polymers are amorphous compounds characterized by high glass transition temperatures (210\u2013250\u00b0C). These polymers are soluble in many organic solvents and form strong transparent films.", 
    "genre": "research_article", 
    "id": "sg:pub.10.1007/bf02494901", 
    "inLanguage": [
      "en"
    ], 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1022309", 
        "issn": [
          "1066-5285", 
          "1573-9171"
        ], 
        "name": "Russian Chemical Bulletin", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "6", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "49"
      }
    ], 
    "name": "Synthesis of phthalide-containing dihalogeno derivatives and polyarylene ether ketones based on them", 
    "pagination": "1093-1096", 
    "productId": [
      {
        "name": "readcube_id", 
        "type": "PropertyValue", 
        "value": [
          "0809a158121014a7022996dcc4f100152f419bab8ff7f90d2b5ec66c10f63666"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/bf02494901"
        ]
      }, 
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1001687749"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/bf02494901", 
      "https://app.dimensions.ai/details/publication/pub.1001687749"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2019-04-11T13:27", 
    "sdLicense": "https://scigraph.springernature.com/explorer/license/", 
    "sdPublisher": {
      "name": "Springer Nature - SN SciGraph project", 
      "type": "Organization"
    }, 
    "sdSource": "s3://com-uberresearch-data-dimensions-target-20181106-alternative/cleanup/v134/2549eaecd7973599484d7c17b260dba0a4ecb94b/merge/v9/a6c9fde33151104705d4d7ff012ea9563521a3ce/jats-lookup/v90/0000000370_0000000370/records_46738_00000000.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "http://link.springer.com/10.1007%2FBF02494901"
  }
]
 

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.10.1007/bf02494901'

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

curl -H 'Accept: application/n-triples' 'https://scigraph.springernature.com/pub.10.1007/bf02494901'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/bf02494901'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/bf02494901'


 

