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991.
Ting Feng Xin Li Yuan‐Yuan An Sha Bai Li‐Ying Sun Yang Li Yao‐Yu Wang Ying‐Feng Han 《Angewandte Chemie (International ed. in English)》2020,59(32):13516-13520
The efficient backbone‐directed self‐assembly of cyclic metalla[3]catenanes by the combination of tetrachloroperylenediimide (TCPDI)‐based dinuclear rhodium(III) clips and 4,4′‐diazopyridine or 4,4′‐dipyridylethylene ligands is realized in a single‐step strategy. The topology and coordination geometry of the cyclic metalla[3]catenanes are characterized by NMR spectroscopy, ESI‐TOF‐MS spectrometry, UV/Vis‐NIR spectroscopy, and X‐ray diffraction studies. The most remarkable feature of the formed cyclic metalla[3]catenane is that it contains π‐aggregates (ca. 2.6 nm) incorporating six TCPDIs. Further studies revealed that cyclic metalla[3]catenanes can be converted reversibly to their corresponding sodium adducts and precursor building blocks, respectively. This strategy opens the possibility of generating unique supramolecular structures from discrete functional π‐aggregates with precise arrangements. 相似文献
992.
Mahalingam Vanjinathan Hong‐Cheu Lin A. Sultan Nasar 《Journal of polymer science. Part A, Polymer chemistry》2012,50(18):3806-3818
A series of conjugated hyperbranched polymers, hyperbranched copolymers, and linear polymers containing 2‐pyran‐4‐ylidenemalononitrile (acceptor) and triphenylamine/fluorene (donor) units were synthesized and characterized by FTIR, 1H NMR, thermogravimetric analyses, differential scanning calorimetry, gel permeation chromatography, UV–visible, photoluminescence, and cyclic voltammetry measurements. All the polymers show red‐light emission in the range of 566–656 nm both in solution and in solid state. The quantum efficiency of the polymers was in the range of 56–82%. Among the six polymers synthesized, only polymers containing fluorene units show Tg and polymers based on triphenylamine not exhibit Tg. The band gap of these polymers were found to be reasonably low; hyperbranched copolymer containing fluorene unit shows lowest band gap of 2.18 eV due to the stabilization of LUMO energy level by the electron withdrawing ? CN groups. The thermal and solubility behavior of the polymers were found to be good. All the EL spectra of the devices (indium‐tin oxide/poly(3,4‐ethylenedioxythiophene):poly(styrenesulfonate)/polymer/2,9‐dimethyl‐4,7‐diphenyl‐1,10‐phenanthroline/tris(8‐hydroxyquinoline)aluminum)/LiF/Al) show red‐light emission, and the device fabricated with P3 and P4 shows maximum luminance and luminous efficiency of 4104 cd m?2 and 0.55 cd Å?1 and 3696 cd m?2 and 0.47 cd Å?1, respectively, indicates that they had the best carrier balance. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012 相似文献
993.
A highly hydrophobic cyclic peptide GG-110824,cyclo(Gly-Leu-Val-Leu-LeuVal-Pro-Ile-Gly-Leu)(C49H86N10O10),has been synthesized by a strategy combined with solid-phase synthesis(SPPS) of linear peptide and cyclization in solution.The structure including the absolute configuration of synthesized GG-110824 was confirmed by CuK radiation X-ray crystallography in the monoclinic system,space group P21 with a = 11.4966(10),b = 18.5286(2),c = 13.3943(10),= 95.03o,V = 2842.20(4)3,F(000) = 1080 and Z = 2. 相似文献
994.
