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The synthesis, characterization, and photovoltaic properties of a series of four conjugated polymers containing 2‐aryl‐2H‐benzotriazoles and “bis(thiopheno)dialkylfluorenes” is described. The polymers were obtained via Suzuki‐polycondensation and comprise alternating electron rich and electron poor building blocks. The impact of systematic structural changes on the electronic and morphological properties and device efficiencies were studied. Application of these polymers as light‐harvesting and electron‐donating materials in organic solar cells using PCBM derivatives as electron accepting materials resulted in power conversion efficiencies up to 1.8%. Both the properties of the pristine polymers and the device performance show that the impact of the substitution farther‐off the backbone is negligible while substitution directly on the backbone has a major impact. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011.  相似文献   
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The purpose of this paper is to extend the symmetric representation of the rigid body equations from the group SO (n) to other groups. These groups are matrix subgroups of the general linear group that are defined by a quadratic matrix identity. Their corresponding Lie algebras include several classical semisimple matrix Lie algebras. The approach is to start with an optimal control problem on these groups that generates geodesics for a left-invariant metric. Earlier work by Bloch, Crouch, Marsden, and Ratiu defines the symmetric representation of the rigid body equations, which is obtained by solving the same optimal control problem in the particular case of the Lie group SO (n). This paper generalizes this symmetric representation to a wider class of matrix groups satisfying a certain quadratic matrix identity. We consider the relationship between this symmetric representation of the generalized rigid body equations and the generalized rigid body equations themselves. A discretization of this symmetric representation is constructed making use of the symmetry, which in turn give rise to numerical algorithms to integrate the generalized rigid body equations for the given class of matrix Lie groups. Dedicated to Professor Arieh Iserles on the Occasion of his Sixtieth Birthday.  相似文献   
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A novel N‐hydroxy succinimide‐based carbonate monomer that allows direct synthesis of polymers incorporating a reactive carbonate group in the side chain was synthesized. This new monomer was copolymerized with methyl methacrylate and poly(ethylene glycol) methylether methacrylate using free‐radical polymerization to obtain organo‐ and water‐soluble reactive copolymers. Copolymerization of the activated carbonate monomer with an azide‐containing monomer and N‐hydroxy succinimide‐containing activated ester monomer provided orthogonally functionalizable copolymers. The pendant reactive carbonate groups of the copolymers were functionalized with amines to obtain carbamates. Polymers capable of orthogonal functionalization could be selectively functionalized as desired using subsequent 1,3‐dipolar cycloaddition or amidation reactions. The novel monomer and the copolymers were characterized by 1H‐NMR, 13C‐NMR, and infrared spectroscopy. The efficient stepwise orthogonal functionalization of the copolymers were examined via 1H‐NMR spectroscopy. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2010  相似文献   
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Since its discovery 5-fluorouracil 1(1,5-FU), an important anticancer drug, has been the subject of study for the preparation of some suitable derivatives2 which may have better therapeutic efficacy. These are prepared through silylation method3, mercuri salt method4 and direct alkylation method5 of 5-FU. It was reported5 that the direct alkylation of 5-FU with saturated and allylic type halides under controlled conditions occur at N3 (3-) and N1 (1-) position respectively in contrast to alkylation of uracil where N1 alkylated products are obtained in both cases. The position of alkylation in 5-FU was determined, with analogy from uracil6, by the bathochromic shift in UV from the neutral pH to alkaline pH of the 3-substituted product compared to no such shift of the 1-substituted product.  相似文献   
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Using an effective lattice gas-like model for B-B′ site ordering we study order-disorder transitions in double perovskite materials A2BB′O6. We motivate this effective model from a microscopic hamiltonian. Using this model, we are able to address several experimentally observed issues including nonmonotonic dependence of the degree of order on annealing temperature, and the rapid decrease of order upon overdoping with either B or B′ species. We also study ordering in the ‘ternary’ compounds A2BB′1−yB″yO6, using a variant of the Blume-Emery-Griffiths model. Several issues related to structural and magnetic ordering are discussed.  相似文献   
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