@prefix foaf: . @prefix wikipedia-en: . @prefix dbr: . wikipedia-en:Phosphazene foaf:primaryTopic dbr:Phosphazene . @prefix dbo: . dbr:Polyphosphazene dbo:wikiPageWikiLink dbr:Phosphazene . dbr:High-refractive-index_polymer dbo:wikiPageWikiLink dbr:Phosphazene . dbr:Hexafluorophosphazene dbo:wikiPageWikiLink dbr:Phosphazene . dbr:Superbase dbo:wikiPageWikiLink dbr:Phosphazene . dbr:Organic_base dbo:wikiPageWikiLink dbr:Phosphazene . dbr:Nontrigonal_pnictogen_compounds dbo:wikiPageWikiLink dbr:Phosphazene . dbr:Cyclodiphosphazane dbo:wikiPageWikiLink dbr:Phosphazene . dbr:Tetraazidomethane dbo:wikiPageWikiLink dbr:Phosphazene . dbr:List_of_inorganic_compounds_named_after_people dbo:wikiPageWikiLink dbr:Phosphazene . dbo:wikiPageWikiLink dbr:Phosphazene . dbr:P4-t-Bu dbo:wikiPageWikiLink dbr:Phosphazene . dbr:Hexachlorophosphazene dbo:wikiPageWikiLink dbr:Phosphazene . dbr:Double_bond_rule dbo:wikiPageWikiLink dbr:Phosphazene . dbo:wikiPageWikiLink dbr:Phosphazene . dbr:Non-nucleophilic_base dbo:wikiPageWikiLink dbr:Phosphazene . dbr:Phosphine_imide dbo:wikiPageWikiLink dbr:Phosphazene . dbo:wikiPageWikiLink dbr:Phosphazene . @prefix rdf: . @prefix yago: . dbr:Phosphazene rdf:type yago:Cognition100023271 , yago:Compound105870180 , yago:PsychologicalFeature100023100 , yago:Whole105869584 , yago:Idea105833840 , yago:Content105809192 , yago:Concept105835747 , yago:WikicatPhosphorusCompounds , yago:WikicatNitrogenCompounds , dbo:ChemicalCompound , yago:Abstraction100002137 . @prefix rdfs: . dbr:Phosphazene rdfs:label "\u0424\u043E\u0441\u0444\u0430\u0437\u0435\u043D\u0438"@uk , "Phosphazene"@en , "Fosfacenos"@es , "\u0424\u043E\u0441\u0444\u0430\u0437\u0435\u043D\u044B"@ru , "Fosfazeny"@cs , "Fosfazeni"@it , "Phosphaz\u00E8ne"@fr , "\u30DB\u30B9\u30D5\u30A1\u30BC\u30F3"@ja ; rdfs:comment "Les phosphaz\u00E8nes sont une classe de compos\u00E9s chimiques comportant au moins une double liaison entre un atome de phosphore pentavalent et un atome d'azote, d'o\u00F9 les synonymes d'iminophosphoranes ou d'imides de phosphine. En synth\u00E8se organique, le terme phosphaz\u00E8ne est souvent utilis\u00E9 pour d\u00E9signer une sous-classe de compos\u00E9s dans lesquels l'atome de phosphore est li\u00E9 \u00E0 trois autres atomes d'azote. Ces compos\u00E9s sont \u00E9tonnamment stables et montrent une remarquable basicit\u00E9, ce qui en fait un des plus remarquables exemples de superbase organique neutre."@fr , "Los fosfacenos son una clase de compuestos organof\u00F3sforicos qu\u00EDmicos en el que un \u00E1tomo de f\u00F3sforo est\u00E1 unido covalentemente a un \u00E1tomo de nitr\u00F3geno por un enlace doble y a otros tres \u00E1tomos o radicales por enlaces simples. Mientras que otras sustituciones producen compuestos relativamente persistentes, en s\u00EDntesis org\u00E1nica, el t\u00E9rmino se refiere principalmente a las especies con tres sustituyentes amina unidos al f\u00F3sforo. Estos compuestos son ejemplos inusualmente estables de la clase fosforano de mol\u00E9culas y tienen una notable afinidad prot\u00F3nica. Como tales, son unos de los ejemplos eminentes de superbases neutras y org\u00E1nicas.