2013-02
AUTHORSD. E. Dmitriev, Yu. A. Strelenko, A. B. Sheremetev
ABSTRACT3-Nitrofurazans with different substituents at position 4 were studied by 1H, 13C, and 14N NMR spectroscopy. A correlation between chemical shifts (CS) in the 13C NMR spectra of furazans and benzene with similar substituents was revealed. Increments for a series of new substituents were determined. The 13C and 14N CS values presented can be used as a reliable set of reference data. More... »
PAGES504-515
http://scigraph.springernature.com/pub.10.1007/s11172-013-0070-9
DOIhttp://dx.doi.org/10.1007/s11172-013-0070-9
DIMENSIONShttps://app.dimensions.ai/details/publication/pub.1044866040
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": "N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation",
"id": "http://www.grid.ac/institutes/grid.439283.7",
"name": [
"N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation"
],
"type": "Organization"
},
"familyName": "Dmitriev",
"givenName": "D. E.",
"id": "sg:person.014213065445.89",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014213065445.89"
],
"type": "Person"
},
{
"affiliation": {
"alternateName": "N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation",
"id": "http://www.grid.ac/institutes/grid.439283.7",
"name": [
"N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation"
],
"type": "Organization"
},
"familyName": "Strelenko",
"givenName": "Yu. A.",
"id": "sg:person.014142606623.54",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014142606623.54"
],
"type": "Person"
},
{
"affiliation": {
"alternateName": "N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation",
"id": "http://www.grid.ac/institutes/grid.439283.7",
"name": [
"N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation"
],
"type": "Organization"
},
"familyName": "Sheremetev",
"givenName": "A. B.",
"id": "sg:person.012630732145.84",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.012630732145.84"
],
"type": "Person"
}
],
"citation": [
{
"id": "sg:pub.10.1023/b:rucb.0000035665.41332.ae",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1008495085",
"https://doi.org/10.1023/b:rucb.0000035665.41332.ae"
],
"type": "CreativeWork"
},
{
"id": "sg:pub.10.1023/a:1020931511013",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1051864739",
"https://doi.org/10.1023/a:1020931511013"
],
"type": "CreativeWork"
},
{
"id": "sg:pub.10.1007/s11172-012-0049-y",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1003143860",
"https://doi.org/10.1007/s11172-012-0049-y"
],
"type": "CreativeWork"
},
{
"id": "sg:pub.10.1007/s11172-006-0058-9",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1014851525",
"https://doi.org/10.1007/s11172-006-0058-9"
],
"type": "CreativeWork"
},
{
"id": "sg:pub.10.1023/a:1024895631593",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1022589460",
"https://doi.org/10.1023/a:1024895631593"
],
"type": "CreativeWork"
},
{
"id": "sg:pub.10.1007/bf00531329",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1018754455",
"https://doi.org/10.1007/bf00531329"
],
"type": "CreativeWork"
},
{
"id": "sg:pub.10.1023/b:rucb.0000035644.16331.f0",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1007786058",
"https://doi.org/10.1023/b:rucb.0000035644.16331.f0"
],
"type": "CreativeWork"
},
{
"id": "sg:pub.10.1007/s11172-012-0132-4",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1027712616",
"https://doi.org/10.1007/s11172-012-0132-4"
],
"type": "CreativeWork"
},
{
"id": "sg:pub.10.1023/a:1015820318686",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1021714409",
"https://doi.org/10.1023/a:1015820318686"
],
"type": "CreativeWork"
},
{
"id": "sg:pub.10.1007/s11172-011-0254-0",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1013962927",
"https://doi.org/10.1007/s11172-011-0254-0"
],
"type": "CreativeWork"
},
{
"id": "sg:pub.10.1007/978-0-387-98070-6",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1042421677",
"https://doi.org/10.1007/978-0-387-98070-6"
],
"type": "CreativeWork"
},
{
"id": "sg:pub.10.1023/a:1015407727307",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1008747546",
"https://doi.org/10.1023/a:1015407727307"
],
"type": "CreativeWork"
},
{
"id": "sg:pub.10.1023/b:cohc.0000010653.01134.a7",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1046041339",
"https://doi.org/10.1023/b:cohc.0000010653.01134.a7"
],
"type": "CreativeWork"
}
],
"datePublished": "2013-02",
"datePublishedReg": "2013-02-01",
"description": "Abstract3-Nitrofurazans with different substituents at position 4 were studied by 1H, 13C, and 14N NMR spectroscopy. A correlation between chemical shifts (CS) in the 13C NMR spectra of furazans and benzene with similar substituents was revealed. Increments for a series of new substituents were determined. The 13C and 14N CS values presented can be used as a reliable set of reference data.",
"genre": "article",
"id": "sg:pub.10.1007/s11172-013-0070-9",
"isAccessibleForFree": false,
"isPartOf": [
{
"id": "sg:journal.1022309",
"issn": [
"1063-5211",
"1026-3500"
],
"name": "Russian Chemical Bulletin",
"publisher": "Springer Nature",
"type": "Periodical"
},
{
"issueNumber": "2",
"type": "PublicationIssue"
},
{
"type": "PublicationVolume",
"volumeNumber": "62"
}
],
"keywords": [
"chemical shifts",
"NMR spectroscopic studies",
"NMR spectroscopy",
"NMR spectra",
"spectroscopic studies",
"different substituents",
"new substituents",
"similar substituents",
"substituents",
"position 4",
"furazan",
"spectroscopy",
"CS values",
"spectra",
"series",
"reliable set",
"shift",
"reference data",
"values",
"study",
"increment",
"correlation",
"data",
"set"
],
"name": "NMR spectroscopic study of 3-nitrofurazans",
"pagination": "504-515",
"productId": [
{
"name": "dimensions_id",
"type": "PropertyValue",
"value": [
"pub.1044866040"
]
},
{
"name": "doi",
"type": "PropertyValue",
"value": [
"10.1007/s11172-013-0070-9"
]
}
],
"sameAs": [
"https://doi.org/10.1007/s11172-013-0070-9",
"https://app.dimensions.ai/details/publication/pub.1044866040"
],
"sdDataset": "articles",
"sdDatePublished": "2022-08-04T17:02",
"sdLicense": "https://scigraph.springernature.com/explorer/license/",
"sdPublisher": {
"name": "Springer Nature - SN SciGraph project",
"type": "Organization"
},
"sdSource": "s3://com-springernature-scigraph/baseset/20220804/entities/gbq_results/article/article_605.jsonl",
"type": "ScholarlyArticle",
"url": "https://doi.org/10.1007/s11172-013-0070-9"
}
]Download the RDF metadata as: json-ld nt turtle xml License info
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/s11172-013-0070-9'
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/s11172-013-0070-9'
Turtle is a human-readable linked data format.
curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/s11172-013-0070-9'
RDF/XML is a standard XML format for linked data.
curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/s11172-013-0070-9'
This table displays all metadata directly associated to this object as RDF triples.
147 TRIPLES
21 PREDICATES
62 URIs
41 LITERALS
6 BLANK NODES