Abstract:Two functional polyurethanes (P1 and P2) bearing a large p electron conjugated chromophoric pendant were synthesized and characterized by FT-IR, 1 H-NMR and UV-Vis absorption spectra. Their optical limiting properties were evaluated. The results show that P1 and P2 show novel optical limiting properties, which are assigned to a long p electron conjugated chromophoric pendant. It was found that their optical limiting properties were affected simultaneously by solution concentration and P2 displays a better opti… Show more
“…It can be found that higher concentration (lower transmittance) solution exhibits better performances. Similar results were also found by Kojima's and our previous publications . Solution with higher concentration has more molecules per unit volume, thereby absorbing the energy of the harsh laser more efficiently.…”
Section: Resultssupporting
confidence: 91%
“…Similar results were also found by Kojima's 48 and our previous publications. 49 Solution with higher concentration has more molecules per unit volume, thereby absorbing the energy of the harsh laser more efficiently.…”
A series of new molecular hybrids with stilbene chromophore (H1-H4) are prepared by hydrosilylation of octahydridosilsesquioxane (T 8 H ). All these stilbene-containing hybrid materials are soluble in common organic solvents, such as chloroform, toluene, THF, and 1,2-dichloroethane, and possess good film-forming properties. Their structures and properties are characterized and evaluated by FT-IR, NMR, UV, PL, TGA, DSC, nonlinear optical (NLO), and optical limiting (OL) analyses. The results show that the thermal decomposition temperatures (T d , 5 mass % loss) of the hybrids are 20-60 °C greater than their corresponding stilbene monomers, and the hybrids show obvious nonlinear absorption (β up to 2.56 Â 10 -11 m/W) and optical limiting properties. The larger excited-state absorption cross sections than corresponding ground-state absorption cross sections of the hybrids indicate that reverse saturable absorption is a major mechanism responsible for the optical limiting of the hybrids.
“…It can be found that higher concentration (lower transmittance) solution exhibits better performances. Similar results were also found by Kojima's and our previous publications . Solution with higher concentration has more molecules per unit volume, thereby absorbing the energy of the harsh laser more efficiently.…”
Section: Resultssupporting
confidence: 91%
“…Similar results were also found by Kojima's 48 and our previous publications. 49 Solution with higher concentration has more molecules per unit volume, thereby absorbing the energy of the harsh laser more efficiently.…”
A series of new molecular hybrids with stilbene chromophore (H1-H4) are prepared by hydrosilylation of octahydridosilsesquioxane (T 8 H ). All these stilbene-containing hybrid materials are soluble in common organic solvents, such as chloroform, toluene, THF, and 1,2-dichloroethane, and possess good film-forming properties. Their structures and properties are characterized and evaluated by FT-IR, NMR, UV, PL, TGA, DSC, nonlinear optical (NLO), and optical limiting (OL) analyses. The results show that the thermal decomposition temperatures (T d , 5 mass % loss) of the hybrids are 20-60 °C greater than their corresponding stilbene monomers, and the hybrids show obvious nonlinear absorption (β up to 2.56 Â 10 -11 m/W) and optical limiting properties. The larger excited-state absorption cross sections than corresponding ground-state absorption cross sections of the hybrids indicate that reverse saturable absorption is a major mechanism responsible for the optical limiting of the hybrids.
“…Water-soluble organic polymeric dyes were also found to possess third-order nonlinearity. Thin films of polymers 433 and 434 (Chart ) showed nonlinear absorption in the IR with a TPA coefficient of 55 and 18 cm/GW, respectively. , Functional polyurethanes 435a , b were synthesized, and their OL properties were evaluated. , These were ascribed to the presence of long π-electron conjugated chromophoric pendants. Polymer 435b displayed better OL properties than 435a at the same value of linear transmittance, although 435a had a larger χ (3) (4.28 × 10 –11 esu) than 435b (0.87 × 10 –11 esu) from RSA mechanism.…”
Section: Organic Materialsmentioning
confidence: 99%
“…959,960 Functional polyurethanes 435a,b were synthesized, and their OL properties were evaluated. 961,962 These were ascribed to the presence of long π-electron conjugated chromophoric pendants. Polymer 435b displayed better OL properties than 435a at the same value of linear transmittance, although 435a had a larger χ (3) (4.28 × 10 −11 esu) than 435b (0.87 × 10 −11 esu) from RSA mechanism.…”
The control of luminous radiation has extremely important implications for modern and future technologies as well as in medicine. In this Review, we detail chemical structures and their relevant photophysical features for various groups of materials, including organic dyes such as metalloporphyrins and metallophthalocyanines (and derivatives), other common organic materials, mixed metal complexes and clusters, fullerenes, dendrimeric nanocomposites, polymeric materials (organic and/or inorganic), inorganic semiconductors, and other nanoscopic materials, utilized or potentially useful for the realization of devices able to filter in a smart way an external radiation. The concept of smart is referred to the characteristic of those materials that are capable to filter the radiation in a dynamic way without the need of an ancillary system for the activation of the required transmission change. In particular, this Review gives emphasis to the nonlinear optical properties of photoactive materials for the function of optical power limiting. All known mechanisms of optical limiting have been analyzed and discussed for the different types of materials.
“…(2) and 4-((4-(bis(2-hydroxyethyl)amino)phenyl)diazenyl) benzaldehyde (3) were synthesised by the methods of Su et al [21] and Ledoux et al [22] respectively. Tetraethyl ((9,9-bis(2-ethylhexyl)-fluorene-2,7-diyl)bis(methylene))bis(phosphonate) was synthesised by an adaptation of the method of Mongin et al [23], while tetraisopropyl ((2-((2-ethylhexyl)oxy)-5-methoxy-1,4-…”
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