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121.
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Poly (3-alkylthiophenes) (P3ATs) have made up of a family of conductive polymerswhich are soluble, fusible and processable, since the introduction of flexible alkyl sidechains"'. It is generally accepted that P3ATs can form similar layered structures. inwhich the thiophene rings possess planarity and the side chains act as spacers'-'. Whenthe number. of 'carbon atoms of alkyl side chains is more than 10, some orderlyarrangements will occur for side chains betWeen the' layers'. It has been w… 相似文献
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Xiu Hui Lu Wei Rong Wu Xin Che Jun Feng Han Le Yi Shi 《International journal of quantum chemistry》2010,110(6):1273-1278
The cycloaddition mechanism of forming a polycyclic compound between singlet dimethylmethylene carbene(R1) and formaldehyde(R2) has been investigated with MP2/6‐31G* method, including geometry optimization and vibrational analysis for the involved stationary points on the potential energy surface. The energies of the different conformations are calculated with CCSD(T)//MP2/6‐31G* method. From the potential energy profile, it can be predicted that the dominant reaction pathway of the cycloadditional reaction between singlet dimethylmethylene carbene and formaldehyde consists of two steps: (1) the two reactants(R1, R2) firstly form an energy‐enricheded intermediate (INT1a) through a barrier‐free exothermic reaction of ΔE = 11.3 kJ/mol. (2) Intermediate (INT1a) then isomerizes to a three‐membered product (P1) via a transition state (TS1a) with an energy barrier of 20.0 kJ/mol. The dominant reaction has an excellent selectivity and differs considerably from its competitive reactions in reaction rate. © 2009 Wiley Periodicals, Inc. Int J Quantum Chem, 2010 相似文献
125.
TiO2/organically modified silane organic–inorganic hybrid films doped with different disperse red 1 contents are prepared by combining
a low-temperature sol–gel method and a spin-coating process. Effects of the disperse red 1 content on the third-order nonlinear
and the planar waveguide properties of the hybrid films are also studied by a z-scan technique and a prism coupling technique.
Results indicate that the nonlinear refractive index of the hybrid films is negative, whose magnitude is of the order of 10−8 esu for the measured samples. It is suggested that both the thermal effect and the photoisomerization process contribute
to the third-order nonlinear optical properties of the hybrid films jointly. It is also found that the refractive index and
the thickness of the hybrid films decrease with an increase of the temperature as the independent variable. In addition to,
optical absorption properties of the hybrid films are characterized by UV–Visible spectroscopy. These results indicate that
the as-prepared hybrid films are promising candidates for photonic applications. 相似文献
126.
The effect of an adsorbed anionic surfactant sodium dodecyl benzene sulfonate(SDBS) on electron transfer(ET) reaction between ferricyanide aqueous solution and decamethylferrocene(DMFc) located on the adjacent organic phase was investigated for the first time by thin layer method.The adsorption of SDBS at the interface resulted in a decay in the cathodic plateau current of bimolecular reaction with increasing concentrations of SDBS in aqueous phase.However,the rate constant of electron transfer(k_(et)) i... 相似文献
127.
Ke Xin Huang Yu Bing Feng Wei Yao Lei Xiang Yang Feng Wang Hai Bo Li Su Zeng Jing Xu Gong Ming Hui Hu Yu Zhao Xiu Mei Wu Xiao Kun Li Jia Qu 《中国化学快报》2009,20(10):1187-1190
Four naturally rare 5,6,7-trimethoxy-2,3-cis-dihydroflavonols(3-6) and two 5,6,7-trimethoxy-2,3-trans-dihydroflavonols(7-8) were designed and synthesized.Their antioxidative properties were evaluated by way of examining their scavenging capacities towards DPPH and O_2~(·-) free radicals,as well as by measuring their inhibitory ability against LPO.Both the 2,3-trans and the 2,3- cis conformers exhibited certain quenching abilities to DPPH and O_2~(·-) radicals,while most of the synthetic dihydroflavonols ... 相似文献
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H-bonding angle angleYHX has an important effect on the electronic properties of the H-bond Y...HX, such as intra- and intermolecular hyperconjugations and rehybridization, and topological properties of electron density. We studied the multifurcated bent H-bonds of the proton donors H3CZ (Z = F, Cl, Br), H2CO and H2CF2 with the proton acceptors Cl(-) and Br(-) at the four high levels of theory: MP2/6-311++G(d,p), MP2/6-311++G(2df,2p), MP2/6-311++G(3df,3pd) and QCISD/6-311++G(d,p), and found that they are all blue-shifted. These complexes have large interaction energies, 7-12 kcal mol(-1), and large blue shifts, delta r(HC) = -0.0025 --0.006 A and delta v(HC) = 30-90 cm(-1). The natural bond orbital analysis shows that the blue shifts of these H-bonds Y...HnCZ are mainly caused by three factors: rehybridization; indirect intermolecular hyperconjugation n(Y) -->sigma*(CZ), in that the electron density from n(Y) of the proton acceptor is transferred not to sigma*(CH), but to sigma*(CZ) of the donor; intramolecular hyperconjugation n(Z) -->sigma*(CH), in that the electron density in sigma*(CH) comes back to n(Z) of the donor such that the occupancy in sigma*(CH) decreases. The topological properties of the electron density of the bifurcated H-bonds Y...H2CZ are similar to those of the usual linear H-bonds, there is a bond critical point between Y and each hydrogen, and a ring critical point inside the tetragon YHCH. However, the topological properties of electron density of the trifurcated H-bonds Y...H3CZ are essentially different from those of linear H-bonds, in that the intermolecular bond critical point, which represents a closed-shell interaction, is not between Y and hydrogen, but between Y and carbon. 相似文献
130.
Jing Wang Xi Chen Xiu Wang Wei-Qiang Zhang Hua-Ming Sun Guo-Fang Zhang Ya Wu Zi-Wei Gao 《Transition Metal Chemistry》2016,41(7):731-738
Tunable organometallic Lewis acid catalysts were developed by combining salicylic acid (H2-Sal) with benzoic acid (H-Ben), 4-fluorobenzoic acid (H-BenF) and 3-thiophenic acid (H-Th), as coligands for mixed bis-carboxylate titanocene complexes. Three air-stable complexes [Cp2Ti(η1-HSal)(η1-Ben)] (1), [Cp2Ti(η1-HSal)(η1-BenF)] (2) and [Cp2Ti[η1-HSal][(η1-Th)] (3) were prepared in high yields by the reaction of salicylato titanocene chelate with carboxylate ligands. The mixed bis-carboxylate titanocene complexes were fully characterized by physicochemical and spectroscopic methods. Single-crystal X-ray diffraction studies revealed Ti–O(H-Sal) bond distances in 1, 2 and 3 of 1.972(3), 1.9245(18) and 1.912(5) Å, respectively, while the bond distances involving the coligands of 1, 2 and 3 are 1.908(3) Å (Ti–OBen), 1.9296(19) Å (Ti–OBenF) and 1.945(5) Å (Ti–OTh), respectively. These bis-carboxylate titanocene complexes showed satisfactory activities and selectivities in Mannich and cross-aldol reactions. Notably, complex 3 bearing the labile thiophene carboxylate ligand gave high yields with a diastereomer ratio (d.r.) as high as 1:99 for the direct Mannich reactions of benzaldehyde, cyclohexanone and aniline. In cross-aldol reaction of benzaldehyde and cyclohexanone, 1 and 2 successfully catalyzed the formation of double-aldol products in up to 99 % yield. 相似文献