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<strong>Con</strong> <strong>profondo</strong> <strong>dolore</strong> <strong>annunciamo</strong> <strong>la</strong> <strong>scomparsa</strong> <strong>del</strong> P rofessor <strong>Gian</strong><br />

P aolo Chiusoli, membro <strong>del</strong>l’Accademia Nazionale dei Lincei e<br />

P rofessore Emerito <strong>del</strong>l’Università di P arma, dove aveva ricoperto <strong>la</strong><br />

cattedra di Chimica Organica Industriale a partire dal 1975. I risultati<br />

<strong>del</strong><strong>la</strong> sua attività di ricerca sono punti di riferimento per <strong>la</strong> comunità<br />

scientifica internazionale e costituiscono vanto per <strong>la</strong> nostra comunità<br />

nazionale.<br />

Born Treviso (Italy), 7 June 1923<br />

<strong>Professor</strong>, Industrial Organic Chemistry, University of Parma, Viale <strong>del</strong>le Scienze, 43100 Parma.<br />

Tel.(521)905554, 905555; FAX (521)905472<br />

Working for almost three decades in Industry <strong>Gian</strong> Paolo Chiusoli has set up the first basic research in an<br />

Italian industrial chemical <strong>la</strong>boratory, the Donegani Research Institute at Novara. Here he discovered new<br />

selective catalytic syntheses based on multiple activation of simple molecules such as carbon monoxide,<br />

acetylene and carbon dioxide under mild conditions. He became Director of the Donegani Institute in<br />

1966. Next he moved to the University of Parma (1975), where with another group he found new<br />

vanguard techniques of chemistry, based on the use of metals in catalytic reaction sequences suitable for<br />

the selective formation and functionalization of organic molecules.<br />

During the industrial period he has set up basic research in Chemistry for the first time in an Italian<br />

research <strong>la</strong>boratory. He discovered new methods for the construction of complex organic molecules under<br />

the catalytic action of metal complexes in ordered sequences. He further extended the concept during the<br />

Academic period with the discovery of several new reactions based on pal<strong>la</strong>dium or rhodium catalysis.<br />

He is the author of more than 250 papers in international Journals and of 127 industrial patents.<br />

He received prizes for his research activity from Italian Chemical Society (1972), from Accademia dei<br />

Lincei (1984), from the Organometallic Division (1992), and from Federchimica (1997). In 1989 he<br />

received a medal from the Ministry of Education. In 1993 he was dedicated a special volume of the<br />

Journal of Organometallic Chemistry. He is or was a member of the Emeritus Editorial board of the<br />

Journal of Organometallic Chemistry, Transition Metal Chemistry, Gazzetta Chimica Italiana. Since 1989<br />

he is a member of the National Academy of Lincei Since 1999 he is Emeritus <strong>Professor</strong> of the University<br />

of Parma, where I continues to work.<br />

Main innovations<br />

· Nickel­catalyzed sequential insertion reactions: Gazz. Chim. Ital., 89, 1332 (1959);<br />

Angew.Chem., 72, 74(1960); Synthesis, 509 (1973); Acc. Chem. Res. 6, 422 (1973).<br />

· C­C coupling of allylnickel complexes: Tetrahedron Lett.,1591 (1963); Chim. Ind. (Mi<strong>la</strong>n), 43,<br />

365 (1961); Ang.Chem.Int.Ed.Engl., 17, 353 (1978).<br />

· Reformatski reaction with CO2: Chem. Ind. (London), 1457 (1966.)<br />

· Carboxy<strong>la</strong>tion of organic substrates with CO2 promoted by alkali phenoxides : Chem. Comm.,<br />

618 (1966); Gazz. Chim. Ital., 103, 105 (1973).<br />

· Cyclization of dienoic acids to phenols : Proc. Chem. Soc., 310 (1963).


· Oxidative carbony<strong>la</strong>tion of acetylene : Chem. Ind. (London), 977 (1968).<br />

· Coupling of acrylonitrile to adiponitrile on cobalt(0): Chem. Comm., 1515 (1968).<br />

· Asymmetric carbony<strong>la</strong>tion of styrene at room temperature and atmospheric pressure: J.<br />

Organomet. Chem., 236, C31 (1982)).<br />

· Che<strong>la</strong>tion­assisted reactions ­ Rearrangement of allyl 3­butenoate :J.C.S.Chem.Comm., 793<br />

(1977); J. Mol. Cat., 41, 75 (1987)); J. Chem. Soc. Perkin Trans. 1, 1347 (1994)).<br />

· Ary<strong>la</strong>tion via aroyl chlorides: Trans. Metal Chem., 4,398 (1979)).<br />

· Multiple insertions terminated by H (de<strong>la</strong>yed hydrogenolysis): J. Organomet. Chem., 199, C21<br />

(1980)).<br />

· Oxidative carbony<strong>la</strong>tion of styrene : J. Organomet. Chem., 181, C14 (1979).<br />

· Catalysis by pal<strong>la</strong>dium(0) of catalysis of diene addition to double bonds by rhodium(I): J. Chem.<br />

Soc. Chem. Comm.,1303 (1990)).<br />

· Metal<strong>la</strong>cycle­promoted reactions. Cobalt(0) metal<strong>la</strong>cycles as catalysts: J. Chem. Soc. Chem.<br />

Comm., 1632 (1990))<br />

· Metal<strong>la</strong>cycle­ promoted reactions. Aromatic and alifatic C­H activation (first paper: J. Organomet.<br />

Chem., 233, C21 (1982); Pure Appl. Chem., 62, 623 (1990)).<br />

· Pal<strong>la</strong>dium(IV) metal<strong>la</strong>cycles: J. Organomet. Chem., 346, C27 (1988); Gazz. Chim. Ital., 123, 1<br />

(1993)).<br />

· Synthesis of pyrrolediacetic acid by oxidative rbony<strong>la</strong>tion : Synthesis, 262 (1989).<br />

· Combination of pal<strong>la</strong>dium­catalyzed oxidative carbony<strong>la</strong>tion with reduction in a single process: J.<br />

Chem. Soc. Chem. Comm., 2429 (1994).<br />

· Carbony<strong>la</strong>tion of alkynes to beta­<strong>la</strong>ctones and <strong>la</strong>ctams: J. Chem. Soc. Chem. Comm., 1429<br />

(1994); Tetrahedron Lett. 36, 7495 (1995)).<br />

· Pal<strong>la</strong>dium­catalyzed multi­component reactions to form heterocyclic rings: J. Organomet. Chem.,<br />

371, C51 (1989); Tetrahedron Lett., 35, 5919,5923 (1994).<br />

· Direct incorporation of carbon dioxide into amines: J. Chem. Soc.Chem. Comm. 1669­1700<br />

(1999); J. Chem Soc Perkin Trans. 1541­1546 (1998).<br />

· Sequential reactions of carbon monoxide and carbon dioxide: Chem. Comm. 1381­1382 (1999);<br />

J. Mol. Cat. A Chemical 143, 297­310 (1999).<br />

· Catalytic carbon­carbon coupling through C­H activation: Coord. Chem. Rev. 254, 456­459<br />

(2010).<br />

The problem of Darwinian evolution in Chemistry has been examined recently: Rend. Fis. Acc. Lincei 20,<br />

199­209 (2009)<br />

Chiusoli also co­edited with Peter Maitlis a book on Metal­catalysis in Industrial Organic Processes<br />

published by RSC in 2006 and 2008

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