Linked Life Data

21258700

Source:http://linkedlifedata.com/resource/pubmed/id/21258700

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
2011-3-31
pubmed:abstractText
A series of symmetrical imidazole- and N-methylated imidazole-based diarylethenes were synthesized, and the structures have been well characterized by NMR spectroscopy and mass spectrometry. Their photochromism were investigated upon UV/vis light irradiation in DMF solution. A significant red-shift of UV absorption was observed after irradiation with UV light when substituents on the benzene ring (such as methoxyl group) were introduced. But N-methylation on the two imidazole rings will result in a blue-shift of UV absorption. The photophysical properties can be adjusted by changing the substituents, which provides a new strategy for the design of diarylethenes with excellent properties.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
1474-9092
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
10
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
587-91
pubmed:meshHeading
pubmed:year
2011
pubmed:articleTitle
Synthesis and photochromic properties of imidazole-based diarylethenes.
pubmed:affiliation
College of Chemistry, Central China Normal University, Wuhan, HuBei, 430079, China.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't