• Rapid Communication in Photoscience
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• v.3 no.1
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• pp.1-15
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• 2014

We summarize recent studies on photoinduced electron- and energy-transfer processes of various supramolecules including imide group(s) as a component. Recently, imides have been employed in various functional molecular systems, because of their excellent photophysical and electron accepting properties. Our research group also employed imides in various supramolecular systems such as donor-acceptor dyads, quantum dots, DNA, and so on. First, we summarize fundamental properties of imides such as photophysical and electrochemical properties. Then, photoinduced processes of imides in the supramolecular systems are described to show their applicability in the various fields.

• Proceedings of the Korean Vacuum Society Conference
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• 2012.08a
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• pp.372-372
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• 2012

We have studied a fabrication of Poly (3,4-ethylenedioxythiophene) (PEDOT) wire arrays and structures with various feature sizes from hundreds micrometers to tens nanometers. PEDOT is well-known as a conducting material, can be grown by a vapor pressure polymerization (VPP) method. The VPP technique is a bottom-up processing method that utilizes the organic arrangement of macromolecules to easily produce ordered aggregates. Also, liquid-bridge-mediated nanotransfer molding (LB-nTM), which was reported as a new direct patterning method recently, is based on the direct transfer of various materials from a mould to a substrate through a liquid bridge between them. The PEDOT nanowires grown by VPP method and transferred on a substrate to use LB-nTM method have been investigated by Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM), Selected Area Electron Diffraction (SAED), X-Ray Diffraction (XRD), X-ray Photoelectron Spectroscopy (XPS), and electrical properties.

• Proceedings of the Korean Vacuum Society Conference
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• 2010.02a
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• pp.317-317
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• 2010

This paper reports syntheses of $TiO_2$ nanocubes and theirs application to DSSC. We synthesized $TiO_2$ nanocubes via solvothermal method using titanium isopropoxide (TTIP) and tetramethylammoiumhydroxide (TMAH). By adding longer alkyl chain ammonium hydroxide that slowed down the growth rate of the crystal, $TiO_2$ nanocubes were obtained with average particle size in the range of 40 nm to 70 nm. By TEM investigation, each particle was found to be single crystal of anatase having six-faces of (001) and {100} crystallographic planes truncated by {101} series of planes, which are clearly distinguishable from spherical nanoparticles. Among various application, utilizing nanocubes as photo-electrode in dye-sensitized solar cell, we investigated photo-electron conversion performances in comparison with spherical shaped $TiO_2$ nanoparticles by I-V characteristics and IPCE measurements, etc.. Photocurrent-transient analysis revealed that $TiO_2$ nanocubes have a higher transient electron transfer rate by more than 10 times compared with spherical particles of similar size. Fast electron transport along the cube edges having small curvature was suggested as a plausible origin of high diffusion coefficient of electron in nanocube $TiO_2$.

• Bulletin of the Korean Chemical Society
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• v.28 no.12
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• pp.2343-2353
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• 2007

We report the application of time-dependent density functional theory (TDDFT) to the calculation of potential energy profile relevant to the excited state intramolecular proton transfer (ESIPT) processes in title molecules. The TDDFT single point energy calculations along the reaction path have been performed using the CIS optimized structure in the excited state. In addition to the Stokes shifts, the transition energies including absorption, fluorescence, and 0-0 transition are estimated from the TDDFT potential energy profiles along the proton transfer coordinate. The excited state TDDFT potential energy profile of SA and 3ASA resulted in very flat function of the OH distance in the range ROH = 1.0-1.6 A, in contrast to the relatively deep single minimum function in the ground state. Furthermore, we obtained very shallow double minima in the excited state potential energy profile of SA and 3ASA in contrast to the single minimum observed in the previous work. The change of potential energy profile along the reaction path induced by the substitution of electron donating groups (-NH2 and -OCH3) at different sites has been investigated. Substitution at para position with respect to the phenolic OH group showed strong suppression of excited state proton dislocation compared with unsubstitued SA, while substitution at ortho position hardly affected the shape of the ESIPT curve. The TDDFT results are discussed in comparison with those of CASPT2 method.

• Journal of Photoscience
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• v.3 no.2
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• pp.49-60
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• 1996

Preparative features of photoinduced single electron transfer (SET) reactions of selected N-silylmethallyl-iminium salts have been probed in the context of strategies for functionally complex spirocyclic amine synthesis.

• Bulletin of the Korean Chemical Society
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• v.24 no.2
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• pp.219-221
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• 2003

Rabi oscillation between bound states of a single potential is well known. However the corresponding formula between the states of two different potentials has not been obtained yet. In this work, we derive Rabi formula between the states of a coupled harmonic oscillator which may be used as a simple model for the electron transfer. The expression is similar to typical Rabi formula for a single potential. This result may be used to describe transitions between coupled diabatic potential curves.

