New chemosensor systems of the benzo-[de]Isoquinoline-1,3-Dione Series View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2012-11-27

AUTHORS

I. E. Tolpygin, E. N. Shepelenko, Yu. V. Revinskii, A. D. Dubonosov, V. A. Bren, V. I. Minkin

ABSTRACT

New derivatives of the benzo[de]isoquinoline-1,3-dione system containing an amino group were synthesized by the reaction of 2-benzyl-6-bromobenzo[de]isoquinoline-1,3-dione with ethylenediamine and hydrazine. Further functionalization of the free amino groups leads to imines, amines, thioureas, and hydrazones. Some compounds exhibit high chemosensor selectivity in the determination of anions.

PAGES

1325-1331

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s10593-012-1140-x

DOI

http://dx.doi.org/10.1007/s10593-012-1140-x

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1046934493


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/2008/0305", 
        "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
        "name": "Organic Chemistry", 
        "type": "DefinedTerm"
      }
    ], 
    "author": [
      {
        "affiliation": {
          "alternateName": "Scientific-Research Institute of Physical and Organic Chemistry, Southern Federal University, 194/2 Stachki Ave., 344090, Rostov-on-the-Don, Russia", 
          "id": "http://www.grid.ac/institutes/grid.182798.d", 
          "name": [
            "Scientific-Research Institute of Physical and Organic Chemistry, Southern Federal University, 194/2 Stachki Ave., 344090, Rostov-on-the-Don, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Tolpygin", 
        "givenName": "I. E.", 
        "id": "sg:person.07764646417.25", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07764646417.25"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Southern Scientific Center, Russian Academy of Sciences, 41 Chekhova St., 344010, Rostov-on-the-Don, Russia", 
          "id": "http://www.grid.ac/institutes/grid.465325.3", 
          "name": [
            "Southern Scientific Center, Russian Academy of Sciences, 41 Chekhova St., 344010, Rostov-on-the-Don, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Shepelenko", 
        "givenName": "E. N.", 
        "id": "sg:person.010123611500.98", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010123611500.98"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Southern Scientific Center, Russian Academy of Sciences, 41 Chekhova St., 344010, Rostov-on-the-Don, Russia", 
          "id": "http://www.grid.ac/institutes/grid.465325.3", 
          "name": [
            "Southern Scientific Center, Russian Academy of Sciences, 41 Chekhova St., 344010, Rostov-on-the-Don, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Revinskii", 
        "givenName": "Yu. V.", 
        "id": "sg:person.07435241541.11", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07435241541.11"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Southern Scientific Center, Russian Academy of Sciences, 41 Chekhova St., 344010, Rostov-on-the-Don, Russia", 
          "id": "http://www.grid.ac/institutes/grid.465325.3", 
          "name": [
            "Southern Scientific Center, Russian Academy of Sciences, 41 Chekhova St., 344010, Rostov-on-the-Don, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Dubonosov", 
        "givenName": "A. D.", 
        "id": "sg:person.015331070355.66", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015331070355.66"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Scientific-Research Institute of Physical and Organic Chemistry, Southern Federal University, 194/2 Stachki Ave., 344090, Rostov-on-the-Don, Russia", 
          "id": "http://www.grid.ac/institutes/grid.182798.d", 
          "name": [
            "Scientific-Research Institute of Physical and Organic Chemistry, Southern Federal University, 194/2 Stachki Ave., 344090, Rostov-on-the-Don, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Bren", 
        "givenName": "V. A.", 
        "id": "sg:person.014142154521.27", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014142154521.27"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Southern Scientific Center, Russian Academy of Sciences, 41 Chekhova St., 344010, Rostov-on-the-Don, Russia", 
          "id": "http://www.grid.ac/institutes/grid.465325.3", 
          "name": [
            "Scientific-Research Institute of Physical and Organic Chemistry, Southern Federal University, 194/2 Stachki Ave., 344090, Rostov-on-the-Don, Russia", 
            "Southern Scientific Center, Russian Academy of Sciences, 41 Chekhova St., 344010, Rostov-on-the-Don, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Minkin", 
        "givenName": "V. I.", 
        "id": "sg:person.07535265367.87", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07535265367.87"
        ], 
        "type": "Person"
      }
    ], 
    "citation": [
      {
        "id": "sg:pub.10.1134/s1070363210040146", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1039141122", 
          "https://doi.org/10.1134/s1070363210040146"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1134/s1070428010080129", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1014846694", 
          "https://doi.org/10.1134/s1070428010080129"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1134/s1070428007030098", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1032593071", 
          "https://doi.org/10.1134/s1070428007030098"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1134/s1070428009020018", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1007772040", 
          "https://doi.org/10.1134/s1070428009020018"
        ], 
        "type": "CreativeWork"
      }
    ], 
    "datePublished": "2012-11-27", 
    "datePublishedReg": "2012-11-27", 
    "description": "New derivatives of the benzo[de]isoquinoline-1,3-dione system containing an amino group were synthesized by the reaction of 2-benzyl-6-bromobenzo[de]isoquinoline-1,3-dione with ethylenediamine and hydrazine. Further functionalization of the free amino groups leads to imines, amines, thioureas, and hydrazones. Some compounds exhibit high chemosensor selectivity in the determination of anions.", 
    "genre": "article", 
    "id": "sg:pub.10.1007/s10593-012-1140-x", 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1429545", 
        "issn": [
          "0132-6244", 
          "1573-8353"
        ], 
        "name": "Chemistry of Heterocyclic Compounds", 
        "publisher": "Springer Nature", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "9", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "48"
      }
    ], 
    "keywords": [
      "amino groups", 
      "determination of anions", 
      "free amino groups", 
      "chemosensor selectivity", 
      "further functionalization", 
      "chemosensor system", 
      "new derivatives", 
      "dione system", 
      "dione series", 
      "functionalization", 
      "anions", 
      "ethylenediamine", 
      "imines", 
      "hydrazine", 
      "hydrazones", 
      "thiourea", 
      "selectivity", 
      "amines", 
      "benzo", 
      "compounds", 
      "dione", 
      "derivatives", 
      "reaction", 
      "determination", 
      "series", 
      "group", 
      "system"
    ], 
    "name": "New chemosensor systems of the benzo-[de]Isoquinoline-1,3-Dione Series", 
    "pagination": "1325-1331", 
    "productId": [
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1046934493"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/s10593-012-1140-x"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/s10593-012-1140-x", 
      "https://app.dimensions.ai/details/publication/pub.1046934493"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2022-12-01T06:30", 
    "sdLicense": "https://scigraph.springernature.com/explorer/license/", 
    "sdPublisher": {
      "name": "Springer Nature - SN SciGraph project", 
      "type": "Organization"
    }, 
    "sdSource": "s3://com-springernature-scigraph/baseset/20221201/entities/gbq_results/article/article_573.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "https://doi.org/10.1007/s10593-012-1140-x"
  }
]
 

