Solvent-assisted proton transfer in catalysis by zeolite solid acids

被引:107
作者
Haw, JF [1 ]
Xu, T [1 ]
Nicholas, JB [1 ]
Goguen, PW [1 ]
机构
[1] PACIFIC NW NATL LAB, ENVIRONM MOL SCI LAB, RICHLAND, WA 99352 USA
关键词
D O I
10.1038/39843
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Intermolecular proton transfer in the gas phase is usually strongly disfavoured because the charged products are highly unstable. It is promoted in aqueous solution, however, because the high dielectric constant (epsilon = 78.3) of water allows efficient stabilization of the corresponding cations and anions. Zeolites-microporous catalysts used in petroleum refining and the synthesis of chemical feedstocks-provide another medium for proton-transfer reactions(1-3), because their anionic aluminosilicate frameworks are highly acidic. The low dielectric constant of zeolites (epsilon approximate to 1.6; ref. 3) suggests, however, that such processes in the zeolite channels should involve concerted action rather than strong charge separation, and thus resemble gas-phase reactions. Here we demonstrate that solution-like proton-transfer behaviour can be induced in zeolites. We find that the co-injection of nitromethane into a catalytic flow reactor clearly enhances the conversion of methanol, isopropanol and acetone over the zeolite catalyst HZSM-5. Conservation of nitromethane during-the course of reaction and its effects on the reactant-zeolite interaction complex seen by solid-state NMR indicate that nitromethane behaves in a manner similar to polar solvents: it promotes proton transfer by stabilizing ion-pair structures. These findings suggest that rationally selected solvents might provide a simple means to increase the efficiency of these industrially important catalysts.
引用
收藏
页码:832 / 835
页数:4
相关论文
共 23 条
  • [1] ANDZELM J, 1991, DENSITY FUNCTIONAL METHODS IN CHEMISTRY, P155
  • [2] Theoretical study of C-C bond formation in the methanol-to-gasoline process
    Blaszkowski, SR
    vanSanten, RA
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (21) : 5020 - 5027
  • [3] Breitmaier E., 1979, ATLAS CARBON 13 NMR
  • [4] HYDROCARBONS FROM METHANOL
    CHANG, CD
    [J]. CATALYSIS REVIEWS-SCIENCE AND ENGINEERING, 1983, 25 (01): : 1 - 118
  • [5] Cl L., 2023, GAUSSIAN94, V14, DOI [10.3389/fimmu, DOI 10.3389/FIMMU]
  • [6] LOW-BARRIER HYDROGEN-BONDS AND ENZYMATIC CATALYSIS
    CLELAND, WW
    KREEVOY, MM
    [J]. SCIENCE, 1994, 264 (5167) : 1887 - 1890
  • [7] Gates B. C, 1992, CATALYTIC CHEM
  • [8] OPTIMIZATION OF GAUSSIAN-TYPE BASIS-SETS FOR LOCAL SPIN-DENSITY FUNCTIONAL CALCULATIONS .1. BORON THROUGH NEON, OPTIMIZATION TECHNIQUE AND VALIDATION
    GODBOUT, N
    SALAHUB, DR
    ANDZELM, J
    WIMMER, E
    [J]. CANADIAN JOURNAL OF CHEMISTRY, 1992, 70 (02) : 560 - 571
  • [9] Physical organic chemistry of solid acids: Lessons from in situ NMR and theoretical chemistry
    Haw, JF
    Nicholas, JB
    Xu, T
    Beck, LW
    Ferguson, DB
    [J]. ACCOUNTS OF CHEMICAL RESEARCH, 1996, 29 (06) : 259 - 267
  • [10] Hibbert F., 1990, ADV PHYS ORG CHEM, V26, P255, DOI DOI 10.1016/S0065-3160(08)60047-7