Hexairidium clusters supported on gamma-Al2O3: Synthesis, structure, and catalytic activity for toluene hydrogenation

被引:46
作者
Zhao, A [1 ]
Gates, BC [1 ]
机构
[1] UNIV CALIF DAVIS, DEPT CHEM ENGN & MAT SCI, DAVIS, CA 95616 USA
关键词
D O I
10.1021/ja952996x
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
[Ir(CO)(15)](2-) was formed by surface-mediated synthesis on gamma-Al2O3 powder by treatment of adsorbed [Ir(CO)(2)(acac)] in CO at 100 degrees C and 1 atm. The supported clusters were characterized by infrared and extended X-ray absorption fine structure (EXAFS) spectroscopies and by extraction into solution by cation metathesis. Treatment of gamma-Al2O3-supported [Ir-6(CO)(15)](2-) in He at 300 degrees C led to decarbonylation without disruption of the cluster frame, giving Ir-6/gamma-Al2O3, as indicated by EXAFS data determining a first-shell Ir-Ir coordination number of 4.05 +/- 0.07 (where the error bounds represent precision, not accuracy), matching that of the supported [Ir-6(CO)(15)](2-), With a first-shell Ir-Ir coordination number of 4.07 +/- 0.03. The supported Ir-6 clusters were found to be catalytically active for toluene hydrogenation at temperatures in the range of 60-100 degrees C; the turnover frequency at 60 degrees C with a toluene partial pressure of 50 Torr and a H-2 partial pressure of 710 Torr was 1.7 x 10(-3) s(-1). The catalyst was stable in operation in a flow reactor, and consistent with this observation, EXAFS results for the used catalyst indicated that the nuclearity of the supported Ir-6 clusters was essentially unchanged during catalysis. The gamma-Al2O3-supported Ir-6 catalyst is an order of magnitude less active (per total Ir atom) for toluene hydrogenation than a catalyst consisting of small aggregates of iridium (with an average of about 50 atoms each) supported on gamma-Al2O3. Because toluene hydrogenation is known to be a structure-insensitive catalytic reaction, the data suggest that the concept of structure insensitivity in catalysis does not extend to clusters as small as Ir-6. However, the relatively low activity of the Ir-6 clusters may be more an indication of an effect of the support as a ligand changing the electronic properties of the iridium in the cluster than an effect of the cluster size.
引用
收藏
页码:2458 / 2469
页数:12
相关论文
共 63 条
  • [1] SOLID-STATE METAL-CARBONYLS .5. TETRAIRIDIUM DODECACARBONYL
    ADAMS, DM
    TAYLOR, ID
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS II, 1982, 78 : 1573 - 1579
  • [2] Anderson J.R., 1975, Structure of metallic catalysts
  • [3] REACTION OF IR4(CO)12 WITH BASES
    ANGOLETTA, M
    MALATESTA, L
    CAGLIO, G
    [J]. JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1975, 94 (01) : 99 - 106
  • [4] [Anonymous], XRAY ABSORPTION PRIN
  • [5] HETEROGENEOUS CATALYSIS BY METALS
    BOUDART, M
    [J]. JOURNAL OF MOLECULAR CATALYSIS, 1985, 30 (1-2): : 27 - 38
  • [6] CATALYTIC-HYDROGENATION OF CYCLOHEXENE - LIQUID-PHASE REACTION ON RHODIUM
    BOUDART, M
    SAJKOWSKI, DJ
    [J]. FARADAY DISCUSSIONS, 1991, 92 : 57 - 67
  • [7] Boudart M., 2014, KINETICS HETEROGENEO
  • [8] Boudart M., 1969, ADV CATAL, V20, P153, DOI DOI 10.1016/S0360-0564(08)60271-0
  • [9] CHANG JR, 1991, J PHYS CHEM-US, V95, P9945
  • [10] NEW TETRAHEDRAL CLUSTER COMPOUNDS OF IRIDIUM - SYNTHESIS OF ANIONS [IR4(CO)11X]- (X=CL,BR,I,CN,SCN) AND X-RAY STRUCTURE OF [PPH4] [IR4(CO)11BR]
    CHINI, P
    CIANI, G
    GARLASCHELLI, L
    MANASSERO, M
    MARTINENGO, S
    SIRONI, A
    CANZIANI, F
    [J]. JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1978, 152 (02) : C35 - C38