Reaction of 3,4-diaminofurazan with carbonyl compounds and their metal complexes View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1986-05

AUTHORS

I. S. Vasil'chenko, S. G. Kochin, V. A. Anisimova, L. I. Khmel'nitskii, A. D. Garnovskii

ABSTRACT

It is shown that when 3,4-diaminofuranzan reacts with formic acid under various conditions there is, along with the mono- and diformylation, an intermolecular reaction leading to a polymeric compound. The diamine under consideration forms a monoazomethine with salicylaldehyde but a bis (azomethine) complex with the salicylaldehydate of divalent nickel.

PAGES

546-549

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf00519537

DOI

http://dx.doi.org/10.1007/bf00519537

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1004953514


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/2008/0306", 
        "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
        "name": "Physical Chemistry (incl. Structural)", 
        "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": "N.D. Zelinsky Institute of Organic Chemistry", 
          "id": "https://www.grid.ac/institutes/grid.439283.7", 
          "name": [
            "M. A. Suslov Scientific-Research Institute of Physical and Organic Chemistry, Rostov State University, Rostov-on-Don", 
            "N. D. Zelinskii Institute of Organic Chemistry, Academy of Sciences of the USSR, Moscow"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Vasil'chenko", 
        "givenName": "I. S.", 
        "id": "sg:person.013456134753.25", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.013456134753.25"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "N.D. Zelinsky Institute of Organic Chemistry", 
          "id": "https://www.grid.ac/institutes/grid.439283.7", 
          "name": [
            "M. A. Suslov Scientific-Research Institute of Physical and Organic Chemistry, Rostov State University, Rostov-on-Don", 
            "N. D. Zelinskii Institute of Organic Chemistry, Academy of Sciences of the USSR, Moscow"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Kochin", 
        "givenName": "S. G.", 
        "id": "sg:person.010173644531.02", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010173644531.02"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "N.D. Zelinsky Institute of Organic Chemistry", 
          "id": "https://www.grid.ac/institutes/grid.439283.7", 
          "name": [
            "M. A. Suslov Scientific-Research Institute of Physical and Organic Chemistry, Rostov State University, Rostov-on-Don", 
            "N. D. Zelinskii Institute of Organic Chemistry, Academy of Sciences of the USSR, Moscow"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Anisimova", 
        "givenName": "V. A.", 
        "id": "sg:person.0623276120.27", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0623276120.27"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "N.D. Zelinsky Institute of Organic Chemistry", 
          "id": "https://www.grid.ac/institutes/grid.439283.7", 
          "name": [
            "M. A. Suslov Scientific-Research Institute of Physical and Organic Chemistry, Rostov State University, Rostov-on-Don", 
            "N. D. Zelinskii Institute of Organic Chemistry, Academy of Sciences of the USSR, Moscow"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Khmel'nitskii", 
        "givenName": "L. I.", 
        "id": "sg:person.014727371351.17", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014727371351.17"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "N.D. Zelinsky Institute of Organic Chemistry", 
          "id": "https://www.grid.ac/institutes/grid.439283.7", 
          "name": [
            "M. A. Suslov Scientific-Research Institute of Physical and Organic Chemistry, Rostov State University, Rostov-on-Don", 
            "N. D. Zelinskii Institute of Organic Chemistry, Academy of Sciences of the USSR, Moscow"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Garnovskii", 
        "givenName": "A. D.", 
        "id": "sg:person.014222624313.54", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014222624313.54"
        ], 
        "type": "Person"
      }
    ], 
    "citation": [
      {
        "id": "https://doi.org/10.1002/9780470166086.ch3", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1000058737"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/jhet.5570050114", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1036175829"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/jhet.5570050114", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1036175829"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/prac.19733150425", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1036543453"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/cr60290a003", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1053764887"
        ], 
        "type": "CreativeWork"
      }
    ], 
    "datePublished": "1986-05", 
    "datePublishedReg": "1986-05-01", 
    "description": "It is shown that when 3,4-diaminofuranzan reacts with formic acid under various conditions there is, along with the mono- and diformylation, an intermolecular reaction leading to a polymeric compound. The diamine under consideration forms a monoazomethine with salicylaldehyde but a bis (azomethine) complex with the salicylaldehydate of divalent nickel.", 
    "genre": "research_article", 
    "id": "sg:pub.10.1007/bf00519537", 
    "inLanguage": [
      "en"
    ], 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1356886", 
        "issn": [
          "0009-3122", 
          "1573-8353"
        ], 
        "name": "Chemistry of Heterocyclic Compounds", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "5", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "22"
      }
    ], 
    "name": "Reaction of 3,4-diaminofurazan with carbonyl compounds and their metal complexes", 
    "pagination": "546-549", 
    "productId": [
      {
        "name": "readcube_id", 
        "type": "PropertyValue", 
        "value": [
          "179acba207eb90c7aa0559597e26c1f5bcad74eda219f172fb8e7a912dd5acf7"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/bf00519537"
        ]
      }, 
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1004953514"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/bf00519537", 
      "https://app.dimensions.ai/details/publication/pub.1004953514"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2019-04-11T13:58", 
    "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/v90/0000000371_0000000371/records_130823_00000000.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "http://link.springer.com/10.1007/BF00519537"
  }
]
 

