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101.
102.
Chang Yeon Lee Dr. Jae Kwon Jang Chul Hoon Kim Dr. Jaehoon Jung Bo Keun Park Dr. Jihee Park Wonyong Choi Prof. Young‐Kyu Han Dr. Taiha Joo Prof. Joon T. Park Prof. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2010,16(19):5586-5599
A new artificial photosynthetic triad array, a [60]fullerene–triosmium cluster/zinc–porphyrin/boron–dipyrrin complex ( 1 , Os3C60/ZnP/Bodipy), has been prepared by decarbonylation of Os3(CO)8(CN(CH2)3Si(OEt)3)(μ3‐η2:η2:η2‐C60) ( 6 ) with Me3NO/MeCN and subsequent reaction with the isocyanide ligand CNZnP/Bodipy ( 5 ) containing zinc porphyrin (ZnP) and boron dipyrrin (Bodipy) moieties. Triad 1 has been characterized by various spectroscopic methods (MS, NMR, IR, UV/Vis, photoluminescence, and transient absorption spectroscopy). The electrochemical properties of 1 in chlorobenzene (CB) have been examined by cyclic voltammetry; the general feature of the cyclic voltammogram of 1 is nine reversible one‐electron redox couples, that is, the sum of those of 5 and 6 . DFT has been applied to study the molecular and electronic structures of 1 . On the basis of fluorescence‐lifetime measurements and transient absorption spectroscopic data, 1 undergoes an efficient energy transfer from Bodipy to ZnP and a fast electron transfer from ZnP to C60; the detailed kinetics involved in both events have been elucidated. The SAM of triad 1 ( 1 /ITO; ITO=indium–tin oxide) has been prepared by immersion of an ITO electrode in a CB solution of 1 and diazabicyclo‐octane (2:1 equiv), and characterized by UV/Vis absorption spectroscopy, water contact angle, X‐ray photoelectron spectroscopy, and cyclic voltammetry. The photoelectrochemical properties of 1 /ITO have been investigated by a standard three‐electrode system in the presence of an ascorbic acid sacrificial electron donor. The quantum yield of the photoelectrochemical cell has been estimated to be 29 % based on the number of photons absorbed by the chromophores. Our triad 1 is unique when compared to previously reported photoinduced electron‐transfer arrays, in that C60 is linked by π bonding with little perturbation of the C60 electron delocalization. 相似文献
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Sun Hwa Lee Li Xu Dr. Byeong Kwon Park Yuri V. Mironov Dr. Soo Hyun Kim Young Ju Song Cheal Kim Prof. Dr. Youngmee Kim Dr. Sung‐Jin Kim Prof. Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2010,16(15):4678-4685
Two new tetranuclear chalcocyanide cluster complexes, [{Mn(saloph)H2O}4Re4Q4(CN)12]?4 CH3OH? 8 H2O (saloph=N,N′‐o‐phenylenebis(salicylidenaminato), Q=Se ( 1 ‐Se), Te ( 2 ‐Te)), have been synthesized by the diffusion of a methanolic solution of [PPh4]4[Re4Q4(CN)12] into a methanolic solution of [Mn(saloph)]+. The structure of 2 ‐Te has been determined by X‐ray crystallography. These rhenium cluster‐supported [MnIII(saloph)] complexes have been found to efficiently catalyze a wide range of olefin epoxidations under mild experimental conditions in the presence of meta‐chloroperbenzoic acid (mCPBA). Olefin epoxidation by these catalysts is proposed to involve the multiple active oxidants MnV?O, MnIV?O, and MnIII? OOC(O)R. Evidence in support of this interpretation has been derived from reactivity and Hammett studies, H218O‐exchange experiments, and the use of peroxyphenylacetic acid as a mechanistic probe. Moreover, it has been observed that the participation of MnV?O, MnIV?O, and MnIII? OOC(O)R can be controlled by changing the substrate concentration. This mechanism provides the greatest congruity with related oxidation reactions that employ certain Mn complexes as catalysts. 相似文献
106.
