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141.
Koji Yamamoto Kazuki Higuchi Masahiro Ogawa Hiromitsu Sogawa Shigeki Kuwata Yoshihiro Hayashi Susumu Kawauchi Toshikazu Takata 《化学:亚洲杂志》2020,15(3):356-359
We synthesised palladium and platinum complexes possessing cyclic and acyclic pincer‐type polyaromatic ligands and investigated their structural effect on the catalysis. The pincer‐type bis(6‐arylpyridin‐2‐yl)benzene skeleton was constructed via Kröhnke pyridine synthesis under transition metal‐free conditions on gram‐scale quantity. Ligand structure significantly influenced catalytic activity toward the platinum‐catalysed hydrosilylation of diphenyl acetylenes, despite the ligand‐independence of the conformations and electronic properties of these complexes. 相似文献
142.
Simultaneous Delamination and Rutile Formation on the Surface of Ti3C2Tx MXene for Copper Adsorption
In this work, we studied the formation of the rutile phase of titanium dioxide (TiO2) on delaminated MXene (d‐Ti3C2Tx) flakes by the reaction of Ti3C2Tx with amino acids in water. Three types of amino acids with varied side‐chain polarity were used to delaminate Ti3C2Tx. d‐Ti3C2Tx flakes formed stable colloidal solutions due to the negative surface charges of chemisorbed amino acids on the d‐Ti3C2Tx. Rutile formed on d‐Ti3C2Tx at room temperature upon the intercalation of aromatic amino acids and subsequent sonication of the solution, while flakes intercalated with aliphatic amino acids did not oxidize. X‐Ray diffraction (XRD), transmission electron microscopy (TEM) and Raman spectroscopy revealed the nanosize rutile formation on the surface of Ti3C2Tx flakes. The XPS results indicated the surface functionalization of histidine on d‐Ti3C2Tx flakes. As‐synthesized histidine functionalized rutile TiO2@d‐Ti3C2Tx hybrid was used for adsorption of Cu2+ ions from aqueous solution with a maximum uptake of 95 mg g?1. 相似文献
143.
Hidemasa Azuma Yuzuru Katagiri Shinichi Yamabe 《Journal of polymer science. Part A, Polymer chemistry》1996,34(8):1407-1414
Transition states (TSs) of radical addition homopolymerization reactions of methyl acrylate, methyl methacrylate, dimethyl itaconate, and N-methyl itaconimide were examined with two-unit radical models using MOPAC (PM3 UHF) semiempirical method. Calculated activation energies (Eas) show good correlations with experimental values. Calculated activation entropies (−ΔS‡s) are found to be well proportional to Eas. The entropy terms play an important role as well as Ea in radical additions. Ea depends on the angle (θrs) between reaction points of radical and of monomer at TS. The bond length between reaction points at TS is constant regardless of monomers studied. The geometries and thermodynamical properties calculated here for TS indicate the importance of steric effects caused by substituted group(s) rather than electronic perturbation energies reported previously. © 1996 John Wiley & Sons, Inc. 相似文献
144.
Shinichi Kinugasa Hisae Nakahara Jun-Ichi Kawahara Yoshinori Koga Haruo Takaya 《Journal of Polymer Science.Polymer Physics》1996,34(3):583-586
Static light scattering measurements were performed on dilute solutions of monodisperse poly(ethylene oxide) (PEO) in methanol at 25°C. PEOs of five different molecular weights ranging from nominal Mw = 8.6 × 104 to 9.13 × 105 were used. Linear Zimm plots were obtained for all the PEO samples: no downturn was observed at small angles, indicating that no large aggregates of PEO molecules exist in the solution. From the plots, values of the weight-average molecular weight, Mw, the radius gyration, RG, and the second virial coefficient, A2, were successfully determined for respective PEOs. Observed relationship between RG and Mw indicates that methanol is certainly a good solvent for the polymer. © 1996 John Wiley & Sons, Inc. 相似文献
145.
Claudia Valverde Larissa Alexandrova Esbaide Adem Takeshi Ogawa D. V. G. L. N. Rao 《先进技术聚合物》1996,7(1):27-30
Some new octa-3,5-diynylene diurethanes were prepared using 3-butyn-1-ol, and all were found to be highly light-sensitive and to undergo topochemical polymerization on exposure to irradiation. The di-n-octyldiurethane was mixed with vinyl polymers such as poly(vinyl acetate) and poly(N,N-dimethylamino-ethyl methacrylate) and the mixtures were made into thin films by spin coating. The films were then irradiated by an electron beam to polymerize the diacetylene. The purple films thus obtained showed third-order nonlinear susceptibility, χ(3), of the order of 10−10–10−11 e.s.u. 相似文献
146.
Masahito Sekiguchi Hiromichi Tanaka Noriaki Takami Akiya Ogawa Ilhyong Ryu Noboru Sonoda 《Heteroatom Chemistry》1991,2(3):427-430
The reduction of elemental selenium by samarium diiodide led to selective formation of selenolate anion species (Se2− and Se22−), the alkylation of which provided dialkyl selenides and diselenides, respectively, in excellent yields. 相似文献
147.
148.
Satoshi Ogawa Yutaka Masutomi Naomichi Furukawa Tomoki Erata 《Heteroatom Chemistry》1992,3(4):423-429
Diaryl tellurides undergo rapid ligand exchange and disproportionation reactions on treatment with phenyllithium at −78°C. Triarylteliuranes [10-Te-3(C3)]− Li+ were identified as discrete intermediates during the reactions by 125Te, 1H, 13C, and CH-COSY NMR studies. 相似文献
149.
150.