1,1′-Azobis-1,2,3-triazole is a moderately explosive but comparatively stable chemical compound which contains a long continuous chain of nitrogen atoms, with an unbroken chain of eight nitrogen atoms cyclised into two 1,2,3-triazole rings. It is stable up to 194 °C. The compound exhibits cis–trans isomerism at the central azo group: the trans isomer is more stable and is yellow, while the cis isomer is less stable and is blue. The two rings are aromatic and form a conjugated system with the azo linkage. This chromophore allows the trans compound to be isomerised to the cis when treated with an appropriate wavelength of ultraviolet light.
Attributes | Values |
---|
rdf:type
| |
rdfs:label
| - 1,1'-Azobis-1,2,3-triazole (en)
- 1,1'-アゾビス-1,2,3-トリアゾール (ja)
|
rdfs:comment
| - 1,1′-Azobis-1,2,3-triazole is a moderately explosive but comparatively stable chemical compound which contains a long continuous chain of nitrogen atoms, with an unbroken chain of eight nitrogen atoms cyclised into two 1,2,3-triazole rings. It is stable up to 194 °C. The compound exhibits cis–trans isomerism at the central azo group: the trans isomer is more stable and is yellow, while the cis isomer is less stable and is blue. The two rings are aromatic and form a conjugated system with the azo linkage. This chromophore allows the trans compound to be isomerised to the cis when treated with an appropriate wavelength of ultraviolet light. (en)
- 1,1'-アゾビス-1,2,3-トリアゾール(1,1'-Azobis-1,2,3-triazole)は、弱い爆発性を持つが、比較的安定な化合物である。8つの窒素原子が2つの1,2,3-トリアゾールに環化した、長い繋がった鎖を持つ。194℃まで安定である。中央のアゾ基の部分で、cis-trans幾何異性体を持つ。trans-異性体は黄色くより安定で、cis-異性体は青色でより安定性が低い。2つの環は芳香族性を持ち、アゾ結合で共役系を形成する。 この発色団は、特定の波長の紫外線を照射することで、trans-異性体をcis-異性体に異性化することができる。 (ja)
|
foaf:depiction
| |
dct:subject
| |
Wikipage page ID
| |
Wikipage revision ID
| |
Link from a Wikipage to another Wikipage
| |
sameAs
| - 1,1'-Azobis-1,2,3-triazole
- 1,1'-Azobis-1,2,3-triazole
- 1,1'-Azobis-1,2,3-triazole
- 1,1'-Azobis-1,2,3-triazole
- 1,1'-Azobis-1,2,3-triazole
- 1,1'-Azobis-1,2,3-triazole
- 1,1'-Azobis-1,2,3-triazole
- 1,1'-Azobis-1,2,3-triazole
- 1,1'-Azobis-1,2,3-triazole
|
dbp:wikiPageUsesTemplate
| |
thumbnail
| |
ImageFile
| |
imagesize
| |
PIN
| |
verifiedrevid
| |
has abstract
| - 1,1′-Azobis-1,2,3-triazole is a moderately explosive but comparatively stable chemical compound which contains a long continuous chain of nitrogen atoms, with an unbroken chain of eight nitrogen atoms cyclised into two 1,2,3-triazole rings. It is stable up to 194 °C. The compound exhibits cis–trans isomerism at the central azo group: the trans isomer is more stable and is yellow, while the cis isomer is less stable and is blue. The two rings are aromatic and form a conjugated system with the azo linkage. This chromophore allows the trans compound to be isomerised to the cis when treated with an appropriate wavelength of ultraviolet light. (en)
- 1,1'-アゾビス-1,2,3-トリアゾール(1,1'-Azobis-1,2,3-triazole)は、弱い爆発性を持つが、比較的安定な化合物である。8つの窒素原子が2つの1,2,3-トリアゾールに環化した、長い繋がった鎖を持つ。194℃まで安定である。中央のアゾ基の部分で、cis-trans幾何異性体を持つ。trans-異性体は黄色くより安定で、cis-異性体は青色でより安定性が低い。2つの環は芳香族性を持ち、アゾ結合で共役系を形成する。 この発色団は、特定の波長の紫外線を照射することで、trans-異性体をcis-異性体に異性化することができる。 (ja)
|
prov:wasDerivedFrom
| |
page length (characters) of wiki page
| |
IUPAC name
| - 1,1-Diazenediyldi(1H-1,2,3-triazole) (en)
|
foaf:isPrimaryTopicOf
| |
is Link from a Wikipage to another Wikipage
of | |
is Wikipage redirect
of | |
is foaf:primaryTopic
of | |