Near infrared absorbing polymerizate

Claim 2

A near-infrared absorbing article of (a) solid transparent synthetic resin of polyol(allyl carbonate) monomer and (b) a near-infrared absorbing amount of the reaction product of tungsten hexachoride and phenol, said amount of the reaction product being soluble in the poly(allyl carbonate) monomer, and said reaction product being formed by heating a mixture of the tungsten hexachloride and liquid phenol at temperatures below about 65° C. until the evolution of hydrogen chloride gas ceases, the mole ratio of phenol to tungsten hexachloride being from about 4:1to 6:1.

Claim 3

The article of claim 1 wherein the near-infrared absorbing amount of reaction product is from about 0.01 to about 1.0 weight percent (calculated as tungsten), based on the synthetic resin.

Claim 4

The article of claim 2 wherein the near-infrared absorbing amount is from about 0.01 to about 0.1 weight percent.

Claim 5

The article of claim 2 wherein the mole ratio of phenol to tungsten hexachloride is about 4:1 to 5:1.

Claim 6

The article of claim 1 wherein the synthetic resin is selected from bis(allyl carbonates) represented by the graphic formula, ##STR14## wherein R 1 and R 3 are each allyl, halo-substituted allyl or C 1 -C 4 alkyl substituted allyl, and R 2 is a C 2 -C 4 alkylene glycol, C 2 -C 4 alkylene ether, or poly(C 2 -C 4 alkylene glycol).

Claim 7

A near-infrared absorbing article of (a) solid transparent synthetic resin of alkylene glycol bis (allyl carbonate) monomer and (b) from 0.01 to 1.0 weight percent (calculated as tungsten) of the reaction product of tungsten hexachloride and phenol, said amount of the reaction product being soluble in the alkylene glycol bis (allyl carbonate) monomer, and said reaction product being formed by heating a mixture of tungsten hexachloride and liquid phenol at temperatures below about 65° C. until the evolution of hydrogen chloride gas ceases, the mole ratio of phenol to tungsten hexachloride being from about 4:1 to 6:1.

Claim 8

A near-infrared absorbing article of (a) solid transparent synthetic resin of alkylene glycol bis (allyl carbonate) monomer and (b) from 0.01 to 1.0 weight percent (calculated as tungsten) of the reaction product of tungsten hexachloride and phenol, said amount of the reaction product being soluble in the alkylene glycol bis (allyl carbonate) monomer, and said reaction product being formed by heating a mixture of tungsten hexachloride and liquid phenol at temperatures below about 65° C. until the evolution of hydrogen chloride gas ceases, the mole ratio of phenol to tungsten hexachloride being from about 4:1 to 6:1.

Claim 9

The article of claim 6 wherein the synthetic resin is poly.

Claim 10

The article of claim 7 wherein the near-infrared absorbing amount of the reaction product is from about 0.01 to 0.1 weight percent (calculated as tungsten), based on the synthetic resin.

Claim 11

The article of claim 7 wherein the mole ratio of phenol to tungsten hexachloride is from about 4:1 to 5:1.

Claim 12

A composition of polyol(allyl carbonate) monomer and from about 0.01 to 1.0 weight percent (calculated as tungsten) of the reaction product of tungsten hexachloride and phenol, said amount of the reaction product being soluble in the polyol(allyl carbonate) monomer, and said reaction product being formed by heating a mixture of tungsten hexachloride and liquid phenol at temperatures below about 65° C. until the evolution of hydrogen chloride gas ceases, the mole ratio of phenol to tungsten hexachloride being form about 4:1to 6:1.

Claim 13

A composition of polyol(allyl carbonate) monomer and from about 0.01 to 1.0 weight percent (calculated as tungsten) of the reaction product of tungsten hexachloride and phenol, said amount of the reaction product being soluble in the polyol(allyl carbonate) monomer, and said reaction product being formed by heating a mixture of tungsten hexachloride and liquid phenol at temperatures below about 65° C. until the evolution of hydrogen chloride gas ceases, the mole ratio of phenol to tungsten hexachloride being form about 4:1to 6:1.

Claim 14

The composition of claim 10 wherein the polyol (allyl carbonate) is represented by the graphic formula, ##STR15## wherein R 1 and R 3 are each selected from the group consisting of allyl, halo-substituted allyl or C 1 -C 4 alkyl substituted allyl and R 2 is a C 2 -C 4 alkylene glycol, C 2 -C 4 alkylene ether, or poly (C 2 -C 4 alkylene glycol).

Claim 15

The composition of claim 10 wherein the polyl(allyl carbonate) is diethylene glycol bis(allyl carbonate).

Claim 16

The composition of claim 11 wherein the mole ratio of phenol to tungsten is from about 4:1 to 5:1.

Claim 17

The composition of claim 12 wherein the mole ratio of phenol to tungsten hexachloride is from about 4:1 to 5:1.

Claim 18

The composition of claim 14 wherein the tungsten hexachloride-phenol reaction product is present in amounts of from 0.01 to 0.1 weight percent (calculated as tungsten) based on the diethylene glycol bis(allyl carbonate).