The fully lithiated form of 5,5,10,10,15,15,20,20-octaethylporphyrinogen (H-4L) synthesized in tetrahydrofuran (thf ) has been structurally characterized in its solvated form Li4L.3thf, while its unsolvated form from n-hexane behaves as a 'superbase' capable of decomposing thf to the lithium enolate identified in the aggregate Li6L(OCH=CH2)2.4thf.

Solvent-dependent Forms of Lithiated 5,5,10,10,15,15,20,20-Octaethylporphyrinogen in Solution and in the Solid State and Reaction with Tetrahydrofuran / S., De Angelis; E., Solari; C., Floriani; A., Chiesi Villa; Rizzoli, Corrado. - In: JOURNAL OF THE CHEMICAL SOCIETY DALTON TRANSACTIONS. - ISSN 0300-9246. - (1994), pp. 2467-2469. [10.1039/DT9940002467]

Solvent-dependent Forms of Lithiated 5,5,10,10,15,15,20,20-Octaethylporphyrinogen in Solution and in the Solid State and Reaction with Tetrahydrofuran

RIZZOLI, Corrado
1994-01-01

Abstract

The fully lithiated form of 5,5,10,10,15,15,20,20-octaethylporphyrinogen (H-4L) synthesized in tetrahydrofuran (thf ) has been structurally characterized in its solvated form Li4L.3thf, while its unsolvated form from n-hexane behaves as a 'superbase' capable of decomposing thf to the lithium enolate identified in the aggregate Li6L(OCH=CH2)2.4thf.
1994
Solvent-dependent Forms of Lithiated 5,5,10,10,15,15,20,20-Octaethylporphyrinogen in Solution and in the Solid State and Reaction with Tetrahydrofuran / S., De Angelis; E., Solari; C., Floriani; A., Chiesi Villa; Rizzoli, Corrado. - In: JOURNAL OF THE CHEMICAL SOCIETY DALTON TRANSACTIONS. - ISSN 0300-9246. - (1994), pp. 2467-2469. [10.1039/DT9940002467]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11381/2313734
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