Ontology type: schema:ScholarlyArticle
2000-03
AUTHORSStephen J. Archibald, Nathaniel W. Alcock, Daryle H. Busch, David R. Whitcomb
ABSTRACTN,N′−Diphenylamidines and the silver(I) complexes of their deprotonated anions have been synthesized. Previously uncharacterized tetrameric structural motifs were produced by the inclusion of alkyl substituents at the amidinate carbon. The addition of a 2-methoxy functional group to the phenyl ring resulted in a cationic silver trimer in which hydrogen bonding links silver(I)-bound water molecules to the methoxy substituents. The thermal stabilities of the tetrameric species vary with alkyl chain length. The new complexes are: tetrakis(N,N′-diphenylpropamidinato) tetra silver(I), 1, tetrakis(N,N′-diphenylbutamidinato) tetrasilver(I) 2, tetrakis(N,N′-diphenylpentamidinato) tetra silver(I) 3, (N,N′-diphenyloctamidinato)silver(I) 4, (tetrakis(N,N′-di(4-n-butyl)phenylpropamidinato)tetrasilver(I), 5, bis(N,N′-di(2-methoxy)phenylacetamidinato)diaquatrisilver(I) nitrate 6 and tetrakis(N,N′-di(4-methoxy)phenylacetamidinato) tetrasilver(I), 7. Compounds 1, 5, 6 and 7 were structurally characterized by X-ray methods. More... »
PAGES261-283
http://scigraph.springernature.com/pub.10.1023/a:1009085319864
DOIhttp://dx.doi.org/10.1023/a:1009085319864
DIMENSIONShttps://app.dimensions.ai/details/publication/pub.1043760923
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/2008/0302",
"inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/",
"name": "Inorganic Chemistry",
"type": "DefinedTerm"
}
],
"author": [
{
"affiliation": {
"alternateName": "Department of Chemistry, University of Kansas, 66045, Lawrence, KS, USA",
"id": "http://www.grid.ac/institutes/grid.266515.3",
"name": [
"Department of Chemistry, University of Kansas, 66045, Lawrence, KS, USA"
],
"type": "Organization"
},
"familyName": "Archibald",
"givenName": "Stephen J.",
"id": "sg:person.01272127236.47",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01272127236.47"
],
"type": "Person"
},
{
"affiliation": {
"alternateName": "Department of Chemistry, University of Warwick, CV4 7AL, Coventry, UK",
"id": "http://www.grid.ac/institutes/grid.7372.1",
"name": [
"Department of Chemistry, University of Warwick, CV4 7AL, Coventry, UK"
],
"type": "Organization"
},
"familyName": "Alcock",
"givenName": "Nathaniel W.",
"id": "sg:person.01145137433.39",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01145137433.39"
],
"type": "Person"
},
{
"affiliation": {
"alternateName": "Department of Chemistry, University of Kansas, 66045, Lawrence, KS, USA",
"id": "http://www.grid.ac/institutes/grid.266515.3",
"name": [
"Department of Chemistry, University of Kansas, 66045, Lawrence, KS, USA"
],
"type": "Organization"
},
"familyName": "Busch",
"givenName": "Daryle H.",
"id": "sg:person.016233633116.55",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016233633116.55"
],
"type": "Person"
},
{
"affiliation": {
"alternateName": "Dry Media Systems Laboratory, Imation Corporation, 55144, St Paul, MN, USA",
"id": "http://www.grid.ac/institutes/None",
"name": [
"Dry Media Systems Laboratory, Imation Corporation, 55144, St Paul, MN, USA"
],
"type": "Organization"
},
"familyName": "Whitcomb",
"givenName": "David R.",
"id": "sg:person.015262263463.15",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015262263463.15"
],
"type": "Person"
}
],
"datePublished": "2000-03",
"datePublishedReg": "2000-03-01",
