Prevalence of the external surface over the internal pores in the spontaneous generation of tetrathiafulvalene radical cation incorporated in the novel delaminated ITQ-2 zeolite

被引:14
作者
Corma, A
Fornés, V
Galletero, MS
Garcia, H
Gómez-García, CJ
机构
[1] Univ Politecn Valencia, CSIC, Inst Tecnol Quim, Valencia 46022, Spain
[2] Univ Valencia, Dept Quim Inorgan, Valencia, Spain
关键词
D O I
10.1039/b009304l
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
ITQ-2 is a novel delaminated zeolite whose crystalline sheets (2.5 nm depth) define a large external surface (similar to 720 g(-1)) having 12-membered ring (MR) open cups together with a reduced microporosity due to a 10 MR channel system. This feature is the reverse of that of classical zeolites (i.e., much larger internal area compared to the external surface). Herein, we have used tetrathiafulvalene and triphenylamine to probe the capability of layered ITQ-2 zeolite to generate persistent organic radical cations compared to conventional Y, mordenite and ZSM-5 zeolites as well as to Al/MCM-41 (3.2 nm diameter) and amorphous silica-alumina. By selective silylation of the external cups, it has been found that formation of a significant concentration of persistent organic radical cations in ITQ-2 is a property that occurs within the open cups of the external surface rather than inside the 10 MR pores.
引用
收藏
页码:1218 / 1222
页数:5
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