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Jun-Ichiro Makiura Takuma Higo Yutaro Kurosawa Kota Murakami Shuhei Ogo Hideaki Tsuneki Yasushi Hashimoto Yasushi Sato Yasushi Sekine 《Chemical science》2021,12(6):2108
Efficient activation of CO2 at low temperature was achieved by reverse water–gas shift via chemical looping (RWGS-CL) by virtue of fast oxygen ion migration in a Cu–In structured oxide, even at lower temperatures. Results show that a novel Cu–In2O3 structured oxide can show a remarkably higher CO2 splitting rate than ever reported. Various analyses revealed that RWGS-CL on Cu–In2O3 is derived from redox between Cu–In2O3 and Cu–In alloy. Key factors for high CO2 splitting rate were fast migration of oxide ions in the alloy and the preferential oxidation of the interface of alloy–In2O3 in the bulk of the particles. The findings reported herein can open up new avenues to achieve effective CO2 conversion at lower temperatures.Efficient activation of CO2 at low temperature was achieved by reverse water–gas shift via chemical looping (RWGS-CL) by virtue of fast oxygen ion migration in a Cu–In structured oxide, even at lower temperatures. 相似文献
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Self‐Replication and Amplification of Enantiomeric Excess of Chiral Multifunctionalized Large Molecules by Asymmetric Autocatalysis 下载免费PDF全文
Prof. Dr. Tsuneomi Kawasaki Mai Nakaoda Yutaro Takahashi Yusuke Kanto Nanako Kuruhara Kenji Hosoi Prof. Dr. Itaru Sato Arimasa Matsumoto Prof. Dr. Kenso Soai 《Angewandte Chemie (International ed. in English)》2014,53(42):11199-11202
Self‐replication of large chiral molecular architectures is one of the great challenges and interests in synthetic, systems, and prebiotic chemistry. Described herein is a new chemical system in which large chiral multifunctionalized molecules possess asymmetric autocatalytic self‐replicating and self‐improving abilities, that is, improvement of their enantioenrichment in addition to the diastereomeric ratio. The large chiral multifunctionalized molecules catalyze the production of themselves with the same structure, including the chirality of newly formed asymmetric carbon atoms, in the reaction of the corresponding achiral aldehydes and reagent. The chirality of the large multifunctionalized molecules controlled the enantioselectivity of the reaction in a highly selective manner to construct multiple asymmetric stereogenic centers in a single reaction. 相似文献
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Masatomo Sumiya Yutaro Kamo Masaki Takeguchi Hideki Yoshikawa Keisuke Kobayashi Minoru Hagino Shunro Fuke 《Applied Surface Science》2010,256(14):4442-4446
Photocathode devices operating in reflection-mode, where the photoemission is detected on the same side as the light irradiation, were developed for the detection of deep ultraviolet light by using p-AlxGa1−xN films grown on Si(1 1 1) substrates. The external quantum efficiencies were as high as 20-15% at 200 nm and 280 nm, while the value was as low as 10−2% at 310 nm. The on-off ratio was more than four orders of magnitude, which represents high solar-blind sensitivity. The escape probability of AlxGa1−xN photocathode was decreased with increase of AlN mole fraction. The effective barrier potential against the photoelectron emission near the surface was reduced due to the upward shift of conduction band of AlxGa1−xN. The photoemission from the AlxGa1−xN films terminated with Cs-O adatoms will be discussed in terms of band diagrams that were evaluated by hard X-ray photoelectron spectroscopy. 相似文献
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Hirofumi Yamamoto Yuichi Takagi Naoto Yamasaki Tadashi Mitsuyama Yusuke Kasai Hiroshi Imagawa Yutaro Kinoshita Naohiro Oka Masanori Hiraoka 《Tetrahedron》2018,74(50):7173-7178
Thallusin is the only known natural product that induces cell differentiation followed by formation of a thallus during the growth of green macroalgae such as Monostroma and Ulva. Herein, various thallusin analogues based on the terpen skeleton were synthesized to study the structure?activity relationships of thallusin. The potency of the synthetic analogues was investigated in an experimental assay, which demonstrated that the 19-methyl group in thallusin is essential for potent morphogenesis-inducing activity. 相似文献
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Near‐Infrared Light‐Driven Hydrogen Evolution from Water Using a Polypyridyl Triruthenium Photosensitizer 下载免费PDF全文
Yutaro Tsuji Keiya Yamamoto Dr. Kosei Yamauchi Prof. Ken Sakai 《Angewandte Chemie (International ed. in English)》2018,57(1):208-212
In order to realize artificial photosynthetic devices for splitting water to H2 and O2 (2 H2O+hν→2 H2+O2), it is desirable to use a wider wavelength range of light that extends to a lower energy region of the solar spectrum. Here we report a triruthenium photosensitizer [Ru3(dmbpy)6(μ‐HAT)]6+ (dmbpy=4,4′‐dimethyl‐2,2′‐bipyridine, HAT=1,4,5,8,9,12‐hexaazatriphenylene), which absorbs near‐infrared light up to 800 nm based on its metal‐to‐ligand charge transfer (1MLCT) transition. Importantly, [Ru3(dmbpy)6(μ‐HAT)]6+ is found to be the first example of a photosensitizer which can drive H2 evolution under the illumination of near‐infrared light above 700 nm. The electrochemical and photochemical studies reveal that the reductive quenching within the ion‐pair adducts of [Ru3(dmbpy)6(μ‐HAT)]6+ and ascorbate anions affords a singly reduced form of [Ru3(dmbpy)6(μ‐HAT)]6+, which is used as a reducing equivalent in the subsequent water reduction process. 相似文献
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Dr. Hayato Fukuda Yuko Nishiyama Shiina Nakamura Yutaro Ohno Prof. Dr. Tadashi Eguchi Prof. Dr. Yoshiharu Iwabuchi Prof. Dr. Takeo Usui Prof. Dr. Naoki Kanoh 《化学:亚洲杂志》2012,7(12):2872-2881
We have developed two syntheses of vicenistatin and its analogues. Our first‐generation strategy included the rapid and sequential assembly of the macrocyclic lactam by using an intermolecular Horner–Wadsworth–Emmons reaction between the C3–C13 fragment and the C1–C2, C14–C19 fragment, followed by an intramolecular Stille coupling reaction. The second‐generation strategy utilized a ring‐closing metathesis of a hexaene intermediate to generate the desired 20‐membered macrolactam. This second‐generation strategy made it possible to prepare synthetic analogues of vicenistatin, including the C20‐ and/or C23‐demethyl analogues. Evaluation of the cytotoxic effect of these analogues indicated the importance of the fixed conformation of aglycon for determining the biological activity of the vicenistatins. 相似文献