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/bf00519537'

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/bf00519537'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/bf00519537'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/bf00519537'


 

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

102 TRIPLES      21 PREDICATES      31 URIs      19 LITERALS      7 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/bf00519537 schema:about anzsrc-for:03
2 anzsrc-for:0306
3 schema:author Nfec7e9206ae44881ad2cd15af55c5c88
4 schema:citation https://doi.org/10.1002/9780470166086.ch3
5 https://doi.org/10.1002/jhet.5570050114
6 https://doi.org/10.1002/prac.19733150425
7 https://doi.org/10.1021/cr60290a003
8 schema:datePublished 1986-05
9 schema:datePublishedReg 1986-05-01
10 schema:description It is shown that when 3,4-diaminofuranzan reacts with formic acid under various conditions there is, along with the mono- and diformylation, an intermolecular reaction leading to a polymeric compound. The diamine under consideration forms a monoazomethine with salicylaldehyde but a bis (azomethine) complex with the salicylaldehydate of divalent nickel.
11 schema:genre research_article
12 schema:inLanguage en
13 schema:isAccessibleForFree false
14 schema:isPartOf N3ffd221594a04d4bb8a39d0030044d7c
15 Na9ca20991524471c8ae079cd768bc77d
16 sg:journal.1356886
17 schema:name Reaction of 3,4-diaminofurazan with carbonyl compounds and their metal complexes
18 schema:pagination 546-549
19 schema:productId N09281f74fa3349128eeaaa13f470c4da
20 N27084c0d69c0444384d54fd4511be9a8
21 N3af119fabf414657b5b8550b477a9f15
22 schema:sameAs https://app.dimensions.ai/details/publication/pub.1004953514
23 https://doi.org/10.1007/bf00519537
24 schema:sdDatePublished 2019-04-11T13:58
25 schema:sdLicense https://scigraph.springernature.com/explorer/license/
26 schema:sdPublisher N547502031c864791b3316fd4e76a8e7e
27 schema:url http://link.springer.com/10.1007/BF00519537
28 sgo:license sg:explorer/license/
29 sgo:sdDataset articles
30 rdf:type schema:ScholarlyArticle
31 N09281f74fa3349128eeaaa13f470c4da schema:name readcube_id
32 schema:value 179acba207eb90c7aa0559597e26c1f5bcad74eda219f172fb8e7a912dd5acf7
33 rdf:type schema:PropertyValue
34 N27084c0d69c0444384d54fd4511be9a8 schema:name doi
35 schema:value 10.1007/bf00519537
36 rdf:type schema:PropertyValue
37 N2abae9cad0594fd79053b3e605047621 rdf:first sg:person.010173644531.02
38 rdf:rest Nc1f5af35aed74d87a590a621c599c151
39 N3af119fabf414657b5b8550b477a9f15 schema:name dimensions_id
40 schema:value pub.1004953514
41 rdf:type schema:PropertyValue
42 N3ffd221594a04d4bb8a39d0030044d7c schema:issueNumber 5
43 rdf:type schema:PublicationIssue
44 N547502031c864791b3316fd4e76a8e7e schema:name Springer Nature - SN SciGraph project
45 rdf:type schema:Organization
46 N5998030ca13149f99eb0b25217e958f3 rdf:first sg:person.014222624313.54
47 rdf:rest rdf:nil
48 N8e76e54f82cc4a148b2f134326926e42 rdf:first sg:person.014727371351.17
49 rdf:rest N5998030ca13149f99eb0b25217e958f3
