Uniform catalytic site in Sn-β-zeolite determined using X-ray absorption fine structure

被引:131
作者
Bare, SR [1 ]
Kelly, SD
Sinkler, W
Low, JJ
Modica, FS
Valencia, S
Corma, A
Nemeth, LT
机构
[1] UOP LLC, Des Plaines, IL 60016 USA
[2] EXAFS Anal, Bolingbrook, IL 60440 USA
[3] Univ Politecn Valencia, CSIC, Inst Tecnol Quim, Valencia 46022, Spain
关键词
D O I
10.1021/ja052543k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The Sri silicate zeolite, Sn-beta, has been shown to be an efficient, selective heterogeneous catalyst for Baeyer-Villiger oxidations. Using primarily a multishell fit to extended X-ray absorption fine structure (EXAFS) data, we show that the Sri does not randomly insert into the beta-zeolite structure but rather occupies identical, specific, crystallographic sites. These sites are the T5/T6 sites in the six-membered rings. Moreover, the Sri is substituted in pairs on opposite sides of these six-membered rings. We believe that it is the specific, uniform crystallographic location of the Sri in the beta crystal structure that leads to sites with uniform catalytic activity, and consequently to the high chemical selectivity demonstrated for this catalyst. This manifests itself in the almost enzyme-like selectivity of this catalyst in Baeyer-Villiger oxidations. This uniform site distribution of the Sn suggests that there is likely a symbiotic relationship between the structure directing agent in the zeolite synthesis and the Sri heteroatoms during the framework formation.
引用
收藏
页码:12924 / 12932
页数:9
相关论文
共 44 条
[1]   Neutron powder diffraction study of orthorhombic and monoclinic defective silicalite [J].
Artioli, G ;
Lamberti, C ;
Marra, GL .
ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE, 2000, 56 (01) :2-10
[2]  
BARE SR, UNPUB REV SCI INSTRU
[3]  
Brunner G. O., 1971, WISS Z TU DRESDEN, V20, P387
[4]   GROUND-STATE OF THE ELECTRON-GAS BY A STOCHASTIC METHOD [J].
CEPERLEY, DM ;
ALDER, BJ .
PHYSICAL REVIEW LETTERS, 1980, 45 (07) :566-569
[5]   Sn-zeolite beta as a heterogeneous chemoselective catalyst for Baeyer-Villiger oxidations [J].
Corma, A ;
Nemeth, LT ;
Renz, M ;
Valencia, S .
NATURE, 2001, 412 (6845) :423-425
[6]  
CORMA A, 2002, Patent No. 6344583
[7]  
GAGNON R, 1994, J CHEM SOC P1, V18, P2537
[8]  
HANDRECK GP, 1989, J CHEM SOC FARAD T 1, V85, P3195
[9]   Structural investigation of TS-1: Determination of the true nonrandom titanium framework substitution and silicon vacancy distribution from powder neutron diffraction studies using isotopes [J].
Henry, PF ;
Weller, MT ;
Wilson, CC .
JOURNAL OF PHYSICAL CHEMISTRY B, 2001, 105 (31) :7452-7458
[10]   The siting of Ti in TS-1 is non-random. Powder neutron diffraction studies and theoretical calculations of TS-1 and FeS-1 [J].
Hijar, CA ;
Jacubinas, RM ;
Eckert, J ;
Henson, NJ ;
Hay, PJ ;
Ott, KC .
JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (51) :12157-12164