Min Ju Cho U Ra Lee Youn Sun Kim Jicheol Shin Young Min Kim Young Wook Park Byeong‐Kwon Ju Jung‐Il Jin Dong Hoon Choi 《Journal of polymer science. Part A, Polymer chemistry》2010,48(9):1913-1918
A functionalized deoxyribonucleic acid (Cz‐DNA) was prepared with carbazolyl ammonium lipid as a triplet host material for phosphorescent material system. It is soluble in organic solvents, which facilitates the sample preparation for the absorption and luminescent properties in solid states. A highly soluble iridium complex, Ir(Cz‐ppy)3 with carbazolyl‐substituted 2‐phenylpyridine ligands was employed for studying the phosphorescence in Cz‐DNA. There is a good overlap between the photoluminescence spectrum of Cz‐DNA and the metal‐to‐ligand charge transfer (MLCT) absorption bands of the iridium complex. This overlap enables efficient energy transfer from the excited state in the host to the MLCT band of Ir(Cz‐ppy)3. In addition, photoluminescence quantum yield of Cz‐DNA was found to be relatively larger than the copolymer (PCzSt) with vinylcarbazole and styrene. Thus, Cz‐DNA was employed as a triplet host material for fabricating multilayered electrophosphorescence devices via modification of its property by doping 5,4‐tert‐butylhexyl‐1,3,4‐oxadiazole (PBD). After doping 30 wt % PBD and 10 wt % Ir(Cz‐ppy)3 into Cz‐DNA, we achieved much improvement in electron injection/transport from an adjacent carrier transport layer, resulting in much improved device performances. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 1913–1918, 2010 相似文献
107.
Min‐Jung Lee Moon Seong Kang Min‐Ki Shin Jong‐Won Park Dae Sung Chung Chan Eun Park Soon‐Ki Kwon Yun‐Hi Kim 《Journal of polymer science. Part A, Polymer chemistry》2010,48(18):3942-3949
New amorphous semiconducting copolymers, poly(9,9‐dialkylfluorene)‐alt‐(3‐dodecylthienyl‐divinylbenzene‐3‐dodecylthienyl) derivatives (PEFTVB and POFTVB), were designed, synthesized, and characterized. The structure of copolymers was confirmed by H NMR, IR, and elemental analysis. The copolymers showed very good solubility in organic solvents and high thermal stability with high Tg of 178–185 °C. The weight average molecular weight was found to be 107,900 with polydispersity of 3.14 for PEFTVB and 76,700 with that of 3.31 for POFTVB. UV–vis absorption studies showed the maximum absorption at 428 nm (in solution) and 435 nm (in film) for PEFTVB and at 430 nm (in solution) and 436 nm (in film) for POFTVB. Photoluminescence studies showed the emission at 498 nm (in solution) and 557 nm (in film) for PEFTVB and at 498 nm (in solution) and 536 nm (in film) for POFTVB. The solution‐processed thin‐film transistors showed the carrier mobility of 2 × 10?4 cm2 V?1 s?1 for PEFTVB‐based devices and 2 × 10?5 cm2 V?1 s?1 for POFTVB‐based devices. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 3942–3949, 2010 相似文献
108.
MD. Daloar Hossain Le Thi Bao Tran Jong Myung Park Kwon Taek Lim 《Journal of polymer science. Part A, Polymer chemistry》2010,48(22):4958-4964
A new, efficient method for synthesizing stable nanoparticles with poly(ethylene oxide) (PEO) functionalities on the core surface, in which the micellization and crosslinking reactions occur in one pot, has been developed. First, amphiphilic PEO‐b‐PS copolymers were synthesized by reversible addition fragmentation chain transfer (RAFT) radical polymerization of styrene using (PEO)‐based trithiocarbonate as a macro‐RAFT agent. The low molecular weight PEO‐b‐PS copolymer was dissolved in isopropyl alcohol where the block copolymer self‐assembled as core‐shell micelles, and then the core‐shell interface crosslink was performed using divinylbenzene as a crosslinking agent and 2,2′‐azobisisobutyronitrile as an initiator. The design of the amphiphilic RAFT agent is critical for the successful preparation of core‐shell interface crosslinked micellar nanoparticles, because of RAFT functional groups interconnect PEO and polystyrene blocks. The PEO functionality of the nanoparticles surface was confirmed by 1H NMR and FTIR. The size and morphology of the nanoparticles was confirmed by scanning electron microscopy, transmission electron microscopy, and dynamic laser light scattering analysis. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2010 相似文献
109.
Kwon Y Choi S Anantharaju N Lee J Panchagnula MV Patankar NA 《Langmuir : the ACS journal of surfaces and colloids》2010,26(22):17528-17531
The utility of the Cassie-Baxter formula to predict the apparent contact angle of a drop on rough hydrophobic surfaces has been questioned recently. To resolve this issue, experimental and numerical data for advancing and receding contact angles are reported. In all cases considered it is seen that contact angles follow the overall trend of the Cassie-Baxter formula, except for the advancing front on pillar type roughness. It is shown that deviations from the Cassie-Baxter angle have a one-to-one correlation with microscopic distortions of the contact line with respect to its configuration in the Cassie-Baxter state. 相似文献
110.