The crystal-structure analyses of the complexes [AlCl3(RNO2)] (R = Me or Ph) and NMR data in solution suggest a stronger Al-O co-ordinative interaction in the case of nitrobenzene compared to nitromethane; this could account for the dramatic solvent effects observed during certain electrophilic acylation processes involving AlCl3 as a promoter.

Dalton communications. Organic nitro compounds as ligands. A comparison between the ligand behaviour of MeNO2 and PhNO2 towards AlCl3 / Lanfranchi, M.; Pellinghelli, M. A.; Predieri, G.; Bigi, F.; Maggi, R.; Sartori, G.. - In: JOURNAL OF THE CHEMICAL SOCIETY DALTON TRANSACTIONS. - ISSN 0300-9246. - :9(1993), pp. 1463-1464. [10.1039/DT9930001463]

Dalton communications. Organic nitro compounds as ligands. A comparison between the ligand behaviour of MeNO2 and PhNO2 towards AlCl3

Lanfranchi M.;Pellinghelli M. A.;Predieri G.;Bigi F.;Maggi R.;Sartori G.
1993

Abstract

The crystal-structure analyses of the complexes [AlCl3(RNO2)] (R = Me or Ph) and NMR data in solution suggest a stronger Al-O co-ordinative interaction in the case of nitrobenzene compared to nitromethane; this could account for the dramatic solvent effects observed during certain electrophilic acylation processes involving AlCl3 as a promoter.
Dalton communications. Organic nitro compounds as ligands. A comparison between the ligand behaviour of MeNO2 and PhNO2 towards AlCl3 / Lanfranchi, M.; Pellinghelli, M. A.; Predieri, G.; Bigi, F.; Maggi, R.; Sartori, G.. - In: JOURNAL OF THE CHEMICAL SOCIETY DALTON TRANSACTIONS. - ISSN 0300-9246. - :9(1993), pp. 1463-1464. [10.1039/DT9930001463]
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/11381/2887150
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