This HTML5 document contains 51 embedded RDF statements represented using HTML+Microdata notation.

The embedded RDF content will be recognized by any processor of HTML5 Microdata.

Namespace Prefixes

PrefixIRI
dctermshttp://purl.org/dc/terms/
dbohttp://dbpedia.org/ontology/
foafhttp://xmlns.com/foaf/0.1/
n12https://global.dbpedia.org/id/
dbthttp://dbpedia.org/resource/Template:
rdfshttp://www.w3.org/2000/01/rdf-schema#
n4http://www.ontologydesignpatterns.org/ont/dul/DUL.owl#
n13http://commons.wikimedia.org/wiki/Special:FilePath/
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
owlhttp://www.w3.org/2002/07/owl#
dbpedia-zhhttp://zh.dbpedia.org/resource/
wikipedia-enhttp://en.wikipedia.org/wiki/
dbchttp://dbpedia.org/resource/Category:
dbphttp://dbpedia.org/property/
provhttp://www.w3.org/ns/prov#
xsdhhttp://www.w3.org/2001/XMLSchema#
wikidatahttp://www.wikidata.org/entity/
dbrhttp://dbpedia.org/resource/

Statements

Subject Item
dbr:Carbonyldiimidazole
dbo:wikiPageWikiLink
dbr:Triphenylphosphine_phenylimide
Subject Item
dbr:Staudinger_reaction
dbo:wikiPageWikiLink
dbr:Triphenylphosphine_phenylimide
Subject Item
dbr:Triphenylphosphine
dbo:wikiPageWikiLink
dbr:Triphenylphosphine_phenylimide
Subject Item
dbr:Triphenylphosphine_phenylimide
rdf:type
n4:ChemicalObject owl:Thing wikidata:Q11173 dbo:ChemicalSubstance dbo:ChemicalCompound
rdfs:label
苯亚氨基三苯基磷 Triphenylphosphine phenylimide
rdfs:comment
苯亚氨基三苯基磷是一种有机磷化合物，化学式为Ph3P=NPh，其中Ph = C6H5。它是白色固体，可溶于有机溶剂。它可在施陶丁格反应中生成。 这种亚氨基磷最初于赫尔曼·施陶丁格的实验室中合成，他通过三苯基膦和叠氮苯的反应制得。 Ph3P + N3Ph → Ph3P=NPh + N2 X射线衍射表明分子中P-N-C的键角为130.4°，P-N键长为160 pm。 Triphenylphosphine phenylimide is the organophosphorus compound with the formula Ph3P=NPh (Ph = C6H5). It is a white solid that is soluble in organic solvents. The compound is a prototype of a large class of Staudinger reagents, resulting from the Staudinger reaction. The phosphine imides were first prepared in the laboratory of Nobelist Hermann Staudinger. His synthesis involved the direct reaction of triphenylphosphine with phenylazide. Ph3P + N3Ph → Ph3P=NPh + N2 X-ray crystallography establishes that the P-N-C angle is bent (130.4°) and the P-N distance is 160 pm.
foaf:depiction
n13:NPh.png
dcterms:subject
dbc:Organophosphorus_compounds dbc:Phenyl_compounds
dbo:wikiPageID
52685532
dbo:wikiPageRevisionID
1104974195
dbo:wikiPageWikiLink
dbr:Staudinger_reaction dbr:Hermann_Staudinger dbr:Phenylazide dbc:Organophosphorus_compounds dbr:X-ray_crystallography dbr:Organophosphorus_compound dbr:Triphenylphosphine dbr:Phenyl dbc:Phenyl_compounds
owl:sameAs
n12:2r4HC wikidata:Q30715385 dbpedia-zh:苯亚氨基三苯基磷
dbp:wikiPageUsesTemplate
dbt:Chembox_Properties dbt:Chembox_Hazards dbt:Chembox_Identifiers dbt:Chembox dbt:Ubl dbt:Fdacite
dbo:thumbnail
n13:NPh.png?width=300
dbp:imagefile
Ph3P=NPh.png
dbp:pin
Tetraphenylphosphanimine
dbo:abstract
苯亚氨基三苯基磷是一种有机磷化合物，化学式为Ph3P=NPh，其中Ph = C6H5。它是白色固体，可溶于有机溶剂。它可在施陶丁格反应中生成。 这种亚氨基磷最初于赫尔曼·施陶丁格的实验室中合成，他通过三苯基膦和叠氮苯的反应制得。 Ph3P + N3Ph → Ph3P=NPh + N2 X射线衍射表明分子中P-N-C的键角为130.4°，P-N键长为160 pm。 Triphenylphosphine phenylimide is the organophosphorus compound with the formula Ph3P=NPh (Ph = C6H5). It is a white solid that is soluble in organic solvents. The compound is a prototype of a large class of Staudinger reagents, resulting from the Staudinger reaction. The phosphine imides were first prepared in the laboratory of Nobelist Hermann Staudinger. His synthesis involved the direct reaction of triphenylphosphine with phenylazide. Ph3P + N3Ph → Ph3P=NPh + N2 X-ray crystallography establishes that the P-N-C angle is bent (130.4°) and the P-N distance is 160 pm.
prov:wasDerivedFrom
wikipedia-en:Triphenylphosphine_phenylimide?oldid=1104974195&ns=0
dbo:wikiPageLength
2713
dbo:iupacName
Tetraphenylphosphanimine
foaf:isPrimaryTopicOf
wikipedia-en:Triphenylphosphine_phenylimide
Subject Item
dbr:Hermann_Staudinger
dbo:wikiPageWikiLink
dbr:Triphenylphosphine_phenylimide
Subject Item
dbr:Phenyl_azide
dbo:wikiPageWikiLink
dbr:Triphenylphosphine_phenylimide
Subject Item
dbr:Ph3P=NPh
dbo:wikiPageWikiLink
dbr:Triphenylphosphine_phenylimide
dbo:wikiPageRedirects
dbr:Triphenylphosphine_phenylimide
Subject Item
dbr:Phenylimidotriphenylphosphine
dbo:wikiPageWikiLink
dbr:Triphenylphosphine_phenylimide
dbo:wikiPageRedirects
dbr:Triphenylphosphine_phenylimide
Subject Item
wikipedia-en:Triphenylphosphine_phenylimide
foaf:primaryTopic
dbr:Triphenylphosphine_phenylimide