Abstract: Helical arrays comprising structurally different chiral non-racemic molecules or molecular entities that control the helical sense of the helical array provide a method for temperature measurement with a unique characteristic in that the temperature dependent chiral biases of the competing structurally different chiral non-racemic entities control the helical sense population since these biases differ in their temperature dependence. By varying the composition of the chiral non-racemic entities, the temperature at which the helical sense population is equal and how the helical sense population varies as a function of temperature can be controlled.

Abstract: Helical arrays comprising structurally different chiral non-racemic molecules or molecular entities that control the helical sense of the helical array provide a method for temperature measurement with a unique characteristic in that the temperature dependent chiral biases of the competing structurally different chiral non-racemic entities control the helical sense population since these biases differ in their temperature dependence. By varying the composition of the chiral non-racemic entities, the temperature at which the helical sense population is equal and how the helical sense population varies as a function of temperature can be controlled. In this way, competing structurally different non-racemic chiral groups can be varied in their composition so that a helical array can be formed under their effect and be sensitive to temperature over a wide temperature range.

Abstract: Forming graft copolymers in water using labeling of water soluble polymers with photoinitiators. Water soluble polymers can form environmentally responsive hydrophobically stimulated cages. The cages, which contain initiating radicals after irradiation, may be “opened” or “closed” by changes in environmental conditions. When the cage is closed, the radicals are trapped inside and thus do not cause substantial polymerization of water soluble monomers in the same solution. When the cage is closed, the radicals escape and cause polymerization. In another variation, hydrogels and graft copolymers are formed by covalently linking phototoinitiator groups to water soluble polymers that do not form cages. Thus, monomers may form grafts to the polymer, allowing formation of physical hydrogels.

Abstract: Forming graft copolymers in water using labeling of water soluble polymers with photoinitiators. The water soluble polymers can form environmentally responsive hydrophobically stimulated cages, which respond to pH, salt concentration, and/or the addition of water miscible solvents to the aqueous solutions. When the cage is “closed,” irradiation leads to radicals that cannot escape from the cage and therefore don't cause substantial polymerization of water soluble monomers in the same solution. When the cage is open via change of pH, salt concentration and/or solvent composition, the photochemically produced free radicals become exposed and cause polymerization. Under certain conditions, only graft copolymers will be formed. These graft copolymers can form a physical hydrogel in which the crosslinks are reversible. Consequently, the gel and sol states are likewise reversible.

Abstract: Forming graft copolymers in water using labeling of water soluble polymers with photoinitiators. The water soluble polymers can form environmentally responsive hydrophobically stimulated cages, which respond to pH, salt concentration, and/or the addition of water miscible solvents to the aqueous solutions. When the cage is “closed,” irradiation leads to radicals that cannot escape from the cage and therefore don't cause substantial polymerization of water soluble monomers in the same solution. When the cage is open via change of pH, salt concentration and/or solvent composition, the photochemically produced free radicals become exposed and cause polymerization. Under certain conditions, only graft copolymers will be formed. These graft copolymers can form a physical hydrogel in which the crosslinks are reversible. Consequently, the gel and sol states are likewise reversible.

Abstract: Helical arrays comprising structurally different chiral non-racemic molecules or molecular entities that control the helical sense of the helical array provide a method for temperature measurement with a unique characteristic in that the temperature dependent chiral biases of the competing structurally different chiral non-racemic entities control the helical sense population since these biases differ in their temperature dependence. By varying the composition of the chiral non-racemic entities, the temperature at which the helical sense population is equal and how the helical sense population varies as a function of temperature can be controlled. In this way, competing structurally different non-racemic chiral groups can be varied in their composition so that a helical array can be formed under their effect and be sensitive to temperature over a wide temperature range. In this way a temperature may be preselected so that a chiral optical property can reach a minimum near to zero at this temperature.

Abstract: Helical arrays comprising structurally different chiral non-racemic molecules or molecular entities that control the helical sense of the helical array provide a method for temperature measurement with a unique characteristic in that the temperature dependent chiral biases of the competing structurally different chiral non-racemic entities control the helical sense population since these biases differ in their temperature dependence. By varying the composition of the chiral non-racemic entities, the temperature at which the helical sense population is equal and how the helical sense population varies as a function of temperature can be controlled. In this way, competing structurally different non-racemic chiral groups can be varied in their composition so that a helical array can be formed under their effect and be sensitive to temperature over a wide temperature range. In this way a temperature may be preselected so that a chiral optical property can reach a minimum near to zero at this temperature.

Abstract: An optical information storage material which can reversibly store said information comprising a polymeric material with a dependence of optical activity on temperature characterized in that the optical activity is substantially invariant at temperatures below Tg of said polymer, and variant at a temperatures at or near or above the Tg.

Abstract: This invention provides a photoswitchable compound comprising interconvertible mirror image units or interconvertible chiral diastereomeric units connected as pendant groups to a stiff polymer having interconvertible left- and right-handed helical portions of its backbone. Further provided by this invention is a photoswitchable compound formed by the method comprising combining an amount of the compound capable of optical activity and capable of changing its optical activity with an amount of a stiff polymer comprised of interconvertible left- and right-handed helical portions. Additionally, this invention provides a method for reversibly storing optical data comprising providing a material comprised of a mixture of a stiff polymer having interconvertible left- and right-handed helical portions and connected units, said units being capable of optical activity and capable of changing its optical activity and irradiating said material with light capable of changing the optical activity of said material.

Abstract: Thermally reversible gels comprising liquid solvents wherein the solvent is converted into a thermally reversible gel upon the addition of a rigid polymer, preferably, a liquid crystal forming polymer. Structural modifications of the rigid polymer, and in particular modifications of the side-chain, adapt the rigid polymer to form thermally reversible gels in any given solvent media.

Abstract: An optical information storage material which can reversibly store said information comprising a polymeric material with a dependence of optical activity on temperature characterized in that the optical activity is substantially invariant at temperatures below Tg of said polymer, and variant at a temperatures at or near or above the Tg.