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941.
Separation of Acetylene from Carbon Dioxide and Ethylene by a Water‐Stable Microporous Metal–Organic Framework with Aligned Imidazolium Groups inside the Channels
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Jaechul Lee Chong Yang Chuah Prof. Jaheon Kim Youngsuk Kim Nakeun Ko Younggyu Seo Prof. Kimoon Kim Prof. Tae Hyun Bae Prof. Eunsung Lee 《Angewandte Chemie (International ed. in English)》2018,57(26):7869-7873
Separation of acetylene from carbon dioxide and ethylene is challenging in view of their similar sizes and physical properties. Metal–organic frameworks (MOFs) in general are strong candidates for these separations owing to the presence of functional pore surfaces that can selectively capture a specific target molecule. Here, we report a novel 3D microporous cationic framework named JCM‐1 . This structure possesses imidazolium functional groups on the pore surfaces and pyrazolate as a metal binding group, which is well known to form strong metal‐to‐ligand bonds. The selective sorption of acetylene over carbon dioxide and ethylene in JCM‐1 was successfully demonstrated by equilibrium gas adsorption analysis as well as dynamic breakthrough measurement. Furthermore, its excellent hydrolytic stability makes the separation processes highly recyclable without a substantial loss in acetylene uptake capacity. 相似文献
942.
Le Ba Vinh Nguyen Thi Minh Nguyet Seo Young Yang Jang Hoon Kim Le Thi Vien Phan Thi Thanh Huong 《Natural product research》2018,32(17):2001-2007
Eight compounds were isolated from the leaves of Clerodendrum inerme, including one new rearranged abietane diterpene, crolerodendrum B (1). Their structures were determined by means of spectroscopic methods including one-dimensional and two-dimensional nuclear magnetic resonance (1-D and 2-DNMR), high-resolution electrospray ionisation mass spectrometry (HR-ESI-MS) and circular dichroism (CD). The DPPH radical scavenging and cytotoxic activities of isolated compounds against MCF7 (breast), HCT116 (colon) and B16F10 (melanoma) cancer cell lines were evaluated. Compounds 1, 3 and 4 exhibited strong DPPH radical-scavenging effects (ED50 values of 17.6 ± 2.1, 10.1 ± 0.8 and 11.3 ± 0.3 μM, respectively) and 4 showed strong cytotoxicity against the HCT116 cell line (IC50 = 3.46 ± 0.01 μM). 相似文献
943.
Enantioselective Denitrogenative Annulation of 1H‐Tetrazoles with Styrenes Catalyzed by Rhodium
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Takayuki Nakamuro Kohei Hagiwara Dr. Tomoya Miura Prof. Dr. Masahiro Murakami 《Angewandte Chemie (International ed. in English)》2018,57(19):5497-5500
Sulfonylation of 1H‐tetrazoles with triflic anhydride in the presence of chiral rhodium(II) carboxylate dimers causes denitrogenation to generate α‐azo rhodium(II) carbenoid species as new types of donor/acceptor carbenoids, which then readily react with styrenes to afford 3,5‐diaryl‐2‐pyrazolines with a high degree of enantioselectivity. 相似文献
944.
Two Aluminophosphate Molecular Sieves Built from Pairs of Enantiomeric Structural Building Units
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Seungwan Seo Taimin Yang Dr. Jiho Shin Dr. Donghui Jo Prof. Xiaodong Zou Prof. Suk Bong Hong 《Angewandte Chemie (International ed. in English)》2018,57(14):3727-3732
Herein we report the synthesis and structures of two new small‐pore aluminophosphate molecular sieves PST‐13 and PST‐14 with mutually connected 8‐ring channels. The structure of PST‐13, synthesized using diethylamine as an organic structure‐directing agent, contains penta‐coordinated framework Al atoms bridged by hydroxy groups and thus edge‐sharing 3‐ and 5‐rings. Upon calcination, PST‐13 undergoes a transformation to PST‐14 with loss of bridging hydroxy groups and occluded organic species. The structures of both materials consist “nonjointly” of pairs of previously undiscovered 1,5‐ and 1,6‐open double 4‐rings (d4rs) which are mirror images of each other. We also present a series of novel chemically feasible hypothetical structures built from 1‐open d4r (sti) or 1,3‐open d4r (nsc) units, as well as from these two enantiomeric structural building units. 相似文献
945.
Hyowon Seo Anne-Catherine Bédard Willie P. Chen Robert W. Hicklin Alexander Alabugin Timothy F. Jamison 《Tetrahedron》2018,74(25):3124-3128
Selective N-monomethylation of anilines has been achieved under continuous flow conditions using dimethyl carbonate as a green methylating agent in the presence of 1,8-diazabicyclo[5.4.0]undec-7-ene. Our methodology takes advantage of the expanded process windows available in the continuous flow regime to safely induce monomethylation in superheated solvents at high pressure. We propose selective N-monomethylation is achieved via an in situ protection-deprotection pathway, which is supported by the observed reactivities of several putative reaction intermediates. The robust and scalable method was applicable to a broad range of primary aniline substrates including ortho-, meta-, and para-substituted anilines, as well as electron-rich and electron-deficient anilines. The synthetic precursor of diazepam, 5-chloro-2-(methylamino)benzophenone, was selectively synthesized under our optimized conditions. 相似文献
946.
