Abstract: The present invention provides a resin for toner binders, which comprises two polyester resins (A) and (B), said resin (A) being a crosslinked modified polyester resin consisting of the reaction product from a crosslinked polyester resin (a) and a polyepoxide (c) and said resin (B) being an acid anhydride-modified linear polyester resin consisting of the reaction product from a linear polyester resin (b) and an acid anhydride (r).

Abstract: The present invention provides a toner binder for developing electrostatic charge images, which binder comprises a polycondensate polyester resin, said polyester resin being a product formed in the presence of at least one titanium-containing catalyst (A) selected from the group consisting of a titanium halides (A1), a titanium diketone enolate (A2), a titanium carboxylate (A3), a titanyl carboxylate (A4), and a titanyl carboxylate salt (A5). Furthermore, the present invention provides a toner binder for developing electrostatic charge images, which binder comprises a polycondensate polyester resin, said polyester resin being a product formed in the presence of at least one tin-containing catalyst (B) selected from the group consisting of dioctyltin oxide (B1), monobutyltin oxide (B2), and dibutyltin oxide (B3), with the content of tributyltin compounds in (B3) being not more than 250 ppm.

Abstract: The present invention provides a resin for toner binders, which comprises two polyester resins (A) and (B), said resin (A) being a crosslinked modified polyester resin consisting of the reaction product from a crosslinked polyester resin (a) and a polyepoxide (c) and said resin (B) being an acid anhydride-modified linear polyester resin consisting of the reaction product from a linear polyester resin (b) and an acid anhydride (r).

Abstract: The present invention provides a toner binder for developing electrostatic charge images,

Abstract: Optically active compounds having the following formulae (1), (2) or (3) ##STR1## wherein R and R' are C.sub.1-20 alkyl groups; X and Y.sub.1 are --, O, S, or divalent groups such as COO, OOC and OCOO; m is 0 or 1; n is 0 to 5; A.sub.2 is a cyclic group, such as p,p'-biphenylene, 2,6-naphthylene, 2,5-pyrimidinylene-1,4-phenylene, A.sub.1 --Y.sub.2 -pyridylene or A.sub.4 --Y.sub.2 --A.sub.5 ; Y.sub.2 is CH.sub.2 CH.sub.2 or C.tbd.C; A.sub.3 is 2,6-naphthylene, A.sub.1 --Y.sub.2 -pyridylene or A.sub.6 --CH.sub.2 CH.sub.2 --A.sub.7 ; and A.sub.1, A.sub.4, A.sub.5, A.sub.6 and A.sub.7 are cyclic groups, such as 1,4-phenylene and/or 4,4'-biphenylene.

Abstract: Optically active compounds having the following formulae (1), (2) or (3) ##STR1## wherein R and R' are C.sub.1-20 alkyl groups; X and Y.sub.1 are --, O, S, or divalent groups such as COO, OOC and OCOO; m is 0 or 1; n is 0 to 5; A.sub.2 is a cyclic group, such as p,p'-biphenylene, 2,6-naphthylene, 2,5-pyrimidinylene-1,4-phenylene, A.sub.1 -Y.sub.2 -pyridylene or A.sub.4 -Y.sub.2 -A.sub.5 ; Y.sub.2 is CH.sub.2 CH.sub.2 or C.tbd.C; A.sub.3 is 2,6-naphthylene, A.sub.1 -Y.sub.2 -pyridylene or A.sub.6 -CH.sub.2 CH.sub.2 -A.sub.7 ; and A.sub.1, A.sub.4, A.sub.5, A.sub.6 and A.sub.7 are cyclic groups, such as 1,4-phenylene and/or 4,4'-biphenylene.

Abstract: Liquid Crystal compounds represented by the following formula are disclosed. ##STR1## wherein R and R' are independently selected from alkyl groups containing 1.about.20 carbon atoms; X is --O--, --O--CO--O-- or direct bond; A.sub.1 and A.sub.2 are independently cyclic groups (such as phenylene and biphenylene), said cyclic groups may be substituted with 1.about.4 fluorine, chlorine or bromine atoms, or 1 or 2 substituent groups selected from the group consisting of cyano, nitro and trifluoromethyl groups; Y is --CO--O--, --O--CO--, --C.tbd.C--, --CH.sub.2 O--, --OCH.sub.2 --, --CH.dbd.N--, --N.dbd.CH--, --N.dbd.N--, --CH.sub.2 S--, --SCH.sub.2 -- or direct bond; and * represents asymmetric atom providing optical activity.