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

113 TRIPLES      21 PREDICATES      28 URIs      19 LITERALS      7 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/bf02494901 schema:about anzsrc-for:03
2 anzsrc-for:0303
3 schema:author Ne3e6feea98954e9e85224be4b546c6f4
4 schema:citation https://doi.org/10.1070/mc1997v007n05abeh000850
5 schema:datePublished 2000-06
6 schema:datePublishedReg 2000-06-01
7 schema:description New activated phthalide-containing dihalogeno derivatives were synthesized, and cardo polyarylene ether ketones based on them were prepared. The effect of the type of the halogen atom (fluorine, chlorine, or bromine) on the efficiency of polycondensation was estimated. It was demonstrated that high-molecular-weight cardo polyarylene ether ketones can be obtained only from the difluoro derivative. The synthesized polymers are amorphous compounds characterized by high glass transition temperatures (210–250°C). These polymers are soluble in many organic solvents and form strong transparent films.
8 schema:genre research_article
9 schema:inLanguage en
10 schema:isAccessibleForFree false
11 schema:isPartOf N5ece93cd67c24ca4bc532180dfdc82e6
12 N6513b23ff1e745489d128cb48b0f6ef3
13 sg:journal.1022309
14 schema:name Synthesis of phthalide-containing dihalogeno derivatives and polyarylene ether ketones based on them
15 schema:pagination 1093-1096
16 schema:productId N2f8c920d38be40eba31a224bd5993393
17 Nb4e0bc653d3d4fdca8b21f837f67091a
18 Nce72bb3db653430799c5acc62794c988
19 schema:sameAs https://app.dimensions.ai/details/publication/pub.1001687749
20 https://doi.org/10.1007/bf02494901
21 schema:sdDatePublished 2019-04-11T13:27
22 schema:sdLicense https://scigraph.springernature.com/explorer/license/
23 schema:sdPublisher N7b83d6b28b2c4ee2a06c93a6ed09dc6a
24 schema:url http://link.springer.com/10.1007%2FBF02494901
25 sgo:license sg:explorer/license/
26 sgo:sdDataset articles
27 rdf:type schema:ScholarlyArticle
28 N02517fcb1a01448895c12d8edd1cdb26 rdf:first sg:person.016132576163.09
29 rdf:rest N3a8ef4c547384ce2a273ec3b485bff4f
30 N193a0970be63401ab1b67205ec1b5724 rdf:first sg:person.012751450542.75
31 rdf:rest rdf:nil
32 N2f8c920d38be40eba31a224bd5993393 schema:name dimensions_id
33 schema:value pub.1001687749
34 rdf:type schema:PropertyValue
35 N317210c0586846148f5234a6631b8ec9 rdf:first sg:person.016143234253.92
36 rdf:rest Nd7da41b8f97b454c938186acb611760a
37 N3a8ef4c547384ce2a273ec3b485bff4f rdf:first sg:person.013223445453.84
38 rdf:rest N193a0970be63401ab1b67205ec1b5724
39 N5ece93cd67c24ca4bc532180dfdc82e6 schema:volumeNumber 49
40 rdf:type schema:PublicationVolume
41 N6513b23ff1e745489d128cb48b0f6ef3 schema:issueNumber 6
42 rdf:type schema:PublicationIssue
43 N7b83d6b28b2c4ee2a06c93a6ed09dc6a schema:name Springer Nature - SN SciGraph project
44 rdf:type schema:Organization
45 Nb4e0bc653d3d4fdca8b21f837f67091a schema:name doi
46 schema:value 10.1007/bf02494901
47 rdf:type schema:PropertyValue
48 Nce72bb3db653430799c5acc62794c988 schema:name readcube_id
49 schema:value 0809a158121014a7022996dcc4f100152f419bab8ff7f90d2b5ec66c10f63666
50 rdf:type schema:PropertyValue
51 Nd7da41b8f97b454c938186acb611760a rdf:first sg:person.014725472203.42
52 rdf:rest N02517fcb1a01448895c12d8edd1cdb26
53 Ne3e6feea98954e9e85224be4b546c6f4 rdf:first sg:person.013234277712.17
54 rdf:rest Ne703a85fc68e4055a73a95ace265f1f6
55 Ne703a85fc68e4055a73a95ace265f1f6 rdf:first sg:person.01171546735.26
56 rdf:rest Nf02c22bb562841e38e5df0ebab5edbed
57 Nf02c22bb562841e38e5df0ebab5edbed rdf:first sg:person.011643514167.72
58 rdf:rest N317210c0586846148f5234a6631b8ec9
59 anzsrc-for:03 schema:inDefinedTermSet anzsrc-for:
60 schema:name Chemical Sciences
61 rdf:type schema:DefinedTerm
62 anzsrc-for:0303 schema:inDefinedTermSet anzsrc-for:
63 schema:name Macromolecular and Materials Chemistry
64 rdf:type schema:DefinedTerm
65 sg:journal.1022309 schema:issn 1066-5285
66 1573-9171
67 schema:name Russian Chemical Bulletin
68 rdf:type schema:Periodical
69 sg:person.011643514167.72 schema:affiliation https://www.grid.ac/institutes/grid.4886.2
70 schema:familyName Donetskii
71 schema:givenName K. I.
72 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.011643514167.72
73 rdf:type schema:Person
74 sg:person.01171546735.26 schema:affiliation https://www.grid.ac/institutes/grid.4886.2
75 schema:familyName Shaposhnikova
76 schema:givenName V. V.
77 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01171546735.26
78 rdf:type schema:Person
79 sg:person.012751450542.75 schema:affiliation https://www.grid.ac/institutes/grid.4886.2
80 schema:familyName Tkachenko
81 schema:givenName A. S.
82 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.012751450542.75
83 rdf:type schema:Person
84 sg:person.013223445453.84 schema:affiliation https://www.grid.ac/institutes/grid.4886.2
85 schema:familyName Genina
86 schema:givenName M. M.
87 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.013223445453.84
88 rdf:type schema:Person
89 sg:person.013234277712.17 schema:affiliation https://www.grid.ac/institutes/grid.4886.2
90 schema:familyName Salazkin
91 schema:givenName S. N.
92 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.013234277712.17
93 rdf:type schema:Person
94 sg:person.014725472203.42 schema:affiliation https://www.grid.ac/institutes/grid.4886.2
95 schema:familyName Petrovskii
96 schema:givenName P. V.
97 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014725472203.42
98 rdf:type schema:Person
99 sg:person.016132576163.09 schema:affiliation https://www.grid.ac/institutes/grid.4886.2
100 schema:familyName Komarova
101 schema:givenName L. I.
102 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016132576163.09
103 rdf:type schema:Person
104 sg:person.016143234253.92 schema:affiliation https://www.grid.ac/institutes/grid.4886.2
105 schema:familyName Gorshkov
106 schema:givenName G. V.
107 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016143234253.92
108 rdf:type schema:Person
109 https://doi.org/10.1070/mc1997v007n05abeh000850 schema:sameAs https://app.dimensions.ai/details/publication/pub.1035885433
110 rdf:type schema:CreativeWork
111 https://www.grid.ac/institutes/grid.4886.2 schema:alternateName Russian Academy of Sciences
112 schema:name A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 117813, Moscow, Russian Federation
113 rdf:type schema:Organization
 




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


...