Synthesis and catalytic activity of Mo(II) complexes of α-diimines intercalated in layered double hydroxides

被引:11
作者
Marreiros, Joao [1 ]
Diaz-Couce, Maria [1 ]
Ferreira, Maria Joao [2 ,3 ]
Vaz, Pedro D. [4 ,5 ]
Calhorda, Maria Jose [1 ,6 ]
Nunes, Carla D. [1 ,2 ,3 ]
机构
[1] Univ Lisbon, Fac Ciencias, Ctr Quim & Bioquim, P-1749016 Lisbon, Portugal
[2] Univ Lisbon, Fac Ciencias, Ctr Quim Estrutural, P-1049001 Lisbon, Portugal
[3] Univ Lisbon, Inst Super Tecn, P-1049001 Lisbon, Portugal
[4] Rutherford Appleton Lab, ISIS Neutron & Muon Source, Didcot OX11 0QX, Oxon, England
[5] Univ Aveiro, Dept Chem, CICECO Aveiro Inst Mat, P-3810193 Aveiro, Portugal
[6] Univ Lisbon, Fac Ciencias, Dept Quim & Bioquim, BioISI Biosyst & Integrat Sci Inst, P-1749016 Lisbon, Portugal
关键词
Catalysis; Molybdenum; BIAN; Epoxidation; Layered double hydroxides; ELECTROSTATIC INTERACTIONS; EPOXIDATION CATALYSTS; AMINO-ACIDS; IMMOBILIZATION; MOLYBDENUM; PRECURSORS; EXCHANGE; BEHAVIOR; ANIONS;
D O I
10.1016/j.ica.2018.10.062
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The two layered double hydroxides ZnAl-LDH and MgAl-LDH were functionalized with bis(4-HOOC-phenyl)acenaphthenequinonediimine) (H(2)BIAN), leading to the intercalation of its dianion, which in a second step reacted with [Mo(CO)(3)X-2(NCMe)(2)] (X = I, Br), affording four new materials. These materials and the two complexes [Mo(CO)(3)X-2 (H(2)BIAN)(2)] (X = I, Br) were tested in the olefin epoxidation reaction with substrates cis-cyclooctene, styrene, 1-octene, trans-hex-3-en-1-ol, and R-(+)-limonene, using tert-butylhydroperoxide (tbhp) as oxidant. The new catalysts were particularly good for cis-cyclooctene and styrene (100% conversions) and at least one heterogeneous catalyst was comparable to the homogeneous ones in the epoxidation of 1-octene and trans-hex-3-en-1-ol. The homogeneous catalysts were the best to oxidize R-(+ )-limonene (higher conversions).
引用
收藏
页码:274 / 282
页数:9
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