• Animal cells and systems
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• v.14 no.2
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• pp.91-98
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• 2010

Male rats were given a single injection of iron, and temporal changes in iron content and iron-induced effects were examined in heart cellular fractions. Over a period of 72 h, the contents of total and labile iron, reactive oxygen species, and NO in tissue homogenate, nuclear debris, and postmitochondrial fractions were mostly constant, but in mitochondria they continuously increased. An abrupt decrease in membrane potential and NAD(P)H at 12 h was also found in mitochondria. The respiratory control ratio was reduced slowly with a slight recovery at 72 h, suggesting uncoupling by iron.While the ATP content of tissue homogenate decreased steadily until 72 h, it showed a prominent increase in mitochondria at 12 h. Total iron and calcium concentration also progressively increased in mitochondria over 72 h. Enzyme activity of the oxidative phosphorylation system was significantly altered by iron injection: activities of complexes I, III, and IV were reduced considerably, but complex II activity and the ATPase activity of complex V were enhanced. A reversal of activity in complexes I and II at 12 h suggested reverse electron transfer due to iron overload. These results support the argument that mitochondrial activities including oxidative phosphorylation are modulated by excessive iron.

• Bulletin of the Korean Chemical Society
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• v.15 no.9
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• pp.743-748
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• 1994

Photochemical reactions of saccharin with tertiary amines were explored. Saccharin was found to undergo an acid-base reaction with N-trimethylsilylmethyl-N,N-diethyl amine to form N-trimethylsilylmethyl-N,N-diethyl ammonium saccharin salt which is in equilibrium with free saccharin and N-trimethylsilylmethyl-N,N-diethyl amine insolution. Photoreaction of N-trimethylsilylmethyl-N,N-diethyl ammonium saccharin in $CH_3OH\;or\;CH_3CN$ results in the generation of desilylmethylated product, N,N-diethyl ammonium saccharin mainly along with benzamide. Photoreaction of N-methylsaccharin with N-trimethylsilylmethyl-N,N-diethyl amine in $CH_3OH$ leads to the production of o-(N-methylcarbamoyl)-N-ethylbenzenesulfonamid e as the major product along with N-methylbenzamide as the minor product. On the other hand, photoreaction of N,N,N-triethyl ammonium saccharin, generated from saccharin and triethylamine, produces N-methylbenzamide as the exclusive product. These photoreactions are quenched by oxygen indicating that triplets of saccharin and N-methylsaccharin are the reactive excited states. Based on the consideration of the redox potentials of saccharin and N-trimethylsilylmethyl-N,N-diethyl amine, and the nature of photoproducts, pathways involving initial triplet state single electron transfer are proposed for photoreactions of the saccharins with the ${\alpha}$-silylamine.

• Proceedings of the Korean Vacuum Society Conference
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• 2011.02a
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• pp.458-458
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• 2011

Graphene, a single atomic layer of sp2-bonded carbon, shows substantial potential for various applications. Chemical manipulation of its electronic properties will be of great importance. In this study, we have investigated interaction between graphene and organic molecular layer of tetrafluorotetracyanoquinodimethane (F4-TCNQ), a strong electron acceptor. F4-TCNQ films of varying thickness were evaporated onto graphene mechanically exfoliated on SiO2/Si substrates. F4-TCNQ molecules increase the frequencies of Raman G and 2D bands of graphene while decreasing the linewidth of G band and 2D/G intensity ratio, which is consistent with increase of hole density in graphene. These results exemplify the possibility of chemical tuning of electronic properties of graphene.

• The Bulletin of The Korean Astronomical Society
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• v.45 no.1
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• pp.70.4-71
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• 2020

One of the distinctive characteristics of the evolution of binary systems would be mass transfer. Close binary systems experience so-called Case A mass transfer during the main-sequence. We have performed calculations of the evolution of massive Case A (with the initial period 1.5 ~ 4.5 days) binary systems with the initial mass of 10 ~ 20 solar masses and mass ratio 0.5 ~ 0.95 using the MESA code. We find that in some systems, after the first mass transfer, the secondary stars evolve faster than the primary stars and undergo so-called 'reverse' mass transfer. Such phenomena tend to occur in relatively low-mass (initial mass < 16 solar masses) and close (initial period < 3 day) systems. Unless a system enters the common-envelope phase, the primary star would become a single helium star after the secondary star ends its life if the system were unbound by the neutron star kick. We find the various evolutionary implications of the remaining primary stars. In addition to the evolution into the compact single helium star progenitor, there is a possibility that the remaining primary star could evolve into a helium giant star, which could be a promising candidate for Type Ibn supernova progenitor, depending on the core mass. Further, we find that some primary stars satisfy the conditions for the formation of electron-capture supernova progenitor.