"description": "N,N\u2032\u2212Diphenylamidines and the silver(I) complexes of their deprotonated anions have been synthesized. Previously uncharacterized tetrameric structural motifs were produced by the inclusion of alkyl substituents at the amidinate carbon. The addition of a 2-methoxy functional group to the phenyl ring resulted in a cationic silver trimer in which hydrogen bonding links silver(I)-bound water molecules to the methoxy substituents. The thermal stabilities of the tetrameric species vary with alkyl chain length. The new complexes are: tetrakis(N,N\u2032-diphenylpropamidinato) tetra silver(I), 1, tetrakis(N,N\u2032-diphenylbutamidinato) tetrasilver(I) 2, tetrakis(N,N\u2032-diphenylpentamidinato) tetra silver(I) 3, (N,N\u2032-diphenyloctamidinato)silver(I) 4, (tetrakis(N,N\u2032-di(4-n-butyl)phenylpropamidinato)tetrasilver(I), 5, bis(N,N\u2032-di(2-methoxy)phenylacetamidinato)diaquatrisilver(I) nitrate 6 and tetrakis(N,N\u2032-di(4-methoxy)phenylacetamidinato) tetrasilver(I), 7. Compounds 1, 5, 6 and 7 were structurally characterized by X-ray methods.",
"genre": "article",
"id": "sg:pub.10.1023/a:1009085319864",
"inLanguage": "en",
"isAccessibleForFree": false,
"isPartOf": [
{
"id": "sg:journal.1130720",
"issn": [
"1040-7278",
"1572-8862"
],
"name": "Journal of Cluster Science",
"publisher": "Springer Nature",
"type": "Periodical"
},
{
"issueNumber": "1",
"type": "PublicationIssue"
},
{
"type": "PublicationVolume",
"volumeNumber": "11"
}
],
"keywords": [
"hydrogen bonding links",
"alkyl chain length",
"new complexes",
"water molecules",
"deprotonated anions",
"bonding links",
"functional groups",
"alkyl substituents",
"methoxy substituents",
"chain length",
"phenyl ring",
"silver trimer",
"tetrameric species",
"structural motifs",
"thermal stability",
"substituents",
"tetra",
"complexes",
"anions",
"molecules",
"trimer",
"carbon",
"ns",
"ring",
"stability",
"species",
"motif",
"addition",
"group",
"length",
"inclusion",
"link"
],
"name": "Synthesis and Characterization of Silver(I) Complexes with C-Alkyl Functionalized N,N\u2032-Diphenylamidinates: Tetrameric and Trimeric Structural Motifs",
"pagination": "261-283",
"productId": [
{
"name": "dimensions_id",
"type": "PropertyValue",
"value": [
"pub.1043760923"
]
},
{
"name": "doi",
"type": "PropertyValue",
"value": [
"10.1023/a:1009085319864"
]
}
],
"sameAs": [
"https://doi.org/10.1023/a:1009085319864",
"https://app.dimensions.ai/details/publication/pub.1043760923"
],
"sdDataset": "articles",
"sdDatePublished": "2022-05-20T07:21",
"sdLicense": "https://scigraph.springernature.com/explorer/license/",
"sdPublisher": {
"name": "Springer Nature - SN SciGraph project",
"type": "Organization"
},
"sdSource": "s3://com-springernature-scigraph/baseset/20220519/entities/gbq_results/article/article_322.jsonl",
"type": "ScholarlyArticle",
"url": "https://doi.org/10.1023/a:1009085319864"
}
]
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.10.1023/a:1009085319864'
N-Triples is a line-based linked data format ideal for batch operations.
curl -H 'Accept: application/n-triples' 'https://scigraph.springernature.com/pub.10.1023/a:1009085319864'
Turtle is a human-readable linked data format.
curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1023/a:1009085319864'
RDF/XML is a standard XML format for linked data.
curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1023/a:1009085319864'
This table displays all metadata directly associated to this object as RDF triples.