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/s10593-012-1140-x'

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/s10593-012-1140-x'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/s10593-012-1140-x'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/s10593-012-1140-x'


 

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

139 TRIPLES      21 PREDICATES      55 URIs      43 LITERALS      6 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/s10593-012-1140-x schema:about anzsrc-for:03
2 anzsrc-for:0305
3 schema:author Nfb6b9d2370ec409191491020450be890
4 schema:citation sg:pub.10.1134/s1070363210040146
5 sg:pub.10.1134/s1070428007030098
6 sg:pub.10.1134/s1070428009020018
7 sg:pub.10.1134/s1070428010080129
8 schema:datePublished 2012-11-27
9 schema:datePublishedReg 2012-11-27
10 schema:description New derivatives of the benzo[de]isoquinoline-1,3-dione system containing an amino group were synthesized by the reaction of 2-benzyl-6-bromobenzo[de]isoquinoline-1,3-dione with ethylenediamine and hydrazine. Further functionalization of the free amino groups leads to imines, amines, thioureas, and hydrazones. Some compounds exhibit high chemosensor selectivity in the determination of anions.
11 schema:genre article
12 schema:isAccessibleForFree false
13 schema:isPartOf N1e72ab0c217f4182b0bf710430376e08
14 N638a70a724b54aaa838f4950849aa119
15 sg:journal.1429545
16 schema:keywords amines
17 amino groups
18 anions
19 benzo
20 chemosensor selectivity
21 chemosensor system
22 compounds
23 derivatives
24 determination
25 determination of anions
26 dione
27 dione series
28 dione system
29 ethylenediamine
30 free amino groups
31 functionalization
32 further functionalization
33 group
34 hydrazine
35 hydrazones
36 imines
37 new derivatives
38 reaction
39 selectivity
40 series
41 system
42 thiourea
43 schema:name New chemosensor systems of the benzo-[de]Isoquinoline-1,3-Dione Series
44 schema:pagination 1325-1331
45 schema:productId N15fcbc206923469eb6883147b84d4365
46 N991a6bd4ac0148e88b24e9a1c0616971
47 schema:sameAs https://app.dimensions.ai/details/publication/pub.1046934493
48 https://doi.org/10.1007/s10593-012-1140-x
49 schema:sdDatePublished 2022-12-01T06:30
50 schema:sdLicense https://scigraph.springernature.com/explorer/license/
51 schema:sdPublisher Nc8871f290c634d178af4a3ffae488792
52 schema:url https://doi.org/10.1007/s10593-012-1140-x
53 sgo:license sg:explorer/license/
54 sgo:sdDataset articles
55 rdf:type schema:ScholarlyArticle
56 N15fcbc206923469eb6883147b84d4365 schema:name doi
57 schema:value 10.1007/s10593-012-1140-x
58 rdf:type schema:PropertyValue
59 N1e72ab0c217f4182b0bf710430376e08 schema:volumeNumber 48
60 rdf:type schema:PublicationVolume
61 N28f9ba5359c747a09380c1ff94650432 rdf:first sg:person.010123611500.98
62 rdf:rest N743862d55e5d484b8ba576bc35a11a42
63 N3b8ec4cb07cd471394f6144902d5f228 rdf:first sg:person.014142154521.27
64 rdf:rest N517bfd7a025c4caf834c12ca5d7beddc
65 N517bfd7a025c4caf834c12ca5d7beddc rdf:first sg:person.07535265367.87
66 rdf:rest rdf:nil
67 N638a70a724b54aaa838f4950849aa119 schema:issueNumber 9
68 rdf:type schema:PublicationIssue
69 N73ac1424f8e0458f8317e10267cca285 rdf:first sg:person.015331070355.66
70 rdf:rest N3b8ec4cb07cd471394f6144902d5f228
71 N743862d55e5d484b8ba576bc35a11a42 rdf:first sg:person.07435241541.11
72 rdf:rest N73ac1424f8e0458f8317e10267cca285
73 N991a6bd4ac0148e88b24e9a1c0616971 schema:name dimensions_id
74 schema:value pub.1046934493
75 rdf:type schema:PropertyValue
76 Nc8871f290c634d178af4a3ffae488792 schema:name Springer Nature - SN SciGraph project
77 rdf:type schema:Organization
