Light Used (light + used)

Distribution by Scientific Domains


Selected Abstracts


Photo-Induced Electron Transfer Between Photosystem 2 via Cross-linked Redox Hydrogels

ELECTROANALYSIS, Issue 10 2008
Adrian Badura
Abstract Photosystem 2 (PS2) that catalyses light driven water splitting in photosynthesis was ,wired' to electrode surfaces via osmium-containing redox polymers based on poly(vinyl)imidazol. The redox polymer hydrogel worked as both immobilization matrix and electron acceptor for the enzyme. Upon illumination, the enzymatic reaction could be switched on and a catalytic current was observed at the electrode. The catalytic current is directly dependent on the intensity of light used for the excitation of PS2. A typical current density of 45,,A cm,2 at a light intensity of 2.65,mW cm,2 could be demonstrated with a significantly improved operational stability. [source]


Reversible Cluster Formation of Colloidal Nanospheres by Interparticle Photodimerization,

ADVANCED FUNCTIONAL MATERIALS, Issue 5 2004
X. Yuan
Abstract Crosslinked spherical nanoparticles based on trimethoxysilane monomers have been prepared by polycondensation in aqueous emulsion. These particles have been labeled chemically at their surface region with two different types of organic dye molecules (cinnamate, coumarin), which both are well known for their ability to undergo a reversible photodimerization if irradiated with light of a suitable wavelength. Upon irradiation of dilute solutions of these nanoparticles with UV light, the photodimerization of labels belonging to different colloidal nanoparticles caused the formation of large colloidal clusters consisting of chemically bound individual nanospheres. This process has been quantitatively investigated using light scattering and atomic force microscopy. Importantly, utilizing the reversibility of the photoreaction, the clusters could be broken up by irradiation of the sample with UV light of shorter wavelengths than the light used for their formation [source]


Computational analyses of singlet,singlet and singlet,triplet transitions in mononuclear gold-capped carbon-rich conjugated complexes

JOURNAL OF COMPUTATIONAL CHEMISTRY, Issue 12 2005
Zexing Cao
Abstract Density functional theory and CASSCF calculations have been used to determine equilibrium geometries and vibrational frequencies of metal-capped one-dimensional ,-conjugated complexes (H3P)Au(CC)n(Ph) (n = 1,6), (H3P)Au(CCC6H4)(CCPh), and H3PAu(CCC6H4)CCAuPH3 in their ground states and selected low-lying ,,* excited states. Vertical excitation energies for spin-allowed singlet,singlet and spin-forbidden singlet,triplet transitions determined by the time-dependent density functional theory show good agreement with available experimental observations. Calculations indicate that the lowest energy 3(,,*) excited state is unlikely populated by the direct electronic excitation, while the low-lying singlet and triplet states, slightly higher in energy than the lowest triplet state, are easily accessible by the excitation light used in experiments. A series of radiationless transitions among related excited states yield the lowest 3(,,*) state, which has enough long lifetimes to exhibit its photochemical reactivities. © 2005 Wiley Periodicals, Inc. J Comput Chem 26: 1214,1221, 2005 [source]


Near-IR spectroscopic imaging for skin hydration: The long and the short of it

BIOPOLYMERS, Issue 2 2002
E. Michael Attas
Abstract Near-IR spectroscopic methods have been developed to determine the degree of hydration of human skin in vivo. Noncontact reflectance spectroscopic imaging was used to investigate the distribution of skin moisture as a function of location. A human study in a clinical setting has generated quantitative data showing the effects of a drying agent and a moisturizer on delineated regions of the forearms of eight volunteers. Two digital imaging systems equipped with liquid-crystal tunable filters were used to collect stacks of monochromatic images at 10-nm intervals over the 650,1050 and 960,1700 nm wavelength bands. Synthetic images generated from measurements of water absorption band areas at three different near-IR wavelengths (970, 1200, and 1450 nm) showed obvious differences in the apparent distribution of water in the skin. Changes resulting from the skin treatments were much more evident in the long-wavelength images than in the short-wavelength ones. The variable sensitivity of the method at different wavelengths has been interpreted as being the result of different penetration depths of the IR light used in the reflectance studies. © 2002 John Wiley & Sons, Inc. Biopolymers (Biospectroscopy) 67: 96,106, 2002 [source]


Topical aminolaevulinic acid- and aminolaevulinic acid methyl ester-based photodynamic therapy with red and violet light: influence of wavelength on pain and erythema

