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101.
Takafumi Osuga Takashi Murase Manabu Hoshino Makoto Fujita 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2014,126(42):11368-11371
A tray‐shaped PdII3AuI3 complex ( 1 ) is prepared from 3,5‐bis(3‐pyridyl)pyrazole by means of tricyclization with AuI followed by PdII clipping. Tray 1 is an efficient scaffold for the modular assembly of [3×n] AuI clusters. Treatment of 1 with the AuI3 tricyclic guest 2 in H2O/CH3CN (7:3) or H2O results in the selective formation of a [3×2] cluster ( 1 ⋅ 2 ) or a [3×3] cluster ( 1 ⋅ 2 ⋅ 1 ), respectively. Upon subsequent addition of AgI ions, these complexes are converted to an unprecedented Au3–Au3–Ag–Au3–Au3 metal ion cluster. 相似文献
102.
Reactive acrylate esters were encapsulated in the cavity of networked molecular capsules in a single‐crystal‐to‐single‐crystal fashion. Owing to the encapsulation effect, acrylates inside the capsules do not undergo polymerization upon irradiation with UV light or heating, while the guest molecules can be quantitatively extracted by treatment with toluene. 相似文献
103.
Brian N. DiMarco Dmitry E. Polyansky David C. Grills Ping Wang Yutaka Kuwahara Xuan Zhao Etsuko Fujita 《Chemphyschem》2021,22(14):1478-1487
In this work, the differences in catalytic performance for a series of Co hydrogen evolution catalysts with different pentadentate polypyridyl ligands (L), have been rationalized by examining elementary steps of the catalytic cycle using a combination of electrochemical and transient pulse radiolysis (PR) studies in aqueous solution. Solvolysis of the [CoII−Cl]+ species results in the formation of [CoII(κ4-L)(OH2)]2+. Further reduction produces [CoI(κ4-L)(OH2)]+, which undergoes a rate-limiting structural rearrangement to [CoI(κ5-L)]+ before being protonated to form [CoIII−H]2+. The rate of [CoIII−H]2+ formation is similar for all complexes in the series. Using E1/2 values of various Co species and pKa values of [CoIII−H]2+ estimated from PR experiments, we found that while the protonation of [CoIII−H]2+ is unfavorable, [CoII−H]+ reacts with protons to produce H2. The catalytic activity for H2 evolution tracks the hydricity of the [CoII−H]+ intermediate. 相似文献
104.
Byelikov A Adachi T Fujita H Fujita K Fujita Y Hatanaka K Heger A Kalmykov Y Kawase K Langanke K Martínez-Pinedo G Nakanishi K von Neumann-Cosel P Neveling R Richter A Sakamoto N Sakemi Y Shevchenko A Shimbara Y Shimizu Y Smit FD Tameshige Y Tamii A Woosley SE Yosoi M 《Physical review letters》2007,98(8):082501
The Gamow-Teller strength distributions below the particle threshold in 138La and 180Ta, deduced from high-resolution measurements of the (3He,t) reaction at 0 degrees, allow us to evaluate the role of charged-current reactions for the production of these extremely rare nuclides in neutrino-nucleosynthesis models. The analysis suggests that essentially all 138La in the Universe can be made that way. Neutrino nucleosynthesis also contributes significantly to the abundance of 180Ta but the magnitude depends on the unknown branching ratio for population of the long-lived isomer. 相似文献
105.
Dual Catalysis with Copper and Rhenium for Trifluoromethylation of Propargylic Alcohols: Efficient Synthesis of α‐Trifluoromethylated Enones
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Dr. Hiromichi Egami Takafumi Ide Masashi Fujita Toshifumi Tojo Prof.Dr. Yoshitaka Hamashima Prof.Dr. Mikiko Sodeoka 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(38):12061-12065
Trifluoromethylation of propargylic alcohols to provide (Z)‐α‐trifluoromethylated enones and β‐unsubstituted α‐trifluoromethylated enones proceeded with high yield and selectivity in the presence of CuI/Re2O7. The Z isomer was formed under kinetic control, though it is less stable than the E isomer in terms of steric repulsion. 相似文献
106.
Dr. Yoshikazu Ito Dr. Yoichi Tanabe Dr. H.‐J. Qiu Dr. Katsuaki Sugawara Dr. Satoshi Heguri Dr. Ngoc Han Tu Dr. Khuong Kim Huynh Dr. Takeshi Fujita Prof. Takashi Takahashi Prof. Katsumi Tanigaki Prof. Mingwei Chen 《Angewandte Chemie (International ed. in English)》2014,53(19):4822-4826
We report three‐dimensional (3D) nanoporous graphene with preserved 2D electronic properties, tunable pore sizes, and high electron mobility for electronic applications. The complex 3D network comprised of interconnected graphene retains a 2D coherent electron system of massless Dirac fermions. The transport properties of the nanoporous graphene show a semiconducting behavior and strong pore‐size dependence, together with unique angular independence. The free‐standing, large‐scale nanoporous graphene with 2D electronic properties and high electron mobility holds great promise for practical applications in 3D electronic devices. 相似文献
107.