117 TRIPLES
21 PREDICATES
58 URIs
50 LITERALS
6 BLANK NODES
Subject | Predicate | Object | |
---|---|---|---|
1 | sg:pub.10.1023/a:1009085319864 | schema:about | anzsrc-for:03 |
2 | ″ | ″ | anzsrc-for:0302 |
3 | ″ | schema:author | Na85b0ec9747845d1ae48a5f8c9257ecd |
4 | ″ | schema:datePublished | 2000-03 |
5 | ″ | schema:datePublishedReg | 2000-03-01 |
6 | ″ | schema:description | N,N′−Diphenylamidines and the silver(I) complexes of their deprotonated anions have been synthesized. Previously uncharacterized tetrameric structural motifs were produced by the inclusion of alkyl substituents at the amidinate carbon. The addition of a 2-methoxy functional group to the phenyl ring resulted in a cationic silver trimer in which hydrogen bonding links silver(I)-bound water molecules to the methoxy substituents. The thermal stabilities of the tetrameric species vary with alkyl chain length. The new complexes are: tetrakis(N,N′-diphenylpropamidinato) tetra silver(I), 1, tetrakis(N,N′-diphenylbutamidinato) tetrasilver(I) 2, tetrakis(N,N′-diphenylpentamidinato) tetra silver(I) 3, (N,N′-diphenyloctamidinato)silver(I) 4, (tetrakis(N,N′-di(4-n-butyl)phenylpropamidinato)tetrasilver(I), 5, bis(N,N′-di(2-methoxy)phenylacetamidinato)diaquatrisilver(I) nitrate 6 and tetrakis(N,N′-di(4-methoxy)phenylacetamidinato) tetrasilver(I), 7. Compounds 1, 5, 6 and 7 were structurally characterized by X-ray methods. |
7 | ″ | schema:genre | article |
8 | ″ | schema:inLanguage | en |
9 | ″ | schema:isAccessibleForFree | false |
10 | ″ | schema:isPartOf | N37eb5f891a0b4f42959910c7053a8f56 |
11 | ″ | ″ | N844cb878fd444e449fac09086117ae17 |
12 | ″ | ″ | sg:journal.1130720 |
13 | ″ | schema:keywords | addition |
14 | ″ | ″ | alkyl chain length |
15 | ″ | ″ | alkyl substituents |
16 | ″ | ″ | anions |
17 | ″ | ″ | bonding links |
18 | ″ | ″ | carbon |
19 | ″ | ″ | chain length |
20 | ″ | ″ | complexes |
21 | ″ | ″ | deprotonated anions |
22 | ″ | ″ | functional groups |
23 | ″ | ″ | group |
24 | ″ | ″ | hydrogen bonding links |
25 | ″ | ″ | inclusion |
26 | ″ | ″ | length |
27 | ″ | ″ | link |
28 | ″ | ″ | methoxy substituents |
29 | ″ | ″ | molecules |
30 | ″ | ″ | motif |
31 | ″ | ″ | new complexes |
32 | ″ | ″ | ns |
33 | ″ | ″ | phenyl ring |
34 | ″ | ″ | ring |
35 | ″ | ″ | silver trimer |
36 | ″ | ″ | species |
37 | ″ | ″ | stability |
38 | ″ | ″ | structural motifs |
39 | ″ | ″ | substituents |
40 | ″ | ″ | tetra |
41 | ″ | ″ | tetrameric species |
42 | ″ | ″ | thermal stability |
43 | ″ | ″ | trimer |
44 | ″ | ″ | water molecules |
45 | ″ | schema:name | Synthesis and Characterization of Silver(I) Complexes with C-Alkyl Functionalized N,N′-Diphenylamidinates: Tetrameric and Trimeric Structural Motifs |
46 | ″ | schema:pagination | 261-283 |
47 | ″ | schema:productId | Ncab04fb2cea740acae71d30b3694998c |
48 | ″ | ″ | Nf75feaf41909412a981513f3635e9008 |
49 | ″ | schema:sameAs | https://app.dimensions.ai/details/publication/pub.1043760923 |
50 | ″ | ″ | https://doi.org/10.1023/a:1009085319864 |
51 | ″ | schema:sdDatePublished | 2022-05-20T07:21 |
52 | ″ | schema:sdLicense | https://scigraph.springernature.com/explorer/license/ |
53 | ″ | schema:sdPublisher | N130ad2035f284e6fa06b0430c467dd51 |
54 | ″ | schema:url | https://doi.org/10.1023/a:1009085319864 |
55 | ″ | sgo:license | sg:explorer/license/ |
56 | ″ | sgo:sdDataset | articles |
57 | ″ | rdf:type | schema:ScholarlyArticle |
58 | N130ad2035f284e6fa06b0430c467dd51 | schema:name | Springer Nature - SN SciGraph project |
59 | ″ | rdf:type | schema:Organization |
