FIELD: fine organic and organometal synthesis. SUBSTANCE: toluene solution of C60 fullerene is reacted with excessive amount of ether solution of n-propylmagnesium bromide (n-PrMgBr) or n-propylmagnesium chloride (n-PrMgCl) at C60 to n-PrMgHal molar ratio of 1:(50-150), in the presence of zirconacene dichloride Cp2ZrCl2 as catalyst in amount of 1.3 mole % with respect to PrMgHal in argon atmosphere under normal conditions for 8-12 h. EFFECT: more efficient preparation method. 1 ex, 1 tbl
Title | Year | Author | Number |
---|---|---|---|
METHOD OF PREPARING 1-(N-PROPYL)-2-HYDRO[6] FULLERENES | 1998 |
|
RU2135446C1 |
METHOD OF SYNTHESIS OF 1-ARYL(ALKYL)-2-MAGNESIUM HALOGEN(60)- -FULLERENES | 1998 |
|
RU2135506C1 |
METHOD FOR JOINT PREPARATION OF MONO(CYCLOALKYL)DIMAGNESIUMBROMIDEFULLERENES(60) AND BIS(CYCLOALKYL)TETRAMAGNESIUMBROMID- EFULLERENES(60) | 1998 |
|
RU2136688C1 |
METHOD OF PREPARING 1-BUTYL-2-MAGNESIUMBUTYLFULLERENES(60) | 1998 |
|
RU2136687C1 |
METHOD OF SYNTHESIS OF 1-ETHYL-MAGNESIUM HALIDE (60)-FULLERENES | 1998 |
|
RU2135505C1 |
METHOD OF SYNTHESIS OF 1-ARYL-(ALKYL)-2-HYDRO[60]-FULLERENES | 1998 |
|
RU2135447C1 |
METHOD OF PREPARING N-BUTYL SUBSTITUTED C. FULLERENES | 1998 |
|
RU2134255C1 |
METHOD OF COMBINED PREPARATION OF MONO[CYCLOALKYL]DIHYDRO[60] FULLERENES AND BIS[CYCLOALKYL]TETRAHYDRO [60] FULLERENES | 1998 |
|
RU2136647C1 |
METHOD OF SYNTHESIS OF 1-ETHYL-2,3-FULLERENEALUMINOCYCLO- -PENTANES | 1997 |
|
RU2132332C1 |
METHOD OF SYNTHESIS OF ETHYLATED FULLERENES | 1997 |
|
RU2119449C1 |
Authors
Dates
1999-08-27—Published
1998-01-12—Filed