Dr. Qing‐Fu Sun Dr. Sota Sato Prof. Dr. Makoto Fujita 《Angewandte Chemie (International ed. in English)》2014,53(49):13510-13513
In the self‐assembly of PdII ions and two different, but similarly shaped, ligands ( 1 and 2 ), neither random mixing nor self‐sorting of the two ligands into two unmixed structures was observed. Instead a mixed, yet sorted, Pd12( 1 )12( 2 )12 cantellated tetrahedron (and its pseudoisomer) was selectively formed, thus revealing a fine example of intramolecular self‐sorting. A case study showed that a homothetic ratio of >2 is necessary to observe cantellated tetrahedra. 相似文献
108.
Shinsaku Fujita 《Journal of mathematical chemistry》2014,52(7):1717-1750
After the RS-stereoisomeric group \(\mathbf{D}_{2d\widetilde{\sigma }\widehat{I}}\) of order 16 has been defined by starting point group \(\mathbf{D}_{2d}\) of order 8, the isomorphism between \(\mathbf{D}_{2d\widetilde{\sigma }\widehat{I}}\) and the point group \(\mathbf{D}_{4h}\) of order 16 is thoroughly discussed. The non-redundant set of subgroups (SSG) of \(\mathbf{D}_{2d\widetilde{\sigma }\widehat{I}}\) is obtained by referring to the non-redundant set of subgroups of \(\mathbf{D}_{4h}\) . The coset representation for characterizing the orbit of the four positions of an allene skeleton is clarified to be \(\mathbf{D}_{2d\widetilde{\sigma }\widehat{I}}(/\mathbf{C}_{s\widetilde{\sigma }\widehat{I}})\) , which is closely related to the \(\mathbf{D}_{4h}(/\mathbf{C}_{2v}^{\prime \prime \prime })\) . According to the unit-subduced-cycle-index (USCI) approach (Fujita, Symmetry and combinatorial enumeration of chemistry. Springer, Berlin 1991), the subduction of \(\mathbf{D}_{2d\widetilde{\sigma }\widehat{I}}(/\mathbf{C}_{s\widetilde{\sigma }\widehat{I}})\) is examined so as to generate unit subduced cycle indices with chirality fittingness (USCI-CFs). Then, the fixed-point matrix method of the USCI approach is applied to the USCI-CFs. Thereby, the numbers of quadruplets are calculated in an itemized fashion with respect to the subgroups of \(\mathbf{D}_{2d\widetilde{\sigma }\widehat{I}}\) . After the subgroups of \(\mathbf{D}_{2d\widetilde{\sigma }\widehat{I}}\) are categorized into types I–V, type-itemized enumeration of quadruplets is conducted to illustrate the versatility of the stereoisogram approach. 相似文献
109.
Dr. Takaaki Mitsuhashi Dr. Lena Barra Zachary Powers Volga Kojasoy Andrea Cheng Feng Yang Dr. Yoshimasa Taniguchi Dr. Takashi Kikuchi Prof. Dr. Makoto Fujita Prof. Dr. Dean J. Tantillo Prof. Dr. John A. Porco Jr Prof. Dr. Ikuro Abe 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(52):23980-23989
Fungal meroterpenoids are a diverse group of hybrid natural products with impressive structural complexity and high potential as drug candidates. In this work, we evaluate the promiscuity of the early structure diversity-generating step in fungal meroterpenoid biosynthetic pathways: the multibond-forming polyene cyclizations catalyzed by the yet poorly understood family of fungal meroterpenoid cyclases. In total, 12 unnatural meroterpenoids were accessed chemoenzymatically using synthetic substrates. Their complex structures were determined by 2D NMR studies as well as crystalline-sponge-based X-ray diffraction analyses. The results obtained revealed a high degree of enzyme promiscuity and experimental results which together with quantum chemical calculations provided a deeper insight into the catalytic activity of this new family of non-canonical, terpene cyclases. The knowledge obtained paves the way to design and engineer artificial pathways towards second generation meroterpenoids with valuable bioactivities based on combinatorial biosynthetic strategies. 相似文献
110.
Adil Anwar Hiba Anwar Takeshi Yamauchi Ryan Tseng Rajesh Agarwal Lawrence D Horwitz Zili Zhai Mayumi Fujita 《Photochemistry and photobiology》2020,96(4):870-876
Ultraviolet B (UVB) radiation is known as a culprit in skin carcinogenesis. We have previously reported that bucillamine (N-[2-mercapto-2-methylpropionyl]-L-cysteine), a cysteine derivative with antioxidant and anti-inflammatory capacity, protects against UVB-induced p53 activation and inflammatory responses in mouse skin. Since MAPK signaling pathways regulate p53 expression and activation, here we determined bucillamine effect on UVB-mediated MAPK activation in vitro using human skin keratinocyte cell line HaCaT and in vivo using SKH-1 hairless mouse skin. A single low dose of UVB (30 mJ cm−2) resulted in increased JNK/MAPK phosphorylation and caspase-3 cleavage in HaCaT cells. However, JNK activation and casaspe-3 cleavage were inhibited by pretreatment of HaCaT cells with physiological doses of bucillamine (25 and 100 µm ). Consistent with these results, bucillamine pretreatment in mice (20 mg kg−1) inhibited JNK/MAPK and ERK/MAPK activation in skin epidermal cells at 6–12 and 24 h, respectively, after UVB exposure. Moreover, bucillamine attenuated UVB-induced Ki-67-positive cells and cleaved caspase-3-positive cells in mouse skin. These findings demonstrate that bucillamine inhibits UVB-induced MAPK signaling, cell proliferation and apoptosis. Together with our previous report, we provide evidence that bucillamine has a photoprotective effect against UV exposure. 相似文献