50 Na9ca20991524471c8ae079cd768bc77d schema:volumeNumber 22
51 rdf:type schema:PublicationVolume
52 Nc1f5af35aed74d87a590a621c599c151 rdf:first sg:person.0623276120.27
53 rdf:rest N8e76e54f82cc4a148b2f134326926e42
54 Nfec7e9206ae44881ad2cd15af55c5c88 rdf:first sg:person.013456134753.25
55 rdf:rest N2abae9cad0594fd79053b3e605047621
56 anzsrc-for:03 schema:inDefinedTermSet anzsrc-for:
57 schema:name Chemical Sciences
58 rdf:type schema:DefinedTerm
59 anzsrc-for:0306 schema:inDefinedTermSet anzsrc-for:
60 schema:name Physical Chemistry (incl. Structural)
61 rdf:type schema:DefinedTerm
62 sg:journal.1356886 schema:issn 0009-3122
63 1573-8353
64 schema:name Chemistry of Heterocyclic Compounds
65 rdf:type schema:Periodical
66 sg:person.010173644531.02 schema:affiliation https://www.grid.ac/institutes/grid.439283.7
67 schema:familyName Kochin
68 schema:givenName S. G.
69 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010173644531.02
70 rdf:type schema:Person
71 sg:person.013456134753.25 schema:affiliation https://www.grid.ac/institutes/grid.439283.7
72 schema:familyName Vasil'chenko
73 schema:givenName I. S.
74 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.013456134753.25
75 rdf:type schema:Person
76 sg:person.014222624313.54 schema:affiliation https://www.grid.ac/institutes/grid.439283.7
77 schema:familyName Garnovskii
78 schema:givenName A. D.
79 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014222624313.54
80 rdf:type schema:Person
81 sg:person.014727371351.17 schema:affiliation https://www.grid.ac/institutes/grid.439283.7
82 schema:familyName Khmel'nitskii
83 schema:givenName L. I.
84 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014727371351.17
85 rdf:type schema:Person
86 sg:person.0623276120.27 schema:affiliation https://www.grid.ac/institutes/grid.439283.7
87 schema:familyName Anisimova
88 schema:givenName V. A.
89 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0623276120.27
90 rdf:type schema:Person
91 https://doi.org/10.1002/9780470166086.ch3 schema:sameAs https://app.dimensions.ai/details/publication/pub.1000058737
92 rdf:type schema:CreativeWork
93 https://doi.org/10.1002/jhet.5570050114 schema:sameAs https://app.dimensions.ai/details/publication/pub.1036175829
94 rdf:type schema:CreativeWork
95 https://doi.org/10.1002/prac.19733150425 schema:sameAs https://app.dimensions.ai/details/publication/pub.1036543453
96 rdf:type schema:CreativeWork
97 https://doi.org/10.1021/cr60290a003 schema:sameAs https://app.dimensions.ai/details/publication/pub.1053764887
98 rdf:type schema:CreativeWork
99 https://www.grid.ac/institutes/grid.439283.7 schema:alternateName N.D. Zelinsky Institute of Organic Chemistry
100 schema:name M. A. Suslov Scientific-Research Institute of Physical and Organic Chemistry, Rostov State University, Rostov-on-Don
101 N. D. Zelinskii Institute of Organic Chemistry, Academy of Sciences of the USSR, Moscow
102 rdf:type schema:Organization
 




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


...