EPR studies on the photofragmentation of 2,2-dialkyl-2-alkylamino-actophenones
- Author
- LEOPOLD, D; FISCHER, H
Univ. Zυ#79rich, Physikalisch-Chemisches Inst., 8057 Zυ#79rich, Switzerland - Source
Perkin transactions. 2. 1992, Num 4, pp 513-517 ; ref : 28 ref
- CODEN
- JCPKBH
- ISSN
- 0300-9580
- Scientific domain
- Organic chemistry; Atomic molecular physics
- Publisher
- Royal Society of Chemistry, Cambridge
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Amine tertiaire Composé aliphatique Composé benzénique Cycle 6 chaînons Cétone Effet solvant Effet substituant Etat triplet Hétérocycle oxygène azote Intermédiaire réaction Photolyse Radical libre organique Spectrométrie RPE Alcanophénone(2-alkyl-2-dialkylamino)
- Keyword (en)
- Tertiary amine Aliphatic compound Benzenic compound Six membered ring Ketone Solvent effect Substituent effect Triplet state Oxygen nitrogen heterocycle Reaction intermediate Photolysis Organic free radical EPR spectrometry
- Keyword (es)
- Amina terciaria Compuesto alifático Compuesto bencénico Ciclo 6 eslabones Cetona Efecto solvente Efecto sustituyente Estado triplete Heterociclo oxígeno nitrógeno Intermediario reacción Fotolisis Radical libre orgánico Espectrometría RPE
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C01 General and physical chemistry / 001C01F Physical chemistry of induced reactions (with radiations, particles and ultrasonics) / 001C01F01 Photochemistry
- Discipline
- General chemistry and physical chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 5364354
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1039/p29920000513 
https://dx.doi.org/10.1039/p29920000513
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