RETAINED PRODUCT FROM REACTION OF 1-HEXENE ON SAPO-34 - FORMATION OF ADAMANTANES

被引:10
作者
ANDERSON, JR [1 ]
CHANG, YF [1 ]
WESTERN, RJ [1 ]
机构
[1] CSIRO,DIV MAT SCI & TECHNOL,CLAYTON,VIC 3168,AUSTRALIA
关键词
D O I
10.1016/0021-9517(90)90121-Y
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
Treatment of the microporous silico-alumino-phosphate SAPO-34 (similar in structure to chabazite) with 1-hexene at 513 K generates retained reaction product in which adamantanes (adamantane, 1-methyl, dimethyl, ethyl derivatives) are major constituents, together with cyclopentadienes, alkanes, and some alkylbenzenes. No adamantanes could be detected in the evolved gaseous products. Adamantanes are maximized at intermediate treatment times (4-28 h), while products related to naphthalene and anthracene/phenanthrene become important at very long times or higher temperatures. Evidence suggests that adamantanes are formed by acid-catalyzed reactions passing from cyclopentadienes (CPDs) via CPDs-dimer and tetrahydro-CPDs-dimer, while products in the naphthalene and anthracene/phenanthrene systems are produced by alternative acid-catalyzed pathways from CPDs and CPDs-dimer. Evidence shows that adamantanes are formed within the SAPO-34 cages, which appear to be uniquely active for this reaction for reasons possibly related to size/shape coincidence between host cage and transition state guest (analogous, it is suggested, to enzyme-substrate (transition state) complementarity in enzyme chemiStry). © 1990.
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页码:259 / 267
页数:9
相关论文
共 33 条
[31]   SEPARATION AND IDENTIFICATION OF BRIDGEHEAD-SUBSTITUTED METHYL AND ETHYL ADAMANTANES [J].
WARREN, RW ;
SCHNEIDE.A ;
JANOSKI, EJ .
APPLIED SPECTROSCOPY, 1968, 22 (02) :115-&
[32]   TRICYCLO[4.4.0.03,8]DECANE TO ADAMANTANE REARRANGEMENT [J].
WHITLOCK, HW ;
SIEFKEN, MW .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1968, 90 (18) :4929-+
[33]  
1973, ORG SYNTH, V5, P16