Cationic cyclopalladated complexes: new catalyst precursors for the telomerization of butadiene with alcohols
Cationic cyclopalladated complexes: new catalyst precursors for the telomerization of butadiene with alcohols
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DOI:
10.1016/1381-1169(96)00024-6
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发表时间:
1996-06
影响因子:
--
通讯作者:
M. Camargo;P. Dani;J. Dupont;R. F. Souza;M. Pfeffer;I. Tkatchenko
中科院分区:
文献类型:
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作者:
M. Camargo;P. Dani;J. Dupont;R. F. Souza;M. Pfeffer;I. Tkatchenko
The cationic cyclopalladated complexes derived from N,N-dimethylbenzylamine 4, N-benzylidene-(S)-(−)-α-methylbenzylamine 5 and 8-methyl quinoline 6 have been prepared and their properties as catalyst precursors for the telomerization of butadiene with methanol were investigated. The butadiene conversion was 60–70% for the three complexes and a mixture of butadiene dimers and telomers containing 2, 4 and 6 butadiene units were formed. The product selectivity is strongly influenced by the nature of the cyclopalladated complex. Thus, with complex 6 the C16 and C24 telomers were formed preferentially (more than 85%). On the other hand, with complex 4 the amount of butadiene dimers is greater than 40%. Complex 6 is also active for the telomerization of other aliphatic alcohols, but in these cases the 1- and 3-alkoxy octadiene telomers were produced preferentially.