225113-41-7Relevant academic research and scientific papers
Multi-armed chromophores with very large two-photon absorption cross-sections
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, (2008/06/13)
Provided are chromophores with very large two-photon absorption cross-sections. One group of these chromophores has the formula: (T—Q)n—N—Phm wherein Q is a single bond or 1,4-phenylene, Ph is a phenyl group, n has a value of 1-3 and m has a value of 3?n, and wherein T is wherein R1and R2are alkyl groups having 1 to 20 carbon atoms, provided that when Q is a single bond, the value of n is 2 or 3. Another group of these chromophores has the formula: (T—Q)n—G—Phm wherein T is as defined above, Q is a single bond or 1,4-phenylene, Ph is a phenyl group, n has a value of 1-4 and m has a value of 4?n, and wherein G is a 4-arm core unit. Yet another group of these chromophores has the formula: (T—Q)n—G—Phm wherein T is as described previously, Q is a single bond or 1,4-phenylene, Ph is a phenyl group, n has a value of 1-6 and m has a value of 6?n, and wherein G is a 6-arm core unit.
Benzothiazole-containing two-photon chromophores exhibiting strong frequency upconversion
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, (2008/06/13)
There are provided asymmetrical two-photon chromophores of the formula: D-Ar-A wherein Ar is selected from the group consisting of wherein Fl is a fluorene group of the formula: wherein R1 and R2 are alkyl groups having 2 to 20 carbon atoms, and wherein R1 and R2 are the same or different; wherein D is wherein Q is selected from the group consisting of -H, -OH and -O-CxH2x+1, wherein x has a value of 1 to 10; and wherein A is selected from the group consisting of wherein Z is selected from the group consisting of -O- and -S-.
