A method of preparing a compound of formula (I): ##STR00001##
is disclosed. The compound of formula (I) can be used as an antioxidant agent. The compound can also be used as an antibacterial agent to inhibit Staphylococcus aureus MRSA 18-222 and Pseudomonas aeruginosa MDR-PA 18-1774.

A method of preparing a compound of formula (I): ##STR00001##
is disclosed. The compound of formula (I) can be used as an antioxidant agent. The compound can also be used as an antibacterial agent to inhibit Staphylococcus aureus MRSA 18-222 and Pseudomonas aeruginosa MDR-PA 18-1774.

[6,6]-Phenyl C.sub.71 butyric acid derivatives (C.sub.70-PCBR.sub.3) having a selectivity of greater than 95 wt % of the α-isomer are provided by reacting fullerene C.sub.70 with a dialkyl sulfonium tetrafluoroborate having the formula:

##STR00001##

[6,6]-Phenyl C.sub.71 butyric acid derivatives (C.sub.70-PCBR.sub.3) having a selectivity of greater than 95 wt % of the α-isomer are provided by reacting fullerene C.sub.70 with a dialkyl sulfonium tetrafluoroborate having the formula:

##STR00001##

[6,6]-Phenyl C.sub.71 butyric acid derivatives (C.sub.70-PCBR.sub.3) having a selectivity of greater than 95 wt % of the α-isomer are provided by reacting fullerene C.sub.70 with a dialkyl sulfonium tetrafluoroborate having the formula:

##STR00001##

Novel Styryl Carboxylate derivatives are provided which exhibit activity for the treatment of immunological diseases, inflammation, obesity, hyperlipidemia, hypertension, neurological diseases, and diabetes.

Novel Styryl Carboxylate derivatives are provided which exhibit activity for the treatment of immunological diseases, inflammation, obesity, hyperlipidemia, hypertension, neurological diseases, and diabetes.

It is an objective of the present invention to provide a novel polymerizable triptycene derivative and a polymer compound as constituent component thereof that has a structure in which three benzene rings arranged at the axis formed by barrelene of the triptycene skeleton can rotate evenly and that has hydrophilicity imparted to it as compared to any of the prior art triptycene derivatives and is thus highly useful in functional materials. The above objective is achieved by the polymerizable triptycene derivative and a polymer compound as constituent component thereof having substituents with an unsaturated bonding functional group at position 9 and/or position 10 of the triptycene skeleton, the polymerizable triptycene derivative having two carboxyl groups and the polymerizable triptycene derivative having one carboxyl group and one amino group.

Provided is a solid catalyst component for olefin polymerization comprising an electron-donating compound other than a phthalate, the solid catalyst component being equal in the olefin-polymerizing activity and in the primary physical properties of the resulting polymer such as stereoregularity and molecular weight distribution to those with use of a phthalate as an electron-donating compound. A solid catalyst component for olefin polymerization comprises a magnesium atom, a titanium atom, a halogen atom, an ester compound (A) represented by a general formula (1) and a diester compound (B) represented by a general formula (2), wherein a ratio represented by the following expression:
(content (mass %) of ester compound (A)/content (mass %) of diester compound (B))
is 0.05 to 50.

Provided is a solid catalyst component for olefin polymerization comprising an electron-donating compound other than a phthalate, the solid catalyst component being equal in the olefin-polymerizing activity and in the primary physical properties of the resulting polymer such as stereoregularity and molecular weight distribution to those with use of a phthalate as an electron-donating compound. A solid catalyst component for olefin polymerization comprises a magnesium atom, a titanium atom, a halogen atom, an ester compound (A) represented by a general formula (1) and a diester compound (B) represented by a general formula (2), wherein a ratio represented by the following expression:
(content (mass %) of ester compound (A)/content (mass %) of diester compound (B))
is 0.05 to 50.