\u200B Dos ejemplos son el hexaclorociclotrifosfazeno y el cloruro de bis(trifenilfosfina)iminio. Los fosfacenos son tambi\u00E9n conocidos como imidas de fosfano."@es , "I fosfazeni sono una famiglia di composti chimici contenenti formalmente un doppio legame tra fosforo e azoto. Si possono considerare derivati da H3P=NH o da HP=NH. I membri pi\u00F9 importanti sono i ciclofosfazeni e i polifosfazeni lineari. Questi ultimi hanno propriet\u00E0 che li rendono interessanti per applicazioni biomediche, per la costruzione di membrane per elettroliti solidi in batterie al litio o celle a combustibile, per materiali ottici, elastomeri per l'industria aerospaziale e materiali antifiamma."@it , "Phosphazenes refer to classes of organophosphorus compounds featuring phosphorus(V) with a double bond between P and N. One class of phosphazenes have the formula R\u2212N=P(\u2212NR2)3. These phosphazenes are also known as iminophosphoranes and phosphine imides. They are superbases. Another class of compounds called phosphazenes are represented with the formula (\u2212N=P(\u2212X)2\u2212)n, where X = halogen, alkoxy group, amide and other organyl groups. One example is hexachlorocyclotriphosphazene (\u2212N=P(\u2212Cl)2\u2212)3. Bis(triphenylphosphine)iminium chloride [Ph3P=N=PPh3]+Cl\u2212is also referred to as a phosphazene, where Ph = phenyl group. This article focuses on those phosphazenes with the formula R\u2212N=P(\u2212NR2)3."@en , "Fosfazeny jsou slou\u010Deniny tvo\u0159en\u00E9 \u0159et\u011Bzci nebo cykly z atom\u016F fosforu a dus\u00EDku, v nich\u017E se pravideln\u011B st\u0159\u00EDd\u00E1 jednoduch\u00E1 a dvojn\u00E1 vazba. Struktura hexachlorcyklotrifosfazenu Nejzn\u00E1m\u011Bj\u0161\u00EDm p\u0159edstavitelem je cyklick\u00FD trimer , kter\u00FD se p\u0159ipravuje reakc\u00ED chloridu fosfore\u010Dn\u00E9ho a chloridu amonn\u00E9ho. Fosfazeny a jejich deriv\u00E1ty nach\u00E1zej\u00ED vyu\u017Eit\u00ED jako pesticidy, , antioxidanty, zpomalova\u010De ho\u0159en\u00ED, apod."@cs , "\u0424\u043E\u0441\u0444\u0430\u0437\u0435\u043D\u0438 (\u0430\u043D\u0433\u043B. phosphazenes, \u0440\u043E\u0441. \u0444\u043E\u0441\u0444\u0430\u0437\u0435\u043D\u044B) \u2014 \u0446\u0438\u043A\u043Bi\u0447\u043Di \u0430\u0431\u043E \u043Bi\u043Di\u0439\u043Di \u0441\u043F\u043E\u043B\u0443\u043A\u0438 \u0430\u0437\u043E\u0442\u0443 \u0439 \u0444\u043E\u0441\u0444\u043E\u0440\u0443 \u0441\u043Fi\u043B\u044C\u043D\u043E\u0457 \u0444\u043E\u0440\u043C\u0443\u043B\u0438 (\u2013>P=N\u2013)n, \u044F\u043A\u0456 \u043C\u0456\u0441\u0442\u044F\u0442\u044C \u0444\u043E\u0441\u0444\u043E\u0440-\u0430\u0437\u043E\u0442\u043D\u0456 \u043F\u043E\u0434\u0432\u0456\u0439\u043D\u0456 \u0437\u0432\u2018\u044F\u0437\u043A\u0438, \u0442\u043E\u0431\u0442\u043E \u043F\u043E\u0445\u0456\u0434\u043D\u0456 H3P=NH \u0442\u0430 HP=NH. \u041F\u0440., \u043F\u043E\u043B\u0456(\u0434\u0456\u0435\u0442\u043E\u043A\u0441\u0438\u0444\u043E\u0441\u0444\u0430\u0437\u0435\u043D), \u0442\u0440\u0438\u0430\u0437\u0430\u0442\u0440\u0438\u0444\u043E\u0441\u0444\u043E\u0440\u0438\u043D\u0438, \u043F\u043E\u043Bi\u0444\u043E\u0441\u0444\u043E\u043Di\u043B\u0442\u0440\u0438\u043B\u0445\u043B\u043E\u0440\u0438\u0434\u0438 (\u2013PCl2=N\u2013)n \u0442\u0430 \u0456\u043D. \u041D\u0430\u0439\u0432\u0456\u0434\u043E\u043C\u0456\u0448\u0456 \u0445\u043B\u043E\u0440\u043E\u0444\u043E\u0441\u0444\u0430\u0437\u0435\u043D\u0438 (\u0441\u0442\u0440\u0443\u043A\u0442\u0443\u0440\u0430 \u043F\u043B\u043E\u0441\u043A\u043E\u0433\u043E \u0448\u0435\u0441\u0442\u0438\u043A\u0443\u0442\u043D\u0438\u043A\u0430), \u044F\u043A\u0456 \u0443\u0442\u0432\u043E\u0440\u044E\u044E\u0442\u044C \u0447\u0438\u0441\u043B\u0435\u043D\u043D\u0456 \u043F\u043E\u0445\u0456\u0434\u043D\u0456 \u043F\u0440\u0438 \u0437\u0430\u043C\u0456\u0449\u0435\u043D\u043D\u0456 \u0445\u043B\u043E\u0440\u0443. \u041E\u0442\u0440\u0438\u043C\u0443\u044E\u0442\u044C\u0441\u044F \u0437\u0430 \u0440\u0435\u0430\u043A\u0446\u0456\u0454\u044E nP\u0421l5 + nNH4\u0421l \u2192 (N\u2261PCl2)n + 4nHCl."@uk , "\u0424\u043E\u0441\u0444\u0430\u0437\u0435\u043D\u044B \u2014 \u0441\u043E\u0435\u0434\u0438\u043D\u0435\u043D\u0438\u044F, \u0441\u043E\u0434\u0435\u0440\u0436\u0430\u0449\u0438\u0435 \u0434\u0432\u043E\u0439\u043D\u0443\u044E \u0441\u0432\u044F\u0437\u044C \u0444\u043E\u0441\u0444\u043E\u0440-\u0430\u0437\u043E\u0442. \u041A \u0444\u043E\u0441\u0444\u0430\u0437\u0435\u043D\u0430\u043C \u043E\u0442\u043D\u043E\u0441\u044F\u0442 \u0441\u043E\u0435\u0434\u0438\u043D\u0435\u043D\u0438\u044F \u043A\u0430\u043A \u043F\u044F\u0442\u0438\u0432\u0430\u043B\u0435\u043D\u0442\u043D\u043E\u0433\u043E \u0444\u043E\u0441\u0444\u043E\u0440\u0430 \u043E\u0431\u0449\u0435\u0439 \u0444\u043E\u0440\u043C\u0443\u043B\u044B R3P=NR, \u0442\u0430\u043A \u0438 \u043F\u0440\u043E\u0438\u0437\u0432\u043E\u0434\u043D\u044B\u0435 \u0442\u0440\u0435\u0445\u0432\u0430\u043B\u0435\u043D\u0442\u043D\u043E\u0433\u043E \u0444\u043E\u0441\u0444\u043E\u0440\u0430 RP=NR. \u0411\u043E\u043B\u044C\u0448\u0438\u043D\u0441\u0442\u0432\u043E \u0438\u0437\u0432\u0435\u0441\u0442\u043D\u044B\u0445 \u0444\u043E\u0441\u0444\u0430\u0437\u0435\u043D\u043E\u0432 \u2014 \u043F\u0440\u043E\u0438\u0437\u0432\u043E\u0434\u043D\u044B\u0435 \u043F\u044F\u0442\u0438\u0432\u0430\u043B\u0435\u043D\u0442\u043D\u043E\u0433\u043E \u0444\u043E\u0441\u0444\u043E\u0440\u0430. \u0424\u043E\u0441\u0444\u0430\u0437\u0435\u043D\u043E\u0432\u044B\u0439 \u0444\u0440\u0430\u0433\u043C\u0435\u043D\u0442 \u0442\u0430\u043A\u0436\u0435 \u044F\u0432\u043B\u044F\u0435\u0442\u0441\u044F \u0441\u0442\u0440\u0443\u043A\u0442\u0443\u0440\u043D\u043E\u0439 \u0435\u0434\u0438\u043D\u0438\u0446\u0435\u0439 \u0441\u043E\u0435\u0434\u0438\u043D\u0435\u043D\u0438\u0439 (R2P=N-)n \u043A\u0430\u043A \u0446\u0438\u043A\u043B\u0438\u0447\u0435\u0441\u043A\u043E\u0433\u043E (\u0446\u0438\u043A\u043B\u043E\u0444\u043E\u0441\u0444\u0430\u0437\u0435\u043D\u044B) \u0438 \u043A\u0430\u0440\u043A\u0430\u0441\u043D\u043E\u0433\u043E \u0441\u0442\u0440\u043E\u0435\u043D\u0438\u044F, \u0442\u0430\u043A \u0438 \u043F\u043E\u043B\u0438\u043C\u0435\u0440\u043E\u0432 \u2014 \u043F\u043E\u043B\u0438\u0444\u043E\u0441\u0444\u0430\u0437\u0435\u043D\u043E\u0432."@ru , "\u30DB\u30B9\u30D5\u30A1\u30BC\u30F3\uFF08\u82F1: Phosphazenes\uFF09\u306F\u3001\u30EA\u30F3\u539F\u5B50\u3068\u7A92\u7D20\u539F\u5B50\u304C\u4EA4\u4E92\u306B\u7D50\u5408\u3057\u305F\u7121\u6A5F\u5316\u5408\u7269\u306E\u7DCF\u79F0\u3067\u3001\u9396\u5F0F\u307E\u305F\u306F\u74B0\u5F0F\u5316\u5408\u7269\u306E\u5F62\u72B6\u3092\u63A1\u308B\u3002\u74B0\u72B6\u30DB\u30B9\u30D5\u30A1\u30BC\u30F3\uFF08\u74B0\u5F0F\u30DB\u30B9\u30D5\u30A1\u30BC\u30F3\uFF09\u306F\u7121\u6A5F\u30D9\u30F3\u30BC\u30F3\u306E\u7570\u540D\u3092\u6301\u3064\u3002\u82B3\u9999\u3092\u6301\u3064\u304C\u4EBA\u4F53\u306B\u306F\u6709\u5BB3\u3067\u3042\u308B\u3002"@ja ; foaf:depiction , , . @prefix dcterms: . @prefix dbc: . dbr:Phosphazene dcterms:subject dbc:Non-nucleophilic_bases , dbc:Phosphorus_compounds , dbc:Nitrogen_compounds , dbc:Phosphazenes , dbc:Superbases ; dbo:abstract "Fosfazeny jsou slou\u010Deniny tvo\u0159en\u00E9 \u0159et\u011Bzci nebo cykly z atom\u016F fosforu a dus\u00EDku, v nich\u017E se pravideln\u011B st\u0159\u00EDd\u00E1 jednoduch\u00E1 a dvojn\u00E1 vazba. Struktura hexachlorcyklotrifosfazenu Nejzn\u00E1m\u011Bj\u0161\u00EDm p\u0159edstavitelem je cyklick\u00FD trimer , kter\u00FD se p\u0159ipravuje reakc\u00ED chloridu fosfore\u010Dn\u00E9ho a chloridu amonn\u00E9ho. Fosfazeny a jejich deriv\u00E1ty nach\u00E1zej\u00ED vyu\u017Eit\u00ED jako pesticidy, , antioxidanty, zpomalova\u010De ho\u0159en\u00ED, apod."@cs , "\u0424\u043E\u0441\u0444\u0430\u0437\u0435\u043D\u044B \u2014 \u0441\u043E\u0435\u0434\u0438\u043D\u0435\u043D\u0438\u044F, \u0441\u043E\u0434\u0435\u0440\u0436\u0430\u0449\u0438\u0435 \u0434\u0432\u043E\u0439\u043D\u0443\u044E \u0441\u0432\u044F\u0437\u044C \u0444\u043E\u0441\u0444\u043E\u0440-\u0430\u0437\u043E\u0442. \u041A \u0444\u043E\u0441\u0444\u0430\u0437\u0435\u043D\u0430\u043C \u043E\u0442\u043D\u043E\u0441\u044F\u0442 \u0441\u043E\u0435\u0434\u0438\u043D\u0435\u043D\u0438\u044F \u043A\u0430\u043A \u043F\u044F\u0442\u0438\u0432\u0430\u043B\u0435\u043D\u0442\u043D\u043E\u0433\u043E \u0444\u043E\u0441\u0444\u043E\u0440\u0430 \u043E\u0431\u0449\u0435\u0439 \u0444\u043E\u0440\u043C\u0443\u043B\u044B R3P=NR, \u0442\u0430\u043A \u0438 \u043F\u0440\u043E\u0438\u0437\u0432\u043E\u0434\u043D\u044B\u0435 \u0442\u0440\u0435\u0445\u0432\u0430\u043B\u0435\u043D\u0442\u043D\u043E\u0433\u043E \u0444\u043E\u0441\u0444\u043E\u0440\u0430 RP=NR. \u0411\u043E\u043B\u044C\u0448\u0438\u043D\u0441\u0442\u0432\u043E \u0438\u0437\u0432\u0435\u0441\u0442\u043D\u044B\u0445 \u0444\u043E\u0441\u0444\u0430\u0437\u0435\u043D\u043E\u0432 \u2014 \u043F\u0440\u043E\u0438\u0437\u0432\u043E\u0434\u043D\u044B\u0435 \u043F\u044F\u0442\u0438\u0432\u0430\u043B\u0435\u043D\u0442\u043D\u043E\u0433\u043E \u0444\u043E\u0441\u0444\u043E\u0440\u0430. \u0424\u043E\u0441\u0444\u0430\u0437\u0435\u043D\u043E\u0432\u044B\u0439 \u0444\u0440\u0430\u0433\u043C\u0435\u043D\u0442 \u0442\u0430\u043A\u0436\u0435 \u044F\u0432\u043B\u044F\u0435\u0442\u0441\u044F \u0441\u0442\u0440\u0443\u043A\u0442\u0443\u0440\u043D\u043E\u0439 \u0435\u0434\u0438\u043D\u0438\u0446\u0435\u0439 \u0441\u043E\u0435\u0434\u0438\u043D\u0435\u043D\u0438\u0439 (R2P=N-)n \u043A\u0430\u043A \u0446\u0438\u043A\u043B\u0438\u0447\u0435\u0441\u043A\u043E\u0433\u043E (\u0446\u0438\u043A\u043B\u043E\u0444\u043E\u0441\u0444\u0430\u0437\u0435\u043D\u044B) \u0438 \u043A\u0430\u0440\u043A\u0430\u0441\u043D\u043E\u0433\u043E \u0441\u0442\u0440\u043E\u0435\u043D\u0438\u044F, \u0442\u0430\u043A \u0438 \u043F\u043E\u043B\u0438\u043C\u0435\u0440\u043E\u0432 \u2014 \u043F\u043E\u043B\u0438\u0444\u043E\u0441\u0444\u0430\u0437\u0435\u043D\u043E\u0432."@ru , "Phosphazenes refer to classes of organophosphorus compounds featuring phosphorus(V) with a double bond between P and N. One class of phosphazenes have the formula R\u2212N=P(\u2212NR2)3. These phosphazenes are also known as iminophosphoranes and phosphine imides. They are superbases. Another class of compounds called phosphazenes are represented with the formula (\u2212N=P(\u2212X)2\u2212)n, where X = halogen, alkoxy group, amide and other organyl groups. One example is hexachlorocyclotriphosphazene (\u2212N=P(\u2212Cl)2\u2212)3. Bis(triphenylphosphine)iminium chloride [Ph3P=N=PPh3]+Cl\u2212is also referred to as a phosphazene, where Ph = phenyl group. This article focuses on those phosphazenes with the formula R\u2212N=P(\u2212NR2)3."@en , "I fosfazeni sono una famiglia di composti chimici contenenti formalmente un doppio legame tra fosforo e azoto. Si possono considerare derivati da H3P=NH o da HP=NH. I membri pi\u00F9 importanti sono i ciclofosfazeni e i polifosfazeni lineari. Questi ultimi hanno propriet\u00E0 che li rendono interessanti per applicazioni biomediche, per la costruzione di membrane per elettroliti solidi in batterie al litio o celle a combustibile, per materiali ottici, elastomeri per l'industria aerospaziale e materiali antifiamma."