About: Stable Triazenes Derived from 2-Alkylaminonaphthalenes and 5 Nitrobenzo[c]-1,2-thiazole-3-diazonium Hydrogensulphate     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : http://linked.opendata.cz/ontology/domain/vavai/Vysledek, within Data Space : linked.opendata.cz associated with source document(s)

AttributesValues
rdf:type
Description
  • A calculation using the DFT method confirmed that the extraordinary stability of the triazenes formed by an azo coupling reaction of 5-nitrobenzo[c]-1,2-thiazole-3-diazonium and primary or secondary aromatic amines is caused by the fact that these substances are protonated at the heterocyclic nitrogen atom and not at the nitrogen atom of the triazene grouping ?N=N?N(R)Ar. Stable triazenes are also formed by reaction of 5-nitrobenzo[c]-1,2-thiazole-3-diazonium with 2-alkylaminonaphthalenes. In the case of the azo coupling reaction with 2-methylamino- and 2-ethylaminonaphthalene the content of triazenes is almost 50 % in the product mixture with the isomeric azo compounds. The structure of triazenes was confirmed by X-ray analysis.
  • A calculation using the DFT method confirmed that the extraordinary stability of the triazenes formed by an azo coupling reaction of 5-nitrobenzo[c]-1,2-thiazole-3-diazonium and primary or secondary aromatic amines is caused by the fact that these substances are protonated at the heterocyclic nitrogen atom and not at the nitrogen atom of the triazene grouping ?N=N?N(R)Ar. Stable triazenes are also formed by reaction of 5-nitrobenzo[c]-1,2-thiazole-3-diazonium with 2-alkylaminonaphthalenes. In the case of the azo coupling reaction with 2-methylamino- and 2-ethylaminonaphthalene the content of triazenes is almost 50 % in the product mixture with the isomeric azo compounds. The structure of triazenes was confirmed by X-ray analysis. (en)
  • Výpočty využívající DFT medodu potvrdily, že mimořádná stabilita triazenů vzniklých azokopulační reakcí 5-nitrobenzo[c]-1,2-thiazol-3-diazonia s primárními a sekundárními aromatickými aminy je způsobena faktem, že tyto látky jsou protonovány na dusíkovém atomu heterocyklického skeletu a nikoliv na dusíku triazenového uspořádání ?N=N?N(R)Ar. Stabilní triazeny vznikaly také reakcí 5-nitrobenzo[c]-1,2-thiazol-3-diazonia s 2-alkylaminonaftaleny. Téměř 50% podíl triazenů v reakční směsi je v případě azokopulační reakce s 2-methylamino- and 2-ethylaminonaftaleny vedle izomerních azosloučenin. Struktury triazenů byly potvrzeny X-ray analýzami. (cs)
Title
  • Stable Triazenes Derived from 2-Alkylaminonaphthalenes and 5 Nitrobenzo[c]-1,2-thiazole-3-diazonium Hydrogensulphate
  • Stabilní triazeny připravené z 2-alkylaminonaftalenů a 5-nitrobenzo[c]-1,2-thiazol-3-diazonium-hydrogensulfátu (cs)
  • Stable Triazenes Derived from 2-Alkylaminonaphthalenes and 5 Nitrobenzo[c]-1,2-thiazole-3-diazonium Hydrogensulphate (en)
skos:prefLabel
  • Stable Triazenes Derived from 2-Alkylaminonaphthalenes and 5 Nitrobenzo[c]-1,2-thiazole-3-diazonium Hydrogensulphate
  • Stabilní triazeny připravené z 2-alkylaminonaftalenů a 5-nitrobenzo[c]-1,2-thiazol-3-diazonium-hydrogensulfátu (cs)
  • Stable Triazenes Derived from 2-Alkylaminonaphthalenes and 5 Nitrobenzo[c]-1,2-thiazole-3-diazonium Hydrogensulphate (en)
skos:notation
  • RIV/00216275:25310/08:00007781!RIV09-MSM-25310___
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • P(LC512), Z(MSM0021627501)
http://linked.open...iv/cisloPeriodika
  • 19
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 396905
http://linked.open...ai/riv/idVysledku
  • RIV/00216275:25310/08:00007781
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • Azo coupling; diazoniums; triazenes; density functional calcultations; amines (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • DE - Spolková republika Německo
http://linked.open...ontrolniKodProRIV
  • [D031CE1188E7]
http://linked.open...i/riv/nazevZdroje
  • European Journal of Organic Chemistry
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...vavai/riv/projekt
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • -
http://linked.open...iv/tvurceVysledku
  • Jansa, Petr
  • Nachtigall, Petr
  • Růžička, Aleš
  • Černý, Michal
  • Macháček, Vladimír
  • Svobodová, Markéta
  • Přikryl, Josef
http://linked.open...n/vavai/riv/zamer
issn
  • 1434-193X
number of pages
http://localhost/t...ganizacniJednotka
  • 25310
Faceted Search & Find service v1.16.118 as of Jun 21 2024


Alternative Linked Data Documents: ODE     Content Formats:   [cxml] [csv]     RDF   [text] [turtle] [ld+json] [rdf+json] [rdf+xml]     ODATA   [atom+xml] [odata+json]     Microdata   [microdata+json] [html]    About   
This material is Open Knowledge   W3C Semantic Web Technology [RDF Data] Valid XHTML + RDFa
OpenLink Virtuoso version 07.20.3240 as of Jun 21 2024, on Linux (x86_64-pc-linux-gnu), Single-Server Edition (126 GB total memory, 36 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software