In one embodiment, the present application discloses a photo-cleavable surface binding compound of the Formula I and Formula II:

##STR00001##

wherein the variables EG, EG1, SP1, SP2, SP3, Ar and BG are as defined herein. In another embodiment, the application discloses a method for forming a coating on a surface of a substrate using the surface binding compound.

The invention relates to a material for use as construction material for energy-pulse-induced transfer printing, which contains (a) at least one polymerizable binder, (b) at least one volume expansion component, (c) at least one initiator for the polymerization and (d) preferably at least one energy transformation component. The invention furthermore relates to a process for producing three-dimensional objects using the material.

The invention relates to a material for use as construction material for energy-pulse-induced transfer printing, which contains (a) at least one polymerizable binder, (b) at least one volume expansion component, (c) at least one initiator for the polymerization and (d) preferably at least one energy transformation component. The invention furthermore relates to a process for producing three-dimensional objects using the material.

To provide one liquid type dental adhesive composition that exhibits excellent adhesive property to glass ceramics, oxide-base ceramics and tooth substance, and has excellent storage stability, which are contrary features. One liquid type dental adhesive composition contains (a) silane coupling agent represented by general formula (1), (b) acidic group-containing polymerizable monomer, (c) volatile organic solvent, and (d) water. ##STR00001##
(In the formula, R.sup.1 represents an organic group having at least one functional group selected from the group consisting of a (meth)acryloyl group, a vinyl group and an epoxy group, R.sup.2 represents C4-C8 linear alkyl group, R.sup.3 represents C1-C8 alkyl group, and n is integer selected from 1 to 3.)

To provide one liquid type dental adhesive composition that exhibits excellent adhesive property to glass ceramics, oxide-base ceramics and tooth substance, and has excellent storage stability, which are contrary features. One liquid type dental adhesive composition contains (a) silane coupling agent represented by general formula (1), (b) acidic group-containing polymerizable monomer, (c) volatile organic solvent, and (d) water. ##STR00001##
(In the formula, R.sup.1 represents an organic group having at least one functional group selected from the group consisting of a (meth)acryloyl group, a vinyl group and an epoxy group, R.sup.2 represents C4-C8 linear alkyl group, R.sup.3 represents C1-C8 alkyl group, and n is integer selected from 1 to 3.)

To provide one liquid type dental adhesive composition that exhibits excellent adhesive property to glass ceramics, oxide-base ceramics and tooth substance, and has excellent storage stability, which are contrary features. One liquid type dental adhesive composition contains (a) silane coupling agent represented by general formula (1), (b) acidic group-containing polymerizable monomer, (c) volatile organic solvent, and (d) water. ##STR00001##
(In the formula, R.sup.1 represents an organic group having at least one functional group selected from the group consisting of a (meth)acryloyl group, a vinyl group and an epoxy group, R.sup.2 represents C4-C8 linear alkyl group, R.sup.3 represents C1-C8 alkyl group, and n is integer selected from 1 to 3.)

The present invention provides a dental curable composition that shows fluorescence sufficient to enable highly aesthetic harmonious restoration almost indistinguishable from surrounding natural teeth, and that, while having sufficient mechanical strength and radiopacity and good ease of polishing as a restorative material, desirably resists discoloration not only in the intraoral environment but under accelerated heating conditions and under xenon light, without losing fluorescence even under these conditions. The present invention also provides a cured product of such a dental curable composition. The present invention relates to a dental curable composition comprising a polymerizable monomer (A), an inorganic filler (B), a polymerization initiator (C), and a fluorescent agent (D), wherein the fluorescent agent (D) comprises a 9- to 11-membered benzo-fused heterocyclic compound containing two or more heteroatoms (excluding benzoimidazole compounds).

The present invention provides a dental curable composition that shows fluorescence sufficient to enable highly aesthetic harmonious restoration almost indistinguishable from surrounding natural teeth, and that, while having sufficient mechanical strength and radiopacity and good ease of polishing as a restorative material, desirably resists discoloration not only in the intraoral environment but under accelerated heating conditions and under xenon light, without losing fluorescence even under these conditions. The present invention also provides a cured product of such a dental curable composition. The present invention relates to a dental curable composition comprising a polymerizable monomer (A), an inorganic filler (B), a polymerization initiator (C), and a fluorescent agent (D), wherein the fluorescent agent (D) comprises a 9- to 11-membered benzo-fused heterocyclic compound containing two or more heteroatoms (excluding benzoimidazole compounds).

To provide a dental photocurable composition which can exhibit excellent mechanical characteristics even after returning from a low temperature to room temperature. To provide a dental photocurable composition, comprising (A) polymerizable monomer, (B) photosensitizer, (C) photoacid generator and (D) photopolymerization accelerator and the (C) photoacid generator may include only (C-1) iodonium salt-based compound of an anion having log S of −4 or less.

To provide a dental photocurable composition which can exhibit excellent mechanical characteristics even after returning from a low temperature to room temperature. To provide a dental photocurable composition, comprising (A) polymerizable monomer, (B) photosensitizer, (C) photoacid generator and (D) photopolymerization accelerator and the (C) photoacid generator may include only (C-1) iodonium salt-based compound of an anion having log S of −4 or less.