BRITISH JOURNAL OF DERMATOLOGY, Issue 5 2009
P. Mikolajewska
Summary Background, Photodynamic therapy (PDT) is based on the combination of an exogenously administered precursor of photosensitizer [protoporphyrin IX (PpIX)] synthesis and exposure to light. Choosing the optimal wavelength is important. Red light penetrates deeper into tissue, while violet light is more efficient in activating PpIX but does not penetrate so deeply. Objectives, We studied PpIX formation and the PDT effect after application to human skin of creams containing aminolaevulinic acid (ALA) and aminolaevulinic acid methyl ester (MAL). The aim of the study was to investigate whether the wavelength of the light used has an influence on pain sensations during topical PDT with the different prodrugs. Methods, ALA cream (10%) and MAL cream (10%) were topically applied on the skin of 10 healthy volunteers. After 24 h the application site was exposed to 8 mW cm,2 violet laser or to 100 mW cm,2 red laser light. The erythema index was monitored up to 24 h after light exposure. For the first time the pain during topical ALA- and MAL-PDT was assessed by measuring the time taken for pain to occur. Also, for the first time, the intensities of the light sources were calibrated so as to have the same relative quantum efficiency. Results, The pain sensation during ALA-PDT with red light came 22 s sooner than during ALA-PDT with violet light, which is statistically significant (P < 0·05). Moreover, ALA-PDT with red light gave stronger and more persistent erythema than ALA-PDT with violet light. ALA induced about three times more PpIX than MAL. No statistically significant differences were found for erythema, or for the time for pain to occur, in the case of MAL-PDT with red vs. violet light. Conclusions, Topical ALA-PDT with violet light allows longer exposure times before pain is induced and gives less erythema as compared with topical ALA-PDT with red light. [source]


All-Optical Integrated Logic Operations Based on Chemical Communication between Molecular Switches

CHEMISTRY - A EUROPEAN JOURNAL, Issue 1 2009
Serena Silvi Dr.
Abstract Molecular logic gates process physical or chemical "inputs" to generate "outputs" based on a set of logical operators. We report the design and operation of a chemical ensemble in solution that behaves as integrated AND, OR, and XNOR gates with optical input and output signals. The ensemble is composed of a reversible merocyanine-type photoacid and a ruthenium polypyridine complex that functions as a pH-controlled three-state luminescent switch. The light-triggered release of protons from the photoacid is used to control the state of the transition-metal complex. Therefore, the two molecular switching devices communicate with one another through the exchange of ionic signals. By means of such a double (optical,chemical,optical) signal-transduction mechanism, inputs of violet light modulate a luminescence output in the red/far-red region of the visible spectrum. Nondestructive reading is guaranteed because the green light used for excitation in the photoluminescence experiments does not affect the state of the gate. The reset is thermally driven and, thus, does not involve the addition of chemicals and accumulation of byproducts. Owing to its reversibility and stability, this molecular device can afford many cycles of digital operation. [source]


Magnifying Superlenses and other Applications of Plasmonic Metamaterials in Microscopy and Sensing

CHEMPHYSCHEM, Issue 4 2009
Igor I. Smolyaninov Dr.
Abstract Every last detail: New advances in the construction of metamaterials enable the creation of artificial optical media, whose use in microscopy can provide resolution that is not determined by the conventional diffraction limit. The picture shows a superposition of an AFM image of a plasmonic metamaterial onto the corresponding optical image obtained using a conventional optical microscope. Over the past century, the resolution of conventional optical microscopes, which rely on optical waves that propagate into the far field, has been limited because of diffraction to a value of the order of a half-wavelength (,0/2) of the light used. Although immersion microscopes have slightly improved resolution, of the order of ,0/2n, the increased resolution is limited by the small range of refractive indices n of available transparent materials. However, now we are experiencing a quick demolition of the diffraction limit in optical microscopy. In the last few years, numerous nonlinear optical microscopy techniques based on photoswitching and saturation of fluorescence have demonstrated far-field resolution of 20 to 30 nm. In a parallel development, recent progress in metamaterials has demonstrated that artificial optical media can be created, whose use in microscopy can provide resolution that is not determined by the conventional diffraction limit. The resolution of linear immersion microscopes based on such metamaterials is only limited by losses, which can be minimized by appropriate selection of the constituents of the metamaterials used and by the wavelength(s) used for imaging. It is also feasible to compensate for losses by adding gain to the structure. Thus, optical microscopy is quickly moving towards resolution of around 10 nm, which should bring about numerous revolutionary advances in lithography and imaging. [source]