A test reaction to assess the presence of Bronsted and the softness/hardness of Lewis acid sites in palladium supported catalysts

被引:18
作者
Corma, A [1 ]
García, H [1 ]
Primo, A [1 ]
Domenech, A [1 ]
机构
[1] Univ Politecn Valencia, CSIC, Inst Tecnol Quim, Valencia 46022, Spain
关键词
D O I
10.1039/b311513e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cyclic ethylene acetal of alpha-bromopropiophenone gives rise to three distinctive products, each one being specific to Bronsted, hard Lewis and soft Lewis sites, respectively. In the presence of Bronsted sites, hydrolysis of cyclic acetal forms the corresponding alpha-bromophenone. Hard or soft Lewis sites promote selectively a rearrangement of the phenyl or ethylenedioxy group to form 2-phenylpropionate ester or dioxine, respectively. This test reaction has been used to assess the influence of the support on the catalytic activity of palladium in zeolites. Three series of supports including alkali-exchanged faujasite, Beta zeolites and sepiolites have been tested. It has been observed that the nature of the zeolite plays an important role on the palladium selectivity, basic supports increasing the softness of the palladium Lewis sites. The catalytic test correlates well with electrochemical data about the reduction potential of supported palladium, XPS characterization of the oxidation state of palladium supported on the surface and activity in the Suzuki reaction.
引用
收藏
页码:361 / 365
页数:5
相关论文
共 20 条
[11]   2,4,6-triphenylpyrylium ion encapsulated into zeolite Y as a selective electrode for the electrochemical determination of dopamine in the presence of ascorbic acid [J].
Doménech, A ;
García, H ;
Doménech-Carbó, MT ;
Galletero, MS .
ANALYTICAL CHEMISTRY, 2002, 74 (03) :562-569
[12]   Aryl-aryl bond formation one century after the discovery of the Ullmann reaction [J].
Hassan, J ;
Sévignon, M ;
Gozzi, C ;
Schulz, E ;
Lemaire, M .
CHEMICAL REVIEWS, 2002, 102 (05) :1359-1469
[13]   HETEROGENEOUS BASIC CATALYSIS [J].
HATTORI, H .
CHEMICAL REVIEWS, 1995, 95 (03) :537-558
[14]  
Heck R.F., 1985, PALLADIUM REAGENTS O
[15]  
Littke AF, 2002, ANGEW CHEM INT EDIT, V41, P4176, DOI 10.1002/1521-3773(20021115)41:22<4176::AID-ANIE4176>3.0.CO
[16]  
2-U
[17]   Palladium-catalysed reactions of aryl halides with soft, non-organometallic nucleophiles [J].
Prim, D ;
Campagne, JM ;
Joseph, D ;
Andrioletti, B .
TETRAHEDRON, 2002, 58 (11) :2041-2075
[18]   ELECTROCHEMICAL SOLID-STATE ANALYSIS - STATE-OF-THE-ART [J].
SCHOLZ, F ;
MEYER, B .
CHEMICAL SOCIETY REVIEWS, 1994, 23 (05) :341-347
[19]   COMPARISON OF ACID-BASE PROPERTIES OF FAU, EMT, LTL AND MOR (NA FORMS) IN BENZENE ADSORPTION AND ALKYLATION OF ANILINE WITH METHANOL [J].
SU, BL ;
BARTHOMEUF, D .
APPLIED CATALYSIS A-GENERAL, 1995, 124 (01) :81-90
[20]  
Tsuji J., 1995, PALLADIUM REAGENTS C