L. V. T. Nguyen M. J. L. Cahill A. J. Lowery D. Novak P. C. R. Gurney D. D. Sampson Dong-Sun Seo 《Optical and Quantum Electronics》1996,28(8):1067-1080
The physical mechanism attributed to producing rabbit-ears on the chirped multimode optical spectra of gain-switched Fabry-Pérot semiconductor lasers is investigated thoroughly. It has been observed experimentally that the short-wavelength rabbit-ears are dominant in the short-wavelength longitudinal modes. However, the long-wavelength rabbit-ears are dominant in the modes near the lasing wavelength, while the short-wavelength rabbit-ears are again dominant in the longest-wavelength modes. In this paper, the unequal rabbit-ears of each mode and the asymmetric chirped spectrum are shown to be a result of the dynamic power transfer between the modes during the gain-switched optical pulse due to carrier-induced modal intermodulation. Such an understanding, and the ability to model accurately this characteristic, is also shown to be essential for designing Fabry-Pérot laser systems, for short-haul applications such as fibre-to-the-home. 相似文献
947.
Jin Keun Seo 《Journal of Fourier Analysis and Applications》1995,2(3):227-235
Let
be a smooth domain in R2 containing a polygon D. The inverse conductivity problem to the the elliptic equation
is considered. We show that D is uniquely determined from boundary measurements corresponding two appropriately chosen Neumann
datas. 相似文献
948.
949.
Alkynyl heteroaromatic compounds reacted with arylboronic acids to give addition products in the presence of a rhodium catalyst. The best results were obtained when a novel pyridine-substituted water-soluble phosphine ligand was used. The reactions proceed to give trisubstituted alkenes from various arylboronic acids and alkynyl heteroaromatic compounds with high regioselectivity. Only alkynes with a nitrogen atom in proximity to the triple bond were converted to the corresponding alkenes, as expected for a chelation-controlled addition. 相似文献
950.
The crystal structure of an ethylene sorption complex of fully vacuum-dehydrated fully Ag(+)-exchanged zeolite X (FAU), a = 24.865(2) A, has been determined by single-crystal X-ray diffraction techniques in the cubic space group Fd at 21 degrees C. It is very different from the ethylene complex of Ag(92)-X that had been dehydrated at 400 degrees C in flowing oxygen, as were the two dehydrated structures. The crystal was prepared by ion exchange in a flowing stream of aqueous 0.05 M AgNO(3) for 3 days, followed by dehydration at 400 degrees C and 2 x 10(-6) Torr for 2 days, followed by exposure to 300 Torr of zeolitically dry ethylene gas for 2 h at 21 degrees C. The structure was determined in this atmosphere and was refined using all data to the final error indices (based upon the 534 reflections for which F(o) > 4sigma(F(o))) R(1) = 0.062 and wR(2) = 0.135. In this structure, per unit cell, 14 Ag(+) ions were found at the octahedral site I (Ag-O = 2.611(9) A), and 32 partially reduced Ag(+) ions fill two different site I' positions deep in the sodalite cavities (Ag-O = 2.601(13) and 2.618(12) A). The sodalite cavities host two different cationic silver clusters. In about 47% of sodalite units, eight silver atoms form interpenetrating tetrahedra, Ag(8)(n+) (n = 4 is suggested), with T(d)() symmetry. The other 53% of the sodalite units host cyclo-Ag(4)(m+) (m = 2 is suggested) cations with near S(4) symmetry. These clusters are very similar to those in vacuum-dehydrated Ag(92)-X. Thirty-two Ag(+) ions fill the single 6-rings, 15 at site II' (Ag-O = 2.492(10) A), and 17 at site II (Ag-O = 2.460(9) A). The latter 17 lie in supercages where each forms a lateral pi-complex with an ethylene molecule. In turn, each C(2)H(4) molecule forms two cis electrostatic hydrogen bonds to framework oxygens. The remaining 14 Ag+ ions occupy three different II' sites. Vacuum dehydration had caused substantial decomposition: per unit cell, 30 of the 92 Ag(+) ions were reduced and 15 of the 384 framework oxide ions were oxidized to O2(g), leaving lattice vacancies. The sorption of C(2)H(4) at 21 degrees C reoxidized about 7 of the 30 Ag(0) atoms to Ag(+) and reduced 1.75 ethylene molecules to give CH(2)(2-) groups which refilled 3.5 of these 15 lattice vacancies. The remaining vacancies may have been filled with H(2)C=C(2-) ions. The unit cell formula, which originally contained 384 oxygen atoms, may be |Ag(92)(C2H4)17|[Si(100)Al(92)O(369)(CH2)3.5] or |Ag(92)H(23)(C2H4)17|[Si(100)Al(92)O(369)(CH2)3.5(C2H2)11.5]. 相似文献