Pyrylocyanines. 33. Pyrylocarbocyanines with bridge groups in the chromophore View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1994-09

AUTHORS

M. A. Kudinova, E. I. Maiboroda, Yu. L. Slominskii, A. I. Tolmachev

ABSTRACT

Salts of 4,4-tetra-, penta-, and hexamethylene-bis-(2,6-diphenylpyrylium) and -thiopyrylium were synthesized and used as the basis for producing trimethylcyanines with ethylene, tri- and tetramethylene bridge groups in the chromophore. Factors influencing the color of these dyes were analyzed. The bis-pyrylium salts were converted to derivatives of pyridine, N-methyl- and N-phenylpyridinium. The structure of the compounds obtained was confirmed by the data of electron spectroscopy and PMR spectroscopy. More... »

PAGES

1024-1028

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf01171156

DOI

http://dx.doi.org/10.1007/bf01171156

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1015059032


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": [
      {
        "familyName": "Kudinova", 
        "givenName": "M. A.", 
        "id": "sg:person.07352674576.66", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07352674576.66"
        ], 
        "type": "Person"
      }, 
      {
        "familyName": "Maiboroda", 
        "givenName": "E. I.", 
        "id": "sg:person.012066043544.14", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.012066043544.14"
        ], 
        "type": "Person"
      }, 
      {
        "familyName": "Slominskii", 
        "givenName": "Yu. L.", 
        "id": "sg:person.012567752001.14", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.012567752001.14"
        ], 
        "type": "Person"
      }, 
      {
        "familyName": "Tolmachev", 
        "givenName": "A. I.", 
        "id": "sg:person.011751300775.35", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.011751300775.35"
        ], 
        "type": "Person"
      }
    ], 
    "citation": [
      {
        "id": "https://doi.org/10.1016/s0040-4020(01)93679-8", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1003777427"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/jhet.5570250508", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1023813251"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/jhet.5570250508", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1023813251"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/prac.19833250514", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1048461041"
        ], 
        "type": "CreativeWork"
      }
    ], 
    "datePublished": "1994-09", 
    "datePublishedReg": "1994-09-01", 
    "description": "Salts of 4,4-tetra-, penta-, and hexamethylene-bis-(2,6-diphenylpyrylium) and -thiopyrylium were synthesized and used as the basis for producing trimethylcyanines with ethylene, tri- and tetramethylene bridge groups in the chromophore. Factors influencing the color of these dyes were analyzed. The bis-pyrylium salts were converted to derivatives of pyridine, N-methyl- and N-phenylpyridinium. The structure of the compounds obtained was confirmed by the data of electron spectroscopy and PMR spectroscopy.", 
    "genre": "research_article", 
    "id": "sg:pub.10.1007/bf01171156", 
    "inLanguage": [
      "en"
    ], 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1356886", 
        "issn": [
          "0009-3122", 
          "1573-8353"
        ], 
        "name": "Chemistry of Heterocyclic Compounds", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "9", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "30"
      }
    ], 
    "name": "Pyrylocyanines. 33. Pyrylocarbocyanines with bridge groups in the chromophore", 
    "pagination": "1024-1028", 
    "productId": [
      {
        "name": "readcube_id", 
        "type": "PropertyValue", 
        "value": [
          "47befc043a38bcca21b1f08d520ac63072b5f2bcf4c126b740cb8d9b5f91b2ee"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/bf01171156"
        ]
      }, 
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1015059032"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/bf01171156", 
      "https://app.dimensions.ai/details/publication/pub.1015059032"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2019-04-11T13:32", 
    "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_46765_00000000.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "http://link.springer.com/10.1007/BF01171156"
  }
]
 

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/bf01171156'

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/bf01171156'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/bf01171156'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/bf01171156'


 