X‐ray structures,spectroscopic, electrochemical,thermal, antibacterial,and DFT studies of two nickel(II) and cobalt(III) complexes constructed from a new quinazoline‐type ligand 下载免费PDF全文
Two two‐dimensional supramolecular Nickel(II) and Cobalt(III) complexes, [Ni( L 2 )2]·2CH3OH ( 1 ) and [2Co( L 2 )2] ( 2 ) ( HL 2 = 1‐(2‐{[(E)‐3‐bromo‐5‐chloro‐2‐hydroxybenzylidene]amino}phenyl)ethanone oxime), were synthesized via complexation of salts acetate with HL 1 (2‐(3‐bromo‐5‐chloro‐2‐hydroxyphenyl)‐4‐methyl‐1,2‐dihydroquinazoline 3‐oxide, H is the deprotonatable hydrogen). During the reaction, the C–N bond in HL 1 is converted into the C=N–OH group in HL 2 . The spectroscopic data of both complexes were compared with the ligand HL 1 . HL 1 and both complexes were determined by single‐crystal X‐ray crystallography. The differently geometric features of the obtained complexes 1 and 2 are observed. In the crystal structure, 1 and 2 form an infinite 1‐D chain‐like and 2‐D supramolecular frameworks. EPR spectroscopy of 2 was investigated. Moreover, electrochemical properties and antimicrobial activities of both complexes were also studied. In addition, the calculated HOMO and LUMO energies show the character of HL 1 , complexes 1 and 2 . The electronic transitions and spectral features of HL 1 and both complexes were discussed by TD‐DFT calculations. 相似文献
995.
Yu Xuan Hu Dr. Jing Zhang Fangfang Zhang Xiaoyan Wang Prof. Dr. Jun Yin Prof. Dr. František Hartl Prof. Dr. Sheng Hua Liu 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(20):4567-4575
Four cyclometalated diiridium complexes, with IrCp*Cl (Cp*=η5-C5Me5−) termini bridged by 1,4- and 1,3-bis(p-tolyliminoethyl)benzene ( 1 , 2 ), or 1,4- and 1,3-bis(2-pyridyl)benzene ( 3 , 4 ), were prepared and characterized by nuclear magnetic resonance (NMR) spectroscopy and single-crystal X-ray diffraction (complexes 1 , 2 , and 4 ). The two iridium centers in complexes 1 and 3 are thus bound at the central benzene ring in the para-position (trans-Ir2), whereas those in complexes 2 and 4 are in the meta-position (cis-Ir2). Cyclic voltammograms of all four complexes show two consecutive one-electron oxidations. The potential difference between the two anodic steps in 1 and 3 is distinctly larger than that for 2 and 4 . The visible–near-infrared (NIR)–short-wave infrared (SWIR) absorption spectra of trans-Ir2 monocations 1 + and 3 + are markedly different from those of cis-Ir2 monocations 2 + and 4 +. Notably, strong near-infrared electronic absorption appears only in the spectra of 1 + and 3 + whereas 2 + and 4 + absorb only weakly in the NIR-SWIR region. Combined DFT and TD-DFT calculations have revealed that (a) 1 + and 3 + (the diiridium-benzene trans-isomers) display the highest occupied spin-orbitals (HOSO) and the lowest unoccupied spin-orbital (LUSO) evenly delocalized over both molecule halves, and (b) their electronic absorptions in the NIR-SWIR region are attributed to mixed metal-to-ligand and ligand-to-ligand charge transfers (MLCT and LLCT). In contrast, cis-isomers 2 + and 4 + do not feature this stabilizing π-delocalization but a localized mixed-valence state showing a weak intervalence charge-transfer (IVCT) absorption in the SWIR region. 相似文献
996.
Virginie Lair Amandine Calmet Valrie Albin Sophie Griveau Michel Cassir 《Electroanalysis》2019,31(1):22-30
Small fiber peripheral neuropathy is an early complication of diabetes. Electric skin response to some stimulus, as electrochemical skin conductance ECS, is a promising route in the early follow‐up of such diseases. It is related to sweat gland innervations and their permeability to chlorides and protons; it is non‐invasive, quantitative and reproducible. In routine clinical use, it could allow to better adapt the treatments and improve the adhesion for preventing pathological progress, thus reducing colossal healthcare costs. To optimize the measurements and understand the electrochemical behavior of electrodes, an original electrolytic cell was designed in lab scale. Thereby, an electrolyte is chosen to mimic sweat composition. For achieving currents range of ESC in vivo measurements, the original idea was to play on electrolyte viscosity by adding sucrose. In this paper, the novel electrolytic lab cell is presented with its limiting kinetics processes. A model of chloride migration to the anode and global electric model dedicated to the cell are proposed. Cell parameters are thoroughly studied, e. g. the resistance, which is equivalent to the inverse of ESC, by exploiting the models and through in vitro experiments, with protocols focusing on reproducibility. This original approach establishes, inter alia, an important result: the resistance is accurately retrieved using linear voltammetry, whereas single voltage measurement fails notably and is, therefore, unsatisfactory. 相似文献
997.
