A Simple and Efficient Mechanochemical Route for the Synthesis of Salophen Ligands and of the Corresponding Zn, Ni, and Pd Complexes
Luca Leoni,
Andrea Carletta,
Luca Fusaro,
Jean Dubois,
Nikolay A. Tumanov,
Carmela Aprile,
Johan Wouters,
Antonella Dalla Cort
Affiliations
Luca Leoni
Università di Roma La Sapienza, Piazzale Aldo Moro 5, 00185 Roma, Italy
Andrea Carletta
Namur Institute of Structured Matter (NISM) and Namur Research Institute for Life Sciences (NARILIS), University of Namur, 61 rue de Bruxelles, B-5000 Namur, Belgium
Luca Fusaro
Namur Institute of Structured Matter (NISM) and Namur Research Institute for Life Sciences (NARILIS), University of Namur, 61 rue de Bruxelles, B-5000 Namur, Belgium
Jean Dubois
Namur Institute of Structured Matter (NISM) and Namur Research Institute for Life Sciences (NARILIS), University of Namur, 61 rue de Bruxelles, B-5000 Namur, Belgium
Nikolay A. Tumanov
Namur Institute of Structured Matter (NISM) and Namur Research Institute for Life Sciences (NARILIS), University of Namur, 61 rue de Bruxelles, B-5000 Namur, Belgium
Carmela Aprile
Namur Institute of Structured Matter (NISM) and Namur Research Institute for Life Sciences (NARILIS), University of Namur, 61 rue de Bruxelles, B-5000 Namur, Belgium
Johan Wouters
Namur Institute of Structured Matter (NISM) and Namur Research Institute for Life Sciences (NARILIS), University of Namur, 61 rue de Bruxelles, B-5000 Namur, Belgium
Antonella Dalla Cort
Università di Roma La Sapienza, Piazzale Aldo Moro 5, 00185 Roma, Italy
A number of salophen ligands and their Zn, Ni, and Pd complexes were synthesized by an efficient one-pot mechanosynthesis protocol. The reaction products were characterized by means of complementary solid-state techniques, i.e., powder X-ray diffraction, single-crystal X-ray diffraction, and solid-state NMR spectroscopy. Four new crystal structures of metal salophen complexes as DMSO solvates are here reported. The described simple and relatively fast (about 1 h for all derivatives) procedure is a good alternative to classical methods performed in organic solvents.