STRUCTURE AND ELECTRONIC STATE OF MOLYBDENUM SUBCARBONYL SPECIES ENCAGED IN ZEOLITE

被引:43
作者
OKAMOTO, Y [1 ]
IMANAKA, T [1 ]
ASAKURA, K [1 ]
IWASAWA, Y [1 ]
机构
[1] UNIV TOKYO,FAC SCI,DEPT CHEM,BUNKYO KU,TOKYO 113,JAPAN
关键词
D O I
10.1021/j100162a049
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The structure and electronic state of molybdenum subcarbonyl species anchored in alkali-metal cation exchanged zeolites were elucidated by means of EXAFS, IR, and XPS analyses. The subcarbonyl species were produced at 373 K by evacuating Mo(CO)6 entrapped in the zeolite. The structure of the Mo-subcarbonyl species was found to be monomeric Mo(CO)3(OZ)3 with a fac configuration (OZ: zeolite framework oxygen). The Mo-C bond distance is very short (0.186-0.189 nm), suggesting strong d --> pi* back donations from the Mo atom to the CO ligands. The electron density of Mo in Mo(CO)3(OZ)3 increases with increasing basic strength of OZ in the order HY approximately LiY < NaY approximately CsY.
引用
收藏
页码:3700 / 3705
页数:6
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