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

84 TRIPLES      21 PREDICATES      30 URIs      19 LITERALS      7 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/bf01171156 schema:about anzsrc-for:03
2 anzsrc-for:0306
3 schema:author N1353f68c7fed4277af0210ecf6b68cf6
4 schema:citation https://doi.org/10.1002/jhet.5570250508
5 https://doi.org/10.1002/prac.19833250514
6 https://doi.org/10.1016/s0040-4020(01)93679-8
7 schema:datePublished 1994-09
8 schema:datePublishedReg 1994-09-01
9 schema:description Salts of 4,4-tetra-, penta-, and hexamethylene-bis-(2,6-diphenylpyrylium) and -thiopyrylium were synthesized and used as the basis for producing trimethylcyanines with ethylene, tri- and tetramethylene bridge groups in the chromophore. Factors influencing the color of these dyes were analyzed. The bis-pyrylium salts were converted to derivatives of pyridine, N-methyl- and N-phenylpyridinium. The structure of the compounds obtained was confirmed by the data of electron spectroscopy and PMR spectroscopy.
10 schema:genre research_article
11 schema:inLanguage en
12 schema:isAccessibleForFree false
13 schema:isPartOf N14240505ec2c4404b0fc8f618e68b2bc
14 Nb573af59bbfd412daf3d36f5abae9fda
15 sg:journal.1356886
16 schema:name Pyrylocyanines. 33. Pyrylocarbocyanines with bridge groups in the chromophore
17 schema:pagination 1024-1028
18 schema:productId N4ca454a31db24ceb9dcb17f9edd53ef2
19 Nad5f113e4abc42ed84ea968994c94d92
20 Nd301a715853a48238743df141543659f
21 schema:sameAs https://app.dimensions.ai/details/publication/pub.1015059032
22 https://doi.org/10.1007/bf01171156
23 schema:sdDatePublished 2019-04-11T13:32
24 schema:sdLicense https://scigraph.springernature.com/explorer/license/
25 schema:sdPublisher N882c41bb4aea4e059d4c69dd249d4d4d
26 schema:url http://link.springer.com/10.1007/BF01171156
27 sgo:license sg:explorer/license/
28 sgo:sdDataset articles
29 rdf:type schema:ScholarlyArticle
30 N1353f68c7fed4277af0210ecf6b68cf6 rdf:first sg:person.07352674576.66
31 rdf:rest Nfc0dc1973c014b5a91b6fbf1d89f5dd3
32 N14240505ec2c4404b0fc8f618e68b2bc schema:volumeNumber 30
33 rdf:type schema:PublicationVolume
34 N4ca454a31db24ceb9dcb17f9edd53ef2 schema:name dimensions_id
35 schema:value pub.1015059032
36 rdf:type schema:PropertyValue
37 N882c41bb4aea4e059d4c69dd249d4d4d schema:name Springer Nature - SN SciGraph project
38 rdf:type schema:Organization
39 N8b19c03004fb41b298325d1cf57684bf rdf:first sg:person.012567752001.14
40 rdf:rest Nb14f18a88b05428cabbd5399c5f23f27
41 Nad5f113e4abc42ed84ea968994c94d92 schema:name doi
42 schema:value 10.1007/bf01171156
43 rdf:type schema:PropertyValue
44 Nb14f18a88b05428cabbd5399c5f23f27 rdf:first sg:person.011751300775.35
45 rdf:rest rdf:nil
46 Nb573af59bbfd412daf3d36f5abae9fda schema:issueNumber 9
47 rdf:type schema:PublicationIssue
48 Nd301a715853a48238743df141543659f schema:name readcube_id
49 schema:value 47befc043a38bcca21b1f08d520ac63072b5f2bcf4c126b740cb8d9b5f91b2ee
50 rdf:type schema:PropertyValue
51 Nfc0dc1973c014b5a91b6fbf1d89f5dd3 rdf:first sg:person.012066043544.14
52 rdf:rest N8b19c03004fb41b298325d1cf57684bf
53 anzsrc-for:03 schema:inDefinedTermSet anzsrc-for:
54 schema:name Chemical Sciences
55 rdf:type schema:DefinedTerm
56 anzsrc-for:0306 schema:inDefinedTermSet anzsrc-for:
57 schema:name Physical Chemistry (incl. Structural)
58 rdf:type schema:DefinedTerm
59 sg:journal.1356886 schema:issn 0009-3122
60 1573-8353
61 schema:name Chemistry of Heterocyclic Compounds
62 rdf:type schema:Periodical
63 sg:person.011751300775.35 schema:familyName Tolmachev
64 schema:givenName A. I.
65 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.011751300775.35
66 rdf:type schema:Person
67 sg:person.012066043544.14 schema:familyName Maiboroda
68 schema:givenName E. I.
69 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.012066043544.14
70 rdf:type schema:Person
71 sg:person.012567752001.14 schema:familyName Slominskii
72 schema:givenName Yu. L.
73 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.012567752001.14
74 rdf:type schema:Person
75 sg:person.07352674576.66 schema:familyName Kudinova
76 schema:givenName M. A.
77 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07352674576.66
78 rdf:type schema:Person
79 https://doi.org/10.1002/jhet.5570250508 schema:sameAs https://app.dimensions.ai/details/publication/pub.1023813251
80 rdf:type schema:CreativeWork
81 https://doi.org/10.1002/prac.19833250514 schema:sameAs https://app.dimensions.ai/details/publication/pub.1048461041
82 rdf:type schema:CreativeWork
83 https://doi.org/10.1016/s0040-4020(01)93679-8 schema:sameAs https://app.dimensions.ai/details/publication/pub.1003777427
84 rdf:type schema:CreativeWork
 




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


...