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国家自然科学基金(20773046)

作品数:4 被引量:5H指数:1
相关作者:李志儒于广涛徐红亮吴迪陈巍更多>>
相关机构:吉林大学日本九州大学山西师范大学更多>>
发文基金:国家自然科学基金更多>>
相关领域:理学自动化与计算机技术更多>>

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配体数与电子化物的一阶超极化率的碱金属原子序数依赖性被引量:4
2009年
用MP2方法得到单配位电子化物M—X(M=Li,Na,K;X=NH3,NCH,HF)和二配位电子化物M—(FH)2(M=Li,Na,K)的几何结构.使用高水平的QCISD/6-311++G(3df,3pd)计算了它们的一阶超极化率β0.在单配位的电子化物中,单调的一阶超极化率的碱金属原子序数依赖性未表现出来,而二配位电子化物M—(FH)2(M=Li,Na,K)的β0值随着碱金属原子序数的增加而增加,这与文献报道的四配位相关体系的情况一致.这表明,电子化物中配位数与一阶超极化率碱金属原子序数依赖性相关.
徐红亮李志儒吴迪陈巍于广涛王钦
关键词:超极化率
两个四硫富瓦烯分子正离子自由基TTF·^+之间的共价吸引作用
2009年
使用MP2/6-311G方法得到了四硫富瓦烯自由基正离子二聚体(TTF·+-TTF·+)能量极小点的结构.这显示这种正离子间的吸引作用存在.这种新的吸引作用是望远镜形状的20中心2电子分子间共价π/π键.这种共价π/π键的键能约为-21kcal·mol-1,它被正离子间的库伦排斥作用掩盖.有负离子围绕的四硫富瓦烯自由基正离子二聚体(TTF·+-TTF·+)体系是稳定的.
王芳芳王义王炳强王银锋马方李志儒
关键词:分子间相互作用TTF
Imitating trumpet shells: Mbius container molecules
2011年
Mbius container molecules C64H8,C60N4H4,and C58N6H2 with topological one-sided characteristics were constructed at the first time by imitating natural trumpet shells.The structure is an open cage with an inner hexagonal bridge.The bridge joints the outer and inner surfaces of the cage to form a new one-sided Mbius structure.The optimized structures of the three molecules in the singlet(the ground state),triplet and quintet states are obtained using the density functional theory(B3LYP).For the ground state structures of the three Mbius molecules,their oxidizabilities are weaker than that of the C60 and reducibilities are close to that of the stable C80 cage and slightly stronger than that of the C60.These may show that the unusual Mbius structures have some stability.Their potential properties were predicted,for example,the special aromaticity of the bridge ring due to the unique interaction between the bridge and the cage wall.These findings enlarge the knowledge of Mbius molecules. The idea of bionic and topological imitating in chemistry may promote the design of new complex-shaped nano-molecules and molecular devices.
MA FangWANG FangFangLI ZhiRuWU DiLI ZeShengGU FengLong
关键词:分子器件BIUB3LYP方法基态结构
A covalent attraction between two molecular cation TTF·^+被引量:1
2009年
The optimized structure of the tetrathiafulvalence radical-cation dimer(TTF·+-TTF·+) with all-real frequencies is obtained at MP2/6-311G level,which exhibits the attraction between two molecular cation TTF·+.The new attraction interaction is a 20-center-2-electron intermolecular covalent π /π bonding with a telescope shape.The covalent π /π bonding has the bonding energy of about -21 kcal·mol-1 and is concealed by the Coulombic repulsion between two TTF·+ cations.This intermolecular covalent attraction also influences the structure of the TTF·+ subunit,i.e.,its molecular plane is bent by an angle θ=5.6°.This work provides new knowledge on intermolecular interaction.
WANG FangFangWANG YiWANG BingQiangWANG YinFengMA FangLi ZhiRu
关键词:DIMMERATTRACTIONBETWEENINTERMOLECULARΠTTF
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