Group 4 dimethylmetallocenes are catalyst precursors for the methylmetallocenium/borate catalyst systems for olefin polymerization, and they are usually prepared by methylation (with MeMgCl or MeLi) of the parent metallocene dichlorides. We describe here a simpler preparation of a series of bisindenyldimethylmetallocenes carried out by reacting the ð-ligand with a 2-fold excess of MeLi, and then MtCl4 (Mt Ti, Zr, Hf). This simple, one-pot method produces the dimethylated complexes in higher overall yield, and saves on reaction time and solvents. Ind2MtMe2 (1,Mt Ti; 2a,Mt Zr; 3,Mt Hf), (4,7-Me2Ind)2ZrMe2 (4), rac/meso-[C2H4(Ind)2]-ZrMe2 (5), meso-[C2H4(4,7-Me2Ind)2]ZrMe2 (m-6a), and meso-[C2H4(4,7-Me2Ind)2]HfMe2 (m-7a) have been prepared in 40 80% isolated yields. 2a reacts with 1 4 equiv of t-BuOH to give the mono-tert-butoxy derivative 2b, Ind2ZrMe(O-t-Bu), while reaction with 2 equiv of C6F5OH cleanly affords Ind2Zr(OC6F5)2 (2c). Analogously, in the presence of 2 equiv of t-BuOH, m-6a gives meso-[C2H4(4,7-Me2Ind)2]ZrMe(O-t-Bu) (m-6b) with replacement of the outward methyl group only, as established by NMR analysis; meso-[C2H4(4,7-Me2Ind)2]Zr(OC6F5)2 (m-6c) is obtained by reaction with 2 equiv of C6F5OH. The molecular structures of m-6a and m-6c are also described.

Group 4 dimethylmetallocenes: Improved synthesis and reactivity studies

GALLI, SIMONA;
2001

Abstract

Group 4 dimethylmetallocenes are catalyst precursors for the methylmetallocenium/borate catalyst systems for olefin polymerization, and they are usually prepared by methylation (with MeMgCl or MeLi) of the parent metallocene dichlorides. We describe here a simpler preparation of a series of bisindenyldimethylmetallocenes carried out by reacting the ð-ligand with a 2-fold excess of MeLi, and then MtCl4 (Mt Ti, Zr, Hf). This simple, one-pot method produces the dimethylated complexes in higher overall yield, and saves on reaction time and solvents. Ind2MtMe2 (1,Mt Ti; 2a,Mt Zr; 3,Mt Hf), (4,7-Me2Ind)2ZrMe2 (4), rac/meso-[C2H4(Ind)2]-ZrMe2 (5), meso-[C2H4(4,7-Me2Ind)2]ZrMe2 (m-6a), and meso-[C2H4(4,7-Me2Ind)2]HfMe2 (m-7a) have been prepared in 40 80% isolated yields. 2a reacts with 1 4 equiv of t-BuOH to give the mono-tert-butoxy derivative 2b, Ind2ZrMe(O-t-Bu), while reaction with 2 equiv of C6F5OH cleanly affords Ind2Zr(OC6F5)2 (2c). Analogously, in the presence of 2 equiv of t-BuOH, m-6a gives meso-[C2H4(4,7-Me2Ind)2]ZrMe(O-t-Bu) (m-6b) with replacement of the outward methyl group only, as established by NMR analysis; meso-[C2H4(4,7-Me2Ind)2]Zr(OC6F5)2 (m-6c) is obtained by reaction with 2 equiv of C6F5OH. The molecular structures of m-6a and m-6c are also described.
Balboni, Davide; Camurati, Isabella; Prini, Giansiro; Resconi, Luigi; Galli, Simona; Mercandelli, Pierluigi; Sironi, Angelo
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/11383/7242
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