IP Library Granted Patent US 7,588,702
Granted Patent B2
US 7,588,702 · App. 12/022,758 · Granted Sep 15, 2009

Method of quenching electronic excitation of chromophore-containing organic molecules in photoactive compositions

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Quick Facts
Patent No.
US 7,588,702
App. No.
12/022,758
Granted
Sep 15, 2009
Kind
B2
Abstract

The photostabilizing electronic excited state energy—particularly singlet state energy from a UV-absorbing molecule has been found to be readily transferred to (accepted by) α-cyanodiphenylacrylate compounds of formulas (I) and (V) having an alkoxy radical preferably in the four (para) position (hereinafter methoxycrylenes) on one or both of the phenyl rings: wherein at least one of R 1 and R 2 is a straight or branched chain C 1 -C 12 alkoxy radical, preferably C 1 -C 8 , more preferably C 1 -C 4 , and most preferably methoxy, and any non-alkoxy radical R 1 or R 2 is hydrogen; and R 3 is a straight or branched chain C 1 -C 24 alkyl radical, preferably C 12 -C 24 , more preferably C 20 ; wherein A and B are the same or different and are selected from the group consisting of oxygen, amino and sulfur; R 1 and R 3 are the same or different and are selected from the group consisting of C 1 -C 30 alkyl, C 2 -C 30 alkylene, C 2 -C 30 alkyne, C 3 -C 8 cycloalkyl, C 1 -C 30 substituted alkylene, C 2 -C 30 substituted alkyne, aryl, substituted aryl, heteroaryl, heterocycloalkyl, substituted heteroaryl and substituted heterocycloalkyl; R 2 is selected from the group consisting of C 1 -C 30 alkyl, C 2 -C 30 alkylene, C 2 C 30 alkyne, C 3 -C 8 cycloalkyl, C 1 -C 30 substituted alkyl, C 3 -C 8 substituted cycloalkyl, C 1 -C 30 substituted alkylene, C 2 -C 30 substituted alkyne; R 4 , R 5 , R 6 and R 7 are the same or different and are selected from the group consisting of C 1 -C 30 alkoxy straight chain or branched and a, b, c and d are each either 0 or 1, and a, b, c and d add up to 1, 2, 3, or 4.

Claims (13)

1. A method of increasing the UV absorbing life of a sunscreen composition containing (a) a dibenzoylmethane derivative that reaches a singlet excited state or fluoresces when exposed to UV radiation and (b) a cinnamate ester comprising adding a compound of formula (I) in an amount effective to quench the singlet excited state energy from the dibenzoylmethane derivative and transfer the singlet excited state energy from the dibenzoylmethane derivative to the compound of formula (I) thereby returning the dibenzoylmethane derivative to its ground state so that the dibenzoylmethane derivative can absorb more photons from ultraviolet light before it undergoes a photochemical reaction destructive to its UV-absorbing capability thereby photostabilizing (a) and (b)

wherein one of R 1 and R 2 is a straight or branched chain C 1 -C 30 alkoxy radical, and the non-alkoxy R 1 or R 2 is hydrogen; and R 3 is a straight or branched chain C 1 -C 30 alkyl radical.

2. The method of claim 1 , wherein the cinnamate ester is an ester of an alkoxycinnamate.

3. The method of claim 2 , wherein the alkoxycinnamate ester is a methoxycinnamate ester.

4. The method of claim 3 , wherein the cinnamate ester is selected from the group consisting of 2-ethyihexyl p-methoxycinnamate, isoamyl p-methoxycinnamate, and a combination thereof.

5. The method of claim 4 , wherein the cinnamate ester is 2-ethylhexyl p-methoxycinnamate.

6. The method of claim 5 , wherein the dibenzoylmethane derivative comprises butylmethoxy dibenzoylmethane.

7. The method of claim 1 , wherein R 1 or R 2 of formula (I) is a methoxy radical.

8. The method of claim 7 , wherein the compound of formula (I) is added in an amount sufficient to absorb the singlet excited state energy of both the dibenzoylmethane derivative and the cinnamate ester when both are subjected to UV radiation.

9. The method of claim 1 , wherein the compound of formula (I) is present in an amount in the weight range of 0.1% to 20%, based on the total weight of the composition.

10. The method of claim 9 , wherein the compound of formula (I) is present in an amount in the weight range of 0.1% to 10%, based on the total weight of the composition.

11. The method of claim 10 , wherein the compound of formula (I) is present in an amount in the weight range of 3% to 8%, based on the total weight of the composition.

12. The method of claim 10 , wherein the compound of formula (I) is present in an amount in the weight range of 0.1% to 5%, based on the total weight of the composition.

Assignments (5)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 28, 2018
From: HALLSTAR INNOVATIONS CORP.
To: HALLSTAR BEAUTY AND PERSONAL CARE INNOVATIONS COMPANY
Reel/Frame 046977/0359 →
SECOND AMENDED AND RESTATED INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Nov 25, 2014
From: HALLSTAR INNOVATIONS CORP.
To: BANK OF AMERICA, N.A., AS AGENT
Reel/Frame 034468/0854 →
AMENDED AND RESTATED INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Feb 21, 2012
From: HALLSTAR INNOVATIONS CORP.
To: BANK OF AMERICA, N.A., AS AGENT
Reel/Frame 027742/0917 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 23, 2008
From: BONDA, CRAIG A.; PAVLOVIC, ANNA
To: HALLSTAR INNOVATIONS CORP.
Reel/Frame 021724/0918 →
SECURITY INTEREST Recorded Oct 16, 2008
From: HALLSTAR INNOVATIONS CORP.
To: LASALLE BANK NATIONAL ASSOCIATION, AS AGENT
Reel/Frame 021709/0286 →