Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
11
pubmed:dateCreated
2006-3-16
pubmed:abstractText
Photoirradiation of the absorption band of the 10-methylacridinium ion (AcrH+) with visible light in deaerated CH3CN/H2O (1:1 v/v) containing pivalic acid (Bu(t)COOH) and less than 1 equiv of NaOH results in the selective formation of 9-tert-butyl-9,10-dihydro-10-methylacridine (AcrHBu(t)). The same product is obtained in O2-saturated CH3CN/H2O under visible light irradiation. Photoirradiation of the absorption band of AcrHBu(t) with UV light in deaerated CH3CN/H2O (1:1 v/v) results in the formation of tert-butyl hydroperoxide (Bu(t)OOH), accompanied by regeneration of AcrH+. This cycle can be repeated several times. When AcrH+ is replaced by the 9-phenyl derivative (AcrPh+), AcrPh+ acts as an effective photocatalyst for the one-pot photooxygenation of Bu(t)COOH in the presence of less than 1 equiv of NaOH relative to Bu(t)COOH with O2 to yield Bu(t)OOH and Bu(t)H. The photocatalytic oxygenation mechanism is discussed based on the detection of radical intermediates by laser flash photolysis and ESR measurements as well as quantum yield determination.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
1089-5639
pubmed:author
pubmed:issnType
Print
pubmed:day
23
pubmed:volume
110
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
3860-7
pubmed:meshHeading
pubmed:year
2006
pubmed:articleTitle
Photocatalytic oxygenation of pivalic acid with molecular oxygen via photoinduced electron transfer using 10-methylacridinium ions.
pubmed:affiliation
Department of Material and Life Science, Graduate School of Engineering, Osaka University, SORST, Japan Science and Technology Agency (JST), Suita, Osaka, 565-0871, Japan.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't