@it , "Les phosphaz\u00E8nes sont une classe de compos\u00E9s chimiques comportant au moins une double liaison entre un atome de phosphore pentavalent et un atome d'azote, d'o\u00F9 les synonymes d'iminophosphoranes ou d'imides de phosphine. En synth\u00E8se organique, le terme phosphaz\u00E8ne est souvent utilis\u00E9 pour d\u00E9signer une sous-classe de compos\u00E9s dans lesquels l'atome de phosphore est li\u00E9 \u00E0 trois autres atomes d'azote. Ces compos\u00E9s sont \u00E9tonnamment stables et montrent une remarquable basicit\u00E9, ce qui en fait un des plus remarquables exemples de superbase organique neutre."@fr , "Los fosfacenos son una clase de compuestos organof\u00F3sforicos qu\u00EDmicos en el que un \u00E1tomo de f\u00F3sforo est\u00E1 unido covalentemente a un \u00E1tomo de nitr\u00F3geno por un enlace doble y a otros tres \u00E1tomos o radicales por enlaces simples. Mientras que otras sustituciones producen compuestos relativamente persistentes, en s\u00EDntesis org\u00E1nica, el t\u00E9rmino se refiere principalmente a las especies con tres sustituyentes amina unidos al f\u00F3sforo. Estos compuestos son ejemplos inusualmente estables de la clase fosforano de mol\u00E9culas y tienen una notable afinidad prot\u00F3nica. Como tales, son unos de los ejemplos eminentes de superbases neutras y org\u00E1nicas.\u200B Dos ejemplos son el hexaclorociclotrifosfazeno y el cloruro de bis(trifenilfosfina)iminio. Los fosfacenos son tambi\u00E9n conocidos como imidas de fosfano."@es , "\u30DB\u30B9\u30D5\u30A1\u30BC\u30F3\uFF08\u82F1: Phosphazenes\uFF09\u306F\u3001\u30EA\u30F3\u539F\u5B50\u3068\u7A92\u7D20\u539F\u5B50\u304C\u4EA4\u4E92\u306B\u7D50\u5408\u3057\u305F\u7121\u6A5F\u5316\u5408\u7269\u306E\u7DCF\u79F0\u3067\u3001\u9396\u5F0F\u307E\u305F\u306F\u74B0\u5F0F\u5316\u5408\u7269\u306E\u5F62\u72B6\u3092\u63A1\u308B\u3002\u74B0\u72B6\u30DB\u30B9\u30D5\u30A1\u30BC\u30F3\uFF08\u74B0\u5F0F\u30DB\u30B9\u30D5\u30A1\u30BC\u30F3\uFF09\u306F\u7121\u6A5F\u30D9\u30F3\u30BC\u30F3\u306E\u7570\u540D\u3092\u6301\u3064\u3002\u82B3\u9999\u3092\u6301\u3064\u304C\u4EBA\u4F53\u306B\u306F\u6709\u5BB3\u3067\u3042\u308B\u3002"@ja , "\u0424\u043E\u0441\u0444\u0430\u0437\u0435\u043D\u0438 (\u0430\u043D\u0433\u043B. phosphazenes, \u0440\u043E\u0441. \u0444\u043E\u0441\u0444\u0430\u0437\u0435\u043D\u044B) \u2014 \u0446\u0438\u043A\u043Bi\u0447\u043Di \u0430\u0431\u043E \u043Bi\u043Di\u0439\u043Di \u0441\u043F\u043E\u043B\u0443\u043A\u0438 \u0430\u0437\u043E\u0442\u0443 \u0439 \u0444\u043E\u0441\u0444\u043E\u0440\u0443 \u0441\u043Fi\u043B\u044C\u043D\u043E\u0457 \u0444\u043E\u0440\u043C\u0443\u043B\u0438 (\u2013>P=N\u2013)n, \u044F\u043A\u0456 \u043C\u0456\u0441\u0442\u044F\u0442\u044C \u0444\u043E\u0441\u0444\u043E\u0440-\u0430\u0437\u043E\u0442\u043D\u0456 \u043F\u043E\u0434\u0432\u0456\u0439\u043D\u0456 \u0437\u0432\u2018\u044F\u0437\u043A\u0438, \u0442\u043E\u0431\u0442\u043E \u043F\u043E\u0445\u0456\u0434\u043D\u0456 H3P=NH \u0442\u0430 HP=NH. \u041F\u0440., \u043F\u043E\u043B\u0456(\u0434\u0456\u0435\u0442\u043E\u043A\u0441\u0438\u0444\u043E\u0441\u0444\u0430\u0437\u0435\u043D), \u0442\u0440\u0438\u0430\u0437\u0430\u0442\u0440\u0438\u0444\u043E\u0441\u0444\u043E\u0440\u0438\u043D\u0438, \u043F\u043E\u043Bi\u0444\u043E\u0441\u0444\u043E\u043Di\u043B\u0442\u0440\u0438\u043B\u0445\u043B\u043E\u0440\u0438\u0434\u0438 (\u2013PCl2=N\u2013)n \u0442\u0430 \u0456\u043D. \u041D\u0430\u0439\u0432\u0456\u0434\u043E\u043C\u0456\u0448\u0456 \u0445\u043B\u043E\u0440\u043E\u0444\u043E\u0441\u0444\u0430\u0437\u0435\u043D\u0438 (\u0441\u0442\u0440\u0443\u043A\u0442\u0443\u0440\u0430 \u043F\u043B\u043E\u0441\u043A\u043E\u0433\u043E \u0448\u0435\u0441\u0442\u0438\u043A\u0443\u0442\u043D\u0438\u043A\u0430), \u044F\u043A\u0456 \u0443\u0442\u0432\u043E\u0440\u044E\u044E\u0442\u044C \u0447\u0438\u0441\u043B\u0435\u043D\u043D\u0456 \u043F\u043E\u0445\u0456\u0434\u043D\u0456 \u043F\u0440\u0438 \u0437\u0430\u043C\u0456\u0449\u0435\u043D\u043D\u0456 \u0445\u043B\u043E\u0440\u0443. \u041E\u0442\u0440\u0438\u043C\u0443\u044E\u0442\u044C\u0441\u044F \u0437\u0430 \u0440\u0435\u0430\u043A\u0446\u0456\u0454\u044E nP\u0421l5 + nNH4\u0421l \u2192 (N\u2261PCl2)n + 4nHCl."@uk ; dbo:wikiPageWikiLink dbr:Amidine , dbr:P4-t-Bu , dbr:Phosphine_imide , dbr:Polyphosphazene , , dbr:Orbital_hybridization , dbr:Superbase , dbr:Pivaldehyde , dbr:Methyl_group , , dbc:Phosphazenes , dbr:PKa , dbr:Annulation , dbr:Organyl_group , dbr:Phenyl_group , dbr:Halogen , dbr:Conjugate_acid , dbr:Hexachlorophosphazene , , dbr:Organophosphorus_compound , dbc:Nitrogen_compounds , dbr:Solvents , dbr:Pyrrolidine , dbr:Arene_compound , , dbr:Cyclodiphosphazane , dbr:Acetonitrile , dbc:Phosphorus_compounds , , dbr:Hexachlorocyclotriphosphazene , dbr:Non-HBD_cations , dbc:Non-nucleophilic_bases , , dbr:Verkade_base , dbr:Phosphorimidic_triamide , dbr:Alkoxy_group , dbr:Nucleophilic_addition , dbr:Amide , dbr:Amine , dbr:Nucleophile , dbc:Superbases , dbr:Nucleophilicity , dbr:Titration , dbr:Butyl_group . @prefix dbp: . @prefix dbt: . dbr:Phosphazene dbp:wikiPageUsesTemplate dbt:Chem2 , dbt:Clarification_needed , dbt:Jargon , dbt:Reflist ; dbo:thumbnail ; dbo:wikiPageRevisionID 1112273099 . @prefix xsd: . dbr:Phosphazene dbo:wikiPageLength "5209"^^xsd:nonNegativeInteger ; dbo:wikiPageID 7445926 . @prefix owl: . dbr:Phosphazene owl:sameAs , , . @prefix wikidata: . dbr:Phosphazene owl:sameAs wikidata:Q3565831 . @prefix dbpedia-cs: . dbr:Phosphazene owl:sameAs dbpedia-cs:Fosfazeny , dbr:Phosphazene , . @prefix dbpedia-it: . dbr:Phosphazene owl:sameAs dbpedia-it:Fosfazeni , . @prefix yago-res: . dbr:Phosphazene owl:sameAs yago-res:Phosphazene . @prefix dbpedia-es: . dbr:Phosphazene owl:sameAs dbpedia-es:Fosfacenos , . @prefix gold: . dbr:Phosphazene gold:hypernym dbr:Compounds . @prefix prov: . dbr:Phosphazene prov:wasDerivedFrom ; foaf:isPrimaryTopicOf wikipedia-en:Phosphazene . dbr:Phosphazenes dbo:wikiPageWikiLink dbr:Phosphazene ; dbo:wikiPageRedirects dbr:Phosphazene . dbr:Phosphazene_base dbo:wikiPageWikiLink dbr:Phosphazene ; dbo:wikiPageRedirects dbr:Phosphazene .
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