Naoto Aoyagi Takeshi Endo 《Journal of polymer science. Part A, Polymer chemistry》2019,57(24):2606-2615
The bicyclic amidinium iodide effectively catalyzed the reaction of carbon dioxide and the epoxy‐containing oxetane under ordinary pressure and mild conditions with high chemoselectivity to give the corresponding oxetane monomer containing five‐membered cyclic carbonate quantitatively. The cationic ring‐opening polymerization of the obtained monomer by boron trifluoride diethyl ether proceeded to give linear polyoxetane bearing five‐membered cyclic carbonate pendant group in high yield. The molecular weight of the polyoxetane was higher than that of polyepoxide obtained by the cationic ring‐opening polymerization of epoxide monomer containing five‐membered cyclic carbonate. The cyclic carbonate functional crosslinked polyoxetanes were also synthesized by the cationic ring‐opening copolymerization of cyclic carbonate having oxetane and commercially available bisoxetane monomers. Analyses of the resulting polyoxetanes were performed by proton nuclear magnetic resonance, size exclusion chromatography, thermogravimetric analysis, and differential scanning calorimetry. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019 , 57, 2606–2615 相似文献
998.
Prof. Dr. Andreas Gansäuer Dr. Daniel von Laufenberg Dr. Christian Kube Tobias Dahmen Antonius Michelmann Dr. Maike Behlendorf Rebecca Sure Meriam Seddiqzai Prof. Dr. Stefan Grimme Dr. Dhandapani V. Sadasivam Godfred D. Fianu Prof. Dr. Robert A. Flowers II 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(1):280-289
An atom‐economical and catalytic arylation of epoxide‐derived radicals is described. The key step of the catalytic system is a sequential electron and proton transfer for the rearomatization of the radical σ‐complex and catalyst regeneration. Kinetic, computational, spectroscopic, and cyclovoltammetric investigations highlight the key issues of the reaction mechanism and catalyst stabilization by collidine hydrochloride. Studies employing radicophiles rule out the participation of cations as reactive intermediates. 相似文献
999.
Naoto Aoyagi Yoshio Furusho Takeshi Endo 《Journal of polymer science. Part A, Polymer chemistry》2013,51(5):1230-1242
Hydroiodides of secondary and primary amines effectively catalyzed the reaction of carbon dioxide and epoxides under mild conditions such as ordinary pressure and ambient temperature, to obtain the corresponding five‐membered cyclic carbonates in moderate to high yields. Detailed investigation showed that the catalytic activity was highly affected by the counter anions of the ammonium salts; the iodides catalyzed efficiently the carbonate‐forming reactions, whereas the bromide and chloride counterparts exhibited almost no catalysis. We also revealed that two important factors on the amine moieties that affected the catalytic reactions. First, the catalytic activity increased with increasing bulkiness of the substituents on the ammonium nitrogen atoms. Second, the catalysis became more efficient as the parent amines become more basic. Dicyclohexylammonium iodide was the best catalyst among the ammonium salts investigated in this study. As an application of this reaction system, we synthesized homo‐ and copolymers bearing epoxide pendant groups as substrates, which were converted with high efficiency into the corresponding homo‐ and copolymers bearing cyclic carbonate pendant groups under 1 atm at 45 °C. All polymers were easily purified simply by precipitation in water, and were isolated in high yields (>95%). © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013 相似文献
1000.