The present invention relates in a first aspect to a method of preparing a crystalline lanthanum-carboxylate coordination polymer and the crystalline lanthanum-carboxylate coordination polymer obtained or obtainable by the method. In another aspect of the present invention, also provides a method of detecting a target nucleic acid sequence in a sample.

The present invention relates in a first aspect to a method of preparing a crystalline lanthanum-carboxylate coordination polymer and the crystalline lanthanum-carboxylate coordination polymer obtained or obtainable by the method. In another aspect of the present invention, also provides a method of detecting a target nucleic acid sequence in a sample.

Polymers, monomers, chromophoric polymer dots and related methods are provided. Highly fluorescent chromophoric polymer dots with narrow-band emissions are provided. Methods for synthesizing the chromophoric polymers, preparation methods for forming the chromophoric polymer dots, and biological applications using the unique properties of narrow-band emissions are also provided.

Polymers, monomers, chromophoric polymer dots and related methods are provided. Highly fluorescent chromophoric polymer dots with narrow-band emissions are provided. Methods for synthesizing the chromophoric polymers, preparation methods for forming the chromophoric polymer dots, and biological applications using the unique properties of narrow-band emissions are also provided.

A flame retardant composition includes a polymers that is the reaction product of a mixture of a chalcogenide halide and one or more organic compounds comprising an unsaturated carbon-carbon bond under reaction conditions sufficient to produce the polymer, wherein the chalcogenide halide comprises a sulfur monohalide, a sulfur dihalide, a selenium monohalide, a selenium dihalide, a selenium tetrahalide, or a combination of any two or more thereof.

A flame retardant composition includes a polymers that is the reaction product of a mixture of a chalcogenide halide and one or more organic compounds comprising an unsaturated carbon-carbon bond under reaction conditions sufficient to produce the polymer, wherein the chalcogenide halide comprises a sulfur monohalide, a sulfur dihalide, a selenium monohalide, a selenium dihalide, a selenium tetrahalide, or a combination of any two or more thereof.

Polymers, monomers, chromophoric polymer dots and related methods are provided. Highly fluorescent chromophoric polymer dots with narrow-band emissions are provided. Methods for synthesizing the chromophoric polymers, preparation methods for forming the chromophoric polymer dots, and biological applications using the unique properties of narrow-band emissions are also provided.

Polymers, monomers, chromophoric polymer dots and related methods are provided. Highly fluorescent chromophoric polymer dots with narrow-band emissions are provided. Methods for synthesizing the chromophoric polymers, preparation methods for forming the chromophoric polymer dots, and biological applications using the unique properties of narrow-band emissions are also provided.

A titanium oxide aerogel particle has absorption at wavelengths of 450 nm and 750 nm in a visible absorption spectrum, a surface to which a metal compound containing a metal atom and a hydrocarbon group is bonded via an oxygen atom, a BET specific surface area in a range of 120 m.sup.2/g to 1,000 m.sup.2/g, and a value A is in the range of 0.03 to 0.3. The value A is calculated by formula: A={(peak intensity of CO bond+peak intensity of CO bond)/(peak intensity of CC bond+peak intensity of CC bond)}. In the formula, the peak intensity is a value determined from a C 1s XPS spectrum.

A titanium oxide aerogel particle has absorption at wavelengths of 450 nm and 750 nm in a visible absorption spectrum, a surface to which a metal compound containing a metal atom and a hydrocarbon group is bonded via an oxygen atom, a BET specific surface area in a range of 120 m.sup.2/g to 1,000 m.sup.2/g, and a value A is in the range of 0.03 to 0.3. The value A is calculated by formula: A={(peak intensity of CO bond+peak intensity of CO bond)/(peak intensity of CC bond+peak intensity of CC bond)}. In the formula, the peak intensity is a value determined from a C 1s XPS spectrum.