The interaction of aliphatic amines with transition-metal complexes of aromatic di-imines. II: Concurrent nucleophilic attack at the central metal and co-ordinated ligand in the reaction between ethylenediamine and dichloro(5-nitro-1,10-phenanthroline)palladium(II) in dimethylformamide
- Author
- BARTOLOTTA, A1 ; CUSUMANO, M; GIANNETTO, A; RICEVUTO, V
[1] Dip. chimica inorganica struttura molecolare, Messina 98100, Italy - Source
Journal of the Chemical Society. Dalton transactions. 1984, Num 12, pp 2785-2787 ; ref : 10 ref
- CODEN
- JCDTBI
- ISSN
- 0300-9246
- Scientific domain
- Inorganic chemistry; Crystallography; Atomic molecular physics
- Publisher
- Royal Society of Chemistry, Cambridge
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Cinétique Complexe aniono Complexe chloro Composé tricyclique Coordinat organique Diamine Hétérocycle azote Mécanisme réaction Métal divalent Complexe Métal transition Complexe Palladium II Complexe Platinoïde Complexe Réaction chimique Solution organique Phénanthroline-1,10(nitro-5)
- Keyword (en)
- Kinetics Acido complex Chloro complex Tricyclic compound Organic ligand Diamine Nitrogen heterocycle Reaction mechanism Divalent metal Complexes Transition metal Complexes Palladium II Complexes Platinoid Complexes Chemical reaction Organic solution
- Keyword (es)
- Cinetica
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C02 Inorganic chemistry and origins of life / 001C02A Kinetics and mechanism of reactions
- Discipline
- Mineral chemistry and origin of life
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 8957968
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/dt9840002785 
https://dx.doi.org/10.1039/dt9840002785
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