Exploring Dinuclear Titanium Complexes in Titanium(III) Catalysis

被引:0
|
作者
Unkrig-Bau, Michael A. [1 ]
Leijendekker, Sara L. [1 ]
Streuff, Jan [2 ]
机构
[1] Albert Ludwigs Univ Freiburg, Inst Organ Chem, Albertstr 21, D-79104 Freiburg, Germany
[2] Uppsala Univ, Dept Chem, BMC, Husargatan 3, S-75237 Uppsala, Sweden
关键词
Catalysis; Metallocenes; Radicals; Reduction; Titanium; REDUCTIVE UMPOLUNG REACTIONS; ETHYLENE POLYMERIZATION; ACTIVE TITANOCENE; KINETIC-ANALYSIS; TI; BINUCLEAR; HYDROSILYLATION; HYDROGENATION; DICHLORIDE; ZIRCONIUM;
D O I
10.1002/cctc.202401337
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The synthesis of one achiral and two chiral propylene-bridged dititanocenes and their evaluation as catalysts in titanium(III) catalyzed ketone-nitrile coupling reactions are reported. A reaction progress kinetics analysis of the cross-coupling between acetophenone and benzyl cyanide reveals that, using a dinuclear titanocene catalyst, the order in catalyst is reduced from two to one in comparison to a mononuclear catalyst. Although the obtained coupling yields and enantioselectivities did not reach the results obtained with the latter, these examples constitute a proof of concept for the templated C & horbar;C coupling through coordination of ketone and nitrile to the two tethered titanium centers of a dinuclear catalyst. In this proof of principle study, the synthesis of one achiral and two chiral dinuclear titanocenes and their evaluation in the catalytic-reductive ketone-nitrile coupling are reported. A reduction in catalyst order compared to mononuclear titanocenes supports the catalyst-templated dual activation in the coupling transition state. image
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页数:10
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