1,3,5,7-Tetramethyl-2,6,9-trioxo-bicyclo[3.3.1]nona-3,7-diene, a dimer of acetylacetone which is formed as a coordinated species through a Pt(II) promoted {A figure is presented} condensation, can be displaced from the complex by sodium cyanide treatment. This new compound forms stable chelate π-complexes with Pd(II) and Rh(I) and has been resolved into optical isomers by fractional crystallization of a diastereoisomeric Rh(I) complex. © 1977.

Isolation, characterization and resolution of 1,3,5,7-tetramethyl-2,6,9-trioxo-bicyclo[3.3.1]nona-3,7-diene / de Renzi, A.; Panunzi, A.; Paolillo, L.; Vitagliano, Aldo. - In: JOURNAL OF ORGANOMETALLIC CHEMISTRY. - ISSN 0022-328X. - STAMPA. - 124:(1977), pp. 221-228.

Isolation, characterization and resolution of 1,3,5,7-tetramethyl-2,6,9-trioxo-bicyclo[3.3.1]nona-3,7-diene

VITAGLIANO, ALDO
1977

Abstract

1,3,5,7-Tetramethyl-2,6,9-trioxo-bicyclo[3.3.1]nona-3,7-diene, a dimer of acetylacetone which is formed as a coordinated species through a Pt(II) promoted {A figure is presented} condensation, can be displaced from the complex by sodium cyanide treatment. This new compound forms stable chelate π-complexes with Pd(II) and Rh(I) and has been resolved into optical isomers by fractional crystallization of a diastereoisomeric Rh(I) complex. © 1977.
1977
Isolation, characterization and resolution of 1,3,5,7-tetramethyl-2,6,9-trioxo-bicyclo[3.3.1]nona-3,7-diene / de Renzi, A.; Panunzi, A.; Paolillo, L.; Vitagliano, Aldo. - In: JOURNAL OF ORGANOMETALLIC CHEMISTRY. - ISSN 0022-328X. - STAMPA. - 124:(1977), pp. 221-228.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/489500
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