78 Nfb6b9d2370ec409191491020450be890 rdf:first sg:person.07764646417.25
79 rdf:rest N28f9ba5359c747a09380c1ff94650432
80 anzsrc-for:03 schema:inDefinedTermSet anzsrc-for:
81 schema:name Chemical Sciences
82 rdf:type schema:DefinedTerm
83 anzsrc-for:0305 schema:inDefinedTermSet anzsrc-for:
84 schema:name Organic Chemistry
85 rdf:type schema:DefinedTerm
86 sg:journal.1429545 schema:issn 0132-6244
87 1573-8353
88 schema:name Chemistry of Heterocyclic Compounds
89 schema:publisher Springer Nature
90 rdf:type schema:Periodical
91 sg:person.010123611500.98 schema:affiliation grid-institutes:grid.465325.3
92 schema:familyName Shepelenko
93 schema:givenName E. N.
94 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010123611500.98
95 rdf:type schema:Person
96 sg:person.014142154521.27 schema:affiliation grid-institutes:grid.182798.d
97 schema:familyName Bren
98 schema:givenName V. A.
99 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014142154521.27
100 rdf:type schema:Person
101 sg:person.015331070355.66 schema:affiliation grid-institutes:grid.465325.3
102 schema:familyName Dubonosov
103 schema:givenName A. D.
104 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015331070355.66
105 rdf:type schema:Person
106 sg:person.07435241541.11 schema:affiliation grid-institutes:grid.465325.3
107 schema:familyName Revinskii
108 schema:givenName Yu. V.
109 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07435241541.11
110 rdf:type schema:Person
111 sg:person.07535265367.87 schema:affiliation grid-institutes:grid.465325.3
112 schema:familyName Minkin
113 schema:givenName V. I.
114 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07535265367.87
115 rdf:type schema:Person
116 sg:person.07764646417.25 schema:affiliation grid-institutes:grid.182798.d
117 schema:familyName Tolpygin
118 schema:givenName I. E.
119 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07764646417.25
120 rdf:type schema:Person
121 sg:pub.10.1134/s1070363210040146 schema:sameAs https://app.dimensions.ai/details/publication/pub.1039141122
122 https://doi.org/10.1134/s1070363210040146
123 rdf:type schema:CreativeWork
124 sg:pub.10.1134/s1070428007030098 schema:sameAs https://app.dimensions.ai/details/publication/pub.1032593071
125 https://doi.org/10.1134/s1070428007030098
126 rdf:type schema:CreativeWork
127 sg:pub.10.1134/s1070428009020018 schema:sameAs https://app.dimensions.ai/details/publication/pub.1007772040
128 https://doi.org/10.1134/s1070428009020018
129 rdf:type schema:CreativeWork
130 sg:pub.10.1134/s1070428010080129 schema:sameAs https://app.dimensions.ai/details/publication/pub.1014846694
131 https://doi.org/10.1134/s1070428010080129
132 rdf:type schema:CreativeWork
133 grid-institutes:grid.182798.d schema:alternateName Scientific-Research Institute of Physical and Organic Chemistry, Southern Federal University, 194/2 Stachki Ave., 344090, Rostov-on-the-Don, Russia
134 schema:name Scientific-Research Institute of Physical and Organic Chemistry, Southern Federal University, 194/2 Stachki Ave., 344090, Rostov-on-the-Don, Russia
135 rdf:type schema:Organization
136 grid-institutes:grid.465325.3 schema:alternateName Southern Scientific Center, Russian Academy of Sciences, 41 Chekhova St., 344010, Rostov-on-the-Don, Russia
137 schema:name Scientific-Research Institute of Physical and Organic Chemistry, Southern Federal University, 194/2 Stachki Ave., 344090, Rostov-on-the-Don, Russia
138 Southern Scientific Center, Russian Academy of Sciences, 41 Chekhova St., 344010, Rostov-on-the-Don, Russia
139 rdf:type schema:Organization
 




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


...