60 | N37eb5f891a0b4f42959910c7053a8f56 | schema:volumeNumber | 11 |
61 | ″ | rdf:type | schema:PublicationVolume |
62 | N7e84f8de39ff4491ba39be2a66627ae8 | rdf:first | sg:person.015262263463.15 |
63 | ″ | rdf:rest | rdf:nil |
64 | N844cb878fd444e449fac09086117ae17 | schema:issueNumber | 1 |
65 | ″ | rdf:type | schema:PublicationIssue |
66 | Na85b0ec9747845d1ae48a5f8c9257ecd | rdf:first | sg:person.01272127236.47 |
67 | ″ | rdf:rest | Nf9790fdd43d14dd2808fa2286e8dd882 |
68 | Nc7136e56d6a3465eb71ea54cacc23d5f | rdf:first | sg:person.016233633116.55 |
69 | ″ | rdf:rest | N7e84f8de39ff4491ba39be2a66627ae8 |
70 | Ncab04fb2cea740acae71d30b3694998c | schema:name | dimensions_id |
71 | ″ | schema:value | pub.1043760923 |
72 | ″ | rdf:type | schema:PropertyValue |
73 | Nf75feaf41909412a981513f3635e9008 | schema:name | doi |
74 | ″ | schema:value | 10.1023/a:1009085319864 |
75 | ″ | rdf:type | schema:PropertyValue |
76 | Nf9790fdd43d14dd2808fa2286e8dd882 | rdf:first | sg:person.01145137433.39 |
77 | ″ | rdf:rest | Nc7136e56d6a3465eb71ea54cacc23d5f |
78 | anzsrc-for:03 | schema:inDefinedTermSet | anzsrc-for: |
79 | ″ | schema:name | Chemical Sciences |
80 | ″ | rdf:type | schema:DefinedTerm |
81 | anzsrc-for:0302 | schema:inDefinedTermSet | anzsrc-for: |
82 | ″ | schema:name | Inorganic Chemistry |
83 | ″ | rdf:type | schema:DefinedTerm |
84 | sg:journal.1130720 | schema:issn | 1040-7278 |
85 | ″ | ″ | 1572-8862 |
86 | ″ | schema:name | Journal of Cluster Science |
87 | ″ | schema:publisher | Springer Nature |
88 | ″ | rdf:type | schema:Periodical |
89 | sg:person.01145137433.39 | schema:affiliation | grid-institutes:grid.7372.1 |
90 | ″ | schema:familyName | Alcock |
91 | ″ | schema:givenName | Nathaniel W. |
92 | ″ | schema:sameAs | https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01145137433.39 |
93 | ″ | rdf:type | schema:Person |
94 | sg:person.01272127236.47 | schema:affiliation | grid-institutes:grid.266515.3 |
95 | ″ | schema:familyName | Archibald |
96 | ″ | schema:givenName | Stephen J. |
97 | ″ | schema:sameAs | https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01272127236.47 |
98 | ″ | rdf:type | schema:Person |
99 | sg:person.015262263463.15 | schema:affiliation | grid-institutes:None |
100 | ″ | schema:familyName | Whitcomb |
101 | ″ | schema:givenName | David R. |
102 | ″ | schema:sameAs | https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015262263463.15 |
103 | ″ | rdf:type | schema:Person |
104 | sg:person.016233633116.55 | schema:affiliation | grid-institutes:grid.266515.3 |
105 | ″ | schema:familyName | Busch |
106 | ″ | schema:givenName | Daryle H. |
107 | ″ | schema:sameAs | https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016233633116.55 |
108 | ″ | rdf:type | schema:Person |
109 | grid-institutes:None | schema:alternateName | Dry Media Systems Laboratory, Imation Corporation, 55144, St Paul, MN, USA |
110 | ″ | schema:name | Dry Media Systems Laboratory, Imation Corporation, 55144, St Paul, MN, USA |
111 | ″ | rdf:type | schema:Organization |
112 | grid-institutes:grid.266515.3 | schema:alternateName | Department of Chemistry, University of Kansas, 66045, Lawrence, KS, USA |
113 | ″ | schema:name | Department of Chemistry, University of Kansas, 66045, Lawrence, KS, USA |
114 | ″ | rdf:type | schema:Organization |
115 | grid-institutes:grid.7372.1 | schema:alternateName | Department of Chemistry, University of Warwick, CV4 7AL, Coventry, UK |
116 | ″ | schema:name | Department of Chemistry, University of Warwick, CV4 7AL, Coventry, UK |
117 | ″ | rdf:type | schema:Organization |